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.
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