Tuesday, 30 August 2016

Walk-in for QC & QA on 03rd September 2016 at API Ankleshwar

Cadila Healthcare Limited - Ankleshwar
2 - 7 yrs
Ankleshwar

Job Description
    Walk-in for Quality Control & Quality Assurance on 03rd September 2016 at Cadila Healthcare Ltd, API Ankleshwar Multi Product Plant
     

    Here is a chance to join Zydus at our API Manufacturing located at Ankleshwar as.


    Qualification: M.Sc /B.Sc (Chemistry)
    Experience : 2 to 6 years API Pharma Candidates only
    Designation : Executive / Sr.Executive / Assistant Manager


    Date : 03rd September 2016 (Saturday)

    Time: 09:30 AM to 04:00 PM

    Venue : Plot No 291, Cadila Healthcare Ltd,
    Industrial Estate , GIDC
    Dist :Bharuch,
    Ankleshwar,
    Gujarat
     
    Key Responsibilities are mentioned as below:


    QUALITY CONTROL : Candidate should have  hands on experience and relevant exposure in handling instruments like HPLC, GC, UV , wet lab, micro lab and chemical analysis of Raw Material . Must be familiar with cGMP requirements. Shop floor Operation in API / Bulk Drug Manufacturing.




    Quality Assurance : : Candidate should be familiar with cGMP requirements/ Data Integrity / Quality Management System (QMS) / Engineering Activity / Technology transfer documentation/ Trending and APR/ shop floor Operation in API / Bulk Drug Manufacturing.

    a) Data Integrity - Responsible for reviewing of HPLC and GC , QC SOP Compliances, Investigation activities, OOS , OOT and Data of quality control instruments.

    b) Quality Management System - Handling change control, process validation, investigations of OOS, OOT, Deviations and of Market Complaint

    . c) Engineering Activity- Review of Equipment qualification documents, Water system, HVAC, Preventive maintenance and Calibrations.

    d) Technology Transfer Documents - Review and issuance TTD to plant , review of master batch record also review of specification and STP of API, Intermediate, RM, In-process.

    e) Trending and APR - Knowledge of Market complaint, Deviation, Incident, Change control for trending and evaluation for improvement in process and system.

    Candidate should possesses excellent communication & interpersonal skills. Hands on exposure with software like SAP, LIMS, Track wise, MS Office etc.



    Candidates having experience of working in regulatory approved plants and possesses sound knowledge of documentation, cGMP and SAP will be preferred.

    Those who are unable to attend the Personal Interview may send their resume through e-mail at reema.patel@zydusmail.com

    Please mention the position applying for on the top of envelope or subject in case of e-mail.

    Preference will be given to candidates having API - Pharmaceutical Industries experience.

    Company Profile:
Cadila Healthcare Limited - Akleshwar
Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. With a core competence in the field of healthcare, Zydus Cadila provides total healthcare solutions ranging from formulations, active pharmaceutical ingredients and animal healthcare products to wellness products. From a turnover of Rs. 250 crores in 1995, the group posted revenues of over Rs. 8600 crores in FY15. The group had posted a turnover of Rs. 4600 crores in FY 11, making it a billion dollar company. Recently, the group launched Exemptia, the world's first biosimilar for Adalimumab, the largest selling therapy worldwide for inflammatory arthritis.

Zydus is also the only Indian pharma company to launch its own patented NCE - Lipaglyn, the world's first drug to be approved for the treatment of diabetic dyslipidemia. The Zydus group was one amongst the top five companies worldwide at the FT ArcelorMittal Boldness in Business Awards 2014 in the Developing Markets category and was declared as the 'Emerging Company of the Year' by the Economic Times Awards for Corporate Excellence 2010. The group aims to be a leading global healthcare provider with a robust product pipeline and aspires to post revenues of Rs. 10000 crore by 2015-16 and be a research-based pharmaceutical company by 2020.  

Urgent Openings for B.pharma Freshers - Mankind Pharma (delhi)


Image result for mankind logo

0 - 1 Years
Delhi

Job Description
Candidate should possess B.Pharma qualification.
Should possess strong computer skills.
Good Communication skills.
Candidate should be responsible for preparation of artwork.

Company Profile

Mankind Pharma, one of the top 5 leading pharmaceutical companies in India, started its journey in 1995. Today, we have 13,000 employees and are heading towards a turnover of INR 50000 million.

Our vast network includes 50 C&F agents and 7500+ stockists. We provide a wide range of products - Antibiotic, Antifungal, NSAIDs, Gastrointestinal, Anthelmintic, Cardiovascular, Dermal, Erectile Dysfunction, and several other categories - across the nation.

Urgent !! Senior Resident - Paeditrics @ Fortis, Faridabad

0 - 4 Years
Faridabad

Image result for fortis

Job Description




JOB DESCRIPTION:


To initiate evaluation and treatment of patients, modify evaluation
and treatment begun by junior medical colleagues in furtherance of
the highest quality of patient care.
To participate in the general management and care of all patients
including undertaking preliminary basis and routine investigations and
treatment (pre-and post-operative care) under supervision.
To see all new cases especially the seriously ill patient immediately
upon admission and to initiate emergency treatment without delay.
To ensure that all investigations and treatment prescribed are carried
out and reviewing cases daily or more frequently including reviewing
the results of investigations and treatments.
To oversee the proper documentation of patients management from
admission to discharge.
To ensure clarity of plan of care for each patient is documented on a
daily basis.
To prepare a comprehensive discharge summary for each patient
which is authenticated by a consultant.
To carry out procedures under supervision.
To attend all department ward rounds.
To check on the pre-operative preparation of patients.
To perform night calls as per the prescribed duty roster.
To completely and accurately fill up all service request forms.
To update casenotes and complete all case records within 24 hours of
the patients discharge.
To inform immediate supervisor on duty as soon as possible of all
problems e.g. new cases, deterioration in condition of patients, cases
where medicolegal problems may arise (assaults, accidents, and
poisonings).
To supervise junior medical colleagues on the performance of
practical procedures like lumbar puncture etc.
To report all deviation or error in any system to the appropriate
superior.
Education & Research To conduct teaching to junior staff.
To participate in the Units Morbidity & Mortality Meetings and other
department or Unit-level CME activities
Actively participate in research projects (SR)

