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Are you an experienced Mental Health Nurse wanting to work in an environment where kindness and teamwork is integral? Where you'll be invested in, with opportunities to develop and grow your career to achieve your goals? Then join the team at. As an experienced Mental Health Nurse from the NHS or pr

Contract: PermanentSalary: Offering base salary up to £45,000 per annum, plus standby & overtime opportunity. increasing earning by a potential £8,000 - £10,000.We have an exciting opportunity for a career-minded person to join our Mill Green (Hatfield) team as an Electrical and Mechanical Technician. Focused mainly on electrical maintenance, you will be required to perform a range of assigned front-line maintenance/operational activities on our sewage pumping stations in the Hertfordshire area. Working in multi-disciplinary teams that are responsible for carrying out scheduled, unscheduled and emergency maintenance work on mechanical and electrical equipment. This is an excellent opportunity to make a real difference to Thames Water's environmental impact, and you will be actively helping to reduce pollution from our sites and networks. What you’ll be doing as an Electrical and Mechanical Technician • Investigate plant failures and perform repairs as quickly and efficiently as possible to avoid interruptions to the process. This may involve investigating and diagnosing complex faults and performing repairs during incidents., • Installing, modifying, and commissioning new plant equipment and diagnosing and repairing faults in systems and plants., • Provide technical advice, refer to up-to-date technical knowledge, and provide training or support for technical trainees if required., • Examples of equipment that you will be working on include motors, gearboxes, screw /chain conveyors & centrifuges, various pumps, and associated control gear, 3-phase motors, starters and controls, electronic control systems such as VSD, automatic valves, flow, level and pressure measurement, variable speed drives and controls, chemical handling, and dosing equipment., • You should be a time-served apprentice with significant experience in mechanical/electrical systems or with NVQ or C&G level 3 in mechanical/electrical engineering., • A problem solver, able to identify potential issues and implement solutions, or escalate if required., • An excellent communicator, providing technical expertise to Internal and External staff and contractors., • Resilient, adapting to the pressures of work and working in a constantly changing environment., • Ability to work with minimum supervision, under own initiative, to design and meet standards., • Knowledge and awareness of Health and Safety issues relevant to the industry., • Team player who can work in many different teams, showing respect for others, providing helpful feedback and supporting the development of others., • IT literate., • Be a self-motivated individual who can immerse themselves into the team around them, you need to be very disciplined, have the desire to learn from those around you and have a can-do attitude. This role can be demanding at times, but very rewarding too., • Take Ownership of responding quickly to faults, being curious to understand the problem fully, and identifying the best solution to resolve it the first time., • Have excellent communication and interpersonal skills to interact with the team., • Teamwork – We are one team, and our end goals are the same., • Proactive – take the lead on recommendations and improvements around the site and communicate effectively., • Must be prepared to be trained in safety procedures., • Offering base salary up to £45,000 per annum, plus standby & overtime opportunity. increasing earning by a potential £8,000 - £10,000. Increasing earnings by a potential £8,000 - £10,000., • A company van, all PPE and tools are provided., • 24 days holiday per year, increasing to 28 with the length of service. (Plus

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.

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 an Associate Director / Director Safety Scientist to join their team. Hybrid - Office 8 times in a month Your new role As a highly motivated individual, you will support early and late phase development activities as a member of the safety team, providing essential safety oversight and input into all aspects of study management across the entire development and marketed portfolio. In the post-market setting, this may include signal evaluation, safety-related activities associated with new drug applications/regulatory filings, benefit-risk assessment and safety risk management • Develop and maintain an understanding of the safety profile of their assigned product(s) or therapy areas, • Responsible for individual and aggregate case reporting activities including ICSR case management (medical review) and aggregate reporting (i.e. DSUR, PBRER), • Responsible for signal detection and management activities and contributing to the strategy and review of safety assessments and drug safety reports for signals or issues (inc, product quality) or in response to Regulatory Authority requests, • Contributing to risk management activities including preparation and maintenance of CCDS, labeling document maintenance, risk communications, RMP, REMS, • Contributing to study management from a safety perspective through SMT/PET and document review and maintenance across the development continuum (early phase to post-marketing studies), including PASS, • Contribute to regulatory authority submissions (Investigational New Drug/IND applications, New Drug Applications/NDAs, Marketing Authorisation Applications/MAAs, Variations, Renewals, etc.) by reviewing safety data and preparing relevant sections of the filing and submission packages in consultation with the team, • Establish and maintain collaborative working relationships with all key stakeholders, and internal and external customers and ensure the same across relevant teams, • Consistently comply with all governing laws, regulations, standard operating procedures (SOPs) and other guidelines What you'll need to succeed Primary life sciences degree and relevant postgraduate degree preferred Proven drug safety, clinical development experience in the pharmaceutical industry, ideally as a Safety Scientist - including signal evaluation, safety-related activities associated with new drug applications/regulatory filings, benefit-risk assessment, safety risk management and aggregate report writing. Understanding of GxP and regulated processes and end-to-end clinical trial lifecycleStrong orientation towards process improvement and cross-functional teamwork Excellent communication skills, both written and verbal Perform data analysis / statistical methods to evaluate, interpret and present scientific data with clarity Good presentation skills, effective at summarising and presenting the key considerations and decision points Understanding of project management methodology What you need to do now Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and residing in the UK. 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

You'll work with your team to drive sales, exceed targets, and host memorable in-store events. Support sales targets through creative promotion and teamwork.

Duties as a KS2 Teaching Assistant:. Strong communication and teamwork skills as a KS2 Teaching Assistant. Upon registration, candidates undergo enhanced DBS checks, full reference verifications, and eligibility confirmations.

Strong communication and teamwork skills as a KS2 Teaching Assistant. Duties as a KS2 Teaching Assistant:. Assist with classroom preparation, displays, and general administrative tasks.

You'll be part of a collaborative and forward-thinking environment that values scientific excellence and cross-functional teamwork. This role requires some time on site (potentially up to 2 days per week though this is flexible for the right person) and all candidates must already hold the right to