Microbiology Specialist Job at Remedium Partners

Microscopy Specialist

We are seeking a motivated, creative, and experienced Research Scientist to join...

Location

United States , Scottsdale

Salary:

85000.00 - 125000.00 USD / Year

Envita Medical Center

Expiration Date

Until further notice

Requirements

PhD degree in biology, microbiology, life sciences, or related field with 5+ years of relevant laboratory experience
Proven in-depth expertise using darkfield microscopy to visualize cells, tumors, as well as living organisms such as bacteria and viruses
Adept at proper handling of human biological samples including infectious disease samples, preparing tissue and liquid biopsy samples for microscopic examination, slide preparation, and staining techniques
Solid experience with other microscopy and slide preparation techniques such as brightfield, fluorescence, and confocal microscopy
Proficient in molecular biology techniques such as nucleic acid extraction from tissue or liquid biopsy samples, purification, quantification, analysis, and PCR
Highly skilled in standard molecular and cellular biology techniques
Ability to learn and adapt to new technologies and platforms
Expertise in image analysis and interpretation of test results
Process and analyze patient samples
Operate, maintain, and troubleshoot lab equipment

Job Responsibility

Develop, validate, and execute workflows for imaging patient samples using darkfield microscopy and other imaging platforms
Process patient samples for isolation of cancer cells and downstream processing
Prepare blood and tissue biopsy samples for imaging analysis
Perform nucleic acid extraction, purification, and other required molecular biology protocols
Help with data collection, analysis of results, record keeping, and integration into the LIMS platform
Maintain meticulous lab records, ensuring all protocols adhere to quality control standards
Collect, prepare, and manage SOPs as well as results
Manage the use of necessary reagents and supplies
Contribute to scientific publications as needed
Perform other duties as assigned

What we offer

Medical
Life
Dental
Vision
401k

Fulltime

GMP QC Specialist, CMC

Reporting to the Director, QA Operations, the GMP QC Specialist, CMC, will be re...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

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

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

health and retirement
PTO
stock option plans

Substantive Microbiologist

An opportunity has arisen for a skilled and experienced Microbiology professiona...

Location

United Kingdom

Salary:

109725.00 - 145478.00 GBP / Year

Remedium Partners

Expiration Date

Until further notice

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

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

MLS Technical Specialist - Microbiology (Molecular Liaison)

The MLS Technical Specialist participates in all departmental responsibilities f...

Location

United States , Kansas City

Salary:

Not provided

The University of Kansas Health System

Expiration Date

Until further notice

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

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

Biomedical Scientist – Microbiology

We are excited to present an excellent opportunity for a Biomedical Scientist to...

Location

United Kingdom , Central London

Salary:

35000.00 - 50000.00 GBP / Year

Hunter Gatherer AHP

Expiration Date

Until further notice

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

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

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

Microbiology Laboratory Technical Specialist

Microbiology Laboratory Technical Specialist - Full Time - 2nd Shift. Department...

Location

United States , West Allis

Salary:

33.05 - 49.60 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

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

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

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

Fulltime

Specialist Quality Control

In this vital role, you will be part of Amgen India’s (AIN) Quality Control (QC)...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

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

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

Senior QA Specialist

The incumbent is a member of the Quality Assurance (QA) Operations team. Under t...

Location

Singapore , Tuas

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Degree in Chemistry, Microbiology, Engineering or other Science related discipline
Minimum 4 years experience (including QA roles) within the pharmaceutical industry
Compliance, regulatory or validation experience is an advantage
Strong written and oral communication skills
Technical report writing skills is an advantage
Demonstrated personal leadership, accountability, and organizational skills with proven ability to operate independently with minimal supervision
Experience working in a cross-functional, matrix environment is an advantage

Job Responsibility

Provide QA oversight to site operations (primarily Production, Quality Control, Warehouse, Engineering) to ensure products produced are in compliance with Pfizer Quality Standards (PQS) and ICH guidelines
Work with supply chain and downstream / drug product sites to ensure timely delivery of quality products
Support regulatory team to file products and address regulatory queries in an accurate and timely manner
Understand regulatory expectations and support site inspection readiness
Drive quality culture and promote GMP compliant behaviors at the site
Drive improvement of quality systems in collaboration with cross functional teams
Contribute to achieve our vision of being best in class manufacturing site, producing highest quality products in the safest way
Deploy and use Imex 'way of working' for day-to-day operations, problem solving, escalation and continuous improvements
Mentor members within the QA team

Fulltime

Microbiology Specialist

Remedium Partners

Location:
United Kingdom

Category:
Health and Beauty

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 12, 2026

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Job Posted:
March 12, 2026