Specialist, Process Technician

Bristol Myers Squibb; Oegstgeest; On-site; EUR 35,000 - 55,000; Full time

Job summary

Bristol Myers Squibb in Oegstgeest is seeking a Specialist Process Technician responsible for maintenance and troubleshooting of GMP process equipment. The ideal candidate will have a technical degree and 3+ years of relevant experience in a biopharmaceutical manufacturing environment.

This role requires keen attention to detail, the ability to work independently, and a commitment to safety protocols. The position includes on-call duty and potential overtime, and is essential for maintaining high production standards.

Qualifications

• 3+ years of experience in maintenance, preferably related to process-lab equipment.
• Proven expertise in troubleshooting and repair of electro-mechanical systems.
• Self-motivated, pro-active, and able to work with minimal supervision.

Responsibilities

• Perform maintenance and troubleshooting of GMP process equipment.
• Execute routine maintenance activities in accordance with SOPs and BMS policies.
• Participate in training to develop maintenance and operations knowledge.

Skills

Troubleshooting electro-mechanical systems

Experience with clean utilities

Attention to detail

Proficient English communication

Education

MBO level 4 diploma or technical degree

Tools

Computerized Maintenance Management Systems

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. Take your career farther than you thought possible.

Position Summary

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 is to be completed safely and to assure minimal impact to production while complying with cGMPs.

Key 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.
• Assure that all documentation is stored in CMMS and Document Management Systems compliant to GxP regulations.
• Participate in a detailed training program, to develop one\'s knowledge in the maintenance and operations field, as well as other areas of the facility.
• Assist in review related SOPs or job plans/work plans for work related areas.
• Provide 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 his supervisory staff for work assignments and coaching.

Qualifications & Experience

Education

• At least an MBO level 4 diploma, technical degree preferred and/or equivalent experience in maintenance, or related technical discipline.
• Proficiency in reading and writing English.

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.

Working Conditions

Basic lifting involved, accessing large manufacturing equipment, gowning for clean/controlled areas, exposure to chemicals, access to secured areas, exposure to confined space, ability to work at different heights.

Reasons to 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 a supportive culture, promoting global participation 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.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

• Site-essential roles require 100% of shifts onsite at your assigned facility.
• Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture.
• For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People With Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Additional Information

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.

Job Reference

R1601750: Specialist, Process Technician