We believe in building something meaningful together. That means investing in people, supporting each other’s growth, and creating a workplace where every role matters.

Whether you’re just starting your career or looking for a new challenge, there’s a place for you here.

We offer real opportunities, honest support, and the chance to be part of something that improves lives every single day.

- Family owned with a clear vision for the future
- Clear progression and career development opportunities
- UK based end-to-end manufacturing
- Producing products improving people’s quality of life

We believe that great things happen when people feel valued and supported. That’s why we put care into everything, from how we manufacture our products to how we support our team. Every journey at ASPAR is unique, but they all begin with a shared purpose: to do good work, for good people. Meet some of our team.

Our culture is rooted in integrity, care, and a strong sense of family. We support each other, celebrate success together, and create space for people to grow.

Whether you’re an operator on the production floor, in the lab, or part of our office team, you’ll be working in a family environment that values integrity, support and aspires to long-term success shared by our colleagues, customers and communities alike.

Aspar is proud to be a place where people stay, thrive, and build meaningful careers.

Aspar represents integrity and authenticity. Our focus is always on driving quality and delivering on our promise.

We put customers at the heart of everything we do. Our wealth of industry experience will be used to effectively support our customers at all times.

As a UK family business, Aspar is focused on developing long term internal and external relationships.

The Aspar family works together as a team, it learns from each other, it supports each other, it recognises and celebrates successes together.

Be responsible for ensuring Quality Management System (QMS) is robust, compliant, and aligned with regulatory requirements in a pharmaceutical setting The post holder will be responsible for ensuring Quality Management System (QMS) is robust, compliant, and aligned with regulatory requirements. This role supports quality oversight across manufacturing, documentation, supplier management, risk assessment, and regulatory submissions to maintain the highest standards of product quality and regulatory compliance.

This list of responsibilities and requirements is not exhaustive, and the employee may be required to perform other duties in line with requirements and at management’s discretion.

Quality Management System

- Ensure the Quality Management System (QMS) is effectively implemented, maintained, and compliant with required accreditations (e.g., MHRA, ISO standards).
- Perform self-inspections/internal audits at defined intervals and ensure corrective and preventive actions (CAPAs) are implemented.
- Conduct quality walks, prepare observation reports, and review departmental responses.

Documentation &
- Controlled Documents

- Manage controlled documents, including version control and database management.
- Author, review, and update-controlled documents such as SOPs, manufacturing logs, and related QA documents.
- Review specifications, methods, and ensure updates are made effective following approval.
- Manage Master Batch Production Records (BPRs) and Batch Assembly Records (BARs), including amendments and issuance.
- Review BPRs to ensure compliance with registered licenses.

Regulatory &
- Compliance

- Support the regulatory team with the compilation of CTD modules for submission to MHRA.
- Assist in regulatory inspections and external audits.
- Update and maintain product artwork and support regulatory submissions.
- Prepare Product Quality Reviews (PQRs).

Quality Operations
- Raise, assess, and manage deviations, change controls, and CAPAs.
- Generate investigation reports, where applicable.
- Review and approve Bills of Materials (BOMs) and work orders in SAGE.
- Perform risk assessments and gap analyses as needed.

Supplier &
- Vendor Quality

- Perform vendor management activities, including collecting and reviewing quality documents from suppliers.
- Manage and maintain technical/quality agreements.
- Handle supplier complaints and follow through investigations and actions.

KPIs &
- Reporting

- Manage and report monthly Quality KPIs for the organisation.
- Provide quality performance insights and support continuous improvement initiatives.

General Responsibilities
- Ensure full compliance and adherence with all company policies, procedures, guidelines and SOP’s.
- Undertake other duties that are commensurate with the level and responsibilities of the role.

Qualifications

- Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Life Sciences, Quality Management, or a related field

Experience

- Strong knowledge of GMP, GDP, ISO standards, and MHRA/FDA regulatory requirements.
- Experience in a pharmaceutical, medical device, or regulated GMP environment.
- Hands-on experience with QMS operations (change control, deviations, CAPAs, document management and preparing for internal/external regulatory audits.
- Experience with batch documentation (BPR/BAR review) and manufacturing quality oversight.
- Experience with ERP systems such as SAGE (desirable)

Skills

- Excellent attention to detail and accuracy.
- Strong organisational and time management capabilities.
- Good communication skills, both written and verbal.
- Ability to work cross functionally with multiple departments.
- Analytical thinking with strong problem solving skills.
- Ability to manage multiple tasks and work under deadlines.

