Senior Manufacturing Engineer
TLDR
Lead end-to-end equipment validation and global rollout for production lines, shaping validation docs and training.
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 jnj.com.
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.
Job Function:
Supply Chain EngineeringJob Sub Function:
Manufacturing EngineeringJob Category:
Scientific/TechnologyAll Job Posting Locations:
Groningen, NetherlandsJob Description:
We are Johnson & Johnson Surgical Vision Groningen, the Netherlands, and member of Johnson & Johnson's Family of Companies.
The department of Manufacturing Engineer, Asset management, is looking for an ambitious and experienced manufacturing engineer for equipment implementation activities. As Sr Manufacturing Engineer, you will work in full collaboration with the engineering teams with focus on technology & equipment development with a strong emphasis on validation. In this role you are the expert that help deliver solutions to meet the design requirements, quality and the business targets and lead the roll out to our production lines. Support the handover to other departments by providing the adequate documentation and training.
Responsibilities:
- Technical writing of protocols and performing validations in collaboration with Subject Matter Expert (SME))
- Gather requirements, and/or user stories, specifications and write (URS, TM, FAT, IQ OQ, PQ.) for machines & equipment including the software component.
- Will be a subject matter expert GXP, GMP & CSV as it pertains to hardware equipment solutions within the medical device arena.
- You are very familiar with change control in a medical device environment and are capable and comfortable in leading validation activity from the creation of CR, URS, VP, etc incl. creating and execution of test protocols, Writing reports of protocol outputs. Up to the closure of VSR and CR.
- Communication with and support of other departments such as R&D, Quality Assurance (QA), Operations, External suppliers etc within the scope of work defined by the project deliverables.
- Implement new equipment validation in a way that enable seamless global scaling of those equipment and processes within our organisation.
- Design, develop and implement test plans, validation documents and be accountable for the delivery and completion of those activities.
Qualifications
Education:
- Mechanical / Electrical / Engineering degree or related fields. Bachelor is a minimum.
Experience and Skills:
Required:
- Minimum of 7 years of experience in a Manufacturing and/or Industrial Engineering role in medium to high volume manufacturing
- Knowledge & application experiences of GMP, GXP fundamentals
- Knowledge & application experiences of CSV fundamentals
- Hands-on mentality and strong collaboration with all teams
- Proven track record as validation SME within a medtech, pharma or other highly regulated (cGMP) sector is a must.
Desired:
- Experience with metrology systems
- Experience of vision system
- Experience of SCADA system deployment & validation
- Experience with Lathing & Milling technologies
Required Skills:
Preferred Skills:
Accelerating, Analytical Reasoning, Coaching, Communication, Facility Management, Good Manufacturing Practices (GMP), Lean Manufacturing Principles, Lean Supply Chain Management, Manufacturing Engineering, Manufacturing Science and Technology (MSAT), Problem Management, Project Engineering, Project Schedule, Report Writing, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy
The anticipated base pay range for this position is:
€53,500.00 - €85,445.00
Benefits:
In addition to base pay, we offer the following 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. Moreover, we offer 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. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.
*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.
Benefits
Health Insurance
employees can participate in several insurance plans, subject to the terms of their respective plans
Service anniversary and recognition awards
Paid Parental Leave
parental leave for a minimum of 12 weeks
Paid Time Off
vacation days
Well-being reimbursement
8808-Mentor Medical Systems B.V. is focused on advancing healthcare through innovative solutions in medicine and technology. Catering to the complex needs of patients and healthcare providers, we develop products that make treatments smarter, less invasive, and tailored to individual health challenges. Our commitment lies in enabling breakthroughs that significantly impact health outcomes globally.
- Founded
- Founded 1887
- Employees
- 500+ employees
- Industry
- hospital & health care
- Funding stage
- Public
- Stock ticker
- Publicly traded (JNJ)