QC Chemist II - MDI

Cipla; Fall River (MA); On-site; USD 75,000 - 94,000; Full time

Job summary

Join a leading global pharmaceutical company as a Quality Control Chemist, where you will play a vital role in ensuring the quality of medicines. In this position, you will conduct advanced testing and calibration of instruments in a cGMP laboratory environment. The role requires strong analytical and organizational skills, along with a Bachelor's degree in physical sciences or chemistry. This is an excellent opportunity to contribute to a company that values its employees and is dedicated to delivering affordable, high-quality medicines worldwide. If you're ready to take on a challenging role with a dynamic team, we encourage you to apply.

Qualifications

• Bachelor's degree in physical sciences or chemistry preferred.
• Proficient in English with strong analytical and organizational skills.

Responsibilities

• Conduct routine and advanced testing in the QC laboratory.
• Calibration and preventive maintenance of instruments.
• Ensure compliance with cGMP practices and data integrity.

Skills

Analytical Skills

Data Analysis

Communication Skills

Organizational Skills

Teamwork

Education

Bachelor's Degree in Physical Sciences

Chemistry Preferred

Tools

HPLC

GC

Karl Fisher

ICP

Microsoft Office

Scientific Software

Job description

Job Title: Quality Control (QC) Chemist

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: $75,400 - $93,600

Job Overview

The Quality Control Chemist is an individual contributor responsible for testing samples using various techniques and equipment in the QC laboratory.

Duties and Responsibilities

• Calibration and preventive maintenance of instruments.
• Communications with vendors for installation, qualification, and maintenance.
• Conduct routine and advanced testing in a specific department.
• Operate specialized equipment and conduct specialized testing.
• Work with raw materials testing and release.
• Operate instruments such as Karl Fisher, HPLC, GC, Particle size, ICP.
• Lead investigation activities.
• Ensure compliance with data integrity, cGMP practices, and good documentation practices.
• Perform other duties as assigned by the department head.

Education and Experience

• Bachelor's degree in physical sciences, Chemistry preferred.
• Proficient in English, both spoken and written, with the ability to understand scientific work.
• Authorized to work permanently in the U.S. without sponsorship.
• Strong organizational, learning, and team skills.
• Ability to analyze complex data sets.
• Knowledge of Microsoft Office and scientific software.
• Experience in Inhalation products (MDI) is a plus.

Working Conditions

Work in a cGMP laboratory or manufacturing environment with PPE. May involve work on shifts, including weekends and holidays.

Physical Requirements

• Stand or walk for 75% of an 8-hour shift; lift up to 10 kg.
• Wear PPE as required.
• Sit at a desk or computer for 75% of the time.

Professional and Behavioral Competencies

• Willing to work in pharmaceutical packaging settings.
• Flexible with shifts, including day, evening, or night.
• Willing to work weekends as needed.
• No remote work or sponsorship available.

About Cipla

Cipla is a leading global pharmaceutical company committed to high-quality medicines. We value our employees as our greatest assets and focus on making affordable, quality medicines worldwide.

InvaGen Pharmaceuticals

A Cipla subsidiary focused on generic prescription medicines across various therapeutic areas.

EEO Statement

Cipla is an Equal Opportunity Employer, considering all qualified applicants without discrimination based on race, color, age, sex, sexual orientation, gender identity, religion, national origin, disability, or veteran status.