Qualifications

• Bachelor's degree in life or physical science with 2 years experience, or a Master's degree in related field.
• Ability to interpret complex instructions and technical documents.
• Strong documentation skills in compliance with regulatory standards.
• Experience in cGMP and SOP adherence is beneficial but not mandatory for Master’s degree holders.
• Physical ability to perform laboratory tasks, including lifting up to 50 lbs.

Responsibilities

• Maintain high quality lab documentation per regulatory guidelines.
• Draft technical documents including lab notebooks and protocols.
• Train team members on laboratory techniques and procedures.
• Execute efficiency improvement projects under guidance.
• Conduct parallel reviews of GMP documents and lab notebooks.
• Lead small team projects with demonstrated capabilities.
• Develop and execute simple yet high-quality manufacturing procedures.

Benefits

• Defined career path with annual performance reviews.
• Diverse and inclusive workplace culture.
• Positive environment geared towards process improvement and innovation.
• Career growth opportunities in a mission-driven organization.
• 152 hours of PTO plus 8 paid holidays.
• Generous 401K matching program.
• Comprehensive medical, dental, and vision benefits from day one.
• Tuition reimbursement for furthering education.