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Quality Assurance Specialist

Corium Innovations

Grand Rapids, MI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

Job description

Due to our continued growth, Corium Innovations is seeking a Quality Assurance Specialist II to provide oversight to manufacturing operations for both commercial and development projects using technical, regulatory, and cGMP knowledge. This is a unique opportunity to take on a key role with a broad range of responsibilities.
Your most Innovative career move is here!
At Corium Innovations, we’ve led the way in innovating drug delivery technologies for millions of patients whose GI systems just can’t tolerate pills, who can’t remember to take their meds as directed, or who have needle-phobia. This is only the beginning! There’s so much more to deliver, and we need YOU to do it!
Our Purpose is to create, develop and manufacture innovative healthcare products for partners that deliver superior value to patients.
Our Goal is to be the best-in-class specialty CDMO through the use of innovative technologies and superior execution.
Our Company Values are core to our positive and people-centric culture which inspires all of us to come to work every day on behalf of our people, our partners, our customers, and our patients. Through our four core values, we put people first and create opportunities to make each day better than the last.
  • Celebrate Individuals: We’re looking for talent who will celebrate the uniqueness of each of our team members by encouraging everyone to bring their authentic self to work.
  • Successful Together: We believe we’re better together, so we prioritize teamwork as we work to achieve our shared vision knowing each one of us has an important role to play.
  • Embrace Innovation: We embrace new challenges and opportunities while encouraging creative thinking and innovative solutions to best meet the needs of our people and our partners.
  • Pride in Ownership: We take pride in owning our progress and successes, feeling empowered to pursue our growth to reach our full potential. And we hope you will too!
Responsibilities:
  • Lead and participate as a team member in investigations (DEV, CA/PA).
  • Review executed operations records; identify and report errors or omissions.
  • Review documentation and release raw materials, WIP, and finished goods to next processing stage.
  • Provide troubleshooting and guidance to manufacturing shop floor employees on quality issues.
  • Serve as a Quality Assurance liaison to internal and external customers for development and commercial products.
  • Receive and execute customer complaint investigations.
Qualifications:
  • Bachelor’s Degree, preferably in a science or technical field.
  • Minimum of 5 years of related work experience.
  • Comprehensive knowledge of Quality Assurance principles, FDA cGMP regulations, FDA guidance documents, and/or regulatory submission requirements.
  • Ability to maintain accurate records.
  • Strong attention to detail.
  • Great interpersonal skills.
Benefits:
  • Highly competitive benefits program including medical, dental, vision, flexible spending accounts, life insurance, disability insurance, and employee assistance program.
  • 401(k) retirement savings account with a company match and immediate vesting.
  • 12 paid holidays.
  • Competitive paid vacation plan plus ~1 additional week of paid time off for our annual holiday shutdown.

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