12 jobs found

Job Title: Cleanroom Technician - Level 1 Location: Leatherhead, Surrey Salary: Competitive Job Type: Full Time, Permanent About Us: MatOrtho is an internationally recognised joint replacement devices innovator dedicated to improving the quality of life of all patients through technical innovation and ethical design click apply for full job details

We are seeking a detail-oriented and dedicated Technician to join our client's Pharmaceutical Manufacturing team. This is an Entry Level position for the candidates who recently graduated from University or College and are passionate about pharmaceutical industry. The successful candidate will be responsible for supporting manufacturing and quality control processes within a cGMP regulated environment usually in a Clean Room. This role offers an excellent opportunity for someone who wants to gain experience within highly advanced manufacturing operation and is prepared to work in a cleanroom environment and ensure compliance with cGMP regulations at all times. The shift pattern is weekly rotating day shift and afternoon shift, Monday to Friday. You will be expected to work 37.5 hours per week. Responsibilities Manufacture of high end consumable products for commercial and clinical trial applications. Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs Recording data appropriately in batch records and supporting documentation Maintaining hygiene standards in all production areas Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing) Set-up, operation and strip down of modern high speed production equipment Working flexibly within a team to ensure adherence to the production schedule Maintaining personal training records Qualifications Previous experience in GMP manufacturing or working in a cleanroom environment would be an advantage (but not essential) Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded Have a high degree of integrity - to maintain compliance with GMP regulations Be reliable, and able to make a positive contribution to the production team Good practical skills Demonstrates good literacy and numeracy skills Able to communicate well via written media with specific emphasis on report writing Able to work with minimal supervision High attention to detail Good levels of physical fitness Must have a keen interest in Life Sciences/Pharma industries Computer skills: Must be competent in the use of MS Office, particularly Excel and Word. Literacy and Numeracy: Must have excellent communication skills particularly, written English and interpretation and Maths. Benefits Private Medical Insurance and Health Cash Plan Group Personal Pension Plan Life Assurance Generous leave entitlement of 33 days per annum A friendly and focused working environment Career development opportunities Potential job share Cycle to work scheme Free parking Health & wellbeing programme On-site parking Discretional annual bonus This role provides an engaging environment for individuals committed to scientific excellence and quality assurance. Candidates should demonstrate a strong work ethic, analytical mindset, and the ability to follow detailed procedures meticulously. Please note: Only candidates with permanent Right to Work in the UK will be considered. Please email your CV today or apply through this website.

We are seeking a detail-oriented and experienced Manufacturing Technician to join our pharmaceutical team. The successful candidate will be responsible for supporting manufacturing and quality control processes within a regulated laboratory environment. This role offers an excellent opportunity for someone who wants to expand experience within highly advanced pharmaceutical operation and is prepared to work in a cleanroom environment and ensure compliance with GMP regulations at all times. The ideal candidate will therefore have a pharmaceutical background and have ideally gained experience within a cGMP, FDA and MHRA regulated environment. The shift pattern is weekly rotating day shift and afternoon shift, Monday to Friday. You will be expected to work 37.5 hours per week. Responsibilities Manufacture of high end consumable products for commercial and clinical trial applications. Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs Recording data appropriately in batch records and supporting documentation Maintaining hygiene standards in all production areas Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing) Set-up, operation and strip down of modern high speed production equipment Working flexibly within a team to ensure adherence to the production schedule Maintaining personal training records Qualifications Previous experience of pharmaceutical manufacturing or working in a cleanroom environment Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded Be flexibile - to ensure production output and client demands Have a high degree of integrity - to maintain compliance with GMP regulations Be reliable, and able to make a positive contribution to the production team Previous GMP (Good Manufacturing Practice) experience Good practical skills Demonstrates good literacy and numeracy skills Required: Able to communicate well via written media with specific emphasis on report writing Able to work with minimal supervision High attention to detail Must have a keen interest in Life Sciences/Pharma industries Computer skills: Must be competent in the use of MS Office, particularly Excel and Word. Literacy and Numeracy: Must have excellent communication skills particularly, written English and interpretation and Maths. Please note: Only candidates with permanent Right to Work in the UK will be considered. Benefits Private Medical Insurance and Health Cash Plan with Bupa Group Personal Pension Plan Life Assurance Generous leave entitlement of 33 days per annum A friendly and focused working environment Career development opportunities Potential job share Cycle to work scheme Free parking Health & wellbeing programme On-site parking This role provides an engaging environment for individuals committed to scientific excellence and quality assurance. Candidates should demonstrate a strong work ethic, analytical mindset, and the ability to follow detailed procedures meticulously. Please email your CV or apply through this website.

