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Monday-Friday, 7am-3pm (Some flexibility needed).Are you an experienced QC professional with a passion for hands-on work and leadership? Do you thrive in a fast-paced, GMP environment? If so, this could be the ideal opportunity for you to lead a small but growing analytical team.The business is a...

CK Group are recruiting for a Quality Manager, in operational QA (GDP), to join a global biotechnology company, on a contract basis for 12 months. Salary: £370 - £450 per day Umbrella. This role is inside IR35. Quality Manager, GDP Operational QA Role: - The Quality Manager is responsible...

QC Manager I am partnered exclusively with an international advanced pharmaceutical company that are continuing to expand operations both in terms of product delivery and site presence across the UK. This specific hire will take management and scheduling responsibilities for all site Qua...

We are seeking a Pensions project administrator to work in our newly created specialist Administration Project Implementations Team. The types of projects you may be asked to work on will include, but is not limited to, the following: GMP reconciliation projects; GMP equalisation projects; benefi...

Key experience: - Experienced QC/Analytical Chemistry manager or supervisor within a pharmaceutical GMP environment - Technical experience will include some of the following – HPLC, GC - Previous people management experience is essential - Excellent understanding of pharmacopoeia - Knowledge and ...

Key experience: - Experienced QC/Analytical Chemistry manager or supervisor within a pharmaceutical GMP environment - Technical experience will include some of the following – HPLC, GC - Previous people management experience is essential - Excellent understanding of pharmacopoeia - Knowledge and ...

This specific hire will take management and scheduling responsibilities for all site Quality Control (QC) activities with strong focus on method development oversight and team leadership. Key experience: - Experienced QC/Analytical Chemistry manager or supervisor within a pharmaceutical GMP envir...

This specific hire will take management and scheduling responsibilities for all site Quality Control (QC) activities with strong focus on method development oversight and team leadership. Key experience: - Experienced QC/Analytical Chemistry manager or supervisor within a pharmaceutical GMP envir...

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 in de-risking projects for clients over time. Directly involved with the management of more junior...

Deliver engaging in-person and virtual training sessions, including inductions and GMP processes. Maintain and evolve the GMP training programme using a learning management system. Previous experience developing and delivering training in a GMP environment.

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 in de-risking projects for clients over time. Directly involved with the management of more junior...

Understand and follow GMP requirements and defined procedures to maintain the requirements of quality standards in the packaging environment. Your Background: Experience of packaging and labelling environment in a GMP environment, preferably within clinical trials. CK Group are recruiting for a G...

Maintain strict compliance with GMP and site SOPs. Prior experience working in a GMP pharmaceutical or clinical packaging environment. One of our most exciting pharmaceutical clients are seeking a detail-oriented and quality-focused Clinical Packaging Operator to join their GMP manufacturing oper...

As a GMP Production Manager, you will lead the GMP production team and oversee the day-to-day management, scheduling, and operations of the facility in compliance with licensing and regulatory standards. As the GMP Production Manager you will oversee production planning, documentation, and proces...

Are you passionate about delivering high-impact training in a cutting-edge GMP environment? We’re looking for a. Deliver engaging in-person and virtual training sessions, including inductions and GMP processes. Maintain and evolve the GMP training programme using a learning management system.

Maintain strict compliance with GMP and site SOPs. Prior experience working in a GMP pharmaceutical or clinical packaging environment. One of our most exciting pharmaceutical clients are seeking a detail-oriented and quality-focused Clinical Packaging Operator to join their GMP manufacturing oper...

As the GMP Production Manager you will oversee production planning, documentation, and process execution in line with GMP and licensing requirements. As a GMP Production Manager, you will lead the GMP production team and oversee the day-to-day management, scheduling, and operations of the facilit...

GMP Rectification Specialist Do you have the skills needed to lead GMP rectification projects? We are looking for a driven individual to join our newly formed Data Solutions Team, within Aon’s UK Retirement business. What the day will look like Overseeing the delivery of a bank of GMP rectificati...

One of our most exciting pharmaceutical clients are seeking a detail-oriented and quality-focused Clinical Packaging Operator to join their GMP manufacturing operations. Ensure accurate completion of batch documentation and logbooks in accordance with GMP. Maintain strict compliance with GMP and ...

KEY DUTIES AND RESPONSIBILITIES Your duties as the GMP Production Manager will be varied however the key duties and responsibilities are as follows: Act as the named Production Manager on the facility’s manufacturing licence, leading GMP operations, qualification of the facility and compliance wi...

As a GMP Production Manager, you will lead the GMP production team and oversee the day-to-day management, scheduling, and operations of the facility in compliance with licensing and regulatory standards. GMP Production Manager / GMP / ATMP / CDMO / Cleanroom / Manufacturing Licence / Fermentation...

Analytical Scientist – Viral Vector Characterisation (GMP/ATMP) Analytical Scientist – Viral Vector Characterisation (GMP/ATMP) Get AI-powered advice on this job and more exclusive features. Key Responsibilities Design and execute experiments; analyse and interpret complex datasets Develop, op

GMP Production Manager / GMP / ATMP / CDMO / Cleanroom / Manufacturing Licence / Fermentation / Fill Finish / Viral Vectors / Biopharma / SOP / Tech Transfer / South West / Clinical Trial Material / Quality Compliance. As the GMP Production Manager you will oversee production planning, documentat...

Job Description: GMP Rectification Specialist - UK Wide GMP Rectification Specialist Do you have the skills needed to lead GMP rectification projects? We are looking for a driven individual to join our newly formed Data Solutions Team, within Aon's UK Retirement business. What the day will look l...

