Full Job Description
This is a great opportunity for a Quality Control Analyst to join dynamic QC Team at a successful pharmaceutical company located in Hertfordshire. Our client is dedicated to developing a wide range of medicines and healthcare products.
Key Responsibilities:
The role will be diverse, with responsibilities including:
- Conducting analytical testing on raw materials, bulk products, and finished goods for both commercial manufacturing and development environments, following strict GMP guidelines.
- Performing analyses in line with established protocols using techniques such as HPLC, GC, FTIR, and Karl Fischer, including data generation, interpretation, and reporting.
- Assisting in the creation and review of laboratory documentation, including Standard Operating Procedures and Work Instructions.
To be considered for this opportunity, candidates will have the following qualifications and skills:
Essential:
- A degree (or similar) in a chemistry or related discipline.
- Strong attention to detail, with an organized and methodical approach to tasks.
- Excellent verbal and written communication skills.
- Ability to work effectively both independently and as part of a small team.
Desirable:
- Some experience with analytical techniques, recent graduates, particularly those with industrial placement experience.
- Hands-on experience with instrumental techniques, including HPLC, GC, and FTIR.
- Familiarity with Laboratory Information Management Systems (LIMS) and Chromatography Data Systems (CDS).
- Knowledge of EP, BP, and USP analytical methods.
To apply for this position, candidates must be living in the UK eligible to work.
Location
Hertfordshire
Job Type
Full Time
Salary
£24,000 - £28,000 per annum
Industry
Medicines Manufacturing
Closing Date
28th November 2024
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