Microbiology Team Leader Job at CK Group (Wokingham)

Quality Lab Associate II - Group Leader

This is where you make a difference in our patients’ safety. As a member of the ...

Location

United States , Marion

Salary:

68000.00 - 93500.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. degree in Sciences: Biology or Microbiology preferred
Minimum 3 years experience in a Quality Control Laboratory, Environmental Monitoring Lab, or Microbiology Lab
Solid understanding of Environmental Monitoring
Computer literate/knowledge of Microsoft office applications (Word, Excel)
Attention to detail and strong organizational skills
Must have advanced understanding of laboratory instrumentation
Good documentation skills and knowledge of GDPs (Good Documentation Practices)
Exhibits writing and document review proficiency
Able to handle multiple tasks/priorities
Strong knowledge of BLAS, BAxLIMS (or equivalent lab system) and TrackWise

Job Responsibility

Perform Environmental Monitoring tests such as surfaces, viable air, non-viable air, air pressures, etc.
Maintain laboratory instruments to ensure proper working order and troubleshoot malfunctions when needed
Follow laboratory safety procedures to ensure compliance or to make improvements as needed
Monitor operational procedures in technical environments to ensure conformance to standards
Operate lab equipment such as SAS machines, CLIMETs, etc.
Review samples received, logs samples, and enter data into computer database
Responsible for general housekeeping of laboratory and test suites
Sustain a clean and safe work environment applying 6S principles
Perform routine laboratory and safety audits
Serve as mentor to Quality Laboratory Associate (QLA) I and II positions

What we offer

Support for Parents
Continuing Education/Professional Development
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

New

Pilot Plant Digital Process Engineer

Pepsi Lipton, a joint venture between Unilever and PepsiCo, combines 125 years o...

Location

United Kingdom , Sharnbrook

Salary:

Not provided

Unilever

Expiration Date

Until further notice

Requirements

Degree in Engineering, Food Technology, or equivalent apprenticeship and experience
Experience supporting pilot plants, process development, or manufacturing environments
Comfortable working with data and digital tools to improve operations (e.g. electronic batch records, dashboards, data visualisation in Excel/Power BI or similar)
Experience coordinating change implementation in a live operational environment: stakeholder alignment, risk assessment, documentation/SOP updates, training, and change adoption
Ability to manage multiple programs of work at any given time, with a keen eye for detail and rigor
Strong communication skills
A strong team player who can also work independently as required
Strong coordination and stakeholder management skills across internal and external interfaces
Working knowledge of equipment servicing, operational planning, and health & safety requirements
Experience with HACCP and Foods safety appreciated

Job Responsibility

Act as the process development leader to ensure On Time in Full (OTIF) delivery of projects including process design, laboratory and pilot plant prototypes and scale up trials
Lead the scoping, implementation and running of ‘non-standard’ or novel pilot plant operations for new innovations, involving cross-functional interaction with R&D, Technical Project Leads, Supply Chain, Microbiology, Site Safety etc., creating new processes and protocols to support novel workstreams
Lead digital enablement of pilot plant trials, including digitising workflows and automating data capture, ensuring data quality and adoption by users
Lead the process safety implementation for all Pilot Plant equipment, ensuring compliance with HSE and Unilever standards
Plan and coordinate equipment inspections, servicing, and remedial work with internal teams and external service providers to enable effective execution of pilot plant activities
Propose, prioritise, and implement continuous improvement opportunities for pilot plant processes and operations using data-led problem solving (e.g. root cause analysis), standardisation, and practical trials
Own the implementation of agreed improvements: develop requirements, coordinate stakeholders, validate in the pilot plant, update SOPs/training, and track benefits (safety, quality, cost, speed, reliability)
Deputise as Group Safety Advisor to the Pepsi Lipton team at Colworth, attending regular meetings with the Site Safety Team and rolling out site wide initiatives as required
Support the Pilot Plant Manager in identifying and implementing future-fit processing capabilities required to deliver the JV’s innovation and growth strategy
Support Pilot Plant Food Safety agenda, including HACCP creation and implementation

What we offer

competitive salary and pension scheme
annual bonus
subsidised gym membership
discounted staff shop
shares
flexible and hybrid working environment
family-friendly and inclusive workplace

Fulltime

Environmental Manager

This is a senior, site‑based leadership opportunity within a well‑established an...

