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Senior Quality Assurance Officer

Hays Specialist Recruitment Limited
Posted 8 hours ago, valid for a day
Location

Abingdon, Oxfordshire OX14 4SB, England

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

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  • Join a dynamic pharmaceutical company in Abingdon, Oxford, focused on developing cutting-edge vaccines and pharmaceutical products.
  • The role of Senior Quality Assurance Officer requires at least three years of experience in pharmaceutical quality and a Bachelor's degree in a life sciences-related field.
  • Key responsibilities include overseeing Quality Assurance functions, ensuring compliance with GMP standards, and managing controlled documents.
  • The position offers a competitive salary and benefits package, along with opportunities for professional development and training.
  • Employees enjoy 28 days of holiday plus bank holidays, as well as a supportive team culture and career growth prospects.

Your new companyJoin a dynamic and innovative pharmaceutical company located in Abingdon, Oxford. This company is dedicated to developing, manufacturing, and testing cutting-edge vaccines and pharmaceutical products. They focus on providing long-term immunity to some of the world's most pressing infectious diseases through advanced vaccine and immunotherapy candidates. Your new roleAs the Senior Quality Assurance Officer, you will:

  • Oversee the routine maintenance and management of Quality Assurance functions at the development, manufacturing, and testing site.
  • Ensure compliance with corporate quality objectives, GMP standards, and company policies.
  • Create and manage controlled documents, including SOPs and validation protocols.
  • Support QC lab staff with the management of analytical equipment.
  • Assist in external audits and regulatory inspections.
  • Maintain reporting systems for Quality Management Review.
  • Manage the company training system and perform internal audits.
  • Support validation activities and ensure compliance with validation protocols.

What you'll need to succeed

  • A Bachelor's degree in life sciences related field.
  • At least three years of experience in pharmaceutical quality.
  • Strong interpersonal and communication skills.
  • Effective investigation skills and creative, adaptable thinking.
  • Knowldge of validation principles and an understanding of tech transfer processes.
  • Knowledge of Eudralex Volume IV is desirable but not essential.
  • Willingness to follow a personal development plan.

What you'll get in return

  • An opportunity to work in a collaborative and innovative environment.
  • Professional development and training opportunities.
  • A chance to contribute to the development of life-saving vaccines and pharmaceutical products.
  • Competitive salary and benefits package.
  • 28 Days holiday + bank holidays
  • Supportive team culture and career growth prospects.

What you need to do nowIf you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

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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.