Microbiologist

3 weeks ago

Ware, United Kingdom SRG Full time

Job Title: Microbiologist Level 1 – Synergy

Location: Ware, UK

contract: 12 Month FTC

working pattern: Fully onsite

Salary: Competitive



Interested in this role You can find all the relevant information in the description below.

Are you a Microbiology or Biomedical graduate looking for your first role in industry? Or do you already have a background in an industrial micro lab but would like to develop your skills further in a GMP environment?


SRG Synergy are currently working with a world-leading pharmaceutical organisation located in Ware with a vacancy for a Microbiologist – Level 1.


Synergy, part of SRG, offer a range of scientific solutions to different Clients in the Life Sciences sector. We can offer a competitive salary, a range of excellent benefits and access to training & development opportunities within the role.


Within this role, you will be part of a team responsible for the microbial analysis of processes and materials associated with the pharmaceutical manufacturing conducted on site.


Responsibilities:

analysis of samples and supports technical investigations/ monitoring, using a range of analytical techniques related to the microbiological testing of medicines and facility’s environmental monitoring.and checks analytical data accurately according to company, customer and regulatory requirements.the quality and accuracy of analytical results and determines if material meets pre-defined acceptance criteria.analysis as required to support process investigations or as part of process qualification and validation exercises.is an Environmental Monitoring Microbiologist role which will require several EM excursions is different site facilities i.e., manufacturing plant rooms and productions areas which could be physically demanding.


Requirements:

BSc qualification in Microbiology or related relevant scientific discipline, or industrial experience in a GMP laboratory setting.aseptic technique, and knowledge/experience of GMP/GLP regulatory standards would be desirable.of endotoxin or bioburden testing would be advantageous.

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