1 to 22 of 22 Contract QA Jobs in the North of England

Review current best practice for benchmarking initiatives, adopt where appropriate and develop new initiatives where gaps are apparent so that they can contribute to Quality Assurance and Improvement agendas across Cheshire and Merseyside. To provide advice and support to the PROSPECT team on Involvement and Co-Production. Work with internal more »

AS9100, ISO9001, EASA, Engineering, Drawings, Technical, First Article Inspection, PPAP, Auditor, Automotive, Medical, Mechanical, Electronic Join Our Team as a Quality Engineer and Drive Quality Assurance to New Heights! Are you a meticulous Quality Engineer with a passion for precision and excellence? Are you ready to play a pivotal role more »

packaging processes, from initial request to final deployment, collaborating with customers, vendors, and IT departments. Key Responsibilities: - Perform technical analysis, requirements gathering, package creation, quality assurance, user acceptance testing, and deployment. - Create documentation for all tasks. Technical Expertise Required: - Deep understanding of Microsoft Windows operating systems, including installation methods, file more »

Subcontractors to deliver the allocated packages of work. Management of a multi-disciple team to support the Subcontractors delivery and site works including Engineering, QA, Expediting, Commercial, Doc Control, Planning, Construction, Commissioning. Ensuring appropriate resourcing is available from all the above disciplines in accordance with scheduled activities Management of change more »

Requirements Review O&M manuals to ensure compliance Raise & close out non-conformities including defects Attend quality meetings Background/Skills; A background in Quality Assurance within the construction industry (within a heavy civils environment) Report Writing/Presentation Skills Good interpersonal skills Experience in a client facing role Able more »

be instrumental in advancing products, bringing your ideas to life through prototyping and driving continuous improvement initiatives - all while adhering to stringent medical device quality assurance and regulatory standards. Day in the life: Create detailed design plans for new medical equipment Transform design concepts into tangible prototypes Verify and test more »

design house engagement on packages according to the contract. Manage a multidiscipline team to support the sub-contractors delivery and site works including Engineering, QA, Commercial, Document Control, Planning, Construction and Commissioning. Ensure appropriate resourcing is available from all above disciplines in accordance with scheduled activities. Manage sub-contractors in more »

packaging applications from initial request to final deployment by working with customers, vendors and IT departments. Experience performing technical analysis, requirements gathering, package creation, quality assurance, user acceptance testing and deployment. Creation of documentation relating to such tasks. Understand Microsoft Windows operating systems at a technical level, e.g. installation methods more »

timelines, milestones, and deliverables to ensure timely product launches. Collaborate effectively with numerous internal local and global functions such as regulatory affairs, Artwork teams, quality assurance and supply chain as well as external partners like CDMOs to achieve objectives and ensure adequate product availability for launch. Ensure compliance with regulatory more »

role holder will be expected to work within the procurement tracking system supported by the Materials team. The role holder will specify the correct QA grading for the materials being specified, and then fill in the appropriate stock holding request forms for procurement of items to stock. The Materials Technical more »

role holder will be expected to work within the procurement tracking system supported by the Materials team. The role holder will specify the correct QA grading for the materials being specified, and then fill in the appropriate stock holding request forms for procurement of items to stock. The Materials Technical more »

commissioning instructions, as agreed with the Assessment Production Office About us Why work as a flexible worker for NCFE? Our flexible workforce provides supportive quality assurance to ensure that learners taking NCFE qualifications are getting the best education possible. If you become a flexible worker with us, youll choose how more »

of derived RCM maintenance • Provide appropriate RCM knowledge and input for Engineering Design Reviews • Initiate amendments to maintenance resulting from design change • Conduct periodic quality assurance checks of Maintenance Task Instructions (MTIs) and initiate appropriate rectification activity/actions • Convene and/or attend maintenance-related meetings with internal and more »

partnerships across the developing world of Apprenticeships and EPA. About us Why work as a flexible worker for NCFE? Our flexible workforce provides supportive quality assurance to ensure that learners taking NCFE qualifications are getting the best education possible. If you become a flexible worker with us, youll choose how more »

partnerships across the developing world of Apprenticeships and EPA. About us Why work as a flexible worker for NCFE? Our flexible workforce provides supportive quality assurance to ensure that learners taking NCFE qualifications are getting the best education possible. If you become a flexible worker with us, youll choose how more »

the intial request to final deployment working with customers, vendors and IT departments. You must have -Experience of Requirements gathering, technical analysis, package creation, QA, UAT and deployment -MSI Application format -Adminstsudio, InstallShield -App V more »

Senior QA Engineer - 6 Months - Inside IR35 - £520 per day - Leeds (1 day per week) Corecom have partnered with a Yorkshire-based company to hire a Senior QA Engineer to help support internal projects for a global company. They are looking for someone who is proactive and can seek out more »

England. Job Description: As the Head of Quality Department, you will be responsible for overseeing and managing all aspects of the Quality Control and Quality Assurance programs. You will ensure compliance with local and international regulations, implement and monitor quality systems, and drive continuous improvement initiatives. Key Responsibilities: Develop and … Pharmacy, Chemistry, or related field. Advanced degree is a plus. Minimum of 10 years of experience in the pharmaceutical industry with a focus on Quality Assurance and Quality Control. Proven leadership skills with a track record of managing high-performing teams. Strong knowledge of GMP, GLP, and ISO standards. Excellent more »

Quality Assurance Manager - Good Clinical Practice Our client, based in Cheshire are recruiting for a contract GCP QA Manager to join them for a 6 month project. This is an exciting opportunity to join a dynamic company with a great culture. Role: Provide strategic direction for quality, standards, and training … to ensure a quality mindset is embedded in the business Requirements: Expert in GCP with working knowledge of GMP 5 years experience in a QA Manager role within a CRO, Biotech or Pharma company Contract: Hours: 3 days a week - can worked across 3-5 days Location: Wilmslow - hybrid working more »

Anderselite are representing a leading cliet dedicated to delivering excellence in every project we undertake. With a commitment to safety, quality, and innovation, we strive to exceed industry standards and client expectations. As we continue to expand our operations, we more »

I am currently working with a client who are looking to bring on board an experienced QA/QC Coordinator on a pharmaceutical project that has recently kicked off in Billingham. The ideal candidate will have: - Experience working in the pharmaceutical sector - Ability to manage all quality aspects of the more »

Quality Engineer required to support ongoing project The primary role involves working closely with Document Control personnel to investigate and resolve issues of non-conformance in legacy products or processes. This involves generating documentation related to Field Change Requests (FCR more »