Average salary: £42,500 /yearly
More statsRegulatory Affairs and Quality Assurance Assistant - Cambridge (RAaQAAMDC06) Cambridge, England
Regulatory Affairs and Quality Assurance Assistant - Medical Devices - Cambridge
Due to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory...
Regulatory
Immediate start
Work visa
Working as a Senior Quality Expert/Manager - GCP, you will act as the advisor to the Clinical Development teams on all quality related GCP... ...in maintaining and monitoring the GxP QMS ensuring it meets all regulatory requirements and standards, with emphasis on GCP compliance....
Regulatory
Flexible hours
£39k - £52k per annumEstimated
...collected closer to the pathology of interest.
Requirements
Contribute to the development, maintenance, and compliance of the Quality Management System (QMS). With understanding of ISO: 13485. This Role is more QA but knowledge of RA beneficial.
Support the...
Regulatory
Full time
Hybrid work
Holiday work
...Weonlysucceedwhenweworktogether.
Job Description
Senior Manager, Quality provides Quality oversight for Bicycle’s... ...to ensure protocol, procedural, GCP / regulatory compliance and inspection readiness... ...Management (EDM) systems and Microsoft Office suite
Position requires both domestic...
Regulatory
Work at office
Flexible hours
Job Description
Quality Assurance Manager
Seeking an experienced QA Manager focused on Good Manufacturing Practices (GMP), to join... ...~5 years in pharmaceutical QA with GMP emphasis.
~ Strong GMP regulatory knowledge.
~ Broad experience of Quality Management Systems....
Regulatory
£32k - £44k per annumEstimated
...our technology and detection capability, we are continually evolving the requirements of our Quality Management System within the business.
We are therefore looking for a QA Officer to join the QA team and support the business with the compliance of our QMS – Currently ISO...
Suggested
Full time
For subcontractor
Worldwide
No agency
Flexible hours
1 day week
...growth, our client is looking to hire a QA Manager to oversee a small team to achieve cGMP compliance and develop + maintain their QMS (Quality Management System). If you are an experienced QA professional within the biotech GMP sector with prior line management experience,...
Suggested
...and environmental monitoring, patient radiation dose assessment, regulatory audits and advice, instrument calibration, radioactive waste... ...operate within both our HSE-recognised RPA Body and our ISO 9001:2015 Quality Management System.
While HCPC registration as a...
Regulatory
Local area
Night shift
£50k per annum
...use a variety of skills to produce high quality, tailor-made outputs. The work we do places... ...within policy consultancy, focusing on regulatory and policy development, implementation processes... ...how often and when they are in the office. We believe this helps our co-owners to have...
Regulatory
Permanent employment
Full time
Part time
For subcontractor
Work at office
Holiday work
Flexible hours
...Antibodies.com is a leading provider of high-quality antibodies and reagents for life science... ...service, logistics, supply chain, and office management.
Monitor order fulfilment... ...shipping costs.
Ensure compliance with regulatory requirements and quality standards for...
Regulatory
Work at office
Flexible hours
...inspection of pressurised equipment, tanks and piping systems to meet regulatory and customer requirements. Responsible for provision of... ...Protection, Pension, 25 days holiday. Permanent full-time position, office, client site, and home based hybrid working. Accredited training...
Regulatory
Permanent employment
Full time
Contract work
Work at office
Work from home
Hybrid work
Holiday work
Working Monday to Friday
£38k - £52k per annumEstimated
...Job Purpose
The Manager, Medical & Regulatory Writing will be an integral part of MoonLake... ...accuracy.
Support QC processes to ensure quality and accuracy within and between... ...Advanced word processing skills, including MS Office (expertise in Word); software and systems...
Regulatory
Permanent employment
Contract work
Work at office
Remote job
Hybrid work
Flexible hours
2 days week
MoonLake Immunotherapeutics
Cambridge, Cambridgeshire
1 day ago
...offering within our Medical Sector, we are recruiting a Human Factors Regulatory Consultant to join our world class team of product developers... ...including uFMEA/UERAs
• Experience of Medical device project quality management in a project-based organisation.
• Knowledge of ISO...
Regulatory
We are interested in speaking with Compliance Engineers to join a dynamic and rapidly growing business. Working closely with Engineering, Procurement, Project Management and Manufacturing teams, your responsibilities are as follows:
Ownership of compliance requirements.
...
Regulatory
...assay development and proficiency in drug discovery and development, including delivering data and documentation supporting IND/CTA regulatory filings
Scientific experience working in oncology, inflammation or metabolism drug discovery and development programs
Ability...
