Quality Assurance Specialist

job summary: The Quality Assurance Specialist is primarily responsible for performing AQL visual inspections of filled syringes and vials following successful qualifications. This role supports Manufacturing and Packaging Operations by ensuring that incoming materials and finished products meet established quality standards and regulatory requirements. The position requires sound judgment, attention to detail, and the ability to work independently within a cGMP-regulated environment.

location:

Ridgefield, New Jersey job type: Contract salary: $20

• 27 per hour work hours: 9 to 5 education: Bachelors responsibilities: Primary Responsibilities
• Primary responsibility is performing AQL visual inspection of filled syringes and vials following successful qualification. Additional Responsibilities
• Make sound, independent decisions regarding packaging inspections, rework operations, and final disposition of incoming materials in accordance with company policies and procedures, with minimal supervision.
• Prioritize incoming inspections of primary, secondary packaging components and printed materials to align with Manufacturing and production needs.
• Act as a liaison with suppliers to resolve quality-related issues efficiently.
• Provide quality oversight and support to Packaging and Manufacturing Operations, including logbook and AQL inspection form review and real-time issue resolution.
• Participate in continuous improvement initiatives to streamline inspection processes and eliminate redundancies.
• Apply

ANSI/ASQ Z1.4

sampling plans, including normal, reduced, and tightened inspection levels and switching rules.

• Ensure compliance with cGMP requirements related to inspection activities.
• Interpret component drawings and perform measurements using tools such as calipers and micrometers.
• Review and evaluate Certificates of Analysis (CoAs) for raw materials, chemicals, and packaging components.
• Collaborate with Purchasing and suppliers to resolve documentation discrepancies and shipping issues.
• Maintain accurate and compliant documentation in accordance with company and regulatory standards.
• Adhere to all company safety policies and promote safe work practices.
• Support cross-functional teamwork and effective communication across departments.

qualifications:

• High school diploma or equivalent required.
• Associate's degree in a scientific or technical field preferred.
• 2+ years of experience in quality inspection, manufacturing, or a related GMP-regulated environment preferred. Work Environment & Schedule
• Monday-Friday schedule with flexibility for early or late hours as needed.
• Occasional weekend support may be required based on business needs.
• Work performed in a manufacturing and/or controlled environment requiring adherence to gowning and safety procedures. Qualifications (Required)
• Knowledge of cGMP regulations as they relate to inspection and quality activities.
• Ability to read and interpret technical drawings and specifications.
• Experience using measurement tools such as calipers.
• Strong attention to detail, organizational skills, and documentation practices.
• Effective communication and teamwork skills.
• Ability to make independent decisions with minimal supervision. Qualifications (Preferred)
• Working knowledge of AQL inspection processes and

ANSI/ASQ Z1.4

sampling standards.

• Familiarity with normal, reduced, and tightened inspection levels and switching rules.
• Experience in pharmaceutical, biotechnology, or medical device manufacturing environments.
• Knowledge of sterile manufacturing or drug/medical device packaging operations.
• Prior experience evaluating Certificates of Analysis (CoAs).

skills:

Good Manufacturing Practices (GMP), Good Documentation Practices (GDP)

Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. job detailssummary$20

• $27 per hourcontractbachelor degreecategorylife, physical, and social science occupationsreference53498job details job summary: The Quality Assurance Specialist is primarily responsible for performing AQL visual inspections of filled syringes and vials following successful qualifications.

This role supports Manufacturing and Packaging Operations by ensuring that incoming materials and finished products meet established quality standards and regulatory requirements. The position requires sound judgment, attention to detail, and the ability to work independently within a cGMP-regulated environment.

location:

Ridgefield, New Jersey job type: Contract salary: $20

• 27 per hour work hours: 9 to 5 education: Bachelors responsibilities: Primary Responsibilities
• Primary responsibility is performing AQL visual inspection of filled syringes and vials following successful qualification. Additional Responsibilities
• Make sound, independent decisions regarding packaging inspections, rework operations, and final disposition of incoming materials in accordance with company policies and procedures, with minimal supervision.
• Prioritize incoming inspections of primary, secondary packaging components and printed materials to align with Manufacturing and production needs.
• Act as a liaison with suppliers to resolve quality-related issues efficiently.
• Provide quality oversight and support to Packaging and Manufacturing Operations, including logbook and AQL inspection form review and real-time issue resolution.
• Participate in continuous improvement initiatives to streamline inspection processes and eliminate redundancies.
• Apply

ANSI/ASQ Z1.4

sampling plans, including normal, reduced, and tightened inspection levels and switching rules.

• Ensure compliance with cGMP requirements related to inspection activities.
• Interpret component drawings and perform measurements using tools such as calipers and micrometers.
• Review and evaluate Certificates of Analysis (CoAs) for raw materials, chemicals, and packaging components.
• Collaborate with Purchasing and suppliers to resolve documentation discrepancies and shipping issues.
• Maintain accurate and compliant documentation in accordance with company and regulatory standards.
• Adhere to all company safety policies and promote safe work practices.
• Support cross-functional teamwork and effective communication across departments.

qualifications:

• High school diploma or equivalent required.
• Associate's degree in a scientific or technical field preferred.
• 2+ years of experience in quality inspection, manufacturing, or a related GMP-regulated environment preferred. Work Environment & Schedule
• Monday-Friday schedule with flexibility for early or late hours as needed.
• Occasional weekend support may be required based on business needs.
• Work performed in a manufacturing and/or controlled environment requiring adherence to gowning and safety procedures. Qualifications (Required)
• Knowledge of cGMP regulations as they relate to inspection and quality activities.
• Ability to read and interpret technical drawings and specifications.
• Experience using measurement tools such as calipers.
• Strong attention to detail, organizational skills, and documentation practices.
• Effective communication and teamwork skills.
• Ability to make independent decisions with minimal supervision. Qualifications (Preferred)
• Working knowledge of AQL inspection processes and

ANSI/ASQ Z1.4

sampling standards.

• Familiarity with normal, reduced, and tightened inspection levels and switching rules.
• Experience in pharmaceutical, biotechnology, or medical device manufacturing environments.
• Knowledge of sterile manufacturing or drug/medical device packaging operations.
• Prior experience evaluating Certificates of Analysis (CoAs).

skills:

Good Manufacturing Practices (GMP), Good Documentation Practices (GDP)

Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.