Microbiology Lead Job at Coca-Cola HBC (Ploiesti)

Sterility Assurance Lead

This is a critical leadership role responsible for ensuring that all marketed an...

Location

Ireland , Cork

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Microbiology, Biology, Pharmaceutical Sciences, or related discipline (Master’s or PhD preferred)
10–15+ years of progressive experience in microbiology within GMP-regulated pharmaceutical or biotechnology environments
Minimum 5 years in leadership roles, with proven ability to influence cross-functional teams and senior stakeholders
Significant hands-on experience supporting aseptic sterile fill-finish operations, preferably with isolator qualification and maintenance
Strong knowledge of EU GMP Annex 1 and global sterility assurance standards
Demonstrated success in leading contamination investigations and regulatory interactions
Strategic thinker with strong problem-solving and decision-making abilities
Excellent communication and influencing skills across all organizational levels
Ability to interpret complex microbiological data and translate into actionable strategies

Job Responsibility

Strategic Leadership: Own and continuously evolve the site’s Contamination Control Strategy, ensuring alignment with global standards and regulatory requirements
Regulatory Compliance & Influence: Implement regulatory expectations, maintain compliance with EU GMP Annex 1, 21 CFR, USP, EP, JP, and ICH guidelines, and stay current with emerging global regulations, audit trends and best practices
Training & Culture: Design and deliver robust training programs on aseptic processing, behaviors, and contamination control principles to embed a culture of sterility assurance across the site
Environmental Monitoring & Utilities: Establish and maintain environmental monitoring and clean utilities programs, ensuring proactive contamination control
Technical Expertise: Provide expert input on gowning, cleaning, sanitization & sterilization strategies, microbiological method transfers, and contamination investigations
Investigations: Lead and guide the investigation of contamination-related deviations, non-conformances, and sterility failures. Perform root cause analysis, define corrective and preventive actions (CAPAs), and ensure timely closure of quality events
Data Analysis & Risk Mitigation: Review microbiological data trends, identify risks, and implement effective mitigation strategies
Global Collaboration: Partner with global Technology and Quality functions to ensure site alignment with industry best practices and BioMarin network standards
Continuous Improvement: Drive initiatives to enhance microbiological quality, operational efficiency, and inspection readiness
Facility Expansion Support: Lead microbiology aspects of facility expansions, including cleanroom qualification and sterilization systems

Technical Manager

Are you a technical leader with a passion for quality and a background in highly...

Location

United Kingdom

Salary:

65000.00 - 70000.00 GBP / Year

Zest Food Jobs

Expiration Date

Until further notice

Requirements

Proven technical or quality leadership experience in a fast-paced food manufacturing environment
Ideally from a highly automated background-drinks, dairy, soups/sauces or similar
In-depth understanding of BRC, HACCP, GMP, and relevant food legislation
Strong leadership and communication skills, with the ability to influence at all levels
Experience of working with cross-functional teams including operations, engineering, and NPD
Ideally degree-qualified in food science, microbiology, or a related discipline

Job Responsibility

Lead the technical and quality functions across the site, promoting a strong compliance and food safety culture
Oversee site technical standards including HACCP, BRC, GMP, and customer-specific requirements
Drive root cause analysis and resolution for quality, microbiology, and food safety issues
Lead audit readiness and manage site response to third-party, customer, and regulatory audits
Work cross-functionally to support process improvements, automation optimisation, and operational efficiency
Manage risk assessments, technical training, and development of team capability
Act as technical lead for new product introductions, site trials, and scale-up projects
Lead the HACCP team and own technical KPI reporting and governance

What we offer

A comprehensive benefits package
A well-invested, modern site with strong backing
A culture that supports ownership, accountability, and continuous improvement

Director QC Operations - Microbiology

The Director of QC Operations - Microbiology provides strategic leadership and s...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

10+ years of relevant working experience in QC Microbiology
5-8 years of management/leadership responsibilities
BS in Microbiology, Biology or related life sciences field
Excellent communication skills, both written and verbal
Strong attention to detail and cross functional team experience
Proven strong leadership skills with ability to motivate, inspire and build a high performing team
In-depth knowledge of US, EU and other international regulations and guideline associated with environmental monitoring programs

