Piper Companies is currently seeking a Scientist I or Sr. Chemist for an opportunity in the Copiague, NY area. The Scientist I / Sr. Chemist will play a key role in maintaining GMP and regulatory standards, through method validation, analytical testing to ensure quality and compliance of raw materials. This is a highly visible, hands-on role ideal for a self-starter who can operate independently and drive validation activities from start to finish.
1. Responsibilities of the Scientist I / Sr. Chemist Lead execution ofmethod validation, verification, and developmentactivities
Perform analytical testing onraw materials and finished products
Supportanalytical method developmentfor OTC formulations
Execute validation protocols in alignment withICH, USP, and cGMP standards
Assist withimplementation of new testing capabilities, including dissolution equipment
Conduct data analysis, interpretation, and technical documentation/reporting
Collaborate closely with QC leadership and cross-functional teams
Support activities within the R&D laboratory environment
Maintain compliance with regulatory requirements and data integrity standards
Work independently with minimal supervision in a fast-paced environment
2. Qualifications of the Scientist I / Sr. ChemistBS or MS in Chemistry or related scientific discipline
4+ years of experience in apharmaceutical or highly regulated QC laboratory
Strong, hands-on experience withmethod validation (critical requirement)
Experience withmethod development and verification
Proven ability towork independentlyand execute validations end-to-end
Strong understanding ofcGMP, USP/compendial testing, and regulatory expectations
Experience withHPLC and GC instrumentation
Excellent problem-solving, communication, and organizational skills
3. Compensation for the Scientist I / Sr. Chemist
Hourly Rate: $40 – $53 per hour (depending on experience level)
Comprehensive Benefits:
Medical (Cigna), Dental (Cigna), Vision (Cigna), 401K with match (ADP Retirement), PTO, and Holidays
4. Keywords Method Validation, Method Development, Method Verification, HPLC, GC, Dissolution Testing, OTC, Solid Oral Dose, Pharmaceutical QC, cGMP, USP, ICH, Analytical Chemistry, R&D Lab, Data Integrity