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Packaging Operator - Shifts
Added 15/07/2026
Reference: CP87165_1784131141

Shift Packaging Operator - St. Albans Are you a Packaging Operator looking to take on a new challenge?... Read more

Shift Packaging Operator - St. Albans

Are you a Packaging Operator looking to take on a new challenge? Do you want to join a company with great opportunities for progression? Then this opportunity with a Pharmaceutical manufacturer is looking for you!

Responsibilities:

Carry out packaging operations to meet daily and weekly production targets in line with company objectives and while working across rotating day and night shifts.Load and feed packaging materials into machinery to maintain continuous line operation.Ensure all products are packed in line with quality standards and regulatory requirements.Monitor production processes and promptly replace components or materials as required.

This list is not exhaustive and you will be expected to carry out additional duties where reasonable.

Requirements:

Previous experience working in a manufacturing, production, or packaging environment.Technical or vocational qualification in manufacturing, engineering, or a related field (desirable).Familiarity with GMP or regulated environments (desirable).Experience operating automated or semi-automated machinery and performing quality checks and completing production documentation (desirable).

NB - This is a shift role and requires flexibility according to business needs

If you are interested in having a confidential chat regarding the role please reach out to Chad Petersen at Smart4 Sciences.

Read less
£12.00 - £15.00
Per hour
Hertfordshire
Permanent
Senior QC Analyst
Added 15/07/2026
Reference: JN -042026-86554_1784130267

Smart4 Sciences is partnering with a leading pharmaceutical manufacturer in St Albans to recruit a Senior QC Analyst... Read more

Smart4 Sciences is partnering with a leading pharmaceutical manufacturer in St Albans to recruit a Senior QC Analyst who will play a key role in supporting Quality Control operations and ensuring products are tested to the highest GMP and regulatory standards.

You'll be joining a collaborative QC team where you'll play a key role in ensuring raw materials, in-process samples and finished products meet the highest quality standards while supporting continuous improvement and regulatory compliance.

The Role

Your responsibilities will include:

Performing analytical testing on raw materials, in-process samples and finished productsOperating and troubleshooting HPLC, Karl Fischer Titration, Dissolution and other analytical equipmentCarrying out physical testing of tablets, capsules and packaging materialsPreparing, reviewing and checking analytical data prior to approvalPeer reviewing laboratory documentation and analytical resultsSupporting the review and update of SOPs, specifications and analytical proceduresEnsuring compliance with GMP, Data Integrity and Good Documentation PracticesMaintaining laboratory equipment, reference standards and consumablesSupporting investigations relating to analytical issues and implementing corrective actionsCompleting allocated training and maintaining competency across analytical techniques
What we are looking for :EssentialDegree, Diploma or Certificate in Chemistry, Analytical Science, Medical Laboratory Science or a related scientific disciplinePrevious experience working within a pharmaceutical QC laboratoryHands-on experience with HPLC analysisExperience using a range of laboratory instrumentation and analytical techniquesStrong understanding of GMP, Data Integrity and Good Documentation PracticesExcellent attention to detail and analytical skillsStrong written and verbal communication skillsDesirableExperience with Agilent HPLC systems and OpenLab softwareExperience with Karl Fischer Titration, Dissolution testing and physical testing of pharmaceutical dosage formsExperience reviewing analytical data and laboratory documentationPrevious experience supporting SOP reviews and method improvements

If you're an experienced QC Analyst looking for your next challenge in pharmaceutical manufacturing, we'd love to hear from you.

Read less
£32,000.00
Per annum
Hertfordshire
Permanent
Microbiologist
Added 13/07/2026
Reference: 87145_1783953840

Smart4Sciences is recruiting for a Microbiologist to join a leading pharmaceutical manufacturer in Basildon. This is an excellent... Read more

Smart4Sciences is recruiting for a Microbiologist to join a leading pharmaceutical manufacturer in Basildon. This is an excellent opportunity to join a Quality Control team, taking responsibility for microbiological testing and ensuring compliance with GMP and regulatory requirements.

