CrawlJobs Logo

Manager, Quality Lab

United States, San Jose 141780.00 - 166800.00 USD / Year · Job Posted December 06, 2025
Apply Position
Job Link Share

Job Description

As the leader of our quality team in San Jose, you will help define the quality requirements and process controls for our first certified aircraft, Midnight. You will help us overcome the challenge of providing airline-like levels of safety while offering urban air transportation at a price accessible to all, setting the bar for the entire nascent advanced air mobility industry. As the Quality Manager for Archer you will report directly to the Director of Supplier Quality, you will have the responsibility for overseeing the Quality Management System and quality functional support for aircraft production, flight operations, and delivery occurring in San Jose.

Job Responsibility

  • Take a key leadership role in the development and deployment of quality procedures, and standards to ensure Archer meets AS9100 and FAA requirements
  • Lead the establishment of an aircraft incoming inspection plan during the test and production phases of the program
  • Execute / Oversee the assurance process for the Midnight program incorporating risk based approach to inspection
  • Responsible for establishing and leading process quality for the purpose of improving process performance and stability through the effective deployment of process quality and statistical process control
  • Responsible for ensuring the quality lab stays within the overall quality budget requirements
  • Develop & support long- and short-term planning, policies, programs and objectives
  • Lead efforts to implement lean management systems, lean tools, and standardize key processes including materials management and quality systems
  • Collaborate and positively influence cross-functional teams to integrate quality into all business processes

Requirements

  • Bachelor's degree (or higher) in Engineering (Aerospace, Mechanical, Electrical or Industrial) with at least 5+ years’ experience leading quality teams within aerospace or other regulated industry
  • Experience hiring, leading and managing salaried & hourly employees
  • Experience with electronic MES systems and driving quality metrics to improve business performance
  • Experience leading all aspects of quality to include: QMS (Quality Management System)
  • Auditing (Internal & External)
  • 3rd Party Certification, Receiving Inspection
  • In-Process Inspection
  • Product Quality Engineering
  • FMEA (Failure Mode Effects Analysis) implementation
  • RCCA (Root Cause Corrective Action)
  • SPC implementation (Statistical Process Controls)
  • APQP (Advanced Product Quality Planning)
  • Deployment of quality inspection technologies
  • Experience overseeing and implementing AS9100 certification with an in-depth understanding of AS9102, AS9103, AS9145, and AS6500
  • Direct experience establishing and leading CAB (Corrective Action Board) & supporting MOR (Monthly Operations Review) quality reviews with senior leadership

Nice to have

  • Experience establishing real time dashboards used throughout the organization
  • Experience with flight line testing and working with the FAA during a production certification process
  • Six Sigma Black/Green Belt, AS9100 Lead Auditor or ASQ Certified Quality Manager
  • Experience with electric powertrain or aerospace composite assembly processes
  • Experience leading multiple manufacturing sites/locations
  • Experience developing complex metrology processing incorporating both CMM and scanning tools
  • Background or experience with airworthiness assignment and customer aircraft acceptance

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Manager, Quality Lab

8 matching positions

Iqf Lab Manager (Cmt Lab Manager)

Atlas is seeking a highly skilled and motivated Construction Materials Testing (...
Location
Location
United States , Loxley
Salary
Salary:
Not provided
oneatlas.com Logo
Atlas
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 7 years of combined laboratory and construction materials testing and laboratory management
  • Bachelor’s degree in Civil Engineering, Materials Science, or a related field not required but preferred
  • Extensive knowledge of AASHTO and ASTM procedures
  • Familiar with Quality Management Systems
  • Strong knowledge of CMT testing methods, equipment, and industry standards
  • Proven experience in setting up and managing a laboratory facility
  • Excellent leadership, organizational, and communication skills
  • Ability to work independently and as part of a team
  • Strong problem-solving skills and attention to detail
  • Knowledge of safety regulations and procedures in a laboratory setting
Job Responsibility
Job Responsibility
  • Laboratory Setup and Management: Design and oversee the setup of the CMT laboratory, including layout, equipment installation, and workflow optimization
  • Develop and implement quality control procedures and practices for materials testing
  • Ensure the laboratory meets all regulatory and safety standards
  • Procure and install necessary equipment and materials
  • Develop and implement standard operating procedures (SOPs) for laboratory operations
  • Testing, Analysis and Reporting: Manage and conduct testing of concrete, soils, and other CMT materials
  • Ensure accurate and timely analysis of test results
  • Maintain and calibrate laboratory equipment to ensure precision and reliability
  • Quality Assurance: Manage Accreditation compliance
  • Implement and enforce quality control procedures to ensure testing accuracy and consistency
What we offer
What we offer
  • health
  • dental
  • vision
  • life
  • AD&D
  • voluntary life / AD&D
  • disability benefits
  • leaves of absence
  • 401k
  • paid time off
Read More
Arrow Right
New

