Sterility Assurance Validation Engineer — Impact in Pharma

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

Paid volunteer time

Paid time off

Paid holidays

Job summary

Grand River Aseptic Manufacturing Inc. (GRAM) is seeking a Sterility Assurance Validation Engineer/Specialist in Grand Rapids, MI. The role involves validating cGMP equipment, supporting sterility assurance processes, and working with internal teams to ensure compliance with industry standards.

Successful candidates will have a strong background in life sciences or engineering, with at least up to 5 years of relevant experience. GRAM offers exceptional benefits from the first day of employment including medical, dental, vision, 401(k), and paid volunteer time.

Qualifications

• Up to 3 years’ related work experience in pharma/biopharma/biotech.
• 3 to 5 years’ experience for Specialist II.
• More than 5 years’ experience for Specialist III.

Responsibilities

• Support validation of cGMP equipment and processes.
• Write, review, and execute sterilization studies.
• Provide sterility assurance support to internal customers.

Skills

Knowledge of cGMPs for API facilities

Proficient in Microsoft Word, Excel, and Outlook

Education

Bachelor’s degree in Engineering

Bachelor’s degree in life sciences or related field

Job description

Grand River Aseptic Manufacturing Inc. (GRAM) is seeking a Sterility Assurance Validation Engineer/Specialist in Grand Rapids, MI. The role involves validating cGMP equipment, supporting sterility assurance processes, and working with internal teams to ensure compliance with industry standards.

Successful candidates will have a strong background in life sciences or engineering, with at least up to 5 years of relevant experience. GRAM offers exceptional benefits from the first day of employment including medical, dental, vision, 401(k), and paid volunteer time.