IQVIA Hiring Bachelor’s Degree in a Life Science for Pharmacovigilance/Medical Information Specialist

Vacancy details:

  • Post Name: Pharmacovigilance/Medical Information Specialist
  • Education : Bachelor’s Degree in a Life Science
  • Experienced:o1 to 3 years
  • Location:  Bratislava, Bratislava
  • Salary :NA
  • Openings :NA

 Job Description: We have requirement for the post of Pharmacovigilance/Medical Information Specialist in IQVIA .

Selection Process: The selection will be on the basis of Interview.

How to Apply Click here for full details and Apply Online

Sanofi Hiring B.Pharm/M.Pharm/M.Sc for QMS Specialist

Sanofi Recruitment July 2020Graduate/Post Graduate – B.Pharm/M.Pharm/M.Sc. for QMS Specialist

Vacancy details:

  • Post Name: QMS Specialist
  • Education : Graduate/Post Graduate – B.Pharm/M.Pharm/M.Sc.
  • Experience: 2 to 3 years
  • Location: Toopran Mandal
  • Salary : NA
  • Openings :NA
  • Contact Person:HR

 Job Description: We have requirement for the post of QMS Specialist in Sanofi.

Responsibility :

  • Responsible for the Site Document Management (Document Issuance and Archival)
  • Review of the cross functional department Document (SOPs/Specifications etc).
  • Documents Issuance and Archival through the Document management system tool.
  • Issuance of Numbering(Equipment/Instrument/Layoutsetc.) and Management of the master lists.
  • Participate in the Investigations resulted due to any Deviations.
  • Ensuring accuracy of all documentation Issuance/Archival related activities.

Selection Process: The selection will be on the basis of Interview.

How to Apply Click here for full details and Apply Online

Dr. Reddy’s Laboratories Recruitment Pharmacovigilance Systems and Safety Data Lead

Dr. Reddy’s Laboratories Recruitment July 2020 B. Pharm, M. Pharm, Life Science Post Graduate. for Pharmacovigilance Systems and Safety.

Vacancy details:

  • Post Name: Pharmacovigilance Systems and Safety Data Lead
  • Education : B. Pharm, M. Pharm, Life Science Post Graduate.
  • Experience: Ideally 6+ years experience in the Pharma industry in either a pharmacovigilance data entry or Pharma IT role, but 2+ years must be in safety database management
  • Location: Hyderabad
  • Address :8-2-337, Road No 3,, Hyderabad, Telangana, India
  • Salary :  INR 20,00,000 – 30,00,000 PA.
  • Openings : NA
  • Contact Person: HR

 Job Description: We have requirement for the post of Pharmacovigilance Systems and Safety Data Lead in Dr. Reddy’s Laboratories.

Responsibilities:

  • Act as the PV Subject Matter Expert for the global safety database and associated systems
  • Act as the primary liaison and first point of contact for:
    • Internal DRL IT in support of safety database maintenance and changes
    • The vendor supplier of the safety database and associated systems
  • Provide system administration support for central safety database applications as appropriate
  • Coordinate, implement and provide training for PV system projects and follow through the full project life-cycle
  • Develop user requirements, functional specifications and propose solutions for unmet safety system business needs
  • Analyze, collect, test, implement, and maintain safety database configuration changes
  • Perform quality control check on configuration changes; identify discrepancies between the request and the implementation and resolve them or initiate their resolution
  • Support testing and validation processes for pharmacovigilance IT projects; including generation of the appropriate documentation
  • Develop, provide support to create complex specialized data outputs from the safety database for various Pharmacovigilance reports/ad hoc queries, as appropriate
  • Ensure understanding of pharmacovigilance requirements and processes to support process improvement initiatives and the implementation of regulatory changes
  • Provide training to new team members on the PV system, as required
  • Provide safety database SME support during audit and Regulatory Authority Inspections

Selection Process: The selection will be on the basis of Interview.

How to Apply Click here for full details and Apply Online

Gufic Biosciences hiring B.sc,M.sc,B.pharm,M.pharm for QA Validation

Gufic Biosciences Limited Recruitment June 2020 B.Pharma in Any Specialization, B.Sc in Chemistry PG :M.Pharma in Any Specialization, MS/M.Sc(Science) in Chemistry for QA Validation @ Vapi, Vadodara, Dadra and Nagar Haveli, Daman & Diu, Ahmedabad, Surat .

Vacancy details:

  • Post Name: QA Validation
  • Education : B.Pharma in Any Specialization, B.Sc in Chemistry PG :M.Pharma in Any Specialization, MS/M.Sc(Science) in Chemistry
  • Experience:2- 5 years
  • Location: Vapi, Vadodara, Dadra and Nagar Haveli, Daman & Diu, Ahmedabad, Surat
  • Address: National Highway No. 8, Near Grid,, SURAT, Gujarat, India
  • Salary :  2,00,000 – 4,00,000 P.A.
  • Openings :05

 Job Description: We have requirement for the post of QA Validation in Gufic Biosciences Limited.

