Quality Assurance Specialist

OASIS Group; Loughborough; On-site; GBP 30,000 - 50,000; Full time

Job summary

An established industry player is seeking a Quality Assurance Specialist to enhance their Pharma Services team. This role is pivotal in ensuring compliance with the Quality Management System and involves conducting audits, facilitating quality investigations, and supporting various projects. Candidates should possess A-Level qualifications and experience in a QA role within a pharmaceutical context. This is a fantastic opportunity to contribute to meaningful projects in a collaborative environment, enhancing your career in a globally recognized firm dedicated to advancing human health.

Qualifications

• Experience in a QA role within a Pharmaceutical Quality System.
• A-Level or equivalent required; Bachelor's preferred.

Responsibilities

• Support compliance of the Quality Management System (QMS).
• Conduct internal and external audits, assist in process improvements.

Skills

Quality systems

Quality risk management

Education

A-Level qualification (or equivalent)

Bachelor’s degree in a scientific or technical discipline

Job description

Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients.

Skills and Attributes

• Quality systems
• Quality risk management

Description

Quality Assurance Specialist

Location: Loughborough

Hours: 37.5 hours

Business Unit: Pharma Services

Open To: Internal & External Applicants

Ref No.: HRJOB10202

The Role

We are currently recruiting for a Quality Assurance Specialist in Almac Pharma Services. In this role, you will be responsible for supporting compliance of the Quality Management System (QMS) and working to facilitate Quality Investigations (Root cause analysis, Deviations, Vendor queries, etc.). Key responsibilities include monitoring operations, conducting internal and external audits, assisting in process improvement initiatives, and providing QA support for various projects.

Key Requirements

Applicants must have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full-time, permanent employment in the UK.

To be successful in this position, you will need A-Level qualification (or equivalent) and experience in a QA role within a Pharmaceutical Quality System.

Whilst not essential, it would be an advantage if candidates have a Bachelor’s degree (or above) in a scientific (Chemistry, Biology or Pharmacy) or technical (Engineering) discipline (or equivalent), previous experience in writing and producing detailed reports, and direct experience in the manufacture of solid oral dosage products.

Apply Now

Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.

Closing Date

We will no longer be accepting applications after 5pm on Sunday 12th January 2025.

RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CVs received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.

Almac Group is an Equal Opportunity Employer.