QC Chemist III -DPI

Job Details Job Title : Quality Control (QC) Chemist III FLSA Classification : Full-Time, Exempt Professional Work Hours : General Shift: 8:30AM – 5:00PM (may vary based on business needs) Reports To : Quality Control Manager Purpose The job of the "Chemist" is described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The role may be modified based on the department, group, education, training, or experience, as applicable. Duties and Responsibilities The general duties and responsibilities of the "Chemist" include but are not limited to the following: Conduct routine testing or other analysis in a specific group or department setting. Conduct advanced testing and/or critical testing, as required. Operate specialized equipment or conduct specialized skill testing. Working knowledge of raw materials testing and release. Working knowledge of instruments such as Karl Fischer, HPLC, GC, Particle size, ICP. Lead investigation activities. Ensure compliance to all data integrity and cGMP practices, procedures, and expectations. Ensure compliance with all good documentation practices. Other duties and responsibilities as assigned by the Head of the Department or Section Head. Education and Experience Bachelor's degree (BS or BA), physical sciences required Master's degree preferred Chemist III - minimum of 8 years' experience. Proficiently speak English as a first or second language Proficiently communicate and understand (read and write) scientific work in English Have excellent organization, learning and teaching skills required to work in teams Ability to understand and analyze complex data sets. Working knowledge of Microsoft Office programs and other scientific based software. Experience in Inhalation products (MDI) is a plus Working conditions This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required. Physical requirements Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to 10 kg, may be required. Able to wear appropriate personal protective equipment at all times, when required. Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period. Professional and Behavioral Competencies Must be willing to work in a pharmaceutical packaging setting. Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday. Must be willing to work some weekends based on business needs as required by management. No remote work available No employment sponsorship or work visas. Global Company Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. EEO Statement Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status. #J-18808-Ljbffr Cipla