Manufacturing Quality Engineer

Actalent; United States; On-site; USD 63,369 - 73,012; Full time

Benefits offered by this job

Medical, dental & vision benefits

401(k) Retirement Plan

Time Off/Leave

Job summary

Actalent is seeking a Manufacturing Quality Engineer to support quality management systems in Minneapolis, MN. This role involves ensuring compliance with regulatory standards while collaborating with design and manufacturing teams. Essential skills include quality assurance experience, risk management, and knowledge of medical device regulations.

The position emphasizes teamwork in a professional environment focused on continuous improvement and hands-on quality control processes. Candidates with 3–5 years of experience in quality assurance are preferred.

Qualifications

• 3–5 years of experience in Quality Assurance.
• Experience in the medical device industry, ideally with catheter products.
• Hands-on experience with design control for medical devices.

Responsibilities

• Act as the quality representative during engineering projects.
• Ensure compliance with Quality System Regulations in product development.
• Lead NCMR and CAPA investigations and reports.

Skills

Quality Assurance

Medical device industry experience

Risk management

Statistical analysis

Root cause analysis

Education

Bachelor of Science degree

Job description

Job Title: Manufacturing Quality Engineer

Job Description

The Manufacturing Quality Engineer supports the Quality Management System by working closely with design and manufacturing teams to ensure products meet design intent, performance requirements, and all applicable regulatory and internal standards. This role applies core quality engineering principles such as design control, process control, risk management, supplier quality, root cause analysis, statistical analysis, and continuous improvement. The engineer participates in day‑to‑day quality activities, including First Article Inspections, CAPA and NCMR investigations, change order reviews, and training, with a strong focus on medical device products, ideally catheter‑related devices.

Responsibilities

• Function as the operations quality representative during the execution of engineering projects, providing quality input and oversight throughout the project lifecycle.
• Ensure product development projects and changes to existing products comply with applicable Quality System Regulations and internal quality procedures.
• Lead and support NCMR and CAPA investigations and reports, including troubleshooting manufacturing problems and ensuring compliance with requirements.
• Collaborate with suppliers on NCMRs and supplier CAPAs to resolve quality issues and drive corrective and preventive actions.
• Participate in cross‑functional teams to review and disposition nonconforming products or components.
• Participate in cross‑functional teams to develop and maintain Product Risk Management Files, including Risk Management Plans, Risk Assessments, DFMEAs, PFMEAs, and Risk Management Reports.
• Prepare and review quality documentation with a high degree of accuracy, completeness, and effectiveness.
• Contribute to the development of Design Verification and Validation test plans and protocols, as well as Process Verification and Validation test plans and protocols.
• Provide guidance on product requirements compliance for verification and validation activities.
• Provide direction on sample size determination and statistical analysis for verification and validation testing.
• Participate in design reviews and FMEA reviews, ensuring that quality and risk considerations are fully addressed.
• Participate in complaint investigations and ensure that all investigations are thoroughly documented and compliant with procedures.
• Provide guidance to project teams on quality policies and procedures, including verification, validation, statistical methods, and design controls.
• Assist in training related to Special Work Orders, Receiving Inspection processes, and First Article Inspections as required.
• Engage in routine daily quality activities such as First Article Inspections (FAI), CAPA, NCMR, change order review, and team training.
• Support continuous improvement initiatives within manufacturing operations and quality processes.

Essential Skills

• 3–5 years of experience in Quality Assurance, including quality systems, standards, metrics, and tools.
• 3–5 years of experience in the medical device industry, ideally with catheter products.
• Alternatively, an associate’s degree with 10 years of experience in Quality Assurance.
• Experience working within a Quality Management System (QMS) in a manufacturing environment.
• Hands‑on experience with design control and process control for medical devices.
• Practical experience in risk management, including PFMEA and other risk assessment tools.
• Experience with supplier quality activities, including collaboration on NCMRs and supplier CAPAs.
• Proficiency in root cause analysis and implementation of corrective and preventive actions.
• Experience with statistical analysis methods for verification and validation testing, including sample size determination.
• Knowledge of manufacturing operations and process verification and validation.
• Ability to read and interpret engineering drawings and specifications, including geometric dimensioning and tolerancing (GD&T).
• Working knowledge of medical device regulations, including FDA 21 CFR 820 and relevant ISO standards.
• Working knowledge of new product design and development processes for medical devices.
• Strong organizational skills with the ability to prioritize workflow across multiple projects and meet established timelines.
• Effective interpersonal skills for working in cross‑functional teams.
• Ability to prepare and review technical and quality documentation accurately and thoroughly.

Additional Skills & Qualifications

• Bachelor of Science degree in Science, Engineering, Technology, or a related field is preferred.
• Experience in the catheter contract manufacturing or CDMO environment is highly beneficial.
• Experience with complaint investigation and documentation in a regulated environment.
• Familiarity with continuous improvement methodologies within manufacturing and quality functions.
• Experience participating in or leading design reviews and FMEA reviews.
• Knowledge of verification testing and sterilization validation is desirable.
• Comfort providing training on quality‑related processes such as Special Work Orders, Receiving Inspection, and FAIs.
• Ability to work effectively in a fast‑paced environment with growing project bandwidth.
• Strong communication skills to clearly convey quality requirements, findings, and recommendations to diverse stakeholders.

Work Environment

This is an onsite role based in a medical device manufacturing environment, requiring presence on‑site five days per week. The team maintains a fun, collaborative atmosphere where people work hard and also enjoy their time together as a group. Standard hours follow a Monday through Friday schedule, with an understanding of the need for flexibility at appropriate times. The culture emphasizes teamwork, cross‑functional collaboration, and continuous learning, supported by a well‑established quality team with extensive experience in the contract manufacturing and CDMO space. The facility supports hands‑on work with manufacturing operations, inspections, and validation activities, and you can expect a professional environment aligned with regulated medical device production.

Job Type & Location

This is a Contract to Hire position based out of Minneapolis, MN.

Pay and Benefits

The pay range for this position is $46.00 - $53.00/hr.

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)

Workplace Type

This is a fully onsite position in Minneapolis, MN.

Application Deadline

This position is anticipated to close on Jul 10 2026.

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 [e-mail] 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.