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Job Location Weybridge Job Description Procter & Gamble (P&G) is a leading global consumer goods company, with Personal Health Care brands including Vicks, Pepto‑Bismol, and Seven Seas. We are seeking a Qualified Person (QP) / Senior Quality Assurance Manager to lead quality and compliance activities across GMP, GDP and HACCP for food supplements and help safeguard consumer trust across our UK Personal Health Care portfolio. If you thrive at the intersection of regulatory excellence, safety, and quality leadership, this role could be your next career step. You will play a key part in ensuring products are manufactured, released, and distributed in full alignment with UK regulatory requirements and global quality standards. In this highly visible role, you will safeguard product quality, protect consumers, and act as a trusted partner to internal teams, suppliers, and regulatory authorities, making a real impact from manufacturing through distribution. *This position will be primarily based in Weybridge (Surrey), with alternative options available in Reading or Skelmersdale. Candidates must be flexible to travel periodically to the Skelmersdale site as required. Role overview As the Qualified Person (QP) for Procter & Gamble UK, you will be accountable for ensuring that products are manufactured, tested, released, and distributed in full compliance with UK legislation and global quality standards. With us, you will: • Act as Qualified Person for Procter & Gamble UK in accordance with UK legislation for Medicinal Products for Human Use, ensuring batch certification, release, and maintenance of the certification register., • Ensure robust GMP, GDP, and HACCP compliance through effective documentation systems, quality and technical agreements, vendor qualification and auditing, and alignment with Marketing Authorisations and Global Healthcare procedures., • Lead quality governance activities, including deviation management, CAPA definition and tracking, quality performance monitoring, and continuous improvement initiatives., • Manage critical quality events such as incidents, complaints, recalls, and withdrawals, acting as the key interface with internal stakeholders, authorities, and drug and food safety bodies., • Prepare for and manage regulatory inspections and approve and oversee annual training plans to ensure personnel are appropriately trained and qualified. What we offer you: • Meaningful Work from Day 1: From Day 1, you’ll step into a role with real accountability where you will directly influence product release, quality outcomes and regulatory confidence for P&G’s UK portfolio, using your expertise to protect consumers and uphold trusted brands. You will be owning your part of the business and helping it grow, with continuous and supportive coaching from your manager and the wider team., • Competitive Benefits: P&G take a Total Rewards approach meaning on top of your competitive salary, which is reviewed annually, you can expect a whole range of benefits including: a double-matched pension scheme, private health insurance, participation in a stock ownership scheme, 25 days holiday and your very own ‘Flex4Me’ Fund which enables you to allocate a portion of your benefits package to the areas that matter most to you., • Flexibility: We operate a flex at work approach, with flexibility built into the role. Our teams spend 3 days of their week collaborating together in our offices or at our external partners. This is balanced with 2 of their days spent on focused work which most tend to do from home. Of course, we do a bit of both every day, but we encourage our teams to choose where they work based on the jobs to be done. Job Qualifications What you’ll bring • Degree in pharmacy or another formal qualification in medicine, veterinary medicine, chemistry, pharmaceutical chemistry and technology or biology., • Registration and approval as a Qualified Person with British Authorities in accordance with local regulations., • Sufficient experience as a Qualified Person under UK regulations and solid experience in Quality Assurance., • Advanced knowledge of GMP and GDP requirements., • Fluency in English, both written and spoken, • Strong communication and collaboration skills with internal teams, suppliers, and regulators., • A results‑driven, quality‑focused mindset with a strong sense of ownership., • Proactivity, organization and ability to operate with urgency in a regulated environment. Right to Work: For this role, P&G are willing to provide sponsorship to those who require a visa to live and work in the UK, subject to meeting all the necessary Home Office requirements. Full details on visa restrictions can be found on the Home Office website and immigration rules are subject to change. P&G is legally required to ensure all candidates have the right to work in the UK from Day 1 of their employment. All applicants will therefore be asked to provide evidence of their right to work at the conclusion of the recruitment process as a condition of employment. At P&G #weseeequal We are an equal opportunity employer and value diversity at our company. At P&G we strive to build a culture where everyone feels welcome, included, and able to bring their full selves to work. We ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Please click ___ if you require an accommodation during the application process. Please make sure to wait to hear back from us regarding your accommodation before proceeding with the online assessment, we thank you in advance for your patience. Job Schedule Full time Job Number R000144335 Job Segmentation Experienced Professionals Starting Pay / Salary Range

