Junior Quality Control Project Lead

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Job description

FUJIFILM Diosynth Biotechnologies :

We have an excellent progressive opportunity for a Junior QC Project Leader to progress to a Senior level here at FUJIFILM. This opportunity is fantastic for someone who has recently graduated within Biology or Chemistry and has experience in a QC Analytical role with the ability to deliver projects as well as problem solving whilst supporting the team.

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 a QC Project Lead 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:
The QC Project Lead drives and owns QC activities within the Quality Control department.
Provides Leadership and knowledge of QC testing and compliance from GMP preparation through to stability testing.
Drives delivery of projects based on technical knowledge to a high, scientifically sound, standard.
Delivers KPIs in the form of stability milestones on time.
Improves the quality system to ensure we continue to keep in line with regulations and also improve productivity and right first time.
Qualifications and Experience:
A minimum of 1 years' experience in a QC GMP analytical role
A good understanding of Biological and Analytical Chemistry techniques and how they are best applied in Stability and Bulk
Drug Substance testing. Able to guide customers in making analytical testing decisions.
Proven experience of delivery 3 or more projects through detailed planning, problem
solving and coordinated teamwork.
Knowledge in and can troubleshoot at least one of the following areas:
- HPLC/UPLC
- Electrophoresis
- UV spectroscopy
Experience of analytical method development to method validation
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 10 December 2021.

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