CrawlJobs Logo

Microbiology Laboratory Technical Specialist

advocatehealth.com Logo

Advocate Health Care

Location Icon

Location:
United States , West Allis

Category Icon
Category:
Health and Beauty

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

33.05 - 49.60 USD / Hour
Save Job
Save Icon
Apply Position

Job Description:

Microbiology Laboratory Technical Specialist - Full Time - 2nd Shift. Department: 60344 WI ACL Laboratories - WI Central Lab: Microbiology. Schedule: 2:30pm -11:00pm. Rotating 1 in 3 weekends and holidays. Hours Per Week: 40.

Job Responsibility:

  • Performs all duties of the bench staff in the specialty as determined by site need (i.e., Medical Technologist, Histotechnologist)
  • Works with the Supervisor to develop and implement quality control and quality assurance policies and procedures, directly responsible for validation of processes
  • Ensures that work is completed in a safe and efficient manner
  • Monitors laboratory safety practices and corrects hazards that exist
  • Monitors workflow and makes necessary adjustments to complete work in an appropriate time frame
  • Monitors the preventive maintenance program and regulatory compliance standards to ensure they are met
  • Participates in the inspection process
  • Provides financial evaluations as part of procedures, instrumentation, and/or reagent evaluations
  • If needed, assists the Supervisor with preparation of work schedules, timecards, and attendance functions
  • Assists supervisor with technical staff development including competency and coaching, correcting performance as needed, coordination and oversight of student and new staff training
  • Provides technical expertise to any site as needed
  • provides technical consultation to both internal and external clients
  • Reviews laboratory results and quality control for accuracy and validity
  • Documents appropriate information for quality assurance/improvement according to established protocol
  • Utilizes all required computer information systems appropriately
  • Assists in improving the quality and efficiency of laboratory procedures, policies, and processes
  • Assists in writing new technical procedures and policies and revising current procedures
  • Must be able to demonstrate knowledge and skills necessary to provide care appropriate to the age of the patients served
  • Must demonstrate knowledge of the principles of growth and development over the life span and possess the ability to assess data reflective of the patient's status and interpret the appropriate information needed to identify each patient's requirements relative to his/her age-specific needs, and to provide the care needed as described in the department's policies and procedures

Requirements:

  • Medical Technologist (MT) or Clinical Laboratory Scientist (MLS) or Histotechnologist (HTL) certification
  • American Society for Clinical Pathology Board of Certification (ASCP BOC) or equivalent
  • Bachelor’s Degree in Medical Technology, Clinical Laboratory Sciences, or Histotechnology
  • Typically requires 2 years of experience as an instrument key operator
  • In-depth knowledge of moderate and/or high complexity testing as defined by CLIA ‘88
  • Excellent interpersonal and written/verbal communication skills
  • Proficient in the use of laboratory computer systems, including use of word processing programs and spreadsheets
  • Thorough knowledge of statistics and ability to apply statistical rules/analysis to laboratory decision-making processes
  • Demonstrated ability to work in a fast-paced environment and to successfully handle multiple tasks simultaneously
  • Demonstrated organizational ability, attention to detail, and accuracy
  • Ability to work well in stressful situations, maintaining professional composure at all times
  • Ability to consistently handle multi-tasking, meet established deadlines, and recognize assignments that may be delegated
  • Ability to articulate knowledge of topics under discussion
  • Ability to build and support a highly cohesive and functional team
  • Frequently required to lift up to 10 lbs. and occasionally required to lift up to 50 lbs.
  • Must be able to sit, stand or walk most of the workday
What we offer:
  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program
  • Opportunity for annual increases based on performance
  • Premium pay such as shift, on call, and more based on a teammate's job
  • Incentive pay for select positions

Additional Information:

Job Posted:
February 04, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
Advocate Health Care - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Microbiology Laboratory Technical Specialist

