Scientist, Analytical Sciences / QC Full Time

Responsibilities:

• Manage CDMO counterparts through analytical aspects.
• Lead drug product analytical development and manufacturing.
• Provide internal and external leadership through quality events.
• Support retest and shelf-life document strategy and execution.
• Work with cross-functional teams to design control strategies.
• Author and review method development and validation documents.
• Support analytical aspects of drug substance development.
• Assist in global regulatory CMC activities and document authoring.

Requirements:

• BS or equivalent in chemistry or related discipline.
• PhD in chemistry with 1-3 years of experience.
• Experience in novel drug development analytical experience.
• Proven technical contributions in a virtual environment.
• Experience with CROs and CDMOs for drug development.
• Ability to solve analytical and QC challenges.
• Excellent organization and multi-tasking skills.
• Strong interpersonal and team collaboration skills.
• Ability to author and review methods, protocols, and reports.

Benefits:

• Equal employment opportunity for all applicants.
• Transparent recruitment process with no fraudulent requests.