Regulatory
Immediate start
Hybrid work
Flexible hours
£130k - £175k per annum
...print to digital, and from products to services, and also the international reach of our work as part of a global organisation with offices in over 50 countries.
We promote work-life balance through flexible work schedules, hybrid work arrangements, and generous paid leave...
Regulatory
Permanent employment
Full time
Contract work
Part time
Work at office
Home office
Overseas
Hybrid work
Flexible hours
Shift work
2 days week
...offering within our Medical Sector, we are recruiting a Human Factors Regulatory Consultant to join our world class team of product developers... ...including uFMEA/UERAs
• Experience of Medical device project quality management in a project-based organisation.
• Knowledge of ISO...
Regulatory
...national team, you will work alongside some of the leaders in this specialist field of law advising sports organisations and athletes on regulatory disputes, dispute resolution within tribunals and with regulators and can expect the work to be both domestic and international in...
Regulatory
Hybrid work
Flexible hours
£30k - £35k per annum
...team management, including ensuring the quality and on time in-full delivery of assigned... ...and experience of applicable quality and regulatory requirements e.g. ISO:9001/ISO:13485, 21CFR... ...troubleshooting.
High level of competency with MS Office (Word, Excel).
Experience of training...
Regulatory
Work at office
Holiday work
Flexible hours
£73k - £98k per annumEstimated
...Global Regulatory and Operations Senior Director page is loaded Global Regulatory and Operations... ...two or three times a month in the office)
Job type: Permanent
At Mundipharma... ...and external stakeholders.
Uphold data quality standards and compliance protocols, overseeing...
Regulatory
Permanent employment
Full time
Work at office
Local area
Hybrid work
Flexible hours
Mundipharma International Limited
Cambridge, Cambridgeshire
5 days ago
...bringing them to a satisfactory resolution
Ensure that knowledge and skills are maintained and developed in line with industry, regulatory and internal requirements by undertaking regular and appropriate CPD in order to reach their full potential (for the wider benefit of...
Regulatory
Holiday work
Senior Manager Regulatory Affairs Writing
A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Manager Regulatory Affairs Writing. You will lead a team responsible for developing the content for submissions to both US and EU regulatory agencies...
Regulatory
Contract work
Senior Regulatory Affairs Manager CMC
A growing Biotech in Cambridge with multiple Phase 3 assets are seeking a Senior Regulatory Affairs Manager CMC. The role will be responsible for the development, execution and tracking of regulatory CMC and medical device activities....
Regulatory
Associate Director - Regulatory Affairs page is loaded Associate Director - Regulatory Affairs
Apply locations United Kingdom - Cambridge time type Full time posted on Posted 17 Days Ago job requisition id R0040532 For Current Gilead Employees and Contractors:
For more...
Regulatory
Full time
For contractors
Local area
Worldwide
Regulatory Affairs Labelling Associate Project Manager contract job
This well-known biopharmaceutical company is looking for a Regulatory Affairs Labelling Associate Project Manager to join their Labelling team on a contracting basis. This is a 12-month contract job with...
Regulatory
Contract work
Remote job
Work from home
Hybrid work
Flexible hours
...growingCDMO have opportunity for an experienced QA officer to join them on-site on a permanent basis... ...you’ll be doing
Writing and reviewing quality documents, SOPs and other policies... ...internal and external audits and other regulatory inspections
Develop and implement...
Regulatory
Permanent employment
Job Purpose
As a Senior Quality Expert (Good Clinical Practices/GCP), you will support... ...ensure that the QMS meets all necessary regulatory requirements, including good-practice guidelines... ...:
~2 days a week in our brand new office in Porto or Cambridge with some travel...
Regulatory
Permanent employment
Work at office
Remote job
Hybrid work
Flexible hours
2 days week
Job Purpose
As a Senior Quality Expert (Good Clinical Practices/GCP), you will support... ...ensure that the QMS meets all necessary regulatory requirements, including good-practice guidelines... ...:
~2 days a week in our brand new office in Porto or Cambridge with some travel...
Regulatory
Permanent employment
Work at office
Remote job
Hybrid work
Flexible hours
2 days week
CK Group are recruiting for a Quality Assurance Assistant to join a growing Cell Therapy CDMO, to be based at their site in Cambridge on... ...responsibility will be providing support to the QA team and contributing to regulatory compliance, continuous improvement and management of the Quality...
Regulatory
Permanent employment
£40k - £50k per annum
...many other benefits. The role will be onsite every day to be able to utilise their state-of-the-art lab facilities, purpose built for their products.
For more information, or to discuss your experience/CV, please do get in touch with Morgan Veness at SoCode - Cambridge Office
Permanent employment
Work at office
Holiday work