Schedule: Fri-Monday 8am-6pm (4x10).
Location ; Norton MA
Duration : 5- months
Overview
The Analyst I in Quality Control Operations will play a critical role in executing assays, generating accurate and reliable data, and supporting the general operations of the laboratory to ensure the quality and compliance of our products from development through to commercialization.
This position is onsite and will be primarily located in Norton, MA. There may occasional responsibilities at a secondary location in Cambridge, MA.
Qualifications
- Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field
- 0 to 2 years of experience in a GMP/GLP regulated laboratory environment, with exposure to pharmaceutical or biotechnology industries preferred
- Understanding of analytical techniques and their application in raw materials, in-process testing, release, and stability studies is preferred
- Strong documentation skills and attention to detail, with an unwavering commitment to quality and compliance
- Basic awareness of regulatory guidelines relevant to pharmaceutical QC (GMP, GLP, ICH) is desirable
- Effective communication and teamwork skills, with the ability to work collaboratively across functions
- Capable of working under supervision and following detailed instructions
