QC Chemist III

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

QC Chemist III

Inva Gen Pharmaceuticals, Inc.

Central Islip, NY

Full Time – Salary/Exempt

$72,800 - $93,600

In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance – medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) – vacation/sick/flex time, paid holidays, short‑term disability (STD), long‑term disability (LTD), parental leave, paid and unpaid family leave, employee discounts, and other benefits.

8:30 AM – 5:00 PM (General Shift)

The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three.

• 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.
• Participate in 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.

• Bachelor's degree (BS or BA), physical sciences preferred.
• Master's or PhD.
• 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.

• 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.

• 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.

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.

Driven by the purpose "Caring for Life", Cipla’s focus has always been on making affordable, world‑class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast‑growing pharmaceutical company with a continued focus on the expanse of our strong legacy.

Over…