Job description
Research Associate
The duties of post: Prepare and review protocol, deviations, change control CoA (CofA) to investigate incidents of out of specification (OOS) results and action appropriately. Plan & Develop information materials and analyseproduct development trials from R&D and controlthe quality of drug products by following GMP, GLPand Provide technical assistance for the maintenanceof lab environment according to GLP and ICHGuidelines, instrument calibration (schedule prepare and updating), performance report checking and AMC (Annual maintenance contract), Communicate and support to the quality officers in the development and completion of QC tasks. Prepare information materials concerning the users, properties, and risks of particular drugs to perform method validation and method transfer activities for finish products. Prepare and review protocol, deviations, change control CoA (CofA) to investigate incidents of out of specification (OOS) results and action appropriately. Retain and apply up to date knowledge of analytical techniques andequipment including HPLC, GC, FTIR, Dissolution, Kirl Fisher, and UV-vis.
The skill, experience and qualifications required for each post: Applicant must have Master's in chemistry or Pharmaceutical science with 12 to 15 year of experience.
· Critical thinking.
· Technical skills.
· Data collection.
· Data analysis.
· Attention to detail.
· Ability to maintain quality.
· Safety and/or infection control standards.
· Planning and scheduling.
Job Type: Full-time
Salary: £35,000.00-£40,000.00 per year
Benefits:
- Company pension
Schedule:
- Monday to Friday
Ability to commute/relocate:
- Edgware, HA8 5AW: reliably commute or plan to relocate before starting work (required)
Education:
- Master's (preferred)
Work Location: In person