Laboratory Operations Supervisor Jobs

New

Laboratory Operations Supervisor

Responsible for the operation of their laboratory area in accordance with establ...

Location

United States , Social Circle

Salary:

86500.00 - 135960.00 USD / Year

BioLife Plasma Services

Expiration Date

Until further notice

Requirements

Have earned a doctoral, master's, or bachelor's degree in a chemical, biological, clinical, or medical laboratory science, or medical technology, or nursing from an accredited institution
Or have earned an associate degree in a chemical, biological, clinical, or medical laboratory science, or medical laboratory technology, or nursing from an accredited institution
Ability to read and follow Standard Operating Procedures (SOPs) and to maintain complete and accurate records
Demonstrate work history of above-average performance and attendance
Excellent interpersonal skills and communication skills, including written, verbal, and oral presentations
Result-oriented with the ability to adapt to changing priorities
Attention to detail and organizational skills with analytical and problem-solving skills
Proficiency in the use of personal computers and software programs, including Microsoft Word, Excel, and PowerPoint
Ability to stand up for 6-8 hours
Ability to lift, carry, and pull up to twenty-five (25) pounds

Job Responsibility

Provides day-to-day supervision of all laboratory operations and moderate or high complexity testing performance in their laboratory area
Functions as a supervisor for testing personnel performing high and moderate complexity testing
Organize and prioritize workloads and assignments in conjunction with donor center requirements
Responsible for maintaining reagent and consumable inventory
Performs annual employee performance reviews and employee counseling
Performs and reviews pre-analytical staff training and competency assessments
Ensures proper training is received under the oversight of the Operations Manager and the CLIA Laboratory Director
Provides technical assistance to staff, operations, and donor centers in laboratory-related issues
Must be accessible to testing personnel at all times testing is performed to provide on-site, telephone, or electronic consultation to resolve technical problems
Performs NCMR, ENC, and CAPA functions

What we offer

Medical, dental, vision insurance
401(k) plan and company match
Short-term and long-term disability coverage
Basic life insurance
Tuition reimbursement program
Paid volunteer time off
Company holidays
Well-being benefits
Up to 80 hours of sick time per calendar year
Up to 120 hours of paid vacation (new hires)

Fulltime

Lab Supervisor - Microbiology

Are you an experienced clinical laboratory professional looking for leadership o...

Location

United States of America , Tampa

Salary:

Not provided

Labcorp

Expiration Date

Until further notice

Requirements

Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or a non-traditional Associate’s degree that meets local regulatory
Minimum 5 years of experience as a Technologist/Technician
FL State Clinical Laboratory Supervisor license required
Strong working knowledge of CLIA, CAP and relevant state regulations
Understanding of laboratory operations as well as policies and procedures
Proficient with Laboratory Information Systems and Microsoft Office
Strong communication skills
both written and verbal
High level of attention to detail with strong organizational skills
Comfortability making decisions in a changing environment

Job Responsibility

Supervise the day to day operations of the Microbiology department
Ensure laboratory tests are accurately performed and results are reported in a timely manner
Directly supervise, train, and mentor laboratory personnel of the department
Monitor daily workflow in the lab and schedule adequate assay coverage
Responsible for ensuring all shifts in the department are properly staffed
Research and resolve any production errors while escalating when necessary
Engage in continuous process and service level improvements
Ensure all equipment is being properly maintained through Quality Control
Prepare and maintain Quality Assurance records and documents
Evaluate new process improvements and make appropriate recommendations

What we offer

$10,000 sign on bonus
Medical
Dental
Vision
Life
STD/LTD
401(k)
Paid Time Off (PTO) or Flexible Time Off (FTO)
Tuition Reimbursement
Employee Stock Purchase Plan

Fulltime

New

Center Supervisor - Technical Consultant

Every day, the donors you meet will motivate you. The high-quality plasma you co...

