Laboratory operations associate Job at Life Science Talent (Copenhagen)

Clinical Laboratory Associate

We are looking for passionate Clinical Laboratory Associates (CLA) to be respons...

Location

United States , Menlo Park or Union City

Salary:

64178.00 USD / Year ▼

BillionToOne

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent in biology or clinical related sciences
At least 6 months of experience with molecular biology techniques in a research or clinical laboratory
Excellent attention to detail
Effective written and verbal communication skills
The ability to multitask and work independently
Previous clinical laboratory experience is preferred

Job Responsibility

Perform sample accessioning and isolation procedures according to the laboratory’s standard operating procedures
Prepare documents for equipment and personnel records
Perform and document routine maintenance of equipment
Prepare other clinical documentation as required and assigned
Clean labware, equipment, and benches
Prepare reagents required for testing
Write and review controlled documents as assigned

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
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

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

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
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
Evaluates laboratory systems, processes, procedures, and equipment as they relate to operating efficiency, effectiveness, and regulatory compliance

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
Sick time (up to 80 hours per calendar year)
Paid vacation (new hires eligible to accrue up to 120 hours)

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

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

Associate Quality Control

The Associate Quality Control will provide analytical testing support for the Qu...

Location

United States , Thousand Oaks

Salary:

66222.00 - 82012.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 2 years Quality Control experience
Associate’s + 6 months Quality Control work experience
Bachelor’s

Job Responsibility

Execution of QC Microbiology assays following assigned procedures
Analysis of analytical test results and reporting of raw data into various laboratory information management systems
Lab support activities such as management of lab consumables and equipment maintenance/work order completion
Operating specialized laboratory equipment
Daily communication and collaboration with cross-functional teams
Implementation of lab improvements to ensure an efficient and productive lab environment
Flexibility in work hours to support demand of work
occasional evening and/or weekend hours may be required

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans

Fulltime

Research Associate

Prominex Inc. is a startup molecular diagnostic company with an experienced team...

Location

United States , San Diego

Salary:

Not provided

Prominex

Expiration Date

Until further notice

Requirements

Basic knowledge of laboratory procedures, established techniques, instruments and equipment
Experience with nucleic acid amplification techniques (PCR) and nucleic acid purification procedures
Able to operate under SOPs for development purposes
Experience with lateral flow technologies
Basic understanding of Universal Precautions and Basic Lab safety
Skilled with use of word processing, spreadsheets, graphical and presentation software applications
Capable of searching scientific literature to gain information about specific topics
Bachelor’s degree in Science and minimum requirement of 2-5 years of experience in a related field
Master’s degree in Science and minimum requirement of 0-2 years of experience in a related field

Job Responsibility

Executes bench experiments
makes detailed and general observations and reports data accurately and effectively
Analyzes data and interprets results
Prepares technical reports, summaries, protocols, and data analyses
Presents and discusses results of experiments within the scientific team
Works well in a team environment by being a productive team member, suggesting creative solutions to problems and providing input to project planning
Maintains high level of professional expertise through familiarity with scientific literature
Investigates, creates and develops new methods and technologies for project advancement
Helps to troubleshoots problems and institutes corrective action
Performs a wide variety of tasks, and exhibits a wide degree of creativity and latitude

Fulltime

Senior Scientist

Merrick & Company, an employee-owned company, is seeking an experienced Senior S...

Location

United Kingdom , London

Salary:

Not provided

Merrick & Company

Expiration Date

Until further notice

Requirements

Applicant must be a U.K. Citizen
Master’s degree or higher in a science related field from an accredited program
Minimum of five (5) years of experience in laboratory operations, biosafety, & biosecurity
Previous experience in high- and maximum-containment laboratories (CL/BSL-3 or higher) is required
Must have technical knowledge of regulatory requirements regarding biosafety, HSE, ACDP, SAPO, GMO, and IATA
Ability to work on multiple projects which includes resourcing, tracking, follow-up and follow-through to project completion
Well-organized, detail-oriented, and self-motivated professional with strong verbal and written communication skills
Strong desire to work in a team environment
Flexibility/adaptability to work in a fast-paced environment
This position may require vaccination as mandated by client polices

Job Responsibility

Provide strategy, development, execution, and technical knowledge for project deliverables related to laboratory operations, biological risk identification, assessment, characterization, management, exposure assessment and control, general safety, occupational hygiene, health and environmental management, animal care and use and regulatory compliance
Ensure adherence to project quality of deliverables, products, and schedule
Address issues related to the interface of laboratory operations, compliance, and operational planning
Prepare complex studies, reports, plans, specifications, and other products for project deliverables
Support document preparation to aid clients in obtaining and maintaining regulatory registrations and permits
Support proposal development and marketing initiatives
Support leadership to ensure that project schedules and budgets are met and communicate with leadership any issues and concerns
Exercise initiative, judgment, and knowledge commensurate with the responsibilities of the position
Adopt and apply all Merrick policies and procedures and apply them on assignments
Educate clients on pertinent regulations, consensus standards, manufacturers use instructions, and best practices concerning their laboratories, operations, safety programs, hazard control systems, biocontainment, equipment, hazardous materials storage, waste treatment and disposal processes, and all associated documents and records

What we offer

Employee Owned - all eligible U.S. employees have an Employee Stock Ownership Account
Robust Employee Referral Program
Annual performance and compensation reviews
Professional Training and Development
Employee Recognition Awards
Peer Mentor Program
health insurance, dental and vision coverage, 401(k), and paid time off (PTO)

Laboratory operations associate

Life Science Talent

Location:
Denmark , Copenhagen

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 15, 2026

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