Validation Laboratory Supervisor Job at BorgWarner (Blonie)

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

Validation Laboratory Supervisor

Our Client is a global product leader delivering innovative and sustainable mobi...

Location

Poland , Błonie

Salary:

Not provided

Advisory Group TEST Human Resources

Expiration Date

Until further notice

Requirements

Master degree in Electrical/Electronic/Mechanical Engineering
Fluency in English
Minimum 8 years of engineering experience in preferably in validation or design engineering within the automotive or related industry
Good knowledge of validation and testing principles and manufacturing processes
Familiarity with industry standards and testing protocols for automotive components
Proven experience in leading technical teams
Experience in working with global organizations
Good project management skills
Strong ability to assess and mitigate technical risks throughout the project lifecycle
Strong leadership and team management skills

Job Responsibility

Lead, coach, and develop a team of validation engineers and technicians
set goals, manage performance, skills, and hiring
Plan, execute, and report validation projects for automotive power electronics, ensuring alignment with program milestones and customer deadlines
Drive the validation process across the full product development cycle (V-model), from concept to production launch
Oversee validation lab infrastructure, test benches, equipment procurement, commissioning, calibration, and maintenance
Analyze test data against requirements and provide technical guidance to design teams
ensure complete and compliant documentation
Ensure compliance with quality standards (IATF 16949, ISO 17025), Lean principles, and 8D problem-solving methodologies
Collaborate closely with global engineering teams and cross-functional stakeholders to support safe, on-time, and high-quality product launches
Support budgeting, resource planning, continuous improvement, and achievement of cost and quality objectives

What we offer

Private Medicover medical care for the employee and their family
Co-financing for the sport card Multisport
Possibility to join the PZU insurance
Flexible working hours
Salary adequate to skills and experience
Co-financing for holidays
Hard and soft training, language courses

New

Validation Laboratory Supervisor

Our Client is a global product leader delivering innovative and sustainable mobi...

Location

Poland , Błonie

Salary:

Not provided

Advisory Group TEST Human Resources

Expiration Date

Until further notice

Requirements

Master degree in Electrical/Electronic/Mechanical Engineering
Fluency in English
Minimum 8 years of engineering experience in preferably in validation or design engineering within the automotive or related industry
Good knowledge of validation and testing principles and manufacturing processes
Familiarity with industry standards and testing protocols for automotive components
Proven experience in leading technical teams
Experience in working with global organizations
Good project management skills
Strong ability to assess and mitigate technical risks throughout the project lifecycle
Strong leadership and team management skills

Job Responsibility

Lead, coach, and develop a team of validation engineers and technicians
set goals, manage performance, skills, and hiring
Plan, execute, and report validation projects for automotive power electronics, ensuring alignment with program milestones and customer deadlines
Drive the validation process across the full product development cycle (V-model), from concept to production launch
Oversee validation lab infrastructure, test benches, equipment procurement, commissioning, calibration, and maintenance
Analyze test data against requirements and provide technical guidance to design teams
ensure complete and compliant documentation
Ensure compliance with quality standards (IATF 16949, ISO 17025), Lean principles, and 8D problem-solving methodologies
Collaborate closely with global engineering teams and cross-functional stakeholders to support safe, on-time, and high-quality product launches
Support budgeting, resource planning, continuous improvement, and achievement of cost and quality objectives

What we offer

Private Medicover medical care for the employee and their family
Co-financing for the sport card Multisport
Possibility to join the PZU insurance
Flexible working hours
Salary adequate to skills and experience
Co-financing for holidays
Hard and soft training, language courses

New

Senior Clinical Laboratory Scientist

The Senior Clinical Laboratory Scientist will be responsible for performing mode...

Location

United States , Madison

Salary:

69000.00 - 122000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Associate degree in a laboratory science (chemical or biological science) or medical laboratory technology from an accredited institution or equivalent laboratory training and experience as defined: 60 semester hours or equivalent from an accredited institution that, at a minimum, includes either 24 semester hours of medical laboratory technology courses, OR 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology, and 12 semester hours of chemistry, biology or medical laboratory technology in any combination
3+ years of high complexity clinical testing experience in a clinical laboratory setting
Demonstrated strong professionalism and leadership skills
Demonstrated intermediate level project management skills
Demonstrated strong technical skills and professional working knowledge of job industry
Demonstrated ability to perform the Essential Duties of the position with or without accommodation
Authorization to work in the United States without sponsorship

Job Responsibility

Perform moderate and highly complex laboratory tests, procedures, and analyses according to the laboratory’s standard operating procedures with minimal supervision
Perform, review, and document laboratory quality control procedures
Identify potential problems, determine potential solutions, and take appropriate action in order to maintain a high level of quality in test processes and results
Achieve and maintain competency on laboratory tasks
Participate in research, validation, and/or implementation of new procedures and/or technologies
Maintain stringent standards for quality, by identifying, investigating, correcting, and documenting any issues which might adversely impact the quality of test results and/or employee safety, and communicating these to the appropriate management representatives as necessary for resolution
Determine appropriate time allocation between daily test processing needs and project needs in a high quality, efficient and effective manner with minimal direction
Demonstrate and maintain effective communication with internal employees, managers, customers, and cross-functional teams
Model behaviors that promote high productivity, quality and maintaining TAT
Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork

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

BQA Technical Specialist - Transfusion and Transplant

The Biological Quality Assurance Technician III is responsible for performing a ...

