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

Meet Life Sciences; Stuttgart; Vor Ort; EUR 80.000 - 100.000; Vollzeit

Zusammenfassung

An international life sciences company is seeking a Director of Quality Control in Stuttgart to lead multiple laboratory teams. The role involves overseeing QC operations, ensuring compliance with regulations, and driving process enhancements. The ideal candidate holds a Master's degree in Biochemistry, speaks fluent German and English, and has significant experience in the pharmaceutical QC sector. Apply now for this impactful position!

Leistungen

Customized consultative assistance in job search

Continuous feedback during the process

Support for interview preparation

Qualifikationen

• Master's degree or higher in a relevant field.
• 4+ years experience in QC within the pharmaceutical industry.
• Proficient in German & English.

Aufgaben

• Lead laboratory teams for multiple QC operations.
• Manage and validate protein analytical methods.
• Ensure compliance with GMP, ICH, and AMWHV regulations.

Kenntnisse

German proficiency

English proficiency

Leadership

Analytical skills

Problem-solving

Ausbildung

Master’s degree in Biochemistry or related field

PhD preferred

Tools

Laboratory Information Management Systems (LIMS)

Data analysis software

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 :

1. Lead and manage teams across multiple laboratories.
2. Oversee the development, validation, and execution of protein analytical methods, including (U)HPLC-SEC, IEX, RP-HPLC, LC/MS, amino acid analysis, and more.
3. Ensure full compliance with GMP, ICH, and AMWHV regulations.
4. Release laboratory results and oversee method transfers, co-validations, and stability studies per ICH guidelines.
5. Supervise the preparation, review, and approval of GMP documents, including SOPs, plans, reports, and deviations.
6. Drive the adoption of new technologies and automation to enhance QC processes.
7. Ensure efficient and cost-effective management of the laboratory, optimizing processes to meet project timelines and customer expectations.
8. 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 :

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

Good to have :

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

Why work with us at MEET?

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

1. Customized consultative assistance in your job search.
2. Support throughout the entire application process (no cover letters or job portals, just your CV!).
3. Access to multiple vacancies in different companies, including unpublished roles like this one!
4. Continuous feedback after each stage of the process.
5. Preparation and support for each interview.
6. Save time :)

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

Apply now and discover if this or other roles we have could be your dream job!

What do you have to lose?

Feel free to recommend someone you know!

Contact us via:

• Email: [e-mail]
• Telephone: [phone]