Location

United States , Kennesaw

Salary:

22.19 - 30.51 USD / Hour

BioLife Plasma Services

Expiration Date

Until further notice

Requirements

High school diploma or equivalent
Cardiopulmonary Resuscitation (CPR) and AED certification
Frequent bending and reaching
Ability to walk and stand for entire shift
Frequent lifting to 32 pounds
Occasional lifting to 50 pounds
Fine motor coordination
Depth perception
Ability to monitor equipment from a distance
Pro-longed glove wear required due to potential exposure to bloodborne pathogens

Job Responsibility

Oversee employee performance and scheduling
Lead Inventory Control efforts and lead in operational efforts
Work with donors to resolve concerns
Analyze opportunities specific to non-conforming events
Perform all tasks for Medical History, Phlebotomy, and Sample Processing areas
Foster teamwork, communicate and resolve conflicts
Oversee the general management of employees assigned to the production areas

What we offer

Retirement benefits
Medical/dental
Family leave
Disability insurance
Short-term incentives
401(k) plan and company match
Tuition reimbursement program
Paid volunteer time off
Company holidays
Well-being benefits

Fulltime

Quality Control Supervisor

This is a senior-level position responsible for overseeing and supporting the wo...

Location

United States , Brookfield, Connecticut

Salary:

Not provided

Greenfield Global

Expiration Date

Until further notice

Requirements

Bachelor’s or master’s degree in chemistry, biochemistry, or a related field
Previous experience in a QC or quality role
3+ years of experience in supervisory or leading role
Strong supervisory, leadership, strategic thinking, and problem-solving skills
Excellent communication and organizational skills, with an ability to effectively communicate complex concepts to diverse stakeholders
Ability to manage multiple priorities under tight deadlines
Effective problem-solving and troubleshooting skills, with the ability to identify and address issues promptly
Excellent communication skills, both written and verbal, allowing for clear and concise reporting and collaboration with team members
Ability to work independently with minimal supervision while being a proactive and reliable team player

Job Responsibility

Conduct routine and non-routine analyses of raw materials, in-process samples, final products, and stability samples for product release
Utilize various analytical testing techniques such as Gas Chromatography (GC), UV-Visible spectroscopy, titrations, and other relevant methods
Provide guidance, support, and mentorship to foster professional growth and development within the team
Monitor compliance with established procedures, protocols, and regulatory requirements
Represent the QC department in cross-functional meetings and project teams
Review and revise quality control protocols and test plans to align with industry standards
Planning, scheduling, and coordinating analytical testing activities
Monitor the generation of analytical data by the QC team to ensure accuracy, integrity, and compliance
Assist the QC team in resolving technical problems related to instrumentation, method development, or other analytical issues
Interacts with internal and external customers to ensure proper sampling, reporting, and resolution of questions and concerns

What we offer

Formal and informal training opportunities
Comprehensive health and dental benefits
Income protection: short- and long-term disability coverage, life insurance, paid personal sick time
Vacation time exceeding industry standards
Company funded retirement savings program with individual contribution opportunities
Meaningful and challenging work
Curated intentional culture focused on growth and development, engagement, and communication

New

Accessioner

We are looking for a detail oriented Accessioner to be responsible for assisting...

Location

United States , Union City

Salary:

21.12 USD / Hour

BillionToOne

Expiration Date

Until further notice

Requirements

Student in pursuit of a Bachelor's Biology degree or related life sciences degree
Laboratory experience within the last year preferred
Able to integrate and apply feedback in a professional manner
Strong attention to detail
Able to manage daily specimen processing needs with high emphasis on quality
Able to analyze and problem solve basic issues that impact test performance
Strong computer skills preferred
Able to proactively communicate consistently, clearly, and honestly

Job Responsibility

Perform specimen receipt and accessioning according to the laboratory’s standard operating procedures
Maintain equipment according to the laboratory’s standard operating procedures
Clean labware, equipment, and benches
Prepare documents and binders for equipment and personnel records
Document all corrective actions taken when test systems deviate from the established performance specifications
Perform and document routine preventative maintenance
Prepare reagents required for laboratory preparation
Communicate effectively with coworkers and non- laboratory personnel
Report all concerns of accessioning quality and/or safety to the Laboratory Director, Supervisor, or Safety Officer
Participate in inspection preparation activities

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Free daily on-site lunches provided from top eateries
Latest and greatest hardware (laptop, lab equipment, facilities)
A variety of perks on campus (state of the art gym, restaurant)
Free on-site EV charging (compatible with all EVs, including Tesla)

Fulltime

Quality Lab Associate I

Conduct microbiological analysis, perform endotoxin and particulate matter testi...

