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Hyper Recruitment Solutions
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Associate Director - External Manufacturing

£80,000 - £100,000 per annum
Job Reference: J5631949
Updated On: 30/09/2019
Status: Under Offer
Hyper Recruitment Solutions
Sectors: Contract Manufacturing Organisation

Skills: Production / Manufacturing - Pharma / Biotech - Head of / Director, Executive - Pharmaceutical, Executive - Biotechnology, Executive - CRO / CMO, Management Consultancy - Manager / Director

Job Information

Role Overview

Hyper Recruitment Solutions (HRS) are currently searching for a Associate Director - External Manufacturing to join a global biopharmaceutical company with European headquarters in London. As the Associate Director - External Manufacturing you will be responsible for maintaining key specific Contract Development and Manufacturing Organisations relationships with the Technical Operations teams.

Key Duties and Responsibilities

Your duties as the Associate Director - External Manufacturing will be varied however the key duties and responsibilities are as follows:

1. Build multi-level relationships with the relevant CMO teams/departments including those at executive level to install strong cross-company relations.

2. Work with the Programme Managers and Subject Matter Experts on each CDMO team to manage the day to day relationship between the allocated CDMO and Technical Operations teams.

3. As the Associate Director - External Manufacturing, you will be the key point of escalation for delivery issues and arrange resolutions through appropriate department/SME or to the OTL Technical Operations senior management team when required.

4. Monitor the CDMO and the associated OTL’s Technical Operations team performance and provide evidence based, timely feedback and periodic reports to both organisations when required.

Role Requirements

To be successful in your application to this exciting opportunity as the Associate Director - External Manufacturing we are looking to identify the following on your profile and past history:

1. Relevant degree in a biological sciences, chemical engineering or similar discipline.

2. Proven industry experience in the development, manufacture or delivery of biological drug products. Cell or Gene Therapy expertise are highly desirable.

3. A working knowledge and practical experience with FDA, EMA, GMP and ICH regulatory requirements.

Key Words: Biopharmaceutical | Associate Director | GMP | Technical Operations | CDMO | Contract Development and Manufacturing Organisations | FDA | ICH | EMA | Gene Therapy | Cell Therapy|
Andrew Davis
Your Recruitment ConsultantAndrew Davisandrew.davis@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.