Description
Title: Analytical Validation Chemist
Responsibilities
- Execute feasibility (pre-validation) studies to support validation experimental design
- Translate technical information and requirements into experimental design
- Generate, review and execute phrase appropriate method
- validation/verification/transfer protocols
- Prepare documentation in support of the sampling, analysis, and reporting of method
- qualification or validation results
- Perform troubleshooting during method qualification or validation.
- Perform data analysis, interpretation and review using statistical methods
- Prepare summaries and reports
Minimum Requirements:
- 8 hour shift, Monday-Friday
- BS or MS in Analytical Chemistry or equivalent
- 2+ years experience in a cGMP pharmaceutical/biotechnology laboratory
- Strong technical knowledge HPLC, GC and MS
Location: Miramar
About Actalent
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.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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