Due to changes in GDPR and increased usability with the website, any candidates registered before 03/05/19 will need to re-register
Hyper Recruitment Solutions
Back to results

Quality Assurance Officer

Bradford, West YorkshirePermanent
Experience Dependant
Job Reference: J5632095
Updated On: 22/08/2019
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Life Sciences, Science

Skills: Quality Assurance - Permanent, Pharmacology - Graduate (BSc / MSc), Quality Assurance - GMP, Quality Assurance - GLP, Quality Assurance - Compliance, Quality Assurance - Validation, Quality Assurance - Auditing, Quality Assurance - UKAS, Quality Assurance - Biologics, Quality Assurance - Administration, Quality Assurance - Archiving, Quality Assurance - Documentation

Job Information

Role Overview

We are currently supporting a key client of ours in their search for a Quality Assurance Officer to join their facility based in the West Yorkshire area. The company are a growing life sciences firm and in order to enhance their current client services, they are developing their existing analytical laboratories in West Yorkshire.

Your role as the Quality Assurance Officer will focus on the independent cGMP review and approval of work conducted at the facility including analytical method development, method verification/validation, release testing and stability studies for clients in the pharmaceutical, healthcare and medical device industries. The role will also include working with the team of Scientists on site to implement, maintain and improve procedures and processes that support GMP compliance. This role will additionally provide the opportunity to cross-train in GLP auditing.

Key Duties and Responsibilities

Your duties as the Quality Assurance Officer will be varied however the key duties and responsibilities are as follows:

1. Undertake routine checking, review and approval of cGMP laboratory reports, data summaries, COAs, performance verifications, validation and method transfer protocols, in addition to routine review of laboratory and project notebooks.

2. Provide assistance in support of Change Controls, Equipment Qualification, Non-Conformances, OOS/OOT and Exception Reports. Additionally, you will hold control of the site archiving facility and be responsible for archiving and retrieval of records.

3. Develop and review QA-related SOPs, policies and pro-formas, and maintain the associated database of quality documentation.

4. Schedule and perform external and internal audits and inspections as assigned, reporting any deficiencies to the Quality Manager and site management. Generate audit reports and follow-up actions.

5. Train other personnel in all aspects of QA systems and procedures as required.

Role Requirements

To be successful in your application to this exciting opportunity as the Quality Assurance Officer we are looking to identify the following on your profile and past history:

1. Relevant degree in a analytical, chemical or related scientific discipline.

2. Proven industry experience in a cGMP analytical environment or with Regulatory GLP, including GLP auditing, ideally within pharmaceutical manufacturing.

Key Words: QA | quality assurance | QC | quality control | GMP | manufacturing | cGMP | GLP | cGLP | audit | pharmaceuticals | API | medical device | healthcare
Jessica McLachlan
Your Recruitment ConsultantJessica McLachlanJessica.mclachlan@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.