Knowledge of ich guidelines and regulatory authority
This role involves working within a functional service provider solution allowing direct onsite experience at pharmaceutical companies while maintaining full-time benefits
Job Summary
This role involves working within a functional service provider solution allowing direct onsite experience at pharmaceutical companies while maintaining full-time benefits.
The position requires adherence to Good Manufacturing Practices (GMP) and safety standards to support clinical trials conducted in over 100 countries.
Employees are expected to train on analytical instrumentation, address QA findings, and communicate project status to leaders in a fast-paced environment.
Matching Summary
This role involves working within a functional service provider solution allowing direct onsite experience at pharmaceutical companies while maintaining full-time benefits.
Salary
Base: $30.14–$40.00 per hour; Bonus/Equity: Variable annual bonus eligible; Benefits: Comprehensive medical, dental, vision, 401(k), PTO, and parental leave
Skills & Requirements
Must-have
Bachelor's degree in lab sciences
2+ years experience in GMP environment
Knowledge of ICH guidelines and regulatory authority
Ability to maintain safe work environment
Proficiency with Microsoft Excel and Word
Nice-to-have
Empower software knowledge
Experience optimizing analytical methods
Strong problem solving and troubleshooting abilities
Collaborative team work environment
Multi-tasking skills under pressure
Key Requirements
Bachelor's degree in Chemistry, Biology, or related field
Masters degree as alternative qualification
Equivalent combination of education and experience
US work authorization required for Massachusetts location