QC Chemist II

Cipla USA; Fall River (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

An established industry player is seeking a Quality Control Chemist to join their dynamic team in a cGMP laboratory. This role involves executing analytical method validation, conducting advanced testing, and ensuring compliance with stringent quality standards. The ideal candidate will possess a Bachelor's degree in physical sciences or Chemistry, along with strong analytical skills and proficiency in various laboratory instruments. Join a forward-thinking company committed to delivering high-quality medicines and be part of a collaborative environment that values your expertise and passion for healthcare.

Qualifications

• Bachelor's degree in physical sciences or Chemistry preferred.
• Proficiency in Microsoft Office and scientific software.

Responsibilities

• Prepare protocols for analytical method validation and verification.
• Conduct routine and advanced testing in the QC lab.
• Ensure compliance with cGMP practices and maintain documentation.

Skills

Analytical Method Validation

Data Analysis

Cleaning Validation

Teamwork

Microsoft Office

Education

Bachelor's degree in Physical Sciences or Chemistry

Tools

HPLC

GC

Karl Fisher

ICP

Particle Size Analyzers

Job description

Job Title: Quality Control (QC) Chemist (Method Validation)

Salary range: $65,000 - $90,000 + bonus

Work Location: Fall River, MA

Work Hours: 8:30AM to 5:00PM (may vary based on business needs)

Reports To: Quality Control Manager

Job Description

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

Responsibilities

1. Prepare protocols and execute analytical method validation, verification, and transfer.
2. Possess working knowledge of cleaning validation (residue analysis).
3. Conduct routine and advanced testing within the department.
4. Operate specialized equipment and conduct specialized tests.
5. Test and release raw materials.
6. Utilize instruments such as Karl Fisher, HPLC, GC, Particle size analyzers, ICP.
7. Lead investigation activities.
8. Ensure compliance with data integrity and cGMP practices and procedures.
9. Maintain good documentation practices.
10. Perform other duties as assigned by the department head.

Qualifications

• Bachelor's degree in physical sciences or Chemistry preferred.
• Proficiency in English, both written and spoken.
• Legal authorization to work permanently in the U.S. without sponsorship.
• Strong organizational and teamwork skills.
• Ability to analyze complex data sets.
• Proficiency in Microsoft Office and scientific software.
• Experience with inhalation products (MDI) is a plus.

Working Conditions

Work in a cGMP laboratory or manufacturing environment requiring PPE, with potential exposure to solvents, powders, and other materials. May include shift work, weekends, or holidays.

Physical Requirements

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

Professional and Behavioral Competencies

• Willingness to work in pharmaceutical packaging settings.
• Availability for various shifts, including weekends as needed.
• No remote work available.

About the Company

Cipla is a leading global pharmaceutical company committed to high-quality medicines. With a presence in India, South Africa, the U.S., and emerging markets, Cipla values employees' knowledge, experience, and passion for healthcare. Our focus is on making affordable, world-class medicines with uncompromising quality standards.

InvaGen Pharmaceuticals, a Cipla subsidiary based in New York, specializes in generic prescription medicines across various therapeutic areas.

EEO Statement

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, disability, or veteran status.