The RolePerform microbiological testing and accurately analyse and interpret resultsOrganise and support the day-to-day activities of the microbiology laboratoryConduct OOS, out-of-trend investigations, and root cause analysisPrepare microbiology protocols and reports where requiredMaintain laboratory equipment, stock levels, and audit-ready standardsSupport self-inspections, audits, and regulatory inspectionsEnsure all testing activities comply with cGMP, pharmacopoeial requirements, and data integrity standardsAssist with continuous improvement initiatives and KPI reporting The CandidatePrevious microbiology laboratory experience within a pharmaceutical or regulated environmentExperience investigating OOS and out-of-trend resultsStrong understanding of data integrity and GMP requirementsExcellent attention to detail and organisational skillsStrong communication skills and ability to work collaborativelyProficient in Microsoft OfficeDegree in Microbiology, Biology, Pharmacy, or a related Life Science discipline desirableExperience within a pharmaceutical manufacturing environment advantageous

If you're looking to develop your career within pharmaceutical microbiology and join a company committed to quality and compliance, Smart4Sciences would love to hear from you.

Read less
£10,000.00 - £20,000.00
Per annum
Basildon
Permanent
QC Analyst
Added 13/07/2026
Reference: 87144_1783953642

Smart4Sciences is recruiting for a QC Analyst to join a leading pharmaceutical manufacturer in Basildon. This is a... Read more

Smart4Sciences is recruiting for a QC Analyst to join a leading pharmaceutical manufacturer in Basildon. This is a fantastic opportunity to work within a GMP-regulated laboratory, supporting the testing of pharmaceutical products and ensuring compliance with quality standards.

The RolePerform QC testing of raw materials and finished productsPrepare samples, standards, and reagents for analysisMaintain accurate laboratory records in line with GMP and ALCOA+ requirementsOperate and maintain laboratory equipment, including HPLC, GC, pH meters, and titratorsSupport OOS investigations, method validations, and method transfersParticipate in audits, inspections, and continuous improvement activitiesEnsure laboratory housekeeping and compliance standards are maintained at all times The CandidateExperience working in a QC or laboratory environmentKnowledge of analytical testing techniques, including HPLC and GCStrong attention to detail and data accuracyGood communication and organisational skillsProficient in Microsoft OfficeDegree in a Life Science discipline desirableKnowledge of GMP and pharmaceutical quality standards advantageous
If you're looking to develop your career within pharmaceutical quality control, Smart4Sciences would love to hear from you

Read less
£10,000.00 - £20,000.00
Per annum
Basildon
Permanent
Production Manager - Pharmaceuticals
Added 10/07/2026
Reference: LS- PR_1783699482

Production Manager - PharmaceuticalsI am currently recruiting for a Production Manager to work within the pharmaceutical industry, for... Read more

Production Manager - Pharmaceuticals

I am currently recruiting for a Production 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 Production Manager - Pharmaceuticals

Lead and manage day-to-day pharmaceutical manufacturing operations to ensure production schedules are achieved.Drive a culture of safety, quality, compliance, and continuous improvement across the production department.Ensure all manufacturing activities comply with GMP, company procedures, and regulatory requirements.Monitor production KPIs, identify performance trends, and implement improvements to maximise efficiency and reduce waste.Work closely with Engineering, Quality, Validation, Supply Chain, and Maintenance teams to optimise manufacturing performance.Drive Lean Manufacturing and continuous improvement initiatives to enhance operational performance.Manage departmental budgets, staffing levels, and resource planning to meet business objectives.

Requirements for the Production Manager - Pharmaceuticals

Degree qualified in Science, Engineering, Pharmacy, Manufacturing, or a related discipline.Strong knowledge of GMP, regulatory compliance, and pharmaceutical manufacturing processes.Experience in a Production Manager or Manufacturing Manager role within the pharmaceutical, biotechnology, or other highly regulated manufacturing industry.

Benefits for the Production Manager - Pharmaceuticals

Good career development.Free ParkingDesirable locationCompetitive salary

To apply for the Production Manager - Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email .

Read less
£50,000.00 - £80,000.00
Per annum
Nottingham
Permanent
Quality Assurance Officer
Added 10/07/2026
Reference: JN -072026-87146_1783697263

About the jobAre you an experienced Quality Assurance professional looking to take the next step in your career?Smart4... Read more

About the job

Are you an experienced Quality Assurance professional looking to take the next step in your career?

Smart4 Sciences is partnering with a growing pharmaceutical manufacturer in Sandwich, Kent, specialising in the production of Cannabidiol (CBD) Active Pharmaceutical Ingredients (APIs) and industrial hemp derivatives for the pharmaceutical and nutraceutical sectors.

They are looking to recruit a QA Officer who will play a key role in maintaining and continuously improving the company's Quality Management System (QMS).

Working closely with Production, Quality Control and the wider business, you'll ensure products are manufactured and released in accordance with GMP standards while supporting a culture of quality and continuous improvement. This is a varied, hands-on role offering exposure across the full Quality Assurance lifecycle, making it an excellent opportunity for someone looking to broaden their experience within a growing pharmaceutical business.

