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R&d Scientist
Actalent
An engineering and sciences services and talent solutions firm connecting specialized experts with industry projects.
Develop and validate analytical methods for pharma products, supporting R&D.
Participate in regular project reviews with Directors.
Ensure all R&D department duties and activities comply with FDA, OSHA, and GMP systems.
Provide technical support within the laboratory and other departments as needed.
Support the calibration of equipment.
Execute Analytical Method Verification and Validation activities for Pharmaceutical Drug Products and raw materials in accordance with current ICH and FDA requirements.
Document analytical activities and results accurately and in a timely manner, ensuring data integrity.
Formulate lab-scale batches of products and placebos to support analytical method validation.
What you bring
hplc
gc-ms
icp-ms
method development
5 years
bsc chemistry
Expertise in Analytical Chemistry techniques, including HPLC, GC, GC-MS, and ICP-MS.
At least 5 years of experience in method development within the Pharmaceutical Industry.
Bachelor of Science Degree in Chemistry or related
Benefits
Time Off/Leave (PTO, Vacation or Sick Leave)
Health Spending Account (HSA)
Employee Assistance Program
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Transportation benefits
Critical Illness, Accident, and Hospital
Medical, dental & vision
Short and long-term disability
401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
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