Smart4Sciences

QC Section Leader- Pharmaceuticals I am currently recruiting for a QC Section Leader for a Sterile Manufacturing organisation based in North Wales, this is an exciting opportunity for an established leader within QC to progress their career. Key responsibilities for the QC Section Leader- Pharmaceuticals Lead and Supervise the QC Team ensuring deadlines are met within cGMP standards. Review any CAPAs, Change Controls and Deviations prior to QA approval. Write, review and develop internal SOPs for the most efficient process. Support method development, method validation and any equipment qualification. Lead batch release within the QC department. Requirements for the QC Section Leader- Pharmaceuticals Bachelor's degree in a Scientific discipline. Good understanding of GMP. 5 years working within QC with Leadership. Benefits for the QC Section Leader- Pharmaceuticals 25 holidays per year + Bank Holidays Christmas shutdown. Early finish on a Friday and flexible working hours. To apply for the QC Section Leader- Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on (phone number removed) or email me at

Role: Customer Service Administrator Location: Runcorn Salary: 25,000 - 27,000 (discretionary 8% bonus) An exciting opportunity for a customer service professional to join a well established pharmaceutical manufacturer based in Runcorn. The company have an excellent reputation within the industry and are looking for a Customer Service Administrator to assist the Sales Department, and provide a vital link between customer service and Sales. Benefits: Early finish on a Friday Competitive salary 23 days holiday, plus bank holidays (this increases with length of service) Discretionary bonus - 8% Free parking Cycle to work scheme Key Responsibilities Raise orders, quotations and process them through the internal system Assist customers with any queries that arise and liaise with the appropriate department to help resolve the query. Prepare and attend daily/weekly update meetings Raise invoices and credit notes The successful candidate: Previous experience within a customer service role Excellent communication skills Ability to deal with external stakeholders Good telephone manner Ability to think proactively To apply for the Customer Service Administrator or for more information, please contact Jack Challinor at Smart4Sciecnes on

Regulatory Technologist - Cosmetics - Cheshire Would you like to work as a Regulatory Technologist for a global leader in cosmetics? This is a great opportunity to work for a market leader in cosmetics and personal care. As a Regulatory Technologist, you will have further career progression opportunities as the business is recording year on year growth. You will be working with a dynamic company and trendsetter in the market who have created their own brand. The successful Regulatory Technologist will have the chance to build technical knowledge and a diverse professional network. The role: The regulatory team focuses on ethical consumer trends. Raw materials are reviewed for cruelty free compliance, plastic-free vegan suitability and sustainability Ensuring that processes are followed with documentary evidence supporting the marketing of cosmetics for global markets Working closely with the NPD and Lab teams Communicating with testing houses, raw material suppliers and regulatory bodies. Ideal requirements: Previous cosmetics or relevant regulatory experience Computer literate, knowledge of the MS Office suite. Ability to work independently and as part team in a fast-paced environment Ideal candidates would come from a BSc/MSc Cosmetic Science or a Chemistry background If you are interested in this Cosmetics Regulatory Technologist role please send me a word version of your CV

Role: QA Specialist Location: Manchester (Salford area) An exciting opportunity has become available for a QA Specialist to join a growing pharmaceutical company that specialise in parallel import. The position will be based in the Salford area of Manchester. This would be a great opportunity for an experienced quality professional with one or two years of experience to join a growing team to accelerate progression within their career Job Description, QA Specialist Responsible for Database control within the department Administrative support to Customers and Colleagues Error Recording, execution of CAPAs and QMS compliance Oversee the quality of all manufactured products and ensure adherence to GMP, GDP and documented procedures. Responsibilities of the QA Specialist Promote compliance with GMP and company policies Reviewing Batch Record and GMP release Provide support to ongoing preparation for Regulation License Approval Develop and Enhance the QMS activities involved with the release of the product Documentation writing including reports, non-compliances and deviations Experience Scientific degree or equivalent Product release experience 2 years' experience working within pharma QA Experience of working within a compliance team working on procedures and policies Hands on approach and a can do attitude Benefits Great Career progression Generous company pension Free car parking Holiday entitlement Annual pay review To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

Role: QC Analyst Permanent Location: Morpeth Competitive Salary + Shift allowance An exciting opportunity has become available due to internal growth in the team. We're looking for a QC Analyst with at least one year of experience within the pharmaceutical industry. This role is working shifts and comes with a very generous shift allowance. The Role: QC Analyst Testing of a range of products using wet chemical and instrumental techniques such as TLC, HPLC, FTIR, UV analysis to agreed timescales Generating valid QC testing data in accordance with Company Policy and regulatory compliance to agreed time scales Carrying out routine equipment maintenance and calibration of laboratory equipment following approved methods and procedures on assigned pieces of equipment The successful candidate: Experience within the pharmaceutical industry Relevant Scientific Degree Experience of using techniques such as TLC, HPLC, FTIR or UV Experience writing and reviewing SOPS To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

