Permanent Quality Management Jobs in Cambridge

9 Permanent Quality Management Jobs in Cambridge

Senior Quality Manager - GCP

Cambridge, England, United Kingdom
Pharma Partners Recruitment Ltd
Job Description Working as a Senior Quality Expert/Manager - GCP, you will act as the advisor to the Clinical Development teams on all quality related GCP activities. This will be an exciting opportunity with a clinical-stage biopharmaceutical company with multiple Phase 3 assets. Key Responsibilities: To … emphasis on GCP compliance. To provide support and advice to Clinical Development teams with regards to: Definition of appropriate compliant procedures within GxP functions Management of quality issues To ensure external contracted organisations supporting GxP activities are selected and responsibilities defined and documented. To monitor the performance of … GxP service providers with regards to the relevant quality standards. To define and manage clinical audit programme and to preform GCP audits if required. Maintain agreed quality metrics and dashboards to enable clear communication to senior management of compliance performance and any risks or issues identified. To more »
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Clinical Data Management Manager

Cambridge, England, United Kingdom
Taleo BE
better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. CLINICAL DATA MANAGEMENT MANAGER LIVE What you will do In this vital role you will responsible for ensuring clinical projects are executed according to set timelines with … quality and consistency. The successful candidate may be responsible for one or multiple products depending on the complexity. You will be responsible to ensure that Data Management (DM) procedures and processes are adhered to by vendor staff through oversight of quality, cycle times, metrics and use the … approach and review of project timelines and metrics to ensure databases are delivered to set timelines, and approve database locks and unlocks. Ensure that quality control checks are occurring such that quality databases are delivered. Develop and co-ordinate project level training for data management staff. Review more »
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PMO Analyst

Cambridge, England, United Kingdom
Pragmatic
Based within the Programme Management Office, we are looking for an experienced PMO Analyst (or Programme Coordinator) to support a wide portfolio of projects, involving internal and external customers. We are seeking an organised and service-focused individual who is driven to provide quality information and documentation that … report into the Senior Director of PMO. Key Tasks Working closely with the Senior Director (PMO), you will be expected to support the Programme Management Office with the following strategic functions: • Project Delivery – ensuring we have the right PMO resources in the right place at the right time for … project and programme, managing the career ladder and competence framework, training and continuing professional development of all PMO staff, forecasting and recruiting, some line management, organising the programme of team meetings and development seminars, providing coaching and mentoring to PMO staff. • Centre of Excellence – ensuring that we have processes more »
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Expression of Interest - Cell Therapy Automation

Cambridge, England, United Kingdom
Cellular Origins
the short application form on our website. We’re interested in hearing from candidates with experience in the following areas: Key Account and Product Management Quality Management Mechanical Engineering Mechanical Design Electronics Engineering Mechatronics Engineering Software Engineering (industrial automation, embedded) Verification and Validation Engineering Cellular Origins Cellular more »
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Project Manager

Cambridge, England, United Kingdom
Cellular Origins
to craft project briefs and develop comprehensive plans for schedules, resources, communication, risks, and quality. Execution & Monitoring : Employ effective delivery methodologies and support team management to ensure project milestones are met. Closure & Documentation: Wrap up projects efficiently, capturing key learnings and delivering tangible outcomes to realise project benefits. We … to ensure smooth project delivery. You’ll develop and maintain project schedules, budgets and forecasts and accurately document every step of the way. Lastly, quality and risk management will also be key aspects of your role, ensuring that project outputs consistently meet stakeholder requirements while proactively mitigating risks … of IT systems at an advanced level, e.g. MS Office and Project, Atlassian JIRA and Confluence, etc. Experience of working within an ISO 9001 Quality Management System, or similar, is desirable. The above list outlines our ideal candidate, but we know some of you may not apply unless more »
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Supplier Quality Engineer

Cambridge, England, United Kingdom
The ONE Group Ltd
Job Description I am looking for an experienced Supplier Quality Engineer for this innovative technology company during an exciting time of growth. Based just outside of Cambridge, although some travel will be involved to suppliers, you need to have experience within a similar role for a technology company with … also required. On a day to day basis, you will work with teams across the business as well as external partners to improve the quality of the business systems & products to drive continuous improvement. What do we need from you? Minimum HND in an engineering related subject (Electronics/… mechanical/software) or equivalent experience in a similar role. Certification/accreditation in a recognised quality standard (e.g. IRCA Certified Auditor) A strong Technical background Experience of applying and developing Quality practices in an engineering based and/or production focussed role Demonstrative Experience of facilitating improvements more »
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Document Controller

Cambridge, England, United Kingdom
LEX Diagnostics
verification and validation team to ensure that the regulated documentation is in place to support with FDA approvals. You will receive support from the Quality Systems Manager and play an integral role as a valued member of the LEX Diagnostics team. What you will be doing: Manage the Quality … system, addressing any errors or discrepancies found. Generate and manage product technical documentation such as Design History Files (DHF), Device Master Records (DMR), Risk Management Files (RMF), and Device Master Files (DMF) in accordance with procedures. Identify and suggest enhancements to document control systems, offering continuous support and training … and Validation (V&V) activities Requirements Previous skills and experience that would be useful to be successful in this role: Confident at using electronic Quality Management Systems Strong communication skills and able to work in a multidisciplinary team. Logical approach to constructing documentation with great attention to detail more »
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Verification Engineer

Cambridge, England, United Kingdom
LEX Diagnostics
Validation Engineer who will actively engage in hands-on testing of the LEX diagnostic system. You will be working closely with the head of Quality and Engineering team and will be responsible for defining, designing, and executing verification and validation activities for the LEX 5-minute PCR diagnostic platform. … for clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures (SOPs). Collaborate with the Engineering, Manufacturing and … forefront of point-of-care diagnostics for over 20 years. Drawing upon the expertise of its consultants in the Life Science sector, and the management experience of a company with a 30-year track record of developing breakthrough technology and creating ambitious tech businesses, TTP Group invested core IP more »
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Deputy Blood Sciences Manager

Cambridge, United Kingdom
Cambridge University Hospital NHS Foundation Trust
responsible for Haematology. You will play an important role in the operations teams working alongside managers responsible Biochemistry, Specimen Reception, Training and Development and Quality Management.You will have a resilient approach to provide leadership and take responsibility for the day-to-day management of the Haematology team. We … are looking for a pro-active individual with excellent people-management abilities and attention to detail. You will also have exceptional leadership and communication skills to ensure continuous quality improvement to strengthen and develop areas across the Haematology team and the wider Blood Sciences Department. Main duties of … Manages and coordinates the day-to-day activities of the team. Leads on service improvement. Processes highly specialist investigations and responsible for standard and quality of results of the service. Provides expert advice, opinions training to own and other professions in specialist area of activity. Provides specialist training in more »
Employment Type: Permanent
Salary: £50952.00 - £57349.00 a year
Posted:
Quality Management
Cambridge
10th Percentile
£34,276
25th Percentile
£42,313
Median
£57,557
75th Percentile
£73,452
90th Percentile
£81,881