QC Operations Specialist

A global manufacturing company is seeking a QC Operations Specialist to join its Quality and Compliance team at a GMP-compliant production site in Hampshire. This permanent position is key to maintaining site-wide adherence to regulatory requirements and driving continuous improvement across the Quality Management System (QMS).

Known for its commitment to product quality and operational excellence, this organisation operates in a highly regulated environment and fosters a culture of collaboration, ownership, and innovation. This role offers the opportunity to make a real impact while developing your expertise in compliance and quality operations within a high-performing site.

Your role as QC Operations Specialist

As part of the site's GMP Compliance team, the QC Operations Specialist will support internal audits, system governance, and the implementation of quality improvements across departments.

Key responsibilities include:

• Ensuring compliance with GMP regulations, internal standards, and corporate policies across the site.

• Leading and supporting audits (GMP, hygiene, QMS) and managing related actions through to resolution.

• Acting as a site representative for Veeva Quality One (eQMS), reviewing and approving CAPAs, deviations, incidents, and change controls.

• Managing controlled documents and system admin duties via OpenText Document Management System.

• Supporting third-party audits and following up on any required corrective actions.

• Promoting continuous improvement using audit data, observations, and KPI trends.

• Participating in the implementation of quality risk assessments and validation protocol reviews.

• Collaborating with global quality teams and contributing to annual product reviews.

Experience and qualifications for the QC Operations Specialist role

This role is ideal for someone with hands-on quality experience in a regulated environment and a practical understanding of QMS processes.

The ideal candidate will have:

• A degree or equivalent professional experience in a relevant scientific or technical field.

• Experience in a GMP-compliant manufacturing environment (pharmaceutical, cosmetics, or similar sectors).

• Strong working knowledge of QMS, audit processes, and document control systems.

• Familiarity with electronic systems such as Veeva Quality One, OpenText, and SAP (preferred but not essential).

• A proactive, detail-focused approach with strong troubleshooting and analytical skills.

• Excellent communication skills and the ability to collaborate across departments.

• Confidence working both independently and as part of a wider compliance team.

Perks and benefits

• Be part of a well-established global company with a strong compliance culture.

• Work within a dynamic and supportive team environment.

• Opportunity to influence quality systems and continuous improvement initiatives.

• Competitive salary and benefits package.

• Long-term career development prospects within a global organisation.

Apply now for immediate consideration.
If this role isn't quite right but you're interested in quality or compliance opportunities within regulated manufacturing, get in touch to learn more.