Compliance contract jobs in HatfieldCreate job alerts

Associate Director – Mental Capacity Act & Deprivation of Liberty Band 8c | £42.32 per hour | Full-time 37.5 hours | Hybrid | NHS Contract: Full-time, 37.5 hours per week (Monday to Friday) Location: Hybrid (with NHS site presence as required) Job Summary We are seeking an experienced and dynamic professional to take up the role of Associate Director – Mental Capacity Act (MCA) & Deprivation of Liberty Safeguards (DoLS). This pivotal leadership role will be responsible for strategically leading, developing, and embedding all aspects of the MCA (2005) and DoLS (2007) across the ICB. You will work collaboratively with safeguarding leads, senior clinicians, and partner agencies to ensure compliance with statutory responsibilities and to protect the rights of individuals across services. Should the legislative framework change (e.g. the implementation of Liberty Protection Safeguards), you will play a key role in driving forward the transition and leading the implementation across the ICB in partnership with multi-agency stakeholders. Key Responsibilities • Provide strategic leadership on all matters relating to MCA and DoLS., • Develop, implement, and oversee policies, systems, and training packages to ensure ICB-wide compliance., • Act as the clinical expert and provide guidance, advice, and training to staff on MCA/DoLS principles and application., • Work in partnership with safeguarding leads and wider stakeholders to embed MCA/DoLS within relevant services and policies., • Lead the design and delivery of comprehensive training programmes to ensure staff understand their responsibilities in protecting patients’ human rights., • Monitor, evaluate, and evidence improvements in practice and outcomes in relation to MCA/DoLS legislation. This role is suitable for a Registered Nurse, Allied Health Professional, or Social Worker with proven expertise in the Mental Capacity Act and DoLS, alongside significant leadership experience in safeguarding, governance, or statutory compliance. Essential Skills & Experience: • Professional registration (NMC, HCPC, or Social Work England)., • In-depth knowledge and practical application of MCA and DoLS legislation., • Strong leadership skills with the ability to influence and drive change across complex systems., • Experience of working with multi-agency partners and stakeholders., • Proven track record of developing policy, systems, and training at scale., • Ability to evidence impact on practice and outcomes.

About the role As an Operative 2 with expertise in Warehouse Administration, you will collaborate with our client's department. You will be responsible for Warehouse Operations. Tell me more, tell me more Our client is currently looking for a recruit in joining their current team. Below are the job details for your reference:You can also ask our friendly recruitment team for any questions you may have about the role, between 09.00am till 17.00pm Monday to Friday. Shifts: Monday to Friday (37.5 hours) Roles and Responsibilities: We have a fantastic opportunity for a Warehouse Dispatch Operative in the Services logistics Warehouse. You will need to have high levels of accuracy, attention to detail and a strong work ethic; previous export compliance knowledge would be beneficial as you will be raising commercial invoices and previous logistical experience would be highly desirable. You will need to have high levels of accuracy, attention to detail and a strong work ethic. You will have experience in ERP systems (preferably SAP and WMCS). To be successful in the role you will be a great team player, have a flexible approach to work, the ability to work in a fast-paced environment, perform against personal performance targets, prioritise workloads against demand to meet our service level agreements with our customers and have excellent communication skills and be able to escalate directly to your management team and internal service providers, both orally and electronically. Main Responsibilities • Using six different courier vendor platforms to ship both UK homeland services and international., • Using escalation routes for different partners, • Liaising with scheduling, • Ensuring SAP queues are cleared., • Producing an end-of-day report, • Effectively escalate where required both orally and electronically., • Producing manifests for the trunk and sharing electronically between internal service providers and management, • Some export compliance knowledge, • Strong attention to detail, • Strong experience in warehouse practices, • Ability to work as part of a team., • Be a quick learner., • Able to prioritise workloads., • Good numerical skills, • Excellent timekeeping and a flexible approach to work demands, • Flexible working approach, • Counterbalance FLT licence advantage, • Stock management, • Picks and Putaways LocationHatfield Avenue Hatfield Business Park - Hatfield Hertfordshire AL10 9TW Contract 7 Months 8th Sep - 8th Mar 2026 Monday - Friday working hours 11:00 - 19:.5 hours per week Next Steps Once you've applied, one of our friendly recruitment consultants will give you a call and talk you through the screening process. If your application is successful, you'll be involved in a live virtual interview with one of our client's hiring managers to get to know you better.We look forward to speaking to you! Hays Talent Solutions is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found on our website.

