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Role: Senior QC AnalystSalary: Circa £35,000 (Negotiable)Monday - FridayLocation: Chester areaThe role: Carry out Analytical testing using a... Read more

Role: Senior QC AnalystSalary: Circa £35,000 (Negotiable)Monday - FridayLocation: Chester areaThe role: Carry out Analytical testing using a range of techniques such as UV, HPLC and GCCoaching/Mentoring junior members of the teamSupport management with timetabling analytical dutiesReporting any issues into Management The candidate: Degree in scientific disciplineUnderstanding and previous experience of working in a GMP EnvironmentExperienced in analytical techniques such as HPLC, GC, EVThe ability to lead a team If you would like to apply for this position or require further information, please email a copy of your CV to Jack Challinor on Read less

Smart4Sciences are currently working with a Pharmaceutical Company in the north of England to recruit a Qualified Person... Read more

Smart4Sciences are currently working with a Pharmaceutical Company in the north of England to recruit a Qualified Person responsible for sign off and release of finished Pharmaceutical productsAs a QP you will be responsible for reviewing and evaluating batch records and performing batch certification and release of solid-dose products in accordance with GMP and the Human Medicines Regulations. Key ResponsibilitiesPerforming QP batch certification of licensed medicines (per applicable regulations) and providing QP support as required for Quality issues.To act as 'Qualified Person' in approving Finished Product for release onto the marketplace.Verify and ensure that the products are manufactured, packed and tested to the requirements of registered MA.Responsible as named QP on the site MIA. To coordinate the preparation and hosting of MHRA and customer inspections.Key RequirementsEligible to act as Qualified person in UK. Strong understanding of small molecule manufacturing with direct experience in solid oral dosage forms.Extensive Pharmaceutical Industry with hands on experience in development/quality in a GxP environment. Knowledge and understanding of drug development process and the Global Regulatory Requirements and regulations related to GxP.Excellent working knowledge of EU GMPs, especially in the interpretation of requirements and guidance for the development, manufacture, control, and distribution of commercial product.This Qualified Person vacancy is an urgent requirement with interviews happening now - if you would be interested please apply today Read less

Formulation/Development Lead - Pharmaceuticals - North London Smart4Sciences are currently recruiting for a Formulation/Development Lead who will be... Read more

Formulation/Development Lead - Pharmaceuticals - North London Smart4Sciences are currently recruiting for a Formulation/Development Lead who will be responsible for working with one of North London's leading CDMOs of pharmaceutical products and lead all NPI and Tech Transfer activity.This Formulation/Development Lead position is a brand new role that has been created due to increased business and is a brilliant opportunity for a Scientist with a strong background in Formulation/Process Development to take a leading role in future projects within the companyKey responsibilitiesLead all Formulation/Development activities, working with clients and customers from the outset to interpret requirements and ensure projects are delivered on time and in a cost effective manner.Formulate Lab batches and Scale-Up to commercial manufacturingTroubleshoot issues found in the Formulation and Scale-Up processesRequirementsBSc or equivalent in a relevant subject matter ( Chemistry, Pharmaceutical Science etc)A strong background in Pharmaceutical Formulation, ideally within a CDMO environment with solid, semi-solid and liquid dose productsStrong written and verbal communication skillsInterviews for this Formulation/Development Lead position are happening now so please apply today or contact Gareth Gooley@ Smart4Sciences for more info Read less

QC Analyst - Pharmaceuticals Smart4Sciences are currently recruiting for a QC Analyst based in North London, working with... Read more

