Quality Control Technician - GMP & SAP Focus

West Pharmaceutical Services, Inc; Denmark; On-site; DKK 347,000 - 442,000; Full time

Job summary

West Pharmaceutical Services, Inc. in Horsens, Denmark, is seeking a Quality Control Technician to visually review items, document results in SAP, and support QA initiatives in a fast-paced manufacturing environment.

This onsite role requires attention to detail, familiarity with GMP principles, and the ability to work 5 days per week onsite. Candidates should be comfortable with routine tasks and collaborative problem solving.

Qualifications

• Knowledge of SAP and other IT systems, including the office package.
• You approach tasks systematically and structured and thrive on routine tasks.
• You are quality-conscious, detail-oriented and have good eyesight (must be able to pass an eye test, possibly using your own glasses).
• You are committed and have a good mood.

Responsibilities

• Visually review items according to applicable specifications and stated customer requirements.
• Independently communicate observations with affected departments.
• Report results in SAP.
• Perform various control measurements on calibrated equipment (note that this is not a laboratory position, although some measurements are made).
• Act as a sparring partner within quality issues related to AQL.
• Support with visual inspections in relation to deviations, projects and complaints.
• Ensure that instructions that support AQL-related work reflect current practice.
• Participate in and contribute to quality improvement initiatives.
• Ensure that QA-related tasks are carried out and documented as agreed.

Skills

SAP

Microsoft Office

Attention to detail

Systematic approach

Tools

SAP

Microsoft Office

Job description

West Pharmaceutical Services, Inc. in Horsens, Denmark, is seeking a Quality Control Technician to visually review items, document results in SAP, and support QA initiatives in a fast-paced manufacturing environment.

This onsite role requires attention to detail, familiarity with GMP principles, and the ability to work 5 days per week onsite. Candidates should be comfortable with routine tasks and collaborative problem solving.