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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 ...
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 ...
Passionate about Pharma GMP? Are you a key voice in the QA department? * Fantastic opportunity to influence the quality culture * Hertfordshire based Verbatim Pharma are looking for a GMP Compliance ...
Support GMP Experts who work with client managers and operations colleagues with multiple client GMP projects including reconciliation, rectification/recalculation and equalisation * Carrying out ...
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
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 ...
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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 ...
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 ...
Or do you already have a background in an industrial micro lab but would like to develop your skills further in a GMP environment? SRG Synergy are currently working with a world-leading ...
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 ...
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 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 ...
Comprehensive knowledge of current CMC and ICH regulatory requirements as well as GMP standards Regulatory Affairs | RA | Head of Regulatory Affairs| GMP | Pharmaceutical | Regulatory | Submission ...
Maintain compliance with GMP, ISO, Quality Assurance, and Health & Safety policies * Provide outstanding customer service by answering inquiries and resolving issues promptly * Perform administrative ...
Understand fully the GMP and Data Integrity principles and their application in the role * Manage or support the scheduling of testing workload and delegate testing activities to the team * Mentor ...
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 ...
You will carry out daily GMP audits of the warehouse, factory exterior and the office block areas and regular checks on the packing lines to ensure that all products are being manufactured to the ...
Must have a current, satisfactory in date annual appraisal in line with the requirements of the General Medical Council's (GMC's) Good Medical Practice (GMP) * Must hold current, valid personal ...