QC Chemist II

at  Cipla

About Cipla
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 the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division.
InvaGen Pharmaceuticals, Inc.
InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla’s respiratory business in the United States.

EDUCATION QUALIFICATIONS

• Bachelor’s degree (BS or BA), physical sciences preferred.
• Masters or (MS) or Doctorate (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

EXPERIENCE

• Must have a minimum of three (3) years of Pharmaceutical QC lab experience.
• Must have a background within the Pharmaceutical industry.
• Understanding of lab equipment and QC testing techniques required.

SKILLS/ COMPETENCIES

• UV, HPLC, DSC, and other tests.
• Know how to use dissolution instruments.
• LIMS and Empower

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.

The job of the “Chemist” is simple 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.

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.
• Participate in investigation activities.
• Ensure compliance to all data integrity and cGMP practices, procedures, and expectations.

• Ensure compliance with all god documentation practices.Other duties and responsibilities as assigned by the Head of the Department.