My client is looking for an experienced Synthetic Organic Chemist to join their production team. Previous experience working... Read more
My client is looking for an experienced Synthetic Organic Chemist to join their production team. Previous experience working with large-scale reactors is highly desirable for this role. If you don't meet every requirement I strongly recommend you still apply - especially if you meet several of the Advanced Experience targets.
Responsibilities
Equipment experience desired
Distillation UnitsPilot-Scale and Production-Scale ReactorsGas Chromatography (GC)High Performance Liquid Chromatography (HPLC)Fourier Transform Infrared Spectroscopy (FTIR)Karl Fischer (KF)Skills
Process development and scale-upDistillationTechnical troubleshooting and problem solvingStrong understanding of chemical process safetyAbility to work effectively in a busy manufacturing environmentStrong organisational and time management skillsHigh attention to detail and documentation standardsProficiency with Microsoft Office, particularly Excel and WordAbility to work flexibly under changing priorities and deliver results in a timely mannerDemonstrated Experience
Successfully supported the scale-up of chemical processes from laboratory or pilot scale into manufacturing environmentsOperated distillation units and process equipment safely and effectively within a chemical production settingWorked with hazardous chemicals while maintaining high safety and compliance standardsContributed to the manufacture, optimisation, or development of fine chemicals, speciality chemicals, pharmaceutical intermediates, or related productsOrganometallic chemistry experience would be advantageousApplied scientific and technical expertise to resolve production, process, or quality-related issuesMaintained accurate technical records, batch documentation, and quality system requirementsWorked collaboratively with different functions to achieve project and operational objectivesDemonstrated the ability to manage multiple priorities and deliver results in a timely mannerAdvanced Experience
Led or played a significant role in process development, optimisation, or technology transfer projects that resulted in improved manufacturing performanceDemonstrated expertise in organic chemistry within industrial manufacturing environmentsExperience operating or scaling processes using production-scale reactors (typically 5L+ and above)Resolved complex process, yield, quality, or operational issues through structured troubleshooting and root cause analysisContributed to the safe introduction of new processes, products, or manufacturing technologies into productionSupported continuous improvement initiatives that improved efficiency, quality, throughput, or process robustnessOperated within fine chemical, speciality chemical, or pharmaceutical manufacturing environments and demonstrated an understanding of the associated technical and regulatory challengesApplied analytical techniques such as GC, HPLC, FTIR, KF, and titrations to support process development, manufacturing, or troubleshooting activitiesProvided technical leadership, mentoring, or specialist expertise to colleagues and cross-functional teamsHolds a PhD, MChem, or equivalent advanced background in Chemistry, with demonstrated application of organic chemistry principles in an industrial settingRead less
Operations Manager - PharmaceuticalsI am currently recruiting for an Operations Manager to work within the pharmaceutical industry, for... Read more
Operations Manager - Pharmaceuticals
I am currently recruiting for an Operations Manager to work within the pharmaceutical industry, for a niche, yet established product, this is a great opportunity for a Production Manager to work standard hours and develop their skillset and work with an expanding business in the Nottinghamshire area
Key responsibilities for the Operations Manager - Pharmaceuticals
Lead the day-to-day operations of the manufacturing facility, ensuring production targets, quality standards, and customer commitments are consistently achieved.Drive a strong culture of safety, quality, compliance, and continuous improvement across all operational areas.Develop and implement operational strategies to improve efficiency, productivity, and overall equipment effectiveness (OEE).Ensure all manufacturing activities comply with GMP, regulatory requirements, and company quality standards.Lead, mentor, and develop cross-functional teams, fostering a high-performance and collaborative culture.Manage operational budgets, resource planning, and cost control initiatives to achieve business objectives.Work closely with Engineering, Quality, Supply Chain, Validation, and Maintenance teams to optimise manufacturingRequirements for the Operations Manager - Pharmaceuticals
Degree qualified in Engineering, Science, Pharmacy, Manufacturing, Operations Management, or a related discipline.Proven experience in an Operations Manager, Manufacturing Manager, or Senior Production Manager role within the pharmaceutical, biotechnology, or other highly regulated manufacturing industry.Strong knowledge of GMP, pharmaceutical regulations, and quality management systems.Strong communication and stakeholder management abilities with the confidence to influence at all levels of the organisation.
Benefits for the Operations Manager - Pharmaceuticals
Good career development.Free ParkingDesirable locationCompetitive salary
To apply for the Operations Manager - Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email .