Job Title: Cleanroom Technician - Level 1 Location: Leatherhead, Surrey Salary: Competitive Job Type: Full Time, Permanent About Us: MatOrtho is an internationally recognised joint replacement devices innovator dedicated to improving the quality of life of all patients through technical innovation and ethical design. About The Role: The purpose of the role will be to maintain a controlled environment in the cleanroom, process components and instruments, pack, label and ship orthopaedic products in compliance with regulatory rules and guidelines. Execute basic environmental monitoring (EM) activities and routine cleaning within cleanroom to support cGMP and ISO 13485 compliance, including sampling, data recording while adhering to site EM procedures. Duties & Responsibilities: Working in accordance with cGMP practices and guidelines to: Work in an ISO Class 7 cleanroom to manufacture products for terminal sterilisation Maintain a controlled environment in the cleanroom, working in accordance with cleanroom procedures including, but not limited to, full body gowning and perform daily cleaning to set standards Complete cleanroom processes to ensure work is cleared before the end of the day Receive and inspect incoming materials according to specifications, while checking for contamination and quality compliance Clean, assemble and package orthopaedic products according to set standards Operate equipment and machinery required in the assembly of orthopaedic products Communicate status of operations to Cleanroom Manager through weekly meetings to report process and or safety issues Ensure training modules and refreshers are completed within set deadlines Report defective materials and/or that of questionable condition according to the Standard Operating Procedure Be a reliable member of the cleanroom production team Prepare the cleanroom (materials, equipment, packaging etc) to eliminate errors in accordance with Good Manufacturing Practices Work closely with Cleanroom Manager to ensure deadlines are met in addition to completing daily tasks required outside of production (including but not limited to validation, maintenance, environmental monitoring, bioburden testing and quality assignments) Perform final quality checks of finished product according to standard procedures Collaborate with Quality Assurance to identify, implement and support continuous improvement of cleanroom processes and procedures Print implant labels and pack components, ensure products are ready for checks and shrink-wrapping Pack and ship batches for terminal sterilisation, ensure batches are ready for dispatch in within set deadlines About You: Personal attributes/competencies: Strong attention to detail, able to focus on accuracy and quality Able to work with precision, manually handling small parts, requiring good eyesight and hand/eye coordination Able to take initiative Able to work independently without being prompted Able to prioritise and plan work activities, manage time efficiently and adapt to changing priorities Ability to work within tight timelines to meet deadlines Must be able to follow detailed instructions Able to effectively communicate with others Strong team ethics, Work efficiently with cleanroom colleagues Able and willing to learn and develop new skills Good personal hygiene. Expect regular full body gowning and repeated surgical hand washing Must be able to meet the physical requirement of lifting and carrying loads, operating mechanical presses and cleaning Skills and experience: Essential: Strong literacy and numeracy abilities Basic computer skills (Microsoft Word and Excel) Desirable: Full training will be provided but experience in the following would be welcome: Working in a controlled environment Working within a GMP environment Undertaking stock counts UK Driver's License Education and qualifications: Essential: Good standard of education with GCSE or equivalent Maths and English. Benefits: Contributory Group Personal Pension scheme (Aviva) Salary exchange scheme Group Life Assurance Group Income Protection Private healthcare Health Cash Plan Discounted Gym Membership Discounts and rewards scheme Cycle-to-work Scheme Interest-free rail or bus season ticket loan Employee Assistance Programme (24/7 helpline) 25 days' annual leave, plus UK statutory bank holidays Second Medical Opinion Scheme myStrength mental health resource Free parking (subject at the discretion of business park owners) Reimbursement of professional membership fees Staff Referral Programme Access to financial planning advice Company Social Events Please Note: We will not be accepting applications from agencies for this vacancy Please click the APPLY button to send your CV and Cover Letter for this role Candidates with experience or relevant job titles of; Cleanroom Technicians, Laboratory Technicians, Sterile Environment Specialist, Cleanroom Operative, Controlled Environment Technicians, Sterile Room Operator, Manufacturing Technician, Manufacturing Operator, Packing Operative may also be considered for this role.

