QC Operations Specialist

SEC Life Sciences; England; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading global manufacturing organization is seeking a QC Operations Specialist to maintain compliance and support quality systems. The ideal candidate should have a degree and experience within GMP-regulated environments. Responsibilities include implementing quality standards and conducting audits. This position offers a competitive salary and opportunities for professional growth within a supportive atmosphere.

Benefits

Competitive salary

Comprehensive benefits package

Opportunities for professional development

Supportive environment for new ideas

Qualifications

• Experience in GMP-regulated manufacturing, preferably cosmetic or pharmaceutical.
• Proven track record in maintaining and improving quality systems.
• Hands-on experience with audits and quality investigations.

Responsibilities

• Implement and enforce site-wide quality standards.
• Conduct internal audits and document outcomes.
• Manage third-party audit activities.
• Oversee document control processes.
• Lead quality risk assessments for improvement.

Skills

Quality compliance

Problem-solving

Team collaboration

Communication skills

Education

Degree-level education or equivalent

Tools

Electronic quality management systems (EQMS)

Veeva

OpenText

Microsoft Office

Job description

This is an exciting opportunity to step into a QC Operations Specialist role at a leading global manufacturing site. Their mission is to uphold the highest standards of quality and compliance, ensuring products consistently meet regulatory requirements and safeguard consumer trust around the world. With a culture grounded in collaboration, continuous improvement, and professional integrity, this organisation offers a chance to be part of work that truly makes an impact - supporting quality systems that enable products to reach international markets.Your role as QC Operations SpecialistAs a QC Operations Specialist, you'll play a pivotal role in maintaining compliance across the site and supporting the smooth running of quality systems. Key responsibilities include:Implementing and enforcing site-wide policies, procedures, and quality standards to ensure regulatory complianceKeeping up-to-date with GMP regulations, corporate quality requirements, and industry best practicesConducting a range of internal audits (GMP, hygiene, QMS), documenting outcomes, and driving corrective actionsManaging third-party audit activities and ensuring timely closure of any follow-up actionsHandling site responsibilities within electronic quality management systems (EQMS), reviewing and approving CAPAs, deviations, investigations, and change controlsActing as a key site contact with global quality teams and subject matter experts to share insights and support compliance initiativesOverseeing document control processes and maintaining accurate quality records in systems like OpenTextLeading quality risk assessments and identifying continuous improvement opportunities through audit trends and observationsReviewing and approving validation protocols and supporting annual product reviewsExperience and qualifications for the QC Operations Specialist roleThe ideal candidate will bring a strong foundation in quality or compliance within regulated manufacturing, along with excellent problem-solving skills and a collaborative mindset. Specifically, they will have:Degree-level education or equivalent experience in a relevant fieldExperience working in a GMP-regulated, high-paced manufacturing environment (cosmetic or pharmaceutical a plus)Proven track record maintaining and improving quality systems, including authoring and managing procedures and work instructionsSolid understanding of compliance requirements aligned to national and international quality standardsHands-on experience conducting audits and driving quality investigations to resolutionConfidence working with electronic quality systems (such as Veeva, OpenText) and proficiency with Microsoft Office and related platformsStrong written and verbal communication skills, with the ability to engage cross-functional teams and stakeholdersA proactive approach, capable of working both independently and within a team to deliver against key prioritiesPerks and benefitsIn return, you'll be part of an organisation that offers:A competitive salary and comprehensive benefits packageOpportunities to grow your expertise within a global quality and compliance frameworkExposure to international best practices and the chance to collaborate across sites and functionsA supportive environment that values new ideas, problem-solving, and ongoing professional developmentFor immediate consideration, please apply now. If this isn't quite the right fit but you're interested in exploring other quality and compliance opportunities, reach out to discuss how we can help you find the right next step.