As a family-run UK pharmaceutical manufacturer, we take pride in the people behind our products. You’ll be joining a team that values integrity, support, and long-term growth. We offer opportunities to develop your career, gain valuable industry experience, and contribute to improving lives through high-quality medicines.

You’ll work in a clean, compliant, and supportive environment with access to ongoing training and clear progression paths in the Quality department and beyond.

Ready to take your next step in pharmaceutical quality control?

Set up and operate manufacturing equipment safely and efficiently within a regulated, environmentally controlled environment, ensuring pharmaceutical products are manufactured to the highest quality standards The Post Holder Will Be Responsible To Set Up And Operate Manufacturing Equipment Safely And Efficiently Within a Regulated, Environmentally Controlled Environment, Ensuring Products Are Manufactured To The Highest Quality Standards In Compliance With CGMP, Health And Safety, And Company Procedures, While Supporting Continuous Improvement.

The Postholder Will Have The Opportunity To Progress Through Grades 1 To 4 Upon:

- Successful completion of all required training
- Demonstrating full understanding of processes and procedures
- Consistently achieving expected performance, quality, and behavioural standards

This list of responsibilities and requirements is not exhaustive, and the employee may be required to perform other duties in line with requirements and at management’s discretion.
- Operate within strictly environmentally controlled areas,



maintaining a high standard of hygiene and strict adherence to current Positive Manufacturing Practice (cGMP), health and safety requirements, and associated documentation.
- Set up and operate automated and semi automated manufacturing equipment in compliance with approved procedures and agreed production programmes.
- Ensure all equipment is used in accordance with maintenance, calibration, and validation requirements.
- Manufacture high quality, high value products right first time, in line with production schedules and quality standards.
- Accurately complete all required documentation in a timely manner.
- Carry out regular cleaning and basic maintenance of all equipment and fabric within the section in accordance with approved schedules.
- Actively support continuous improvement initiatives and contribute to meeting departmental and section objectives.
- Assist in coordinating section activities, liaising with other departments as required, and supporting the organisation of daily work operations.
- Support process and supervisory activities where required.
- Assist with on the job training to ensure designated tasks are performed effectively and compliantly.
- Contribute to the review and revision of Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and associated documentation.
- Report any health and safety concerns or issues that could impact product quality or manufacturing compliance to the Supervisor or Manager.
- Adhere at all times to GMP, health and safety, hygiene, environmental control, and safe working practices.
- Ensure full compliance and adherence with all company policies, procedures, guidelines and SOP’s.
- Undertake other duties that are commensurate with the level and responsibilities of the role.

Qualifications

- Engineering and/or HSE qualifications (desirable)

Experience

- Experience working in a manufacturing or production environment, within a regulated industry.
- Familiarity with automated or semi automated equipment and controlled environments.
- Working knowledge of cGMP, hygiene, and health and safety requirements.
- Experience completing documentation accurately and on time.

Skills Strong attention to detail with a focus on quality and right first time production.

- Ability to follow procedures, work effectively as part of a team, and support continuous improvement.
- Good written and verbal communication skills
- Willingness to learn
- Manual handling – ability to left heavy materials (25kgs)

As a family-run UK pharmaceutical manufacturer, we take pride in the people behind our products. You’ll be joining a team that values integrity, support, and long-term growth. We offer opportunities to develop your career, gain valuable industry experience, and contribute to improving lives through high-quality medicines.

You’ll work in a clean, compliant, and supportive setting with access to ongoing training and clear progression paths in the Quality department and beyond.

Ready to take your next step in pharmaceutical quality control?

Play a key role in supporting day-to-day engineering operations across packaging and manufacturing lines.

The post holder will be responsible for playing a key role in supporting day-to-day engineering operations across packaging and manufacturing lines. This is a hands-on position focused on technical problem-solving, operational support, and equipment maintenance.

This list of responsibilities and requirements is not exhaustive, and the employee may be required to perform other duties in line with requirements and at management’s discretion.