Location

United Kingdom , Liverpool

Salary:

48000.00 GBP / Year

The People Co.

Expiration Date

Until further notice

Requirements

Degree qualified in a relevant scientific discipline (e.g. food science, microbiology, chemistry or similar)
Proven experience in a quality leadership role within food, feed or FMCG manufacturing environments
Strong laboratory background with hands‑on experience in microbiology, PCR methods and aseptic techniques
Demonstrable experience managing ISO‑based management systems and regulatory audits
Working knowledge of environmental management systems, ideally ISO14001
Confident and credible leader with the ability to influence, coach and develop cross‑functional teams
Highly organised, detail‑focused and comfortable operating in a fast‑paced, regulated environment
A proactive problem solver with a strong commitment to continuous improvement and sustainability

Job Responsibility

Lead all site quality assurance, laboratory and environmental compliance activities
Manage and develop QC laboratory operations, ensuring scientific integrity across microbiological, PCR and analytical testing
Maintain and continuously improve integrated management systems aligned to ISO9001, ISO14001, ISO45001, UFAS, FEMAS and FAMI‑QS
Own internal and external audit programmes, ensuring ongoing audit readiness and timely closure of non‑conformances
Act as the site expert for HACCP, VACCP and TACCP, maintaining robust feed safety, defence and vulnerability frameworks
Oversee non‑conforming product management, root cause investigations and CAPA implementation
Manage site‑wide document control systems in line with quality and compliance policies
Lead environmental management systems, ensuring compliance with permits, legislation and regulatory requirements
Monitor and report on environmental KPIs, including energy, waste, water and emissions
Drive environmental and sustainability initiatives focused on waste reduction, efficiency and continuous improvement

Fulltime

Food Safety and Quality Auditor-Sr. leader

The Food Safety and Quality Sr. Leaders role is part of the PFNA Corporate Quali...

Location

United States , Plano

Salary:

80200.00 - 134250.00 USD / Year

Pepsico

Expiration Date

Until further notice

Requirements

Bachelor's degree required in Chemistry, Food Science, Microbiology, Engineering or related field
Quality and Food Safety background preferably in field manufacturing for at least 5 years, with strong understanding of food safety regulatory requirements and core PFNA quality and food safety programs
Able to travel 50 to 60% and support the PFNA Network (USA, Canada, and Mexico)
must have a valid passport
Authorized to work in the US, and able to obtain a Canadian work permit as needed
Must be PCQI trained or able to successfully complete PCQI training
Understanding of applicable food regulations: FSMA, cGMP, HACCP, Food Safety Standards in accordance with FDA, USDA, CFIA, etc.
Strong systematic problem-solving skills and demonstrated aptitude for structured root cause analysis with demonstrated ability to identify critical data, develop corrective actions, and drive issue resolution
Strong written and verbal communication skills with ability to influence at all levels, including senior leadership
Agile, self-starter with the ability to work with independently in scheduling, planning and managing competing priorities in a fast-paced environment

Job Responsibility

Lead the monitoring and verification of compliance to the PFNA Quality and Food Safety Policies and Standards across internal and contract manufacturing facilities through effective execution of QAS Audits, ensuring consistency and calibrated assessment
Lead close-out discussions with the site
Establish and maintain effective communication with plants assigned for auditing and manage schedule to ensure robust and efficient completion of these audits
Evaluate trends, identify systematic gaps and recurring themes across the QFS Management Systems to proactively develop and implement strategies to strengthen processes and overall performance across all PFNA facilities
Prepare, distribute management reports for the audits and specific program details, and share updates on corrective action progress and strategies to leadership
National ownership and SME of assigned Quality and Food Safety Management Systems and strategic point assignments
effectively collaborate with cross-functional teams across the HQ QFS, R&D, MCOE, and the field teams to develop or enhance PFNA standardization of policies, protocols, procedures, work instructions, job-aids, training content, etc. for these systems
Support training, education and capability-building initiatives that strengthen quality and food safety performance and culture across PFNA
Provide leadership in systematic problem solving and project management to address QFS issues
develop and drive sustainable improvement strategies and deliver effective change management

