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Quality Assurance Manager 6 Months Ware (Hybrid) £233p/d PAYE OR £306p/d via Umbrella Role Brief: We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 million vaccine doses in 2021. We continue to modernise, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together. Are you a Quality Assurance Professional seeking an opportunity to leverage and/or build upon your expertise in validation (inclusive of equipment, utilities, facilities, computer systems) working with internal and external business partners for R&D? Do you enjoy a varied day dealing with challenges and answering the call for advice on different scenarios? If yes, this role in Pharma R&D may be the right opportunity for you to explore. This is a great opportunity where you will deal with various situations, which you will need to provide solutions, so good problem solving skills are a must. Within QA you will be presented with issues and business proposals which you will be asked your advice to ensure quality and the patient is not affected while allowing us to grow and develop as a competitive business. You will work cross functionally with different teams, gaining experience of providing key project management direction, pilot plant systems, analytical systems, medical devices, utilities and facilities. Job Purpose In this QA role in Pharma R&D, Infrastructure and Validation team, you will perform the quality assurance activities and quality oversight of the Validation and GMP facilities management activities performed within Pharma R&D across the UK sites. In this role you will be key in the following areas... Providing review and approval of validation lifecycle documents from a variety of QMS within the company. Provide meaningful comments to ensure compliance with regulatory expectations/requirements. Provide quality oversight of internal business groups and external services partners inclusive of the following quality processes: Change control Deviation investigation inclusive of CAPA. May support project work as a QA representative, quality program or team activities. Provide advice and consultancy to GSK project teams, internal business groups and external partners to reduce regulatory risk to GSK. Preferred Qualifications & Skills: Proven working experience in biopharma/pharmaceutical Industry related to Quality Assurance Job scope. Experience of validation of analytical systems, cold chain storage, secondary manufacturing equipment, utilities and infrastructure. Computer validation if possible for networked systems and corporate facing applications. Ability to manage workload prioritisation in a fast paced changing environment. Excellent organisational skills Strong interpersonal skills. Strong written and verbal communication skills. A good team player and able to work independently. Experience with key Quality activities (i.e. Deviations Change Controls)
Parts Quality Engineer Parts Quality Engineer, Temporary, ongoing basis where you will be engaged via Hays Location: Chichester Working Environment: Hybrid, part office based on site at client offices/ part home based Pay type: Competitive hourly pay rate Our Client Hays are delighted to be working with our global client, one of the world's most successful premium manufacturers of cars, motorcycles, and provider of premium services. Our client demonstrates a commitment to innovation, sustainability, and product responsibility all the way from development to production. Their aim is to play a dynamic and innovative role in shaping the face of mobility. Our client highly values each and every person; their passion, commitment, uniqueness and contribution to shaping the future success of their business. The Role Hays are recruiting for an exciting opportunity for a Parts Quality Engineer to join our client on an ongoing long term temporary assignment for an approximate duration of 12 months (rolling, reviewed annually). As a Parts Quality Engineer (QMT), you'll use your manufacturing process knowledge and exceptional leadership skills to efficiently manage suppliers to achieve product and process maturity, capability, and ongoing efficiency improvements Key Responsibilities As part of a multi-discipline 'cloverleaf' team, you will be responsible for identifying, evaluating, and ultimately nominating new suppliers. You will steer the supplier launch and quality departments to develop and manage the pre-serial activities in line with project milestones. You will be responsible for the approval of parts quality prior to launch and in serial production Your duties will include the management of critical supplier concerns, ensuring in series the supplier is adhering to the standards and targets defined by process partners. You will be responsible for problems associated with your supplier scope, conducting root cause analysis to determine long and short-term solutions in a timely manner and escalating issues as appropriate Your expertise will enable us to uphold, and further enhance, the high quality associated with the brand - as well as to work alongside global teams and strengthen your network Skills and Qualifications: Whilst not essential, an Apprenticeship and/or Degree (or equivalent) in a Mechanical/Electrical Engineering discipline would be beneficial. Language skills would also be an advantage to support international supplier contact A strong knowledge of manufacturing processes, production quality control methods and systems, quality management systems, tools and maturation processes An ability to take ownership of problems and find solutions, with the confidence to make, and enforce, decisions within pressurised situations Proven leadership skills with the ability to steer and influence cross functional teams Excellent conflict management and diplomacy skills General IT skills (Microsoft Office) as well as Business Process IT knowledge Benefits: Competitive hourly rate along with an annual performance related bonus. Hybrid working. Hybrid parking on-site with access to a subsidised restaurant. Hays Go1 training platform which offers a library of over 70,000 courses. Access to Ben - a flexible employee benefits portal offering support across wide range of topics such as mental health well-being, financial or legal matters. 34 days annual leave (including bank holidays) What next? If you are interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now on . Hays Talent Solutions is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk