Chemist B

Division Overview Aurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical product development and manufacturing. Aurolife has a 10‑year history of extraordinary manufacturing practices in the solid oral dose arena. The support and expertise of our parent organization has given Aurolife a jump start in building a solid pharmaceutical portfolio very quickly. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, quality assurance and quality control and regulatory affairs. In addition to several formulations in manufacture, we have a robust pipeline of products. Aurolife’s aim is to provide healthcare at economical prices to make this a healthier world to live in. Job Overview Chemist B is responsible for ensuring that products and materials meet established quality standards and regulatory requirements by conducting laboratory tests, analyzing results, and maintaining accurate documentation. They perform testing on raw materials, in‑process samples, and finished goods using various analytical techniques, while adhering to standard operating procedures (SOPs), standard test procedures and Good Manufacturing Practices (GMP). QC Analysts also investigate discrepancies such as out‑of‑specification results, support corrective actions, maintain laboratory equipment, and ensure compliance with regulatory guidelines. This role requires strong attention to detail, technical expertise, and the ability to work in regulated environments. Responsibilities Perform physical, chemical and instrumental tests on raw materials, active pharmaceutical ingredients, in‑process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV‑Vis, IR, particle size analyzer, KF auto‑titrator, bulk density, and other routine QC instruments) as per USP monograph/In‑house/any other compendial monographs. Independently plan and make adequate inventory of test reagents and solutions to perform work, and assure supplies are ordered as needed. Independently plan and execute testing to meet established timelines; perform complicated testing with supervisory direction. Record data and results as specified in documentation procedures; document work clearly and perform tests accurately. Prepare and/or review test procedures, SOPs and protocols as assigned. Perform maintenance and calibrations of laboratory instruments/equipment with supervisory direction/training. Perform troubleshooting and investigations under the direction of a supervisor. Comply with all regulatory/in‑house requirements (including but not limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity. Review analytical documents as required. Qualifications – Skills & Requirements Minimum 3‑5 years experience in pharmaceuticals and must have 2‑4 years experience in analytical testing. Experience in generic pharmaceutical industries would be preferable. Knowledge in good documentation practices. Knowledge in USP/ICH/FDA. Ability to learn quickly and strong decision‑making skills. Education & Experience Minimum BS with a scientific field. BS in Chemistry is preferred. Benefits Medical and Rx benefits: choice of four medical plans through Horizon; Rx automatically provided with medical benefits. Dental benefits: three dental plan options through CIGNA. Vision plan: two plan options through VSP. Life Insurance (basic life and AD&D) and supplemental life insurance. Disability insurance: voluntary short‑term disability and state disability; long‑term disability (LTD) and state (short term) disability where applicable. FSA (flexible spending accounts) – both health care & dependent care available. HSA (health savings account). 401(k) plan – through Fidelity with employer match and fully vested after three years. Employee Assistance Program (EAP) – 100% confidential and fully company‑paid. Critical illness and accidental insurance. Legal and identity‑theft insurance. Paid time off: paid vacation, PTO, holiday. Compensation USD 65,000.00 / yr (minimum) – USD 75,000.00 / yr (maximum). Physical Requirements Work in a temperature‑controlled office environment or travel via vehicle or commercial transportation. Occasionally required to handle or feel objects, talk, hear, and walk during the course of employment. Position requires some degree of travel for business purposes. May use computer, phone, copier and other office equipment regularly. Specific vision abilities: close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Work is sedentary: predominantly sitting; may stand or walk only occasionally. Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects, including the human body. Blood/Fluid Exposure Risk Category III: Tasks involve no exposure to blood, body fluids or tissues. Category I tasks are not a condition of employment. #J-18808-Ljbffr Aurobindo Pharma USA, Inc.