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Wednesday 31 August 2016

Admissions open for Clinical Research & Pharmacovigilance Fast Track Classroom Training | Next Batch: 19th Sept 2016


Image result for clini india

Clini India invites applications from Pharma & Life science Graduates for Advanced Program in Clinical Research, Clinical Data Management, Pharmacovigilance, Medical writing & Medical Coding.
<<<Learn More>>>
Fresh Batch commencing from 19th September 2016 (4 Months Fast Track training)

Who we are?
CLINI INDIA is a premier Clinical Research Training institute offering advanced training:
  • Clinical Research
  • Records Management
  • Regulatory affairs
  • CDM
  • Pharmacovigilance
  • Medical Writing
Are you eligible? - <<>>

Upcoming Batches: 19th SEPTEMBER 2016.
Location: Bangalore.
Number of seats - 10 Candidates.
CLICK HERE to view our latest placements.
"The future depends on what you do today"

What's Included:
  • Classroom Training / Online Training from Qualified & experienced Industrial Experts.
  • Printed Study Material - Different Books for each subject.
  • Unlimited Classes - We do not limit on your classes, attend as many classes as you can, no limits because our goal is your success.
  • 24X7 Email & Chat Support for Quick query.

If you wish to attend Demo Session <<>>

Students who enrol for 4 Months regular classroom training have the following advantages:
  • Industry Oriented Program
  • 100% Industry Visiting Faculty
  • Placement Support
  • Free Study Material
  • Soft Skills & Communication Skill training
  • Resume/Cover letter customization


For more details contact our Centre Coordinator at 8050040004 or <>
Go for our Hassle Free Distance Learning Training at Home. <>
Clini India is committed to provide you best facility for Clinical Research & Pharmacovigilance Training and we stand by it.
Call or WhatsApp on +91-8050040004  for more details.

WNS Hiring for B.pharm Research Analyst - Meet HR Pooja 02240112935


Image result for wns
0 - 5 Years
Mumbai

Job Description

Greeting from WNS!!

WNS Hiring for Pharma Research Analyst

Walkin from 31st Aug
 
2nd Sep 
Contact HR Pooja 02240112935.

Job description and key accountabilities:

Research and analyze business impacting and time sensitive business information in the Biopharmaceutical Industry.
BioPharmaceutical Databases Development through Business Research, Information analysis and profiling in given format for:
1. Drug database:
Researching through various company websites and collecting the details (such as molecule, chemical structure & properties, mechanism of action, therapeutic area, clinical phases etc) of marketed drugs and drugs under developmental pipelines

2. Life science conference Database:
Searching and capturing details on upcoming biopharmaceutical/ Life science conferences. Details about the location, conference title, speakers, sponsors, exhibitors or media involved are captured

3. Active Intel:
Researching & tagging the Biopharmaceutical Industry news/articles to the database

4. Clinical Trials:
Understanding & tagging the Conditions, Interventions & Sponsors to the Clinical Trial Database
.
5. Pharmaceutical Licensing agreements:
Capturing the details of pharmaceutical licensing transactions from company websites or Securities and Exchange Commission (SEC) files, annual reports etc

6. Ad Hoc Tasks:
Working on any Ad Hoc, short duration assignments/projects assigned by clients related to Biopharmaceutical Industry.


B.Pharma Grad
Minimum work experience: 0

Candidate Boundary Limits: Churchgate / CST till Mira Road, Kharghar and Kalyan
Drop / Pick Up Points: Dadar / Borivli / Vashi / Thane.

Special skills:
Excellent Communication Skills
Keen Interest in Secondary Research
Ability to interpret data and aid in arriving at the key findings
Decision making and judgment
Proficient in MS Office

Shift Timings: Rotations Shifts (7am 2.30pm, 2.30pm 10pm )

Interview Venue:
WNS Global Services,Plant 5, Gate NO 2, Godrej Compound,LBS Marg, Vikhroli West. Near Caf Coffee Day. Landmark: Caf Coffee Day.

