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PHARMA JOBS POST > Hiring > Seeking Top Talent for Fresenius Kabi’s Global Vigilance Centre and Regulatory Affairs
HiringR&DRegulatory Affairs

Seeking Top Talent for Fresenius Kabi’s Global Vigilance Centre and Regulatory Affairs

ADMIN
Last updated: August 2, 2024 1:01 pm
ADMIN 2 years ago
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FRESENIUS KABI multiple openings for Executive/ Research Scientist / Sr. Research Scientist- Analytical Development, Procurement, Chemical Research, Global Vigilance Centre, Regulatory Affairs

Research Scientist / Sr. Research Scientist- Analytical Development

Qualifications: M.SC/ M. Pharm in chemistry.

Experience required: 3-5 yrs 2 to 5 years in analytical development for method development, method validation and other analytical skills.

Job Description:

Routine analysis of API, intermediate and raw material for reaction monitoring, chromatographic purity and assay by UPLC, HPLC, IC.

  • Stability analysis of API & intermediates for related substances, assay by UPLC & HPLC

Standard qualifications (reference/working) of drug substances intermediates, impurities and raw materials UPLC, HPLC, IC.

  • Calibration & Maintenance of HPLC, UPLC, KF, Weighing balances pH meter in given calibration schedule as per GLP & follow the GLP in laboratory in respect of e-LNB writing, cleanliness, Log book entries.

Research Scientist / Sr. Research Scientist – Chemical Research

Qualifications: M.Sc/ PhD in Organic Chemistry.

Experience required: 1-6 years of experience in chemical process development for M.Sc and 1- 3years experience for PhD.

Job Description:

Planning and execution of lab experiments for feasibility, process optimization, validation studies indicative stability, critical process parameter identification/risk-assessment & lab

  • Preparation of study protocols, study reports, RM/Intermediate/API specifications, Technology Transfer Documents etc.
  • Technology transfer to internal and external production units

Sr. Research Scientist-II- Regulatory Affairs

Qualifications: M.Sc (Chemistry)

Experience required: 7-8 years

Job Description:

  • Review of research & development documents of API
  • Assessment and Review of Technical package / DMF
  • Evaluation of impurities

Research Scientist/ Sr.Research Scientist Global Vigilance Centre

Qualifications: M.Pharm

Experience required: 2-5 yrs in Medical Writing

Job Description:

  • Authoring and quality review of aggregate reports including PADERS, PSURS, and PBRERS
  • Author risk management plans and signal management reports.

Executive – Procurement

Qualifications: B.Pharm/ B.Tech/ M.SC/ M.Pharm.

Experience required: Graduate and Post Graduate Diploma in Materials Management

Share your referrals to aruna.tanwar@fresenius-kabi.com by 7th August, 2024

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TAGGED: Regulatory Affairs, Regulatory Affairs Jobs Vacancy
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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
Previous Article Join Titan Laboratories: Walk-In Interviews for Regulatory Affairs Department on Aug 3, 2024!
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