Engineering Technician III, Quality Manager

Responsible for the overall quality system and its implementation and management...
Location
Location
Kuwait , Kuwait City
Salary
Salary:
Not provided
amentum.com Logo
Amentum
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • An associate’s degree in engineering, engineering technology, physics or a related technical field from an accredited college or university, with at least ten (10) years of field experience. Includes qualification requirement OR Completion of a U.S. military precision measurement and calibration program, a precision measurement and calibration school at an accredited school, or within a specialized calibration firm, and have twelve (12) years of work experience in the calibration field with extensive experience in QA. Includes qualification requirement C
  • Demonstrated knowledge of the requirements of calibration laboratory compliance and accreditation to ISO 17025
  • Must have or be able to obtain and maintain a US Government Secret Security Clearance. NOTE: US Citizenship is required to obtain a Secret Clearance
Job Responsibility
Job Responsibility
  • Responsible for the overall quality system and its implementation and management for the KAF Metrology Program
  • Exercises independent judgment on issues concerning ISO 17025 and KAF related Quality documents
  • Performs trend analysis quarterly
  • Develops and maintains the laboratory quality manual and quality system using KAF command directives and standardized templates
  • Assessing requirements, developing and maintaining a complete QA Program for the KAFMB
  • Developing and maintaining a Quality Control program that ensures a high-quality product from all sections of the KAFMB
  • Coordinating with KAF management, QA, Laboratory Supervisors and Inspectors, Material/Production Control personnel and technicians to resolve problems and ensure an integrated effort
  • Develop, maintain, and implement a Quality Assurance Program as per ISO 17025 directives that ensures involvement of all management and technical levels in the implementation, updating and utilization of a quality-oriented program at the KAFMB labs
  • Developing a QA Program for laboratory facility and related environmental control, development, operation and maintenance
  • Assisting the Metrology Engineering Department in researching and developing a Primary Standards capability
  • Fulltime
Read More
Arrow Right
New

Quality Lab Associate III - Investigations

The MO Investigator leads the investigation of microbial out of limits that occu...
Location
Location
United States , Marion
Salary
Salary:
80000.00 - 110000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor or Master’s degree in science, preferably in Microbiology, with minimum 2 years of experience conducting root cause investigations in the pharmaceutical/medical products industry
  • Minimum of 5 years of experience in Quality Operations, Microbiology Laboratory, and/or Quality
  • Strong communication and project management skills
  • Must have thorough understanding of pharmaceutical/medical device manufacturing and current Good Manufacturing Practices and Good Documentation Practices
  • Must have good analysis, troubleshooting, and investigation skills including knowledge and understanding of problem-solving methodologies (e.g. DMAIC)
  • Must have strong technical writing skills and able to put complex thoughts and issues into writing in such a manner that can be understood by the reader
  • Must be able to interact with, and influence others at various levels in multiple departments
  • Must have knowledge of FDA quality systems regulations
  • Must have working knowledge of TrackWise system
Job Responsibility
Job Responsibility
  • Determines scope, product impact, root cause, corrective and/or preventive actions
  • Assembles cross-functional teams, conducts interviews, observes operations to complete investigations and lead process improvement CAPA projects to timely and effective closure
  • Fosters collaborative relationships focused on high-quality and timely investigations, effective corrective actions and the reduction of out-of-limit generation rate
  • Closes investigations in a timely manner to meet business and compliance needs
  • Works with minimal supervision to drive investigations to closure
  • Works with Subject Matter Experts and Quality Approvers to determine scope, identify root cause(s), and implement corrective/preventive actions
  • Manages investigation and CAPA documentation in TrackWise in compliance with Baxter practices and procedures
  • Understands and implements procedures that support implementation of CAPAs
  • Presents and defends investigations during regulatory inspections, as required
What we offer
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
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right
New

