QC Chemist III - MDI

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

Job Title: Quality Control (QC) Chemist III
FLSA Classification: Full-Time, Exempt Professional
Work Location: Fall River, MA
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
Reports To: Quality Control Manager
Salary Range: $96,000 - $103,000

Purpose:
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.

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 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

Education and Experience:
Bachelor's degree (BS or BA), physical sciences preferred
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... For full info follow application link.

Cipla USA and its US Affiliates 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.