Substantive Microbiologist

An opportunity has arisen for a skilled and experienced Microbiology professiona...
Location
Location
United Kingdom
Salary
Salary:
109725.00 - 145478.00 GBP / Year
remediumpartners.com Logo
Remedium Partners
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Full HCPC registration
  • Biomedical Science degree or equivalent
  • Minimum 1 year NHS experience
  • Significant experience working in a microbiology laboratory
  • Strong theoretical knowledge and practical expertise in specialist microbiology procedures
  • Experience in Quality Management Systems and risk assessment
  • Ability to work independently and lead specialist services
  • Excellent communication, organisational, and problem-solving skills
Job Responsibility
Job Responsibility
  • Provide specialist microbiology diagnostic services, including interpretation and validation of results
  • Offer expert advice to clinicians on appropriate investigations, test selection, and turnaround times
  • Lead on designated specialist areas within microbiology, working independently where required
  • Resolve complex technical, equipment, or process-related issues
  • Ensure high standards of infection control, laboratory safety, and quality compliance
  • Participate in research, service evaluation, and the introduction of new diagnostic techniques
  • Lead and supervise a section of the microbiology laboratory where required
  • Delegate tasks effectively and support the smooth day-to-day running of the service
  • Act as a mentor and supervisor for junior scientific and support staff
  • Contribute to workforce training, competency assessment, and professional development
  • Fulltime
Read More
Arrow Right

Biomedical Scientist – Microbiology

We are excited to present an excellent opportunity for a Biomedical Scientist to...
Location
Location
United Kingdom , Central London
Salary
Salary:
35000.00 - 50000.00 GBP / Year
https://hg-ahp.com Logo
Hunter Gatherer AHP
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • HCPC-registered Biomedical Scientist (Microbiology discipline)
  • Demonstrable post-registration experience in a UKAS-accredited Microbiology laboratory
  • Strong technical skills in clinical bacteriology, virology, or related disciplines
  • Experience using LIMS systems and handling sensitive patient data
  • Committed to teamwork, service excellence, and continuous improvement
Job Responsibility
Job Responsibility
  • Conduct routine and specialist diagnostic microbiology tests, including bacteriology, virology, parasitology, and mycology
  • Process a wide variety of clinical samples accurately and efficiently
  • Operate and maintain a range of microbiological laboratory equipment after competency training
  • Participate actively in internal and external quality assurance schemes
  • Support stock control, equipment evaluations, and method development initiatives
  • Adhere to laboratory policies, procedures, and UKAS accreditation requirements
  • Work collaboratively with senior biomedical scientists and multidisciplinary teams
What we offer
What we offer
  • Contributory pension scheme (up to 20% total contribution)
  • Private medical healthcare
  • 33 days annual leave (inclusive of bank holidays)
  • Season ticket loan and family-friendly benefits
  • Access to retail and service discounts
  • Clear career development pathways and training support
  • Fulltime
Read More
Arrow Right

