Job Title: Senior Microbiology Technician
Location: Runcorn, United Kingdom, WA7 3FA
Company: Teva Pharmaceuticals
Job ID: 59291
Who We Are
Teva Pharmaceuticals touches the lives of over 200 million patients daily, providing high-quality, affordable healthcare worldwide. At our Runcorn site, we specialize in developing, manufacturing, and marketing innovative sterile liquid products for respiratory conditions and injectable Combination Products, such as Copaxone for MS treatment. We are currently seeking a Senior Microbiology Technician to join our team on a permanent basis and contribute to our mission of increasing access to essential medicines.
A Day In The Life Of A Senior Microbiology Technician
As a Senior Microbiology Technician, you will be responsible for guiding and directing a team of technicians in all aspects of microbiology testing and laboratory tasks. You will work in a regulated pharmaceutical environment and have a key role in ensuring compliance with Good Manufacturing Practices (GMP). Your primary responsibilities will include:
Key Responsibilities:
Documentation:
Review and approve batch documentation for product and starting materials, ensuring compliance with CGMP standards.
Regularly review data and data management systems to maintain performance and compliance.
Testing Support:
Provide microbiology testing support for raw materials, bulk products, and finished products when required.
Assist with the coordination of testing activities and ensure the proper execution of tests.
Investigation & Continuous Improvement:
Lead complex investigations using root cause analysis and trend results to identify corrective or preventive actions.
Drive continuous improvement within the laboratory to enhance performance.
LIMS & Data Review:
Trend and review LIMS results or product review reports according to company procedures.
Training:
Train laboratory and site personnel in microbiology techniques and regulatory knowledge.
Quality Control Oversight:
Review and approve microbiology data and other relevant documentation.
Support the Microbiology Department and deputize for the Team Leader when required.
Act in a QC Quality Assurance capacity for raw material/component release.
Who We're Looking For
Do you have the following qualifications and experience?
Qualifications:
A degree in a relevant scientific discipline.
Experience:
Significant experience working within a pharmaceutical microbiology environment.
Technical expertise in a regulated microbiology laboratory and a thorough understanding of GMP, EP requirements, and regulatory expectations.
Skills:
Strong knowledge of aseptic techniques.
Experience with technical report writing (desirable).
Computer literate, with experience in Laboratory Information Management Systems (LIMS) and Quality systems such as Deviation, Change Control, CAPA support, and documentation.
Personal Traits:
A keen eye for detail and strong analytical thinking skills.
Driven by continuous improvement and well-organized with strong time-keeping skills.
What We Offer
23.5 paid shift holidays per year, with the option to buy and sell up to 3.5 days of annual leave.
Private healthcare scheme through Bupa.
A formal training and development program specific to your role and department.
Flexible pension contributions from both employee and employer.
Competitive salary and shift allowance.
Employee assistance program and a range of health benefits, including Life Assurance, Critical Illness Insurance, and Income Protection.
Additional flexible benefits through salary sacrifice, including the Cycle to Work scheme, discounts, and more.
Teva’s Equal Employment Opportunity Commitment
Teva is committed to creating a diverse and inclusive workplace where everyone feels comfortable being their true self. We value diversity and embrace differences, which strengthens our company and helps us provide better service to our customers and patients. We are committed to building a fairer society free from discrimination and prejudice.
If you have a passion for microbiology, compliance, and continuous improvement in a pharmaceutical environment, we’d love to hear from you!
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