Pfizer virtual interview for Vaccine & Device Regulatory CMC Team

pfizer virtual interview for vaccine device regulatory cmc6957101626327058932

hiring experienced professionals for our Vaccine Regulatory CMC Team & Devices CMC Regulatory Team at Chennai location

Work Location: Chennai

Pfizer virtual Recruitment Details

Regulatory CMC Team

  • Pfizer setting up a dedicated Vaccines Regulatory CMC Team and invite applications for Manager/Principal Manager (Individual Contributor) positions from Regulatory Affairs professionals.
  • Experience: 10-15 years of experience in Pharmaceutical Industry, mostly in Global Regulatory Affairs function
  • Hands-on experience of developing strategy and authoring CMC content for initial registrations or post-approval variations, preferably for Vaccines
  • Education: Postgraduate degree (or above) in Pharmacy/ Life Sciences

Application Process : Interested candidates may please send their resumes to India [email protected] and [email protected], following which our People Experience team will contact the suitable candidates for a virtual 1:1 interaction.

Devices CMC Regulatory Team

Work Location: Chennai

  • Pfizer hiring experienced professionals for our Devices CMC Regulatory Affairs team
  • If you are passionate about creating an impact in Medical Dences and Combination Product CMC space, in a company that creates breakthroughs that changes patients lives, here is a great opportunity
  • expanding our Devices CMC Regulatory Affairs team and looking to fill positions at Manager (Individual Contributor) level.
  • These positions will provide an exposure of leading & executing successful
  • global submissions of combination products/devices in conjunction with sterile injectables, vaccines, biologics / biosimilars and potentially other platforms in future.
  • Join us if you believe you are right fit to explore and to make a positive impact on patients lives.

Experience & Education Details : Candidates with engineering, biotech and pharmacy background with 7-10 years of experience in 21 CFR 820, EU MDD, ISO 13485, ISO 14971, Combination Product filings and Medical Devices reporting (MDR) are encouraged to send their resumes to [email protected] and
[email protected]

Suitable candidates will be contacted by our Candidate Experience team for a virtual 1:1 interview

pfizer virtual interview for vaccine device regulatory cmc6957101626327058932
Pfizer virtual interview for Vaccine & Device Regulatory CMC Team
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