Jobs in the United States

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Added 9 mins ago
Test Technician II
Novanta Corp
Bedford, MA
High School diploma or its equivalent, or an Associate degree in Electrical Engineering/Technology, and/or related areas and/or minimum of 2-3 years working experience in manufacturing…
Added 9 mins ago
Test Technician II
Novanta Corp
Bedford, MA
High School diploma or its equivalent, or an Associate degree in Electrical Engineering/Technology, and/or related areas and/or minimum of 2-3 years working experience in manufacturing…
Added 9 mins ago
Validation Engineer II
AAIPharma Services Inc
Pepperell, MA
BA/BS in technical or science related field of study. Candidates with an HSD/GED, technical training, or an Associate's degree combined with mechanical aptitude or relevant industry…
Added 55 mins ago
Materials Coordinator Inventory Control Specialist II
Peterson Farms Inc
Ellington, CT
Associate’s degree from a two-year college in a related field, preferred.
Added 2 hours ago
F-15 Mission Systems Software Engineer (Associate, Experienced, & Senior)
The Boeing Company
Berkeley, MO
The Boeing Company is looking for a Software Engineer (Associate, Experienced, & Senior) to join the F-15 Mission System Software Development Team located in Berkeley, MO. This position…
Added 3 hours ago
BM
Associate II, Shop Floor Quality Assurance Cell Therapy
Bristol Myers Squibb
Devens, MA
- $35.45 to $42.95 USD / hour
…oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, and Supply Chain…
Added 3 hours ago
Pharmacy Technician II - Sterile Compounding
Tufts Medicine
Boston, MA
Assists in keeping the Pharmacy neat and clean by caring for equipment and cleaning after compounding prescriptions, manufacturing bulk medications, unit dosing, etc.
Added 4 hours ago
Technician II - Commercial and Regulated - Monday-Thursday, 9:00pm - 7:30am
INTEGRATED DNA TECHNOLOGIES, INC.
Coralville, IA
A Technician II is a skilled manufacturing technician who is responsible for development and manufacturing of products tailored to a customer’s specific requirements. This position requires…
Added 5 hours ago
KU
Machine Operator - 1st Shift
KPR US LLC
Deland, FL
- $17 USD / hour
The Associate II, Assembly plays a key role in the manufacturing process of Cardinal Health medical products. The Associate II, Assembly operates multiple machines at once and performs…
Added 5 hours ago
Administrative Associate II (AWO Secretary) - Warren Correctional Institution
Adult Correction
Warren County, NC
Reporting directly to the Associate Warden of Custody Operation at a medium custody male correctional facility, this position is responsible for providing administrative assistance and…
Added 5 hours ago
Associate II, Quality Assurance (Night Shift)
RESILIENCE US INC
Fairfield, OH
…We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more…
Added 11 hours ago
QC Lab Technician II
BD (Becton, Dickinson and Company)
Mebane, NC
Minimum of 2 years’ experience in current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), or medical device Quality Assurance role. (Associate’s degree in quality,…
Added 11 hours ago
Automation Engineer I/II (MES)
Novo Nordisk
Clayton, NC
May consider an Associate’s degree in engineering or related field from an accredited university with a minimum of five (5) years of engineering experience in process-based manufacturing,…
Added 11 hours ago
KM
Inspector II
Kurt Manufacturing
Minneapolis, MN
- $26.29 to $35.05 USD / hour
At Kurt Machining our employee experience and ability to solve complex manufacturing challenges set us apart. We provide precision CNC-machining services utilizing state-of-the-art…
Added 11 hours ago
KM
Inspector II
Kurt Manufacturing
Minneapolis, MN
- $26.29 to $35.05 USD / hour
At Kurt Machining our employee experience and ability to solve complex manufacturing challenges set us apart. We provide precision CNC-machining services utilizing state-of-the-art…
Added 11 hours ago
CNC Machinist II
Kurt Manufacturing
Minneapolis, MN
At Kurt Machining our employee experience and ability to solve complex manufacturing challenges set us apart. We provide precision CNC-machining services utilizing state-of-the-art…
Added 11 hours ago
CNC Machinist II
Kurt Manufacturing
Minneapolis, MN
At Kurt Machining our employee experience and ability to solve complex manufacturing challenges set us apart. We provide precision CNC-machining services utilizing state-of-the-art…
Added 11 hours ago
CNC Machinist II
Kurt Manufacturing
Minneapolis, MN
At Kurt Machining our employee experience and ability to solve complex manufacturing challenges set us apart. We provide precision CNC-machining services utilizing state-of-the-art…
Added 11 hours ago
CNC Machinist II
Kurt Manufacturing
Coon Rapids, MN
…reputation and allowed us to expand into a variety of other manufacturing sectors including 5-axis vises, workholding towers, automation and quality control. Kurt Workholding also provides…
Added 11 hours ago
CNC Machinist II (2nd Shift)
Kurt Manufacturing
Minneapolis, MN
At Kurt Machining our employee experience and ability to solve complex manufacturing challenges set us apart. We provide precision CNC-machining services utilizing state-of-the-art…
Added 12 hours ago
Quality Associate II
Baxter Healthcare Corporation
Round Lake, IL
Analyze manufacturing, laboratory, engineering, and quality-system data to identify facts, evaluate evidence, and develop well-supported conclusions.
Added 12 hours ago
CP
Materials Control Associate III
Catalent Pharma Solutions LLC
Harmans, MD
- $26.44 to $31.25 USD / hour
We have an opportunity for a Material Control Associate III to join our team. In this role, you will support GMP materials control and warehousing operations for a Phase II/III biopharma…
Added 12 hours ago
Distribution Associate II
Catalent Pharma Solutions LLC
Kansas City, MO
We have an opportunity for a Distribution Associate II to join our team supporting clinical trial projects through accurate picking and packing of clinical site and depot shipments. This…
Added 12 hours ago
CP
Associate II, Materials Control
Catalent Pharma Solutions LLC
Harmans, MD
- $21.63 to $26.44 USD / hour
We have an opportunity for a Material Control Associate II to join our team. In this role, you will support GMP materials control and warehousing operations for a Phase II/III biopharma…
Added 13 hours ago
CT
Quality Assurance Associate II - Night Shift
Capricor Therapeutics
United States
- $75,000 to $90,000 USD / year
This is an overnight (graveyard) shift role supporting off-hours GMP manufacturing. As a Quality Assurance Associate II at Capricor, you will serve as the primary Quality representative…

