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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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