Head of Quality Operations – Pharma Manufacturing – Newcastle Pharma Manufacturing

Greenlsr; Newcastle upon Tyne; On-site; GBP 100,000 - 125,000; Full time

Job summary

A pharmaceutical company in Newcastle Upon Tyne seeks a Head of Quality Operations to ensure compliance with global standards while driving innovation in formulation and product quality. The role involves overseeing QA/QC activities, leading teams, and managing regulatory inspections. Candidates should have over 12 years of pharma manufacturing experience with leadership in quality roles. Competitive compensation and strategic leadership opportunities are offered.

Benefits

Competitive compensation

Leadership role with strategic impact

Opportunity to drive quality and innovation in healthcare

Qualifications

• 12+ years of experience in pharmaceutical manufacturing, particularly in quality and formulation roles.
• Strong understanding of cGMP and ICH guidelines, along with regulatory requirements.
• Experience with regulatory inspections and international filings is essential.

Responsibilities

• Oversee all QA/QC activities to ensure cGMP compliance.
• Lead formulation development for pharmaceutical products.
• Manage tech transfers and process validations.

Skills

Leadership in quality and formulation

Knowledge of cGMP

Regulatory compliance

Job description

Head of Quality Operations – Newcastle Upon Tyne

About The Job

The Head of Quality will ensure compliance with global regulatory standards (e.g., FDA, EMA, WHO GMP) while driving formulation innovation and product quality across the organisation.

Key Responsibilities

• Oversee all QA/QC activities, ensuring cGMP compliance and robust Quality Management Systems.
• Lead formulation development for new and existing pharmaceutical products.
• Manage tech transfer, process validation, and regulatory readiness.
• Direct internal audits, external inspections, and CAPA implementation.
• Build and mentor high-performing quality and R&D teams.
• Collaborate with Manufacturing, Regulatory, and Supply Chain for seamless operations.

Qualifications

• 12+ years of experience in pharma manufacturing, with leadership in quality and formulation.
• Strong knowledge of cGMP, ICH guidelines, QbD, and regulatory requirements.
• Experience with regulatory inspections and international filings (e.g., ANDA, NDA).

What We Offer

• Competitive compensation
• Leadership role with strategic impact
• Opportunity to drive quality and innovation in healthcare

How To Apply

Send your CV to Charlie Wallbank at: [e-mail]