Stabilty Testing QC Chemist II

Job Title

Chemist - Stability Testing - Quality Control

Full-Time

Fall River, MA - on-site daily

8 AM - 5 PM (May vary based on business needs)

$75,000 - $105,000 (DOE)

Bi-Weekly Pay, Paid Time Off, Health Insurance Benefits start on day 1 (Medical, Dental, Vision), Disability Insurance, Shift Differential, Overtime, 401K Match, company sponsored events, career advancement, training, etc.

Cipla is seeking a Stability QC Chemist who will provide support to the Quality Control Department in drug quality assessments under the influence of environmental factors.

The general duties and responsibilities of the job 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 Fisher, HPLC, GC, Particle size, ICP
• Lead investigation activities.
• Ensure compliance to all data integrity and cGMP practices, procedures, and expect
• Ensure compliance with all good documentation practices.
• Other duties and responsibilities as assigned by the Head of the Department or Section Head

• Bachelor's degree (BS or BA), physical sciences preferred
• Proficiently speak English as a first or second language
• Have at least 3 years' experience with formulations stability testing.
• 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
• Must be authorized to work permanently in the United States
• Must be able to work on-site

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.

• Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 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.

Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

About Inva Gen Pharmaceuticals, a Cipla subsidiary Inva Gen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on metered dose inhaler (MDI). The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, Inva Gen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.

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