Biotech Jobs at Curia- Apply for Analytical Operations Specialist Position
Curia, a global CDMO (Contract Development and Manufacturing Organization), is seeking an Analytical Operations Specialist II to join its biologics team in Hopkinton, MA. This role offers hands-on experience in analytical development for biological programs, supporting pharmaceutical and biotech projects from process development to commercialization. Ideal candidates have a background in biology, biotechnology, or analytical chemistry, experience in GMP environments, and a commitment to quality, safety, and scientific excellence.
- Job Position: Analytical Operations Specialist II
- Location: Hopkinton, MA
About the Company:
Curia is a global Contract Development and Manufacturing Organization (CDMO) with over 30 years of experience in partnering with pharmaceutical and biotech companies. Curia develops and manufactures life-saving therapies, supporting customers across drug discovery, development, and manufacturing stages. With a commitment to quality, innovation, and patient impact, Curia provides comprehensive services in biologics, small molecules, and advanced therapies. Employees benefit from a collaborative, professional culture focused on career growth, training, and making a difference in patients’ lives worldwide.
Biotech Jobs at Curia- Role:
The Analytical Operations Specialist II supports analytical development efforts for multiple biological programs, ensuring high-quality testing and documentation within a GMP environment. The role involves both hands-on laboratory work and liaison with management to maintain operational excellence.
Biotech Jobs at Curia- Key Responsibilities:
- Enroll batches in non-GMP stability programs, author protocols, obtain samples, and summarize data.
- Perform USP compendial testing of biologics, including appearance, pH, conductivity, osmolality, UV, subvisible particles, and endotoxin analysis.
- Apply aseptic techniques for bioburden testing and aliquoting in biosafety cabinets.
- Maintain laboratory operations including sample logging, ordering supplies, and creating material specifications.
- Ensure laboratory compliance with safety, quality, and documentation standards.
- Communicate effectively with management and program teams regarding results and progress.
- Exhibit safety awareness and adhere to the Chemical Hygiene Plan.
Required Qualifications for Analytical Operations Specialist:
- BA/BS in Biology, Biotechnology, Analytical Chemistry, or related field with 3 years of relevant pharmaceutical experience in biologics drug substance or product manufacturing.
OR - MA/MS in Biology, Biotechnology, Analytical Chemistry, or related field with 1 year of relevant pharmaceutical experience.
- Experience in GMP laboratory operations.
- Strong communication, organizational, and problem-solving skills.
Preferred Qualifications:
-
Direct experience in GMP Quality Control labs.
Work Schedule & Benefits:
- Full-time position with opportunities for career growth and training.
- Generous benefits including medical, dental, vision, 401(k) with matching contributions, paid vacation and holidays, and education reimbursement.