Contact Person: Miss Pooja.P

Synopsis about WNS:
WNS is a leading global KPO and BPO company. WNS has a strong horizontal focus with its Finance & Accounting, Contact Center and Research & Analytics solutions. WNS 'extends the enterprise' of some of the world's best brands by providing vertical-led solutions for Travel & Leisure, Banking & Financial services, Insurance, Shipping & Logistics, Utilities, Healthcare, Manufacturing, Telecommunications, and Retail & Consumer Packaged Goods industries.
 Company Profile
WNS is a leading global KPO and BPO company. WNS has a strong horizontal focus with its Finance & Accounting, Contact Center and Research & Analytics solutions. WNS 'extends the enterprise' of some of the world's best brands by providing vertical-led solutions for Travel & Leisure, Banking & Financial services, Insurance, Shipping & Logistics, Utilities, Healthcare, Manufacturing, Telecommunications, and Retail & Consumer Packaged Goods industries

Practice Tips and Activities
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1. There are a number of different interview settings you may encounter and it's essential to see and know how to respond in every scenario. Do one interview with a friend or colleague, where you speak to this one individual. Then answer the questions in front of five to 10 friends or colleagues. And finally, answer the same questions speaking straight to the camera. Notice how each can take on a different tone, but try to keep up the trust and likeability you portray in each scenario.

2. No matter what the interview, the most common question is in reference to you and your personal traits. Practice describing yourself with language and tones that come across as confident but not cocky. Make sure you know your strengths and key characteristics you'd like your audience to know about you. Lastly, ask the practice interviewer if he or she thought your answer was believable.

3. Ask a friend to put three random topics in a hat. Pull one out at a time and practice your impromptu responses. Have the friend include one question in which you might not know the answer. It's better to rehearse how you'll handle an answer you don't know before you are in a critical interview.

4. Watch a taped interview of a polished interviewee and pause the video before they give their responses to the questions. Try your hand at the answers and see how your responses differ from the actual subject. Look for differences in dialogue, eye contact, body language and expressions.

5. Your body language can often tell more to your audience than your words do. Take one of your practice videos and watch it through with the volume turned off. See what your expressions and body language is portraying to the public. Ask a friend or colleague to watch the muted video as well and see if they can interpret the mood and impressions of your interview. Try playing around with different facial and body expressions in your next test interview from the feedback you receive.

6. Interviews can come in varying lengths and it's good to have experience knowing how to draw out an answer and how to edit it down to the key points. Ask a friend to come up with three different questions. First answer each question within a 30-second period. Then give yourself 60 seconds. And finally, give yourself two minutes to answer the same questions. Make sure the shortest answer doesn't exclude your most important points and make sure that your longest answer doesn't detract from the main topic.

7. In many interviews, you can't control what the interviewer is going to ask you, but you often have an agenda you want to accomplish or a point you want to make. Have a friend ask you an obscure question and try to work in a natural sounding transition to incorporate the point you want to make. Politicians are experts at this. Watch a few of their interviews to see how they always work an answer in the direction they want it.

8. Try being the interviewer and ask someone else the questions. It often helps to be on the other side of the microphone. It gives us a new perspective on how to answer questions.

9. Start putting in the numbers. As previously stated, nothing replaces practice and experience. Contact a local school, organization, radio station or TV station and ask them if you can perform a question-and-answer session. There is a different pressure when you answer questions for a stranger than when you answer for a friend or close colleague. The more interviews or Q&A's you can do, the better off you'll be.

10. Have fun! Even when you practice, put a smile on and try to focus on the positive aspects of your answers so you always portray an affable demeanor. Your good mood can influence others so keep the positive energy coming.
Interviews can be extremely important and can be quite influential in the outcome of your career. Knowing how important an interview can be, isn't it worth putting in the time to perfect your skills? Your interest in the improvement shows you are already halfway there.  

What is Group Discussion


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Group Discussion! Is a methodology or in a simple language you may call it an interview process or a group activity. It is used as one of the best tools to select the prospective candidates in a comparative perspective. GD may be used by an interviewer at an organization, colleges or even at different types of management competitions.

A GD is a methodology used by an organization to gauge whether the candidate has certain personality traits and/or skills that it desires in its members. In this methodology, the group of candidates is given a topic or a situation, given a few minutes to think about the same, and then asked to discuss the topic among themselves for 15-20 minutes. Freshersworld.com brings you an elaborate section for GD as you had ever seen anywhere else. It is a very useful tool to screen the candidate’s potential as well as their skills.

