drjobs Quality Assurance Officer - Supplier Quality (11513)

Quality Assurance Officer - Supplier Quality (11513)

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Job Location drjobs

Barnstaple - UK

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Role Details

Quality Assurance Officer Supplier Quality

Role: Full-time Permanent

Location: Barnstaple North Devon

Salary: Competitive bonus benefits

The Role

Were seeking a methodical and meticulous QA Officer to support work within our Third-Party Compliance division. Supporting our Head of Quality UK Third Party youll work efficiently across a range of Quality Assurance activities to ensure our Suppliers continually achieve the Quality standards we expect from them (across our portfolio of medicinal products and medical devices) nd maintaining both QA regulatory and business requirements by cultivating good Supplier relationships through collaborative and pragmatic working.

In this broad-ranging department your day-to-day workload could include liaising with third party Suppliers or Service Providers (from raw materials manufacturers to contract laboratories) managing product compliance updating relevant documentation to uphold best practice (including product quality reviews complaint investigations reviewing technical agreements or standard operating procedures) leading Quality-based projects to drive Continuous Improvement across the business maintaining our Pharmaceutical Quality System to ensure compliance conducting investigations assisting with product recalls and following-up on any corrective or preventative actions required or performing manufacturing packing or QC testing site audits. Youll also have the opportunity to work closely with other departments across the business to promote a strong QA culture providing advice and guidance on multi-disciplinary projects resolving artwork queries and reporting on key performance metrics.

The Person

  • Experience in a similar Quality Assurance role within the pharmaceutical industry with good knowledge of related EU/UK Quality Regulations Product Quality Review requirements and administering change control or validation activities.
  • Knowledge of multiple dosage forms would be an advantage.
  • Good experience using electronic document management systems and writing clear and concise reports; used to conducting quality-based investigations root cause analyses and self-inspections.
  • Experience of supporting customer / regulatory audits or performing internal audits of departments / GxP requirements.
  • Ability to interpret GxP requirements and new regulations / guidance to develop and implement new processes to ensure compliance.
  • Proficient technical report writing able to facilitate and document complex investigations desirable.
  • Good communication skills able to build relationships with ease but can diplomatically negotiate and persuade when necessary.
  • Well organised able to manage multiple tasks to deadline and maintain an eye for detail even in a busy and changeable work environment; able to think of solutions on your feet.
  • Good IT skills across the Microsoft Office suite.
  • Higher level science qualification (degree level beneficial).

The Rewards

In return we offer a competitive salary and rewards package. Not to mention the opportunity to genuinely make a difference in this dynamic role within a progressive and expanding business at an exciting time of growing international reach.

How to Apply

If you have the experience passion and ability to make this role a success then we would love to hear from you. Please send your CV with cover letter by 15th June 2025 to

Accord Healthcare Europe is one of the fastest growing pharmaceutical companies in Europe. Accord has one of the largest market footprints of any European generic and biosimilars companies selling generic medicines in over 80 countries around the world. This global footprint enables us to deliver vital affordable medicines to national health systems supporting healthcare professionals to transform patient lives worldwide. The approach of Accord is agile and inventive always seeking to improve products and patients access to them. Accord are driven to think differently and deliver more for the benefit of patients worldwide.

To continue our growth were looking for the best and brightest technical minds and forward-thinking business professionals. Keeping our people at the heart of all we do we offer rewarding opportunities for those looking for continued personal and professional growth investing in training and development tailored to each individuals focus. So if youre looking for an inclusive company to take your career to the next level youre certainly in the right place; come and join us to make it better.

If you would like to request this information in an alternative language please get in contact with us on Si vous souhaitez demander ces informations dans une autre langue veuillez nous contacter Jeli chciaby otrzyma te informacje w innym jzyku prosimy o kontakt pod adresem Se desejar esta informao num idioma alternativo entre em contato conosco em Pokud si pejete tyto informace vydat v jinm jazyce kontaktujte ns prosm na adrese Qualora desiderassi ricevere queste informazioni in una lingua alternativa contattaci cortesemente allindirizzo Si desea solicitar esta informacin en un idioma alternativo pngase en contacto con nosotros en Dac dorii s solicitai aceste informaii ntr-o alt limb v rugm s ne contactai la adresa Als u deze informatie in een andere taal wilt ontvangen neem dan contact met ons op via Wenn Sie diese Informationen in einer anderen Sprache anfordern mchten setzen Sie sich bitte unter: mit uns in Verbindung.

All applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin or disability.

Requisition ID: 11513


Required Experience:

Unclear Seniority

Employment Type

Full Time

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