What are the responsibilities and job description for the Research Associate II (Quality Control) position at Zenith LifeScience LLC?
Job Description
This position provides Quality Control testing of in process and final product testing. Looking for experience with cell culture, RT-qPCR, Immunofluorescence, cell based assays etc. this is an onsite role
ESSENTIAL JOB RESPONSIBILITIES:
Perform routine in-process and release QC testing of cell products.
Execute analytical method validations and transfers including drafting technical protocols, reports and troubleshooting.
Maintain, calibrate and operate equipment and instruments supporting cell bioassays, Flow Cytometry, ELISA and PCR assays.
Track and test products according to stability protocols. 5) Work with internal and external resources to maintain lab in an optimal state.
Monitor and trend data, complete routine record review of test data and related documents for in-process testing, drug substance and drug product release.
Develop, revise and review SOPs, qualification/validation protocols and reports. 8) Conduct investigations regarding out of specifications (OOS) results. Address and manage deviations related to analytical procedures.
Monitor the GMP systems currently in place to ensure compliance with documented policies. Perform other lab duties as required.
REQUIRED:
Bachelor or Master's degree in biotechnology or related field with 5 years of Quality Control experience.
Knowledge of GMP, SOP?s and quality control process
Experience in the biotech and/or pharmaceutical industry.
Ability to work weekends.
Job Types: Contract, Temp-to-hire
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Experience:
- Quality assurance: 1 year (Preferred)
Ability to Commute:
- Westborough, MA 01581 (Required)
Ability to Relocate:
- Westborough, MA 01581: Relocate before starting work (Required)
Work Location: In person
