Unfortunately, we are unable to offer visa sponsorship for this role.
This is a permanent full time position, working a 35 hour week, 7 hours per day flexibly between 7am & 7 pm on 5/7 days as per business needs.
As a Pharmaceutical Analyst you will perform analysis of pharmaceutical raw materials, drug substance, and finished product and produce accurate results within an acceptable timeframe.
Job Responsibilities that you be covering:
- You will perform routine and non-routine analysis using both traditional and modern analytical techniques, including HPLC, Dissolution, and Karl Fischer determination, ensuring all work is completed within a GMP framework and in line with client requirements.
- You will review analytical data to confirm compliance with GMP standards, ensuring accuracy, completeness, and adherence to approved methods and procedures.
- You will initiate, investigate, and follow up on OOS results and action limits in accordance with client procedures, ensuring timely escalation and appropriate documentation.
- You will document all data in line with current client policies and procedures, maintaining accurate, traceable, and compliant laboratory records.
- You will monitor and report productivity through agreed performance metrics, including test volumes, cycle times, laboratory or product related issues, and hours worked per project.
- You will prepare and approve analytical results for tests in which you are trained and deemed competent, ensuring data integrity and adherence to all regulatory and client expectations.