Senior Quality Assurance Associate

Cure Talent; Sevenoaks; On-site; GBP 50,000 - 65,000; Full time

Job summary

A leading Pharmaceutical CDMO is seeking a Senior Quality Assurance Associate to maintain and develop their Pharmaceutical Quality System across UK and Ireland. The role involves providing QA support, hosting audits, and training QA Officers in a collaborative environment.

Qualifications

• Proven experience in QA within a GMP-regulated pharmaceutical environment.
• Strong knowledge of PQS management including quality systems.

Responsibilities

• Maintain and develop the company’s global PQS in line with regulations.
• Support and host internal, supplier, and regulatory audits.

Skills

Leadership

Communication

Problem Solving

Education

Scientific degree (e.g. Chemistry, Pharmaceutical Sciences)

Job description

1 day ago Be among the first 25 applicants

This range is provided by Cure Talent. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

Direct message the job poster from Cure Talent

Connecting the best talent in QARA with Innovative MedTech & STEM Organisations

Cure Talent is thrilled to partner with a leading Pharmaceutical CDMO who, due to their exceptional continued growth, have an exciting opportunity for a Senior Quality Assurance Associate to join their team.

In this role, you will take a lead in maintaining and developing the Pharmaceutical Quality System across UK and Ireland operations. You will provide specialist QA support across the full range of Quality Systems, including deviations, CAPA, change control, validation, supplier audits, and document control. You’ll also play a key role in hosting audits, training QA Officers, and supporting cross-functional teams to ensure operational compliance with GMP and GDP regulations.

Key Responsibilities:

• Maintain and develop the company’s global PQS in line with current regulations and internal standards
• Oversee core PQS elements including change controls, CAPAs, deviations, complaints, document control, and risk management
• Provide QA support for validation, environmental monitoring, and technical documentation
• Review and approve batch records, QC test data, and finished product specifications
• Support and host internal, supplier, and regulatory audits
• Mentor and train QA Officers, delivering internal training on GMP and GDP requirements
• Collaborate with production and technical teams to ensure compliance across manufacturing, storage, and distribution
• Contribute to management reviews and present KPIs on Quality System performance

What You Will Need:

• Proven experience in QA within a GMP-regulated pharmaceutical environment
• Strong knowledge of PQS management, including quality systems such as CAPA, change control, and deviations
• Experience supporting audits, document control, and product quality reviews
• Excellent team leadership, communication, and problem-solving skills
• A scientific degree (e.g. Chemistry, Pharmaceutical Sciences) or equivalent relevant experience
• Experience working with sterile and non-sterile products highly desirable
• Internal or Lead Auditor qualification preferred

If you are passionate about Quality Assurance and want to work in a dynamic and collaborative pharmaceutical setting, we would love to hear from you!

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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