Pharma

If you’re an experienced QP, this is a fantastic opportunity to join a progressive pharmaceutical company in one of their core locations in the East Midlands.

Working with a market leading, global brand, you will join a growing UK operation that has exciting development plans set over the coming years. This specific position is a hands on QP role that will require versatility, flexibility and outstanding stakeholder skills, working with teams at all levels.

This will be a site based role on a 40hr week, Monday to Friday. However, given the expansion plans in manufacturing, flexibility around the working hours and days is critical.

For further information, please contact Mark Bux-Ryan.

If this role sounds of interest, but the location is not right, please still get in contact as we have other similar positions live and pipelined for Q1 2026.

 
Key experience:

• Eligibility to perform as a QP within the UK
• Ideally, strong understanding and experience of GMP aseptic and sterile manufacturing conditions, although non-sterile manufacturing will be considered.

Flexibility in approach to working hours and demands of the role 

We’re partnering exclusively with a growing pharmaceutical company embarking on an exciting phase of site transformation and investment. Although a smaller facility, it forms part of a wider European network and continues to receive strong backing to expand its operations and modernise its infrastructure.

As the site prepares for the installation of new equipment and the enhancement of its operational capabilities, we’re seeking a motivated professional to join the Engineering team.

This position will take the lead on CQV activities, primarily focusing on commissioning and qualification. The ideal candidate will bring a flexible, hands-on approach – ready to contribute to key site projects in a collaborative, fast-evolving environment, and in compliance with GMP standards.

 

Requirements

• Pharmaceutical industry experience with an understanding of GMP
• Minimum 2 years’ engineering experience within a CQV capacity
• Knowledge and understanding of automation and computerised systems is a strong advantage
• Flexibility in being on site as required for additional work (overtime / TOIL available) as the site transforms

We’re working with a leading pharmaceutical company entering an exciting phase of growth, with new product introductions, operational scale-ups, and site expansions underway. This is a unique opportunity to join a small, hands-on site where you’ll play a key leadership role in shaping its engineering function. As Engineering Manager, you’ll take full accountability for a compact team, overseeing maintenance, servicing, and contributing directly to engineering projects. This is a varied, practical role ideal for someone who enjoys being close to the action and making a tangible impact day-to-day. You don’t need decades of experience – what matters most is your willingness to get stuck in and lead by example. Full training will be provided on pharmaceutical equipment and processes. Standard hours are 7am–3pm, Monday to Friday, but flexibility is essential due to occasional call-outs (including nights and weekends). Overtime/TOIL is available. Requirements: Minimum 2 years’ hands-on engineering/maintenance experience in a manufacturing environment Mechanical and electrical engineering capability preferred Supervisory experience is ideal, but strong technical depth and leadership potential will also be considered Pharmaceutical and/or GMP experience is a plus, but not essential Must live (or be willing to relocate) within one hour of the site due to call-out requirements

Quality Assurance Manager – Greater Manchester

We’re working with a leading pharmaceutical company entering an exciting phase of growth, with new product introductions, operational scale-ups, and expansions at their brand-new site. This is a unique opportunity to join a small, hands-on site where you’ll play a key leadership role in shaping its QA function.

As QA Manager, you’ll manage operational and project teams to ensure compliance with GMP, support product development, and maintain inspection readiness. You’ll also play a key role in implementing digital systems like eQMS and LIMS and contribute to global quality initiatives.

This is a fantastic opportunity for a quality professional with a strong background in pharmaceuticals who is ready to lead, mentor, and make a lasting impact.

Key Responsibilities:

• Lead site QA activities and represent QA in the Site Management Team.

• Oversee internal and external audits, deviations, CAPAs, change controls, and OOS/OOT investigations.

• Maintain contamination control strategy and ensure Data Integrity principles are upheld.

• Drive continuous improvement and support globalisation of SOPs and quality systems.

• Manage and mentor QA staff, ensuring training and development plans are in place.

• Support regulatory inspections (MHRA, HSE) and ensure compliance with licenses and GMP.

• Collaborate on new product development and system implementations (eQMS/LIMS).

Requirements:

• Degree or equivalent in a relevant scientific discipline.

• Minimum 5 years’ experience in Quality Assurance, ideally within steriles.

• Previous managerial or supervisory experience with proven leadership skills.

• Strong regulatory knowledge (GMP, MHRA, HSE).

• Excellent communication, organisation, and interpersonal skills.

• Proficiency in Microsoft Office and understanding of PrOFS.

​QC Chemist

 

Join a dynamic team as a QC Chemist/ Analyst at an esteemed international pharmaceutical company. The QC team is expanding at our client’s cutting-edge facility in Surrey.

In this role, you'll be at the forefront of pharmaceutical analysis, contributing to a rapidly growing niche field. You'll have the opportunity to develop your skills and advance in your career while enjoying competitive remuneration.

These positions involve shift work, including nights, so flexibility is key. The shifts would be rotating weekly; 3am-11am, 6am-2pm and 8am-4pm.

 

Key requirements:

·       A degree in a Life Sciences discipline or equivalent

·       Previous work experience in a Quality Control Laboratory

·       Familiarity with chromatography techniques such as HPLC and GC is essential

·       Understanding of GMP principles or willingness to adhere to regulated procedures

·       Flexibility to work shifts

·       Applicants must have full permanent right to work in the UK

 

If you're ready to join a supportive team and make your mark in the pharmaceutical industry, apply below or contact Jolie Trahar for more information.

 

Keywords: QC, quality control, analyst, analytical, laboratory, GMP, entry level, graduate, science, pharmaceutical, biotechnology, manufacturing, shift work.

 

 

 

​QC Chemist - 18 month FTC

 

Join a dynamic team as a QC Chemist/ Analyst at an esteemed international pharmaceutical company. The QC team is expanding at our client’s cutting-edge facility in Surrey.

In this role, you'll be at the forefront of pharmaceutical analysis, contributing to a rapidly growing niche field. You'll have the opportunity to develop your skills and advance in your career while enjoying competitive remuneration.

These positions involve shift work, including nights, so flexibility is key. The shifts would be rotating weekly; 3am-11am, 6am-2pm and 8am-4pm.

 

Key requirements:

·       A degree in a Life Sciences discipline or equivalent

·       Previous work experience in a Quality Control Laboratory

·       Familiarity with chromatography techniques such as HPLC and GC is essential

·       Understanding of GMP principles or willingness to adhere to regulated procedures

·       Flexibility to work shifts

·       Applicants must have full permanent right to work in the UK

 

If you're ready to join a supportive team and make your mark in the pharmaceutical industry, apply below or contact Jolie Trahar for more information.

 

Keywords: QC, quality control, analyst, analytical, laboratory, GMP, entry level, graduate, science, pharmaceutical, biotechnology, manufacturing, shift work.