- Maintain all plant, machinery, and equipment in compliance with GMP, Health &
- Safety, and regulatory standards.
- Support production by carrying out routine and preventative maintenance.
- Diagnose and resolve equipment faults to minimise downtime.
- Provide hands-on engineering support across all site equipment.
- Identify and implement improvements to enhance reliability and performance.
- Collaborate with engineering colleagues, internal stakeholders, and external contractors on maintenance and upgrade activities.
- Maintain accurate records of maintenance activities, faults, and compliance documentation.
- Adhere to all GMP, Health &
- Safety, and company procedures and SOPs.
- Support site quality and safety standards through best engineering practices.
- Participate in CAPA (Corrective and Preventative Actions) activities.
- Provide guidance and basic training to operators on equipment use.
- Support contractor activities, including installations and repairs.
- Ensure full compliance and adherence with all company policies, procedures, guidelines and SOP’s.
- Undertake other duties that are commensurate with the level and responsibilities of the role.

Qualifications

- NVQ Level 3 or equivalent in engineering (desirable).

Experience

- Experience in a fast-paced, regulated manufacturing environment (FMCG, pharmaceutical, or similar)
- Strong practical experience in mechanical and electrical fault finding
- Good understanding of preventative maintenance and reliability practices
- Experience working with contractors and external service providers
- Familiarity with basic electrical systems and instrumentation
- Exposure to TPM, root cause analysis, or continuous improvement methodologies

Skills

- Ability to read and interpret mechanical and electrical drawings
- Working knowledge of GMP or regulated environments
- Experience using PLC machine interfaces
- Strong communication and teamwork skills
- High attention to detail, particularly in record-keeping
- Flexible approach to shift work and emergency callouts
- Familiarity with packaging and manufacturing machinery

As a family-run UK pharmaceutical manufacturer, we take pride in the people behind our products. You’ll be joining a team that values integrity, support, and long-term growth. We offer opportunities to develop your career, gain valuable industry experience, and contribute to improving lives through high-quality medicines.

You’ll work in a clean, compliant, and supportive environment with access to ongoing training and clear progression paths in the Quality department and beyond.

Ready to take your next step in pharmaceutical quality control?

Join a packaging team pursuing excellence The post holder will be responsible for carrying out the efficient operation of production and packaging lines, ensuring that products are packed to the highest quality standards while meeting production targets, complying with Health &

- Safety and GMP requirements, and maintaining excellent housekeeping standards.

This list of responsibilities and requirements is not exhaustive, and the employee may be required to perform other duties in line with requirements and at management’s discretion.
- 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.




- Operate packaging lines efficiently in full compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and company guidelines.
- Carry out machine set-up, changeovers, and clean-down activities within specified timelines.
- Load and feed packaging materials into machinery to maintain continuous line operation.
- Monitor production processes and promptly replace components or materials as required.
- Ensure all products are packed in line with quality standards and regulatory requirements.
- Perform in-process quality checks, ensuring adherence to Good Documentation Practices (GDP).
- Accurately complete batch documentation and reconciliation processes.
- Identify minor mechanical issues and take corrective action where possible or escalate as necessary.
- Maintain optimal line efficiency by minimising downtime and waste.
- Follow all start-up, operational, and cleaning procedures to ensure consistent production performance.
- Maintain a high standard of cleanliness and housekeeping across the production and packaging areas.
- Safely move pallets and materials within the production area using appropriate equipment.
- Work collaboratively with colleagues to achieve team objectives and targets.
- Participate in training programs, continuous improvement initiatives, and internal audits.
- Strictly adhere to all Health &
- Safety, Quality, and Compliance policies.
- Flexibility is required to work across shifts, weekends, and overtime as needed to meet production demands.
- Ensure full compliance and adherence with all company policies, procedures, guidelines and SOPs.
- Undertake other duties that are commensurate with the level and responsibilities of the role.

Qualifications

- Technical or vocational qualification in manufacturing, engineering, or a related field (desirable)
- GCSEs (or equivalent), including English and Maths.

Experience

- Previous experience working in a manufacturing, production, or packaging environment
- Experience operating automated or semi-automated machinery (desirable)
- Familiarity with GMP (Good Manufacturing Practice) or regulated environments (desirable)
- Experience performing quality checks and completing production documentation (desirable).

