GMP Batch Release QA Analyst

Boehringer Ingelheim; Pirbright; On-site; GBP 30,000 - 45,000; Full time

Job summary

Boehringer Ingelheim is seeking a Quality Assurance Analyst in Pirbright, England. This critical role ensures batch release activities comply with regulatory requirements and quality standards, focusing on documentation review and coordination. You will collaborate across functions to support timely product releases while maintaining a high standard of data integrity.

Ideal candidates have a background in quality systems within the pharmaceutical industry, strong attention to detail, and effective communication skills. A scientific degree is preferred.

Qualifications

• Understanding of Good Manufacturing Practice (GMP) principles.
• Experience in quality systems within a regulated industry is advantageous.
• Ability to manage multiple tasks in a dynamic environment.

Responsibilities

• Prepare and review batch-specific documentation for QP certification.
• Perform production checks and formulation sheet reviews.
• Participate in internal audits and quality system maintenance.

Skills

Understanding of Good Manufacturing Practice (GMP)

Experience in a quality system environment

Familiarity with batch record reviews

Attention to detail

Effective communication skills

Microsoft Office proficiency

Education

Degree in a scientific or related field

Tools

LIMS

SAP

Job description

Boehringer Ingelheim is seeking a Quality Assurance Analyst in Pirbright, England. This critical role ensures batch release activities comply with regulatory requirements and quality standards, focusing on documentation review and coordination. You will collaborate across functions to support timely product releases while maintaining a high standard of data integrity.

Ideal candidates have a background in quality systems within the pharmaceutical industry, strong attention to detail, and effective communication skills. A scientific degree is preferred.