Selection Process: The selection will be on the basis of Interview.

How to Apply : Click here for full details and Apply Online

GVK Biosciences Recruitment Senior Research Associate

Important Vacancy details:

  • Post Name: Senior Research Associate
  • Location: Hyderabad
  • Salary : NA
  • Openings :NA

 Job Description: We have requirement for the post of Senior Research Associate in GVK Biosciences.

Selection Process: The selection will be on the basis of Interview.

How to Apply : Click here for full details and Apply Online

Alivira Animal Health Ltd hiring B.sc,M.sc,B.phrm,M.pharm for Analytical Scientist-R&D

Alivira Animal Health Ltd Recruitment June 2020 BSc/MSc or BPharm/MPharm for Analytical Scientist @ Ambernath, Maharashtra.

Vacancy details:

  • Post Name: Analytical Scientist
  • Education : BSc/MSc or BPharm/MPharm
  • Experience:2-5 years
  • Location: Ambernath, Maharashtra
  • Salary : NA
  • Openings :NA

 Job Description: We have requirement for the post of Analytical Scientist in Alivira Animal Health Ltd.

Responsibilities:

  • Complete Analysis of Raw materials, finished products & Stability samples Analysis.
  • Hands on experience in Analytical Method Development-Assay, Related substances and Dissolution
  • Hands on experience in Analytical Method Validation-Assay, Related substances and Dissolution
  • Hands on experience in Analytical Method Transfer-Assay, Related substances and Dissolution
  • Operation and Calibration of various instruments (Analytical balances, HPLC, Dissolution etc.)
  • GLP Compliance in the Lab
  • Independently design, execute, monitor, interpret and document analytical activities related to method development, validation and technology transfer
  • Detailed documentation of analytical activities, method development and validation activities
  • Prepare review and maintenance of documents such as SOPs, Protocols and reports
  • Perform analysis and timely provide analytical support for R&D/PD samples as per existing methods and Specifications

If this vacancy interests you, please send your resume to bhavini.mamtani@sequent.in

Selection Process: The selection will be on the basis of Interview.

How to Apply : Click here for full details and Apply Online

Pfizer Recruitment Data Manager-Clinical Data Sciences/Senior Data Manager

Pfizer Recruitment June 2020Bachelor’s degree minimum requirement. for Data Manager – Clinical Data Sciences/Senior Data Manager @ India- Chennai.

Vacancy details:

  • Post Name: Data Manager – Clinical Data Sciences/Senior Data Manager
  • Qualification: Bachelor’s degree minimum requirement.
  • Experienced:At least 3-4 year experience in Clinical Data Management, performing complete data review activities, in a CRO or a Pharma Company.
  • Location: India- Chennai
  • Salary :NA
  • Openings :NA

 Job Description: We have requirement for the post of Data Manager – Clinical Data Sciences/Senior Data Manager in Pfizer.

ROLE RESPONSIBILITIES

  • Participate in DMM activities including data review and query management, assist with quality database design including documentation, testing, validation, and implementation of clinical data collection tools, CRF and non-CRF, using an electronic data capture (EDC) system and/or other data collection systems, supporting the database set up activities as assigned by Senior Data Manager or Clinical Data Scientist.
  • Ensure work carried out in accordance with applicable SOPs and working practices.
  • Assist with the required study-specific DMM documents in the Trial Master File (TMF) are of high quality and are filed contemporaneously to support downstream inspection and submission readiness activities.
  • Assist with operational excellence in collaboration with Data Manager and CDS for application of standards, data acquisition, proactive data review and query management, data cleaning, e-data processing, data access and visualization, DM metrics reporting, database release, and submission related activities

Selection Process: The selection will be on the basis of Interview.

How to Apply : Click here for full details and apply online

Sun Pharmaceutical Industries Ltd Recruitment June 2020

Sun Pharmaceutical Industries Ltd Recruitment June 2020 B.Pharma in Pharmacy, Diploma in Mechanical, Any Specialization, Electrical, Electronics/Telecommunication PG :M.Pharma in Pharmacy for PRODUCTION -OFFICER / SR. OFFICER @ India- Dadra and Nagar Haveli. 

Vacancy details:

  • Post Name: PRODUCTION -OFFICER / SR. OFFICER
  • Qualification: B.Pharma in Pharmacy, Diploma in Mechanical, Any Specialization, Electrical, Electronics/Telecommunication PG :M.Pharma in Pharmacy
  • Experienced:2 – 5 years
  • Location: India- Dadra and Nagar Haveli
  • Salary :NA
  • Openings :20

 Job Description: We have requirement for the post of PRODUCTION -OFFICER / SR. OFFICER in Sun Pharmaceutical Industries Ltd.

