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Senior Technician - Microbiology & Sterility Laboratory – Quality Control - Fixed Term
Full-timeSeniorResearch & DevelopmentVaccines
Market Rate — Biochemists and Biophysicists
25th
$70K
Median
$107K
75th
$144K
BLS 2024 data (national)
Description
<p style="text-align:left">Job Description</p><p style="text-align:inherit"></p><p><span><b>Senior Technician - Microbiology & Sterility Laboratory – Quality Control</b></span></p><p><span><b>Fixed term: 2 years</b></span></p><p></p><p><span><b>Join Our Team</b></span></p><p><span>Are you passionate about microbiology and ensuring the highest standards of product quality? We’re looking for a <b>Senior Microbiology & Sterility Technician</b> to play a key role in our Quality Control laboratories. This is an exciting opportunity to combine hands-on laboratory experience with senior-level responsibility, supporting aseptic manufacturing and contributing to the reliable supply of vaccines to customers worldwide. The role would be ideal for candidates with a background in Microbiology and previous exposure to aseptic manufacturing processes looking to step into a more senior role within the laboratory.</span></p><p></p><p><span><b>Purpose of the Role</b></span></p><p><span>The Senior Microbiology & Sterility Technician will perform microbiological and sterility testing within the Quality Control laboratories, ensuring compliance with cGMP, pharmacopoeia, and dossier requirements. As a senior member of the team, you will be involved in batch release activities, cross-functional investigations, data analysis and preparation of technical documentation, while promoting a strong culture of safety and compliance. You will also become an SME in the use of LIMS and/or SAP to support users across the site. </span></p><p>As a<span> </span><b>Senior Microbiology & Sterility Technician</b>, you will perform and oversee microbiological and sterility testing within our QC laboratories, ensuring full compliance with<span> </span><b>cGMP</b>,<span> </span><b>pharmacopoeia</b><span> </span>and<span> </span><b>regulatory dossier</b><span> </span>requirements.</p><p>You will be a senior member of the lab team, contributing to:</p><ul><li><p>Batch release activities</p></li><li><p>Cross-functional investigations</p></li><li><p>Data analysis and reporting</p></li><li><p>Technical documentation and SOP updates</p></li><li><p>Continuous improvement initiatives</p></li></ul><p>You will also develop as a<span> </span><b>subject matter expert (SME)</b><span> </span>in<span> </span><b>LIMS</b><span> </span>and/or<span> </span><b>SAP</b>, providing support and guidance to colleagues across the site.</p><p></p><p>Key responsibilities</p><p>In this role, you will:</p><ul><li><p>Perform and oversee microbiology and sterility testing of submitted samples.</p></li><li><p>Ensure all testing is carried out in line with GMP, pharmacopoeia, dossiers and internal quality standards.</p></li><li><p>Identify and support continuous improvement initiatives to enhance compliance, productivity and/or cost efficiency.</p></li><li><p>Assist with the introduction and validation of new methods, laboratory equipment and biomaterials.</p></li><li><p>Support batch release activities according to production priorities, escalating potential supply risks when required.</p></li><li><p>Provide data and summaries for Product Quality Reviews and environmental monitoring meetings/reports.</p></li><li><p>Update and maintain SOPs and other documentation to keep them current, clear and compliant.</p></li><li><p>Support the training and coaching of new and existing staff, maintaining accurate training records.</p></li><li><p>Investigate OOS (out-of-specification) and OOT (out-of-trend) results, contributing to root cause analysis and CAPA actions.</p></li><li><p>Promote and maintain safe working practices within the laboratory.</p></li><li><p>Help ensure the laboratory is always in an audit-ready state; participate in regulatory audits and support closure of any observations.</p></li><li><p>Assist with scheduling laboratory work, including participation in weekend and holiday cover as required.</p></li></ul><p></p><p>About you</p><p>Qualifications</p><ul><li><p>Degree in<span> </span><b>Microbiology</b><span> </span>or a related<span> </span><b>Biological Science</b><span> </span>(or equivalent experience).