QA Officer - Pharmaceuticals

Smart4Sciences; United Kingdom; On-site; GBP 30,000 - 40,000; Full time

Job summary

Join Smart4Sciences as a QA Officer in Hull, a role pivotal to quality assurance in a growing pharmaceutical company. This position offers a chance to influence quality standards while working collaboratively in a modern facility focused on continuous improvement and employee development.

Benefits

Competitive salary and benefits package

Opportunities for progression and development

Positive, quality-driven culture

Qualifications

• Prior experience in a GMP-compliant pharmaceutical environment.
• Strong understanding of regulatory guidelines.

Responsibilities

• Support Quality Management System (QMS) implementation and maintenance.
• Conduct batch record review and assist in product release activities.
• Handle deviations, CAPAs, and customer complaints.

Skills

Attention to detail

Communication skills

Knowledge of pharmaceutical quality systems

Education

Science degree or relevant qualification

Job description

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