Career at Johnson & Johnson "A"

Johnson & Johnson is the world’s most comprehensive and broadly based manufacturer of health care products. The organization is comprised of more than 250 operating companies with over 128,000 employees located in some 60 countries. With Global sales of USD 67.2 billion in 2012, Johnson & Johnson is recognized as one of the most admired and respected companies in the world. In India, Johnson & Johnson operates as a single legal entity and consists of the 3 strategic business units: Consumer Products, Pharmaceuticals and Medical Devices & Diagnostics, which are independently managed and report into their respective Global business segments.
Job Title: Quality Control Officer – Microbiology (Regional Title: Q&C Engineer)
Function: Quality & Compliance
Organization: Johnson & Johnson Limited, Consumer, INDIA

Location: Johnson & Johnson Ltd., Hyderabad, INDIA



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Recruitment drive at Novartis, Bangalore "A"

Job Description

Novartis Healthcare is hiring ...!



Job location : Hyderabad.
Golden opportunity to meet us directly in Bangalore over a weekend - 12 NOV 2016 @ 9:00 AM

Venue: Will be updated here soon.
.

1. Trainee / Junior Programmers - 1 - 3 Yrs..
2. Statistical Programmer -      3- 5 Yrs.

Job Description:
Locally coordinate and take responsibility for trial level programming activities (analysis datasets, pooled datasets, listings, tables and figures) of individual Phase I-IV clinical trials to support program programmers and statistician in project level activities.
Be responsible for statistical tasks on assigned clinical trials e.g. RAP.
Maintain efficient interfaces with internal and external customers with support of ONC Biometrics management and the Program Programmer/Statistician.
Make certain that documents and specifications are consistent and comply with company standards by providing input into CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities.
Program and deliver, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for pooled analysis with high quality and within milestones.
In consultation with the statistician, develop specifications for analysis datasets, pooled datasets, and listings
Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation.
Provide input on process improvement initiatives and participate in non-clinical project activities with support from GH
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Jobs for Clinical SAS programmers "A"

Job Description

Novartis Healthcare is hiring ...!

Job location : Hyderabad.

Golden opportunity to meet us directly in Pune on 21st OCT 2016 @ 9:00 AM

Interview Venue:
Hotel IBIS Pune
Survey No 32, Viman Nagar, Nagar Road, Pune 411 014.
Tel.: +91 20 4018 4018

POC: Priyanka Thatoi (HR)
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Walk In for Pharmacovigilance on 1st October @ Hyderabad "A"

Job Description

Dear All,

We are pleased to inform you that we have multiple positions opened for Pharmacovigilance.

Experience - 2 to 8 years
Skills Required - Case Processing
Job Location - Bangalore
Date & Time - 1st October 2016
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Jobs at Novartis "A"

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 them one of the most rewarding employers in their field.

Post: Senior Clinical Manager




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Walk In for Pharmacovigilance on 1st October @ Hyderabad "A"

Job Description

Dear All,

We are pleased to inform you that we have multiple positions opened for Pharmacovigilance.

Experience - 2 to 8 years
Skills Required - Case Processing
Job Location - Bangalore
Date & Time - 1st October 2016
Apply here

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20 posts vacant at Vivimed "A"

Vivimed Labs Limited, uses chemistry as a base to create ingredients which touch human life on daily basis. The Company manufactures active ingredients which are used in Home & Personal care segments like hair, skin, oral care and anti-microbial preservatives. The Company’s presence in manufacturing of Active Pharmaceutical Ingredients (API) , Finished Dosage Formulation (FDF) and Retail Branded Formulation caters  to the inner health of people. It is also present in the Industrial care segments like photo chromic dyes and imaging chemicals. The Company has global reach with 12 manufacturing units (9 domestic and 3 overseas), 5 R&D centers (3 domestic and 2 overseas) and workforce of over 1,650 people.





No of Posts : 20

Job Description
1. R&D Research Associate.
2. ARD Associates.
3. Purchase Executive.
4. SCM Executive.
5. PMO and BD Professionals.

Send your CV at :shravan.kulakarni@vivimedlabs.com

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Novartis hiring Pharmacovigilance Scientist "A"

Job Description :

• Subject Matter Expert
• Contribute to DS&E projects
• Assess seriousness, causality and labeling of serious adverse events and quality check ICSRs to ensure accurate and consistent Argus data entry from source documents.
• Author/co-author, along with Global Medical Safety Physicians, regulatory periodic safety re- ports (Periodic Safety Update Reports, US Periodic Reports) for Novartis mature portfolio: collecting, organizing, analyzing and presenting the data by means of DS&E templates and procedures.
• Lead/co-lead cross functional expert teams to fulfill Periodic Safety Report accountabilities (DRA, Clinical, Marketing).
• Review global marketing programs and establish process for AEs collection with global marketing teams.
• Review Risk Management Plans in coordination with Global Medical Safety groups and assess the operational feasibility and implications of Pharmacovigilance commitments.
• Collaborate with Electronic Data Management team to reconcile Serious Adverse Events be- tween the Clinical and Safety databases to meet joint accountabilities and enable locking of Clinical database.
• Alert the Medical Safety Physicians of potential safety issues and assist the Medical Safety Physicians in monitoring the safety profile of products.
• Member of Safety Profiling Teams to ensure that case reports are accurately evaluated and database, authoring or contributing to Product Specific Guidelines for assigned products.
• Contribute to the preparation of Standard Operating Procedures and Argus processing conventions (MAP).