QC Analyst - Pharmaceuticals Smart4Sciences are currently recruiting for a QC Analyst based in North London, working with one of North London's leading contract manufacturers of pharmaceutical products. This QC Analyst position is a great opportunity for a candidate with GMP experience to further develop their career and gain experience with QA activities and non-routine analysis Key responsibilitiesRoutine testing on finished products, via HPLC, GC, FTIR, UV-vis and Wet ChemistryAssist with continuous improvement and work with the QC Team Leader/Manager to implement this.Write technical/scientific reports.Assist with analytical testing for the NPD team and provide input how to improve this.Leadership within the laboratory for the analyst within the team.Assist with CAPAs and Deviations (When required) RequirementsBSc or equivalent in a relevant subject matter ( Chemistry, Pharmaceutical Science etc)Prior experience in Pharmaceutical QCStrong written and verbal communication skills. Interviews for this QC Analyst position are imminent so please apply today or contact Gareth Gooley at Smart4Sciences for more information Read less

Role: Quality Assurance Officer Location: WirralSalary: £35,000 (negotiable) An exciting opportunity has become available for a QA Specialist... Read more

Role: Quality Assurance Officer Location: WirralSalary: £35,000 (negotiable) An exciting opportunity has become available for a QA Specialist to join a growing pharmaceutical company that specialise in pharmaceutical manufacturing. The position will be based on the Wirral. 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, Quality Assurance Officer Conduct regular audits and inspectionsAssist in training staff on quality standards and best practicesError Recording, execution of CAPAs and QMS complianceOversee the quality of all manufactured products and ensure adherence to GMP, GDP and documented procedures. Responsibilities of the Quality Assurance Officer Promote compliance with GMP and company policiesReviewing Batch Record and GMP releaseProvide support to ongoing preparation for Regulation License ApprovalDevelop and Enhance the QMS activities involved with the release of the productDocumentation writing including reports, non-compliances and deviations Experience Scientific degree or equivalentProduct release experience2 years' experience working within pharma QAExperience of working within a compliance team working on procedures and policiesHands on approach and a can do attitude Benefits Great Career progressionGenerous company pensionFree car parkingHoliday entitlementAnnual pay review To apply for the Quality Assurance Officer or here more information, please contact Jack Challinor at Smart4Sciecnes on Read less

Quality Engineer Location: AltonSalary: £35,000 - £41,000 A fantastic opportunity for a Quality Assurance specialist to join a... Read more

Quality Engineer Location: AltonSalary: £35,000 - £41,000 A fantastic opportunity for a Quality Assurance specialist to join a growing team in the pharmaceutical industry. You'll play a crucial role in maintaining high standards, supporting new product introductions, and ensuring compliance with regulatory expectations.The Role: QMS Internal Audit Programme: Plan, assign, and carry out audits. Ensure timely production and sign-off of audit reports and log corrective actions.Support Operations Team: Investigate internal non-conformities and quality issues. Advise on problem-solving techniques to establish root causes and identify corrective/preventative actions promptly.Change Control Process Management: Oversee and manage the change control process efficiently.Customer Quality Issues and Complaints: Investigate and provide timely responses to customer quality issues and consumer complaints.Deviations Review: Complete deviations in a timely manner and allocate actions to the QC department as necessary.CAPA Monitoring: Ensure proposed actions are relevant and applicable, carry out verifications, and perform effectiveness checks on CAPAs.The successful candidate: Internal Auditor Experience: Essential qualification and experience as an internal auditor.Pharmaceutical Manufacturing background: Highly DesirableQuality Analytical Tools: Proficient in quality analytical/problem-solving tools and techniques gained through practical experience.Multitasking Ability: Capable of handling multiple demands, self-managing, and working under pressure.Technical Knowledge: Demonstrated technical knowledge and transferable skills to gain respect and credibility within the team.Communication Skills: Strong verbal communication and interpersonal skills. Ability to listen, discuss, and advise effectively. If you would like more information or to apply for this role, please contact Jack Challinor at Read less

Role: QC Analyst Location: HullFull timeSalary: Around £30,000 - £32,000A fantastic opportunity has arisen for Senior QC Analysts... Read more

Role: QC Analyst Location: HullFull timeSalary: Around £30,000 - £32,000A fantastic opportunity has arisen for Senior QC Analysts to join a sterile manufacturing facility in Hull. The role: QC Analyst As an Analyst you will:Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verificationSupport 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 qualificationUnderstanding of current GMP, Health and Safety and COSHH regulationsExperience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervisionThe ability to take on a limited supervisory role would be an advantageRelevant 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 Read less

