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.

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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.

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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

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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 รข„¢. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.

Direct Walk - In from 15th August - 26th August Time - 11.00 AM to 3.00 PM Address : 1st Floor, Capital Building , Ameerpet,, Hyderabad, 500016,India Connolly has acquired iHealth ( including iSpace,Hyd) in 2014. Our Global Locations : United States of America, UK , Canada

Image result for cotiviti
Designation Medical Coding Freshers - Policy Support Analyst - 30 Opening(s)
Job Description Direct Walk In - Immediate Requirement 

Required Skills :-

 - Any Science graduate with 0-2 years Coding Experience

- Medical coding freshers with coding training

- Coding experience is added advantage

- Formal Medical Coding training is mandatory

 - Coding certification is desirable

 - Good subject knowledge Anatomy & Physiology, Medical Terminology, ICD/CPT , Modifiers

 - Willing to learn and give a long term commitment

 - Good communication skills

Wipro - Hiring for Pharmacovigilance Officer

Wipro 
0 - 5 yrs
Delhi


Job Description


    Dear Candidate,

    Wipro BPS is Hiring for Pharmacovigilance Business.

    - CANDIDATE SHOULD BE COMFORTABLE FOR NON-VOICE/VOICE PROCESS

    - CANDIDATE SHOULD BE OKAY FOR NIGHT SHIFTS & REGISTERED PHARMACIST.

    Please find the JD below, if interested please walk-in to the below address with the required documents.

    Interview Address:

    Wipro,A- 23, Mathura Road, Sarita Vihar, Near Sarita Vihar Metro Station, New Delhi - 44

    Walk-in Date: 25th & 26th August 2016

    Walk-in Time: 11am - 4pm

    Contact Person: Rupshikha Ray

    Qualification: Education:

    * Bachelors / Masters in Pharmacy + Registered Pharmacist

    * Valid PAN CARD available

    * minimum 1 year experience required in case processing
    * Freshers can also apply.

    Skills:
    - Excellent English Communication both written and Spoken
    Performing preliminary step of Pharmcovigiliance that case intake
    - Doing research work on adverse events or product complaints, or with an inquiry about the human health product
    - Receiving calls from consumers and health care professionals with reports
    - Verbal Probing for necessary information including but not limited to the adverse event(s), the patient's medical history, - Suspect product, concomitant drugs involved if any, and medication history of patient
    - Answering to the inquiries, and respond to inquiries in a knowledgeable manner
    - Completing various safety reports regarding the contact through computer based database system
    - Receiving adverse drug reaction or adverse event information Medical coding of terms according to Med DRA. WHO medical dictionary Filling AEM (Adverse event management) forms and generating adverse event reports according to ICH-guidelines E2A, E2B, E2E Writing narratives for adverse events
    - Ability to work under pressure and deliver

    - Comfortable working in Voice Process
    - Comfortable with night shifts
    - Immediate Joining

    Documents Required -

    - Updated and Printed Resume
    - 2 Passport Sized Colored Photographs
    - Govt. Photo ID
    - Certificate of Registration

    MENTION RUPSHIKHA RAY ON THE TOP OF YOUR RESUME.

Company Profile:
Wipro BPS (A division of Wipro Limited)
Wipro BPS
At Wipro BPS, you will get a in-depth understanding about the best way to service the customer requirements by leveraging Quality, Innovation, a self-sustaining Process Framework, IT expertise and Domain knowledge.
In addition to our intensive new-hire training program and our scheduled development-oriented programs, we provide Learn and Earn options to fast track your career by offering a variety of paid education programs (SEED) affiliated with various reputed universities - these programs include both graduate and post-graduate options.
While best-of-breed facilities and infrastructure is a given, we believe that our iconic brand, our industry leading position and the exciting career opportunities differentiate us from the rest of the industry.  

