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QA Officer, Pharmaceutical

Russell Taylor
Posted 9 days ago, valid for 20 days
Location

Stevenage, Hertfordshire SG2 7BG

Salary

£30,000 - £36,000 per annum

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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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  • The position is for a QA Officer or Senior QA Officer at a pharmaceutical company in Stevenage, offering a salary between £35,000 and £45,000 based on experience.
  • The role involves managing quality assurance processes, ensuring product compliance, and maintaining the Quality Management System (QMS).
  • Candidates should have a degree in a STEM subject and essential GMP QA experience, preferably in a pharmaceutical environment.
  • Experience in CAPA, deviations, change controls, and internal auditing is preferred, along with strong communication skills in English.
  • This is a permanent position that provides an opportunity to contribute to the development of a positive change culture within the company.
QA Officer/Senior QA Officer, Pharmaceutical Location: Stevenage Type: Permanent Salary: £35000 - £45000 depending on experienceRussell Taylor Group is working exclusively with an established pharmaceutical manufacturing company who is looking to recruit for an experienced QA Officer or a Senior QA Officer (depending on experience) to work as part of an established team (onsite) & will play a key role in the furthered development of the QMS & the positive change culture that the QM is introducing; this is a great time to join a company very much on the up!The Role:- ØThe Quality Assurance Officer will be responsible for quality management, quality assurance, and quality auditing tasks related to pharmaceutical products.ØEnsuring products are fit for purpose before release for use or commercial sale.ØMaintaining and improving QMS' performance by ensuring items such as deviations, CAPA and change control for which you are the owner are progressed in a compliant and timely manner and all other items are reviewed and/or approved in accordance with internal procedures.ØEnsure customer or supplier complaints are satisfactorily investigated and communicated.ØEnsure all customer requests and queries are dealt with in a timely manner in line with company procedures.ØParticipate and/or host internal and external audits inclusive of customer and regulatory audits.ØCompetent to author and approve routine QMS activities.ØPerforming Root Cause Analysis using problem solving tools such as Fishbone, 5 Whys etc.ØAuthors, reviews, and approves Controlled Documents in accordance with procedures.ØWill support in delivering the site GMP training as required.ØWill conduct the internal audit programme.ØWill support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department and across site as required.ØEnsure customer or supplier complaints are satisfactorily investigated and communicated.The Person:-ØThe ideal Candidate will hold a degree in a STEM related subject ØGMP QA experience is essential! Ideally in a Pharmaceutical setting or similar ØExperience in CAPA, deviations, change controls, internal auditing (preferred) etcØStrong interpersonal skills, we are looking for Candidates who are good communicators ØStrong written and verbal use of English language essential due to the nature of the role Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.

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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.