QC Analyst II

Why Join Bend Bioscience?

Mission And Culture

At Bend Bioscience, we Advance Health Through Innovation by developing and manufacturing therapies that improve patients' quality of life. We believe every employee plays a vital role in our mission to advance human health through innovative client partnerships. Whether you’re involved in development, manufacturing, testing, or contributing your expertise in other areas, your work will have a meaningful, positive impact on countless lives.

Do You

• Love finding new and better ways to do things?
• Want to help develop medicines that improve patients' lives?
• Have a passion for learning and growth?
• Nerd out on science and technology?
• Value collaboration and teamwork?
• Embrace audacity and entrepreneurial thinking?
• Prioritize safety and lead by example?
• Care deeply about doing the right thing?
  
  

At Bend Bioscience, we foster a diverse, inclusive, challenging, and supportive culture. We are committed to continuous improvement, both as individuals and as an organization, and we encourage personal and professional development at every level. Join us to make a real difference in patients’ lives through your work.

Your New Role At Bend Bioscience

• Performs relevant QC testing, such as HPLC, GC, Dissolution, Malvern and wet chemistry testing as required in compliance with cGMP requirements, compendia standards, and internal procedures
• Ensures testing is properly conducted and documented for all performed activities with emphasis on data integrity
• Prepare test solutions, volumetric solutions, and samples used in analysis
• Performs assigned physical tests, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished, and stability products in an FDA regulated lab environment
• Perform analysis with a practical understanding of the test procedure and instrument operation
• Perform laboratory analysis right first time, contemporaneous documentation, analyze and document the results
• Conducts laboratory investigation under the supervision of laboratory manager.
• Complies with all regulatory/ in-house requirements may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, documentation
• Maintain required level of training needed to perform a GMP task
  
  

Education & Experience

• Experience in UPLC/HPLC GMP operations
• Knowledge with analytical equipment and Part 11 compliant software, such as Chemstation™, Chromeleon™, EMPOWER™, and Laboratory Information Management System.
• Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment
• Proficient in Microsoft Office Suite or similar software