Quality Assurance Senior Inspector

Job Title: Quality Assurance Senior Inspector

Location: New Jersey, USA (Open to U.S. Citizens; locals preferred)

Position Type: Contract

Pay Rate: $35 to $40 per hour

Duration: 6 Months

Shift: Monday to Friday, 8:30 AM - 5:00 PM (Onsite)

About ProQuality Network

ProQuality Network is a trusted recruiting partner for the pharmaceutical, biotech, and medical device industries. We connect top-tier professionals with rewarding contract opportunities. As a consultant with ProQuality Network, youll represent our core values and commitment to excellence at our clients site.

This is a contract opportunity where you will play a vital role as a Quality Assurance Senior Inspector supporting our client, a leader in the pharmaceutical industry.

Position Overview

The Quality Assurance Senior Inspector will provide critical quality support to the manufacturing department, ensuring compliance with cGMP, DEA regulations, and internal SOPs. This role demands precision, attention to detail, and the ability to operate in a dynamic, fast-paced environment.

Key Responsibilities

• Conduct facility audits to ensure compliance with cGMP, DEA, and internal SOPs.
• Perform QA room releases, line clearances, equipment releases, and AQL inspections as required.
• Provide Quality Floor support during batch manufacturing through routine auditing.
• Support manufacturing activities for clinical and commercial batches.
• Audit executed batch records and raw material documentation for cGMP compliance.
• Prepare customer audit responses and facilitate interdepartmental communication for obtaining and correcting audit-related information.
• Participate in investigations and provide detailed documentation for batch discrepancies as required.
• Comply with Health, Safety, and Environmental responsibilities.
• Assist in other duties assigned by the department manager to support departmental and business needs.
• Be available for weekend work and extended hours as required.
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Qualifications

Education:

• High school diploma or equivalent (GED) with 8 years of relevant experience in Quality Assurance, Compliance, or Manufacturing within the pharmaceutical industry.

Skills & Knowledge Requirements:

• Strong understanding of compliance regulations, including FDA, cGMP, and DEA requirements for pharmaceutical manufacturing.
• Knowledge of quality auditing and evaluation techniques.
• Proficient in evaluating facilities, records, processes, and procedures for regulatory compliance.
• Excellent mathematical, oral, and written communication skills.
• Ability to multitask effectively under pressure in a fast-paced environment.
• Proficiency with documentation control and quality assurance procedures.

Physical Requirements

• Ability to sit, stand, and work for extended periods.
• Capacity to lift 15-30 pounds as needed.
• Comfortable wearing Personal Protection Equipment (PPE), such as safety glasses and respirators, when required.

Work Environment

This position operates in a high-pressure, fast-paced manufacturing facility requiring exceptional attention to detail, communication, and interpersonal skills. Interaction with cross-functional teamsincluding manufacturing, facilities, and QAis essential to meeting production schedules and quality standards. Flexibility for weekend work and extended hours may be required to support business needs.

Why Join Us?

This role offers the opportunity to make a meaningful impact in the pharmaceutical industry while gaining valuable experience with a renowned client. If you are detail-oriented, thrive under pressure, and possess strong regulatory knowledge, we encourage you to apply.

Apply today inside the job description with your updated resume or share this opportunity with your network! Lets shape the future of quality assurance together.