</p></li></ul><p></p><p>Skills & experience</p><p>You will bring:</p><ul><li><p>Previous practical<span> </span><b>laboratory experience</b>, ideally in a GMP-regulated environment.</p></li><li><p>Strong working knowledge of<span> </span><b>GMP</b><span> </span>and quality systems.</p></li><li><p>Experience using<span> </span><b>LIMS</b><span> </span>with the ability to troubleshoot and train others.</p></li><li><p>Experience using<span> </span><b>SAP</b>, with confidence in supporting and training colleagues.</p></li><li><p>Strong written English skills and the ability to produce clear, accurate documentation.</p></li><li><p>Proven ability to troubleshoot and support resolution of complex deviations.</p></li><li><p>Clear, confident communicator, able to explain technical concepts to both technical and non-technical audiences.</p></li><li><p>Excellent time management and the flexibility to adapt to changing priorities.</p></li><li><p>High attention to detail and accuracy, both in performing tests and in recording/reviewing data.</p></li><li><p>A strong commitment to<span> </span><b>laboratory safety</b><span> </span>and<span> </span><b>GMP compliance</b>.</p></li></ul><p></p><p>What we offer</p><ul><li><p>The chance to directly contribute to the reliable supply of vaccines to patients worldwide.</p></li><li><p>A senior, hands-on laboratory role with clear opportunities to develop SME status and broader quality skills.</p></li><li><p>Exposure to cross-functional teams (Production, QA, Validation, etc.) and regulatory interactions.</p></li><li><p>A collaborative, supportive environment focused on scientific excellence, safety and continuous improvement.</p></li></ul><p></p><p>Ready to make an impact?</p><p>If you’re excited by the opportunity to apply your microbiology expertise in a senior QC role and support the delivery of high-quality vaccines, we’d love to hear from you.</p><div></div><p>Closing date for applications: 13/03/2026</p><p></p><p><b>Required Skills: </b></p>Batch Releases, GMP Compliance, GMP Laboratory, Laboratory Analytical Techniques, Laboratory Information Management System (LIMS), Laboratory Investigations, Laboratory Operations, Microbiological Test, Microbiology, Quality Control Management, Quality Management, Quality Standards<p></p><p><b>Preferred Skills: </b></p><p style="text-align:inherit"></p><p style="text-align:left">Current Employees apply <a target="_blank" href="https://wd5.myworkday.com/msd/d/task/1422$6687.htmld">HERE</a></p><p style="text-align:inherit"></p><p style="text-align:left">Current Contingent Workers apply <a target="_blank" href="https://wd5.myworkday.com/msd/d/task/1422$4020.htmld">HERE</a></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Search Firm Representatives Please Read Carefully </b><br />Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. </p><p style="text-align:inherit"></p><p style="text-align:left"><b>Employee Status: </b></p>Temporary (Fixed Term)<p style="text-align:inherit"></p><p style="text-align:left"><b>Relocation:</b></p>No relocation<p style="text-align:inherit"></p><p style="text-align:left"><b>VISA Sponsorship:</b></p>No<p style="text-align:inherit"></p><p style="text-align:left"><b><span>Travel Requirements:</span></b></p>No Travel Required<p style="text-align:inherit"></p><p style="text-align:left"><b>Flexible Work Arrangements:</b></p>Not Applicable<p style="text-align:inherit"></p><p style="text-align:left"><b>Shift:</b></p>Not Indicated<p style="text-align:inherit"></p><p style="text-align:left"><b>Valid Driving License:</b></p>No<p style="text-align:inherit"></p><p style="text-align:left"><b>Hazardous Material(s):</b></p>N/a<p style="text-align:inherit"></p><p style="text-align:left"><b>Job Posting End Date:</b></p>03/14/2026<p style="text-align:left"><b><span>*A job posting is effective until 11:59:59PM on the day <u>BEFORE</u> the listed job posting end date. Please ensure you apply to a job posting no later than the day <u>BEFORE</u> the job posting end date. </span></b></p>
Verona Pharma
PHARMACEUTICAL
Small molecules for respiratory indications
LocationUK - London
Open Jobs687
Respiratory
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