Asst Manager Radiology Speciality Medical Coding - DELL - Coimbatore

Dell International Services India Private Limited
6 - 11 yrs
Coimbatore



Job Description


    • To work with a variety of medical records and assigns appropriate codes based on medical documentation using CPT-4 and/or ICD-9 and ICD-10 coding guidelines
    • Handle a team of around 30 medical coders and responsible for their work delivarables. 
    • Develop training materials and update the contents that are relevant to the specialty.
    • Closely work with clients and sort out queries from them (If Any) 
    • provide training to the team members and guide them accordingly

Company Profile:
Dell International Services India Private Limited
Dell is a Technology driven company with a unique Dell Direct model. Dell Information Technology department (Dell I/T) plays a key role in enabling the Dell Direct model by creating, deploying and supporting global industry-leading I/T assets and services that reliably deliver the best customer experience and competitive edge.  

Thursday, 25 August 2016

Pharmacovigilance Data Manager

Novartis Healthcare Pvt. Ltd.
3 - 5 yrs
Hyderabad / Secunderabad

Job Description

 
- To retrieve data and prepare outputs from the Pharmacovigilance database to support the analysis of drug safety related tasks. - Uses their experience of pharmacovigilance data management to mentor and train other data managers. - Identify process improvements and lead data management related activities.

Major Accountabilities: Support DS&E customers or other external line units by providing them with retrieved data from the Pharmacovigilance database. Understand and translate data retrieval need into query request, create query criteria, retrieve data from the Pharmacovigilance database and provide the results to DS&E staff or external line functions. Generate regulatory reports, standard reports, tabulations and retrievals in preparation for regulatory submission Perform QC check on data retrieved; Identify errors/inconsistencies in outputs and resolves them or initiates their resolution. Train and mentor new Pharmacovigilance Data Management personnel as appropriate. To Provide Input and review of database design, validation checks and necessary reports to ensure high quality and consistent data during retrievals. Identifies opportunities for improvement of DS&E business processes and proposes and implement new solutions. Assist Department Head in defining Pharmacovigilance data management strategy and guidelines in order to establish common rules for assessing adverse event reports. Support testing and validation processes in DS&E IT projects.



Company Profile:
Novartis Healthcare Pvt. Ltd.

A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes us one of the most rewarding employers in our field. 

Job Description


Greetings from Magna!!!

This is Archana Singh from Magna InfoTech.

An excellent opportunity engulfs you with one of our most renowned clients

About Us:
Magna InfoTech is a division of USD 400 + million Quess Group which in turn is a subsidiary of USD 37+ billion - Canadian Multinational, Fairfax Financial Holding Group.
Magna Infotech is the largest staff Augmentation and Solutions Company in India, USA and APAC regions.
We are a team of 10,000 + associates and 350 + recruiters servicing 250 + clients across all domains (BFSI, Services & Consulting, Automotive, Engineering and Telecom, Products, FMCG, Retail & Healthcare)
Today we are recognized as the most compliant partner by our customers (300 + client audits on a yearly basis)


About Role:
Designation : Pharma Benefit Analyst (2013-2015 Passedout)
Required Skills : Pharmacist, Pharmacology, Fresher, B Pharmacy, M Pharmacy
Experience : 1 4 years Only
Working Location :Hyderabad
NP : Immediate Joinee
Salary : 2.4 lpa

NO BE / B Tech NO Technical Background


Only F2F No Telephonic round

Shift timing: Night Shift (Cab facility is there)

NO TELEPHONIC ROUND WILL BE THERE

Note: Interested candidates please share your updated profile along with the details mentioned below:

Name
DOB
Highest Qualification
Current Company
NP
Current CTC
Exp CTC
Current Location
Reason To Change

Mail to: archana.singh@magna.in
080-30485441
9343218425

SR Infotech Building, Thaverekere Main road, SG Palya, DRC Post, Bangalore- 29
Landmark Opposite to forum mall (Koramangala)


Salary: INR 1,00,000 - 2,50,000 P.A
Industry: BPO Call Centre ITES
Functional Area: ITESBPOKPOLPOCustomer ServiceOperations
Role Category: Associate/Senior Associate -(NonTechnical)
Role: Associate/Senior Associate -(NonTechnical)
Keyskills:


Job Description


Greetings from Magna!!!

This is Archana Singh from Magna InfoTech.