Actalent

Quality Engineer

Eden Prairie, MN, United States

$43 to $52 USD / hour

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Job details

Pay: $43 to $52 USD / hour
Posting language: English
Posted: Nov 4, 2026

Original job description

Job Title: Lead Quality EngineerJob DescriptionThe Lead Quality Engineer will oversee day-to-day quality systems for a Class II medical device within a small, collaborative team in the Twin Cities. This role manages the Quality Management System (QMS), including CAPAs, change reports, continuous improvement initiatives, and test method validations for on-market products. The position focuses on post-market quality and quality assurance, while offering the opportunity to grow into design assurance responsibilities and gain hands-on leadership experience in a smaller medical device organization.

Responsibilities

Oversee and manage the Quality Management System (QMS) for Class II medical devices, ensuring compliance with applicable standards and regulations.
Lead and maintain Corrective and Preventive Action (CAPA) processes, including investigation, root cause analysis, implementation of corrective actions, and effectiveness verification.
Review and manage change reports and quality documentation to ensure accurate, compliant, and timely updates to quality records.
Drive continuous improvement activities focused on enhancing safety, improving quality cycle times, and reducing lead times to minimize waste.
Lead the implementation and effectiveness evaluation of continuous improvement systems and methodologies across the quality function.
Develop, conduct, and control production processes in collaboration with manufacturing teams and quality inspectors to ensure products meet specifications and quality standards.
Improve measurement and process capability through activities such as gage R&R, test method validation (TMV), statistical process control (SPC), and design of experiments (DOE).
Initiate and manage nonconforming product or material review board activities, including disposition decisions and follow-up actions.
Support post-market quality activities for on-market products, including monitoring product performance and implementing quality improvements.
Collaborate closely with manufacturing and other cross-functional development teams to support product and process improvements.
Provide day-to-day guidance and oversight to a quality associate, helping to manage workload, priorities, and professional development.
Work alongside another quality engineer and report to the director of quality, contributing to a cohesive and high-performing quality team.
Participate in audits and quality control activities to maintain robust quality assurance practices.
Support and potentially expand into design assurance responsibilities, contributing to risk management and design-related quality activities as experience grows.

Essential Skills

35 years of experience as a Quality Engineer in a regulated environment.
At least 3 years of hands-on experience managing and executing CAPA processes.
Minimum of 3 years of experience working within a formal Quality Management System (QMS).
At least 5 years of experience in the medical device industry, preferably with Class II devices.
Strong knowledge of quality engineering principles, including quality control and quality assurance in a manufacturing environment.
Experience with test method validation (TMV), gage R&R, statistical process control (SPC), and design of experiments (DOE).
Demonstrated ability to lead continuous improvement initiatives focused on safety, quality, and waste reduction.
Experience with audits and compliance activities related to medical devices.
Proven ability to collaborate with manufacturing and cross-functional teams to improve processes and product quality.

Additional Skills & Qualifications

Exposure to or experience in design assurance is a plus, with the potential to grow into a dedicated design assurance role.
Experience supporting post-market quality activities for on-market products.
Ability and interest in gaining management experience by overseeing and mentoring a quality associate.
Strong analytical and problem-solving skills with a focus on root cause analysis and data-driven decision-making.
Effective communication skills for working with quality, manufacturing, and other internal teams.
Motivation to work in a smaller medical device company environment with opportunities for broader responsibility and career growth.

Work EnvironmentThe role is based onsite in an office located in Eden Prairie, working Monday through Friday. The quality team is small and collaborative, currently consisting of a director of quality and a quality associate, with this position joining as the third team member. The Lead Quality Engineer will work closely with another quality engineer, the associate, and cross-functional teams such as manufacturing and development. After initial training, there may be some flexibility in work arrangements. The environment offers exposure to a broad range of quality activities, opportunities to gain leadership experience, and close collaboration across departments within a growing medical device organization. Job Type & LocationThis is a Contract to Hire position based out of Eden Prairie, MN. Pay and BenefitsThe pay range for this position is $43.00 - $52.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & LocationThis is a Contract to Hire position based out of Eden Prairie, MN. Application DeadlineThis position is anticipated to close on Nov 18, 2026. Workplace TypeThis is a fully onsite position in Eden Prairie,MN.About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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More about this job

Skills

Quality control systems
Leadership
Quality assurance procedures
Medical devices
Regulatory compliance
Root cause analysis
Documentation
Process improvement
Control production
Statistical process control
SPC
Quality control
Quality assurance
Risk management
Engineering principles
Improve business processes
Coaching
Problem solving
Decision making
Communication skills
Collaboration

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