QA Engineer

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

**Job Function:**

Quality

**Job Sub** **Function:**

Quality Assurance

**Job Category:**

Business Enablement/Support

**All Job Posting Locations:**

Groningen, Netherlands

**Job Description:**

**Are you ready to take on a unique and exciting opportunity as a Quality Assurance Engineer? Johnson & Johnson is seeking a highly motivated individual to join our team in Groningen, Netherlands with a 1 year fixed-term contract. This is your chance to be part of a world-class organization that is committed to innovation and delivering flawless quality in everything we do.**

**As the** **Quality Assurance Engineer** **, you will play a crucial role in ensuring that our operations meet the highest standards of quality and compliance. You will have the opportunity to work with a team of exceptional professionals and contribute to the success of our goals.**

**Your role will be to provide support for product and process development projects and the production process, as well as support in the implementation, improvement and development of the quality policy and the quality system in order to guarantee the quality of the goods produced by AMO Groningen. This role is for** **1 year fixed-term** **contract.**

**Duties & Responsibilities**

**Ensure quality assurance within product and process development projects**

**Perform and assess statistical analyzes and support the implementation of statistical process control techniques, sampling schemes and other quality techniques**

**Assess and partly determine specifications for raw materials and consumables, processes, semi-finished products and end products in relation to internal and external quality standards**

**Drafting and reviewing protocols and reports**

**Review all changes to product specifications**

**Advising, reviewing and approving changes in products/processes or systems, in line with the applicable procedures. Approving all QMS related procedures and work instructions**

**Continuous improvement of the focus area in response to regulatory developments, trends, deviations or other data-driven inputs.**

**Support Quality Operations by:**

**Addressing non-conformities within production and taking care of internal escalations**

**Guiding planned deviations from the production process**

**Advising, reviewing and (approving) changes in production processes, in line with the applicable procedures**

**Analyzing data on rejects within the production process for continuous improvement and reducing or eliminating sources of variation within the production process**

**Education**

**Bachelor level**

**Technical area or business administration**

**Experience**

**2-4 years in a similar quality role**

**experience in a GmP environment within Pharma or Medtech is a pro**

**Skillset**

**Pro-active**

**Analytical**

**Good writing skills**

**Flexible and accurate**

**Work independently and in teams**

**Fluent in Dutch, verbal and in writing**

**Proficient in English, verbal and in writing**