What we offer

Bonus based on performance and eligibility target payout is 8% of annual salary paid out annually
Paid time off subject to eligibility, including paid parental leave, vacation, sick, and bereavement
Medical, Dental, Vision, Disability, Health, and Dependent Care Reimbursement Accounts
Employee Assistance Program (EAP)
Insurance (Accident, Group Legal, Life)
Defined Contribution Retirement Plan

Fulltime

Fsqa Microbiology Technician

The Microbiology Technician (Micro Tech) will be responsible for conducting micr...

Location

United States , Toluca

Salary:

Not provided

Ajinomoto Foods North America, Inc.

Expiration Date

Until further notice

Requirements

A Bachelor of Science (B.S.) degree in Microbiology or Food Technology, Food Science or related field of study required
Broad experience in food manufacturing Food Safety and Quality Assurance and/or food plant production operations, processes, and policies strongly preferred
Certifications in HACCP, SQF, or through ASQ and other professional quality associations are preferred
Must be able to pass quarterly proficiency testing for microbial analysis
Understanding of a micro lab process is strongly preferred
Demonstrated laboratory technique to perform serial dilutions, maceration of sample matrices, and plating technique required
Must possess good analytical, investigative and problem solving skills as well as the ability to integrate activities in the processing environment to cause and effect for bacteriological risk assessments and root cause analysis
Good working knowledge of Root Cause Analysis (i.e. 5Y, Ishikawa). Lean Manufacturing, Kaizen, PDCA, DMAIC and other quality tools strongly desired
Strong communication skills (reading, writing, verbal) are essential to interface with various levels of plant management, co-workers, and suppliers
A high level of organizational, mathematical, and recordkeeping skills required

Job Responsibility

Perform required microbiological tests and apply the related technological knowledge to the implementation and maintenance of bacteriological testing and quality assurance programs
Orchestrate the collection of environmental, ingredient and finished product samples for bacteriological testing as needed
Maintain a current and comprehensive knowledge of microbiological testing and analysis procedures
Assist or independently conduct raw material/ingredient hazard analysis and risk assessments that may require microbial analysis, Certificates of Analysis, or export certification
Inspect equipment and facilities for cleaning deficiencies and other food safety issues
Participate on the positive swab investigative team as the leader, investigator or swab tech and maintain all records required for investigations
Assist in the training or instruction of laboratory personnel, and monitor assigned bacteriological tests
Ensure proper maintenance and operation of all bacteriological equipment, Good Laboratory Practices (GLPs) and maintain the cleanliness of the laboratory at all times
Prepare and maintain necessary records and reports and keep leadership advised on all technical matters within the facility pertaining to microbiological procedures, bacteriological analyses reports, etc.
Responsible for updating and maintaining the laboratory manual with all current policies and procedures, including the environmental site program and all related Corporate FSQA policies and procedures

Fulltime

Validation Manager

The validation department performs sterilisation validation activities to ensure...

