NL - Quality Engineer

Johnson & Johnson Worksense (via Randstad Sourceright) is responsible for finding, engaging and contracting talent for the Johnson & Johnson contingent workforce.

Currently we are looking for Quality Engineers to expand our pool. On a regular basis we have Quality Engineering positions open in Leiden for Mentor, a Johnson & Johnson Medical Device company!

If you are interested in working for Johnson & Johnson, do not hesitate to apply! Once you are in our pool, you will be the first person we contact when we have an open vacancy.

As a Quality Engineer, you will use Quality Engineering principles, tools and techniques to develop, optimize, and support systems and processes that are aligned with the overall company strategy and mission affecting continuous quality improvement.

Duties & Responsibilities:

• Support the leading Quality Operations department to ensure all quality objectives and goals are met and help develop and drive strategic direction of the organization.
• Capable of developing junior quality engineers and quality technicians in the use of Process Excellence tools and Quality Systems to make data-driven, risk-based decisions that ensure the quality of the product.
• Support and lead quality improvement projects throughout the life cycle of Mentor products, including product design and development, and manufacturing.
• Utilize Quality Engineering tools and techniques to establish sampling plans, develop quality plans, conduct and participate in FMEA activities, support reliability engineering activities, conduct process and systems audits and support specification development.
• Analyzes routine and test data looking for improvement opportunities.
• Designs and implements experiments (DOE's) for process and product improvement and validation testing.
• Provides expertise and support for sampling plan analysis, DOEs, Pareto, ANOVA, and SPC applications, and other statistical applications as the need arises.
• Evaluate manufacturing quality performance capability and develop criteria to monitor and improve existing processes.
• Serves as a technical review for validation activities, i.e. protocols and reports.
• Investigate nonconforming material and the determination of cause, corrective action and recommendation of disposition Apply research and benchmarking activities to build innovative solutions, validate their efficiency and facilitate their implementation.
• Comprehension of the quality System Regulation (21 CFR PART 820), ISO 13485 requirements, MDD, Canadian Regulation and other applicable regulations.
• Serves as the Quality Engineering specialist on assigned responsibility areas and has conceptual understanding of all Quality functions and business areas.
• Responsible for presenting business related issues or opportunities to next management level.

Qualifications:

• Bachelor’s degree (B.S.) in engineering, science, ... is required.
• Proven knowledge of good manufacturing principles and practices, and procedures.
• Medical device or pharmaceutical manufacturing experience is required.

EXTRA INFORMATION:

• You will work on-site in Leiden.
• This is a contracting position, with the possibility of an extension after the end date. You will receive a contract via our partner YACHT. They can offer you a contract for the duration of the assignment at J&J, a one year contract or a freelance contract (ZZP).