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Are you a detail-oriented technician with a passion for precision and quality? Join a leading medical device manufacturer where innovation and compliance meet excellence. We are seeking a Calibration Technician to maintain, improve, and ensure the reliability of critical production and lab equipment. This is a dynamic role that offers exposure to high-tech environments and the opportunity to directly support life-saving technology.

• Perform scheduled and ad-hoc calibrations on production and facilities equipment per approved procedures.
• Identify and manage Out-of-Specification (OOS) conditions; initiate Calibration Alerts and inform QA as required.
• Document all calibration activities in accordance with internal procedures and regulatory requirements.
• Develop and revise Standard Operating Procedures (SOPs) for calibration processes and new equipment.
• Support manufacturing and laboratory operations by ensuring accurate, reliable equipment performance.
• Establish and maintain calibration and test methods for both new and existing assets.
• Troubleshoot calibration issues and perform root cause analyses to ensure continuous improvement.
• Ensure all records are accurately completed and easily retrievable for audit readiness.
• Actively participate in cross-functional teams, projects, or initiatives that contribute to company goals.
• Attend relevant training and report any tasks requiring additional qualification or supervision.
• Perform other duties as assigned by the supervisor.

Functie-eisen

Minimum Requirements:

• Associate Degree in Industrial, Electrical, Mechanical, Instrumentation, Electronics or related field.
• Professional certifications as required by local regulations.
• Proficient in MS Office and SAP; comfortable working with digital systems.
• Excellent written and verbal communication skills.
• Ability to work independently under tight deadlines with a proactive, positive attitude.

Technical Competencies:

• Strong technical understanding of pharmaceutical or medical device production equipment.
• Proficient in reading and interpreting mechanical drawings, electrical schematics, and technical documents.
• Demonstrated ability to perform root cause analysis and implement corrective actions.
• Basic knowledge of aseptic techniques and cGMP compliance.
• Automation and instrumentation knowledge preferred (depending on functional area).
• Familiarity with safety, health, and environmental regulations in a manufacturing setting.

Arbeidsvoorwaarden

What We Offer:

• Be part of a team dedicated to advancing healthcare and improving lives.
• Work in a collaborative, safety-focused environment with cutting-edge equipment.
• Opportunities for professional growth, training, and development.
• Competitive salary and benefits package.

Bedrijfsinformatie

Apply today to become a key contributor in maintaining the integrity and reliability of equipment that shapes the future of medical innovation.

Why YACHT?

Because of challenging positions at leading companies, a large network and development opportunities! These are the advantages of working via YACHT.

With us, you will get all the space to grow further. Together we will look for assignments that suit your ambitions and help you to realize your goals. Through coaching, for example, but also by inviting you to interesting courses, knowledge sessions and inspiring meetings.

Through us, you will get access to a large network of professionals and companies that are happy to share their knowledge and opportunities with you.

We are currently seeking an experienced and driven Automation Engineer (BMS/EMS) to join the Execution Systems (MAM-ES) Department at Janssen Biologics BV in Leiden. This is an exciting opportunity to work at the forefront of pharmaceutical manufacturing automation in a collaborative, highly professional, and fast-paced environment.

As part of a team of 60 passionate automation professionals, you will be instrumental in designing, implementing, and supporting cutting-edge Building Management Systems (BMS) and Environmental Monitoring Systems (EMS), contributing directly to the production of life-saving medicines.

• Lead the design, implementation, and installation of the Building Automation System (BAS) and Environmental Monitoring System (EMS – Honeywell), aligned with cGMP standards.
• Provide expert-level maintenance and ongoing support for BMS systems, ensuring safety, quality, and regulatory compliance.
• Act as liaison for external vendors, subcontractors, and system integrators, ensuring smooth and compliant delivery of automation solutions.
• Manage and coordinate automation change activities within a multidisciplinary engineering team.
• Develop and execute commissioning protocols, test plans, validation documentation, and system lifecycle deliverables.
• Review, update, and maintain system documentation, SOPs, and work instructions in compliance with GxP standards.

