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QA Associate

Berkshire, BerkshireContract
Experience Dependant
Job Reference: J5632892
Updated On: 18/02/2020
Status: Under Offer
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Life Sciences, Science

Skills: Biochemistry - QC / Stability, Biochemistry - Production / Manufacturing, Quality Assurance - Qualified Person - Permanent, Quality Assurance - Qualified Person - Contract, Quality Assurance - Permanent, Quality Assurance - Contract, Biochemistry - Biomedical Scientist (non HPC), Life Sciences - Molecular Biology, Quality Assurance - Qualified Person - Trainee, Biochemistry - Manufacturing / Plant Scale Purification, Quality Assurance - GMP, Quality Assurance - GDP, Quality Assurance - GCP, Quality Assurance - GLP, Quality Assurance - ISO13485, Quality Assurance - HACCP / BRC, Quality Assurance - Compliance, Quality Assurance - Validation, Quality Assurance - Auditing, Quality Assurance - ISO17025, Quality Assurance - ISO9001, Quality Assurance - UKAS, Quality Assurance - Quality Manager, Quality Assurance - Quality Director / Head Of Quality, Quality Assurance - Energy, Quality Assurance - Clinical Supplies, Quality Assurance - Biologics, Quality Assurance - CSV, Quality Assurance - Administration, Quality Assurance - Archiving, Quality Assurance - Documentation, Quality Assurance - IMP, Quality Assurance - ATMPs, Quality Assurance - ISO27001

Job Information

Role Overview

To ensure that Quality is maintained at an appropriate level meeting, customer and regulatory expectations. This will be achieved by assessing compliance to site PQS and principles of GMP auditing documentation generated during manufacturing processes, development and laboratory processes and where required escalating non-compliances through the PQS, site governance mechanisms and senior QA leadership.

Key Duties and Responsibilities

Your duties as the QA Associate will be varied however the key duties and responsibilities are as follows:

1. In the role of a QA Associate, you will be responsible for auditing documentation generated during manufacturing processes and for ancillary areas of manufacturing, co-ordinating of review and any follow-up actions/corrections of GMP documentation.

2. Auditing documentation generated during development and laboratory processes, including protocols, assays/raw data and validation reports while ensuring current GMP requirements for all areas are met.

3. As a QA Associate, you will perform basic document reviews of SOP’s, batch records, test methods, and logbooks.

4. Expand and utilise knowledge of quality procedures to identify and report non-conformances and resolve issues arising in the area via interaction with the relevant personnel.

Role Requirements

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

1. Relevant degree in biochemistry or related field (BSc or equivalent)

2. Proven experience in QA / GMP role within the pharmaceutical industry (approximately 2 years).

3. A working knowledge and practical experience working in GMP compliant environments, identifying deviations and raising CAPAs while auditing, reviewing and correcting documents and SOPs generated during manufacturing and development.
Huseyn Hajiyev
Your Recruitment ConsultantHuseyn Hajiyevhuseyn.hajiyev@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.