Stabilty Testing QC Chemist II

Cipla USA; Fall River (MA); On-site; USD 65,000 - 105,000; Full time

Job summary

An established industry player is seeking a dedicated Stability Testing QC Chemist to join their dynamic team. This role involves performing critical testing of samples using advanced laboratory techniques and equipment. You will be responsible for ensuring compliance with cGMP standards and supporting drug stability assessments. The ideal candidate possesses strong analytical and organizational skills, with a Bachelor's degree in physical sciences and experience in stability testing. Join a collaborative environment where your contributions will make a significant impact on pharmaceutical quality control.

Qualifications

• 3+ years of experience in formulations stability testing.
• Proficiency in English communication and analytical skills.

Responsibilities

• Conduct routine and advanced testing in the QC laboratory.
• Lead investigation activities related to stability testing.

Skills

Analytical Skills

Organizational Skills

Communication Skills

Education

Bachelor's degree in physical sciences

Tools

HPLC

GC

Karl Fisher

ICP

Microsoft Office

Scientific software

Job description

Job Title: Stability Testing 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: $65,000 - $105,000

Purpose:

The Chemist performs testing of samples using various techniques and equipment in the QC laboratory. Responsibilities may vary based on department, group, education, training, and experience.

Scope:

This description outlines the general nature of the work, responsibilities, and expectations. It is not exhaustive and may be modified based on department, group, or individual assignments, considering education, training, and experience.

Duties and Responsibilities:

• Conduct routine and advanced testing in the QC laboratory.
• Operate specialized laboratory equipment such as HPLC, GC, Karl Fisher, ICP, and particle size analyzers.
• Lead investigation activities related to stability testing.
• Ensure compliance with data integrity, cGMP, and good documentation practices.
• Support the quality control department in drug stability assessments, especially under environmental influences.

Education and Experience:

• Bachelor's degree in physical sciences (BS or BA).
• Minimum of 3 years' experience in formulations stability testing.
• Proficiency in English communication (reading and writing).
• Experience with inhalation products (MDI) is a plus.
• Strong organizational and analytical skills, with ability to understand complex data.
• Proficiency in Microsoft Office and scientific software.

Working Conditions:

Work is performed in a cGMP laboratory or manufacturing environment requiring PPE such as lab coats, safety glasses, and respirators. Work may involve solvents, powders, and other materials typical of pharmaceutical labs. Shifts may include day, evening, night, weekends, or holidays.

Physical Requirements:

• Standing or walking for 75% or more of an 8-hour shift. Lifting up to 10 kg may be required.
• Ability to wear PPE as required.
• Sitting at a desk or computer for 75% or more of an 8-hour shift.

Professional and Behavioral Competencies:

• Willingness to work in pharmaceutical packaging and manufacturing settings.
• Flexibility to work various shifts, including weekends, as needed.
• No remote work available.