Quality Associate Manager

☞ FUJIFILM Diosynth Biotechnologies

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Update day: 04-06-2024

Location: Billingham Yorkshire and the Humber

Category: Pharmaceutical / Chemical / Biotech

Industry: Manufacturing

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Job content

FUJIFILM Diosynth Biotechnologies :
We are a trusted CDMO partner for life. At FUJIFILM Diosynth Biotechnologies (FDB), we encourage you to discover what inspires you every day, to follow your passion and your power – what we call Genki.

The work we do has the potential to transform people’s lives and to impact where it matters most. Each day is an opportunity to push the boundaries of your potential, so join us as QA Associate Manager and become part of a fast-growing global company, united by Genki.
About Us:

We are a dynamic global company and our focus is to combine technical leadership in cell culture, microbial fermentation and gene therapies with world class cGMP manufacturing facilities to advance tomorrow’s medicines.


We are growing and we are growing fast. With sites in Billingham & Wilton UK, Hillerod Denmark, North Carolina and Texas USA, the size and breadth of our business will open up huge opportunities for you, whether you want to move to a different role in the UK, relocate, or progress and take on more responsibility.


Our teams are proud to partner with innovative companies reimagining what’s possible in biopharmaceuticals. Every day at FDB is a day for improvement, each challenge is an opportunity for growth, and every moment is a chance to evolve together.

Role & Responsibilities:
Reporting to the QA Manager, the position will be a key member of the QAAS team, reviewing Quality Control data, in line with local procedures to ensure the data is to both a high technical and quality standard. In addition, the position will cover various QA systems, such as Laboratory Investigations, Trackwise Events, Data Integrity (DI) and Qualification and Validation. The position will be expected to build and maintain good relationships between the QAAS team and the sub-divisions of Quality Control.
Qualifications and Experience:
  • Chemistry/Microbiology/Biochemistry degree or a related subject - desirable
  • A minimum of 5 years’ experience in a GMP/GLP environment - essential
  • Good understanding of analytical techniques, such as: HPLC, SDS-PAGE, UV Spectrophotometry etc. - essential
  • Demonstrate a sound knowledge of how the principles and practices of GMP are applied to QC data - essential
  • Competent in QA systems such as events/deviations, laboratory investigations - essential
  • Experience in line management - desirable
  • Ability to plan effectively over a period of up to 3 months - desirable
  • Excellent written and verbal communication skills - essential
  • Ability to influence and negotiate as well as managing conflict - essential
  • Able to work effectively and accurately when balancing conflicting priorities or handling a large amount of documentation - essential
  • Ability to work without close supervision yet able to judge when advice and support is required - desirable
  • Good attention to detail - essential
  • Ability for flexible working - essential
Why work with us?:
At FDB, your passion – your Genki – is your power and we empower you to define what Genki means to you.
When you join us, we will train, develop and support you to become the best you can possibly be. We offer a structured new starter induction programme as well as on-going development training. In addition to this, we offer:
  • Competitive salary plus company bonus scheme
  • Up to 35 days of holiday, plus bank holidays.
  • Salary Sacrifice scheme offering, healthcare, bikes, dental etc.
  • Generous pension scheme
  • Free parking
Closing date 26 November 2021.

QA Associate Manager JD
QA Associate Manager PS
Why Work in Billingham
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Deadline: 19-07-2024

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