GMP QC Specialist, CMC

Reporting to the Director, QA Operations, the GMP QC Specialist, CMC, will be re...
Location
Location
United States , Philadelphia
Salary
Salary:
Not provided
cabalettabio.com Logo
Cabaletta Bio Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in scientific discipline
  • Advanced degree preferred
  • Minimum of 5 years’ hands-on experience in biopharmaceutical technical operations, QC operations and/or quality operations
  • Minimum of 2 years’ hands-on experience in GMP laboratory environment, with specific familiarity with cell and gene therapy release assay development, performance, and qualification
  • Specific experience performing or reviewing microbiological assays, including compendial methods (sterility, endotoxin, mycoplasma assays, APS, APV and Environmental Monitoring)
  • Experience interacting with external testing laboratories preferred
  • Working knowledge of GMP and ICH guidance and both US and international regulatory requirements
  • Highly organized, effective, and proactive communicator verbally and in writing. Able to work independently to appropriately prioritize work
  • Strong team orientation and passion for continuous self-development
  • Experience in industry or in a startup industrial setting is preferred
Job Responsibility
Job Responsibility
  • GMP Compliance: Ensure that all internal laboratory activities are maintained in accordance with internal data integrity practices and standards. Ensure that external laboratory activities comply with GMP regulations and guidelines. Stay current with regulatory requirements and industry standards related to GMP
  • Batch Review / Release: Perform full batch record review of all types of investigations
  • perform appropriate quality control review of all QC data generated by third parties
  • draft, review, and approve CoA (internal/external)
  • Investigations: Identify issues of non-compliance and work directly with the third party to resolve prior to batch release. Review and approve any out-of-specification investigations in a timely manner
  • Quality Control Procedures: Develop, implement, and maintain quality control procedures to monitor and assess internal laboratory processes, as well as the processes employed by external laboratories used to generate QC data. Conduct regular reviews to identify areas for improvement and initiate corrective action(s) as needed
  • Audits and Inspections: Assist in the planning and conducting of internal audits to assess compliance with data integrity standards and approved procedures (e.g. SOPs, test methods). Support audits of external laboratories as needed
  • Assay Qualification / Validation: Review and approve assay development, qualification and validation plans, data generated and reports. Provide primary QC support for all activities
  • Documentation Management: Oversee the creation, review, and approval of laboratory documentation, including SOPs, test methods, protocols, and reports. Ensure that the documentation is accurate, complete, and in compliance with GMP requirements. Ensure all Process Development (Analytical Development and Manufacturing Sciences & Technology) related documentation and data are reviewed and archived in a timely and accurate manner
  • Training and Education: Assist in providing training and guidance to Process Development personnel on GMP principles, procedures, and compliance requirements. Ensure that all team members are informed and adhere to quality control measures
What we offer
What we offer
  • health and retirement
  • PTO
  • stock option plans
Read More
Arrow Right

Specialist Quality Control

In this vital role, you will be part of Amgen India’s (AIN) Quality Control (QC)...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Industry related Microbiology and Environmental Monitoring experience
  • Quality Control laboratory experience
  • Degree in Microbiology or other Life Science
  • High school diploma / GED and 12 years of related experience
  • Associate’s degree and 10 years of related experience
  • Bachelor’s degree and 8 years of related experience
  • Master’s degree and 6 years of related experience
  • Doctorate degree and 2 years of related experience
  • Strong technical writing skills within a highly regulated environment
  • Working knowledge of cGMP regulations, practices, and trends pertaining to Quality Control
Job Responsibility
Job Responsibility
  • Managing document requests from the global QC Network, including intake, prioritization, and tracking to completion
  • Creating, authoring, revising, and coordinating workflows for a variety of controlled document types, ensuring completion within agreed timelines and in compliance with procedural requirements
  • Collecting, organizing, and analyzing data from multiple repositories (e.g., LIMS, electronic laboratory notebooks) to support document management activities
  • Facilitating information gathering and alignment across the QC Network and cross-functional partners to support document updates and process harmonization
  • Driving project deliverables to ensure timely and high-quality completion of assigned tasks and initiatives
  • Supporting issue identification and resolution, collaborating effectively across sites and functions to maintain operational continuity
  • Ensuring all controlled documents meet Amgen’s quality standards and comply with cGMP, safety, and other applicable regulatory requirements
  • Ensuring all assigned training requirements are completed, current, and compliant with cGMP standards
  • Identifying opportunities for continuous improvement to ensure alignment in document structure, formatting standards, and data retrieval/compilation practices across the network
Read More
Arrow Right

MLS Technical Specialist - Microbiology (Molecular Liaison)