Key Responsibilities:Maintain and continuously improve the Quality Management System (QMS)Review and approve batch manufacturing documentation prior to batch releaseReview and approve SOPs, controlled documents and quality recordsManage Deviations, CAPAs, Change Controls, Complaints and Out of Specification (OOS) investigationsSupport internal, supplier and regulatory auditsAssist with supplier qualification activities and Quality AgreementsSupport product recalls and quality investigations where requiredMaintain GMP training records and ensure compliance across the businessWork collaboratively with Production, QC and other departments to drive continuous quality improvementsSupport validation activities and lead quality improvement initiatives where appropriateWhat We're Looking For:Minimum of 3 years' experience within a GMP pharmaceutical Quality Assurance environmentStrong understanding of GMP and wider GxP regulationsExperience managing QMS activities including CAPAs, Deviations, Change Controls and batch record reviewExperience supporting internal or supplier auditsStrong investigation, root cause analysis and problem-solving skillsExcellent technical writing and documentation skillsGood working knowledge of Microsoft OfficeStrong organisational skills with the ability to manage multiple prioritiesExcellent communication skills and the confidence to work across multiple departmentsDesirable Experience:Validation activitiesSupplier Quality ManagementTraining and mentoring colleaguesContinuous Improvement projectsExperience supporting regulatory inspectionsPersonal Attributes:Highly organised with excellent attention to detailProactive with a continuous improvement mindsetStrong communicator and collaborative team playerAble to take ownership and work independentlyCommitted to maintaining the highest quality and compliance standards

This is an excellent opportunity to join a growing pharmaceutical manufacturer where you'll gain broad exposure across the full Quality Assurance function, take ownership of key quality systems and contribute directly to the company's continued growth and success. If you're looking for a role where you can make a genuine impact while developing your career, we'd love to hear from you.

Read less
£29,000.00 - £35,000.00
Per annum
Sandwich
Permanent
Production Engineer (Nights)- Pharmaceuticals
Added 10/07/2026
Reference: LS- PR_1783688468

Production Engineer (Nights)- PharmaceuticalsI am currently recruiting for a Production Engineer for a leading pharmaceutical manufacturer based in... Read more

Production Engineer (Nights)- Pharmaceuticals

I am currently recruiting for a Production Engineer for a leading pharmaceutical manufacturer based in the Yorkshire area to work on a night shift. This will be a great opportunity for someone who has experience working for the Engineering department for a pharmaceutical manufacturer looking at different production machines, and lines. Completing shift handover and improving production efficiency.

Key responsibilities for the Production Engineer (Nights)- Pharmaceuticals

Provide day-to-day engineering support to pharmaceutical manufacturing operations.Identify and implement process improvements to increase productivity, efficiency, and product quality.Monitor production performance using KPIs and recommend continuous improvement initiatives.Ensure all engineering/ Production activities comply with GMP, health & safety, and regulatory requirements.Support and implement change control, deviation investigations, and risk assessments where required.

Requirements for the Production Engineer (Nights)- Pharmaceuticals

Relevant engineering qualification2 years minimum experience working within Pharmaceutical Manufacturing/ Production.Knowledge of GMP, regulatory compliance, and engineering/ production best practices.Excellent analytical, problem-solving, and project management skills..

Benefits for the Production Engineer (Nights)- Pharmaceuticals

Good career development.Impacting life changing pharmaceutical manufacturing.Competitive salary

To apply for the Production Engineer (Nights)- Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email .

Read less
£45,000.00 - £46,000.00
Per annum
North Yorkshire
Permanent
HVAC Engineer- Pharmaceuticals
Added 10/07/2026
Reference: LS- H-ENG_1783683698

HVAC Engineer- PharmaceuticalsI am currently recruiting for a HVAC Engineer for a leading pharmaceutical manufacturer based in the... Read more

HVAC Engineer- Pharmaceuticals

I am currently recruiting for a HVAC Engineer for a leading pharmaceutical manufacturer based in the Yorkshire area. This will be a great opportunity for someone who has experience with commonising, preventive and corrective engineering within a pharmaceutical HVAC operation.

