Microbiology Analyst

Curia

Milton

On-site

GBP 24,000 - 34,000

Full time

8 days ago
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Job summary

Curia in Glasgow is inviting applications for a Microbiology Analyst to join our growing team. You will work in a GMP environment in a high-throughput microbiology lab, performing environmental monitoring, microbial identifications, and product testing to support sterile manufacturing.

You will receive comprehensive training and have a clear development path in microbiology, with responsibilities including sample handling, data recording, equipment checks, and adherence to SOPs.

Qualifications

  • Ideally, recently educated to degree level, or equivalent, in a Science related discipline, preferably Biology or Microbiology
  • Any experience in operating laboratory equipment is an advantage
  • GMP environment knowledge and regulatory commitments (GMP, ICH, COSHH) is desirable

Responsibilities

  • Enumerate microbial growth from environmental monitoring plates and other microbial samples
  • Microbial identification via Gram stain, spore stain & Vitek
  • Sampling of process water and TVC/TOC and pH testing of process water samples
  • Environmental and product testing to support sterile IMP manufacture
  • Downloading and assessment of particle counts
  • Perform ‘at rest’ environmental monitoring
  • Perform training and gowning monitoring of cleanroom operators and maintain gown qualification
  • Inspection and growth promotion of pre-prepared and PST media
  • Perform checks including airflow, temperature checks of incubators, fridges and freezers, pipettes, water bath etc
  • Identifying system failures and reporting to senior members in a timely manner
  • Reporting of OOS / atypicals to key personnel
  • Providing good housekeeping and safety at all times including cleaning and disinfectant testing
  • Bioburden validation
  • Ensures completion and filing of relevant certificates/documentation/reports in adherence with GMP
  • Product and water endotoxin testing by kinetic turbidometric method
  • Sterility testing & validation using membrane filtration

Skills

Microbiology
Environmental monitoring
Sterility testing
Gram staining
Vitek
Documentation
Lab equipment

Education

Bachelor's in Microbiology/Biology

Tools

Vitek

Job description

Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. We have a fantastic opportunity to come and join our growing Microbiology team here in Glasgow. If you are looking to develop your experience in pharmaceutical drug manufacturing within a microbiology team, this is the perfect opportunity to join Curia as we enter our next stage of Growth and work towards the gold standard in pharmaceuticals. We provide excellent training in a fast-paced environment, provide variety and progression. We pursue excellence because our work has the power to improve patient’s lives with the pharmaceuticals we develop and manufacture.

Our Micro team operates is a support function for the facility, ensuring that all samples (API, excipients, in-process samples, finished product samples, stability samples, and water testing) are sampled, received, controlled, and tested in a timely fashion. As part of production support, effective environmental monitoring, sterility suite, staff gown monitoring, and overall direction regarding the maintenance of effective microbial control are performed. All work is performed within the Glasgow facility and operates to ensure that sterile products are manufactured to GMP.

Curia provides a great platform for learning. Here is an example of tasks you will be trained in and have responsibility for:
  • Enumeration of microbial growth from environmental monitoring plates and other microbial samples
  • Microbial identification via Gram stain, spore stain & Vitek
  • Sampling of process water and Total Viable Count (TVC), Total Organic Carbon (TOC) and pH testing of process water samples
  • Environmental and product testing to support sterile IMP manufacture
  • Downloading and assessment of particle counts
  • Perform ‘at rest’ environmental monitoring
  • Perform training and gowning monitoring of cleanroom operators and maintain gown qualification personally
  • Inspection and growth promotion of pre-prepared and PST media
  • Perform relevant checks including airflow, temperature checks of incubators, fridges and freezers, prodigy checks and trending and equipment calibration checks (e.g. pipettes, water bath etc)
  • Identifying system failures and report to more senior members of department and line management in a timely manner and following departmental SOPs.
  • Reporting of OOS / atypicals to key personnel
  • Providing good housekeeping and safety at all times including performing cleaning and cleanroom disinfectant testing.
  • Bioburden validation
  • Ensures completion and filing of relevant certificates/documentation/reports is performed in adherence with GMP and departmental procedures
  • Product and water endotoxin testing by kinetic turbidometric method
  • Sterility testing & validation using membrane filtration (e.g. Steritest)
Skills and Qualifications
  • Ideally, recently educated to degree level, or equivalent, in a Science related discipline, preferably Biology or Microbiology
  • Any experience in operating laboratory equipment is an advantage.
  • It is highly desirable if you can demonstrate Good practical skills in Microbiology and it is an advantage to have knowledge and/or experience in a GMP environment and, understanding of regulatory commitments, e.g. GMP, ICH, COSHH, etc.

Learning and Development is a key focus at Curia, therefore, we would like an ongoing commitment to training and development in Microbiology or related field. The role involves a high throughput of samples and therefore the Analyst must be able to:

  • Effectively organise their own workload with guidance from your line manager.
  • Adapt to changing priorities in workload without compromising quality.
  • Remain aware of workload levels and priorities within the lab and communicate these to line management where necessary.
  • Ensure good levels of documentation; legible writing; clear structure.
  • Adopt right first time culture

This position will be well-suited to someone with a minimum of 2 years industry experience. A full, training program will be provided.

Hours: 8-hour shifts including breaks, paid overtime, excellent staff benefits
Hours: 37.5 hours per week - flex from 8.30am to 5.30pm Monday to Friday
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