Job Title: Documentation Analyst
Location: New Brunswick, NJ (Hybrid)
Job Summary:
- Join our team as a Documentation Analyst where you’ll play a crucial role in compiling scientific information, authoring regulatory documents, and conducting data integrity checks. This role is integral to the timely submission of both investigational and marketing applications for small and large molecules.
Job Responsibilities:
- Compile information from scientists for document preparation
- Author the chemistry, manufacturing, and controls (CMC) sections of regulatory documents
- Perform data integrity checks
- Evaluate analytical data critically
- Collaborate constructively with team members for problem-solving
Skills Required:
- Experience in Regulatory Documentation and/or Authoring (beyond just formatting)
- Ability to multitask effectively
- Strong oral and written communication skills
- Background in the pharmaceutical industry
- Solid knowledge of organic or medicinal chemistry
Education:
- A B.S. in Chemistry is required. Candidates with an M.S. or Ph.D. in Organic or Medicinal Chemistry are strongly preferred.
About SSi People:
With over 26 years of industry experience, SSi People has built its reputation and expertise on putting people first. Everything we do works toward delivering an exceptional experience for our consultants, our clients, and our internal team. Through a genuine commitment to people in everything we do. We have developed refined processes and a stellar internal team to deliver talent quickly. More importantly, we focus on building long-term relationships, not transactions. Putting people first is just what we do well.
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