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Manufacturing Associate

Manufacturing Associate

Bristol-Myers SquibbLeiden, Zuid-Holland, Netherlands
11 dagen geleden
Functieomschrijving

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.

Bristol Myers Squibb Netherlands

Bristol Myers Squibb has been active in the Dutch market for over 50 years, employing people across a range of activities and business units in Utrecht, The Netherlands.

The Netherlands is also home to our first European Cell Therapy facility, located at the Leiden Bio Science Park, the largest life sciences cluster of The Netherlands. This new state-of-the-art facility is focused on commercial manufacturing with capabilities for multi-product Cell Therapy manufacturing. You can become part of this exciting journey.

Would you like to become an important chain in our worldwide network to bring this new personalized treatment to patients suffering from blood cancer? Join us and be a game changer!

The primary purpose of the Manufacturing Associate role is to complete production assignments with high quality and timely output in a cellular therapeutic manufacturing environment.

Job Responsibilities :

  • Works on routine manufacturing assignments per written procedures, where ability to recognize deviation from accepted practice is required.
  • Adheres to Good Manufacturing Practices and standard operating procedures.
  • Measures and checks raw materials. Assembles, cleans and sanitizes process equipment and / or assemblies.
  • Completes work instructions and maintains clean room environment to comply with regulatory requirements.
  • Trains for proficiency in the operation of primary production equipment within the assigned functional area.
  • Trains for proficiency in process systems (i.e. Syncade MES and SAP interfaces) and some supporting business systems (i.e. Maximo, DeltaV, etc.).
  • Assists with the revision and / or creation of process documents, such as SOPs and electronic work instructions.
  • Assists in maintaining material and components inventory level.
  • Supports safe work environment.
  • Works on assignments that are routine in nature where judgment is required in resolving problems and making routine recommendations.

WORKING CONDITIONS :

  • Should be able to work in a cleanroom environment that requires gowning.
  • Should be able to stand for extended periods of time.
  • Required to move manufacturing material bags several times a day while handling production equipment and / or materials.
  • Work in areas that may have magnets.
  • Work in areas where handling human blood products (ML-II) may be required.
  • May work in areas with exposure to vapor phase liquid nitrogen.
  • Should be able to work nights, weekends, and in shift rotation that can be up to 24 / 7 / 365.

    • Qualifications and Education Requirements :

  • MBO 3 or 4 in sciences is Minimum and / or equivalent combination of education and experience is required.
  • 0-3 years of cGMP manufacturing experience is desired or equivalent in work experience or education. Validated experience working on teams where combined contribution, collaboration, and results were expected.
  • Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web-based applications. Experience where attention to detail and personal accountability were critical to success.
  • Maintains a professional and productive relationship with area management and co-operators.
  • Ability to work in a later stage in 24 / 7 operation shift.
  • Attention to detail and follow-through.
  • Unwavering commitment to implement and follow safety protocols and work practices.
  • Experience in working with Computerized Maintenance Management Systems.
  • Self-motivated, proactive, and able to work with minimal supervision.
  • Excellent written and verbal communication skills in English.

    • Why You Should Apply

    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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