PRODUCTION :- OFFICER / SR. OFFICER  Candidates having educational qualification of B. Pharm/  M. Pharm with 2 to 5 years of experience in manufacturing section Granulation / Compression / Coating & Packing.

PRODUCTION TECHNICIAN :- Candidates having educational qualification of ITI (Any Trade) / D.Pharm , DME , Diploma in I & C ,Diploma in E & C etc with 2 to 5 years of experience in Compression, Coating, Granulation, Packing.Details Of Walk In Interview Date : 27th June 2020 (Saturday) Time : 10 :00 AM to 09. 00 PMVenue :-  Plot No.C/1-2710, 3rd Phase, GIDC, Vapi, Gujarat – 396195

Selection Process: The selection will be on the basis of Interview.

How to Apply : Click here for full details and apply online

Lupin Limited Recruitment Manager QC

Lupin Limited Recruitment June 2020 B.Sc – Chemistry PG:MS/M.Sc(Science) – Chemistry, Any Specialization, Bio-Chemistry, Microbiology, Organic Chemistry for Manager QC @ Visakhapatnam. 

Vacancy details:

  • Post Name: Manager QC
  • Qualification: B.Sc – Chemistry PG:MS/M.Sc(Science) – Chemistry, Any Specialization, Bio-Chemistry, Microbiology, Organic Chemistry
  • Experienced:9 – 14 Years
  • Location: Visakhapatnam
  • Salary :NA
  • Openings :NA
  • Recruiter Name:Ridhi Prasad

 Job Description: We have requirement for the post of Manager QC in Lupin Limited.

Experience of handling overall activities of QC dept. as team lead

& Planning and supervising daily activities of QC function.

1. Capable to lead a team & consistent performer with people management skills

2. Successfully leading QC team for regulatory audits like USFDA, EU, ENVISA, WHO etc. in a leading role and should have working experience at managerial cadre of not less than 02-06 years

3. Well versed in handling of QC related OOS,OOT, deviation and incidence investigations, Train Staff, Operators and update their capabilities on cGMP, Safety, etc…

4. Planning, Implementing, prioritizing Quality Control Systems and jobs as per Plant requirements w.r.t. Raw Materials, in process materials and Finished Products in coordination with PDL, R & D, Production, Warehouse, Purchase, RA and QA and

5. Documentation and validation of process and analytical methods as per cGMP norms.

6. Responsible for stability management.

7. Responsible from Lab commissioning to improvement of  systems and practices.

8. Responsible for CAPA management and Change management procedures (Change control).

9. Responsible for receiving and conducting Analytical method transfers to other locations.

10. Implementation of Pharmacopoeia changes as and when required.

11. Conducting periodic audits & identify the areas of improvement

12. evaluating the requirement for the training  of Quality control personnel, further continuous training on the quality systems improvements & changes and skill level enhancement, Periodic cGMP trainings and ensure their qualifications

13. Handling of market complaints in coordination with cross functional departments14. Responsible for Analytical Method Verifications

15. Responsible for Cost control and inventory effective utilisation

16. Ensuring the safety of laboratory and personnel through best GLP practices

Selection Process: The selection will be on the basis of Interview.

How to Apply : Click here for full details and apply online

Dr.Reddy’s Laboratories Ltd Recruitment MSAT Associate – Upstream process

Dr.Reddy’s Laboratories LtdRecruitment June 2020 M Sc for MSAT Associate – Upstream process @ Biologics Divison, Dr.Reddy’s Laboratories Ltd, Bachupally, Hyderabad, Telangana, India. 

Vacancy details:

  • Post Name: MSAT Associate – Upstream process
  • Department:Biologics
  • Qualification: M Sc
  • Experienced:2 to 7 Years
  • Location: Biologics Divison, Dr.Reddy’s Laboratories Ltd, Bachupally, Hyderabad, Telangana, India
  • Salary :NA
  • Openings :03

 Job Description: We have requirement for the post of MSAT Associate – Upstream process in Dr.Reddy’s Laboratories Ltd.

  • Ensure that manufacturing processes are capable, compliant, in control, cost-effective, and continuously improved.
  • Regularly evaluate MSAT operations, developing and implementing recommended and/or necessary improvements and changes
  • Provide a science-based approach for the resolution of deviations, investigations, and process issues through analysis of historical data and scale-down studies.
  • Data collection and statistical data analysis, understanding of CPV (Continued process verification), process & equipment related investigations, experience of upstream manufacturing process, technology transfer and scale up, trouble shooting and root cause analysis, sound knowledge of cGMP.

Selection Process: The selection will be on the basis of Interview.

How to Apply : Click here for full details and apply online

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