Aspire Laboratories is expanding and we’re seeking a motivated, detail-oriented, and driven individual, with excellent communication and organisational skills to join our team.
This is a full time, 5 days on site position.
You will receive hands-on training, mentorship, and exposure to real-world GMP operations in a dynamic, supportive environment.
Job Description
- Support the QA and QC departments in ensuring all laboratory activities are conducted in accordance with GMP, SOPs, and pharmacopoeial requirements.
- Support audits and inspections (MHRA, customer, and Home Office).
- Ensure laboratory compliance with GMP
- Use and maintain electronic systems such as LIMS and Eupry.
- Logging in of laboratory samples and consumables
- Dual responsibility for supply chain - ensuring all materials are available before they are needed by the labs
- Supplier management, ensuring costing, quotations and core lists are in place
- Maintaining supplier KPIs
- Organising and managing the lab waste
- Manage document control activities including archiving and issuing controlled documentation.
- Manage and organise document destruction and send off
- Maintaining change controls
- Keep up to date with relevant legislative and regulatory requirements and communicate implications to the team.
- Contribute positively to a collaborative and proactive team environment.
- Perform other QA and QC-related duties as assigned.
Mandatory Candidate Requirements:
- Bachelor’s degree in sciences (chemistry / microbiology or similar) or related discipline
- A brilliant communicator
- Proactive can-do and will-do attitude
- Experience with Scientific and/or Pharmaceutical terms preferred
- Excellent Microsoft Office skills.
In return, the opportunities for personal and career development within the business are vast.
You will benefit from exceptional training and development opportunities, in addition to extensive cross-training within the business.
Aspire Laboratories provided the following inclusive hiring information:
We are an equal opportunity employer and considers all qualified applicants equally without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
Job Types: Full-time, Permanent
QA, QC, quality, control, assurance, analytical, microbiology, testing, solid, dose, raw materials, laboratory, analyst, GMP, manufacturing, HPLC, chromatography, GC, chemistry, development, validation, transfer, assurance
Job Types: Full-time, Permanent
Pay: £12.25 per hour
Benefits:
- Casual dress
- Company pension
- On-site parking
Application question(s):
- MANDATORY QUESTION (applicants who do not answer this are automatically rejected):
We do not provide sponsorship. Describe your right to work documentation and any expiry dates (if applicable)
- MANDATORY QUESTION (applicants who do not answer this are automatically rejected):
Have you used AI in any part of the application process for this position including your CV? Applicants found to have used AI for CV, phone interviews or other stages will be rejected immediately.
- MANDATORY QUESTION (applicants who do not answer this are automatically rejected):
How long would it take for you to commute to Dagenham East RM107FN? (in minutes); would that be public transport or car?
- MANDATORY QUESTION (applicants who do not answer this are automatically rejected):
Please confirm you have read and accept the salary offered for this position
- MANDATORY QUESTION (applicants who do not answer this are automatically rejected):
We are looking for a passionate individual - a great communicator with a can-do attitude and attention to detail. How do you believe you fit this description? (max 150 words)
- MANDATORY QUESTION: This position requires background in chemistry or pharmaceutical microbiology. Unfortunately we do not accept biomedical sciences / biotechnology / biology/ medical based degrees. Please write down your degree and what degree mark was achieved.
Work authorisation:
- United Kingdom (required)
Work Location: In person