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Dr. Reddy's hiring for Regulatory Affairs "A"

Job Description

Participate in the regulatory activities of full spectrum of formulation development, from clinical trials to marketing to post approval activities.
Ensure the appropriate licensing, marketing and legal compliance of the finished dosages.
Review the documents at each stage of formulations development.
Highlight the regulatory issues that can be there and try to resolve them.
Coordinate with R&D, AR&D, QA, etc. to collect the complete set of documents.
Compile the ANDA document to be submitted to FDA.
Ensure the documents are error free and have minimum deficiencies.
Prepare annual reports and send them to FDA.
Manage change controls and deviation controls.
Keep themselves abreast of international legislation, guidelines and customer practices
Develop and write clear arguments and explanations for new product licenses and license renewals.
Advise PDTs on regulatory requirements.
Respond to the queries of Regulatory authorities and customers on time.
Review the process change proposals and provide guidance on change proposals.

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Inventiv Health hiring Drug Safety Physician "A"

Sr. Drug Safety Physicians

Job Description

Responsibilities
Medical review of adverse events reported to investigational and marketed products including identification of event/s, confirmation of seriousness, ensure that events are coded and mapped to the appropriate terms in MedDRA, provide assessment of expectedness per reference safety information, assessment of causality, review of narrative for chronology and medical content and provide medical evaluation comment.
Ensure that appropriate medical interpretation and consistency are applied to adverse event case assessment.
Ensure regulatory compliance with respect to the evaluation, reporting and surveillance of safety information.
Identify, communicate, and effectively manage potential safety issues.
Provide medical safety analysis and interpretation for periodic safety aggregate reports (e.g. DSUR, PSUR/PBRER, PADER, bridging reports, and other relevant aggregate report/analyses).
Interact with clients safety/medical personnel as appropriate to ensure above.
Maintain a working knowledge of projects in the functional area for which inVentiv Health Clinical safety is responsible for safety reporting.
Stay abreast of clinical and drug development information relevant to contracted programs by review of literature and by maintaining training.
Serve as a mentor for other internal safety staff including case processing staff.

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Novartis Healthcare hiring Medical Writers "A"

 Submission/regulatory Medical Writer

Novartis Healthcare Pvt. Ltd.

1 - 6 yrs

Hyderabad / Secunderabad

Job Description

1. To author and review independently or assist senior writers in the team to manage high quality clinical and safety documents: Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), Clinical Trial Registry Database (CTRD), Risk Management Plans (RMP), CTD summaries and other special safety/clinical reports.
2. Assist/Lead outsourced Narrative projects. Assist/ Coordinate other outsourced activities.
3. Member of Clinical Trial Team (CTT)/ participate in Safety Management Team (SMT).
4. Actively participate in planning of data analyses and presentation to be used in study reports or summary documents.
5. Act as documentation consultant in CTTs and SMTs to ensure compliance of documentation to internal company standards and external regulatory guidelines.
6. May act as Program Writer ensuring adequate medical writing resources are available for assigned program and consistency between documents.
7. Act as liaison between Clinical Trial Teams, Clinical Submission Teams and publishing teams to ensure timely delivery of final documents for publishing.
8. Support the development of the team through participation in initiatives, training/mentoring and other related activities.
9. Contribute to development of processes and may contribute to cross-functional initiatives.
10. Fostering cross-functional communication to optimize feed-back and input towards high quality documents.
11. Maintain audit, SOP and training compliance.

Key Performance Indicators (Indicate how performance for this role will be measured)
1. Delivery of high quality clinical and safety documents in accordance with standard processes with respect to timelines and in compliance with internal and external standards.
2. Completion of an adequate number of documents (taking into account complexity) per year.
3. Adequate representation on the clinical team or submission team, and effectiveness of communication and guidance.
4. Appropriate communication of project resource needs and status.

Ideal Background (State the preferred education and experience level)

Education:

Minimum university life science degree or equivalent is required. Advanced degree or equivalent education/degree in life sciences/healthcare is desirable.
Masters with 1-8 years of relevant experience.
PhD or degree in medicine (MBBS/MD or Alternative medicine) with 1-8 years of relevant experience.
Languages: Fluent English (oral and written).
Experience / Professional Requirement: 1 year medical writing experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus strong knowledge of the medical writing processes.
Excellent communication skills (written, verbal, presentations)
Operational knowledge of clinical trial reporting.
Understanding of biostatistics principles.
Ability to prioritize and manage multiple demands and projects.
Knowledge of and some experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements).
Ability to define and solve complex problems (Problemsolver)
Proven track record in matrix environment
Experience in contributing to global, cross functional projects.
Global, cross-cultural perspective and customer orientation. 

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.  

