Quality Assurance Specialist

JR United Kingdom; Colchester; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading global pharmaceutical company is looking for a motivated Quality Assurance Specialist in Colchester. This role involves ensuring compliance with GMP standards, conducting reviews of clinical batch records, and collaborating with teams globally to support clinical supply chains. The ideal candidate will possess a relevant scientific degree and strong organizational skills, with potential experience in QA environments preferred.

Qualifications

• Bachelor's degree in Chemistry, Biology, or Pharmacy required.
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal abilities.

Responsibilities

• Perform final review of clinical batch records for GMP compliance.
• Compile and approve data packs for Qualified Person release.
• Manage issue resolution and maintain documentation accuracy.

Skills

Attention to detail

Organizational skills

Communication

Interpersonal abilities

Ability to work independently

Education

Bachelor's degree in a scientific discipline

Job description

Social network you want to login/join with:

Quality Assurance Specialist, colchester

col-narrow-left

Client:

Planet Pharma

Location:

colchester, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

1

Posted:

04.06.2025

Expiry Date:

19.07.2025

col-wide

Job Description:

An exciting opportunity is available for a motivated and detail-oriented Quality Specialist to join a Global Development Quality team. This role offers exposure to a wide range of investigational medicinal products, from small molecules to advanced immunotherapies, contributing directly to the delivery of life-saving treatments to patients.

Key Responsibilities:

• Perform final review of clinical batch records to ensure compliance with GMP and regulatory filings.
• Compile and approve data packs for Qualified Person (QP) release.
• Collaborate with global clinical supply chain teams and manufacturing sites (internal and external).
• Manage issue resolution and ensure timely documentation and communication.
• Maintain high standards of accuracy and compliance throughout the review process.

Qualifications & Skills:

Required:

• Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy).
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal abilities.
• Ability to work independently and manage multiple priorities.

Preferred:

• Prior experience in a QA or GMP-regulated environment.
• Familiarity with clinical manufacturing and regulatory compliance processes.