About Us Touchlight pioneers scalable, cell-free DNA technology, transforming gene therapy and genetic medicine. With a commitment to innovation, excellence, and a diverse team, we push boundaries to deliver safer, more efficient solutions for the future. At Touchlight, we’ve reimagined DNA production to meet the evolving needs of innovators like you. Our patented synthetic DNA vector, dbDNA™, and cell-free enzymatic manufacturing platform deliver DNA with unmatched speed, scale, and purity, helping you move faster from discovery to clinic. Whether you’re developing mRNA, viral vector, or vaccines, Touchlight helps you overcome the limits of plasmid manufacturing. No fermentation. No antibiotics. No cell banking. Just high-quality RUO or GMP DNA, ready when you need it. DNA is our DNA™ Role Overview: Touchlight is currently seeking a skilled & highly organised Laboratory Technician to support our CDMO lab. The Laboratory Technician is responsible for the completion of essential tasks such as reagent preparation, equipment verification, facility cleaning, stock control and QMS actions. The Lab Technician reports to the dbDNA Team Lead. Your key responsibilities will be: generation of reagents, within a Grade D manufacturing facility and R&D facility where required, for laboratory methods and processes for both GMP and research grade activities. Additionally, you will be responsible for regular equipment calibration and verification checks. You will help maintain our laboratories to enable it to operate at its highest level of performance, as well as maintaining stocks and organising logistics. You will also be expected to identify ongoing challenges and develop solutions to maintain an optimal work environment and ensure compliance with good H&S practices and company policies. We'd like to hear from you, if you have a scientific background and/or proven experience working in a laboratory, ideally in a GMP or production setting. Skills and Experience: Required: • Laboratory or relevant industry experience, • Strong verbal and written communication skills, • Proactive attitude Desirable: • Science degree or relevant academic experience, • Experience in GMP, • Working knowledge of SAP (or other ERP) Touchlight Benefits Touchlight is a successful scale-up business with a record of world-leading innovation and a welcoming, entrepreneurial culture. We make Touchlight an extraordinary place to work by providing our employees with incredible facilities, flexible working and a competitive benefits and remuneration package. A Place for Everyone We believe diversity drives innovation and for that reason we strongly encourage those from all backgrounds to apply for roles at Touchlight. We are an equal opportunity employer and aim to build a workforce that is truly representative of the communities in which we operate and our customers. If you need reasonable adjustments at any point in the application or interview process, please speak with the HR team who will be happy to support you.

Candidates should have a relevant scientific degree and experience in GMP environments, and will have the chance to influence quality culture in a respected organization.

A global specialty pharmaceutical company in Byfleet is seeking a Quality Release Specialist to ensure compliance with Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP).

Documentation Officer New Malden ⏰ Hours: Monday–Friday, 9:00am–5:00pm We are currently recruiting a Documentation Officer to join a busy team based in New Malden. This role sits within a GMP‑regulated production environment and is ideal for someone with hands‑on experience handling documentation within manufacturing. This position could also particularly suit an experienced Production Operative or Production Officer who has taken responsibility for GMP paperwork, batch records, or quality documentation as part of their role and is looking to move into a more documentation‑focused position. Key Responsibilities • Preparing, reviewing, and maintaining GMP documentation, • Completing and checking batch records, logs, and production paperwork, • Ensuring documentation is accurate, compliant, and completed on time, • Maintaining document control systems (paper‑based and/or electronic), • Supporting production and quality teams with documentation queries, • Raising and correcting documentation errors in line with procedures, • Ensuring compliance with GMP, SOPs, and data integrity standards Skills & Experience Required • Previous experience working with GMP documentation, • Background within an FMCG manufacturing environment (e.g. food, pharmaceutical, cosmetics, chemical, or similar), • Strong attention to detail and accuracy, • Good understanding of SOPs, batch records, and controlled documents, • Confident using basic IT systems (Word, Excel, document systems), • Organised, reliable, and comfortable working to deadlines, • Able to work independently and as part of a team What’s on Offer • Stable, Monday–Friday day hours (9am–5pm), • Clear transition pathway from production into a documentation‑led role, • Supportive team environment, • Training and ongoing development, • Opportunity to work within a regulated, quality‑focused organisation If you have GMP documentation experience from any FMCG manufacturing setting and are looking for a structured, office‑based role in New Malden, we would love to hear from you. Apply today to be considered