The MLS Technical Specialist participates in all departmental responsibilities f...
Location
Location
United States , Kansas City
Salary
Salary:
Not provided
kansashealthsystem.com Logo
The University of Kansas Health System
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor of Science
  • High School Graduate
  • Meets the CLIA requirements for high complexity testing required
  • Medical Laboratory Scientist (MLS) - American Medical Technologists (AMT) within 180 Days
  • Technologist in Molecular Biology (MB (ASCP))
Job Responsibility
Job Responsibility
  • Analyzes patient, control and proficiency testing specimens and records results in a timely manner according to laboratory policy
  • Assists with departmental management tasks including, but not limited to the following: a) Maintains an adequate inventory of all supplies and reagents as assigned. b) Schedules and coordinates departmental staffing as assigned. c) Participates in departmental financial planning and oversight with the supervisor/manager. d) Contributes to content included in competency training and reviews
  • Coordinates quality assurance and quality improvement activities for the department
  • Ensures compliance with regulatory requirements and maintains a laboratory of constant readiness
  • Ensures all departmental policies and procedures are kept up to date
  • Ensures compliance with regulatory, accreditation, safety and hospital standard, policies and procedures
  • Instructs, orients and mentors students, employees, residents, patients and other health care providers as applicable
  • Completes continuing education and submits appropriate documentation where applicable
  • Oversees calibration, maintenance, troubleshooting and quality control for instrument issues in addition to the review and management of the appropriate documentation
  • Provides oversight for the review and correlation of results to each other and with the patient's condition recognizing abnormal results and critical/alert values
  • Fulltime
Read More
Arrow Right

Microbiology Specialist

An exciting opportunity has arisen for a Specialist Doctor in Microbiology to jo...
Location
Location
United Kingdom
Salary
Salary:
Not provided
remediumpartners.com Logo
Remedium Partners
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Full GMC registration with a licence to practise
  • Eligibility to work in the UK
  • MBBS or equivalent medical qualification
  • FRCPath is Essential
  • RCPath Part 2 examination completed
  • Minimum 1 year NHS experience
  • Experience working within a Clinical Microbiology laboratory at a Speciality Doctor level or equivalent
  • Significant postgraduate experience in microbiology or a related speciality
  • Demonstrated clinical judgement, risk management, and decision-making ability
  • Ability to prioritise workload and recognise when to seek senior input
Job Responsibility
Job Responsibility
  • Contribute to the delivery of a comprehensive microbiology service, including bacteriology, virology, mycology and parasitology
  • Provide clinical advice and interpretation of laboratory results to clinicians across hospital and primary care settings
  • Attend ward rounds, including Intensive Care Unit rounds, to support management of complex infections
  • Use clinical knowledge and laboratory data to guide diagnosis, investigation, and treatment decisions
  • Participate in MDT meetings, incident reviews, and root cause analyses where required
  • Participate in the 24/7 microbiology on-call rota and achieve autonomous working within 3 months
  • Act as an active member of the Infection Prevention and Control team
  • Support outbreak investigation, infection control management, and action planning to reduce healthcare-associated infections
  • Liaise with infection control teams regarding alert organisms and emerging risks
  • Contribute to daily laboratory operations and ensure compliance with UKAS standards
Read More
Arrow Right

