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QA Officer - Pharmaceutical Manufacturing - HULL

Join a Growing Pharmaceutical Company with a Passion for Quality and Innovation!

We are partnering with an ambitious and rapidly expanding pharmaceutical manufacturing company based in Hull to recruit a QA Officer. This is an exciting opportunity to be part of a company making significant investments in their facilities, people, and future.

As a QA Officer, you'll play a vital role in ensuring that quality standards are upheld across all stages of manufacturing and supply. Whether you're an experienced QA Associate looking to take the next step, or already operating as a QA Officer, this role offers the chance to grow in a supportive and collaborative environment.

Key Responsibilities:

Support the implementation and maintenance of the Quality Management System (QMS) in line with GMP and regulatory requirements.

Conduct batch record review and assist in product release activities.

Handle deviations, CAPAs, change controls, and customer complaints.

Assist with internal audits and regulatory inspections.

Support document control processes and SOP management.

Collaborate with manufacturing, QC, and supply chain teams to promote a culture of continuous improvement.

Ideal Candidate Profile:

Prior experience in a GMP-compliant pharmaceutical environment, ideally within a CDMO.

Strong understanding of pharmaceutical quality systems and regulatory guidelines.

Excellent attention to detail and communication skills.

Ability to work both independently and as part of a team.

Science degree or relevant qualification preferred.

Why Join?

Be part of a growing business with exciting expansion plans.

Modern facilities and a forward-thinking team.

Genuine opportunities for progression and development.

Competitive salary and benefits package.

Positive, quality-driven culture.

Ready to take your QA career to the next level in a company that's going places?
Apply now or contact Gareth Gooley on for more info

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Project Automation Engineer-Contract- Pharmaceutical- ABB- ABB800XA

I am currently recruiting for a Project Automation Engineer with proven experience in ABB control systems to join a global pharmaceutical company on a contract basis.

Key responsibilities for the Project Automation Engineer-Contract

Review technical documentation for automation and engineering activities.Design, configure, and troubleshoot ABB DCS/PLC/SCADA systems (e.g., ABB 800xA), communicating with the client directly.Develop and review documentation, system architecture, and detailed design documentsEnsure automation systems meet GxP and GMP compliance standards

Requirements for the Project Automation Engineer-Contract

Bachelor's degree in Electrical, Automation, or Control Engineering (or related discipline)Hands-on experience with ABB control systems, preferably ABB 800xAExcellent communication and stakeholder management skills

To apply for the Project Automation Engineer-Contract or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email

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Validation Engineer - Pharmaceuticals - Hull

Salary negotiable

Are you looking for your next step in Pharmaceutical Validation ?

This company is experiencing an exciting period of growth, known for internal progression & variation, this is great place to progress your skills & expertise in Validation Engineering.

As the Validation Engineer, you will benefit from working on various projects including exposure to the full validation life from Design Qualification through to operational handover & inclusive of CSV.

Desirable Experience & Qualifications

Broad validation experience in GMP Experience in cGMP Annex 11, 21 CFR Part 11, GAMP 5. Able to write URS and VMP (DQ, OQ, IQ, PQ)

would like to discuss please get in touch & apply now or contact Simon Fowler at NGAGE Smart4Sciences

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Role: QC Analyst

Location: Hull

Full time

Salary: Around £30,000 - £32,000

A fantastic opportunity has arisen for Senior QC Analysts to join a sterile manufacturing facility in Hull.

The role: QC Analyst

As an Analyst you will:

Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verificationSupport the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis.

The successful QC Analyst will have:

A relevant science degree or equivalent qualificationUnderstanding of current GMP, Health and Safety and COSHH regulationsExperience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervisionThe ability to take on a limited supervisory role would be an advantageRelevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation

To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

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