Quality Lab Associate I - Environmental Monitoring

This is where your work makes a difference. At Baxter, we believe every person—r...
Location
Location
United States , Marion
Salary
Salary:
68000.00 - 93500.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • B.S. degree in Microbiology, Biology, or related science
  • Minimum 1 year experience in Pharmaceutical/Medical Device industry preferred
  • Strong communication and project management skills
  • Possess knowledge of core manufacturing and support systems
  • Computer literate/knowledge of Microsoft office applications (Word, Excel)
  • Must have good interpersonal skills and able to work optimally and efficiently in a team-based environment
  • Proficient in the aseptic use and handling of media plates and swabs for EM sampling
  • Must be a dedicated individual who requires minimal direction
  • Attention to detail and strong organizational skills
  • Must have a basic understanding of laboratory instrumentation
Job Responsibility
Job Responsibility
  • Conduct microbiological analyses on raw materials, in-process and finished products
  • Use laboratory instrumentation and computer systems to collect and record data
  • Complete all testing, including special project / protocol testing in a timely following local procedures and cGMP regulations
  • Maintain data integrity and ensure compliance with regulatory agencies
  • Operate equipment such as SAS Air Sampler and Climet Particle Counter for the purpose of collecting air/particulate samples
  • Perform surface sample testing using plate and/or swab method
  • Collect water samples throughout the facility on a weekly/monthly basis
  • Perform weekly and monthly HEPA inspections to ensure integrity of HEPA filters in clean-rooms
  • Performs weekly Real Time Risk Assessments (RTRA) to identify potential contamination issues in clean-rooms
  • Perform IMD (Instantaneous Microbial Detection) Testing
What we offer
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
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right
New

Quality Lab Associate III - Investigations

The MO Investigator leads the investigation of microbial out of limits that occu...
Location
Location
United States , Marion
Salary
Salary:
80000.00 - 110000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor or Master’s degree in science, preferably in Microbiology, with minimum 2 years of experience conducting root cause investigations in the pharmaceutical/medical products industry
  • Minimum of 5 years of experience in Quality Operations, Microbiology Laboratory, and/or Quality
  • Strong communication and project management skills
  • Must have thorough understanding of pharmaceutical/medical device manufacturing and current Good Manufacturing Practices and Good Documentation Practices
  • Must have good analysis, troubleshooting, and investigation skills including knowledge and understanding of problem-solving methodologies (e.g. DMAIC)
  • Must have strong technical writing skills and able to put complex thoughts and issues into writing in such a manner that can be understood by the reader
  • Must be able to interact with, and influence others at various levels in multiple departments
  • Must have knowledge of FDA quality systems regulations
  • Must have working knowledge of TrackWise system
Job Responsibility
Job Responsibility
  • Determines scope, product impact, root cause, corrective and/or preventive actions
  • Assembles cross-functional teams, conducts interviews, observes operations to complete investigations and lead process improvement CAPA projects to timely and effective closure
  • Fosters collaborative relationships focused on high-quality and timely investigations, effective corrective actions and the reduction of out-of-limit generation rate
  • Closes investigations in a timely manner to meet business and compliance needs
  • Works with minimal supervision to drive investigations to closure
  • Works with Subject Matter Experts and Quality Approvers to determine scope, identify root cause(s), and implement corrective/preventive actions
  • Manages investigation and CAPA documentation in TrackWise in compliance with Baxter practices and procedures
  • Understands and implements procedures that support implementation of CAPAs
  • Presents and defends investigations during regulatory inspections, as required
What we offer
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
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right
New