An excellent opportunity engulfs you with one of our most renowned clients

About Us:
Magna InfoTech is a division of USD 400 + million Quess Group which in turn is a subsidiary of USD 37+ billion - Canadian Multinational, Fairfax Financial Holding Group.
Magna Infotech is the largest staff Augmentation and Solutions Company in India, USA and APAC regions.
We are a team of 10,000 + associates and 350 + recruiters servicing 250 + clients across all domains (BFSI, Services & Consulting, Automotive, Engineering and Telecom, Products, FMCG, Retail & Healthcare)
Today we are recognized as the most compliant partner by our customers (300 + client audits on a yearly basis)


About Role:
Designation : Pharma Benefit Analyst (2013-2015 Passedout)
Required Skills : Pharmacist, Pharmacology, Fresher, B Pharmacy, M Pharmacy
Experience : 1 4 years Only
Working Location :Hyderabad
NP : Immediate Joinee
Salary : 2.4 lpa

NO BE / B Tech NO Technical Background


Only F2F No Telephonic round

Shift timing: Night Shift (Cab facility is there)

NO TELEPHONIC ROUND WILL BE THERE

Note: Interested candidates please share your updated profile along with the details mentioned below:

Name
DOB
Highest Qualification
Current Company
NP
Current CTC
Exp CTC
Current Location
Reason To Change

Mail to: archana.singh@magna.in
080-30485441
9343218425

SR Infotech Building, Thaverekere Main road, SG Palya, DRC Post, Bangalore- 29
Landmark Opposite to forum mall (Koramangala)


Salary: INR 1,00,000 - 2,50,000 P.A
Industry: BPO Call Centre ITES
Functional Area: ITESBPOKPOLPOCustomer ServiceOperations
Role Category: Associate/Senior Associate -(NonTechnical)
Role: Associate/Senior Associate -(NonTechnical)
Keyskills:



 Janmashtami, the birthday of Lord Krishna is celebrated with great devotion and enthusiasm in India in the month of July or August. According to the Hindu calendar this religious festival is celebrated on the Ashtami of Krishna Paksh or the 8th day of the dark fortnight in the month of Bhadon.
Sri Krishna is considered as the one of the most powerful human incarnations of the Lord Vishnu. He was born around 5,200 years ago in Mathura. The sole objective of Sri Krishna's birth was to free the Earth from the evilness of demons. He played an important role in Mahabharata and propagated the theory of bhakti and good karma which are narrated deeply in the Bhagwat Geeta.
Image result for story behind janmashtami celebration
Sri Krishna was born in a prison in the custody of Kansa. Vasudev, His father immediately thought of his friend Nand and decided to hand over his child to him to save Krishna from the clutch of Kansa. Krishna grew up in Gokul and finally killed his uncle, King Kansa.

The actual celebration of Janmashtami takes place during the midnight as Sri Krishna is believed to be borned on a dark, stormy and windy night to end the rule and violence of his uncle, Kansa. All over India this day is celebrated with devotional songs and dances, pujas, arti, blowing of the Conch and rocking the cradle of baby Sri Krishna.

The Janmashtami celebration of Mathura and Vrindavan, the places where Sri Krishna had spent his life, are very special. On this day temples and homes are wonderfully decorated and illuminated. Night long prayers are offered and religious mantras are sung in the temples.

Celebrated on the eighth day of Savana month, Janmashtami marks the birth of Lord Krishna, an avatar of Lord Vishnu. The festival is celebrated across the length and breadth of India, by people following Hinduism. In fact, it is an important day for Hindus. The celebration goes on for two days. On the first day, the Raslila (dance drama) is performed, which depicts the important phases of Shri Krishna's life. The merrymaking reaches it peak at midnight stroke, when aarti is performed and bhajans are sung to praise the Lord. Small children are dresses as the young Krishna and his playmate Radha. Then there are folklores and stories which are recited on the occasion, they are generally connected to the history of Janmashtami, which can be traced back to the ancient era. Read the following lines to get information on the history of Janmashtami.