GD evaluation is done by the subject experts based on the discussions. A report will be prepared on analyzing the facts at the end of the discussion.

Some of the personality traits the GD is trying to gauge may include:


* Communication skills
* Interpersonal Skills
* Leadership Skills
* Motivational Skills
* Team Building Skills
* Analytical /Logical Skills
* Reasoning ability
* Different Thinking
* Initiative
* Assertiveness
* Flexibility
* Creativity
* Ability to think on ones feet
* Why GDs are implemented commonly:

The reason why institutes put you through a Group discussion and an interview, after testing your technical and conceptual skills in an exam, is to get to know you as a person and gauge how well you will fit in their institute. GD evaluates how you can function as a part of a team. As a manager or as a member of an organization you will always be working in teams. Therefore how you interact in a team becomes an important criterion for your selection. Managers have to work in a team and get best results out of teamwork. That is the reason why management institutes include GD as a component of the selection procedure.

Company's Perspective:

Companies conduct group discussion after the written test to know more about your:

* Interactive Skills (how good you are at communication with other people)
* Behavior (how open-minded are you in accepting views contrary to your own)
* Participation (how good an active speaker you are & your attention to the discussion)
* Contribution (how much importance do you give to the group objective as well as your own)

Aspects which make up a Group Discussion are:

* Verbal Communication
* Non-verbal behavior
* Confirmation to norms
* Decision making ability
* Cooperation

You should try to be as true as possible to these aspects.

Senior Research Associate Trainee - DMPK

0 - 1 YearsBengaluru/Bangalore Openings: 3

Image result for syngene

Job Description

  1. To support in life PK studies of NCEs in rodents
  2. Rodent surgery, pre-formulation analysis, dosing and sampling of plasma for bioanalysis 

Company Profile

Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

Over the past 16 years, Syngene has successfully partnered with leading pharmaceutical companies, large biotech companies, crop protection companies and cosmetics companies. Syngene together with  Bristol-Myers Squibb has set up a dedicated research facility in Bangalore to help advance Bristol-Myers Squibb's work in discovery and early drug development.

To advance its programs and expand its capabilities, Syngene is looking to recruit outstanding scientific talents.

So come and join us in our journey of scientific innovation.

For further details, please visit www.syngeneintl.com.

 QA Clinic - Ba/be


0 - 1 yrs
Job Description
     System Audit, Study Specific Audit, Vendor Audit, Review of protocol, Review of Calibration/ Validation documents & Review of Clinical Reports
Company Profile:
Cliantha Research Ltd

Cliantha Research, a leading life science company, is a global full service Contract Research Organization with integrated offerings in Clinical, Bioanalytical, Dermatology, Biometrics, Pathology and Formulation services.

Our facilities are inspected and audited by global regulatory bodies like USFDA, ANSM (French regulatory agency), MCC (South African regulatory agency), AGES (Austrian regulatory agency), AEMPS (Spanish regulatory agency), WHO, UK-MHRA, Thai MoPH, MOH Turkey and various international companies  

Opening for Clinical Data Management for Mumbai and Kolkata

Image result for cognizant

4 - 9 Years

Job Description

Hi!!


We have an urgent opening for Clinical Data Management for Mumbai and Kolkata location.


Qualification: Graduate/Post Grraduate in Science/Life Sciences/B.Pharm/M.Pharm


Experience : 4years+  in Clinical Data Management.


Job Description:


End to End CDM activities
Relevant experience in Clinical Data Management
Perform data management activities on the assigned project in a timely and efficient manner
Generate queries to clarify and improve the quality of the data
Test and execute validation procedures



**Candidate should be open for rotational shifts.




Interested candidates kindly mail your resume to:
pooja.rajapurkar2@cognizant.com


Regards,


HR Team




Company Profile

Cognizant (NASDAQ: CTSH) is a leading provider of information technology, consulting, and business process outsourcing services, dedicated to helping the world's leading companies build stronger businesses. Headquartered in Teaneck, New Jersey (U.S.), Cognizant combines a passion for client satisfaction, technology innovation, deep industry and business process expertise, and a global, collaborative workforce that embodies the future of work. With over 100 development and delivery centers worldwide and approximately 221,700 employees as of December 31, 2015, Cognizant is a member of the NASDAQ-100, the S&P 500, the Forbes Global 2000, and the Fortune 500 and is ranked among the top performing and fastest growing companies in the world. Visit us online at www.cognizant.com or follow us on Twitter: Cognizant.

