Quality Control Associate I

Integrated Resources Inc.; Durham (NC); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking a Quality Control Associate I to support critical functions within the Quality Control Chemistry group. You will be responsible for performing sampling and testing, ensuring compliance with regulations, and providing technical expertise. This role requires a Bachelor’s degree in Chemistry or a related field, along with relevant hands-on experience, and offers opportunities for growth within a dynamic team environment.

Qualifications

• 1-2 years experience required with Bachelor’s degree, or 3+ years with Associate or High School Diploma.
• Ability to lift 10-20 pounds and stand for long periods.
• Exposure to chemicals, dust, fumes, and hazardous waste.

Responsibilities

• Perform QC Raw Material sampling and testing.
• Adhere to GLP/GMP requirements.
• Provide technical support and comply with FDA/EMEA regulations.

Skills

Knowledge of scientific principles

Data analysis

Laboratory safety

Strong communication skills

Education

Bachelor’s degree in Chemistry or related field

Associate degree/High School Diploma with equivalent experience

Tools

HPLC

GC

UV-vis

Dissolution

FT-IR

Job description

Job Description

Client: Direct Client

Location: Research Triangle Park, NC

Job Title: Quality Control Associate I

Duration: 1 Year+

Summary:

The Quality Control Associate I supports key functional, tactical, and operational aspects of the Quality Control Chemistry group.

Responsibilities:

1. Perform QC Raw Material sampling and testing, including all associated activities.
2. Support sampling, training, testing of raw materials, transfer qualification, validation activities, and maintain compliant cGMP documentation.
3. Provide technical support as a subject matter expert in key functional areas.
4. Process documentation and computer system entries.
5. Apply understanding of Quality Systems in daily functions.
6. Adhere to GLP/GMP requirements and understand FDA/EMEA regulations.
7. Interact effectively with Quality management, support investigations, and participate in employee training and compliance activities.
8. Work effectively within the team and across the site, demonstrating strong communication skills.
9. Support activities such as interviewing, training, and corrective actions.
10. Work weekends and overtime as required.

Requirements:

• Bachelor’s degree in Chemistry or related field with 1-2 years of experience, or Associate degree/High School Diploma with equivalent experience (typically 3+ years).
• Knowledge of scientific principles and data analysis.
• Experience with laboratory instrumentation (HPLC, GC, UV-vis, Dissolution, FT-IR).
• Understanding of cGMP/cGLP requirements and laboratory safety.
• Ability to lift 10-20 pounds and stand for extended periods.
• Exposure to chemicals, dust, fumes, and hazardous waste.

Weekend and overtime work may be required.

Additional Information:

Feel free to share this opportunity with colleagues.

Thanks!

Warm Regards,

Amrit Singh

Clinical Recruiter

Integrated Resources, Inc

Tel: [phone]

http://www.irionline.com

This job posting is active and available.