QC Chemist - MDI

Job Title

Quality Control (QC) Chemist

Fall River, MA

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

Quality Control Manager

QC Chemist I – $66,300 - $86,000

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.

Generally, modifier designation with respect to experience for Chemist are as follows. However, combination of education, training and special skills will determine the assignment of Level I - III to a specific individual.

• 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 expectations.
• 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.
• 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.

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.

• Must be willing to work in a pharmaceutical packaging setting.
• Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday.
• Must be willing to work some weekends based on business needs as required by management.
• 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.