QC Chemist III - MDI
Listed on 2026-06-03
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Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager
Eligibility Notice
The posting is for local applicants only and is not for those applying for a global assignment or employees working outside of Cipla's U.S. subsidiaries or affiliates.
Job Summary- 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
The Chemist is an individual contributor who performs testing of samples of various types using a range of techniques or equipment in the QC laboratory. The role may be modified by department or group assignment and by individual education, training, experience, or a combination thereof.
Duties and Responsibilities- 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.
- Work‑knowledge of raw materials testing and release.
- Work‑knowledge of instruments such as Karl Fisher, HPLC, GC, particle size, ICP.
- Lead investigation activities.
- Ensure compliance with 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.
- Proficient in speaking English as a first or second language.
- Strong written and verbal scientific communication skills in English.
- Excellent organization, learning and teaching skills required for teamwork.
- Ability to understand and analyze complex data sets.
- Working knowledge of Microsoft Office programs and other scientific software.
- Experience with inhalation products (MDI) is a plus.
This role works in a cGMP laboratory or manufacturing environment where personal protective equipment is required, including uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. The employee may work with solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility. The role may be assigned on a work‑shift basis (day, evening, night) and weekend or holiday work may be requested or required.
Physical Requirements- Work standing or walking unassisted for 75% or greater of an 8‑hour period.
- Unassisted lifting up to 10kg, may be required.
- Ability to wear appropriate personal protective equipment at all times when required.
- Sitting at a desk and/or working at a computer or other screen for 75% or greater of an 8‑hour period.
- Willing to work in a pharmaceutical packaging setting.
- Willing and able to work any assigned shift (first or second shift).
- Work schedule may be Monday to Friday.
- 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.
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