Manager, Process Development and Automation

The Manager, Process Development and Automation provides leadership support to t...
Location
Location
United States , Redwood City
Salary
Salary:
124000.00 - 200000.00 USD / Year
exactsciences.com Logo
Exact Sciences
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's Degree in Engineering, Technology, Molecular Biology, Clinical Laboratory science, Chemical, biological, Electronics, or related field and 2 years’ experience as outlined in the essential duties
  • or Associates Degree in a Microbiology field or Engineering Science and 4 years’ experience as outlined in the essential duties in lieu of Bachelor's degree
  • 2+ years in a role with progressively increasing responsibilities such as laboratory management, quality and control, lead technologist, or technical specialist
  • 8+ years’ experience in process development, laboratory automation, service engineering, laboratory setting, or related industry as outlined in the essential duties
  • Successful track record of leading projects holistically from inception to successful implementation with cross-functional participation in a matrixed environment
  • Proficient in computer aided design software (SolidWorks) or statistical analysis programs (JMP), Microsoft Office Word, Excel, PowerPoint, and similar software
  • Working knowledge of regulatory requirements to make sure the laboratory is in compliance with all applicable laws and regulations, including applicable CLIA, CAP, California, New York (CLEP), and other requirements
  • Experience in the design, development, and implementation of solutions comprised of integrated automated and manual workflows, including software components in a highly regulated environment (ISO 13485 or 21 CFR Part 820, or cGMP using 21 CFR Part 210, 21 CFR Part 211)
  • Understanding and application of user requirements, system requirements, risk assessments, trace matrices, FMEA, etc. translating into a successful track record in understanding complex end-user applications, collecting and clearly documenting end-user needs, and translating those into clear, concise, and testable requirements
  • 1+ years in a leadership role with staff and team accountability
Job Responsibility
Job Responsibility
  • Provide leadership on best practices for the development of processes and products in a regulated environment
  • Lead the team in continuous improvement projects and support other areas’ needs dependent on demand
  • Coach, mentor, and raise the team's ability to deliver and exceed expectations while creating opportunities for team member development
  • Consistent demonstration of exceptional leadership qualities
  • Effectively manage, support, and guide your team
  • Serve as a resource for employees by sharing and knowledge transfer of best practices for experiment design and execution
  • Ensure that any incoming support requests from outside of the normal channels are properly routed
  • Ensure that assigned support requests from cross-functional project teams or business units are being actively addressed
  • Assist and coordinate training methodology and training documentation in conjunction with other leadership
  • Provide mentoring and technical guidance to PDA engineers and scientists
What we offer
What we offer
  • Paid time off (including days for vacation, holidays, volunteering, and personal time)
  • Paid leave for parents and caregivers
  • A retirement savings plan
  • Wellness support
  • Health benefits including medical, prescription drug, dental, and vision coverage
  • Bonus eligibility
  • Fulltime
Read More
Arrow Right

BQA Technical Specialist - Transfusion and Transplant

The Biological Quality Assurance Technician III is responsible for performing a ...
Location
Location
United States , Norcross, Georgia
Salary
Salary:
Not provided
werfen.com Logo
werfen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree/Science (BS/BA) from four-year college or university
  • or equivalent combination of education and experience
  • 1+ years’ experience in a highly Regulated/GMP environment
  • 3-4 years of experience in Environmental Microbiological laboratory setting including experience in laboratory techniques
Job Responsibility
Job Responsibility
  • Reviews data generated by the BQA Department
  • Ensures all department employees follow applicable laboratory SOPs, OSHA regulations and cGMP regulations
  • Assists Biological Quality Assurance Supervisor in assessing compliance gaps and implementing corrective actions
  • Ensures employee training is documented and completed in a timely manner
  • Performs laboratory tests in BQA when necessary
  • Assists Biological Quality Supervisor in assigning tasks to BQA personnel
  • Assists Biological Quality Supervisor in collecting monthly departmental metrics and quarterly metric data
  • Ensures microbiological testing, investigation and documentation is performed in a timely manner
  • Performs data entry of test results into database
  • Performs and interprets calculations as needed
Read More
Arrow Right
Jobs by Category
Art and Entertainment Jobs Banking Jobs Call Center Jobs Construction Jobs Consulting Jobs Customer Service Jobs Education Jobs Energy Jobs Finance Jobs Gastronomy Jobs Health and Beauty Jobs Hospitality and Tourism Jobs Human Resources Jobs Insurance Jobs IT - Administration Jobs IT - Software Development Jobs Legal Jobs Logistics Jobs Manufacturing Jobs Marketing, Digital Marketing, SEO, SEM Jobs Media Jobs Nursing Jobs Office Administration Jobs Pharmacy Jobs Physical Work Jobs Public Relations Jobs Public Sector Jobs Purchasing Jobs Quality Control Jobs Real Estate Jobs Research and Development Jobs Sales Jobs
Job Positions Jobs by Country
United States Jobs United Kingdom Jobs India Jobs Canada Jobs Australia Jobs Germany Jobs Ireland Jobs Poland Jobs
Company
Blog About Us Contact
Follow Us
Facebook
X (Twitter)
LinkedIn
Instagram
CrawlJobs Group
ITFlashcards AllDevBlogs
© 2026 CrawlJobs Ltd. All Rights Reserved
Terms & Conditions Privacy Policy