Manufacturing Quality Engineer

DPS Group Global; Groningen; On-site; EUR 65,000 - 90,000; Full time

Job summary

DPS Group Global is seeking a QA specialist to oversee quality assurance in the factory, supporting operations and manufacturing engineering on deviations, changes and escalations.

The role focuses on addressing non-conformities, guiding deviations, approving changes, analyzing process data, CAPAs, and driving continuous improvement in line with regulatory requirements. Fluency in Dutch and English is essential; collaboration in cross-functional teams is expected.

Qualifications

• 4-6 years of relevant work experience in pharma or medical-device industry.
• Able to function both independently and in a team.
• Excellent command of Dutch and English.

Responsibilities

• Quality assurance oversight in the factory, close support to operations and manufacturing engineering in deviations, changes and escalations
• 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
• Generates, identifies, and suggests improvements in significant performance trends. Reports them to management and appropriate cross functional teams.
• Investigates and resolves Corrective and Preventive actions (CAPAs).
• Ensures continuous improvement of the focus area in response to regulatory developments, trends, deviations or other data-driven inputs.
• Writes and assists others in writing new or updated operating procedures.

Skills

Communicative

Flexible

Accurate

Team player

Dutch language

English language

Education

University/Bachelor's Degree or Equivalent

Job description

Quality assurance oversight in the factory, close support to operations and manufacturing engineering in deviations, changes and escalations

• 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
• Generates, identifies, and suggests improvements in significant performance trends. Reports them to management and appropriate cross functional teams.
• Investigates and resolves Corrective and Preventive actions (CAPAs).
• Ensures continuous improvement of the focus area in response to regulatory developments, trends, deviations or other data-driven inputs.
• Writes and assists others in writing new or updated operating procedures.

Education:

• University/Bachelor's Degree or Equivalent

Work Experience:

• 4-6 years of relevant work experience, preferably in the pharmaceutical or medical-device industry
• Communicative
• Flexible and accurate
• Able to function both independently and in a team
• Excellent command of Dutch and English language