Ensure accurate completion of batch documentation and logbooks in accordance with GMP. Maintain strict compliance with GMP and site SOPs. Prior experience working in a GMP pharmaceutical or clinical packaging environment.

Key Responsibilities Design and execute experiments; analyse and interpret complex datasets Develop, optimise and validate analytical methods Write and maintain SOPs and lab documentation to ISO13485 and GLP standards Contribute to design control and technical transfer processes Lead or support d...

Join Our Team as an Actuarial Consultant - GMP Equalisation and Project Work (Nationwide) Are you a talented and ambitious actuary with a strong background in GMP rectification and equalisation? At Mercer, we are excited to expand our dynamic team by welcoming skilled part-qualified or qualified ...

KEY DUTIES AND RESPONSIBILITIES Your duties as the Senior GMP Production Scientist will be varied however the key duties and responsibilities are as follows: Supervise GMP cleanroom production operations, lead tech transfer activities from process development, and manage production planning for a...

Senior Technical Actuary (GMP Equalisation) View more categories View less categories Sector Insurance Role Senior Executive Contract Type Permanent Hours Full Time Senior Technical Actuary GMP Equalisation Hybrid Full Time or Part Time Permanent Ref: 002846 This role could be based from any

Social network you want to login/join with: Analytical Scientist – Viral Vector Characterisation (GMP/ATMP), Bedford Client: BioTalent Location: Bedford, United Kingdom Job Category: Other EU work permit required: Yes Job Views: 3 Posted: 10. Key Responsibilities Design and execute experiments; a...

Join Our Team as an Actuarial Consultant - GMP Equalisation and Project Work (Nationwide) Are you a talented and ambitious actuary with a strong background in GMP rectification and equalisation? At Mercer, we are excited to expand our dynamic team by welcoming skilled part-qualified or qualified ...

Skills and experience that will lead to success Be proactive and self-motivated, with a desire to own and deliver the best solutions for Aon An ability to improve processes and adapt to change Have experience of similar projects, such as pensions change projects and/or GMP equalisation Have stron...

We’re Looking For Essential: Degree in Chemistry, Biology, Physics, Engineering, or a related field At least 2 years’ industry experience in a lab-based role Hands-on experience with HPLC or comparable analytical techniques Strong data interpretation and troubleshooting abilities Familiarity wit

Are you a part-qualified or qualified pensions actuary with GMP experience, looking for your next fully remote role within a rapidly growing team of a major global consultancy? Then look no further! This is a fantastic, client-facing opportunity in which you will work on projects relating to GMP ...

Perform start-up, execution, and cleaning of clinical packaging and labelling operations Operate a range of equipment for primary and secondary packaging of oral solid dosage forms Assemble, label, and inspect clinical trial supplies — including automated walleting and labelling lines Ensure accu...

Job profile for Senior Technical Actuary (GMP Equalisation) Senior Technical Actuary (GMP Equalisation) The job requirements are detailed below. Regular liaison and communication with the GMP team, client team and other departments in XPS. Basis: Full time Job category/type: XPS Pensions Date pos...

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 in de-risking projects for clients over time. Directly involved with the management of more junior...

Join Our Team as an Actuarial Consultant - GMP Equalisation and Project Work (Nationwide) Are you a talented and ambitious actuary with a strong background in GMP rectification and equalisation? At Mercer, we are excited to expand our dynamic team by welcoming skilled part-qualified or qualified ...

Prestigious UK law firm is seeking a professional and personable part-time Legal Receptionist to join its London office, located in a prime City location.Generous employee benefits to include wellbeing fund, gym membership contribution, holiday buy / sell etc.The successful candidate will work fr...

We will count on you to: Work as part of a great multi-disciplinary team on complex defined benefit modelling using advanced actuarial skills and techniques, specialising in complex UK pension solutions You will be responsible for checking and reviewing complex calculations, as well as communicat...

Our US powerhouse law firm client is seeking to hire a highly polished and professional Legal Receptionist to join their London office on a part-time basis.Superb employee benefits, including gym membership contribution, fertility & family planning services, 27 days annual leave (FTE) after 2 yea...

Key Responsibilities: Collating and analysing scheme information Identifying data gaps and managing data rectification Running calculations using GMPe workbooks and interpreting results Producing and issuing project reports and trustee updates Leading and managing end-to-end project delivery Data...

Junior Operations Manager LONDON BASED.Working in the SPORTS EVENTS MARKET.You will be responsible for managing a range of international and routine business Summits, Market Visits and networking events.The business support is for 3 communities:.Expert or new to market multi-sector companies seek...

Key Duties And Responsibilities Your duties as the Senior GMP Production Scientist will be varied however the key duties and responsibilities are as follows: Supervise GMP cleanroom production operations, lead tech transfer activities from process development, and manage production planning for a...

To support scientific staff by monitoring and maintaining levels of consumables within GMP manufacturing areas. To manage garments required for GMP areas, ensuring adequate garments are available in all change areas as well as effective control over the laundering process. The Role Contribute to ...

OMODA Motors is a new brand built by Chery Group, which is a leading Chinese automobile company.OMODA operates individually from other brands of Chery Group.Its business scope covers the R&D, production and sales of passenger cars.Since founded, Chery has always taken adhering to technology-drive...

The safety of our patients and our people is paramount to us at Ramsay Health Care UK.That’s why our work in the Decontamination Unit is so vital.It’s here that we sterilise all the instruments and equipment needed to deliver a wide variety of surgical procedures and treatments across the hospit

Must have art/luxury experience.Our client, a leading international art gallery that specialises in modern and contemporary art, is looking for an experienced Warehouse Operative to work within their logistics center in North West London.Handling, moving, packing and unpacking all artwork and ins...