Read lessCapital Project Engineering Manager - PharmaceuticalsI am currently recruiting for a Capital Project Engineering Manager for a leading... Read more
Capital Project Engineering Manager - Pharmaceuticals
I am currently recruiting for a Capital Project Engineering Manager for a leading pharmaceutical manufacturer based in the Yorkshire area. This will be a great opportunity for someone who has experience with capital projects, with a strong engineering background.
Key responsibilities for the Capital Project Engineering Manager - Pharmaceuticals
Lead the planning, execution, and delivery of capital engineering projects from concept through to commissioning and handover.Manage CAPEX budgets, project schedules, resources, and contractor performance to ensure successful project delivery.Develop project scopes, engineering specifications, tender documentation, and business cases.Oversee equipment procurement, installation, commissioning, qualification, and validation activities.Ensure all engineering projects comply with GMP, EHS, and pharmaceutical regulatory standards.Lead multidisciplinary teams, including Engineering, Production, Quality, Validation, Maintenance, and external contractors.Identify project risks and implement mitigation strategies to ensure successful outcomes.Drive continuous improvement initiatives, incorporating innovative engineering solutions and best practices.Provide regular project updates to senior stakeholders, ensuring effective communication throughout the project lifecycle.Support site master planning, asset management, and long-term capital investment strategies.
Requirements for the Capital Project Engineering Manager - Pharmaceuticals
Degree qualified in Mechanical, Electrical, Chemical, Process, or Industrial Engineering (or equivalent).Significant experience managing capital projects within the pharmaceutical, biotechnology, or other highly regulated manufacturing industries.Proven experience delivering complex CAPEX projects from concept through completion.Strong understanding of GMP, pharmaceutical regulations, and engineering compliance.Experience managing multidisciplinary teams, engineering contractors, and external suppliers.Excellent project management, financial, and stakeholder management skills.Benefits for the Capital Project Engineering Manager - Pharmaceuticals
Good career development.Impacting life changing pharmaceutical manufacturing.Competitive salary
To apply for the Capital Project Engineering Manager - Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email .
Read lessSenior Automation Engineer - PharmaceuticalsI am currently recruiting for a Senior Automation Engineer for a leading pharmaceutical manufacturer... Read more
Senior Automation Engineer - Pharmaceuticals
I am currently recruiting for a Senior Automation Engineer for a leading pharmaceutical manufacturer based in the Yorkshire area. This will be a great opportunity for someone who has experience working on various SCADA, Simens, PLCs and DCS systems for a pharmaceutical manufacturer.
Key responsibilities for the Senior Automation Engineer - Pharmaceuticals
Lead the design, development, implementation, and optimisation of automation and control systems across manufacturing operations.Provide technical expertise for PLC, SCADA, HMI, and DCS systems, ensuring optimal system performance and reliability.Collaborate with internal department such as, Production, Engineering, Validation, Quality, and IT teams on continuous improvement initiatives.Troubleshoot automation and control system issues, implementing effective solutions to minimise production downtime.Manage external vendors and contractors to ensure successful project delivery.Support the delivery of capital projects, including system design, commissioning, qualification, and validation.Support and lead the junior automation Engineer for operational excellence within the team.Requirements for the Senior Automation Engineer - Pharmaceuticals
Degree qualified in Automation, Electrical, Electronic or Controls Engineering or equivalent qualification.Strong knowledge of PLC programming (Siemens, Allen-Bradley, or similar), SCADA, HMI, and DCS platformsStrong communication and stakeholder management abilities.Experience with delivering automation projects from concept through to implementation.Benefits for the Senior Automation Engineer - Pharmaceuticals
Good career development.Impacting life changing pharmaceutical manufacturing.Competitive salary
To apply for the Senior Automation Engineer - Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email .
Read less
ResponsibilitiesPerform quality control testing of raw materials, intermediates, and finished products using a range of analytical techniquesDocument and... Read more
Read less
Junior Regulatory Coordinator Location: West YorkshireSalary: £28,000 - £30,000 + BenefitsOur client is seeking a Junior Regulatory Affairs... Read more
Junior Regulatory Coordinator
Location: West Yorkshire
Salary: £28,000 - £30,000 + Benefits
Our client is seeking a Junior Regulatory Affairs Administrator to join their Technical team based in Bradford.
This is an excellent opportunity for an organised and detail-focused individual looking to develop a career within Regulatory Affairs. Working alongside an experienced Regulatory professional, you will receive full training and support whilst gaining exposure to a broad range of UK, EU and international compliance requirements.
This is a predominantly desk-based role and would suit someone who enjoys working with data, systems and technical information whilst supporting the wider business on regulatory and compliance matters.
