We are looking for Quality Assurance Specialist for our client in Ridgefield, NJ
Job Title: Quality Assurance Specialist
Job Location: Ridgefield, NJ
Job Type: Contract
Job Overview:
Pay Range: $22hr - $27hr
Responsibilities:
- Make independent decisions regarding packaging inspections, rework operations, and material disposition in accordance with policies and procedures.
- Prioritize and perform inspections of primary and secondary packaging components and printed materials based on production needs.
- Act as a liaison with suppliers to resolve quality-related issues in a timely manner.
- Provide quality oversight to packaging and manufacturing operations, including review of logbooks and AQL inspection forms.
- Support real-time issue resolution during production and packaging activities.
- Participate in continuous improvement initiatives to enhance inspection processes and efficiency.
- Apply ANSI/ASQ Z1.4 sampling plans, including normal, reduced, and tightened inspection levels.
- Ensure compliance with cGMP requirements related to inspection and quality activities.
- Interpret technical drawings and perform measurements using tools such as calipers and micrometers.
- Review Certificates of Analysis (CoAs) for raw materials, chemicals, and packaging components.
- Collaborate with purchasing and suppliers to resolve documentation discrepancies and shipment issues.
- Maintain accurate and compliant documentation per regulatory and company standards.
- Adhere to safety policies and promote safe work practices.
- Support cross-functional collaboration across teams and departments.
Required Skills And Experience:
- High school diploma or equivalent.
- Knowledge of cGMP regulations related to quality and inspection activities.
- Ability to read and interpret technical drawings and specifications.
- Experience using measurement tools such as calipers and micrometers.
- Strong attention to detail and documentation practices.
- Ability to make independent decisions with minimal supervision.
- Effective communication and teamwork skills.
Preferred Qualifications:
- Associate s degree in a scientific or technical field.
- 2+ years of experience in quality inspection or manufacturing in a GMP-regulated environment.
- Working knowledge of ANSI/ASQ Z1.4 sampling standards and AQL inspection processes.
- Familiarity with inspection levels (normal, reduced, tightened) and switching rules.
- Experience in pharmaceutical, biotechnology, or medical device manufacturing.
- Knowledge of sterile manufacturing or packaging operations.
- Experience reviewing Certificates of Analysis (CoAs).
Soft Skills:
- Strong analytical and problem-solving abilities.
- Detail-oriented with a focus on quality and compliance.
- Good organizational and time management skills.
- Ability to work independently and collaboratively.
- Proactive mindset with continuous improvement focus.