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

Meet Life Sciences; Stuttgart; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

An established industry player is seeking a Director of Quality Control to lead multiple laboratory teams and optimize processes for quality assurance. This pivotal role involves overseeing compliance with regulatory standards, driving technological advancements, and collaborating across departments to ensure project success. With a focus on leadership and innovation, this position offers a unique opportunity to make a significant impact in the life sciences sector. If you're ready to take your career to the next level and contribute to groundbreaking advancements, this role is designed for you.

Leistungen

Customized job search assistance

Interview preparation and support

Continuous feedback

Access to unpublished roles

Qualifikationen

• 4+ years in QC within the pharmaceutical industry, with leadership experience.
• Experience with protein analytical techniques and regulatory compliance.

Aufgaben

• Lead and manage QC teams across multiple laboratories.
• Ensure compliance with GMP, ICH, and AMWHV regulations.

Kenntnisse

German proficiency

English proficiency

Leadership skills

Analytical skills

Problem-solving skills

Ausbildung

Master's degree in Biochemistry

PhD in related field

Tools

Laboratory Information Management Systems (LIMS)

(U)HPLC-SEC

LC/MS

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. Oversee the release of laboratory results, 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. Manage the laboratory efficiently and economically, optimizing processes to meet project timelines and customer expectations.
8. Collaborate with R&D, Manufacturing, and Regulatory Affairs to achieve project objectives and ensure timely analytical reporting.

Your Profile: MUST Have:

• Master’s degree in Biochemistry, Molecular Biology, Biotechnology, or a related field; PhD preferred.
• Proficiency in German and English.
• At least 4 years of experience in QC within the pharmaceutical industry, with 2+ years in a leadership role preferred.
• Experience with 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 high-performing teams.
• Strong analytical and problem-solving skills, with successful CAPA implementation experience.
• Excellent communication and interpersonal skills for cross-organizational collaboration.
• Experience with QC lab management, equipment qualification, and method validation.
• Strong organizational skills to manage multiple priorities in a fast-paced environment.

Why choose us?

By clicking "apply" or contacting us, you will enjoy:

• Customized job search assistance.
• Support throughout the application process (no cover letters or job portals needed; just your CV).
• Access to multiple vacancies, including unpublished roles.
• Continuous feedback after each stage.
• Interview preparation and support.
• Time-saving benefits.

Our client is looking for someone to start as soon as possible. The position may close within a month, so don’t miss out!

Apply now to 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!