Specialist, Process Technician

Qabird; Leiden; On-site; EUR 45,000 - 60,000; Full time

Job summary

Qabird in Leiden, Netherlands is seeking a Specialist Process Technician responsible for maintaining, installing, and troubleshooting GMP process equipment at the production site. The ideal candidate possesses at least an MBO level 4 diploma and 3+ years of maintenance experience, particularly in GMP facilities. Strong attention to detail and excellent communication skills in English are essential. The position requires onsite presence for all shifts as part of the company’s operational structure, and the role may involve on-call duties and overtime.

Qualifications

• 3+ years of maintenance experience, preferably related to process and lab equipment.
• Direct experience working in GMP facilities with knowledge of record keeping and documentation.
• Self-motivated, pro-active, and able to work with minimal supervision.

Responsibilities

• Execute routine to intermediate level maintenance activities.
• Operate clean utility and process equipment to sustain a biopharmaceutical manufacturing facility.
• Provide basic troubleshooting of clean utilities and equipment systems.

Skills

Troubleshooting and repair of electro-mechanical systems

Attention to detail

Excellent written and verbal communication skills in English

Proficiency in Computerized Maintenance Management Systems

Education

MBO level 4 diploma or technical degree

Job description

We offer a wide variety of competitive benefits, services and programs that provide 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 and providing maintenance, installation, and troubleshooting of GMP process equipment used in manufacturing, warehouse and analytical labs at the production site. All work is 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.
• Ensure 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.
• Require on-call duty and, if needed, overtime and weekend hours. Work 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.
• Have daily contact with 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.

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.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [e-mail]. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.