Skills

- Reliable, punctual, and committed to meeting deadlines.
- Positive attitude with a willingness to learn and develop new skills.
- Strong work ethic and attention to detail.
- Team-oriented with a collaborative approach to work.
- Flexible and adaptable to changing production demands.

As a family-run UK pharmaceutical manufacturer, we take pride in the people behind our products. You’ll be joining a team that values integrity, support, and long-term growth. We offer opportunities to develop your career, gain valuable industry experience, and contribute to improving lives through high-quality medicines.

You’ll work in a clean, compliant, and supportive environment with access to ongoing training and explicit progression paths in the Quality department and beyond.

Ready to take your next step in pharmaceutical quality control?

The post holder will be responsible to support the QC Supervisor and Senior Analysts by performing routine laboratory sampling, preparation, and testing of pharmaceutical products The post holder will be responsible to support the QC Supervisor and Senior Analysts by performing routine laboratory sampling, preparation, and testing in compliance with SOPs, GMP, GDP, Data Integrity, and EHS standards. Entry-level role with independent work in sampling/preparation and supervised analytical work.

This list of responsibilities and requirements is not exhaustive, and the employee may be required to perform other duties in line with requirements and at management’s discretion.

- Perform routine sampling, sample preparation, physical testing, and analytical testing as per workplans or supervisor direction.
- Ensure all activities comply with SOPs, GMP, GDP, Data Integrity, and EHS standards.
- Assist in drafting, reviewing, and verifying SOPs and specifications to meet regulatory and customer requirements.
- Prepare analytical data and ensure documentation is complete, accurate, and available for peer review.
- Coordinate with QC Senior Analysts to ensure timely delivery of assigned work.
- Escalate issues relating to:


- Equipment calibration, qualification, and validation status


- Availability of protocols, reports, and specifications


- Reagents, reference standards, consumables, and lab supplies

- Maintain strict adherence to data integrity and documentation requirements.
- Prepare retention and reference samples for raw materials, finished products, and packaging.
- Implement immediate corrections and corrective actions identified during data review.
- Complete assigned training on time and apply learning effectively (e.g., HPLC, KF titration, dissolution, physical testing).
- Carry out EHS-related tasks including waste disposal and glassware cleaning and ensure awareness of EHS responsibilities before work begins.
- Perform raw material sampling, including safe manual handling of materials (>25kg) using appropriate equipment where required.
- Support general laboratory upkeep, including equipment care, minor maintenance, and cleanliness.
- Undertake additional duties as directed by senior staff in line with role requirements.
- Ensure full compliance and adherence with all company policies, procedures, guidelines and SOP’s.
- Undertake other duties that are commensurate with the level and responsibilities of the role.

Qualifications

- Diploma/BSc in Chemistry, Analytical Sciences, or related field

Experience

- Experience working in a QC or laboratory environment (pharmaceutical preferred)
- Hands-on experience with analytical techniques (e.g., titration, spectroscopy)
- Experience following SOPs, GMP, and quality standards
- Familiarity with lab equipment, sampling, and testing processes

Skills

- Good verbal and written communication
- Strong organisation and time management
- IT skills (Microsoft Office)
- Able to work independently and in a team
- Problem-solving and effective escalation skills
- Committed to quality, compliance, and improvement
- Use of lifting equipment for lifting materials over 25kg

As a family-run UK pharmaceutical manufacturer, we take pride in the people behind our products. You’ll be joining a team that values integrity, support, and long-term growth. We offer opportunities to develop your career, gain valuable industry experience, and contribute to improving lives through high-quality medicines.

You’ll work in a clean, compliant, and supportive environment with access to ongoing training and clear progression paths in the Quality department and beyond.

Ready to take your next step in pharmaceutical quality control?

We don’t just make products, we build careers. We support, we train, and we celebrate success together. At ASPAR, your work matters, your growth matters, and you matter.

Ready to join the family?

Whether you’re looking for a manufacturing partner, a new role, or simply want to learn more about our approach and commitment to quality we’d love to hear from you.

Report a Problem To report an issue or adverse reaction related to one of our products, please click here. Your feedback is vital to ensuring product safety and continuous improvement.

Aspar Pharmaceuticals Ltd, Albany House, Acrewood Way, St Albans AL4 0JY

Registered in England No: 2658906 / VAT Registered No: GB 587 0621 24

📌 About the role (Amreli)
🏢 Aspar Pharmaceuticals
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