Paraplanner (Fixed-Term Contract – 6 to 12 Months) Immediate Start Available Location: Offices Near St Albans (Hertfordshire) Contract: Full-time | Fixed Term (6–12 months) Salary: £45,000 – £55,000 (Depending on Experience) Are you an experienced Paraplanner looking for a fixed-term opportunity with a dynamic and supportive team? We’re working with a highly regarded independent financial planning firm who are looking to appoint a Paraplanner on a 6–12 month fixed-term contract. This is an excellent opportunity to join a firm known for its personal, high-quality service to clients with portfolios ranging from £750,000 up to £70 million. You'll play a key role in supporting advisers through a busy period, helping to ensure the continued delivery of accurate, compliant, and high-value advice. Key Responsibilities: • Writing suitability reports and financial plans, • Conducting in-depth product and fund research, • Supporting advisers with pensions, investments, protection, and estate planning cases, • Liaising with clients, providers, and internal teams to ensure seamless service delivery, • Ensuring compliance with FCA regulations and internal procedures About You: • Diploma qualified (Level 4) or close to completion, • At least 2–3 years’ experience in a Paraplanning role, • Strong knowledge of financial planning software, tools, and platforms, • Excellent written communication and attention to detail, • Proactive and self-sufficient with a collaborative approach What’s On Offer: • Competitive salary: £45,000–£55,000, • Flexible working options (hybrid or remote considered), • Work alongside a highly respected team with an exceptional reputation, • Immediate start for the right candidate Please send your CV or get in touch with Sam at to find out more.

Design Manager St Albans, Hertfordshire £30m+ Projects We are seeking a proven Design Manager to take ownership of a major build project in St Albans. This scheme is within the life sciences sector, so previous experience in this area would be highly beneficial. However, candidates with strong backgrounds in commercial, industrial, or data centre projects will also be considered. You will be responsible for managing the full design process, coordinating consultants and contractors, and ensuring projects are delivered to the highest standards of quality, compliance, and safety. About the role: • Oversee design stages from inception through to completion – lead design meetings, carry out technical reviews., • Maintain compliance with life sciences regulations (BREEAM, manage contract specifications, drawings, O&M and H&S file collation)., • Interface effectively with stakeholders – clients, contractors, and colleagues – resolve issues and deliver to schedule Requirements: • Experience working as a Design Manager (or similar role), • Successful track record on projects valued at £25m+, • Life sciences experience preferred, or strong exposure to commercial, industrial, or data centre builds, • Strong leadership, communication, and problem-solving skills What’s on offer: • The chance to work on technically complex, high-value projects, • A collaborative and supportive environment, • Competitive salary and benefits with genuine scope for career growth If you have the experience and ambition to deliver at this level, we’d love to hear from you. Please apply with your updated CV for consideration.

Applications outside a 10 miles radius of South Mimms, Hertfordshire will not be considered. Laboratory Assistant – Temporary Contract (3 Months Minimum) 📍 Location: South Mimms – must be commutable 5 days per week 🕒 Hours: Full-time, 37 hours per week (excluding lunch break) 📅 Contract: Ongoing temporary role, minimum 3 months 🚀 Start Date: Must be available to start immediately Are you experienced in laboratory operations and looking for a hands-on role in a scientific environment? We’re seeking a proactive Laboratory Assistant to support essential lab services including sterilisation, equipment maintenance, and hygiene management. Key Responsibilities: • Operate and maintain autoclaves, glasswashers, and sterilising ovens, • Ensure safe decontamination of hazardous materials, • Manage laundry and hygiene services for lab and cleanroom wear, • Coordinate with contractors and lab staff to resolve equipment and supply issues, • Minimum 3 years’ experience in a similar lab-based role, • Strong knowledge of sterilisation and decontamination techniques, • Skilled in operating and maintaining industrial lab equipment, • Organised, adaptable, and a collaborative team player This is a great opportunity to contribute to a vital scientific service in a dynamic and supportive environment.

CK Group are recruiting for a Clinical Study Manager, to join a company in the Pharmaceutical industry, at their site based in Welwyn Garden City, on a contract basis for 6 months. Salary: Daily: £339 - £376.97 PAYE or £450 - £500 per day Umbrella. Clinical Study Manager Role: • Drive Operational Excellence by developing operational plans, creating & managing clinical study budget & overseeing the consistency of operations., • Manage vendors & stakeholders by managing relationships with vendors & cross-functional stakeholders., • Oversee performance of vendors and third-party providers., • Provides direction and leadership to the local study team, including Clinical Research Associates (CRAs) to ensure delivery of the study., • Ensure timely delivery of the study within the UK while ensuring quality and compliance and diversity plan., • Collaborate with the relevant colleagues to ensure timely feasibility, start-up, site payments etc. Your Background: • Previous experience in UK clinical trial management., • Study start-up experience highly desirable., • Hold a university degree or equivalent years of experience, preferred focus in life sciences., • Possess strong working knowledge of drug development process and respective regulations, including ICH and GCP guidelines. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Location: This role is based at our clients site in Welwyn Garden City, for 2 or 3 days a week, then offers home working for the remainder of the week. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 151 198 in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.

