Packing operator

Great Yarmouth
8 months ago
Applications closed

Related Jobs

View all jobs

Clone - CNC Programmer/Setter/Operator

Medical Secretary *IMMEDIATE START

Mechanical Engineer

Business Development Executive (part-time)

Multi-skilled Maintenance Engineer (Days)

European Technical Services Manager

Packing Operator

Our client, a successful and dynamic Pharmaceutical Manufacturing company, is currently seeking a Packing Operator to join their Production team.

This is a full-time position, based in Great Yarmouth.

Hours:

Week one

Monday to Thursday 6am to 2pm

Friday 6am to 1pm

Week two

Monday to Thursday 1.45pm to 10pm

Friday 12.45pm to 6.45pm

Benefits:

  • Competitive salary, salary reviewed annually with an annual bonus payable in May depending on Company performance

  • Holiday is 25 days less 3 to cover Christmas closure plus bank holidays.

  • Pension offered at 5%, increasing to 6% after 5 years’ service, this is offered on a matched / salary exchange basis.

  • Life Assurance, payable at 4 times basic salary

  • AXA PPP private health offered after a qualifying period.

  • Employee Assistance Programme

  • A great working environment

  • Full initial and on-going training and career development

  • Free lunch offered daily, plus tea / coffee etc

  • Free onsite parking

    Key Knowledge & Skills:

  • Good numeracy and verbal and written communication skills.

  • Previous experience in a similar role within a manufacturing environment.

  • Strong health and safety awareness

  • Be a competent computer user.

  • Have a high attention to detail, with codes and quantities.

  • Competent with documentation

    Key responsibilities:

  • Identifying continuous improvement and waste reduction opportunities and supporting their implementation.

  • Ensure self is always occupied remaining flexible across the department and site.

  • Show respect when dealing with colleagues and external parties.

  • Be trained and qualified in all relevant Health and Safety procedures.

  • Maintain high standards of general line tidiness and housekeeping to ensure safe and effective working.

  • Ensure that all Production Line operations are conducted in a safe manner.

  • Ensure any H&S hazards or incidents are reported on a timely basis and take part in subsequent investigations.

  • Ensure that Production and GMP operations are carried out in line with cGMP, Medicines, Medical Devices and Cosmetics regulations.

  • Ensure compliance with local procedures on the Production Lines Delivery

  • Performance of the Production Line (Output vs Plan and Product Quality).

  • Support G3 Packing Operator in moving stock to and from the line as required.

  • Identify problems with equipment/components that affect running performance and product quality.

  • Assist with training of any new team members in a safe and effective operation of the line

    For further details of this exciting opportunity please forward a copy of your CV today!

    Todd Hayes Ltd is an equal opportunities employer. Due to the large number of applications we receive I’m afraid we are unable to respond to everyone individually however your details will remain on file should another suitable opportunity become available moving forward.

    If we can take your application further we will of course be in touch.

    Todd Hayes is acting as an Employment Business in relation to this vacancy.

    Todd Hayes Ltd

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.

Neurodiversity in Medical Technology Careers: Turning Different Thinking into a Superpower

Medical technology sits at the intersection of health, engineering & innovation. From imaging & diagnostics to digital health apps, wearables & surgical robotics, medtech is about solving complex real-world problems that directly affect patients’ lives. To do that well, the sector needs people who think differently. If you live with ADHD, autism or dyslexia, you may have been told your brain is “too distracted”, “too literal” or “too disorganised” for a regulated, safety-critical industry. In reality, many traits that made school or previous jobs difficult can be huge strengths in medical technology – from pattern-spotting in clinical data to meticulous attention to detail in device testing. This guide is for neurodivergent job seekers exploring medical technology careers in the UK. We’ll cover: What neurodiversity means in a medtech context How ADHD, autism & dyslexia strengths map to common medtech roles Practical workplace adjustments you can ask for under UK law How to talk about your neurodivergence in applications & interviews By the end, you’ll have a clearer sense of where you might thrive in medical technology – & how to turn “different thinking” into a genuine superpower.

Medical Technology Hiring Trends 2026: What to Watch Out For (For Job Seekers & Recruiters)

As we move into 2026, the medical technology (MedTech) jobs market in the UK is changing fast. Hospitals and health systems are under pressure to do more with less. Diagnostics and devices are becoming smarter, more connected and more regulated. AI, robotics and remote monitoring are no longer “future tech” – they’re being built into mainstream care pathways. At the same time, budgets are tight, funding cycles are uneven and some healthtech start-ups are consolidating or being acquired. That means fewer vague “innovation” roles and more focus on medical technology jobs that directly support regulatory approval, patient safety, NHS adoption and commercial growth. Whether you are a MedTech job seeker planning your next move, or a recruiter building teams for medical device, diagnostics or digital health companies, this guide breaks down the key medical technology hiring trends for 2026.

Medical Technology Recruitment Trends 2025 (UK): What Job Seekers Need To Know About Today’s Hiring Process

Summary: UK medical technology hiring has shifted from title‑led CV screens to capability‑driven assessments that emphasise regulatory‑aware product delivery (QMS, ISO 13485), software lifecycle & risk (IEC 62304/14971), usability (IEC 62366), clinical & regulatory strategy (MDR/UKCA), device cyber security & privacy, and measurable patient/clinical and commercial impact. This guide explains what’s changed, what to expect in interviews & how to prepare—especially for SaMD engineers, AI/ML in medical devices, product & quality engineers, regulatory/clinical affairs specialists, validation/verification, manufacturing/operations, and digital health roles. Who this is for: Software/firmware engineers in medtech, SaMD/AI engineers, systems & verification engineers, quality & regulatory affairs (QARA), clinical evaluation/PMCF specialists, human factors engineers, medical device cyber security & privacy, test/validation, manufacturing & operations, field/service engineers, and medtech product managers in the UK.