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Quality Technician

41105efb-bc19-43f8-b35a-09bf3b22851d
Posted 6 hours ago
Location

Eden Prairie, MN, US

Salary

$27 - $30 per hour

Contract type

Full Time

Paid Time Off

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Location: Eden Prairie, MN

Annual Bonus Opportunity up to $2,500


Evergen is a global industry-leading contract development and manufacturing organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is headquartered in Alachua, FL, and has manufacturing facilities in West Lafayette, IN; Eden Prairie and Glencoe, MN; Neunkirchen, Germany; Glasgow, UK; and Marton, New Zealand.


We are proud to be Great Place to Work® Certified in 2026, reflecting our commitment to creating an exceptional employee experience and workplace culture. Evergen currently has full-time career opportunities available across multiple locations.

Our comprehensive benefits package includes:

  • Paid Time Off (PTO)
  • 401(k) with company match
  • Holiday pay
  • Medical, dental, and vision insurance
  • Short-term and long-term disability coverage
  • Paid parental leave and much more!

Read more about this change and Evergen’s commitment to advancing regenerative medicine here: https://www.linkedin.com/company/evergenbio

The Promotional Review Specialist will manage the day-to-day operation of the promotional review process and serve as the central liaison for internal teams and external business partners submitting promotional materials for review. This role will work cross-functionally with Compliance, Marketing, Medical, Legal, Regulatory Affairs and Commercial teams to coordinate review workflows, facilitate reviewer feedback and revisions, maintain approval and lifecycle documentation, and support timely, consistent execution of the promotional review process.

RESPONSIBILITIES

  • Provides quality support for the Quality Engineering functions such as manufacturing, sterility assurance, or supplier quality.
  • Performs investigations for product or supplier nonconformance and process noncompliance issues and documents exceptions appropriately in the Corrective Action 
  • Performs CAPA investigations using problem solving methodologies and a high attention
  • to detail
  • Participates in the review and disposition of non-conforming product or controlled process
  • inputs including the Product Quality Review Board (PQRB), returns, and complaints
  • Assists in the Change Management function including maintaining relevant work
  • instructions, Standard Operations Procedures (SOPs), and other quality documentation
  • Performs product acceptance testing, quality inspections, data entry, and data corrections
  • quickly and efficiently
  • May provide support for environmental monitoring investigations, documentation of quality
  • inspections on controlled suppliers, or supports the Approved Supplier List monitoring
  • activities
  • Identifies and supports process improvement initiatives and implementation
  • Performing laboratory analysis of in-process and finished good samples of microbial growth
  • Attend meetings as requested by management
  • May support projects as a quality resource as assigned
  • Other duties as assigned

REQUIREMENTS

Education

  • High School diploma or equivalent

Experience

  • 3-6 years of experience in Quality Assurance or Quality Control
  • Additional education may substitute for experience requirement

Certification

  • No certification required

Skills

  • Strong verbal and written communication skills
  • Microsoft Office Suite, Basic Excel
  • Technical Writing

Travel

  • N/A


SAFETY


Physical Requirement

  • Move or lift objects up to 25 pounds
  • Frequent (>75%) stationary position (standing or sitting) while utilizing digital displays
  • Frequent (>75%) fine manipulation using hands and fingers (typing, opening, writing, clicking, paper sorting, etc.)


Working Environment

  • Onsite: Office environment with assigned workstation
  • Remote positions only: Home office environment with minimum distractions


More about Evergen:

Evergen provides customers across a diverse set of market segments with leading-edge expertise, scale, and flexibility across end-to-end services including design, development, regulatory support, verification and validation, manufacturing, and supply chain management. 


 Evergen is rooted in a steadfast commitment to quality, integrity, and patient safety with a focus on five key values:

  • Accountable: We own our actions and decisions.
  • Agile: We embrace change to stay ahead of the curve and evolve to drive innovation and growth. 
  • Growth Mindset: We embrace challenges as opportunities for continuous learning.
  • Customer-Centric: We prioritize customers at every touch point. 
  • Inclusive: We thrive on the richness of our diversity and ensure every voice is heard, respected, and celebrated. 

At Evergen, we are committed to fostering an inclusive workplace where we embrace the richness of our diversity and ensure that every voice is heard, respected, and celebrated. We believe that by embracing diversity and promoting inclusivity, we not only uphold our values but also strengthen our position as the CDMO of Choice in regenerative medicine solutions. We recognize that cultivating a growth mindset is essential to our success, and we are dedicated to continuous learning and improvement in our diversity, equity, and inclusion efforts. Through accountability and action, we strive to create an environment where individuals can thrive, innovate, and contribute their unique perspectives to drive our collective success.

Montagu Private Equity (“Montagu”), a leading European private equity firm, acquired RTI in 2020 and has supported the transformation of the company to its next level of potential.


#LI-Onsite




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