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Associate Director of Analytical Services
- Posted 22 March 2023
- LocationNottingham
- Job type Permanent
- Discipline Research & Development
- Reference82253
- Contact NameLewis Besbeech
Job description
-BioTalent are working in collaboration with an outstanding CDMO who are operating within a modern, highly functional cGMP facility based in Nottingham, UK. The company is known for their standout abilities to tailor pharmaceutical services for clients of all sizes, whilst delivering results to the highest of qualities.
We are on the search to fill an exciting post for an Associate Director, who will be coordinating and supporting Analytical Development and QC professionals in their daily achievements. You will be expected to have worked within a like-minded setting, be capable of troubleshooting and have a passionate for safety, compliance, quality and cohesion.
This role will offer you:
You will be responsible for:
You will bring the following:
If you would like to learn more about this unique opportunity or to recommend a valued professional from your network, please reach out using the contacts below.
lewis.besbeech@biotalent.com // +44 (0)2033438780
BioTalent Ltd are acting as an employment agency in relation to this opportunity.
We are on the search to fill an exciting post for an Associate Director, who will be coordinating and supporting Analytical Development and QC professionals in their daily achievements. You will be expected to have worked within a like-minded setting, be capable of troubleshooting and have a passionate for safety, compliance, quality and cohesion.
This role will offer you:
- Competitive salary, bonus, private medical insurance and more.
- Flexibility of working to balance personal and professional commitments.
- High-performing colleagues, supportive leadership and professional development opportunities.
You will be responsible for:
- Quality system, GMP, Regulatory and H&S compliance during all Analytical/Quality activities.
- Managing the operational exercises and supporting a culture of continuous improvement.
- Demonstrate troubleshooting abilities across a range of analytical techniques.
- Task and resource project management for Quality projects/Analytical services and technical guidance during Customer projects.
- Client and regulatory audit support/representation, QMS documentation management, contribution to business development.
- Lead/contribute to root cause analysis meetings, change controls and deviations as required.
- Support with competency and compliance training of Analytical/QC staff.
You will bring the following:
- Extensive experience working in a CDMO (Contract, Development and Manufacturing Organisation).
- Proven experience working with medicinal products in clinical trials.
- Experience working in Quality Control and/or Analytical Services.
- Ability to lead effectively, communicate with purpose and organise efficiently.
If you would like to learn more about this unique opportunity or to recommend a valued professional from your network, please reach out using the contacts below.
lewis.besbeech@biotalent.com // +44 (0)2033438780
BioTalent Ltd are acting as an employment agency in relation to this opportunity.