Job Responsibility

Provide strategic direction, leadership, and oversight for all QC Microbiology operations across NH sites
Develop and implement long-term QC microbiology strategies, technologies, and process improvements
Oversee and continuously improve core QC Microbiology programs including Environmental Monitoring (EM), Utility Monitoring, Product Microbiology Testing, and Contamination Control initiatives
Ensure microbiology programs, methods, and systems remain compliant, scientifically sound, and optimized
Provide review and approval of microbiology data, technical assessments, and quality documents
Lead, mentor, and develop QC Microbiology managers and staff
Provide executive oversight and guidance for microbiology-related deviations, investigations, CAPAs, and quarterly/trend reports
Drive proactive contamination control strategies and risk mitigation plans
Ensure all microbiology operations adhere to cGMP, global regulatory expectations, corporate policies, and quality standards
Partner closely with Operations, Facilities, Validation, Quality Assurance, and other key functions

Fulltime

Quality Manager

Our client, a leading manufacturer in the food industry is seeking a driven Qual...

Location

United Kingdom , Greater Manchester

Salary:

45000.00 - 50000.00 GBP / Year

Zest Food Jobs

Expiration Date

Until further notice

Requirements

Proven experience in a Quality Management or Senior Quality Assurance role within food manufacturing
A strong understanding of HACCP principles and BRC standards
Previous experience working to major retailer standards
Excellent leadership skills with the ability to develop, coach, and motivate a team
Exceptional attention to detail and the ability to influence at all levels
A degree in a relevant field (e.g., Food Science, Microbiology, or related discipline)

Job Responsibility

Lead and manage the Quality Assurance team, driving a culture of excellence and accountability
Report directly to the Technical Manager and act as deputy in their absence
Maintain and develop the site's Quality Management Systems, ensuring all procedures and documentation are current and compliant
Ensure the site remains audit-ready at all times and meets all customer, BRC, and regulatory standards
Lead the HACCP team and manage the site's HACCP plans effectively
Oversee the internal audit programme, ensuring timely completion and follow-up of actions
Support external audits and customer visits
Drive and promote continuous improvement initiatives across all areas of quality and food safety

Sterility Assurance Lead

Senior QA Subject Matter Expert role for a full-time contract of approximately 6...

Location

United Kingdom , Swindon

Salary:

50.00 - 75.00 GBP / Hour

Randstad

Expiration Date

February 17, 2026

Requirements

Master Degree in Microbiology
At least 5 proven years experience in microbiology in pharmaceutical industry
Practical knowledge in GMPs and Regulatory Compliance, especially for sterility assurance (EU GMP annex 1)
Extensive background on sterility assurance, process and cleaning validation concepts and contamination control strategy
Strong interpersonal and communications skills
Ability to make scientific decisions
Able to coach and mentor more junior employees
Participates and/or leads meetings
On-call services, remote, based on department organization
Fluency in English

Job Responsibility

Own and drive the Contamination Control Strategy and Sterility Assurance strategy for the site
Assure the surveillance plan of operational activities
Collaborate on the floor on the management of quality events with an impact on sterility
Owns and maintains the site microbiology risk assessment and Sterilization-in-place concept
Responsible for writing and/or review of SOPs related to sterility assurance
Support the EM review/evaluation including the relevant action plan

Fulltime

New

Site Food Safety Lead

The role is responsible for ensuring full food safety and regulatory compliance ...

Location

United Kingdom , Kendal

Salary:

50000.00 GBP / Year

Cooper Lomaz

Expiration Date

Until further notice

Requirements

Degree in Food Science, Microbiology, Food Technology, or a related discipline
Formal qualifications in HACCP, PCQI, and/or food safety auditing (HACCP Level 4 required)
Minimum of 5 years’ experience in food safety or quality within a food manufacturing environment, ideally within infant formula or high-care dairy
Strong working knowledge of FDA regulations, PCQI responsibilities, and U.S. export compliance
Proven experience leading validation programs for cleaning, allergen control, and thermal processes
In-depth understanding of FSMS principles, food microbiology, allergen management, and hygienic design
Demonstrated capability across the full validation lifecycle, from protocol development to data analysis and interpretation
Knowledge of BRC, ISO 22000, Codex Alimentarius, and CFR Title 21
Excellent analytical, communication, and leadership skills, with the ability to influence cross-functional teams
Lead Auditor qualification

