Pharmaceutical Inspector - 3rd Shift

Corium Innovations; Grand Rapids (MI); On-site; USD 25,000 - 30,000; Full time

Benefits offered by this job

Medical, dental, vision

401(k) with company match

12 paid holidays

Paid time off for shutdown

Life insurance

Disability insurance

Employee assistance program

Job summary

Corium Innovations in Grand Rapids, MI is seeking a Pharmaceutical Inspector for the 3rd shift to inspect products and components, document production records, and support general manufacturing tasks. The role emphasizes adherence to cGMP guidelines, quality standards, and accurate labeling and inventory processes. A high school diploma or GED and GMP experience are preferred.

Qualifications

• High school diploma or GED required.
• Minimum 1 year in manufacturing environment preferred; GMP experience preferred.
• Strong attention to detail and ability to follow written instructions.

Responsibilities

• Inspects product/components to meet specifications and quality standards.
• Counts, packages and labels components and finished product per specifications.
• Completes cGMP documentation accurately.
• Performs digital inventory material transactions.
• Cleans equipment and manufacturing facility per cGMP procedures.
• Assists in other general manufacturing duties as required.

Skills

Attention to detail

Communication skills

Team player

Follow procedures

Education

High school diploma or GED

Job description

We're growing! Corium Innovations is seeking a Pharmaceutical Inspector for 3rd shift who will inspect products and/or components during and after assembly and packaging to meet cGMP product specifications and quality standards. This position also maintains accurate documentation of production and/or assembly records, following cGMP guidelines and company policies.

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:

• Inspects product/components to meet specifications outlined in documentation and quality standards.
• Counts, packages and labels components and finished product per product specifications.
• Accurately completes cGMP documentation to meet quality requirements.
• Performs digital inventory material transactions.
• Cleans equipment and manufacturing facility following cGMP procedures.
• Assists in other general manufacturing duties as required.

Qualifications:

• High school diploma or GED.
• Minimum of 1 year of experience in a manufacturing environment preferred, GMP experience preferred.
• Strong attention to detail.
• Ability to follow written instructions and procedures.
• Ability to communicate effectively.
• Ability to identify defects in components and final products as outlined in quality standards.
• Ability to accurately complete documentation.
• Strong team player.
• Ability to complete all training requirements.
• Ability to work 10pm - 6am Monday-Friday.
• 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.