Production Operative New Malden ⏰ Shift: Monday–Friday, 6:30am–3:00pm We are currently seeking a Production Operative to join a growing manufacturing team based in New Malden. This is a hands‑on role within a regulated production environment, ideal for someone with previous GMP manufacturing experience from any industry. Key Responsibilities • Operating on the production line in accordance with GMP standards, • Following standard operating procedures (SOPs) accurately, • Weighing, mixing, packing, or assembling products as required, • Completing production and quality records clearly and correctly, • Maintaining a clean, safe, and organised work area, • Complying with health & safety, hygiene, and quality procedures at all times Skills & Experience Required • Previous experience working in a GMP production environment (e.g. food, pharmaceutical, cosmetics, chemical, or similar), • Experience operating manufacturing equipment, • Good understanding of cleanliness, hygiene, and quality standards, • Ability to follow instructions and work to procedures, • Reliable, punctual, and able to work an early morning shift, • Good attention to detail and a strong work ethic, • Able to work independently and as part of a team What’s on Offer • Consistent day shift hours (6:30am–3:00pm), • Monday to Friday work–life balance, • Supportive team environment, • Training and ongoing support, • Opportunity to work in a stable, regulated manufacturing setting If you have experience working in a GMP production environment and are looking for a steady day shift role in New Malden, we would love to hear from you. Apply today to be considered

Ideal candidates will have experience in aseptic services and quality assurance, a keen eye for detail, and understand GMP.

NHS is looking for a Radiopharmacy Technician/Scientist at St.Bartholomew's Hospital in London.Candidates should possess relevant qualifications, such as a BTEC in Pharmaceutical Sciences and experience in aseptic manufacturing and quality control.Strong organizational and communication skills are e

NHS Blood and Transplant is seeking an Eye Services Technical Officer to support our Eye Bank team in maintaining high-quality services.This role includes preparing samples, maintaining equipment, and ensuring compliance with standards.The position offers a supportive work environment, flexible work

Deze rol vereist minimaal 2 jaar labervaring, een MLO opleiding, en kennis van GMP/GcLP.

A global pharmaceutical leader is seeking a Packaging Operator to join their production team in England.This mid-senior level role involves operating packaging equipment and ensuring compliance with safety and quality standards.Ideal candidates will have experience in pharmaceuticals or similar regu

The role involves running the packaging line, ensuring compliance with GMP, and maintaining quality standards while packaging pharmaceuticals.

A recruitment agency is seeking a full-time Sales and Lettings Negotiator to manage property sales and rental transactions in the Forest of Dean.The successful candidate will build relationships with clients, offer advice, and promote properties through various channels.A driving licence is often ne

Entrust Resource Solutions is seeking a Manufacturing Manager to oversee site-wide management of manufacturing projects in a GMP environment.

The role offers substantial advancement opportunities within a renowned organization, emphasizing problem-solving and teamwork in compliance with GMP standards.

The ideal candidate will possess a degree in engineering, experience in lead process engineering, and an understanding of GMP compliance.

Hiring #GMP #GoogleMarketingPlatform #Data #Leadership. Provide thought leadership and expert consultancy on the GMP platform and activation of use cases to drive successful outcomes. Strong GMP experience (7+ years).

A leading NHS trust in London is seeking an enthusiastic Band 5 Radiopharmacy Technician to join their Radiopharmacy team.Candidates should have attention to detail, effective communication skills, and the ability to work under pressure.Experience in aseptic manufacturing and working with radioactiv

A leading consultancy in the United Kingdom seeks a qualified or part qualified Actuary to provide advice on GMP equalisation and benefit rectification projects.

A leading digital marketing agency in Greater London is seeking a professional for technical support roles focusing on Google Cloud projects.The ideal candidate should possess extensive experience with Google Cloud products, especially BigQuery and Firestore.Responsibilities include integrating tech

This senior leadership position involves overseeing all engineering and technical operations within a GMP-regulated manufacturing facility.

