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

ZipRecruiter; Baden-Baden; Vor Ort; EUR 80.000 - 120.000; Vollzeit

Zusammenfassung

A dynamic international life sciences company is looking for a Director of Quality Control to lead laboratory teams and optimize quality processes. This role involves ensuring regulatory compliance, managing QC operations, and driving process improvements while collaborating with R&D and manufacturing teams. The ideal candidate will have a Master’s or PhD in a relevant field and substantial experience in the pharmaceutical industry.

Leistungen

Customized job search assistance

Support throughout the application process

Access to multiple job vacancies

Continuous feedback

Interview preparation support

Qualifikationen

• Minimum 4 years of experience in QC within the pharmaceutical industry.
• Full professional proficiency in German and English required.
• Experience with protein and peptide analytical techniques.

Aufgaben

• Lead and manage teams across multiple laboratories.
• Ensure regulatory compliance and optimize QC processes.
• Drive adoption of new technologies for QC.

Kenntnisse

Leadership skills

Analytical skills

Problem-solving

Data analysis

Communication skills

Ausbildung

Master’s degree in Biochemistry, Molecular Biology, Biotechnology

PhD in related field

Tools

Laboratory Information Management Systems (LIMS)

Jobbeschreibung

Job Description

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 economical 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:

• 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 choose us at MEET?

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

• Customized consultative assistance in your job search
• Support throughout the application process (no cover letters or job portals needed, 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 support for each interview
• Saved time :)

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

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

What do you have to lose?

Feel free to recommend someone you think might be interested!

Contact via:

Email: [e-mail]

Telephone: [phone]