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About the vacancy
Production
Process Automation
Manufacturing Engineering
Process Engineering
Maintenance
Electrical & Mechanical
Facility & Equipment
Repair & Maintenance
Oncology & Hematology
Cell Therapy
About Your Next Job
The Specialist Process Technician is responsible for performing/providing maintenance, installation, and troubleshooting of GMP process equipment used in manufacturing, warehouse and analytical labs at the production site. All work to be completed safely and to assure minimal impact to production while complying with cGMPs.
About Your Next Colleagues
Our employees are passionate about making a difference in patients’ lives. This unwavering commitment gives us a distinct advantage in delivering life-saving treatments to patients, faster.
About Your Tasks and Responsibilities
- Execute routine to intermediate level maintenance activities and operate plant clean utility and process & lab equipment to sustain a cell therapy biopharmaceutical manufacturing facility in accordance with CFRs, SOPs, job plans, and BMS policies.
- Assures that all documentation is stored in CMMS and Document Management Systems compliant to GxP regulations.
- Participates in a detailed training program, to develop one’s knowledge in the maintenance and operations field, as well as other areas of the facility.
- Assists in review related SOPs or job plans/work plans for work related areas.
- Provides basic troubleshooting of clean utilities and process & lab equipment/systems.
- Requires on-call duty and if needed overtime and weekend hours. Works on assignments that are moderately complex in nature where judgment is required in resolving problems and making routine recommendations.
- Contact with F&E Team, Manufacturing, Warehouse & Lab Operators and Vendors.
- Will have daily contact with her/his supervisory staff for work assignments and coaching.
About Your Skills and Experience
- 3+ years of experience in maintenance, preferably related to process-,lab equipment and clean utilities.
- Direct experience working in GMP facilities, including understanding of GMP record keeping and documentation practices.
- Proven expertise in troubleshooting and repair of electro-mechanical systems and instrumental equipment.
- 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, pro-active, and able to work with minimal supervision.
- Excellent written and verbal communication skills in English
Where Molecules Meet Opportunities
Mentorship, leadership, growth and inclusion. These are just some of the benefits of a career with BMS.
Contact person
Talent Acquisition
At Bristol Myers Squibb, your work helps people prevail over serious diseases. From the scientists behind the microscope to the analysts behind the data, everyone at BMS is working to make an impact. And while our work transforms the lives of patients, it also transforms the lives and careers of our people.
This isn’t easy work, but it is uniquely interesting. You’ll rewrite the rules, solve the toughest challenges, and create miracles.
The BMS Leiden manufacturing facility is our first European site for CAR T cell therapies, joining our global network of facilities transforming care for patients with blood cancer and other serious diseases. Equipped with the latest technology and state-of-the-art production facilities, the facility represents our commitment to ensuring supply of CAR T therapies.