Location: South of England (Harwell) Type: Full-time Sector: Life Sciences Engineering High-Performance Environments The Mechanical Project Manager will be responsible for the successful delivery of cleanroom and laboratory projects from concept through to commissioning and handover. This role focuses on managing the mechanical services associated with controlled environments, Mechanical Project Manager ensuring projects are delivered safely, on time, within budget, and in compliance with all relevant industry standards and client requirements. What You Will Be Doing Overseeing all stages of the project lifecycle, including conception, design, development, and implementation Managing and coordinating project teams, including engineers, designers, technicians, and subcontractors Develop, manage and maintain Design, Procurement, Construction and Commissioning (DPC&C) programmes in Microsoft Project Responsible for full mechanical cost control, including budgeting, estimating, package procurement, subcontract account management, and agreement of final accounts to meet project targets Chairing weekly subcontractor progress meetings and keeping accurate meeting minutes Ensuring projects are delivered on time and within budget Identifying project risks, implementing mitigation strategies, and resolving issues or delays Managing project resources and materials to support successful delivery Developing and maintaining strong relationships with clients, contractors, and key stakeholders Ensuring compliance with health & safety requirements and relevant industry standards Completing tender reviews and comparison reports to document the equalisation of compliant tender returns Producing building services quality plans (ITPs), including detailed commissioning plans and schedules What We Are Looking For At least 5 years of relevant project management experience within the construction or engineering industry Strong technical knowledge of building services and HVAC systems Sound industry knowledge and understanding of best practice Experience managing projects through the full lifecycle, from pre-construction through to delivery Understanding of cleanroom standards and regulatory requirements (beneficial) Knowledge of GMP environments and validation processes (beneficial) Experience delivering multiple projects concurrently (beneficial) Experience working on fast-track or live operational sites Excellent organisational, communication, and stakeholder management skills with the ability to track and file information efficiently and effectively. Able to achieve results in a client-focused, collaborative manner Ambitious and capable, with a professional and articulate manner and a strong drive to deliver results. Able to work under pressure and meet tight deadlines Qualifications - Site Management Safety Training Certification (SMSTS) (Mandatory) - Construction Skills Certification (CSCS) (Mandatory) - Engineering degree or equivalent qualification in Mechanical Engineering or Building Services (Desirable) Benefits - 31 days holidays (inclusive of public holidays) - Annual Bonus scheme linked to Company performance - Life Insurance - Company Pension - Employee Discounts - Referral Programme - Subsidised Health Assessments

Join Our Team as a Manufacturing Technician! Are you ready to make a difference in the world? We are looking for dedicated individuals to join our client's team in Cramlington, where you will contribute to producing life-saving medical products that help create a healthier, cleaner, and safer world. Position: Manufacturing Technician Contract Type: Temporary Hourly Rate: 15.18 Start Date: ASAP Contract Length: 6 months with a view to become permanent Working Pattern: Full-Time (Continental Shift: 4 days on, 4 days off, 6am - 6pm) Why Join Us? Be part of a dynamic team that values innovation and quality. Enjoy a supportive environment where full training will be provided, even if you don't have previous clean room experience. Opportunity for the role to become permanent after the initial contract period. Key Responsibilities: As a Manufacturing Technician, your day-to-day tasks will include: Safely and efficiently producing high-quality single-use medical products in a cGMP compliant cleanroom. Complying with safe working practises and using the required personal protective equipment (PPE). Maintaining product quality and ensuring compliance with cGMP standards. Handling critical components and setting up raw materials. Reading, following, and understanding detailed assembly drawings and standard operating procedures (SOPs). Performing manual assembly of critical components on a defined production line. Inspecting finished goods in line with approved customer specifications. Accurately detailing and recording critical cGMP data in the batch record. Requirements: We are looking for candidates who: Are capable of working safely in a clean room environment. Can read and accurately follow Batch Record Sheets and Standard Operating Procedures. Preferably have GMP and manufacturing assembly experience. Have a good understanding of the English language, both written and verbal. Possess basic mathematical skills. Ready to Make an Impact? If you are enthusiastic about contributing to the production of essential medical products and are eager to learn and grow in a vibrant environment, we want to hear from you! How to Apply: Don't miss out on this exciting opportunity! Submit your application today and take the first step towards a fulfilling career in manufacturing. Join us in making a positive impact on health and safety across the globe! We are an equal opportunity employer and welcome applications from all backgrounds. Your future starts here! Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser (url removed)