The history of Janmashtmi dates back to thousand years. There are also several legends and stories associated with this festival. If you start exploring the origin of the festival, you will end up listening to thousands of folklores related to Krishna and his birth. It is believed that Lord Krishna was the incarnation of Vishnu, one of the three most important Hindu Gods. It is commonly believed that he took birth for killing Kansa, the unreligious demon king of Mathura and other demons, to establish a kingdom of peace, prosperity and religion on earth and to spread the message of brotherhood and humanity.

In his preaching to Arjuna in the Holy Bhagvad Gita he says Whenever the balance of the universe is disturbed by external interference from any of its parts, then I reveal myself as the Power of eternal balancing. For the protection of those who are in harmony, and the rectification of everything disharmonious, I incarnate myself at every juncture of time. So, it is assumed that the form of God will return back on earth for the establishment of peace, religion and prosperity in society once again when required. The celebration of Janmashtami is also a way to commemorate his holy deeds on earth for the mankind.

Historians calculate that the birth of Lord Krishna goes back to the Dwapar Yug. It is in the year of Visvavasu around 3227 BC when Lord Krishna was born. He was born on a dark, stormy night on the day eight day of the second fortnight of the month of Shravana which now corresponds to the month of August-September in the Gregorian calendar. Born in the prison of Demon Kansa, from Kansas sister Devaki and Vasudeva, Krishna was declared to be the savior of mankind and the end of Kansa even before his birth. Krishna, right from the day of birth exhibited that he was a special child and there was extraordinary powers with him. Throughout his childhood and adolescence in Gokul, he did many things which made people believe that he was a form of God. Since then, the people of Nandgaon celebrated the birth of Krishna as a day of fortune. 
Image result for story behind janmashtami celebration

Even thousands of years after his heavenly abode, people observe this day as a day of fortune and commemorate the birth of Lord Krishna by fasting and feasting. People believe Krishna to be the ultimate savior of the world. One who unlike other gods, can be regarded, as a lover, friend, divine guru or ones own child. People mesmerized with Krishnas persona and deeds can be seen singing and dancing in the name of Krishna to eternity on the day of Janmashtami. It is the deep faith and devotion of people towards him that the festival is still celebrated with a great honor, joy as well as elation as it was celebrated thousands of years back.                          

Mega Walk-In Drive For QA / QC Positions @ Sun Pharma | 50 openings Available

Image result for sun pharma
Sun Pharma an international, specialty pharmaceutical company headquartered in India with a global manufacturing network across 25 countries. We manufacture and market a large basket of pharmaceutical formulations as branded generics & generics in India, US and across the world. Our leadership is approachable, encourages transparency & strong work ethics to ensure that people get the best opportunities to learn and grow. We encourage our employees to challenge themselves for highest level of performance through greater bandwidth of work responsibilities and growth opportunities. Apply to us if you wish to be part of Sun Pharma growth story.
A Walk-in Interview is scheduled for multiple Formulation (Solid Orals/Parenterals) Post at Manufacturing plants near Baroda.
Job Title: QA/QC Positions
Qualification & Experience :
Candidates having educational qualification of BSc / MSc / BPharm / MPharm with required subject of Specialisation (as mentioned below) with more than 2 years of experience.
Posts Vacant in :
  • Quality Control: Specialisation in Chemistry/Organic Chemistry / Analytical Chemistry With Experience in Calibration /Analysis / Analytical method validation in QC /PM/Stability labs. Working knowledge of instruments like HPLC /GC / Dissolution / UV Spectrophotometer etc. is essential.
  • Quality Control (Microbiology): Specialization in Microbiology with experience in Microbiology testing like sterility testing, bacterial endotoxin, particular matter, MLT, Environment monitoring, water sample analysis etc.
  • Quality Control (QA of Laboratory): Specialization in chemistry with experience of review of analytical data and records, chromatographic data and audit trails, investigation of OOS /OOT result.
  • Quality Assurance : Experience in IPQA /QA Microbiology /QA Documentation /Quality Engineering /CSV /Compliance / QMS /Batch Release / Validation etc in solid orals /parenteral / injectable dosage forms.
  • Production & Packing : B.Pharm having experience in production /packing of solid orals/parenteral & injectable
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