Functie-eisen

• A Bachelor’s degree (HBO level) or higher in Industrial Automation, Electrical Engineering, or related technical discipline.
• 2–5 years of hands-on experience in automation within the biotech or pharmaceutical industry.
• 3+ years of solid experience with modern BMS platforms; Honeywell systems (HC900, EBI R600) and/or Priva experience is highly preferred.
• Working knowledge of GAMP 5, control philosophies, functional specifications, and lifecycle documentation.
• Ability to read and interpret P&IDs and work with instrumentation and control equipment in an industrial setting.
• Strong communication skills in English (written and verbal), Dutch is a Plus.
• VCA and NEN 3140 certifications (mandatory).
• A proactive, detail-oriented, and collaborative mindset, capable of working independently and as part of a dynamic team.

Arbeidsvoorwaarden

What We Offer:

• Be part of a leading global healthcare organization under the Johnson & Johnson umbrella.

• Work in a mission-driven environment contributing to innovative therapies that impact global health.

• Collaborate with some of the brightest minds in automation and pharmaceutical manufacturing.

• Enjoy a long-term project (12+ months) with high potential for extension or transition to future opportunities.

Bedrijfsinformatie

Apply now and bring your expertise to one of the most dynamic and impactful teams in the pharmaceutical industry.

Why YACHT?

Because of challenging positions at leading companies, a large network and development opportunities! These are the advantages of working via YACHT.

With us, you will get all the space to grow further. Together we will look for assignments that suit your ambitions and help you to realize your goals. Through coaching, for example, but also by inviting you to interesting courses, knowledge sessions and inspiring meetings.

Through us, you will get access to a large network of professionals and companies that are happy to share their knowledge and opportunities with you.

Join Janssen Biologics B.V., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and become part of a world-leading organization dedicated to the development, production, and marketing of vaccines and antibodies to combat infectious diseases.

At our Leiden site, As a Technical Specialist, you will be the driving force behind quality and compliance in our laboratory operations. You’ll manage medium- and high-priority compliance issues, lead investigations, and serve as the subject matter expert during audits and product transitions. You’ll also play a pivotal role in maintaining cGMP compliance, leading continuous improvement projects, and guiding your team with safety, compliance, and reliability as your core values.

• Lead investigations for deviations and non-conformances, coordinating corrective and preventive actions (CAPAs).
• Act as Subject Matter Expert (SME) during audits and inspections.
• Serve as the single point of contact (SPOC) for new product introductions, lab investigations, and equipment qualifications.
• Own and manage technical systems related to (analytical) lab equipment.
• Review and update lab documentation, particularly in support of new product introductions (NPIs).
• Provide hands-on technical support and collaborate with local/global customers and service teams.
• Champion and lead continuous improvement (LEAN) initiatives.
• Foster strong communication and trusted relationships with lab technicians, cross-functional teams, and leadership.

Functie-eisen

We’re looking for a detail-oriented, technically strong individual who can independently handle complex lab quality challenges while actively contributing to a high-performance, collaborative environment.

• Bachelor’s degree (HLO) or higher in Life Sciences, Molecular Biology, or related fields.

• Proficient in English (written & verbal).

• Demonstrated ability to work independently and within cross-functional teams.

• Experience with microbiological techniques (e.g., bioburden, endotoxin, sterility) is highly preferred.

• Analytical mindset with strong technical problem-solving skills.

• Prior GMP experience is a plus.

Arbeidsvoorwaarden

What We Offer:

• Flexible working hours
• Opportunities to work on exciting projects with real impact
• A collaborative, inclusive, and inspiring workplace
• Global career development pathways and educational support
• Competitive salary and benefits package
• Being part of a purpose-driven, diverse, and motivated team

Bedrijfsinformatie

Join our team and help shape the future of healthcare. Apply today and become part of a company that’s not just leading the industry but also changing lives around the world.

Why YACHT?

Because of challenging positions at leading companies, a large network and development opportunities! These are the advantages of working via YACHT.

With us, you will get all the space to grow further. Together we will look for assignments that suit your ambitions and help you to realize your goals. Through coaching, for example, but also by inviting you to interesting courses, knowledge sessions and inspiring meetings.

Through us, you will get access to a large network of professionals and companies that are happy to share their knowledge and opportunities with you.