Welding Production Technician required to join a precision aerospace production team to work in a cleanroom environment on the assembly, integration and testing of aerospace devices. Our international Aerospace and Defence client is going through a continued period of expansion and looking for Precision Mechanical Assembly Technicians. The ideal candidate will have experience as a Mechanical fitter experience ideally through apprenticeship with exposure to and of the following; non return valves, flow control valves, solenoid valves, cold gas thrusters or any fluidic components for the space industry. Training and skills development will be provided, extended working hours may be required to meet production targets. Responsibilities Precision assembly and test activities in a Class 8 clean room. Testing the integrity of assembled systems using high pressure gases and leak detection equipment such as helium mass spectrometers. Cleaning components in preparation for assembly and test activities using automatic particle counting equipment and patch sample counting techniques. Electrical testing Gas flow testing of valves, thrusters and fluidic components to ensure components are within tolerance prior to assembly. Digital voltmeters, oscilloscopes, data acquisition systems, high voltage dielectric and insulation resistance test equipment. Material joining processes including manual TIG (Tungsten Inert Gas) welding, orbital welding, and compiling weld inspection reports on parts and test pieces.

Berry Recruitment are NOW hiring for a committed and ambitious Trainee Pharmaceutical Manufacturing Operative to work for a company in Kidlington, Oxford. Role: Trainee Pharmaceutical Manufacturing Operative Salary: 29,000 Per Annum Location: Kidlington, Oxfordshire Hours: 08:30 - 17:30 (Monday - Friday) Key Responsibilities of the Trainee Pharmaceutical Manufacturing Operative : Training & Cleanroom Operations (First 6 Months) During the first phase, you will gain a strong foundation in pharmaceutical manufacturing by learning the importance of hygiene, precision, and safety within a controlled environment. Learn and maintain compliance with cleanroom and GMP procedures. Carry out routine cleaning duties - sweeping, mopping, vacuuming floors, and disinfecting surfaces. Ensure work areas are maintained to the highest cleanliness and safety standards. Assist in equipment preparation and basic maintenance under supervision. Record data accurately and follow standard operating procedures (SOPs). Manufacturing Training & Production (Ongoing Development) After successfully completing your initial training, you will progress to the next stage - learning the full process of pharmaceutical production. Receive comprehensive training in the manufacturing of pharmaceutical products, including tablets, liquids, gels, and powders. Operate and monitor production equipment following GMP and safety guidelines. Measure, mix, and prepare raw materials according to precise formulations. Carry out in-process quality checks to ensure product consistency and compliance. Collaborate with senior technicians and production leaders to meet production targets. Maintain accurate production records and follow documentation standards. About you: A strong interest in science, production, or pharmaceuticals. Excellent attention to detail and commitment to high-quality work. Ability to follow procedures precisely and work safely in a controlled environment. A proactive and positive attitude towards learning new skills. GCSEs (or equivalent) in English, Maths, and Science preferred. No candidate will meet every single desired qualification we have listed. If your experience looks a little different but you think you can role; value to the role, we'd love to learn more about you!" For more information and to apply, contact the Oxford branch of Berry Recruitment - (phone number removed) or click 'Apply Now' to submit your application. Please note that no terminology in this advert is intended to discriminate on the grounds of a person's gender, marital status, race, religion, colour, age, disability or sexual orientation. Every candidate will be assessed only in accordance with their merits, qualifications and ability to perform the duties of the job.