 

Company Profile
Fortis Healthcare Limited is committed to clinical excellence and patient-centric healthcare, which is manifest in hospital design, patient services, medical programmes and the compassionate approach of medical and non-medical hospital staff. Fortis commissioned its first hospital in 2001 at Mohali, near Chandigarh, and has expanded its operations to become a network with an over 10,000 bed capacity across 68 hospitals

Product Specialist - Critical Care - Sales

1 - 4 YearsMumbai Openings: 4

Image result for biocon

Job Description

To attain or exceed the targeted sales volume in the assigned territory for the antibiotics and anti-infective portfolio.
Maintain healthy secondary to primary sales ratio.
To develop relations with the select doctors in the assigned territory.
Ensuring liquidation of stocks
To implement HO strategies on the field.
Providing feedback to HO on sales figures, activities, competition, etc.Company Profile
Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting world. Today, Biocon together with group companies employs more than 5000 employees with approxmimately Rs 2500 crore turnover and is expected to grow further during the current financial year .

Analytical R & D Job in Bangalore

2 - 5 YearsBengaluru/Bangalore

Image result for apotek

Job Description

1. M Sc (Organic/ Analytical/ Industrial Chemistry  or M pharmacy with 1-5 years Analytical R & D experience, familiarity with method development & validation is essential.

2. Experience in technical trouble-shooting, technical literature search & review and experience on conducting stress study, stability studies, characterization, etc. are a must.

3. To follow cGMP, Good Laboratory Practices as laid down in procedures.

4. Operating of the instruments such as HPLC, GC, IR -Spectrophotometer, UV-Visible Spectrophotometer, NMR etc.
5. Should have worked for regulatory audits like USFDA, TGA and MHRA
6. Good understanding of documentation review along with exposure to regulatory audit is required


Interested candidate can send resume to this mail ID (umashank@apotex.co.in)

Company Profile

Apotex Inc., founded in 1974, is the largest Canadian-owned pharmaceutical company. We employ over 6,000 people worldwide in research, development, manufacturing and distribution. We produce more than 300 generic pharmaceuticals in approximately 4000 dosages and formats and export to over 115 countries around the globe.

APOTEX RESEARCH PRIVATE LIMITED (ARPL) based at Bangalore is a 100% owned subsidiary of Apotex Inc., and is engaged in the development, bio-clinical evaluation, manufacturing and distribution of safe and efficacious generic pharmaceutical formulations for the global market.

As a part of this dynamic team, you will get to work in our state-of-the-art facilities, which include sophisticated equipments', high standard processes and the opportunity to work alongside some of the world's top professionals.

Apotex encourages the new technological developments in the field of research, manufaturing and distribution and embraces all the new techniques and technologies available in our area of concentration, our new manufaturing facility has been inaugurated in June 2012 and uses some of the most sophisticated technologies and machines available today.

Biomedical Engineer

Alexis Multi-Specialty Hospital
2 - 5 yrs
Nagpur

Image result for Alexis Hospital
Job Description
    Looking for Biomedical Engineer with 2-4 years of experience.
Company Profile:
Alexis Multi-Specialty Hospital
Alexis Multi-Specialty Hospital is a subsidiary hospital of Zulekha Hospitals, UAE. It is bringing quality healthcare to Nagpur, Central India offering secondary and tertiary care services in various disciplines.

It is a 210 bedded hospital with state-of-the-art facility at par with International standards. Our facility includes 6 Operation Theatres, Cath Lab, 60 bedded critical care unit, ultra-modern laboratory & radiology set-up.  

Freshers Govt Job @ ACTREC | Studentship / Traineeship in Bioinformatics & Scientists Post Vacant With Attractive Salary

Image result for govt job

Positions :
  1. Scientist (One position)
  2. Studentship  in Bioinformatics (1)
  3. Traineeship  in Bioinformatics (1)
Title of the Project : Bioinformatics centre DBT- Sub-DIC at ACTREC
Funding Agency : DBT Grant No.232
Principal Investigator : Dr. Ashok Varma
Duration of the Project:
  • For Sl. No. 1: Six Months from the date of appointment can be extended further for six months.
  • For Sl. No. 2 & 3: Three Months only
Consolidated Salary:
  • Rs. 35,000/- p.m. (For Sl. No. 1)
  • Rs. 8,000/- p.m. (for Sl. No.2 & 3)
Essential Qualifications and Experience:

  • For Sl. No. 1: 1st Class Master’s Degree in Bioinformatics or Life Sciences equivalent degree from a recognized University with 4 years R&D experience in Bioinformatics or relevant subjects from recognized institutes. OR Ph.D. degree in Bioinformatics or Life Sciences from recognized University.  M.Sc. degree obtained after a one year course will not be considered. Experience: Research/teaching experience in Bioinformatics or relevant subjects form recognized Institute(s).
  • For Sl. No. 2: Pursuing PG degree in Bioinformatics.
  • For Sl. No. 3: Completed PG degree in Biotechnology or Life Sciences and willing work/learn bioinformatics based project.
How to Apply :
Candidates fulfilling these requirements should pre-register by sending their application in the prescribed format with recent CV and contact details of 2 referees by e-mail to ‘program.office@actrec.gov.in’ latest by 17.00 hrs on 04-09-2016.
The interviews would be held on 06-09-2016 and only for the pre-registered candidates will be eligible to appear for interview. Candidates should report between 09.30 to 10.00 a.m. in Steno Pool, 3rd floor, Khanolkar Shodhika, ACTREC, Kharghar, Navi Mumbai. No T.A./D.A. will be admissible for attending the interview.
At the time of Interview the candidate should bring original certificates along with CV with contact details of 2 referees and submit the photocopies (attested) of the certificates, with a recent passport size photograph.
Date & Time: 6th September, 2016, at 10.00 a.m.
Venue: Meeting Room, 3rd floor, Khanolkar Shodhika, ACTREC


 Walkin Lifescience Freshers For Medical Coding@ Vee Technologies Salem

Vee Technologies
0 - 1 yrs
Salem


Job Description


    Walkin Life Science Freshers for Medical Coding @ Vee Technologies, Salem on August 30th to September 6th.

