Analytical Development Analyst II

Curia

12d • Onsite

About The Position

Build your future at Curia, where our work has the power to save lives. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives. The principal responsibility of the Analytical Development Analyst II is method development and the analysis of biological molecules including proteins, DNA and RNA. The Analyst II is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry and cell based assays. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture.

Requirements

• Bachelor’s degree in Chemistry or related field and a minimum 3 years’ relevant experience, or a Master’s degree in Chemistry or related field and a minimum 1 year relevant experience, or a Ph.D. in Chemistry or related field
• Must pass a background check
• Must pass a drug screen
• May be required to pass Occupational Health Screening

Responsibilities

• Subject matter expert for testing, troubleshooting and complex problems
• Develop and write analytical method procedures for biological assay including ELISA, cIEF, CE-SDS, HPLC/UPLC, qPCR, PA800, cell based assays
• Write analytical development reports, validation protocols and reports meeting ICH guidelines
• Perform assays, analyze data effectively and under minimal supervision.
• Perform peer data review. Provide corrections and good documentation coaching
• Enter data on form per Good Documentation Practices site policy
• Demonstrate proficiency in interpreting data sets and providing summaries to customers
• Manage workload and time to perform multiple projects effectively, and ensure all necessary paperwork is completed on a timely basis
• Maintain a detailed and accurate recording of activities and results
• Author quality investigations, change controls and data summaries.
• Understand and utilize risk assessment and root cause tools
• Track and trend data as applicable
• Lead departmental projects
• Participate in research and development team meetings to understand process changes and potential impact to assays
• Follow responsible actions regarding chemical disposal.
• Maintain compliance with all regulations at the federal, state, and local levels
• Exhibit safety awareness and safe work practices
• Participate in self-development activities and training of others

Benefits

• Generous benefit options (eligible first day of employment)
• Paid training, vacation and holidays (vacation accrual begins on first day of employment)
• Career advancement opportunities
• Education reimbursement
• 401K program with matching contributions
• Learning platform

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree