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Job summary
A fast-growing biotechnology firm in Salt Lake City is seeking a Stability Coordinator to manage cGMP stability programs for a 12-month contract. This role supports the QC team, ensuring compliance with regulations and effective data management. Candidates should possess a Bachelor’s degree in a relevant field and have at least 2 years of relevant experience. Strong organizational and communication skills are critical. The position involves extensive partnership with internal teams and external organizations to meet quality assurance goals.
Qualifications
2+ years in cGMP QC/stability/analytical operations required.
Familiarity with biologics and cold-chain/accelerated stability is advantageous.
Experience supporting GMP testing/equipment qualification is a plus.
Responsibilities
Draft and maintain stability protocols per SOPs.
Plan and stage studies including sample handling.
Compile data and issue periodic stability trending reports.
Coordinate with internal teams and CROs/CDMOs.
Skills
Detail-oriented
Strong organization skills
Excellent communication skills
Data integrity principles
Knowledge of ICH Q1A–Q1F
Education
BS/BA in Chemistry, Biochemistry, or related field
Tools
LIMS/ELN
Excel/JMP
Empower
Job description
A fast-growing biotechnology firm in Salt Lake City is seeking a Stability Coordinator to manage cGMP stability programs for a 12-month contract. This role supports the QC team, ensuring compliance with regulations and effective data management. Candidates should possess a Bachelor’s degree in a relevant field and have at least 2 years of relevant experience. Strong organizational and communication skills are critical. The position involves extensive partnership with internal teams and external organizations to meet quality assurance goals.