Site microbiologist Work, Jobs in Southport, Msy (with Salaries)

Site Microbiologist
Teva —County
- Team management
- Relocation assistance
Quality Control Microbiologist
Teva —County
- £2,200 - £2,600 a month
- Weekend availability
- English
- Quality control
14d

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Quality Control Microbiologist
Teva —County
Employee rewards and recognition programs, events and social activities. Perform bioburden, bacterial endotoxins, TOC analysis of samples (water samples, drug…
£2,200 - £2,600 a month
14d
Laboratory Technician (Microbiology)
Cheshire Scientific LTD —Wirral
Support sample checking, storage and quality control. Whether you have previous laboratory experience or are completely new to the field, if you have the…
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1d

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Site Microbiologist

Teva -
County

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Job details

Permanent

Benefits

Relocation assistance

Qualifications

Microbiology
Cost control
Performance management
Team management

Full job description

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

The Opportunity

We would like to invite applications for the role of Site Microbiologist at our Waterford site. This is a Permanent Position.

The Site Microbiologist is responsible for the Management of the Microbiology Lab and defines the microbiology strategy for the site in order to meet TEVA Waterford Operational and Quality objectives.

The successful person will be managing the full micro team for the site along with reviewing departmental performance and acting as the site main contact for all micro related queries.

There is no relocation support offered for this role.

How You’ll Spend Your Day

Responsible for all micro queries and investigations around the site
Liaising with senior management on all queries relating to the micro team
Proactively plans for, develops and implement new projects and systems for the micro team on an ongoing basis
Being a subject matter expert on all matters relating to micro
Supports and drives the Contamination Control Strategy for the site in accordance with Annex 1 requirements
Develop and train the micro analysts on the team to the best standards
Deliver Customer Service (both internal and external) in accordance with Quality standards, ‘TEVA Best Practices’ and Cost Control.
Ensure that operational schedules are met with all batches being ready as needed
Ensure GMP compliant, cost effective systems are developed in place and operational in order to ensure all work carried out by Microbiology personnel is in compliance with required standards conforming to TEVA, cGMP, and Health and Safety, TEVA Best Practice and Environmental requirements.
Ensure the team are fully ready for all audits and inspections as required

Your Skills and Experience

Are you:

Third Level qualified in Microbiology (essential)

Do you have:

Extensive management experience in a high throughput Microbiology Laboratory within the Pharma industry
Excellent Knowledge of Regulatory USP/Ph.Eur/JP harmonised microbiological methods, method verification/development ensuring the site is in compliance with all micro regulations
Comprehensive Knowledge of Microbiology and Microbiological Techniques in the Pharma Industry
Knowledge of Steam Sterilisation and microbiological media.
Knowledge of environmental control, routine monitoring and method validation.
Understanding of microorganisms and bioburden/contamination control and the risk associated with non-sterile inhalation products.
Knowledge of PW systems and microbial control
Knowledge of microbial identification methods
Good understanding of Contamination Control Strategy and Annex 1 requirements

Already Working @TEVA?

Teva designs eligibility to empower and enable employees to manage their careers internally and provides an easy and smooth process to view and apply. To be considered for an open internally posted position, an employee must:

Be a current employee of Teva
Meet the basic requirements for the job
Have received a rating not lower than “Successful” on their most recent performance review and must not currently be on a performance improvement plan
Apply to the posted requisition within the allotted time frame
Have been in their current position for a minimum tenure of twelve (12) months

Unless explicitly stated in the job description, no company sponsored work authorisation or relocation assistance should be assumed.

Deadline for internal applications will close on Friday 8th May 2026 #TJ

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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site microbiologist jobs in southport, msy

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