Key Responsibilities
Support regulatory and compliance activities across a range of products and packaging formats.Collect, maintain and process technical and regulatory data to ensure compliance with relevant legislation.Assist with the management and maintenance of product and packaging information.Maintain internal databases and ensure information remains accurate, current and readily accessible.Support the preparation and completion of compliance documentation for customers and external stakeholders.Assist with the completion of technical questionnaires and customer information requests.Monitor and maintain regulatory records and documentation.Support the wider business by communicating updates relating to regulatory requirements.
About You
We are looking for someone who is:
Highly organised with exceptional attention to detail.Confident using Microsoft Excel and other IT systems.Comfortable working with large volumes of data and technical information.Able to prioritise workloads and manage multiple tasks effectively.A strong communicator with excellent administrative skills.Keen to learn and develop within a regulatory and compliance environment.
Experience & Qualifications
A degree in Chemistry, Environmental Science, Regulatory Affairs or another scientific discipline would be advantageous.Previous experience within a regulatory, compliance, technical administration or similar office-based environment is desirable.Recent graduates with strong organisational and IT skills are encouraged to apply.Experience within manufacturing, chemicals, FMCG or another regulated industry would be beneficial but is not essential.
What's on Offer?
Salary of £28,000 - £30,000 depending on experience.Company pension scheme.24 days annual leave.Optional private medical insurance.Genuine progression opportunities within Regulatory Affairs.The opportunity to learn from an experienced regulatory professional.Flexible working arrangements may be considered for the right candidate.
This is an exciting opportunity to join a successful and growing organisation and develop a long-term career within Regulatory Affairs and Compliance.
To apply, please submit your CV for immediate consideration.
Read lessNPD / Project Manager - Household - Worcestershire | Site-BasedA growing manufacturing business within the FMCG and consumer... Read more
NPD / Project Manager - Household - Worcestershire | Site-Based
A growing manufacturing business within the FMCG and consumer chemicals sector is looking to appoint an experienced NPD / Project Manager to support ongoing product innovation and development activity across its expanding product portfolio.
Working closely with the Technical Director, you'll play a key role in driving projects from concept through to commercial launch, ensuring products are delivered efficiently, compliantly, and to the highest standards. The role also offers the opportunity to lead and develop a small technical team while collaborating with departments across the wider business.
This position would suit someone who enjoys a varied and hands-on environment where no two projects are the same and where strong organisation, technical understanding, and stakeholder management are essential.
The Opportunity
* Manage the full lifecycle of new product development projects from brief through to launch
* Coordinate activity across technical, manufacturing, procurement, quality, packaging, and commercial teams
* Support formulation updates, product enhancements, and cost-saving initiatives
* Oversee manufacturing trials, pilot batches, and first production runs to ensure smooth scale-up activity
* Maintain compliance with relevant industry legislation and internal quality standards
* Ensure technical records, specifications, and supporting documentation are accurately maintained
* Identify opportunities for continuous improvement across products, processes, and operational practices
* Provide guidance and support to junior members of the development team
What We're Looking For
* Experience gained within FMCG, household products, cosmetics, detergents, chemicals, or a similar manufacturing environment
* Previous involvement in product development, technical projects, or formulation-led activities
* Strong ability to manage workloads, deadlines, and multiple stakeholders effectively
* Understanding of relevant regulations and compliance requirements including REACH, CLP, COSHH, and associated industry standards
* Confident communication skills with a proactive and solutions-focused approach
* Comfortable working within a fast-moving manufacturing setting where priorities can change quickly
* Knowledge of product trials, manufacturing processes, or commercialisation activities would be advantageous
Why Apply?
* Join a business continuing to invest in innovation and product development
* Work closely with senior leadership and contribute to key strategic projects
* Opportunity to make a visible impact within a collaborative and supportive team environment
* Genuine scope for involvement in continuous improvement and future product direction
Benefits
* Bupa EAP
* Death in Service cover from day one
* Digital health and wellbeing services
* Cycle to Work scheme
* Quarterly attendance bonus
* Internal incentive schemes
For more information or to apply, please send your CV to Rick Metcalfe @Smart4 Sciences.
Read lessAutomation & CSV Engineer (Permanent) - West YorkshirePharmaceutical Manufacturing | High-Tech GMP Environment | Career Growth OpportunityAn exciting... Read more
Automation & CSV Engineer (Permanent) - West Yorkshire
Pharmaceutical Manufacturing | High-Tech GMP Environment | Career Growth Opportunity
An exciting opportunity is available for an Automation & Computer System Validation (CSV) Engineer to join a highly regulated manufacturing environment within the pharmaceutical/life sciences sector.
This role is ideal for an engineer who enjoys working at the intersection of automation, validation, digital systems, and manufacturing operations. You'll play a key role in supporting critical production systems, driving continuous improvement initiatives, and ensuring compliance across computerized and automated processes.
