Quality Control Microbiologist
Posted Today by PE Global
£21 Per hour
Undetermined
Undetermined
Wokingham, England, United Kingdom
Summary: The role of Scientist - Microbiologist involves working as a junior team leader within a cross-functional team to deliver RDQ activities for projects focused on consumer experience. The position requires organizing and executing projects under the guidance of a manager, ensuring compliance with GMP standards, and producing technical reports based on data analysis. This is an opportunity for individuals looking to enhance their leadership experience in a pharmaceutical microbiology environment.
Key Responsibilities:
- Deliver RDQ activities for project and productivity projects.
- Organize and execute projects in line with client requirements.
- Communicate project status and risks effectively.
- Plan and conduct projects according to GMP requirements.
- Write technical reports analyzing results and providing recommendations.
- Create and maintain accurate consumer-led specifications.
Key Skills:
- 3+ years in a GMP Pharmaceutical Microbiology Environment.
- Technical expertise in microbiology.
- Experience as a line manager for at least 1-2 people.
- Ability to work independently and make decisions without supervision.
Salary (Rate): £20.94/hr
City: Wokingham
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: Mid-Level
Industry: Other
PE Global are currently recruiting for a Scientist - Microbiologist for an initial 6 contract role with a leading company based in Wokingham. This position is a junior team leader position, not a manager. It’s a good opportunity for someone wanting to further their team leader experience.
Responsibilities
- Working as part of a cross functional team, you deliver the RDQ activities required to complete project and/or productivity projects with an emphasis on meeting the desired consumer experience.
- With the support and guidance of a manager, you will organize and execute projects in line with client requirements, effectively communicating status and risks.
- You will plan and conduct projects in accordance with good manufacturing practice and GMP requirements and validation activities
- You will also write technical reports that will require the analysis and interpretation of results and that lead to conclusions and recommendations and create and maintain accurate consumer-led specifications.
Requirements
- 3 Years + in a GMP Pharmaceutical Microbiology Environment – with testing and data review responsibilities. (please make sure this is clearly evidenced on their CV)
- Must have a technical mind in microbiology
- Must have been a line manager of at least 1-2 people and experience doing 1:1’s
- Need to be able to work without supervision and be able to make decisions without a manager around.
Interested candidates should submit an up to date CV.