    Current Requirement : Medical Coder Trainee

    Eligibility : Freshers (Life Science Graduates) + Ready to work in Night Shift

    Work Location :Salem
    Date: August 30th - September 6th

    Job Description :
    # Coders will be involved in Coding charts of different specialties

    Skills Required : Graduates/Postgraduates in B.Sc with specialization in Zoology, Biology, Botany, Bsc-Nursing,
    Biotechnology (Bsc ,Msc,BTech / MTech), Micro-Biology, BDS, BHMS, BSMS,B-Pharm and M-Pharm

    Ability to multi-task Willingness to be a team player and show initiative where needed

    If interested kindly Walk in for Interview on weekdays between 10.30am - 5pm

    Venue :
    No. 4/14, Maamangam PO,
    Reddipatti Road,
    Jagir Ammapalayam,
    Salem.

    Regards,
    Mayura
    Mobile:9488781064
    rajamayura.p@veetechnologies.com
Company Profile:
Vee Technologies
http://www.veetechnologies.com
Vee Technologies a Sona Group Company has been operating in the BPO space for in various domains like Insurance, Healthcare, Logistics, Engineering Services, Finance & Accounts and News tracking successfully for the last 14 years.

The Sona Valliappa Group owns and runs a group of educational institutions like the Sona College of Technology, Sona School of Management and Thiagarajar Polytechnic. The Valliappa Software Technological Park is a pioneer in the infrastructure and incubation services.
We work with major physician groups, billing companies and hospitals   

Excellent Opportunity for Clinical Data Management Role in Mumbai

Image result for tcs

2 - 4 YearsMumbai

Job Description
Work Location:- Mumbai Mahape/ Vikhroli
Night Shift/ Rotational Shifts:- Yes
Educational Qualifications:- B. Sc / B. Pharm/M.Sc /M. Pharm
Not more than 3 years of experience for B. Pharm/ B. Sc & 2 years in case of M. Pharm /M. sc
Desired Experience Level in Years:- 1-3 yrs of relevant CDM experience for BPO 2.
Skills required: CDM experience and can work effectively in big teams. Should have exposure to discrepancy
management and other aspects of Conduct and close out for studies like vendor reconciliations, SAE
reconciliations and database locks. InForm or Rave knowledge mandatory.

    Company Profile
TCS -Established in 1968 | 2nd largest Service Provider in the ITES/BPS Industry in India |183 Offices worldwide in 43 countries | 300,000+ employees|100,000 women employees' |Revenues US$ 14.44 billion (2013-14) |Traded as BSE: 532540, NSE: TCS
The TCS Business Process Services (BPS) organization, provides domain centric business process transformation, consulting and analytics services to over 200 global clients across various verticals like Aerospace | BFS | Insurance & Healthcare | Life Science | Manufacturing | Energy & Resource Utilities | Government | Hi Tech | Media & Information Services | Retail & CPG | Telecom | Travel & Transportation

 CRA - Clinical Research Associate - On Site Monitoring

Quintiles
3 - 8 yrs
Bengaluru/Bangalore , Mumbai
Job Description
    Hiring for CRA - Clinical Research Associate - On Site Monitoring



    Candidates with Site Monitoring Visits (TRIALS) only need to apply

    No BA- BE Studies



    Job Location : Mumbai / Bangalore

    Multiple openings across grades.

    Exp: 3-7 yrs.

    Jd as follows.:

    JD

    POSITION SUMMARY:

    Conduct monitoring visits at assigned sites for protocols that are complex and/or require knowledge in advanced therapeutic areas. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements

    RESPONSIBILITIES

    Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
    Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
    Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
    Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Project Manager (CPM), Clinical Research Specialist CRS) and/or line manager.
    Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
    Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
    Act as a mentor for clinical staff including conducting co-monitoring and training visits.
    May provide assistance to the Clinical Project Manager and/or CRS with design of study tools, documents and processes.

    REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

    Strong knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
    Strong therapeutic and protocol knowledge as provided in company training
    Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
    Strong written and verbal communication skills including good command of English language
    Strong organizational and problem-solving skills
    Effective time management skills
    Ability to manage competing priorities
    Good mentoring and training skills
    Ability to establish and maintain effective working relationships with coworkers, managers and clients

    MINIMUM REQUIRED EDUCATION AND EXPERIENCE

    Bachelor's degree in a health care or other scientific discipline or educational equivalent and 2 5 years of on-site monitoring experience; or equivalent combination of education, training and experience.
Company Profile:
Quintiles

Quintiles is the world's largest provider of biopharmaceutical development and commercial outsourcing services. We bring a fully integrated approach to build biopharma and life sciences solutions - from pipeline through portfolio to population health â„¢. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.  

Monday, 29 August 2016

Sun Pharma enters dermatology segment to expand retail offering


Sun Pharmaceutical Industries Ltd said on Wednesday it had entered the dermatology segment as part of an initiative to further expand its retail offerings.
The world's fifth biggest generic drug maker launched a new dermatology product - Suncros - a sunscreen brand which was earlier available only as a branded prescription product.

Image result for sun pharma

The product will form the fourth part of its global consumer healthcare business vertical which currently markets dietary supplements, analgesics and antacids.
The company also said it was evaluating options to grow the vertical further through new product categories and acquisitions.


Medical Scribe at Hyderabad


1 - 5 Years
Hyderabad / Secunderabad
Image result for elico healthcare

Job Description

Position: Medical Scribe

An opportunity that will change your life! Are you ready for the change?

