(hybrid) Director of Quality Control (m / f / d)

Meet Life Sciences; Baden-Württemberg; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

An innovative life sciences company is seeking a Director of Quality Control to lead multiple laboratory teams. This pivotal role involves overseeing QC operations, ensuring compliance with regulations, and driving process improvements. The ideal candidate will have extensive experience in protein analytical techniques, strong leadership skills, and a passion for optimizing laboratory processes. Join a dynamic team that values collaboration and innovation, and make a significant impact in the life sciences industry. If you are ready to take the next step in your career, this opportunity could be your dream job!

Leistungen

Customized consultative assistance

Continuous feedback

Interview preparation assistance

Access to unpublished roles

Qualifikationen

• Minimum 4 years experience in QC within the pharmaceutical industry.
• Full proficiency in German & English required.

Aufgaben

• Lead and manage multiple laboratory teams in QC operations.
• Ensure compliance with GMP, ICH, and AMWHV regulations.

Kenntnisse

Protein Analytical Techniques

Leadership

Data Analysis Software

Regulatory Compliance (GMP, FDA, EMA)

Problem-Solving

Ausbildung

Master’s degree in Biochemistry

PhD in a related field

Tools

Laboratory Information Management Systems (LIMS)

Jobbeschreibung

Are you tired of only firefighting? Are you ready to make a real impact and optimize the Quality Control process for an international company?

Our client, a dynamic and growing international life sciences company, is seeking a Director of Quality Control to lead and develop multiple laboratory teams. Reporting directly to the Vice President, this leadership role will oversee all QC operations, ensuring regulatory compliance, process improvements, and alignment with company objectives.

Your Responsibilities :

• Lead and manage teams from multiple laboratories
• Oversee the development, validation, and execution of protein analytical methods, including (U)HPLC-SEC, IEX, RP-HPLC, LC/MS, amino acid analysis, and more
• Ensure full compliance with GMP, ICH, and AMWHV regulations
• Release laboratory results and oversee method transfers, co-validations, and stability studies per ICH guidelines
• Supervise the preparation, review, and approval of GMP documents, including SOPs, plans, reports, and deviations
• Drive the adoption of new technologies and automation to enhance QC processes
• Ensure efficient and economical management of the laboratory, optimizing processes to meet project timelines and customer expectations
• Collaborate closely with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs, to achieve project objectives and ensure timely delivery of analytical reports

Your Profile : MUST Have :

• Minimum Master’s degree in Biochemistry, Molecular Biology, Biotechnology, or a related field; PhD is preferred
• Full professional proficiency in German & English
• Minimum of 4 years of experience in QC within the pharmaceutical industry, with at least 2 years in a leadership role is preferred
• Experience in a broad range of protein and peptide analytical techniques, including (U)HPLC-SEC, IEX, RP-HPLC, LC/MS, and amino acid analysis
• Extensive knowledge of biologics manufacturing, regulatory requirements (GMP, FDA, EMA), and QC systems
• Proficiency in data analysis software and Laboratory Information Management Systems (LIMS)

Good to have :

• Proven leadership skills with a track record of managing and developing high-performing teams
• Strong analytical and problem-solving abilities, with a history of successful CAPA implementation
• Excellent communication and interpersonal skills, capable of collaborating across all organizational levels
• Experience with QC lab management, equipment qualification, and method validation
• Strong organizational skills and the ability to manage multiple priorities in a fast-paced environment

Why through us MEET?

By simply clicking "apply" or contacting us, you will enjoy the following benefits :

• Customized consultative assistance in your job search
• Assistance throughout the application process (no cover letters or job portals, just your CV!)
• Access to multiple vacancies in different companies (including unpublished roles like this one!)
• Continuous feedback after each stage of the process
• Preparation and assistance for each interview
• Saved time :)

Our client is looking for someone to start as soon as possible, and the position can be filled within a month, so don’t miss out!

Apply now and discover if this or other jobs I have could be your dream job!

What do you have to lose?

Feel free to recommend someone!