Back to searchSenior QA Officer, Pharmaceutical
Russell Taylor Group Ltd
Posted 21 hours ago, valid for a month
Hitchin, Hertfordshire SG5 1EP, England
£48,000 - £57,600 per annum
Full Time
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Sonic Summary
- The Senior QA Officer position is located in Stevenage and requires full onsite attendance five days a week.
- This permanent role offers a salary range of £35,000 to £45,000, depending on experience, with potential for exceptional candidates to negotiate a higher salary.
- The ideal candidate should have experience in batch review and batch release, with a strong background in GMP QA, preferably within a pharmaceutical setting.
- Key responsibilities include managing quality assurance tasks, conducting internal and external audits, and maintaining the QMS performance.
- A degree in a STEM-related subject is required, along with strong interpersonal and communication skills.
Location: Stevenage (fully onsite x5 days a week)- days
Type: Permanent
Salary: £35000 - £45000 depending on experience possible scope on this for exceptional candidates
Russell Taylor Group is working exclusively with an established pharmaceutical manufacturing company who is looking to recruit for an experienced Senior QA Officer (depending on experience) to work closely with the QA Manager and deputize when needed. They 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:-
The Quality Assurance Officer will be responsible for quality management, quality assurance, and quality auditing tasks related to pharmaceutical products.
Ensuring products are fit for purpose before release for use or commercial sale.
Maintaining 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.
Ensure customer or supplier complaints are satisfactorily investigated and communicated.
Ensure all customer requests and queries are dealt with in a timely manner in line with company procedures.
Participate and/or host internal and external audits inclusive of customer and regulatory audits.
Competent to author and approve routine QMS activities.
Performing Root Cause Analysis using problem solving tools such as Fishbone, 5 Whys etc.
Authors, reviews, and approves Controlled Documents in accordance with procedures.
Will support in delivering the site GMP training as required.
Will conduct the internal audit programme.
Will support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department and across site as required.
Ensure customer or supplier complaints are satisfactorily investigated and communicated.
The Person:-
The ideal Candidate will hold a degree in a STEM related subject
Experienced in batch review and batch release
GMP QA experience is essential! Ideally in a Pharmaceutical setting or similar
Experience in CAPA, deviations, change controls, internal auditing (preferred) etc
Strong interpersonal skills, we are looking for Candidates who are good communicators
Strong 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.