We have exciting opportunity for Experienced Medical Coders and Medical Transcriptionists to become Virtual Doctors .Enter into the exciting field of Medical Scribing .We will train you and place you as Medical Scribes which is the ultimate role in the entire chain of US healthcare domain. You will have excellent opportunity to master the US healthcare domain and grow rapidly in your career .Take the plunge and change your destiny.
Eligibility: Minimum one year experience in the field of Medical coding and Medical Transcription. Willingness to work in Night shift.
Competency required:
i) Good English skills, written and spoken.
ii) Good knowledge in Medical Terminology and Language of Medicine.
iii) Good decision making skills.
iv)Good in reasoning and analytical skills.
Perks: i) Salary 20000- 60000 per month depending on experience plus incentives.
ii) Pick up and drop 
iii) 5 days a week
ivi)Health Insurance coverage
v)Good allowance
If you have faith in yourself walk-in with your resume

Contact Person: Ms. Lakshmi / Ms. Pushpalatha

Company Profile

ELICO, an ISO 9001 and IEC 27001 certified company with history of 50 years. ELICO has been serving the science and technology domain for over decade. Elico Health care Services is a part of its division serving the US Healthcare clients for over 10 years. We take pride in banding with our clients as strategic technology partners.

Opportunity for Pharmacovigilance Role in Mumbai

2 - 4 Years
Mumbai
Image result for tcs

Job Description

Experience in Pharmacovigilance (Case processing ICSRs) is mandate.
Good Analytical approach and problem solving proficiency.
Knowledge of Medical Terminology
An understanding of the principles and concepts associated with Patient Safety case-handling process, including regulatory reporting requirements for single case expedited reporting, Patient safety policies, processes and procedures.
Be fully competent to perform all steps within the case-handling process from triage to case submission to regulatory for cases.
Contribute to the development and implementation of new safety-related systems, processes and procedures within the process
 
Company Profile
TCS -Established in 1968 | 2nd largest Service Provider in the ITES/BPS Industry in India |183 Offices worldwide in 43 countries | 300,000+ employees|100,000 women employees' |Revenues US$ 14.44 billion (2013-14) |Traded as BSE: 532540, NSE: TCS
The TCS Business Process Services (BPS) organization, provides domain centric business process transformation, consulting and analytics services to over 200 global clients across various verticals like Aerospace | BFS | Insurance & Healthcare | Life Science | Manufacturing | Energy & Resource Utilities | Government | Hi Tech | Media & Information Services | Retail & CPG | Telecom | Travel & Transportation and Hospitality| offering specialized platform expertise in the F&A, SCM, CIM and HRO space.

Mega Walk in on 29th & 30th Aug for Pharmacovigilance for SME Level

Image result for accenture

3 - 6 YearsMumbai

Job Description
Hi,

Accenture is hiring for Pharmacovifilance in the Healthcare Domain for Subject Matter Expert (SME) role.We have multiple positions for this role.

Mega walk-in is on 29th & 30th  Aug 12pm-2pm Please get your friends along to participate in this special hiring.



Must Skills:

Must be a B.Pharm graduate who have experience in Pharmacovigilance work in last 2-3 years.
The Pharmacist must have must have acted as a floor-walker/ mentor to guide the agents on which is a better drug.
Monitoring side effects and suggesting better substitutes etc.

Experience: 3-6 years

Shifts: Rotational/Night Shifts

Job Location: Airoli (Transport provided)

Transport Boundaries:

Western up to Borivali - Dadar
Central Ambernath
Harbour New Panvel

Interview Details:

Venue:
Accenture
Bldg. No. 10,
5min walking from Airoli railway station
Mindspace, Airoli.

Date & Time: 29th & 30th Aug ,between 12:00PM- 2:00PM

Source: Kripa (Please write this on top of your resume)

Interviewer: Neha/Hema

Please get you ID proof and updated resume and write "Kripa" on top of your resume (Mandatory)


Regards,
Kripa Thakkar
kripa.thakkar@accenture.com


Accenture is an equal opportunities employer and welcomes applications from all sections of society and does not discriminate on grounds of race, religion or belief, ethnic or national origin, disability, age, citizenship, marital, domestic or civil partnership status, sexual orientation, gender identity, or any other basis as protected by applicable law
 

Company Profile
Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functions-underpinned by the world's largest delivery network-Accenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With approximately 373,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives. Visit us at www.accenture.com.

Join as Executive/Senior Executive– DSP @ Panacea Biotec
Panacea Biotec is a leading research based Health Management Company. We are engaged in research, development, manufacture & marketing of Vaccines, Bio-Pharmaceuticals and Pharmaceuticals (Rx & OTC) of international quality and Health Services. All Panacea Biotec plants are accredited by international agencies and they follow current Good Manufacturing Practices, as per WHO guidelines.
We offer stimulating work environment & a career that spells growth. In tune with our plans, we require young, aggressive, dynamic, high performing and result oriented professional.
Job Title: Executive/Senior Executive– DSP
Image result for panacea biotec

Job Description:
  • Perform and manage Down Stream Process development activities.
  • Review of scientific literature related to the process or technology.
  • Knowledge of Purification Techniques.
  • Media, buffers and assemblies preparation
  • Concentration – TFF & Hollow fiber
  • Sanitization & integrity testing of filters
  • Preparation of matrix and column packing
  • Size exclusion chromatography (SEC)
  • Ion Exchange chromatography (IEC)
  • Affinity chromatography
  • Drug substance preparation
  • Development of methods for yield improvement at different steps of DSP
  • Scale up / scale down of process as per requirement
  • Experience of Working in GMP conditions & Documentation accordingly.
Qualification: MSc Lifesciences, Biochemistry, Biotechnology, Microbiology, M.Tech.
Experience: 1-5 years
Age: 25-40 Years

Location: R&D Mohali

Apply now
Thermo Fisher Scientific Hiring Biological Science Candidates For Scientist Post
When you’re part of the team at Thermo Fisher Scientific, you’ll do important work. Surrounded by collaborative colleagues, you’ll have the support and opportunities that only a global leader can give you. Our respected, growing organization has an exceptional strategy for the near term and beyond. Take your place on our strong team, and help us make significant contributions to the world.

