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Weekend Qa Manager Jobs (NOW HIRING)

Central Point Partners

QA Manager

Denver, CO · On-site

Quality Assurance Manager The Quality Assurance (QA) Manager works as part of a dynamic team in a rapidly growing company. The QA Manager will be responsible for developing, leading and evolving the ...

FPC Decatur

Quality Assurance Manager

Houston, TX · On-site

Quality Assurance Manager Salary Range: $95K-$125K+ 12% Bonus Summary Of Job: We are seeking an experienced Quality Assurance Manager to lead quality management and continuous improvement initiatives ...

Eagle Railcar Management, LLC

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Quality Assurance Manager

Orange, TX · On-site

$85K - $95K/yr

The Quality Assurance Manager is responsible for leading the quality assurance program at the respective Eagle Railcar Services facility. The Quality Assurance Manager implements and maintains ...

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JRG Partners

Quality Assurance Manager

Mobile, AL · On-site

$90K/yr

Quality Assurance Manager - Job D escription The Quality Assurance Manager ensures all regulatory, customer, and internal quality standards are met. This role leads the QA and Sanitation teams ...

Soni Resources

QA Manager

Conshohocken, PA · On-site

$165K/yr

We are seeking an experienced QA Manager to lead quality assurance efforts in a player-coach environment , combining hands-on automation work with team leadership. This role will oversee end-to-end ...

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As of Aug 15, 2026, the average yearly pay for weekend qa manager in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 per year, depending on experience, location, and employer.
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Infographic showing various Weekend Qa Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

Quality Assurance Manager

Filtration Group Corp

Louisville, CO • On-site

$120K - $140K/yr

Other

Re-posted 16 days ago

Filtration Group rating

6.6

Company rating: 6.6 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

Job description

Overview
Molecular Products makes specialized air-treatment and gas-processing products-basically technology that helps people breathe safely in environments where air is limited or contaminated.
Provides technologies such as CO₂ absorbers, oxygen generators, and activated carbon filters for healthcare, defense, and industrial use.
We are a global leader focused on maintaining safe, breathable air in high-risk and enclosed settings.
Purpose of job
  • To evaluate QMS processes and ensure they are efficient and scalable with the growth of the business for both MPI and OC Lugo businesses.
  • To lead the maintenance and continual improvement of the QMS
  • To lead the effectiveness and compliance of MPI with ISO, ITAR and FDA requirements
  • To lead in the education of staff and ensure their knowledge of the QMS
  • To verify the quality of all products and that all required records are being maintained
Organization
  • The QA Manager will be part of Operations, reporting directly to the Business Unit Leader; any conflicts between Operations and Quality will be addressed through the Group Business Unit Leader.
  • All quality assurance and laboratory personnel will report directly to the QA Manager

Responsibilities
Scope
  • The QA Manager will have the authority to stop any production process if he/she feels that there is any issue with the quality of materials being used or produced. The QA Manager will have the authority to stop any shipments he/she feels do not meet quality requirements until the quality of the shipment can be verified.
  • The QA Manager coordinates the operation of the QA laboratory in order to fulfil its' primary function which is to provide accurate, on-time quality control services to the company and our customers, comply with all standards, keep accurate well organized records, stay aligned with corporate goals, and keep the lab operations in a state to deliver on that mission.
  • The QA Manager will, as necessary, schedule meetings and training sessions with all personnel to insure continued compliance with established quality standards.
  • The QA Manager will oversee the following processes: Internal Auditing, Customer Feedback, Change Orders/Document Control, Non-conforming Material, Deviations, Employee Training, Product Acceptance, Corrective Action and Preventive Actions, and calibration.
  • The QA Manager will establish focus groups and ensure effectiveness of said groups to drive the continuous improvement of the QMS.
  • The QA Manager will oversee the collection and reporting of product trending data to monitor for negative trends and/or process improvements.
  • The QA Manager ensures effective root cause analysis in regards to corrective actions or supplier corrective actions and recommends supplementary actions.
  • The QA Manager will schedule and conduct audits of the QMS to the ISO 9001, ISO 13485, MDSAP standards and ITAR requirements as required, including those requested by customers.
  • The QA Manager in coordination with the Logistics Manager will schedule supplier audits as necessary to insure continued supply of high quality raw materials to MPI.
  • The QA Manager has the authority to approve purchases for supporting QA activities including training, documents, and external testing up to $1000. The QA Manager has the authority to approve purchases for laboratory related expenses up to $1200, including laboratory equipment, repairs, supplies, contract laboratory testing, etc.
Measurement and review
The success of this role will be measured via the delivery of the following:
  • Maintenance of ISO 9001, ISO 13485 and MDSAP registration
  • Effectiveness of the QMS (as evidenced by successful audits)
  • Timely completion of corrective actions
  • Customer Feedback Metrics
  • Awareness and understanding of the QMS and quality standards by all staff
  • Quality Goals as defined by the Management Team
  • Compliance to company policies including EH&S, ITAR and QMS

Qualifications
  • A minimum 5 years of experience in Quality System management
  • A minimum of 5 years experience maintaining an ISO 9001, ISO 13485 and MDSAP QMS
  • A minimum of 3 years experience in conducting audits of an ISO 9001, ISO 13485 and MDSAP system
  • Bachelors degree ideally in Engineering
  • Must demonstrate a working knowledge of ITAR restrictions, Technical Data protection, and restricted visitor protocols.
  • MS Office ¾ Intermediate to Expert knowledge
  • Excellent written and verbal communication skills

Pay: $120,000 - $140,000 USD Annual + 15% annual bonus potential
Location: This position is fully onsite in Louisville CO. Travel once a quarter to the facility in PA.

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