QA Validation Engineer

Overview

We are seeking a dedicated and detail-oriented QA Validation Engineer to join our diverse team within the pharmaceutical industry. In this role, you will play a critical part in ensuring the quality and compliance of our manufacturing processes through robust method validation and protocol oversight. We are committed to fostering an inclusive work environment that values diverse perspectives and promotes equal opportunity for all individuals.

Responsibilities

• Lead and execute method validation activities in accordance with industry standards and regulatory requirements within a pharmaceutical plant setting.
• Oversee the development, review, and approval of validation protocols and reports to ensure accuracy and compliance.
• Identify, document, and manage deviations during validation processes, driving root cause analysis and corrective actions.
• Collaborate cross-functionally with Quality Assurance, Production, and Regulatory teams to maintain validation standards.
• Continuously improve validation procedures and support compliance audits.
• Promote a culture of quality, diversity, equity, and inclusion across all validation activities.

Qualifications

• Bachelor?s degree in Engineering, Life Sciences, or a related field; advanced degrees or certifications are a plus.
• Strong knowledge of regulatory guidelines (e.g., FDA, EMA, ICH) as they pertain to validation and quality systems.
• Excellent skills in protocol development, review, and approval processes.
• Ability to manage deviations thoughtfully and collaboratively to ensure compliance and continuous improvement.
• Strong communication and teamwork skills, with a demonstrated commitment to fostering inclusive and equitable work environments.
• Detail-oriented with excellent organizational and problem-solving abilities.

We encourage applications from candidates of all backgrounds and are committed to building a team that represents a variety of experiences and perspectives. Join us in shaping the future of quality assurance in pharmaceutical manufacturing.

To apply, please email your CV

CMC is an equal opportunity employer. We welcome applications from individuals of all ages and backgrounds and assess candidates solely on merit, skills, and potential. No terminology in this advert is intended to discriminate in any way.

We welcome applications/enquiries from individuals of all backgrounds and are committed to providing equal access to employment opportunities across all regions in which we operate.