Image result for thermo fisher
Job Title : Scientist I
Job ID : 38709BR
Location : Bangalore
Qualification : MS/MSc in life sciences (cell biology/molecular biology/biotechnology/biochemistry) with research (academic/industry) experience is a must.
Responsibilities :
  • The candidate would be working with a team on research projects using standard techniques and protocols.
  • Responsible for designing experiments, data analysis and diligent maintenance of records
  • Presenting data to a larger group on a regular basis and troubleshoot as needed.
Skills & Experience :

  • Should have a thorough understanding of immunocytochemical and fluorescence microscopy techniques in mammalian cell and tissue systems.
    Working knowledge of basic biochemical, cellular & molecular biologic techniques is essential.
  • Experience with image processing, image analysis, densitometric quantitation using relevant software, flow cytometry, Western blotting and technical writing skills is desired.
  • Handling high throughput imaging systems, and experience with multiplexed immunophenotyping by flow cytometry, compensation settings, as well as publications in peer-reviewed journals is a bonus.
  • Attention to detail, ability to work in a fast paced environment and strict adherence to deadlines is essential
Plant Biotechnologist Required @ HiMedia Laboratories Pvt. Ltd.
HIMEDIA LABORATORIES is a leading manufacturer of products for microbiology, parasitology, immunology, serology, molecular biology, virology and biotechnology. Our product portfolio includes over 4000 line items. Our customers include clinical, industrial, research and academic laboratories around the world.
Job Title : Plant Biotechnologist
Experience : 2 – 5 yrs
Location  : Mumbai , Mumbai Suburbs
Image result for HiMedia Laboratories
Job description : 
  • The candidate shall be responsible for handling activities of the QA & R & D Department of Plant Tissue Culture.
  • The candidate should possess hands on experience from any reputed Organization. He / She should be well versed with basic Plant Tissue Culture techniques. The candidate must be able to assist & design the product literature / publications.
  • The Candidate shall be responsible for achieving Continual Improvement of the department as per the Quality Standards.
  • Female candidates from Mumbai region preferred
Desired :
    1) The candidate should be post Graduate in Botany / Plant Biotechnology having 2-5 years of experience in similar capacity.
    2) He/ She must have good communication & presentation skills along with good command over English Language.
    3) He / She should have clear thinking & a focused approach in work & planning.
    4) Working knowledge of computer is essential.

    5) Female candidates from Mumbai region preferred
How to Apply :
Interested candidates can send their resume to hrd@himedialabs.com

Join as a Quality Control Associate @ Accenture | Apply Online
Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functions underpinned by the worlds largest delivery network. Accenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With approximately 373,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives.
Job Title: NH – Quality Control Associate

Image result for accenture


Job Number: J4010
Job Description: 
  • Train newly joined hires on Pharmacovigilance related work and also help in creating training documents.
Responsibilities/Authorities :

  • Conduct more complex job-training programs.
  • Develop and Conduct training programs for new and experienced resources in conjunction with training team and build an evaluation system to assess the trainees.
  • Provide feedback to trainees and the supervisors to ensure ongoing development of the trainee.
  • Required to learn Adverse event processing (AEP) & systems, to be an effective information source to new hires.
  • Identify additional training needs and assist in planning to address them.
  • Assure proper training documentation is maintained.
  • Assess effectiveness of training program and suggest change.
  • Maintain competency in areas being trained.
  • Teach, qualify, and mentor staff in the Trainer I role.
  • Provide assistance to Management team in improving the quality.
  • Provide regular updates on new tools and processes.
  • Responsible for generating reports regarding the trainees.
  • Assist HR in recruitment and selection process for new hires.
Earn Upto Rs. 1,32,005/- p.m As Associate / Assistant Professor @ IIT Indore


Advertisement for Recruitment of Associate Professor, Assistant Professor and Assistant Professor (on-contract). This is a rolling advertisement.
IIT Indore invites applications from outstanding, highly-motivated Indian nationals (and those of Indian origin / holding PIO cards) for faculty positions at the levels of Associate Professor, Assistant Professor and Assistant Professor (on-contract) in the disciplines of Centre for Biosciences and Biomedical Engineering and only at level of Associate Professor in Chemistry.

Image result for iit indore
Qualifications and Experience:
Associate Professor: Ph.D. degree with first class or equivalent at the preceding degree in the appropriate branch with a very good academic record throughout and at least six years of post-Ph.D. experience in teaching / industry / research, of which at least three years of experience should be at the level of Assistant Professor / Senior Scientific Officer / Senior Design Engineer, or equivalent.

Assistant Professor: Ph.D. in relevant areas of specializations with a first class or equivalent at the preceding degree in the appropriate branch with a very good academic record throughout and at least three years of post-Ph.D. Research/Teaching/Industry experience. Candidates not satisfying the required post-PhD experience criterion for direct recruitment as Assistant Professor may be put on tenure track as Assistant Professor (on-contract).

Apply now

 Walkin Lifescience Freshers For Medical Coding@ Vee Technologies Salem

Vee Technologies
0 - 1 yrs
Salem


Job Description

    Walkin Life Science Freshers for Medical Coding @ Vee Technologies, Salem on August 30th to September 6th.

    Current Requirement : Medical Coder Trainee

    Eligibility : Freshers (Life Science Graduates) + Ready to work in Night Shift

    Work Location :Salem
    Date: August 30th - September 6th

    Job Description :
    # Coders will be involved in Coding charts of different specialties

    Skills Required : Graduates/Postgraduates in B.Sc with specialization in Zoology, Biology, Botany, Bsc-Nursing,
    Biotechnology (Bsc ,Msc,BTech / MTech), Micro-Biology, BDS, BHMS, BSMS,B-Pharm and M-Pharm

    Ability to multi-task Willingness to be a team player and show initiative where needed

    If interested kindly Walk in for Interview on weekdays between 10.30am - 5pm

    Venue :
    No. 4/14, Maamangam PO,
    Reddipatti Road,
    Jagir Ammapalayam,
    Salem.

