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GMP Production Manufacturing Technician Opportunity - Kent Opportunity: An exciting opportunity has been created due to company growth. My client a global pharmaceutical manufacturing company are ...
The role will form part of the projects team with the current focus being around delivering GMP Equalisation projects on the proposition to clients, which can incorporate or lead onto being involved ...
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 ...
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
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
... GMP) or FMCG to be considered for this role What you want to know about this Client: * Highly reputable Global manufacturer renowned for their leading research and technology * A corporate business ...
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
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 ...
Ensure that own work, and that of the team, complies with GMP, Good Documentation Practice (GDP) and GxP Data Integrity guidance's, and is undertaken in accordance with applicable procedures (e.g ...
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 ...
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 ...
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 ...
Knowledge of GMP * Team player but able to work autonomously * Competency of use of Microsoft office
As such, I am interested in speaking with people from Production and QC GMP settings, as well as fresh graduates looking to get that key break. This team is very open to your background - it is all ...
As the Radiopharmacy Production Technician you will be responsible for manufacturing of PET Radiopharmaceuticals to GMP standards. KEY DUTIES AND RESPONSIBILITIES:Your duties as the Radiopharmacy ...
Candidates will be responsible for all aspects of GMP reconciliation and equalisation work including preparing / analysing data, calculations and reports etc. Experience: - Candidates need to have ...
... 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 ...
Previous GMP experience
You will be working on a variety of projects to assist schemes as they prepare for buy-out/buy in, assisting with GMP data preparedness and the future Pensions Dashboard. You will take an active role ...
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 ...
Maintain compliance with GMP, ISO, Quality Assurance, and Health & Safety policies * Provide outstanding customer service by answering inquiries and resolving issues promptly * Perform administrative ...
Be the guardian of quality, ensuring every launch meets the gold standard of GMP and GDP regulations. * Tackle challenges head-on, turning obstacles into opportunities for innovation and growth
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 ...