Quality Assurance Engineer

Alton
1 year ago
Applications closed

Related Jobs

View all jobs

Quality Assurance Manager – Pharmaceuticals / life sciences

Sterility Assurance Manager (12 Month Fixed Term Contract)

Medical Devices Consultant - Senior Mechanical Engineer

Business Development Manager - Biotech CDMO

Technical Training Specialist - Medical Devices

Senior Scientist Mass Spec

Quality Assurance Engineer

I am working with a cosmetic and pharmaceutical manufacturing site based in Hampshire, with manufacturing of multiple dosage products, this is a fantastic opportunity for someone looking to develop their skillset and career within pharmaceuticals.

Key responsibilities for the Quality Assurance Engineer

Ensure the manufacturing on the site in accordance with cGMP and any regulatory requirements.
Collaborate and work closely with multiple different departments to ensure customer satisfaction.
Ownership and execute of outstanding and new CAPAs for the manufacturing facility.
Assist and sometimes lead any investigations for non-conformances.
Perform internal audits to ensure cGMP.
Review and validate SOPs and other process to ensure cGMP Compliance.Requirements for the Quality Assurance Engineer

Hold a Scientific Degree.
2 Years' experience working within Quality Assurance in the pharmaceutical industry.
Strong written and verbal communication skills.

Benefits for the Quality Assurance Engineer

Free on-site parking.
Subsidised canteen
Healthshield cash plan/counselling
No weekends.
25 + 8 bank holidays.

To apply for the Quality Assurance Engineer or here more information, please contact Liam Shannon at Smart4Sciences on (phone number removed)

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Jobs

CSL Behring Jobs UK: Careers, Salaries, Locations & How to Get Hired

CSL Behring is one of the world’s leading biopharmaceutical companies specialising in plasma-derived therapies, recombinant proteins, gene therapy, vaccines, and rare disease treatments. If you’re a UK job seeker looking for a career with real purpose, strong scientific standards, and long-term progression, CSL Behring roles can be an excellent fit, especially if you have experience in biotech, pharma manufacturing, quality, engineering, supply chain, clinical operations, regulatory, pharmacovigilance, or commercial. This guide is written for UK candidates who want to understand what CSL Behring jobs typically involve, which roles to target, where opportunities may be based, what skills recruiters look for, and how to tailor your application to stand out.

Careers

How Many Biotechnology Tools Do You Need to Know to Get a Biotech Job?

If you are trying to break into biotechnology or progress your career, it can feel like the list of tools you are expected to know is endless. One job advert asks for PCR, another mentions cell culture, another lists bioinformatics pipelines, automation platforms or GMP systems. LinkedIn makes it worse, with people sharing long skills lists that make you wonder if you are already behind. Here is the reality most biotech employers will not say out loud: they are not hiring you because you know every tool. They are hiring you because you understand biological systems, can work accurately and safely, follow protocols, interpret results and contribute reliably to a team. Tools matter, but only when they support those outcomes. So how many biotechnology tools do you actually need to know to get a job? The answer depends on the role you are targeting, but for most job seekers it is far fewer than you think. This article breaks down what employers really expect, which tools are essential, which are role-specific, and how to focus your learning so you look employable rather than overwhelmed.

Jobs

What Hiring Managers Look for First in Biotechnology Job Applications (UK Guide)

Hiring managers in biotechnology do not start by reading your CV word for word. They scan for credibility, relevance and risk. In a regulated, evidence-driven sector like biotech, the first question is simple: is this person safe, competent and genuinely capable of contributing in this environment? Whether you are applying for roles in research, manufacturing, quality, regulatory, clinical, bioinformatics or commercial biotech, the strongest applications make the right signals obvious in the first 10–20 seconds. This in-depth guide explains exactly what hiring managers in UK biotechnology look for first, how they assess CVs, cover letters and portfolios, and why capable candidates are often rejected. Use it as a practical checklist before you apply.

🍪 We use cookies to enhance your browsing experience on our website. By continuing to use this site, you consent to the use of cookies as described in our Cookie Policy. You can review our Cookie Policy for more information.