    Regards,
    Mayura
    Mobile:9488781064
    rajamayura.p@veetechnologies.com
Company Profile:
Vee Technologies
http://www.veetechnologies.com
Vee Technologies a Sona Group Company has been operating in the BPO space for in various domains like Insurance, Healthcare, Logistics, Engineering Services, Finance & Accounts and News tracking successfully for the last 14 years.

The Sona Valliappa Group owns and runs a group of educational institutions like the Sona College of Technology, Sona School of Management and Thiagarajar Polytechnic. The Valliappa Software Technological Park is a pioneer in the infrastructure and incubation services.
We work with major physician groups, billing companies and hospitals  

Friday, 26 August 2016





FDA approves first absorb able stent for coronary artery disease


The U.S. Food and Drug Administration today approved the first fully absorbable stent to treat coronary artery disease. The Absorb GT1 Bioresorbable Vascular Scaffold System (BVS), which releases the drug everolimus to limit the growth of scar tissue, is gradually absorbed by the body in approximately three years.
Image result for absorb able stent for coronary artery disease
“The FDA’s approval of the Absorb GT1 BVS offers a new treatment option for individuals who are candidates for angioplasty, but would prefer an absorbable device rather than a permanent metallic coronary stent,” said Bram Zuckerman, M.D., director of the division of cardiovascular devices at the FDA’s Center for Devices and Radiological Health.

Coronary heart disease is responsible for about 370,000 deaths each year in the U.S., according to the National Heart, Lung, and Blood Institute. The condition develops when cholesterol-containing deposits build up and narrow the coronary arteries, decreasing blood flow to the heart. This can cause chest pain (angina), shortness of breath, fatigue or other heart disease symptoms. Doctors often treat coronary artery disease with a procedure called angioplasty to widen the artery using a metal stent. Scar tissue can form within the stent causing the artery to narrow again (restenosis). Drug-eluting stents temporarily release a drug, typically for a few months after stent placement, to combat the formation of scar tissue.

The Absorb GT1 BVS is manufactured from a biodegradable polymer called poly(L-lactide), which is similar to materials used in other types of absorbable medical devices, such as sutures. The device’s absorption by the body gradually eliminates the presence of foreign material in the artery once the stent is no longer needed. After absorption, there are only four very small platinum markers embedded in the walls of the artery, which help cardiologists identify where the Absorb GT1 BVS was originally placed.
In approving the Absorb GT1 BVS, the FDA evaluated data from a randomized trial of 2,008 patients, which compared the rate of major adverse cardiac events between the Absorb GT1 BVS and a drug-eluting metallic stent. After one year, the Absorb GT1 BVS group showed a major cardiac adverse event rate of 7.8 percent, which was clinically comparable to the rate of 6.1 percent observed in the control group. In addition, after one year, the rate of blood clots forming within the devices was 1.54 percent for the Absorb GT1 BVS and 0.74 percent rate for the control.
Possible adverse events that may be associated with the procedure to insert the Absorb GT1 BVS or with the Absorb GT1 BVS itself include allergic reactions to materials in the device or medications used during the procedure, allergic reaction to the drug everolimus, infection or irritation at the catheter insertion site, internal bleeding, the development of abnormal connections between arteries and veins, embolism, or other coronary artery complications that may require medical intervention and that could lead to death.

The Absorb GT1 BVS is contraindicated for patients who have a known hypersensitivity or allergy to everolimus or the materials used in the device, such as poly(L-lactide), poly(D,L-lactide), or platinum. It is also contraindicated for those who are not candidates for angioplasty, have sensitivity to contrast, or who cannot take long-term aspirin therapy along with other blood-thinning medications (antiplatelet agents).
The Absorb GT1 BVS is manufactured by Abbott Vascular in Santa Clara, California.

Associate Regulatory Affiars

1 - 2 Years

Delhi
Image result for parexel
Job Description
Experienced with preparation/ review of Clinical Trial Application Packages for Asian countries including India.

Awareness of regulatory requirements

Review and evaluate technical and scientific data and reports required for submission

Monitor applicable regulatory requirements; assure compliance with the companys and external standards Co-ordinate with global team for documentation

Responding to queries raised by regulatory authorities

Maintain regulatory files in a format consistent with requirements

Label reviews

Tracking submissions

CTRI registrationCompany Profile
PAREXEL International Corporation is a leading global biopharmaceutical services organization, providing a broad range of expertise-based contract research, consulting, medical communications, and technology solutions and services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. PAREXEL Informatics provides advanced technology solutions, including medical imaging, to facilitate the clinical development process. Headquartered near Boston, Massachusetts, PAREXEL has offices nearly 80 locations in over 50 countries around the world, and has approximately 18,000 employees.

In India, PAREXEL has seven offices spread across five cities: Bengaluru, Hyderabad, Chandigarh, New Delhi and Mumbai. These offices are home to more than 3,000 employees.
Our two new offices in Bengaluru, called IndiQube and EcoWorld, were strategically designed to support a variety of work styles. There are collaboration zones in bright colors, freestanding high tables with stools to serve as informal meeting spaces, quiet rooms for group meetings, and private booths for phone calls. This innovative workspace encourages teamwork, and allows for sufficient flexibility to utilize the office beyond workstations.