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 actuaries to a vital role that not only drives revenue but also fosters professional growth a

A leading digital marketing technology firm in Greater London is seeking a professional to develop and support its Google Marketing Platform clients.The role requires over 5 years of PPC experience and strong communication skills.You will manage client onboarding, provide technical support, and deli

LUNAR LABS LIMITED is seeking a Quality Management System (QMS) specialist to oversee and support the Quality Management System in compliance with GMP standards. A Bachelor's degree in Pharmaceutical Sciences or related field is required along with experience in a GMP-regulated environment.

The role involves maintaining batch documentation, supporting production equipment, and ensuring compliance with cGMP and health standards.

You will oversee maintenance activities, manage technical documentation, and ensure compliance with GMP regulations. The ideal candidate has experience in GMP environments and relevant engineering education.

Applicants should have a pharmacist qualification, experience in GMP environments, and a passion for driving continuous improvement.

Integrating new capabilities for prototyping of tech solutions for both Assembly and GMP Clients. Be an evangelist to help our clients be at the top of their game by helping with their technical solutions of the GMP & GCP tools. Experienced throughout the GMP tech stack.

You will manage projects from concept to completion, ensuring compliance with GMP standards while optimizing plant infrastructure.

Candidates must have a degree in a relevant scientific discipline and prior experience in highly regulated environments such as cGMP or ISO.

Ideal candidates should have experience in radiopharmaceutical or aseptic production, work well in teams, and comply with GMP regulations.

Required: degree in engineering or a related field, extensive GMP experience, and significant leadership experience.

The successful candidate will ensure GMP compliance, conduct laboratory experiments, and support project initiatives.

This role entails overseeing validation project activities while ensuring compliance with GMP guidelines.

A growing global pharmaceutical manufacturer in the UK is seeking a Microbiology Manager to lead microbiology activities ensuring compliance in a GMP-regulated environment.

Candidates must have at least 7 years of GMP experience and a strategic mindset to engage with senior clients successfully. A leading digital recruitment agency in the UK is seeking a senior professional with extensive experience in the Google Marketing Platform (GMP).

A leading pharmaceutical company in the United Kingdom is seeking a highly motivated Manufacturing Technician.This role entails operating and maintaining manufacturing equipment, ensuring adherence to safety and quality standards, and supporting production efficiency.Candidates should have a High Sc

A leading biotechnology firm in the UK seeks a QC Analytical Scientist to oversee testing of gene therapy products, adhering to EU and FDA GMP requirements. Ideal candidates will have a degree in Human Health or Sciences and prior experience in a GMP environment.

The ideal candidate will have over 7 years of experience in the Biotech or pharmaceutical sectors, particularly in cGMP environments.

A leading recruitment firm in Greater London is seeking a detail-oriented QC Materials Technician to ensure compliance and quality standards in a GMP-regulated environment. The ideal candidate should have at least 1 year of experience in a GxP or GMP setting, possess strong communication skills, and

The GMP Production Manager will be responsible for establishing the GMP production team and taking a lead role in the operation of the GMP production suites. The GMP Production Manager will lead and develop the GMP production team and will be responsible for leading the day-to-day management, operat

The role involves operating filling and packing equipment in a GMP environment, ensuring compliance with quality standards.

A healthcare agency is seeking an experienced Pharmacist with NHS Hospital experience to join their team in Greater London.The ideal candidate will be GPhC registered, compliant with regulations, and able to work flexible hours, both part-time and full-time.In return, the agency offers excellent pay

Ideal candidates will have strong knowledge of GMP, HACCP, and tracing in manufacturing environments.

Key responsibilities include preparing, compounding, and dispensing aseptic products under GMP standards.

A global ecommerce group is hiring a Machine Operative for their production team in Blackpool, England.In this role, you will ensure safety and quality standards while operating and maintaining high-speed production equipment.Ideal candidates possess strong communication skills, attention to detail,

A leading medical technology company in Cirencester is seeking a Senior Validation Engineer to maintain the validated state of critical medical device manufacturing processes.The role involves leading validation projects, supervising a team, and ensuring compliance with regulatory standards.Candidat

This role involves managing validation compliance activities and ensuring all processes meet GMP and corporate standards.