Location

United States , Norcross, Georgia

Salary:

Not provided

werfen

Expiration Date

Until further notice

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

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

Medical Laboratory Scientist II

Baptist Health is looking to add a highly motivated and skilled Medical Lab Scie...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

Valid Medical Technologist - Generalist license in the State of Florida before hire
Associate's Degree
2 years Medical Technologist Experience
Licensed Medical Technologist or Licensed Clinical Laboratory Technician

Job Responsibility

Processing and collecting specimens
Working in the LIS
General clerical duties in the general (main) lab
Maintaining expertise and performing technical, specimen collection/processing, LIS, general department, and clerical functions
Maintaining records of performance as defined in the SOP manuals
Performing all responsibilities without on-site supervision
Supervising MLTs as General Supervisor
Serving as Charge Technologist in the absence of other lab supervisors or MTs
Instructing new employees and students

What we offer

$6,000 Sign-On Bonus Offered
Relocation Assistance Available

Fulltime

Analyst 1

Results oriented to produce high quality defensible analytical data, safely and ...

Location

Canada , Mississauga

Salary:

Not provided

Bureau Veritas Certification CZ, s.r.o.

Expiration Date

Until further notice

Requirements

Post-Secondary school education or equivalent experience
Demonstrated success in the role of a Laboratory Technician
Sound knowledge of sample handling procedures to ensure continuity and integrity of samples through compliance with laboratory procedures and quality assurance protocols
Knowledge of, and experience with laboratory Occupational Health and Safety practices to handle hazardous materials by taking the necessary precaution and using the appropriate PPE
Excellent manual dexterity, record keeping, calculations and problem solving abilities
Flexible to perform varying duties to accommodate changing priorities
Accurately follows Standard Operating Procedures (SOP’s) and instructions
Detail oriented with accurate record keeping skills
Good time-management, communication, multi-tasking and priority setting skills
Strong computer skills

Job Responsibility

Review task board to plan and organize daily work
Follow Standard Operating Procedures (SOP’s) when conducting following work: Perform sample preparation and procedure prior to analyses
Analysis of results. Where applicable, this may include statements of conformity or opinions and interpretations
Identify any non-routine samples and seek guidance on procedures for handling
Prepare standards and reagents and ensure adequate supplies are available by monitoring quantities
Ensure a high level of accuracy in sample preparation and analysis
Operate and maintain all necessary instruments and equipment to complete tasks
Assess and correct problems with all laboratory operations according to SOP guidelines and ISO 17025 regulation criteria
Meet quality and TAT specifications required by the client and ensure samples are analyzed within holding time requirements
Identify and document all known sample deviations, non-conformances, and/or process deviations and report to the Supervisor and or Manager

Fulltime

Lead Clinical Laboratory Scientist

Join a team of brilliant, passionate innovators who wake up every day determined...

Location

United States , Union City

Salary:

228788.00 USD / Year ▼

BillionToOne

Expiration Date

Until further notice

Requirements

Bachelor's degree in the chemical, physical or biological sciences
Minimum of 4 years of CLS experience in a clinical setting (molecular and/or high-complexity laboratory experience preferred)
A current California Clinical Laboratory Scientist License that meets requirements for Testing Personnel under CLIA regulations (42 CFR, part 493) (ASCP, CGMBS or generalist license is required)
Hands-on training and experience with manual molecular biology protocols, including DNA extraction, PCR, and automated liquid handlers
Advanced knowledge of Google Docs, Word, Excel, basic statistics and familiarity with LIMS systems and Next-Generation Sequencing
Strong attention to detail and ability to work flexibly and well under given timeframes.
Self-starter and dynamic team player with excellent verbal and written skills.

Job Responsibility

Lead clinical laboratory daily supervision in alignment with company values and mission
Hold General Supervisor delegation and responsibilities including oversight and support of day-to-day operations, scheduling, and troubleshooting
Manage CLIA direct reports including licensed and/or unlicensed staff (CLS, Clinical Laboratory Assistants)
Contribute to continuous process improvement projects including tech transfer, troubleshooting, training, and validations
Perform clinical laboratory assays to provide data for diagnosis, treatment, and prevention of disease
Perform quality control studies to ensure the accuracy of clinical data
Verify instrument performance by checking and calibrating specific lab instruments and documents data

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

Validation Laboratory Supervisor

BorgWarner

Location:
Poland , Blonie

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 18, 2026

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