Senior QC Analyst - 24 Month Secondment/FTC

About the Company

Responsibilities

• ● As a Senior QC Analyst, you will:
• ● Provide technical leadership and subject matter expertise across microbiology testing and environmental monitoring activities.
• ● Support microbiology laboratory operations while ensuring compliance with cGMP, GLP, regulatory, and company requirements.
• ● Lead and support method validation and qualification activities for microbiological test methods and systems.
• ● Partner with colleagues to develop, implement, and optimise Laboratory Information Management Systems (LIMS).
• ● Lead and participate in Quality Risk Assessments and continuous improvement initiatives.
• ● Investigate out-of-specification and out-of-trend results, identify root causes, and implement effective corrective and preventive actions.
• ● Review, interpret, and author technical documentation, including validation protocols, reports, investigations, and standard operating procedures.
• ● Perform technical review and approval of microbiological data.
• ● Support internal and external regulatory inspections and customer audits.
• ● Provide technical guidance and training to laboratory personnel.
• ● Contribute to project activities supporting manufacturing operations, new technologies, and laboratory improvements.
• ● Act as a key escalation point for troubleshooting complex laboratory issues.
• ● Support laboratory scheduling and operations, including deputising for the Laboratory Supervisor when required.

Requirements

• ● Degree or equivalent experience in Microbiology or a related scientific discipline.
• ● Significant experience within a cGMP-regulated pharmaceutical, biotechnology, or life sciences environment.
• ● Strong understanding of microbiology and sterility assurance requirements within regulated manufacturing operations.
• ● Expertise in microbiological method validation, endotoxin testing, and sterility testing.
• ● Knowledge of LIMS and experience supporting system implementation or optimisation.
• ● Strong technical writing, documentation, and data review skills.
• ● Desired skills and experience
• ● Sophisticated technical knowledge of sterility assurance, aseptic processing, and microbiological testing methodologies.
• ● Ability to build strong collaborative relationships across multiple functions and sites.
• ● Excellent problem-solving and root cause analysis capabilities.
• ● A continuous improvement attitude with experience driving efficiency and compliance enhancements.
• ● Strong planning, organisation, and prioritisation skills.
• ● Ability to coach, mentor, and develop colleagues.
• ● Excellent written and verbal communication skills.
• ● Strong digital literacy, including experience with digital platforms and a working knowledge of AI tools and technologies.

Benefits

• ● You'll be part of a collaborative and supportive team where your expertise will directly contribute to product quality, patient safety, and operational perfection. We value diverse perspectives and encourage innovation, continuous learning, and professional growth.
• ● If you're passionate about microbiology, quality, and driving improvements in a fast-paced pharmaceutical environment, we'd love to hear from you.
• ● Inclusive hiring statement
• ● We are committed to creating an inclusive workplace where everyone can thrive. We welcome applications from candidates of all backgrounds, experiences, and perspectives. If you don't meet every requirement listed but believe your skills and experience would enable you to succeed in this role, we encourage you to apply.
• ● Date Posted 28-Aug-2026
• ● Closing Date 11-Sept-2026