Quality Assurance Specialist

Home Quality Assurance Specialist Healthcare & Life Sciences $ 24 - $ 27 / Hour location_on Ridgefield, New Jersey acute Contract/Temporary favorite_border

JOB ON CANDIDATE PORTAL

COPY LINK link Adecco Healthcare & Life Sciences is hiring a Quality Assurance Specialist for our Medical Supply partner in Ridgefield, NJ. The anticipated hourly wage for this position is between $24 and $27. Hourly wage may depend upon experience, education, geographic location, and other factors. Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program,muter benefits, Daily Pay, and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, w required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria 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 iing 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. Key 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 iing materials in accordance with policies and procedures, with minimal supervision.
• Prioritize iing inspections of primary, secondary packagingponents and ed 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.

ANSI/ASQ Z1.4

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

• Ensurepliance with cGMP requirements related to inspection activities.
• Interpretponent drawings and perform measurements using tools such as calipers and micrometers.
• Review and evaluate Certificates of Analysis (CoAs) for raw materials, chemicals, and packagingponents.
• Collaborate with Purchasing and suppliers to resolve documentation discrepancies and shipping issues.
• Maintain accurate andpliant documentation in accordance withpany and regulatory standards.
• Ad to all safety policies and promote safe work practices.
• Support cross-functional teamwork and effectivemunication across departments. 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,anizational skills, and documentation practices.
• Effectivemunication 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). Education & Experience
• High school diploma or equivalent required.
• Associates 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 adnce to gowning and safety procedures.

Pay Details:

$24.00 to $27.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program,muter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay w applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to adecco/en-us/candidate-privacy The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance

Massachusetts Candidates Only:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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US_EN_99_106405_2538233