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GMP Pensions Specialist (Split with other specialist area)LondonReputable and well known consultancy seeking a GMP consultant to work in a split role across GMP and another specialist area of their ...
Reputable and well known consultancy seeking a GMP consultant to work in a split role across GMP and another specialist area of their choosing | National role which can be based completely remotely ...
Senior & Pensions Project Consultant - GMP, Buyout Equalisation, TPR Reporting Hybrid or Fully Remote Home Working - £competitive + Flexible Working & Excellent Package. An award-winning Pensions ...
Job Description * for day-to-day operation and manufacture of the RPE ATMPs in a GMP facility * batch records, equipment logs and other production records to comply with cGMP in collaboration with ...
TechYard Recruitment is currently working with a global consultancy who are building a new GMP practice. They are hiring for a Programmatic Consultant. This person will be a programmatic subject ...
Your main responsibility will be to ensure that all materials are tested according to agreed specifications and procedures, in agreed time frames and in accordance to GMP and company guidelines
Maintain processes (GMP documentation lifecycle, Change Control, Deviation, CAPA, self-inspections, Complaints, GMP document control and training) needed for successful site compliance to the PQS
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Design and develop comprehensive training programs on GMP regulations, procedures, and best practices. * Collaborate with experts and leaders to identify training needs and create engaging content
Ensuring Compliance with GMP and GDP: Monitoring, assessing, and ensuring compliance with Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) to uphold product quality, safety ...
This Senior Quality Assurance Associate position demands a candidate with a good understanding of the GDP and GMP, who is capable of working as part of a team to ensure the highest standards of ...
Knowledge of GMP * Team player but able to work autonomously * Competency of use of Microsoft office
As the Senior MSAT Scientist, you will be responsible for owning of cell therapy manufacturing processes from process development into GMP. Your responsibilities as the Senior MSAT Scientist will be
The successful individual has a working knowledge of Quality, GMP and GLP practices. The Quality Control Specialist will play a vital role in ensuring adherence to quality standards, GMP (Good ...
Ensure that training programs align with current GMP regulations, industry standards, and company policies. * Emphasize the importance of adherence to GMP principles in all training materials and ...
Key activities will include manufacturing dbDNA at both, feasibility and GMP grades , applying best practices and regulatory guidance, ensuring and maintaining high standards of H&S , adhering to all ...
To ensure GMP are fully complied Essential Skills * Excellent attention to detail * Min Level 3 HACCP training * Experience in food safety, legality, quality and authenticity aspects of food ...
... GMP documentation, H&S documentation and Risk assessments, designing of layout fit for operational use, maintenance and calibration. Ownership of project related activities and tasks as delegated by ...
Ensure that contracts for GMP and non GMP vendors are managed and updated as required. * Liaise with utilities providers, landlord and maintenance contractors to ensure that the facility is serviced ...
Supporting specialist teams and gaining exposure to areas such as Risk Transfer, GMP Equalisation and Member Options * Assisting with training and mentoring junior colleagues to build the expertise ...
GMP reconciliation projects; GMP equalisation projects; benefit analysis and rectification work; new scheme implementations; individual technical or high priority cases; scheme events; support and ...
Experience of method development and troubleshooting analytical assays is highly beneficial to this role.3. A working knowledge and practical experience working with AAV gene therapy within a GMP ...
Management of GMP and GDP compliance * Management of complaints, CAPAs, risk assessments, and validation protocols * Review and manage the QMS system * Able to manage non-compliance issues and ...
Develop, implement & maintain a comprehensive QA strategy aligned with GDP, GMP, GxP, Pharmacy & Regulatory standards * Responsible for operations licences at all sites; namely WDA(h) & MS licenses