Omega is the premier offshore provider of healthcare outsourcing services We specialize in medical billing, coding, accounts receivable management, and other healthcare related services

Image result for omega healthcare
Designation Omega Healthcare - Sr. Executive - Recruitment - Bhimavaram - 2 Opening(s)
Job Description
  • End to end recruitment which includes Sourcing, Screening, Salary Negotiation, Offer & On boarding.
  • Understanding the background of the Job and Its Scope.
  • Collecting source from various sources like Colleges, Consultancies, Job Portals, Referrals and lining up the candidates for the interview.
  • Should co ordinate with interview Panel for interviews
  • Should interact with Recruitment Vendors and process their profiles
Desired Profile
  • Should have a strong sourcing knowledge 
  • Should have excellent verbal & written communication skills.
  • Need to be flexible with timings when required.
  • Experience 2 - 3 Years of Recruitment Preferably ITES
  • Candidates should be willing to relocate to Bhimavaram - Andhrapradesh

Experience 2 - 4 Years

Apply here
 Acetaminophen, also known as paracetamol or APAP, is a drug commonly used to alleviate mild to moderate pain and reduce fever. It is present in more than 600 over-the-counter (OTC) and prescription medications, including Tylenol and Vicodin.
Headache, muscle aches, back pain, toothache, colds, menstrual pain, and arthritis are among the numerous conditions acetaminophen is used for.

According to the Consumer Healthcare Products Association (CHPA), each week, around 23 percent of adults in the U.S. - or 52 million Americans - use a medication containing acetaminophen.
At recommended doses, acetaminophen is considered one of the safest OTC medications.
Unlike other common pain relievers, such as nonsteroidal anti-inflammatory drugs (NSAIDs), acetaminophen does not raise the risk of stomach or heart problems, making it a go-to medication for people who are unable to tolerate NSAIDs.
Image result for Acetaminophen risk
What is more, healthcare providers consider acetaminophen as one of the few pain relievers that is generally safe to use during pregnancy; a 2010 study from the Centers for Disease Control and Prevention (CDC) found the drug causes no increased risk of major birth defects when used in the first trimester of pregnancy.

But, as with all medications, there are risks, and researchers are finding that the risks of acetaminophen use may be more serious than we realize.
Last year, a review published in Annals of the Rheumatic Diseases concluded that the possible risks of acetaminophen have been "underestimated," with some studies suggesting the drug could raise the risk of cardiovascular events and mortality.
In this spotlight, we take a look at some of the well-established risks of acetaminophen use, as well as some that may come as a surprise.

Acetaminophen overdose and liver damage

Liver damage is perhaps the most well-known risk of acetaminophen use, and such damage can arise through overdosing on the drug.
After taking acetaminophen, most of the drug is metabolized by the liver and excreted through urination. However, some of the drug is converted into a toxic metabolite that can harm liver cells. Taking too much acetaminophen raises the risk of liver damage, and in severe cases, it can lead to death.
According to the Food and Drug Administration (FDA), between 1998-2003, acetaminophen was the leading cause of acute liver failure in the U.S., and almost half of liver failure cases during this period were a result of accidental overdose.
Furthermore, the FDA state that, during the 1990s, unintentional acetaminophen overdose was responsible for around 56,000 emergency department visits, 26,000 hospitalizations, and 458 deaths each year.
Because acetaminophen is present in such a wide range of OTC and prescription drugs at varying doses, it can be quite easy to accidentally take too much, particularly if using multiple acetaminophen-containing medications at once.
Current guidelines recommend taking no more than 4,000 milligrams of acetaminophen daily. Considering a single Extra Strength Tylenol tablet contains 500 milligrams, it is easy to see how one may accidentally overdose on the drug.
What is more, acetaminophen-induced liver damage occurs slowly, often going unnoticed until it is too late, so people may think that taking a little extra acetaminophen than recommended is posing no harm.
With this in mind, in 2011, the FDA asked prescription drug manufacturers to voluntarily limit the amount of acetaminophen in each tablet or capsule to no more than 325 milligrams, in order to reduce consumers' risk of accidental overdose.
As of 2014, the organization reported that just half of prescription drug manufacturers had voluntarily complied with the request, prompting them to launch proceedings to withdraw approval of prescription combination drugs containing more than 350 milligrams.
Additionally, the FDA recommend that healthcare providers consider prescribing combination drugs containing less than 350 milligrams of acetaminophen per dose.
Severe skin allergies and blood cancers

A number of studies have associated acetaminophen use with severe skin allergies, and the FDA Adverse Event Reporting System (FAERS) revealed that between 1969-2012, 107 such cases occurred in the U.S., resulting in 67 hospitalizations and 12 deaths.
[A bottle of acetaminophen]
In rare cases, acetaminophen can cause severe skin reactions.
As such, in 2013, the FDA issued a warning that acetaminophen use, in rare cases, can cause a number of potentially fatal skin reactions, including Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN).
"FDA's actions should be viewed within the context of the millions who, over generations, have benefited from acetaminophen," said Dr. Sharon Hertz, deputy director of FDA's Division of Anesthesia, Analgesia and Addiction. "Nonetheless, given the severity of the risk, it is important for patients and healthcare providers to be aware of it."
In 2011, a study published in the Journal of Clinical Oncology uncovered a link between regular acetaminophen use and increased risk of certain blood cancers.
The study, which reviewed the painkiller use of more than 64,000 men and women aged 50-76, found that individuals who used acetaminophen four or more times a week for at least 4 years were at a twofold risk of some blood cancers, including lymphoma and leukemia.
However, study co-author Emily White, of the Fred Hutchinson Cancer Research Center in Seattle, WA, noted that the risk of such cancers was still small among regular, long-term acetaminophen users, at around 2 percent over a 10-year period.
Autism, ADHD, and asthma

Despite acetaminophen use during pregnancy being considered generally safe, a number of studies have suggested this may not be the case.
In February this year, a study that found expectant mothers who used acetaminophen were more likely to have children who developed asthma by the age of 3 years.
The researchers - including Dr. Maria Magnus of the Norwegian Institute of Public Health in Oslo, Norway - say the findings are of public health importance, uncovering the possible adverse effects of acetaminophen use in pregnancy.
However, they say the results do not warrant changes to current acetaminophen recommendations for use during pregnancy, which state that pregnant women should consult with their doctor prior to using the drug.
But asthma is not the only risk that may arise with acetaminophen use in pregnancy.
Earlier this month, MNT reported on a study that uncovered a link between prenatal exposure to acetaminophen, autism, and attention deficit hyperactivity disorder (ADHD).
From an analysis of more than 2,600 pregnancy women, the researchers found that women who used acetaminophen in the first 32 weeks of pregnancy were 30 percent more likely to have offspring with attention impairments at the age of 5, which are often seen in children with autism or ADHD.
Additionally, the researchers - including study co-author Jordi Julvez of the Center for Research in Environmental Epidemiology (CREAL) in Barcelona, Spain - found that boys prenatally exposed to the drug were more likely to have clinical symptoms of autism.
Taking to MNT, Julvez said he believes doctors need to better inform patients - particularly expectant mothers - about the potential risks associated with acetaminophen use.
"We need to tell them this possibility [of developmental problems in offspring] and to be cautious on its use, maybe taking the least possible dose and also only when it is strictly necessary," he told us. 