We re expanding an engineering team for a global high tech manufacturer in South Wales, and we re looking for multi skilled professionals who want long term growth in a clean, modern, and highly structured environment. If you re hands on, technically trained, and confident working across both mechanical and electrical systems, this is a strong next step. We welcome people from the forces, automotive, engineering, manufacturing, or any practical technical background; your transferable skills matter. What You ll Be Doing You ll work in a cleanroom facility on PC based equipment (minimal PLC work), carrying out: Strip downs and rebuilds Calibrations and precision adjustments Fault recovery and problem solving Procedure driven, repeatable tasks to high-quality standards This is a well organised, planned environment, ideal for someone who enjoys structure, consistency, and technical challenge without chaos. What We re Looking For A formal engineering/technical qualification (C&G, NVQ, HNC, etc.) Ideally, a completed apprenticeship (any discipline considered) Strong mechanical and electrical capability Experience with pneumatics or vacuum systems is a bonus Open minded, adaptable candidates from any hands on technical field Shift Pattern & Pay 4 and 3 day weeks rotating (one week you have 3 days off, the next 4 days off) 12 hour shifts: permanent days (7am 7pm) or nights (7pm 7am) Fixed pattern, no rotation Shift allowance: Days (Sun/Mon/Tue + alt Sat): % Days (Wed/Thu/Fri + alt Sat): % Nights (all patterns): % Why Join? Stable, well paid role in a cutting edge manufacturing environment Clear development pathways as part of a major site expansion Work with modern equipment in a clean, well run facility Supportive team culture with long term progression built in If you re multi skilled, motivated, and ready for a high tech environment where you can grow, we d love to speak with you. Apply with an up to date CV for a confidential conversation

We are recruiting for an experienced Production Technician to join a leading pharmaceutical company based in Worthing. This role requires working in a regulated environment, adhering to Good Manufacturing Practice (GMP) and Standard Operating Procedures (SOPs). You will be required to wear full Personal Protective Equipment (PPE) to prevent contamination. As part of this role, you will contribute to the production of healthcare products that improve people's lives. Working in Grade A and B cleanroom environments, you will follow strict batch records and SOPs while ensuring first-time quality and timely product delivery. As a Production Technician, your key responsibilities will include: Completing GMP training Batches to be manufactured on time and in compliance to GMP standards Conduct detailed investigations for non-conformances, identifying root causes Apply Good Manufacturing Principles in all areas of responsibility Adhering to filling procedures at all times Requirements: Excellent communication skills both written and verbally Previous experience of a production environment Experience working within a GMP-regulated setting An interest in or prior experience with scientific processes Previous experience working in full PPE Benefits: Bonus scheme 25 days holiday Free parking Pension & life insurance scheme Private healthcare Discounted gym membership This is a full time permanent position working Monday to Friday 7am to 3pm based in Worthing on an annual salary of 27,230, increasing to 30,230 after successful 3 months training to grade B. Wild Recruitment Ltd T/A First Recruitment Services is acting as an employment agency in relation to this vacancy.