Location

Ireland , Dun Laoghaire

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree with 5+ years of experience in Validation, Engineering
BS degree with 7+ years of experience in Validation, Engineering, Microbiology or Quality

Job Responsibility

Provide leadership and guidance to the validation team, with clear goals and expectations for the day-to-day activities for Validation, Re-Qualification and Periodic Review programs
Support Operations from a Validation perspective to deliver and maintain equipment in a qualified state in the most efficient manner possible
Develop and ensure internal policies, procedures and practices associated with maintenance of the Site Validation Master Plan and Requalification Plans specific to area of responsibility
Responsible for managing and co-ordinating the aseptic process simulation program, including aseptic intervention review, protocol and summary report review, MES hold time support
Collate and report on relevant validation data and metrics
Provide validation support for Amgen’s quality management system, including change control, deviation and CAPA processes
Participate and deliver regulatory filings and RTQ’s for validation
Provide expert technical validation support to meet site objectives, comprising of the full validation lifecycles process
Work on moderately complex to complex problems, where analysis of situations or data requires in-depth evaluation of various factors
Writes and/or implements, owns and approves changes to controlled documents (e.g., SOPs, Specifications, Master Protocols, etc.) as needed

Head of Quality Control

Location

United Kingdom , Dundee

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

Bachelor's degree in Science (Chemistry
Pharmacy
Biology) or equivalent experience
MSc. in Science, Pharmacy or Chemical Engineering, Pharmaceutical Technology or equivalent experience
Minimum 5 years experience leading a QC laboratory function within a Pharmaceutical business with advanced knowledge of relevant cGMP requirements
Experience in various analytical techniques, including method development, validation and transfer, wet chemistry and instrument techniques, chromatography systems and microbiological testing
Well-developed leadership skills, with a proven track record of leading teams, performance management, and coaching
Excellent interpersonal, written and verbal communication skills
High energy and commitment to company values
Commitment to continuous improvement and driving efficiency

Job Responsibility

Key member of Site Leadership Team (SLT). Works with Site Senior Leadership Team to develop site strategy, implement site performance KPI’s, and translate these into specific annual performance goals
Overall responsibility for Argenta’s Quality Control performance including testing of starting materials, finished products, stability samples, validation samples, data review and investigations
Implements safe and GMP compliant working practices in the function, and ensures team perform their duties accordingly
Lead the development of Argenta’s Quality Control systems, ensuring on time delivery of valid results
Drive staff engagement and a positive culture within the Quality Control department to achieve high-performing results
Grow, develop and support your leaders and extended analytical staff
Demonstrate leadership on quality, compliance and HS&E culture
Management of QC budget
Drive improvements in operational quality performance to enhance the customer experience and minimise the 'cost of poor quality'
Provide QC support for analytical method transfers and Validation, ensuring a smooth introduction of new analytical methods, timely generation of data and ensure transfer documentation (protocols and report) are appropriately supported

Fulltime

Site Leader - Project Manager

Comecer is seeking a skilled and customer-focused Site Leader - Project Manager ...

Location

United States , Raleigh; Philadelphia

Salary:

100000.00 - 125000.00 USD / Year

ATS Automation Tooling Systems Inc.

Expiration Date

Until further notice

Requirements

Bachelor's degree in Engineering, Nuclear Medicine, Microbiology, or related field
5 - 7 years of relevant professional experience
PMP certification preferred
Experience with PKO meetings and Project Execution Planning
Strong cross-functional collaboration skills under pressure and tight deadlines
Highly organized, detail-oriented, and process driven
Fluency in English (Italian language skills a plus)
CRM experience and strong understanding of customer documentation requirements
Excellent time-management and ability to manage multiple complex projects
Proficiency with Microsoft Project, Excel, Outlook, Word, PowerPoint

Job Responsibility

Plan, coordinate, and oversee installation and commissioning activities to meet project deadlines
Manage budgets, cost tracking, progress reporting, and contract documentation
Coordinate all North American project commitments in alignment with Comecer SpA
Support SAT, IQ/OQ, validation, and both warranty and non-warranty service needs
Maintain strong customer communication and satisfaction throughout the project lifecycle
Prepare quotations and assist with pre-order meetings as needed
Coordinate travel for Comecer and ATS personnel
Travel frequently, including extended on-site support
Identify, assess, and mitigate project risks
Manage project schedules, resources, and labor/material budgets

Fulltime

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Microbiology Team Leader

Job Description

Job Responsibility

Requirements

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