Key responsibilities for the HVAC Engineer- Pharmaceuticals

Carry out planned preventative maintenance and reactive maintenance on HVAC and associated building services systems.Assist with HVAC upgrades, capital projects, commissioning, qualification, and validation activities.Ensure all work complies with GMP, health & safety, and pharmaceutical industry standards.Work closely with Production, Facilities, Validation, and Quality teams to ensure uninterrupted manufacturing operations.Work closely with Production, Facilities, Validation, and Quality teams to ensure uninterrupted manufacturing operations.Monitor system performance and recommend energy efficiency and continuous improvement initiatives.

Requirements for the HVAC Engineer- Pharmaceuticals

Relevant engineering qualification in Mechanical Engineering, Building Services, HVAC, or equivalent.2 years minimum experience working within Pharmaceutical Manufacturing.Knowledge of GMP, regulatory compliance, and engineering best practices.Good fault-finding, problem-solving, and communication skills.

Benefits for the HVAC Engineer- Pharmaceuticals

Good career development.Impacting life changing pharmaceutical manufacturing.Competitive salary

To apply for the HVAC Engineer- Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email .

Read less
£40,000.00 - £45,000.00
Per annum
North Yorkshire
Permanent
Project Engineer- Pharmaceuticals
Added 10/07/2026
Reference: LS- PE_1783680082

Project Engineer- PharmaceuticalsI am currently recruiting for a Project Engineer for a leading pharmaceutical manufacture based in the... Read more

Project Engineer- Pharmaceuticals

I am currently recruiting for a Project Engineer for a leading pharmaceutical manufacture based in the Yorkshire area. This will be a great opportunity for someone who has experience with both capital and internal projects, with a strong engineering background.

Key responsibilities for the Project Engineer- Pharmaceuticals

Manage engineering projects from concept through to completion, ensuring delivery on time and within budget.Ensure all projects comply with GMP, health & safety, and regulatory requirements.Oversee equipment installation, commissioning, qualification, and handover.Prepare and maintain project documentation, reports, and technical records.Drive continuous improvement initiatives across manufacturing and engineering operations.

Requirements for the Project Engineer- Pharmaceuticals

Hold a degree of equivalent qualification within Engineering2 years of experience working within Project Engineering for a GMP regulated facility.Experience managing CAPEX projects from design through implementation.Ability to work independently while collaborating effectively with multidisciplinary teams.Strong written and verbal communication skills.

Benefits for the Project Engineer- Pharmaceuticals

Good career development.Impacting life changing pharmaceutical manufacturing.Competitive salary

To apply for the Project Engineer- Pharmaceuticals or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email

Read less
£50,000.00 - £55,000.00
Per annum
North Yorkshire
Permanent
Jnr QC Analyst
Added 07/07/2026
Reference: 87100_1783409379

Smart4Sciences is supporting a leading manufacturing organisation in recruiting a QC Analyst to join their Quality Control team.... Read more

Smart4Sciences is supporting a leading manufacturing organisation in recruiting a QC Analyst to join their Quality Control team. This role offers an excellent opportunity to work within a laboratory environment, carrying out quality control testing to ensure raw materials and finished products meet both company and customer specifications.

The RolePerform quality control testing of raw materials, finished goods, and other samples as requiredPrepare and analyse samples in accordance with established laboratory proceduresSupport the Quality Manager and Quality Control Manager with routine and ad hoc testing activitiesFollow Good Laboratory Practice (GLP), health and safety regulations, and maintain laboratory housekeeping standardsEnsure the correct storage and disposal of retained production and laboratory samplesValidate laboratory instruments in line with company proceduresManage laboratory consumables and solvent stock, carrying out regular stock checks and arranging replenishment where requiredIssue Certificates of Analysis (CoAs) and maintain accurate laboratory records and filing systemsSupport Production, Customer Service, Technical Service, Purchasing, R&D, and Commercial teams through timely and accurate testingIdentify and implement process improvements to enhance laboratory performance and efficiencyUtilise Microsoft Word, Excel, and internal systems including Epicor, BOS, COSHH databases, Torque databases, and email systemsThe CandidateExperience working within a laboratory environmentPrevious experience in a Quality Control roleA Levels or equivalent qualifications in one or more scientific subjectsProficient in Microsoft Word and ExcelStrong attention to detail and commitment to quality standardsAbility to manage workloads effectively and work flexibly to meet business needsExcellent communication skills with the ability to build strong working relationships across departmentsKnowledge of laboratory health and safety practices and quality procedures

If you're looking to develop your career within a quality-focused laboratory environment and contribute to the delivery of high-quality products, Smart4Sciences would love to hear from you.

Read less
£10,000.00 - £20,000.00
Per annum
Greater Manchester
Permanent
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