Quality Assurance Inspector - 3rd Shift

Amneal Pharmaceuticals; Piscataway Township (NJ); On-site; USD 28,000 - 33,000; Full time

Job summary

Amneal Pharmaceuticals is seeking a QA Inspector to sample, inspect and test incoming materials, packaging components and returned goods to ensure compliance with specifications. The role covers all manufacturing phases, including release and control of labels and outserts, with a 12-hour rotating shift from 6:00 PM to 6:30 AM, including every other weekend.

The position emphasizes meticulous documentation, material release checks, and calibration of QA equipment.

Qualifications

• High School diploma or GED is required.
• At least 1 year of QA or related experience.
• Strong math skills and meticulous attention to detail; capable of detailed recordkeeping.

Responsibilities

• Inspect and test incoming raw materials, packaging components and returned goods per procedures.
• Prepare samples for chemical and microbiological analysis and deliver to QC lab.
• Perform line checks and in-process testing per batch records.
• Prepare labeling components and release reports; maintain related logs.
• Maintain calibration records for weighing and measuring equipment.
• Monitor warehouse areas and environmental conditions.

Skills

Attention to detail

Mathematics

Recordkeeping

Education

High School or GED

Tools

Hardness tester

Weight variation system

Balances

Label counting machine

Kirby Lester tablet counters

Job description

Description:

The QA Inspector monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run.

Job Description

The QA Inspector monitors and ensures all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. The QA Inspector must monitor and ensure all phases of drug manufacturing are in compliance with established specifications; receive, inspect, release and control of labels and outserts, to ensure quality compliance before, during and after each packaging run. This role follows a 12-hour rotating schedule, working from 6:00 PM to 6:30 AM. (Requires every other weekend.)

Essential Functions:

• Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. Preparation of samples for chemical and microbiological (where required) analysis and delivering them to the QC lab. Inspection and test of packaging components utilizing various measuring devices such as scales, micrometers and height gauges to determine conformance to specifications. Maintaining detailed records of sampling, inspections and testing activities. Assigning and verification of expiry date and retest date for all the GMP raw materials through vendor COA and in-house COA. Collection of packaged product samples for annual stability.
• Perform room, equipment, and packaging line checks (where applicable) prior to each stage of manufacturing following detailed written procedures. Conduct in process testing per manufacturing and packaging batch record instructions. Prepare controlled / uncontrolled / packaged finished product samples for QC lab and QA retains, following detailed documentation procedures. Maintenance of standard weights required to perform daily verification of balances.
• Labeling component receipt, visual examination, counting, preliminary inspection and sampling. Preparation of labeling components/outverts inspection reports; quarantine and release labels and maintaining incoming components log and corresponding inventory cards. Issuance of labeling components/outverts according to packaging order and regular monitoring and auditing of label room. Fill out the QA final labeled product inspection report, final line clearance which includes labeling and packaging reconciliation paperwork.
• Compliance of Warehouse area in terms of Isolation of Quarantine, Released, In-Process, Finished Product, Packaged Product, Returned Goods, and Rejected areas.
• Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record.
• Monitor facility and product environmental operating conditions

Additional Responsibilities:

• Operate, maintain and calibrate Hardness tester, Fabricator, Weight Variation system, weighing scales and balances, label counting machine, and Kirby Lester tablet counters according to established schedules and maintain detailed calibration records
• Collection of samples to reassay bulk finished product before expiration
• Work in a Contained Manufacturing area/facility following all precautions and procedures
• Visual inspection and preparation of report of all products for APR
• Other duties as assigned by management.

Qualifications

Education

• High School or GED - Required

Experience

• 1 year or more in 1 year in QA or related field

Specialized Knowledge

• Good basic math knowledge and excellent attention to details.
• Records observations for improving processes.

The hourly rate for this position ranges from $19.50 to $23.50 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award with this position within the first 12 months. Amneal ranges reflect the Company’s good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills.

At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life’s many other commitments and opportunities.

About Us

Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at [e-mail] . Requests will be handled confidentially and in accordance with applicable laws.