Your new company My client is a global biopharmaceutical company with a goal of contributing to healthcare innovation and environmental sustainability. They are focused on improving people's quality of life, specialising in Oncology, neurology, rare diseases, ophthalmology and immunology. There is an opportunity for a Senior Pharmacovigilance Scientist to join their Patient Safety Operations - Data Transformation team on an initial 12-month rolling contract. OUTSIDE IR35 Hybrid -2 days in office per week Your new role As a highly motivated individual, you will use your pharmacovigilance expertise, particularly individual case safety report (ICSR) knowledge, to ensure safety data is processed and reported in a high-quality, compliant manner, so it can be used to understand and communicate the product benefit risk to protect patients' safety. • Performing oversight of service providers who execute ICSR tasks (and Medical Device reports), • Answering queries and proactive sharing of your subject matter expertise to stakeholders (internally, at the service provider, business partners, auditors and inspectors), • Conducting process reviews to design and implement process improvements, • Identifying root causes of non-compliance to agree Corrective Actions and Preventative Actions (CAPAs), which you may be responsible for implementing, • Life sciences degree, • Proven Pharmacovigilance experience in the pharmaceutical industry - Demonstrated experience in a breadth of areas pertaining to pharmacovigilance, and pharmacovigilance legislation; good knowledge of international regulations (ICH, EU GVP Modules, FDA) and an understanding of the pharmaceutical industry (product development and the commercial environment) and of rapidly evolving personalised healthcare environment and ecosystem., • Medical Device processing experience, knowledge., • Evidence of leading complex, time-pressured projects, working with a wide range of stakeholders. If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on 03330106292

Job Title: Packaging Operator Location: Hatfield, UK Company: Leading Global CDMO We are connecting with a leading Contract Development and Manufacturing Organisation (CDMO) dedicated to supporting the pharmaceutical and biotechnology industries. Their Hatfield facility plays a key role in delivering high-quality products that improve patient lives worldwide. The Role As a Package Operator, you will be responsible for the efficient and compliant operation of packaging equipment, ensuring products are packaged to the highest quality standards. This is a hands-on role in a fast-paced GMP-regulated environment, offering the opportunity to develop your skills within a global pharmaceutical organisation. Key Responsibilities • Operate, monitor, and maintain packaging equipment in line with SOPs and GMP requirements., • Carry out line clearance, changeovers, and equipment cleaning to ensure smooth production flow., • Complete accurate documentation of all packaging activities., • Support quality checks to ensure compliance with company and regulatory standards., • Contribute to a safe and clean working environment, reporting any issues promptly., • Collaborate with colleagues across Production and Quality to meet output targets. Requirements • Previous experience in pharmaceutical, biotech, or FMCG packaging operations preferred (training will be provided)., • Understanding of GMP and health & safety standards (advantageous)., • Strong attention to detail and ability to follow procedures precisely., • Good communication and teamwork skills., • Flexibility to work shifts if required. What We Offer • Competitive salary and benefits package., • Training and career development opportunities within a global organisation., • A supportive, collaborative, and safety-focused workplace., • The chance to contribute to life-changing medicines. How to Apply If you are looking to take the next step in your career with a company that makes a real difference in global healthcare, we’d love to hear from you. Please submit your CV and a short cover letter via the application link. About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

View more categories View less categories Sector Advisory Tax ,Corporate Tax ,Compliance ,Direct Tax ,Mixed Tax ,Personal Tax Role Flexible hours ,Manager ,Semi Senior ,Tax Senior ,Full-time ,Permanent Contract Type Permanent. Mixed Tax or Personal Tax Senior- Stoke on Trent. As Tax Senior, you will

Ethics and Compliance Analyst, Ethics and Compliance Analyst. Senior Compliance Officer - 12 Months Fixed Term Contract. Senior Compliance Officer - 12 Months Fixed Term Contract.

We are looking for a Property Compliance Officer to assist our Compliance Assurance team with responsibility for keeping our customers and employees safe through delivering effective administration of all statutory, compliance and similar servicing contracts and by actively coordinating the relation

Asset Compliance Contracts Manager – Lifts. As our Asset Compliance Contracts Manager (Lifts), you’ll take the lead on making sure every one of our lift systems is fully compliant, reliable, and well looked after. Contract: Full-time, Permanent.

Get notified about new Corporate Tax Manager jobs in.Senior Tax Manager - Private Credit (Up to $250K base).Tax Manager - REMOTE(must be based in AZ) - $150k-175k DOE.Senior Director, Tax – Indirect (Specialty Tax Operations).Manager, Global Reporting and Strategic Tax Initiatives.Tax Manager - RE

We are looking for a bright, motivated associate with a keen interest in financial services regulation to join the Compliance Advisory Team in London on a short-term contract. Compliance Associate (6 Month Contract). You will be supported by an experienced team and will collaborate with Marketing, S