GMP Manufacturing Scientist

Quotient Sciences; Alnwick; Vor Ort; GBP 32.000 - 52.000; Vollzeit

Zusammenfassung

Quotient Sciences is seeking an Aseptic Manufacturing Scientist to join our GMP manufacturing team. You will help manufacture, dispense and package clinical products in a regulated pharmaceutical setting, ensuring high quality, compliant documentation and traceability.

You will work with API materials, excipients and packaging components, maintaining stock, assisting with process development, and supporting cross‑functional teams to meet client expectations.

Qualifikationen

• BSc or equivalent in a scientific discipline.
• Strong written and verbal communication skills.
• Excellent attention to detail and ability to follow procedures.
• Experience in a GMP-regulated facility or GMP manufacturing environment.
• Organised, with the ability to manage multiple tasks and priorities.
• Committed to health, safety and GMP standards.

Aufgaben

• Manufacture, dispense and package oral and intravenous clinical products in line with GMP and procedures.
• Prepare and complete documentation related to manufacture and supply of clinical products.
• Dispense APIs, excipients, drug products, IMPs and packaging materials.
• Maintain GMP stock levels and assist with ordering, goods receipt and storage.
• Support cleaning, maintenance and upkeep of the GMP facility, utilities and equipment.
• Record work accurately in line with regulatory requirements and client needs.
• Support process development studies and non-clinical batch manufacture when required.
• Collaborate with Quality Control, microbiology and purchasing teams for material management.
• Adhere to health and safety procedures and work across the site as needed.

Kenntnisse

Attention to detail

Documentation discipline

Communication skills

Procedural compliance

Organised workload management

Health & GMP awareness

Team collaboration

Ausbildung

BSc or equivalent in a relevant scientific discipline

Jobbeschreibung

The Role

We are looking for anAseptic Manufacturing Scientist to join our GMP manufacturing team, supporting the manufacture, dispensing and packaging of clinical products within a regulated pharmaceutical environment. This is an excellent opportunity for someone with a scientific background who is looking to build experience in aseptic manufacturing, clinical supplies and pharmaceutical development.

Working as part of a skilled manufacturing team, you will help ensure clinical products are prepared to high quality standards, in line with GMP requirements, internal procedures and client expectations. This role would suit someone who is detail-focused, organised and comfortable working in a regulated environment where accuracy, safety and documentation are essential.

Key responsibilities

• Manufacture, dispense and package oral and intravenous clinical products in accordance with GMP requirements and company procedures.
• Prepare and complete documentation relating to the manufacture and supply of clinical products.
• Dispense APIs, excipients, drug products, IMPs and packaging materials for clinical use.
• Maintain GMP stock levels, including supporting ordering, goods receipt, storage and stock control.
• Support the cleaning, maintenance and general upkeep of the GMP manufacturing facility, utilities and equipment.
• Record all work accurately and in line with regulatory requirements, internal policies, procedures and client requirements.
• Support process development studies and the manufacture of non-clinical batches where required.
• Work closely with Quality Control, microbiology teams and purchasing colleagues to support effective material management.
• Follow health and safety procedures at all times to protect yourself, colleagues and the wider working environment.
• Work flexibly across the site to support business and client needs.

Skills and experience required

Essential:

• BSc or equivalent qualification in a relevant scientific discipline.
• Good written and verbal communication skills.
• Strong attention to detail and the ability to follow procedures accurately.
• Ability to work in a regulated environment where documentation, quality and compliance are important.
• Organised approach with the ability to manage a range of tasks and priorities.
• Positive and flexible approach to new work challenges.
• Commitment to health, safety and GMP standards.
• Experience working in a GMP regulated facility or GMP manufacturing environment.

Desirable:

• Experience manufacturing clinical formulations or pharmaceutical products.
• Knowledge of the drug development process.
• Experience working with APIs, excipients, IMPs or clinical packaging materials.
• Experience supporting stock control, goods receipt or materials management within a regulated setting.

Eligibility to Work in the UK

Please note that this position isnot eligible for sponsorship under the UK points-based immigration system. If you require sponsorship, we will be unable to progress your application or make an offer of employment.

As this is apermanent role, we are also unable to accept applications from candidates on a Graduate Visa.