Specialist Process Technician

Bristol Myers Squibb; Netherlands; On-site; EUR 50.000 - 70.000; Full time

Job summary

A global biopharmaceutical company in the Netherlands is seeking a Specialist Process Technician to be responsible for maintenance and troubleshooting of GMP process equipment. The ideal candidate will have at least 3 years of maintenance experience, specifically in GMP facilities, and a MBO level 4 diploma. This role involves ensuring compliance with safety protocols and operating in a 24/7 operational environment.

Qualifications

• 3+ years of experience in maintenance, preferably related to process and lab equipment.
• Direct experience working in GMP facilities with understanding of GMP practices.
• Ability to work in a 24/7 operation shift and follow safety protocols.

Responsibilities

• Execute maintenance activities and operate clean utility and process equipment.
• Ensure compliance with GxP regulations and store documentation in CMMS.
• Provide troubleshooting for clean utilities and lab equipment.

Skills

Troubleshooting and repair of electro-mechanical systems

Attention to detail

Excellent communication skills in English

Proficient in Computerized Maintenance Management Systems

Education

MBO level 4 diploma or technical degree

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.

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.

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 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.
• 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.

Qualifications & Experience

Education:

• Requires at least a 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.

Bristol Myers Squibb is an equal employment opportunity employer and is committed to providing equal employment opportunities to all qualified applicants. We will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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.