Analytical Development Analyst II

Analytical Development Analyst II – Hopkinton, MA 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. 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 401(k) program with matching contributions Learning platform Essential Job Duties 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, and 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 applicableLead 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 Education, Experience, Certification, & Licensures 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 Other Qualifications Must pass a background check Must pass a drug screen May be required to pass Occupational Health Screening Pay Range $76,000‑$95,300/yr. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer. #J-18808-Ljbffr