Mega Walkin for Females Freshers/t.y Appeared on 27th Aug_airoli

Image result for accenture
0 - 1 YearsMumbai

Job Description

Hi,

Accenture is hiring for Female Freshers for B.Pharma / B.Sc Microbiology / B.Sc Chemistry / Diploma Pharma / B.Sc. Zoology / B.Sc. Botany / B.Sc Biochemistry / B.Sc. Nursing / Bio-Technology/ M. Pharma/ B.COM/ BA/ BMS field- T.Y. Appeared / Results Awaited / Freshers for Healthcare Backend Operations role.

Mega walk-in event on 27th Aug between 12:00 PM- 2:00 PM at Airoli


Below are the Job Details:

Job Title: Associate -Healthcare Backend Process

Shift Timing: Night Shifts (Transport facility will be provided)

Salary: 13,000 Gross

Transport boundaries:
Western up to Borivali - Dadar
Central Ulhasnagar
Harbour New Panvel

Job location: Airoli/Thane

Must Skills:

Education: B.Pharma / B.Sc Microbiology/ B.Sc. Chemistry / D.Pharma / B.Sc. Zoology / B.Sc. Botany/ B.Sc Biochemistry / B.Sc. Nursing / Biotechnology/ M.Pharm / BCOM/ BA/ BMS- T.Y. Appeared / Results Awaiting / Freshers.

Experience-0-1 year

Role and Responsibility -

-Healthcare Backend Operation.
-Healthcare Process Transactions.
-Non-voice Backend process.
- Medical Biiling

Please get your updated resume and an ID proof for the drive, on the top of the resume write "Vijeyta"(Mandatory)

Please carry Photo ID and Address Proof, without this you cannot attend the drive
.

Interview Location:


Accenture
Bldg. No. 10,
5min walking from Airoli railway station
Mindspace, Airoli.

Date and Time: 27th Aug, between 12:00:PM-2:00PM

Source Person- Vijeyta (Please write this on top of the resume compulsory)

Contact Person - Vijeyta and Neha Sinha

In case you have the same interview before please do not attend it again.


Thanks & Regards,
Vijeyta Kataria
vijeytakataria@accenture.com


 Company Profile
Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functions-underpinned by the world's largest delivery network-Accenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With approximately 373,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives. Visit us at www.accenture.com.

Thermo Fisher hiring for the Post of Sr. Manager, Manufacturing Operations


Image result for Thermo Fisher


Manager, Manufacturing and Operations Site Lead
This position will report to the Director of Operations for the Protein Biology business and be responsible for leading and developing the manufacturing team and influencing significant supply chain improvements. The manufacturing team’s primary focus is to deliver high quality production on time and on budget. This position will be responsible for providing key intermediate bulk formations to the Protein Biology product lines out of the Eugene, OR Frederick, MD and Rockford, IL sites.
Essential Functions
  • Train and develop the manufacturing team. Define and establish clear objectives and expectations, provide direct feedback routinely for performance management.
  • This position will be responsible for delivery high quality products on time and within budget.
  • Responsible for ensuring a proactive safety environment at the site.
  • Establish key performance indicators that drive change and visibility to the team and leadership. Track, trend, and monitor routinely with active data analysis rigor performed to drive results.
  • Effectively uses prioritization mechanisms to utilize resources across teams to complete the work on-hand and/or rise to Leadership so that resource needs can be addressed.
  • Responsible for establishing and maintaining manufacturing budget; including spending, scrap, inventory, variances, etc. and reporting up through senior management.
  • Documents SOP’s and work instructions to capture and document processes and procedures.
  • Serves as the cells and antibodies network operations product approval committee (PAC) member for new product introductions in the PCP process.
  • Lead manufacturing representative in all customer facing site events, such as customer audits, technology sharing, quality audits and regulatory audits.
  • Promote a working environment that encourages employee involvement to achieve operational excellence.
Nature and Scope
Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Ensures schedules and budget requirements are met. Erroneous decisions will result in critical delay(s) in large scrap and may may jeopardize overall business activities. Regularly interacts with senior management or executive-levels on matters concerning several functional areas, platforms, and/or customers. Requires the ability to lead change and gain acceptance of others in sensitive situations.

Education:
  • M Tech in Biotechnology or related disciplines
  • MBA a plus
Experience:
  • Minimum of 7 years experience in a manufacturing or technical environment performing production/operations and/or project management functions.
  • Experience in product development and manufacturing of consumable reagents and kits desired
  • Practical application experience of Six Sigma and Lean. Green Belt / Black Belt Certification desired.
Contacts:
Has contact with all levels of company employees as well as occasional interaction with vendors and customers.
Working Conditions:
Works in an office environment. Will be required to work in operational areas such as manufacturing, QC, distribution, etc. An element of travel will be required to support other Life Technologies US and International sites.

Apply here

 JOB Opening FOR Freshers | Pharmacovigilance

Quintiles
0 - 1 yrs
Bengaluru/Bangalore


Job Description

    Dear All,

    We are pleased to inform you that we are hiring freshers for PV.
    Please revert if you are interested.

    Role - Pharmacovigilance


Company Profile:
Quintiles
Quintiles is the world's largest provider of biopharmaceutical development and commercial outsourcing services. We bring a fully integrated approach to build biopharma and life sciences solutions - from pipeline through portfolio to population health â„¢. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.

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