Manager, Lab Support

In this role, you will be responsible for managing a team that supports the Inno...
Location
Location
Sweden , Stockholm
Salary
Salary:
Not provided
alfalaval.com Logo
Alfa Laval
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Proven leadership experience, preferably within Maintenance/ Production environments
  • Strong technical understanding of utilities and technical environments
  • Experience or knowledge in chemical handling and safety regulations
  • Strong interpersonal and change management skills
  • Ability to develop and implement structured and efficient processes
  • A holistic mindset with strong problem-solving skills
Job Responsibility
Job Responsibility
  • Lead and guide your team to deliver high-quality support for testing activities
  • Ensure center equipment, chemical handling, and facilities meet safety, quality, and sustainability standards
  • Collaborate with your team to create and improve workflows and structured processes aligned with organizational goals
  • Oversee resource allocation, including people, equipment, materials, and chemicals, to support project needs
  • Work closely with different R&D teams to integrate testing into product development
  • Ensure safe and sustainable practices, including responsible chemical management, are implemented across all center activities
What we offer
What we offer
  • Join a team of highly competent and motivated colleagues
  • Work in a technically challenging and dynamic environment
  • Fulltime
Read More
Arrow Right
New

Quality Lab Associate I - Environmental Monitoring (7pm-7am)

This is where you make a difference in our patients' safety. As a member of the ...
Location
Location
United States , Marion
Salary
Salary:
68000.00 - 93500.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • B.S. degree in Microbiology, Biology, or related science
  • Minimum 1 year experience in Pharmaceutical/Medical Device industry preferred
  • Strong communication and project management skills
  • Possess knowledge of core manufacturing and support systems
  • Computer literate/knowledge of Microsoft office applications (Word, Excel)
  • Must have good interpersonal skills and able to work optimally and efficiently in a team-based environment
  • Proficient in the aseptic use and handling of media plates and swabs for EM sampling
  • Must be a dedicated individual who requires minimal direction
  • Attention to detail and strong organizational skills
  • Must have a basic understanding of laboratory instrumentation
Job Responsibility
Job Responsibility
  • Conduct microbiological analyses on raw materials, in-process and finished products
  • Use laboratory instrumentation and computer systems to collect and record data
  • Complete all testing, including special project / protocol testing in a timely following local procedures and cGMP regulations
  • Maintain data integrity and ensure compliance with regulatory agencies
  • Operate equipment such as SAS Air Sampler and Climet Particle Counter for the purpose of collecting air/particulate samples
  • Perform surface sample testing using plate and/or swab method
  • Collect water samples throughout the facility on a weekly/monthly basis
  • Perform weekly and monthly HEPA inspections to ensure integrity of HEPA filters in clean-rooms
  • Performs weekly Real Time Risk Assessments (RTRA) to identify potential contamination issues in clean-rooms
  • Perform IMD (Instantaneous Microbial Detection) Testing
What we offer
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
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Flexible Spending Accounts
  • educational assistance programs
  • commuting benefits
  • Fulltime
Read More
Arrow Right
New

Quality Lab Senior Supervisor

This is where you make a difference in our patients’ safety. As a member of the ...
Location
Location
United States , Marion
Salary
Salary:
96000.00 - 132000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • B.S. Degree in Life Science Field (e.g. Biology, Microbiology, related)
  • Minimum of 5 years of experience or Master’s Degree in biological science with applied experience, preferably in the pharmaceutical or medical device industry
  • Knowledge of aseptic technique and microbiological testing according to FDA, cGMP, GLPs, and USP testing methodology
  • Computer skills including knowledge of Microsoft office applications (Word, Excel)
  • Able to manage multiple tasks/priorities in a timely manner
  • Able to work independently and manage time to complete assigned tasks
  • Ability to create an environment that values people, encourages trust, and open communication through feedback and recognition
  • Applicants must be authorized to work for any employer in the U.S.
Job Responsibility
Job Responsibility
  • Coordinate all activities required to occur for assigned shift responsibilities relative to the QC Laboratory including but not limited to: Personnel management
  • Conducting non-conformance investigations within TrackWise 8 for procedural non-compliances and non-conforming results
  • Assign tasks, set priorities, and ensure effective performance and development of team members
  • Conduct regular training for staff
  • Conduct ACE Check-ins with staff and additional communications as needed
  • Ensure testing is performed accurately and efficiently, following established protocols and standards
  • Oversee the accurate recording and analysis of test results, review results, and address documentation errors in accordance with procedural requirements
  • Ensure results are provided to document control within specified timeframes for release
  • Cross train in all areas of the QC Microbiology Laboratory which has staffing represented on night shift to enable troubleshooting of issues and/or guidance as necessary
  • Perform documentation review of all areas of QC Microbiology Laboratory as assigned by the Quality Manager
What we offer
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
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • Fulltime
Read More
Arrow Right