Senior Specialist Process Technician at BristolMyers Squibb
Leiden, Zuid-Holland, Netherlands -
Full Time


Start Date

Immediate

Expiry Date

09 Jun, 25

Salary

0.0

Posted On

10 Mar, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

English, Mechanical Systems, Gmp, Maintenance

Industry

Mechanical or Industrial Engineering

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

The Sr. 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.

Job Responsibilities:

  • Maintain/execute routine to intermediate level maintenance activities, and operate plant clean utility and process & lab equipment in order to sustain a cell therapy biopharmaceutical manufacturing facility in accordance with CFRs, SOPs, job plans, and BMS policies
  • Ensures that all documentation for work tasks is completed with accurate information following good documentation practices (GDP)
  • Participates in a detailed training program, in order to develop one’s knowledge in the maintenance and operations field, as well as other areas of the plant
  • Assists in the development and revision, and 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, coaching and general management discussions
  • Occasional contact with other line management staff relating to specific project responsibilities may be expected

Qualifications and Education Requirements :

  • Requires at least a MBO level 4 diploma, technical degree preferred and/or equivalent experience in maintenance, or related technical discipline
  • Ability to work in a later stage in 24/7 operation shift
  • Proficiency in reading and writing English
  • 5+ years total related experience in process & lab equipment and clean utilities maintenance
  • Direct experience working in GMP facilities, including a thorough understanding of GMP record keeping and documentation practices
  • Proven expertise in troubleshooting and repair of electro-mechanical systems and instrumental equipment
  • Attention to detail and follow-through
  • Unwavering commitment to implement and follow safety protocols and work practices
  • Knowledge of Computerized Maintenance Management Systems

LI-Onsite

Disclaimer: For any third parties or external agencies, please, be informed we do not accept unsolicited requests, proposals, applications or profiles for any of our roles at BMS.

Responsibilities
  • Maintain/execute routine to intermediate level maintenance activities, and operate plant clean utility and process & lab equipment in order to sustain a cell therapy biopharmaceutical manufacturing facility in accordance with CFRs, SOPs, job plans, and BMS policies
  • Ensures that all documentation for work tasks is completed with accurate information following good documentation practices (GDP)
  • Participates in a detailed training program, in order to develop one’s knowledge in the maintenance and operations field, as well as other areas of the plant
  • Assists in the development and revision, and 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, coaching and general management discussions
  • Occasional contact with other line management staff relating to specific project responsibilities may be expecte
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