What are the responsibilities and job description for the Quality Assurance Specialist position at Jobs via Dice?
Dice is the leading career destination for tech experts at every stage of their careers. Our client, Cynet Systems, is seeking the following. Apply via Dice today!
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:
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.
- 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.
- 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).
- 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.
Salary : $22 - $27