QC Technician (Medical Device)

Actalent; Saint Paul (MN); Vor Ort; USD 62.000 - 79.000; Vollzeit

Benefits dieser Stelle

Medical, dental, vision, and life保险

401K with company match

Profit sharing

Zusammenfassung

Actalent is seeking a Quality Control Technician to support process and product quality testing in a fully on-site role in Saint Paul, MN. You will prepare equipment, samples, and materials for analysis, conduct measurements, and manage batch records and nonconformance investigations.

The ideal candidate has 4+ years in a regulated industry, experience with third-party labs or contract testing labs, and a science-based degree.

Qualifikationen

• 4+ years of quality experience in a regulated industry (medical device, pharmaceutical, cosmetic, aerospace, food).
• Ability to follow Standard Operating Procedures (SOPs) and demonstrate a quality mindset.
• 1+ years of experience in investigation, technical reports, and analysis.

Aufgaben

• Perform incoming, in-process, final, and finished product inspections.
• Conduct measurement and verification activities using calibrated inspection equipment.
• Review manufacturing documentation, supplier-provided data, and Certificates of Analysis.
• Verify product labeling, packaging, and acceptance criteria.
• Identify, document, and control nonconforming materials and products.
• Maintain quarantine areas and segregate returned products to prevent unintended use.
• Prepare samples, submit them for analysis, collect and analyze data, and interpret results.
• Perform environmental monitoring of cleanrooms.
• Collect, prepare, and submit samples to various labs.
• Verify and analyze test results.
• Prepare and mix chemical formulations for production use.
• Perform in-process quality control tasks and maintain equipment maintenance records.
• Conduct daily pre-operational QC checks of passivation chemistry.
• Perform package visual inspection, seal strength, and integrity testing.
• Review sterilization certificates for full release.
• Engage in QC investigations and corrective action plans (CAPAs).

Kenntnisse

Quality control experience

Investigation & reports

Ausbildung

Associates or Bachelors degree in science

Jobbeschreibung

Quality Control Technician

Device Industry | Non-Contract | Long-term Growth

As a Quality Control Technician, you will play a pivotal role in supporting process and product quality testing. Your responsibilities will include preparing equipment, samples, and materials for analysis, as well as performing environmental monitoring in cleanrooms. You will also partner with third-party testing laboratories and manage batch record reviews, non-conformance investigations, and data entry.

Responsibilities

• Perform incoming, in-process, final, and finished product inspections.
• Conduct measurement and verification activities using calibrated inspection equipment.
• Review manufacturing documentation, supplier-provided data, and Certificates of Analysis.
• Verify product labeling, packaging, and acceptance criteria.
• Identify, document, and control nonconforming materials and products.
• Maintain quarantine areas and segregate returned products to prevent unintended use.
• Prepare samples, submit them for analysis, collect and analyze data, and interpret results.
• Perform environmental monitoring of cleanrooms.
• Collect, prepare, and submit samples to various labs.
• Verify and analyze test results.
• Prepare and mix chemical formulations for production use.
• Perform in-process quality control tasks and maintain equipment maintenance records.
• Conduct daily pre-operational QC checks of passivation chemistry.
• Perform package visual inspection, seal strength, and integrity testing.
• Review sterilization certificates for full release.
• Engage in QC investigations and corrective action plans (CAPAs).

Essential Skills

• 4+ years of quality experience in a regulated industry (medical device, pharmaceutical, cosmetic, aerospace, food).
• Ability to follow Standard Operating Procedures (SOPs) and demonstrate a quality mindset.
• 1+ years of experience in investigation, technical reports, and analysis.

Additional Skills & Qualifications

• Associates or Bachelors degree in science.
• Experience in the medical device industry.
• Experience with third-party sterilization labs or contract testing labs.
• 6+ months of sterilization/environmental monitoring experience in a regulated environment.

Work Environment

This position is fully on-site operating from 8:00 AM to 4:30 PM, Monday through Friday. The role is primarily focused on quality control functions (80%) with the remaining time dedicated to documentation tasks (20%).

Job Type & Location

This is a Permanent position based out of Saint Paul, MN.

Pay And Benefits

The pay range for this position is $62400.00 - $79040.00/yr.

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.

• medical, dental, vision and life insurance
• 401K, with company match of up to 4%
• profit sharing

Application Deadline

This position is anticipated to close on Oct 28, 2026.

Workplace Type

This is a fully onsite position in Saint Paul,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 [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.