Back to search
We have an exciting opportunity for a QC Microbiology and Sterility Technician to join our global pharmaceutical client in Milton Keynes. This full-time, temporary position is initially set for one year, with the potential for extension. It’s a great chance to work in the animal health sector with a reputable organisation. The role is a full-time site based role offering an hourly rate up to £18 per hour depending on experience.
To perform microbiology testing, isolator and clean room testing as well as doing investigations for deviations, implementation of CAPA’s and change controls. This role also involves testing of finished products and intermediates in accordance with GMP, dossier and relevant pharmacopoeia requirements.
Role Responsibilities and Duties include:
- To perform and oversee testing of intermediate and finished products in accordance with GMP, dossier and where relevant, as per pharmacopoeia requirements.
- Microbiology testing and Training of personnel (Bioburdens, water testing, plate reading, sterility testing, growth promotion, Lungworm testing and Inactivation’s) in accordance with SOP’s.
- Ensure all activities are performed in compliance with GMP, company quality guidelines and pharmacopeia.
- Release of batches in accordance with LROT, escalating any potential affect to supply.
- Raising of deviations in the Quality Management System.
- Supporting with investigations to identify root-cause and implementation of appropriate CAPA’s in the Quality Management System.
- Facilitate change management by being a change owner/manager for full change controls and actioning change control tasks generated in the Quality Management System.
- Completion and review of COSHH assessments and either Risk or Manual handling assessments.
- Provide training of test procedures to new members of the team.
- Entering and locking of test results in SAP.
- Update SOP's, and Specs ensuring they are current and relevant.
- Promote safety within the laboratory areas, by carrying out safety observations, ensuring correct signage and maintaining COSHH documentation to prevent or reduce unnecessary exposure to hazardous substances.
- Completion of safety actions within assessnet and Enablon within agreed timelines.
- Other responsibility
- To upload company procedures regarding GMP and always comply with UK pharmaceutical regulations.
- To comply with company’s health and safety practices and procedures
The above list of duties is not exhaustive and is subject to change. The post holder may be required to undertake other duties within the scope and grading of the post.
Skills, Experience, Knowledge and Qualifications:
Knowledge
- Microbiology lab experience
- GMP Compliance
Experience
- Experience in Quality Control testing
- Laboratory investigations
- (DESIRABLE ONLY) Previous roles include interaction with Production/Manufacturing departments.
Skills and Ability
- MS Word and Excel
- Ability to identify deviations and raise events in the Quality Management System.
- Ability to support with troubleshooting to help resolve issues.
- Protocol, hypothesis, and Report writing
- Ability to troubleshoot resolve issues
Personal Attributes
- Able to communicate at all levels and across all functions
- Ability to communicate concise technical information with clarity
- Good Time Management in a high flow through laboratory
- Flexible approach to changing priorities
- Attention to detail
Qualifications:
- Science related Degree
