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Production Specialist

Production Specialist

Bristol-Myers SquibbMoreton, England, United Kingdom
4 days ago
Job type
  • Full-time
Job description

Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more : careers.bms.com / working-with-us

Position Summary

We are looking for a dynamic Production Specialist to join our experienced team in the packaging and labeling of clinical supplies.

In this role, you will oversee the GMP, safety, and procedural aspects of producing supplies in a state-of-the-art cGMP production area. Your expertise will ensure that our high standards are consistently met.

We are seeking candidates with prior experience in the pharmaceutical industry, ideally with a background in clinical trials packaging.

If you have a keen eye for detail and a commitment to excellence, we want to hear from you!

Key Responsibilities

  • 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.

Required Skills

  • 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 .

    • If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

    Uniquely Interesting Work, Life-changing Careers

    With a single vision as inspiring as “Transforming patients’ lives through science,” every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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