Laboratory Analyst – Micronised Substances (MSQC)

GSK; Ware; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking a Laboratory Analyst to join their Ware manufacturing site. The role involves conducting product testing and ensuring compliance with Good Manufacturing Practices, while working collaboratively to maintain product supply and drive improvements. Ideal candidates will have GMP experience and strong problem-solving skills, contributing to a dynamic team focused on producing high-quality respiratory devices and medicines.

Benefits

Competitive salary

Annual bonus based on performance

Training opportunities

Industry conference participation

Support for professional development

Healthcare and wellbeing programs

Recognition programs

Qualifications

• GMP experience required.
• Strong interpersonal skills essential.
• Motivated individual thriving in fast-paced environments.

Responsibilities

• Carry out product testing and analysis.
• Ensure compliance with GMP and EHS regulations.
• Collaborate with lab and external departments.

Skills

Problem-solving

Teamwork

Attention to detail

Communication

Education

Minimum 2 A levels or equivalent qualifications

Tools

IT and computer systems

Job description

We are looking for a forward-thinking person to join our world-class team to support the Ware manufacturing site’s laboratories. We seek someone who can innovate processes and work collaboratively to drive the lab forward, while maintaining product supply.

Job Purpose:

The Laboratory Analyst is central to our site operations. You will carry out product testing and analysis to support the laboratory team in providing a consistent flow of safe, efficacious, and compliant products. You must ensure compliance with Good Manufacturing Practice (GMP) and EHS regulations. The role involves teamwork within the lab and with external departments to maintain supply, solve problems, and drive improvements.

About You:

This role suits a motivated individual with GMP experience. You should thrive in a fast-paced environment, enjoy problem-solving, and be committed to continuous improvement. Strong interpersonal skills, teamwork, and good communication are essential. Attention to detail and a mindset for ongoing improvement are also required.

About Ware Manufacturing Site:

Our site produces Respiratory devices and Oral Solid Dose medicines, employing approximately 1,500 staff. It is a key site for launching new medicines and high-volume production of respiratory devices.

Application Deadline:

Wednesday, 4th June 2025 (COB).

Basic Qualifications:

1. Minimum 2 A levels or equivalent qualifications in a relevant subject
2. Experience with IT and computer systems

Preferred Experience:

1. Knowledge of current Good Manufacturing Practice (cGMP)
2. Experience testing micronised materials, e.g., Particle Size Distribution

Benefits:

• Competitive salary
• Annual bonus based on performance
• Training opportunities
• Industry conference participation
• Support for professional development
• Healthcare and wellbeing programs
• Recognition programs

Learn more about our benefits at Life at GSK.

Why GSK?

GSK is committed to uniting science, technology, and talent to combat disease, positively impacting billions of lives and fostering a thriving workplace. We focus on vaccines, medicines, and data-driven innovations across key therapeutic areas.

Our success depends on our people. We aim to create an inclusive environment where everyone can thrive, feel valued, and grow. Join us in our journey to get Ahead Together.

Equal Opportunity Employer:

GSK provides equal employment opportunities regardless of race, gender, age, disability, or other protected characteristics. We support flexible working arrangements. For adjustments during the application process, contact [e-mail] or call 0808 234 4391 (hours apply).

Additional Notes:

For agency inquiries, prior authorization from GSK is required. US healthcare professionals should be aware of compliance and reporting obligations related to expenses and disclosures.