QC Chemist III - MDI
Cipla USA, Fall River, MA, United States
NOTICE
The posting is for local applicants only and is not for those applying for a global assignment 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: 8:30 AM – 5:00 PM (may vary based on business needs)
Reports To
Quality Control Manager
Salary Range
$96,000 – $103,000
Purpose
The chemist is an individual contributor who performs testing of samples of various types using a variety of techniques or equipment in the QC laboratory. The role may be further modified by the department, group, education, training or experience.
Duties and Responsibilities
Conduct routine or advanced testing in a specific group or department setting.
Operate specialized equipment or perform specialized skill testing.
Have knowledge of raw materials testing and release.
Use instruments such as Karl Fisher, HPLC, GC, particle size, ICP.
Lead investigation activities.
Ensure compliance with data integrity and cGMP practices, procedures, and documentation.
Follow good documentation practices.
Other duties as assigned by the Head of Department or Section Head.
Education and Experience (Qualifications)
Bachelor's degree (BS or BA) in physical sciences preferred.
Proficient in English as a first or second language.
Strong written and verbal communication in scientific work.
Excellent organizational, learning, and team‑working skills.
Ability to analyze complex data sets.
Working knowledge of Microsoft Office and other scientific software.
Experience in inhalation products (MDI) is a plus.
Working Conditions
Work in a cGMP laboratory or manufacturing environment. Personal protective equipment such as lab coat, safety glasses, respiratory protection, hearing protection is required. Work may be on Day, Evening, or Night shifts; weekends or holidays may be requested or required.
Physical Requirements
Stand or walk unassisted for at least 75% of an 8‑hour shift.
Lift up to 10 kg unassisted as required.
Wearing appropriate personal protective equipment at all times.
Use a computer or other screen for at least 75% of an 8‑hour shift.
Professional and Behavioral Competencies
Willingness to work in a pharmaceutical packaging setting.
Willingness to work any assigned shift, including Monday–Friday, and some weekends as needed.
No remote work available.
No employment sponsorship or work visas.
EEO Statement
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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The posting is for local applicants only and is not for those applying for a global assignment 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: 8:30 AM – 5:00 PM (may vary based on business needs)
Reports To
Quality Control Manager
Salary Range
$96,000 – $103,000
Purpose
The chemist is an individual contributor who performs testing of samples of various types using a variety of techniques or equipment in the QC laboratory. The role may be further modified by the department, group, education, training or experience.
Duties and Responsibilities
Conduct routine or advanced testing in a specific group or department setting.
Operate specialized equipment or perform specialized skill testing.
Have knowledge of raw materials testing and release.
Use instruments such as Karl Fisher, HPLC, GC, particle size, ICP.
Lead investigation activities.
Ensure compliance with data integrity and cGMP practices, procedures, and documentation.
Follow good documentation practices.
Other duties as assigned by the Head of Department or Section Head.
Education and Experience (Qualifications)
Bachelor's degree (BS or BA) in physical sciences preferred.
Proficient in English as a first or second language.
Strong written and verbal communication in scientific work.
Excellent organizational, learning, and team‑working skills.
Ability to analyze complex data sets.
Working knowledge of Microsoft Office and other scientific software.
Experience in inhalation products (MDI) is a plus.
Working Conditions
Work in a cGMP laboratory or manufacturing environment. Personal protective equipment such as lab coat, safety glasses, respiratory protection, hearing protection is required. Work may be on Day, Evening, or Night shifts; weekends or holidays may be requested or required.
Physical Requirements
Stand or walk unassisted for at least 75% of an 8‑hour shift.
Lift up to 10 kg unassisted as required.
Wearing appropriate personal protective equipment at all times.
Use a computer or other screen for at least 75% of an 8‑hour shift.
Professional and Behavioral Competencies
Willingness to work in a pharmaceutical packaging setting.
Willingness to work any assigned shift, including Monday–Friday, and some weekends as needed.
No remote work available.
No employment sponsorship or work visas.
EEO Statement
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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