Location

United States , Marion

Salary:

56000.00 - 77000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. degree in Microbiology, Biology, or related science
2-5 years of experience or Master’s Degree in biological sciences with 0-3 years experience, preferably in the pharmaceutical or medical device industry
computer literate/knowledge of Microsoft office applications (Word, Excel)
proficient in quality based computer systems such as LIMS, POMS, Endoscan-V software, Sampler Sight Pharma, and AS400
attention to detail and ability to prioritize multiple tasks
proficient in the operation of laboratory instrumentation and equipment such as laminar flow hoods, micro-pipettors, pH meters, analytical balances, and instruments used to perform particulate matter and endotoxin testing
good documentation skills and knowledge of GDPs (Good Documentation Practices)
knowledge of aseptic sampling and testing techniques and microbiological testing according to FDA, cGMP, GLPs and USP testing methodology
must be able to communicate effectively with supervisors and peers
must be experienced in executing general microbiology procedures

Job Responsibility

Prepare samples and perform endotoxin testing on raw materials, solution, and water for bioburden
perform particulate matter testing on solution
perform daily pH meter, balance, and pipette verification
perform daily Honeywell automated temperature checks and manual temperature monitoring
perform peptidoglycan and gel clot testing as needed
manage reagent inventory
generate monthly trend reports
calibration of micro-pipettes, analytical balance, water bath, dry heat bath, depyrogenation ovens, light obscuration particle counters and spectrophotometer
responsible for daily lab upkeep including cleaning, glassware washing and depyrogenation, supply replenishment, syringe and endotoxin prep
assist in method validation and protocol testing as needed

What we offer

Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
short-term and long-term disability insurance
Employee Assistance Program
childcare benefits

Fulltime

Information Management Coordinator

Full-time Information Management Coordinator position available in Maddington WA...

Location

Australia , Maddington

Salary:

76515.00 - 90000.00 AUD / Year

11 Recruitment

Expiration Date

Until further notice

Requirements

Bachelor qualification in Business, Information Management, Project Administration or related discipline
Minimum 3 years’ experience in information coordination, data management or administrative roles
Experience working in construction, engineering, laboratory services or field-based operations
Strong understanding of information management processes, documentation control and compliance requirements
High level of accuracy, attention to detail and organisational skills
Strong communication and stakeholder coordination capabilities
Ability to manage multi-site workflows, competing priorities and time-sensitive data tasks
Proficiency in Microsoft Office, digital filing systems and operational documentation tools

Job Responsibility

Maintain accurate testing records, sampling logs and project documentation, ensuring timely submission of results to engineers and supervisors for analysis and reporting
Collect, verify and transfer concrete and materials testing data between multiple project sites across WA, ensuring high standards of accuracy and timeliness
Manage operational information systems, including electronic filing structures, version control and document standardisation to support auditing and compliance requirements
Coordinate with site supervisors, foremen, engineers and field technicians to support smooth testing procedures, timely communications and adherence to project schedules
Follow strict on-site safety protocols and regulatory guidelines to ensure safe and compliant data collection, documentation handling and reporting practices
Manage logistical planning for sample data movement, scheduling and route optimisation across multiple testing locations to support operational efficiency
Prepare and update internal reports, testing summaries and procedural documentation, communicating key information to relevant stakeholders to support operational decision-making
Support continuous improvement of information management processes, recommending system and workflow enhancements to improve accuracy, efficiency and compliance

What we offer

superannuation

Fulltime

Laboratory Technician Separations

The Separation laboratory within the QC laboratories of Johnson & Johnson Innova...

Location

Netherlands , Leiden

Salary:

2965.00 - 3200.00 EUR / Month

Randstad

Expiration Date

August 20, 2026

Requirements

Good written and oral communication skills in English
MLO / Associate or Bachelor’s degree in Life Sciences, Biology, Chemistry, Biochemistry, or comparable
Pro-active, able to work independently as well as in a team, flexible and organized
GMP / GLP experience is beneficial

Job Responsibility

Training on and understanding basic testing and laboratory practices
Providing support to the laboratory by performing operational tasks such as equipment maintenance and calibration, preparation of samples and reagents, document management
Generating results data, analyzing data, and reviewing with peers and supervisor
Delivering test activities in line with the schedule and lab priorities with a good record of first-time testing
Displaying knowledge of products manufactured at specific location and some understanding of the QC methods relative to product quality

What we offer

Opportunities to develop yourself
A workplace at an international organization
Full compensation for public transport
A pleasant working environment
A full time job
5.5% ADV allowance on top of salary

Fulltime

Laboratory Operations Supervisor

BioLife Plasma Services

Location:
United States , Social Circle

Category:
Research and Development

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 26, 2025

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