Job Responsibility

Lead the development, implementation, and ongoing maintenance of the site Food Safety Management System (FSMS) in accordance with HACCP principles and international infant formula standards
Ensure compliance with all relevant UK, EU, and U.S. FDA regulatory requirements
Plan and conduct internal audits, inspections, and risk assessments to identify, manage, and mitigate food safety risks
Act as the site subject matter expert for FDA, FSMA, and PCQI requirements to maintain continuous export readiness to the United States
Manage and maintain all food safety documentation, records, and processes required for FDA compliance
Collaborate closely with Regulatory Affairs to ensure alignment with current and emerging U.S. regulatory expectations
Lead the design, execution, and documentation of validation activities across the FSMS
Oversee validation programs including Clean-in-Place (CIP) systems, allergen cleaning and controls, and thermal process validations (e.g. pasteurisation, UHT)
Ensure validation activities are scientifically robust, risk-based, and compliant with FDA, Codex, and EU standards
Maintain validation master plans, protocols, and reports, ensuring timely review, approval, and revalidation

Fulltime

Senior GMP Quality Auditor

Proclinical is seeking a Senior GMP Quality Auditor to join a team in the UK. Th...

Location

United Kingdom , London

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Degree in Chemistry, Pharmacy, Microbiology, or equivalent
General auditing qualification: external lead auditing qualification is desirable
Proven experience in a similar role within the pharmaceutical industry
Familiarity with directives and guidelines for medical devices, sterile manufacturing facilities, and biosimilars
Strong organizational and time management skills with the ability to prioritize multiple tasks
Excellent communication skills, both written and verbal, including the ability to engage with senior management at third-party suppliers
Sound problem-solving skills and the ability to make decisions based on risk
Willingness and ability to travel globally
Proficient in working independently and collaboratively as part of a team

Job Responsibility

Mentor team members and support their professional development
Oversee the lifecycle management of approved vendors and suppliers in compliance with industry regulations
Establish and monitor KPIs, evaluating and reporting associated metrics
Manage a risk-based audit program for vendors and suppliers, excluding pharmacovigilance partners
Conduct risk analysis based on audit outcomes and collaborate with QPs and management on necessary actions
Ensure audits provide assurance for vendors and suppliers in line with EU GMP, EU GDP, or equivalent standards and marketing authorizations
Monitor and maintain CAPAs internally and with external suppliers
Maintain vendor validity within the SAP ERP system
Evaluate and interpret global regulations for audit purposes
Create, revise, and review QA documentation, including audit checklists, questionnaires, SOPs, and guidance documents

Fulltime

Senior Research Scientist microbiome assay and metaproteomics

We’re looking for a Senior Research Scientist to join the Laboratory of Prof Dan...

Location

United Kingdom , Norwich

Salary:

45450.00 - 56750.00 GBP / Year

Quadram Institute

Expiration Date

February 15, 2026

Requirements

PhD in Biochemistry, Microbiology, Molecular Biology or relevant fields
Knowledge of experimental microbiology relevant to live microbiome studies, metaproteomics and bioinformatic analysis of data
Significant previous experiences in microbiome laboratory experiments and metaproteomic

Job Responsibility

Advance function based study of the interactions of prebiotics, drugs and other xenobiotics with the gut microbiome
Utilisation of microbiome assays in precision prebiotic microbiome intervention trials aimed at promoting healthy aging
Support the Group Leader with day-to-day running of the lab, including line management of staff, overseeing budgets, and leading the scientific direction

What we offer

Family, faith and diversity friendly working arrangements
Disability Confident employer (interview guarantee for disabled applicants meeting essential criteria)
Visa application support

Fulltime

Microbiology Lead

Coca-Cola HBC

Location:
Romania , Ploiesti

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 26, 2026

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