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Summary
About the Role
About You
- Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or related field from an accredited institution.
- 1-3 years of experience in analytical quality assurance.
- Strong command of English language communication skills, both verbal and written.
- Solid documentation and technical writing skills.
- Experience with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDP).
- Master’s degree in a relevant field.
- Experience in analytical quality assurance in pharmaceutical manufacturing.
- Knowledge of analytical laboratory activities related to active pharmaceutical ingredients (API) and drug products.
- Experience with inhalation products (MDI).
- Ability to work any assigned shift.
Benefits
- Health, Vision, Dental insurance.
- 401K retirement plan.
- Relocation assistance up to $6,000.
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Our expertise spans capabilities in engineering including product and manufacturing, systems and software, construction management, environmental, architecture and civil; and power and utilities. We focus on sciences capabilities in laboratory sciences, healthcare, and clinical research.
Actalent is an operating company of Allegis Group, the global leader in talent solutions.