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About the vacancy
Engineering
Process Automation
Process Automation
Quality
Quality Control
Quality Assurance
Compliance
Quality Control
Quality Assurance
Compliance
About Your Next Job
- Lead the technical implementation of new laboratory systems with cross-functional teams.
- Create and maintain administrative, technical installation, and maintenance procedures.
- Provide timely support and troubleshoot issues involving computerized systems.
- Ensure equipment implementations comply with 21 CFR Part 11 requirements.
- Contribute to laboratory systems initiatives and projects in collaboration with the global organization and in line with business needs.
- Support the team in resolving day-to-day technical challenges.
- Lead or support investigations into non-conformances involving systems, testing of raw materials, in-process materials, drug substance and drug product, and related processes.
- Define, coordinate, and implement corrections, corrective and preventive actions, and effectiveness checks.
- Act as a Subject Matter Expert and participate in inspections when required.
About Your Next Colleagues
- Work closely with cross-functional teams across departments to maintain product quality and compliance.
- Collaborate with the global organization on laboratory systems initiatives and projects.
About Your Tasks and Responsibilities
- Perform, document, and manage investigations related to quality records.
- Identify root causes and define and implement corrective actions.
- Lead the technical implementation of new laboratory systems.
- Create and maintain administrative, technical installation, and maintenance procedures.
- Provide timely support and troubleshoot issues involving computerized systems.
- Ensure equipment implementations comply with 21 CFR Part 11 requirements.
- Contribute to laboratory systems initiatives and projects.
- Support the team in resolving day-to-day technical challenges.
- Lead or support investigations into non-conformances involving systems, testing of raw materials, in-process materials, drug substance and drug product, and related processes.
- Define, coordinate, and implement corrections, corrective and preventive actions, and effectiveness checks.
- Act as a Subject Matter Expert and participate in inspections when required.
About Your Skills and Experience
- Bachelor’s degree (HBO) in Life Sciences, Computer Science, or equivalent experience in a similar role.
- Good knowledge of relevant local and global procedures, with a basic understanding of GMP regulations, FDA and EMA guidelines, and quality-control and compliance best practices.
- At least two years of experience in the pharmaceutical industry, including GMP and automation responsibilities.
- Hands-on experience in software development and programming. Laboratory experience is an advantage.
- Experience with computerized system validation in a GxP environment.
- Strong analytical, technical problem-solving, planning, and prioritization skills.
- Proven ability to build productive relationships at all levels of the organization.
- Excellent written and spoken English; Dutch is desirable.
- Proactive and able to work independently, take initiative, and prepare protocols, reports, and procedures.
About Your Benefits
- An annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions.
- Vacation days.
- Parental leave for a minimum of 12 weeks.
- Bereavement leave.
- Caregiver leave.
- Volunteer leave.
- Well-being reimbursement.
- Programs for financial, physical and mental health.
- Service anniversary and recognition awards.
- Subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans.
Where Molecules Meet Opportunities
- At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
- As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
- Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Only apply if...
- Bachelor’s degree (HBO) in Life Sciences, Computer Science, or equivalent experience in a similar role.
- Good knowledge of relevant local and global procedures, with a basic understanding of GMP regulations, FDA and EMA guidelines, and quality-control and compliance best practices.
- At least two years of experience in the pharmaceutical industry, including GMP and automation responsibilities.
- Experience with computerized system validation in a GxP environment.
- Excellent written and spoken English.
Contact person
Frank Helmus
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com