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MSG
Bristol Myers
Production Specialist
Full-Time
England, United Kingdom
Health & Biotech
Health & Biotech
12 March 2025
Description
- Demonstrate knowledge of cGMPs in clinical supply packaging and labeling.
- Review and prioritize production schedules and orders.
- Ensure compliance with cGMPs and SOPs, using SAP for documentation.
- Generate COSHH, safety risk assessments, procedures, and guidelines.
- Liaise with Packaging & Labeling, Quality, Logistics, and Quality Control teams.
- Ensure adherence to health and safety guidelines.
Qualifications
- Supervisory experience in production, with skills in scheduling, organizing, and team building.
- Knowledge of cGMP requirements in clinical packaging and labeling.
- Excellent attention to detail and adherence to procedures and regulations.
- Understanding of the pharmaceutical development process.
- Effective communication and leadership in a team environment.
- Ability to manage competing priorities, adapt to change, and handle additional responsibilities.
- Proficiency in MS Office, MS Outlook, and industry software (e.g., SAP, Veeva).
- Ability to schedule multiple jobs/orders effectively.
- Required Education and Experience
- Bachelor of Science or a Mechanical Engineering Degree, ideally
- Demonstrated experience in a pharmaceutical industry, required
- Experience in Pharmaceutical manufacturing with a focus in the production of Clinical Trial Supplies, preferred
- Extensive experience of progressive leadership or supervisory experience in the pharmaceutical industry, required .
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