5 Month Contract working in the Filling team. 4 on 4 off shift pattern days and nights. Based in Speke in Liverpool. Working under the Team Leader, the Process Technician is responsible for executing the manufacturing processes in the Aseptic Filling department in accordance with written procedures. The role holder will provide (be trained in) the technical skill sets necessary to manufacture high quality vaccines in a compliant, efficient and cost-effective manner. Responsibilities Carries out all sterile filling process operations using local SOPs and batch documentation whilst in full compliance with cGMP to meet production schedule demands. To work in a safe manner in compliance with all pertinent UK legislation, Seqirus mandatory policies, guidelines and site procedures for Health, Safety and Environment. When manufacturing ensure that all Departmental SOPs and MIs are followed and: Ensure appropriate control, monitoring and delivery of activities in their area of work. Ensure that all documentation is completed correctly, accurately in a timely manner and signed by the relevant personnel. Carry out final documentation review and sign off to ensure documentation is right first time. Ensure compliance to Health and Safety regulations. Consistently demonstrating the behaviours necessary to create a safe working environment for themselves and their colleagues. To actively maintain and promote a cGMP compliant culture, ensure that the highest standards of housekeeping and safety are applied within the area in accordance with the Orange Guide and CFR regulations and to apply the principles of Lean Manufacturing, Problem Solving, 5S ,Waste Elimination and Energy Efficient Activities in support of Continuous Improvement. To maximise their individual contribution so that team objectives are achieved. To work as a team member, providing and receiving feedback to team members and their team leader. To communicate and liaise with members of other teams in order to meet the business's objectives. When required, to flexibly support other departments - providing adequate training is received and it is safe to do so. Attend all compulsory and allocated training courses required for the role. Ensure that all training is completed in a timely manner and that personal training records are kept up to date. To continue to develop new skills, competencies and behaviours to fulfil both current and future business needs. The role holder will be able to demonstrate the application of the skills required for their role. To contribute ideas and action in order to improve team, process and equipment performance. To support process improvement and uphold Seqirus Values and Behaviours. Support organisation change and process improvements. Aseptic Filling - Specific Tasks Include: Movement of materials using pallet trucks (manual and electric) to ensure manufacturing operations are efficient and production demands are met. Cleaning and disinfection of production rooms and equipment to maintain cleanroom, cGMP and HSE standards. Cleaning, preparation, sterilisation, assembly and disassembly of production equipment Performance of In Process Control checks and Environmental Monitoring to ensure the isolator environment is maintained and products are made within specification. Operation of the Filling production line including use of machine interfaces, performing VHP/CIP/SIP cycles, monitoring the batch and performing interventions Knowledge, Skills & Competencies Filling of sterile products / Aseptically qualified (e.g. sterile connections, sterility assurance) / Use of Isolator technology. Attention to detail and high personal concern for standards, integrity, communication, and discretion. Proven knowledge of cGMP. Basic mechanical aptitude or knowledge of electronic/mechanical equipment Competent in using multiple computer systems e.g. PCS, GLIMS, SAP and production line machine interfaces Education Requirements Relevant degree qualification preferred Experience Requirements 1+ years' experience and competence in cGMP and sterile product production operations in the Biotech or Pharma industry preferred Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser (url removed)

Mechanical Assembly Technician Cleanroom Location: Hailsham, BN27 4EL Salary: Competitive, DOE Contract: Full time, Permanent Benefits: A competitive salary, private medical insurance, 25 days holiday, salary sacrifice company pension, life insurance, a state-of-the-art working environment! Take Your Career to the Next Level with VACGEN! For over 60 years, VACGEN has been driving innovation in ultra-high vacuum (UHV) technology, supporting cutting-edge research across the globe. From NASA and the European Space Agency to CERN, our high-precision products are trusted by world-leading institutions and researchers to deliver results. We are now recruiting for an Assembly Technician to assume responsibility for assembling mechanical and electrical components and building complex systems, according to engineering drawings. In addition to this, as our Mechanical Assembly Technician you will be responsible for: Carrying out specialist UHV compatible instrument wiring & electrical testing. Maintaining UHV clean process standards with all in vacuum component parts and sub-assemblies. Supporting transition of new hardware from NPI through to routine production including writing any required manufacturing information documents & guides Maintaining and updating existing manufacturing instructions. Supporting the maintenance of departmental records, particularly test data, quality control information and serial numbering of instruments. In order to be successful in this role you should have: Ideally a relevant engineering degree/HND/HNC e.g., Mechanical Engineering, Electromechanical Engineering, QBE or time served apprenticeship candidates can be considered. Familiarity with the production of UHV compatible devices & instrumentation that utilises electron optics & ion optics principals would be advantageous. Previous experience in a low volume customised product manufacturing environment is preferred. Ideally yielding a broad understanding and appreciation of precision hand fitting techniques, specialist wiring and product test procedures. Resilience under pressure, able to adhere to the predetermined timescales and deadlines. Basic IT skills, including MS Office Mechanical engineering Level 3 Previous experience in a high technology manufacturing environment or clean room. No agencies please. Click on APPLY today! Vacgen Limited is committed to fostering an inclusive and diverse workplace. We are proud to be an equal opportunity employer and do not discriminate based on race, ethnicity, religion, gender, gender identity, sexual orientation, disability, age, or any other protected status under the Equality Act 2010. Please Note: We cannot accept applications from Overseas.