Gmp Qc Inspector
3 days ago
We’ve an exciting opportunity for a hard-working individual who is capable of working independently as well as within a team. Our GMP QC department are looking to recruit a GMP QC Inspector based in Manchester. As part of the onboarding training program and continued development; training is based in Leeds and will last from 3 to 6 months.
MAC is a full-service global Contract Research Organisation (CRO). We also own a network of research sites. Our mission is to serve with honesty and integrity to make an outstanding contribution to human health.
This is a full-time permanent position
Main Responsibilities
- Inspection and approval of clinical trial medicinal products
- Review of associated documentation
- Ability to prioritise workload and deal with changes to priorities to support a fast-paced ever changing manufacturing environment
- Liaise and communicate with multiple departments to facilitate the on-time release of products.
Key Skills and Requirements
- GMP Production experience (e.g. pharmacy or medical devices) - essential
- Good interpersonal skills
- Very good skills with Microsoft Office (eg Word, Excel)
- The ability to write clear and concise reports
- Good attention to detail and excellent organisational ability
- Sufficient initiative to be able to work alone and with a team
- Background in Microbiology, Chemistry or similar life science would be an advantage
- Some experience in a clinical environment would be useful
BENEFITS:
- Competitive salary in keeping with pharmaceutical industry standards and will reflect experience
- Health Insurance
- Free onsite parking
- 25 days annual leave (increasing in increments to 30 days after 6 years service)
- Your birthday off work
Application question(s):
- are you able to commit to 3-6 months of travelling to Leeds for training?
- Do you have experience with Good Manufacturing Practice (Pharmaceutical or Medical Devices)?
Work authorisation:
- United Kingdom (required)
Work Location: In person
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