QC Lab Technician I

Davita Inc.; North Great River (NY); On-site; USD 45,000 - 65,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Quality Control Lab Technician to manage lab samples and maintain compliance in a cGMP environment. The successful candidate will be responsible for various laboratory tasks, ensuring high standards of quality, and must have a strong background in laboratory work and relevant educational qualifications.

Qualifications

• At least 2 years of laboratory experience.
• Preferred: Associate's or Bachelor's degree in relevant fields.
• Strong organizational and analytical skills.

Responsibilities

• Manage samples for incoming raw materials, in-process, and finished products.
• Coordinate chemical inventories and verify expiration.
• Conduct sample loading and submit stability samples.

Skills

Organizational skills

Analytical skills

Fluency in English

Education

High School Diploma or equivalent

Associate's degree in Chemistry, Laboratory Science, or related field

Bachelor's degree in physical sciences

Tools

Microsoft Office Suite

Job description

NOTICE:

The posting is for local applicants only and is not for those applying for a global assignment or employees outside of Cipla's U.S. Subsidiaries or Affiliates.

Job Title

Quality Control (QC) Lab Technician

FLSA Classification

Full-Time, Non-Exempt/Hourly Professional

Work Location

Central Islip, NY

Work Hours

General Shift: 9:00 AM - 5:30 PM (may vary based on business needs)

Reports To

Quality Control Director

Purpose

This job description outlines the general responsibilities, expectations, and level of work for the QC Lab Technician position. It is not exhaustive and may be modified based on department needs and individual qualifications.

Scope

The scope of this role is to describe the general nature of the work and the skills required. It may be adjusted according to the department, testing group, education, training, and experience.

Duties and Responsibilities

• Manage samples for incoming raw materials, in-process, finished products, and stability samples, including receipt, logging, distribution, and destruction.
• Coordinate chemical and reference standard inventories, verify expiration, and discard expired chemicals as per procedures.
• Update sample information in SAP and complete data entry as required.
• Maintain lab consumables and place orders as needed.
• Monitor temperature and humidity in stability chambers.
• Conduct sample loading and submit stability samples as scheduled.
• Assist in shipping samples to contract labs.
• Maintain laboratory housekeeping and perform other duties as assigned.

Education and Experience

• High School Diploma or equivalent required.
• Proficient in Microsoft Office Suite.
• At least 2 years of laboratory experience.
• Associate's degree or higher in Chemistry, Laboratory Science, or related field preferred.
• Bachelor's degree in physical sciences preferred.
• Fluent in English.
• Strong organizational and analytical skills.
• Experience with oral solid dosage is a plus.

Professional and Behavioral Competencies

• Hourly, full-time position.
• Willing to work in a pharmaceutical packaging environment.
• Flexible to work shifts, including weekends as needed.
• Positive attitude and team cooperation.
• No remote work, sponsorship, or visas available.

Working Conditions

Work in a cGMP laboratory or manufacturing environment with PPE required. May involve working with solvents, powders, and other materials. Long periods of standing, ladder use, and lifting up to 35 pounds are expected. Work shifts may include day, evening, or night, and weekend or holiday work may be required.