QC Chemist II - DPI

NOTICE: The posting is for local applicants only and is not for those applying for a global assignment or for employees working outside Cipla's U.S. Subsidiaries or Affiliates.

Quality Control (QC) Chemist II)

Full-Time, Exempt Professional

Hauppauge, NY (Unit
1)

General Shift: 8:30 AM – 5:00 PM (may vary based on business needs)

Quality Control Manager

$72,800 - $93,600

The job of the "Chemist" is 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 upon department, group, education, training, and experience as assigned.

The scope of this job description describes the general nature and level of work and provides a basic understanding of the role, responsibilities, and expectations. It is not intended to provide an exhaustive list of all duties, tasks, skills, or qualifications. The role may be modified with respect to department, group, and individual assignments based on testing needs and education, training, and experience.

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.
• Demonstrate working knowledge of raw materials testing and release.
• Demonstrate working knowledge of instruments such as Karl Fischer, HPLC, GC, particle size, ICP.
• Lead investigation activities.
• Ensure compliance with data integrity and cGMP practices, procedures, and expectations.
• Ensure compliance with good documentation practices.
• Perform other duties as assigned by the Head of the Department or Section Head.

• Bachelor's degree (BS or BA) in physical sciences required.
• Master's degree preferred.
• Chemist III – minimum of 5 years' experience.
• Proficiently speak English as a first or second language.
• Proficiently communicate and understand (read and write) scientific work in English.
• Excellent organization, teamwork, and learning abilities.
• Ability to understand and analyze complex data sets.
• Working knowledge of Microsoft Office programs and other scientific software.
• Experience in Inhalation products (DPI) is a plus.

This role works in a cGMP laboratory or manufacturing environment, where PPE is required (uniforms, lab coats, safety glasses, respiratory protection, 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 (Day, Evening, Night). Weekend or holiday work may be requested or required.

• Stand or walk for 75% or more of an 8-hour period. Lifting up to 10 kg may be required.
• Able to wear appropriate PPE at all times when required.
• Sit at a desk or work at a computer for 75% or more of an 8-hour period.

• Willing to work in a pharmaceutical packaging setting.
• Willing and able to work any assigned shift (Day or Evening); schedule may be Monday to Friday.
• Willing to work some weekends based on business needs.
• No remote work available.
• No employment sponsorship or work visas.

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.

CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.) Inva Gen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company is based in Central Islip and Hauppauge, New York.