Smart4Sciences - Head of Quality - PharmaceuticalsSmart4Sciences are currently working with a Pharmaceutical Manufacturing company in Hertfordshire to... Read more

Smart4Sciences - Head of Quality - PharmaceuticalsSmart4Sciences are currently working with a Pharmaceutical Manufacturing company in Hertfordshire to recruit an experienced Head of Quality to lead and the develop an experienced Quality team and ensure all products are manufactured inline with GMP and MHRA Regulations.As the Head of Quality you will be part of the SLT; essential in driving the business forward, developing current processes and delivering continuous improvement throughout the Quality function.Key ResponsibilitiesVerify and ensure that all processes and procedures to include effective data management systems, policies, processes and programmes to provide assurances of ongoing statutory, regulatory and MA compliance.As a key member of the SLT escalate any quality issues that are detected during batch review.Host MHRA inspections, writing the responses and liaising with the MHRA Inspectorate.Provide effective oversight of all remediation projects from a quality perspective.Responsible for the review and closure of Deviations, OOS, CAPA and Change controlKey RequirementsBSc or above in a suitable Scientific/Pharmaceutical DisciplineSignificant experience in a Quality Management/Leadership position within the Pharmaceutical IndustryIn-depth working knowledge of EU GMP guidelines and other regulatory requirementAbility to act as a Qualified Person is desirable but not essential.This Head of Quality position is an immediate need to please apply now or contact Gareth Gooley at Smart4Sciences for more information Read less

Role: QA OfficerLocation: WidnesSalary: £30,000 - £32,000 Due to expansion we are looking to build our team! We're... Read more

Role: QA OfficerLocation: WidnesSalary: £30,000 - £32,000 Due to expansion we are looking to build our team! We're expanding our team and need to recruit a QA Officer for our team based in Widnes. The role: Reviewing Batch records and creating the associated checklists to support batch certificationArchiving GMP critical documents in line with company policyEnsuring current versions of controlled documents are available to site personnelAssist in AuditsProactively identifying risks within the QMS and supporting the development of action plans to address and drive continuous improvementTo foster collaborative working with sister departments across the globeTo perform out of specification / out of trend investigations The successful candidate: At least 2 years of experience in a similar QA roleExperience or knowledge of the pharmaceutical industryRelevant scientific degreeAbility to prioritise work If you would like more information or to apply please contact Jack Challinor at Read less

Role: Engineering TechnicianShifts: Monday - Friday 6am-2pm and 1:30pm - 9:30pmSalary: Starting at £39,924 rising to £44,364 following... Read more

Role: Engineering TechnicianShifts: Monday - Friday 6am-2pm and 1:30pm - 9:30pmSalary: Starting at £39,924 rising to £44,364 following successful training periodLocation: Deeside We're looking to expand our team! We need an Engineering Technician with experience within Sterile Products to help support our Deeside team. The role:Operate in accordance with current engineering procedures and compliance with cGMP and all applicable UK lawsSize and component changeovers on washing, filling and sealing machines for vial and ampoule parenteral product productionDay to day maintenance on washing, filling and sealing machines for amps and vial parenteral product production in compliance with cGMPScheduled Preventative Maintenance and reliability on washing, filling and sealing machines for amps and vials for parenteral productPrevent engineering issues by pro-actively managing the lines to maximise line running and reduce line set up and changeover times.The successful candidate:Recognised Engineering Apprenticeship (Multi-Skilled would be an advantage)The ability to work alone or as part of a team and have excellent fault finding, rectification and communication skillsWill require an intimate understanding of pharmaceutical engineering, pharmaceutical industry standards and regulatory expectationsRelevant experience of working in Grade A, B and C Pharmaceutical environment is essential.Has practical experience in reliability engineering and various reliability strategies. If you would like further information or to apply, please contact Jack Challinor on Read less