Experienced CMC Regulatory Affairs Scientist
Join us to apply for the Experienced CMC Regulatory Affairs Scientist role at Johnson & Johnson Innovative Medicine.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, profoundly impacting health for humanity. Learn more at https://www.jnj.com
Job Function: Discovery & Pre-Clinical/Clinical Development
Job Sub Function: Regulatory Science
Job Category: Scientific/Technology
All Job Posting Locations: Warsaw, Masovian, Poland
Job Description
We are searching for the best talent for an Experienced CMC Regulatory Affairs Scientist to be in Warsaw, Poland.
Purpose
The CMC Regulatory Affairs Scientist contributes to the development of global CMC regulatory strategies, dossier plans, and submissions in collaboration with other CMC RA personnel.
You Will Be Responsible For
- Assist in execution of the development strategy that meets global regulatory requirements over the lifecycle of the product.
- Support global regulatory filings for development compound and marketed products in collaboration with/under supervision of other CMC RA senior personnel.
- Develop CMC content and dossier plans.
- Assist in the preparation of dossiers for submission to Health Authorities (NDA/BLA/MAA/IND/CTA and post approval variations).
- Assist in preparing country‑specific required documents to global submissions.
- Assist with CMC RA submissions for renewals and annual product submissions.
- Assist in preparing responses to Health Authority questions or other communications.
- Provide CMC Regulatory support to Health Authority inspections.
Qualification / Requirements
- BS in engineering, biology, pharmaceutical or chemical sciences with generally a minimum of 0–2+ years of experience inclusive of post‑graduate education and/or pharmaceutical or health care industry experience. MS, PhD, or Pharm. D. degrees preferred.
- Good verbal and written communication skills.
- Good organizational skills.
- Strong attention to detail.
- Proficient understanding of biology, chemistry and/or engineering relevant to pharmaceutical products.
- Understanding scientific principles for the manufacture of drug substance and drug product and/or devices.
- General knowledge of drug development and lifecycle management.
Seniority Level
Not Applicable
Employment Type
Full‑time
Job Function
Legal
Industries
Pharmaceutical Manufacturing
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