Quality Specialist (m/f/d)

Quality Specialist (m/f/d) - Pharmaceutical Industry | Saarland

For one of our international clients in the pharmaceutical manufacturing sector, we are currently seeking a Quality Specialist (m/f/d) to strengthen the Quality Control team at a production site in Saarland.

Our client is a globally active, innovation-driven company operating in the development and manufacturing of high-quality pharmaceutical products. With a strong presence across multiple international markets, the organization is committed to quality, compliance, and continuous improvement.

Your Responsibilities

• Support the GMP-compliant approval process for raw materials, intermediates, and finished products by assessing analytical data

• Evaluate and interpret laboratory test results, ensuring compliance with defined specifications and quality standards

• Oversee laboratory activities to guarantee adherence to GMP regulations and internal procedures

• Perform independent checks of analytical data, ensuring accuracy and consistency with product requirements

• Contribute to the investigation of out-of-specification (OOS) results, including identifying root causes and implementing corrective and preventive actions (CAPAs)

• Identify opportunities for process improvements within quality control and assist in implementing new analytical techniques or systems

• Draft, update, and maintain standard operating procedures (SOPs) in line with regulatory requirements

• Assist in the preparation and execution of internal and external audits, including follow-up on identified actions

• Ensure proper documentation and reporting of all QC activities in accordance with GMP standards

• Deliver training and guidance to laboratory staff and support onboarding of new methods and technologies

• Participate in or coordinate quality control-related projects, including digital or system-related initiatives

Your Profile

• Degree in Pharmacy or another qualification in line with §15 AMG (or equivalent regulatory requirements)

• Initial experience in pharmaceutical quality control within a GMP-regulated environment

• Knowledge of analytical techniques such as HPLC, GC, UV/VIS is an advantage

• Strong understanding of GMP, ICH guidelines, and regulatory expectations

• High level of analytical thinking and precision in handling test results and deviations

• Strong communication skills and ability to collaborate across departments

• Experience with laboratory information systems and standard software tools (e.g., MS Office)

• Fluent German (C1 level) and good English skills (B1 or higher)

What You Can Expect

• A stable position within an international and quality-focused environment

• Opportunities for professional development and growth

• A collaborative and inclusive working culture

• Exposure to modern pharmaceutical production and quality systems

If you are interested in this opportunity, we look forward to receiving your application and discussing the role with you in more detail.