Key Responsibilities
Support and maintain automation and control systems across manufacturing operationsTroubleshoot equipment and process-related automation issuesParticipate in computerized system validation (CSV) activities within a GMP-regulated environmentAssist with qualification, commissioning, and lifecycle management of automated systemsSupport continuous improvement and process optimization projectsCollaborate with engineering, production, quality, and external vendorsMaintain technical and validation documentation in line with regulatory expectationsContribute to data integrity and compliance initiativesProvide technical support and training to operational teamsIdeal Background
Degree qualified in Automation, Electrical, Electronics, Mechatronics, or related Engineering disciplineExperience working with PLC, HMI, SCADA, or industrial control systemsExposure to regulated industries such as pharmaceuticals, biotech, medical devices, or food manufacturing preferredUnderstanding of GMP and computerized system validation principlesStrong troubleshooting and problem-solving skillsAbility to work both independently and within cross-functional teamsExcellent communication and technical documentation abilitiesDesirable Experience
PLC/SCADA programming or supportSystem integration projectsEquipment qualification or validation activitiesKnowledge of data integrity and regulatory compliance requirementsExperience supporting utilities, manufacturing systems, or process equipmentWhat's on Offer
Opportunity to work in a modern, highly automated manufacturing environmentExposure to cutting-edge pharmaceutical technologiesCareer progression within engineering and digital manufacturingCollaborative and technically focused cultureCompetitive salary and benefits packagThis is an excellent opportunity for an ambitious engineer looking to develop within a fast-paced and growing technical operations environment.
For a confidential discussion or to learn more, please contact Simon Fowler on
+44 (0)1925 239 725 or
Read lessLaboratory Manager - Fragrance Development - East SussexWe are seeking an experienced Laboratory Manager to lead the development... Read more
Laboratory Manager - Fragrance Development - East Sussex
We are seeking an experienced Laboratory Manager to lead the development of fragrance products in a dynamic and results-driven environment. This is an exciting opportunity for a proven leader who has successfully implemented change and managed large teams, delivering measurable results in previous roles.
Key Responsibilities:
Key Skills & Experience:
Proven leadership experience in a technical management or product development role, with a strong track record of managing large teams and driving change.3-5 plus years of relevant experience in the fragrance or consumer products industry, with a deep understanding of fragrance composition and its application in consumer goods.In-depth knowledge of sustainability practices and trends within the fragrance industry, with a focus on practical application in product development.Strong experience in sensory evaluation methodologies and consumer testing, with a keen eye for delivering products that resonate with target audiences.A degree in Chemistry (Bachelor's or Master's), or a related field, would be an advantage.If you are an experienced leader, ideally in fragrance development with a proven ability to manage teams and implement successful changes, we'd love to hear from you. Please submit your CV along with a cover letter outlining why you're the right fit for this role.
Contact Rick Metcalfe @smart4 sciences for more information -
Read lessAre you a detail-driven scientist with a passion for analytical testing and pharmaceutical development? Smart4 Sciences are working... Read more
Are you a detail-driven scientist with a passion for analytical testing and pharmaceutical development?
Smart4 Sciences are working with an established and innovative pharmaceutical services provider to recruit a Pharmaceutical Development Analyst into their Pharmaceutical Development team.
The Role
This is an exciting opportunity to carry out high-quality analytical testing for complex pharmaceutical products in a GMP-regulated environment. You'll be an integral part of a specialist team working on product development projects with a focus on respiratory and inhalation drug products.
Key Responsibilities:
Perform experimental testing of pharmaceutical products using validated analytical methods.Prepare and handle solutions, mobile phases, and reagents in line with internal SOPs.Accurately record and analyse data in accordance with GMP and ALCOA+ principles.Use analytical equipment (e.g., HPLC) with appropriate training and calibration.Communicate results clearly with senior scientific staff and cross-functional teams.Maintain an up-to-date training record and follow health & safety protocols at all times.Ensure all work meets regulatory standards including GMP, ICH, and COSHH.
About You
Essential:
A degree in a scientific field such as Chemistry, Pharmaceutical Sciences, or a related discipline.Experience working in a laboratory setting.A strong sense of organisation and attention to detail.Excellent data recording and documentation skills.
Desirable:
Experience with HPLC or similar analytical instrumentation.Knowledge of GMP/GLP standards and pharmaceutical regulatory guidelines.Previous work in respiratory or inhalation product development.
You'll be joining a motivated team and a business that values integrity, innovation, and continuous improvement.
Read less
All your saved jobs are no longer available or you've already applied.
for the following search criteria
