QC Chemistry Associate I

Summary: Entry level position, individual contributor responsible for conducting routine analysis of raw materials, proteins, peptides, and small molecules under general supervision for in‑process, release, and stability testing. May focus on a specialized area and provide routine analysis and testing according to standard operating procedures in any of the following areas: raw materials, in‑process, and finished formulations. Essential Duties and Responsibilities Perform routine analysis and testing in a GMP environment (including compendial assays, AQL inspections, and USP identification test methods, ensuring compliance with industry standards). Participate in qualification/verification of assays. Perform assay and documentation review. Write and review product specifications as required. Collect and dispose of laboratory waste according to established procedures. Contribute to laboratory readiness including lab cleaning, glass washing, and inventory management. Maintain personal training records and attend all required training. Demonstrate regular and reliable attendance on a full‑time basis. Exhibit professional behavior with internal and external business associates that reflects positively on the company. Align daily actions with department goals and company culture. Special Demands Constantly sit and reach to use computers and other office equipment. Constantly stand for extended periods of up to four (4) hours per day. Frequently lift up to 40 pounds. Frequently view objects at close and distant ranges with hand‑eye coordination. Frequently communicate with others. Subject to passing a Visual Acuity test, depending on the standard operating procedure being performed. Work Environment Employee will work with a moderate noise level, experience numerous interruptions, and may occasionally be exposed to fumes, airborne particles, toxic chemicals, vibration, and bio‑hazardous materials. The work environment is fast‑paced and demanding. Off‑shift, weekend and overtime duties may be required. Qualifications High School Diploma required. Bachelor’s degree in Life Sciences discipline or equivalent preferred. Zero to two years of relevant work experience. Ability to perform testing in a highly accurate and reproducible manner. Follow GMP guidelines and detailed direction in a laboratory environment. Familiarity with cGMP, manufacturing, instrument operations, troubleshooting, and data entry. Strong communication and teamwork skills. Needs regular supervision to deliver goals and objectives. Compensation & Benefits Hourly rate: $24.08–$27.09, plus eligibility for an annual performance bonus. Competitive benefits package includes paid time off, health insurance coverage (including dental and vision), a flexible spending account, and a 401(k) plan. Equal Employment Opportunity Statement PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, equity and inclusion are at the core of our company’s purpose. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture. #J-18808-Ljbffr