Job Title: EC&I Technician Full time (shifts) Location: Speke Permanent The Shift EC&I Technician is a multi-skilled role that works as a core member of the site Maintenance Team, providing critical support to operations across site during core and non-core hours. The Shift Technician will be self-directed, making decisions on priorities during breakdown situations, in often time critical high-pressure situations. The role: EC&I Technician Carry out multiskilled, planned and corrective maintenance and repairs to relevant standards. Ensure equipment is available to meet safety and quality standards Use diagnostic tools to identify modes of failure Complete records, work orders, datasheets, equipment logs The successful candidate NVQ level 3 or equivalent in Electrical, Instrument or Control discipline Experience of assisting installation and upgrading of plant equipment to improve reliability and performance Experience of safe working practices Experience of operating and maintaining of process control equipment To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

Job title: Process Safety Engineer Industry: Pharmaceutical Location: Speke The role: Process Safety Engineer Provides safety consultation and direction to the organisation. Specific areas of primary responsibility include technical leadership, direction and consultation for process safety management. Provides safety consultation, direction and support for both new product introduction projects and ongoing manufacturing processes and is responsible for ensuring that the Speke process safety systems remain compliant with external regulatory safety standards and guidelines. Responsibilities Responsible for monitoring and ensuring implementation to ensure site compliance with the COMAH Regulations and site PSM requirements. Support site compliance with local regulations e.g. DSEAR ATEX, Pressure Safety regulations etc Lead communication with external competent authorities in order to ensure optimum compliance with COMAH Regulations and notification of incidents and changes to the Health & Safety Executive. Monitoring and coordinating the implementation of the PSM system and reporting to senior management, ensuring appropriate resources are allocated to PSM activities Developing the process safety business plan and providing leadership for its implementation. Lead/Chair Process Safety Activities as required e.g. PHRs, facility siting, incident investigations, project/change assessments. The successful candidate: Process Safety Engineer Chemical Engineering degree IChem accreditation Experience of providing expertise on site To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

Automation Engineer (Permanent) Pharmaceutical Manufacturing Liverpool 55- 60k Experience in Automation of Delta-V OR Rockwell from Pharmaceutical or a transferable manufacturing facility If you are an Automation Engineer with experience of Delta V or Rockwell operating systems, this could be the challenging next step for you. Pharmaceutical site working through a process of change & transformation. As the Automation Engineer, you will act as Subject Matter Expert and site Administrator for continual improvement projects & optimisation of Delta V & Rockwell operating systems. What you will get in return is a career advancing role with multiple projects & an above average benefits package with training, development and a clear path of progression. Please apply now or contact Simon Fowler at Smart4Sciences

Role: Senior QC Analyst Location: North Wales, Wrexham Full time Salary: Around 30,000 A fantastic opportunity has arisen for Senior QC Analysts to join a sterile manufacturing facility in North Wales. We offer a fantastic package plus benefits such as: 7 % matched pension Discounts on common retail outlets through our rewards platform Generous holidays Salary sacrifice scheme Subsidised canteen Free parking The role: QC Analyst As an Analyst you will: Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verification Support the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis. The successful QC Analyst will have: A relevant science degree or equivalent qualification Understanding of current GMP, Health and Safety and COSHH regulations Experience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervision The ability to take on a limited supervisory role would be an advantage Relevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation To apply for the Senior Quality Control Analyst or here more information, please contact Jack Challinor at Smart4Sciecnes on

Senior Formulation Chemist - Cosmetics - Staffordshire Would you like to work as a Formulation Chemist for a global leader in cosmetics and personal care? This is a great opportunity to work for a market leader in cosmetics and personal care. As a Senior Formulation Chemist, you will have further career progression opportunities as the business is recording year on year growth. You will be working with a dynamic company and trendsetter in the market who have created their own brand. As the senior formulation chemist you will be leading the product development and have plenty of autonomy in your role! Day to day duties will include: Leading the design of advanced cosmetic products Formulating and reformulating a variety of well-known cosmetic products Managing multiple projects from initial concept to launch Drive technical advancements. Researching and evaluating raw materials and ingredients for technical and product enhancements Laboratory Management Trend analysis Requirements: Degree educated within a relevant science discipline. Preferably 5 years plus formulation experience Current or recent cosmetics experience is essential. The ideal candidate would have experience with mascaras, colour cosmetics or SPF Ability to work in a fast-paced environment Able to mentor and manager junior staff If you are interested in joining the market leader as a senior formulation chemist please send me a word version of your CV