At a Glance
- Tasks: Join our Microbiology team to support pharmaceutical manufacturing and ensure product quality.
- Company: Curia, a leading global contract research and manufacturing service provider.
- Benefits: Paid overtime, excellent staff benefits, and a commitment to training and development.
- Other info: Dynamic role with opportunities for growth and learning in a GMP environment.
- Why this job: Make a real impact on patient lives while developing your skills in a fast-paced environment.
- Qualifications: Degree in Science, preferably Biology or Microbiology; lab experience is a plus.
The predicted salary is between 28000 - 34000 £ per year.
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 patients’ lives with the pharmaceuticals we develop and manufacture.
Our Micro team operates as 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. 37.5 hours per week - flex from 8.30am to 5.30pm Monday to Friday.
Pharmaceutical Microbiology Analyst in Glasgow employer: Curia
Curia is an exceptional employer, offering a vibrant work culture in Glasgow that fosters innovation and collaboration within the pharmaceutical and biotechnology sectors. With a strong commitment to employee development, we provide comprehensive training and clear pathways for career progression, ensuring that our team members can thrive in a fast-paced environment while contributing to life-changing pharmaceutical advancements.
StudySmarter Expert Advice🤫
We think this is how you could land Pharmaceutical Microbiology Analyst in Glasgow
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We think you need these skills to ace Pharmaceutical Microbiology Analyst in Glasgow
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Curia!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Curia that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Curia!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Curia, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Curia
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Curia that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Curia’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.