Pharmacovigilance Expert

Novartis Healthcare Pvt. Ltd.
1 - 5 yrs
Hyderabad / Secunderabad


Job Description

    Provide support to the Brand Safety Leader/ Pharmacovigilance Leader (PVL/ BSL) in monitoring the safety profile of assigned products by providing quality deliverables within agreed timeframes and adhering to a high standard of accuracy in compliance with IMS business rules, standard operating procedures and global and local regulatory requirements.

    1. Assist the BSL/ PVL in monitoring the safety profile of products potentially including activities such as literature review, evaluation of individual cases or signal detection. Medical review of single case reports will be performed by associates possessing medical degree.

    2. Together with the BSL/ PVL, co-author the PSUR including analytical input to PSUR for known and potential risks defined in the RMP.

    3. Together With BSL/ PVL, assist in the development, maintenance and implementation of the RMP including the coordination with other line functions for associated activities such as updates, management of large datasets for analysis purposes and the ongoing tracking of commitments and effectiveness measures

    4. Assist in evaluating and writing other safety deliverables including but not limited to clinical overviews, ad hoc health authority queries, drug safety product profile (DSPP), drug safety update report (DSUR)

    5. Assist in providing safety input to DRA and clinical documents (e.g. core data sheet and investigator brochure)

    6. Play an active role in standing and ad hoc Safety Management Team (SMT) and Safety Project Team (SPT) meetings

    7. Play an active role in SIGDET and MSRB meetings including preparatory activities

    8. Interface with the clinical team for safety matters including follow-up on events of interest and input into site queries regarding adverse events, updating on PVO requirements

    9. Quality of work delivered (attention to details, thoroughness, medical sound judgment, writing)

    10. Timeliness of deliverables according to established directives

    11. Compliance with Internal and external regulations and procedures

    12. High level of independence
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

Genpact Urgent Opening for Senior Medical Underwriter (30-31august)


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2 - 7 YearsDelhi/NCR(National Capital Region)

Job Description

GENPACT HIRING FOR SENIOR  MEDICAL UNDERWRITER (30-31 AUGUST 2016)

Interview location - Genpact Noida, stellar building ,7th floor sec 135, nearest metro station is Botanical garden
Take  "CITY LIFE" shuttle

 Profile : Medical Underwriter / Summarizer

Shifts : Day Shift 
Work Location : Noida

contact person-
                            AMBIKA@ 9643820484

Education and Experience-
Resource preferred to be a licensed Professional (MBBS, BHMS, BAMS, BPT, BDS, B.Pharma) or Life Sciences graduate.
Must have minimum 2-3 years of Life Insurance Underwriting / Medical Summarization / Clinical Research experience with in depth knowledge of underwriting requirements, analysis and decision making based on information and assessing mortality risk

Medical Knowledge-
Thorough knowledge of human physiology, familiarity with medical conditions, treatments, medical tests/investigations, and medicines

Analytical Skills
Ability to understand complex situations, to synthesize available contextual information. Exhibit good knowledge of medical conditions, medical terminology. Ability to analyze medical reports and treatment regimen
Good documentation skills, medical and English writing skills required
Required Skills:

For Senior Underwriter


Must have minimum 2-3 years of Life Insurance Underwriting / Medical Sunmarization / Clinical Research experience with in depth knowledge of underwriting requirements, analysis and decision making based on information and assessing mortality risk 





Note - Carry one updated resume, one original identity proof, one
passport size photograph.
(Mention  AMBIKA  on top of the C.V as HR Reference


AMBIKA


 Company Profile
Genpact (NYSE: G) designs, transforms, and runs intelligent business operations including those that are complex and specific to a set of chosen industries. Our hundreds of long-term clients include more than one-fourth of the Fortune Global 500. Founded as a division of GE in 1997 and then spun off in 2005, Genpact earned 2014 revenues of $2.28 billion and has more than 67,000 employees in 25 countries, with key management and a corporate office based in New York City.

 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  

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
    â€Æ’
    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.  

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