Staff QC Chemist

Staff Synthetic Chemist

At Par Health, we believe great healthcare is built on getting the essentials right. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. The Staff Synthetic Chemist position within the Par Health API Development and Support organization synthesizes small molecule analytical reference standards in support of Active Pharmaceutical Ingredient (API) and Drug Product businesses. Beyond bench execution, you will serve as the technical lead for our Reference Standards Program, collaborating closely with Analytical R&D, Quality Control, and Regulatory Affairs to ensure compliance with ICH guidelines and cGMP requirements. to confirm chemical structures.

Reference Standard Program Technical Leadership: Oversee the lifecycle of the reference standard inventory. Drive the generation, review and approval of Certificates of Analysis (CoAs) and manage requalification schedules in alignment with regulatory standards.

Partner with process chemistry team to identify potential process impurities and with analytical chemistry team / QC to develop specifications and test methods for purity determination and standard qualification.

Regulatory & Quality: Contribute to the preparation of technical reports and regulatory filings.

Mentorship & Safety: Provide technical guidance and mentorship to junior synthetic chemists. Champion a culture of rigorous lab safety, proactive hazard assessment, and immaculate chemical hygiene.

Compliance: Remains compliant with Company, Quality, Environmental Health & Safety, and Drug Enforcement Administration (DEA) policies and procedures.

Inventory: Helps maintain system used to track reference standards inventory.

D. in Organic Chemistry with a minimum 3 years of related industrial experience; MS (thesis preferred) in Organic Chemistry with a minimum 5 years of related industrial experience; BS in Chemistry with a minimum of 8 years of related industrial experience.

Demonstrated proficiency in advanced purification techniques (normal/reverse-phase flash chromatography, prep-HPLC, crystallization).

Analytical Acumen: Able to interpret complex NMR spectra and mass spectrometry data for structural elucidation of unknown or complex organic molecules.

Strong understanding of pharmaceutical development, API manufacturing, and the role of reference standards in analytical method development and validation. Familiarity with cGMP, FDA, and ICH regulatory guidelines.

Excellent technical writing skills for maintaining laboratory notebooks, drafting CoAs, and authoring comprehensive technical reports.

Proven ability to work independently in a fast-paced environment, adapt to shifting priorities, and creatively overcome difficult synthetic roadblocks.

Standard laboratory conditions within a DEA-regulated environment. Employees must wear eye protection, lab coat, and safety shoes while in the lab area. Occasional handling of potent compounds or hazardous chemicals may require the use of additional PPE. We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.