SonicJobs Logo
Left arrow iconBack to search

Associate Director, Quality

Cpl Life Sciences
Posted 6 days ago, valid for 11 days
Location

Cambridge, Cambridgeshire CB2 8AG, England

Salary

£60,000 - £72,000 per annum

info
Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

info
  • The role is for an AD, Quality position in Cambridge, requiring an experienced candidate to oversee quality aspects of production.
  • The candidate must ensure products meet quality standards and work closely with production and compliance teams for quality improvements.
  • A Bachelor's degree in a relevant field or equivalent experience is required, along with experience in product quality management in the life sciences sector.
  • Familiarity with GxP standards, change control processes, and CAPA is essential, along with strong problem-solving and leadership skills.
  • The salary for this full-time, permanent position is not specified, but several years of relevant experience in the industry is expected.

AD, Quality

Cambridge

Full time, Permanent

Overview:

We are seeking an experienced candidate to oversee the quality aspects of production, ensuring that products meet quality standards, are consistent, and satisfy customer expectations. This role involves close collaboration with production and compliance teams to drive quality improvements across the product lifecycle, from development to distribution.

Key Responsibilities:

Ensure product quality standards are met and maintained.

Oversee quality control processes, including data review, supply chain oversight, and complaint management.

Drive continuous improvement initiatives and product quality plans.

Conduct root cause analyses, manage quality records, and implement corrective actions.

Provide training, lead quality review meetings, and participate in product team discussions.

Qualifications and Experience:

Bachelor’s degree in a relevant field or equivalent experience.

Experience in product quality management within the life sciences sector, preferably with biological, stem cell or vaccine products.

Familiarity with GxP standards, change control processes, and CAPA.

Strong problem-solving and leadership skills, with the ability to work independently and collaboratively.

If interested then please send your CV to

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.