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QA BMR Reviewer at Sterling Engineering

Position QA BMR Reviewer
Posted 01 Jul 2026
Expired 31 Jul 2026
Company Sterling Engineering
Location Dublin | IE
Job Type Full Time

Job Description:

Latest job information from Sterling Engineering for the position of QA BMR Reviewer. If the QA BMR Reviewer vacancy in Dublin matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.

Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at Sterling Engineering for the position of QA BMR Reviewer below matches your qualifications.

QA BMR Reviewer / Technician We are currently recruiting for a QA BMR Reviewer / Technician to join the Quality Assurance team of a leading pharmaceutical manufacturing company. This role is ideal for a quality-focused professional with experience in GMP-regulated environments who is passionate about ensuring compliance, documentation accuracy, and product quality. Working within the QA department, you will play a key role in reviewing Batch Manufacturing Records (BMRs), supporting batch release activities, and maintaining quality systems in line with regulatory requirements. Key Responsibilities: Review Intermediate and Finished Product Batch Manufacturing Records (BMRs) and associated documentation for completeness, accuracy, and compliance. Verify Critical Process Parameters (CPPs) to ensure manufacturing processes have been executed in accordance with approved procedures. Raise and support the completion of quality records, including Deviations, CAPAs, Change Controls, Non-Conformances, and Document Change Requests (DCRs). Prepare and collate documentation to support Qualified Person (QP) batch release activities in line with regulatory requirements. Issue and manage Batch Manufacturing Records and logbooks using electronic document management systems. Maintain document control activities, including reconciliation, archiving, retrieval, and record management. Support QA/GMP compliance programmes and quality system initiatives. Manage the retention of product samples and quality documentation. Participate in internal and external audits, providing QA support as required. Deliver training and guidance on GMP procedures and quality-related activities where appropriate. Contribute to continuous improvement initiatives and cross-functional projects. Provide updates on documentation review status and collaborate effectively with Production, QC, Engineering, and other departments. About You: The successful candidate will have: A third-level qualification in a scientific discipline (BSc or equivalent preferred). Previous experience within a pharmaceutical or highly regulated manufacturing environment. A solid understanding of cGMP requirements and Good Documentation Practices (GDP). Knowledge of FDA and EMA regulatory expectations. Excellent attention to detail with a methodical and organised approach. Strong communication and interpersonal skills. The ability to prioritise workloads and meet deadlines in a fast-paced environment. Experience using electronic quality management or document management systems is advantageous. For a confidential conversation about the role please apply for the role or contact Owen Clancy at By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose

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Job Info:

  • Company: Sterling Engineering
  • Position: QA BMR Reviewer
  • Work Location: Dublin
  • Country: IE

How to Submit an Application:

After reading and understanding the criteria and minimum qualification requirements explained in the job information QA BMR Reviewer at the office Dublin above, immediately complete the job application files such as a job application letter, CV, photocopy of diploma, transcript, and other supplements as explained above. Submit via the Next Page link below.

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