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Openings For Medical Coding "A"

Openings For Medical Coding!!!

1 - 5 Years

Job Description

Greeting from Sutherland Health care Services!!!

We are currently hiring for E&M-inpatient & outpatient (min 1year of exp).

Job Description:

Good written and verbal communication skills.
Good analytical and domain skills
Well versed in MS office and ability to work online with multiple navigation systems and various coding software(s).
Coding Certification (CPC/CCS): Preferred
ICD-10 training completed - Preferred

Free transportation 

Sat & Sun- Fixed off

Salary: As per company norms

Work Location: Hyderabad

Interested candidates mail your resume to marysandana.nikhita @sutherlandglobal.com

Regards,

HR Team

Sutherland Global Services

Hyderabad

Company Profile

Apollo Health Street (AHS) is an end-to-end healthcare outsourcing focused services company, with impeccable credentials, proven track record and unwavering commitment aimed at delivering value added services to its clients

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Dr. Reddy's hiring Scientists "A"

Scientist

Job Description

1. Execution of downstream purification activities by chromatography and all filtration techniques for process development.
2. To document lab note book and present the experimental findings in the form of reports and presentations.
3. Maintaining the equipments, instrument logs and relevant records.
4. Adherence to all safety norms in the lab.
5. Upkeep of general maintenance of the lab area
6. To lead a small team for purification process development of monoclonal antibodies.

Company Profile

Dr. Reddy's Laboratories Ltd. (NYSE: RDY) is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Through its three businesses - Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products - Dr. Reddy's offers a portfolio of products and services including APIs, custom pharmaceutical services, generics, biosimilars and differentiated formulations. Major therapeutic focus is on gastro-intestinal, cardiovascular, diabetology, oncology, pain management and anti-infective. Major markets include India, USA, Russia-CIS and Europe apart from other select geographies within Emerging Markets. For more information, log on to: www.drreddys.com

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Inventiv health hiring Sr. Drug Safety Physicians "A"

 Sr. Drug Safety Physicians

inVentiv International Pharma Services Pvt. Ltd

3 - 5 yrs

Hyderabad / Secunderabad , Pune

Job Description

Responsibilities
Medical review of adverse events reported to investigational and marketed products including identification of event/s, confirmation of seriousness, ensure that events are coded and mapped to the appropriate terms in MedDRA, provide assessment of expectedness per reference safety information, assessment of causality, review of narrative for chronology and medical content and provide medical evaluation comment.
Ensure that appropriate medical interpretation and consistency are applied to adverse event case assessment.
Ensure regulatory compliance with respect to the evaluation, reporting and surveillance of safety information.
Identify, communicate, and effectively manage potential safety issues.
Provide medical safety analysis and interpretation for periodic safety aggregate reports (e.g. DSUR, PSUR/PBRER, PADER, bridging reports, and other relevant aggregate report/analyses).
Interact with clients safety/medical personnel as appropriate to ensure above.
Maintain a working knowledge of projects in the functional area for which inVentiv Health Clinical safety is responsible for safety reporting.
Stay abreast of clinical and drug development information relevant to contracted programs by review of literature and by maintaining training.
Serve as a mentor for other internal safety staff including case processing staff.

Company Profile:

inVentiv International Pharma Services Pvt. Ltd

PharmaNet/i3 is recognized as a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. Our expertise includes therapeutically specialized capabilities for Phase I-IV clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team (FSP).

We seek individuals with a desire to excel in their fields, pursue excellence, and develop intelligent solutions by applying their knowledge and experience. Our employees focus on meeting our clients' requirements, work in a culture of mutual respect, and demonstrate a commitment to quality in everything they do. PharmaNet/i3 employees are empowered to think independently, be accountable, make decisions quickly, and use the resources of our global organization on our customers' behalf.

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Medical Coding Freshers Job "A"

Medical Coding Freshers - Policy Support Analyst

Cotiviti India Pvt Ltd

0 - 2 yrs

Hyderabad / Secunderabad

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

Company Profile:

Cotiviti India Pvt Ltd

Direct Walk - In from 15th August - 26th August

Time - 11.00 AM to 3.00 PM

Address : Cotiviti India Private Limited
4th & 5th Floors, Western Pearl
Survey Number 13, Kondapur
Hyderabad - 500084, Telangana, India


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M. Pharma Walk-in Drive on 1st Sept "A"

M. Pharma Walk-in Drive on 1st Sept-2016 at 11 AM

0 - 1 Years

Hyderabad / Secunderabad

Openings: 3

Walkin Interview from 1st September to 2nd September from 11 AM

Job Description

 Healthcare related market Research work

Company Profile

UK based MNC dealing with Healthcare Research

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Novartis hiring for Pharmacovigilance "A"

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

Apply now

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Medical Scribe required at Hyderabad "A"

Medical Scribe at Hyderabad

1 - 5 Years

Hyderabad / Secunderabad

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.

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Novartis Healthcare Jobs for Pharmacovigilance "A"

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. 

Apply here 

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Medical Coding Freshers required "A"

Direct Walk - In from 18th July to 12th 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

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 Apply now

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