
Job Overview
Compensation
Hourly
Range $22.00 - $23.00
Work Schedule
Rotating Shifts
Benefits
Health Insurance
Dental Insurance
Paid Time Off
Retirement Plan
flexible schedule
Professional Development
Employee assistance program
Job Description
This job opportunity is with a reputable manufacturing company specializing in the pharmaceutical, cosmetic, and nutriceutical industries. The company is committed to producing high-quality products that comply with stringent regulatory standards, ensuring consumer safety and satisfaction. Operating under current Good Manufacturing Practices (cGMPs) and following meticulous Standard Operating Procedures (SOPs), they maintain a rigorous quality assurance framework that supports their dedication to excellence and compliance. They employ a team of dedicated professionals who play vital roles in maintaining product integrity and regulatory adherence. This position is full-time and offers a rotating weekly shift schedule between 1st and 2nd shifts, providing flexibility within the production environment.
The role of Quality Assurance (QA) Line Inspector is integral to the company’s Quality Assurance department. Reporting directly to the QA Manager, the QA Line Inspector is responsible for ensuring daily compliance with cGMPs, SOPs, and all applicable regulatory guidelines. This position demands sharp attention to detail and a strong understanding of quality assurance best practices specific to pharmaceutical, cosmetic, and nutriceutical manufacturing processes. The QA Line Inspector inspects finished goods on the packaging line, audits item details against descriptions, and ensures compliance with established quality standards. They contribute to the overall production quality by checking product attributes such as fill levels, weights, labeling, barcodes, and packaging integrity.
In addition to routine inspections, the inspector handles documentation including daily reports, retains logs, and quarantine metrics. They apply release and quarantine stickers to product pallets, estimate batch yields, and support cross-departmental quality activities. Part of their responsibilities includes preparing samples for laboratory approval, reviewing and finalizing batch records, and processing quality-related documentation such as Questionable Material Reports (QMRs), Material Destruction Records (MDRs), and Reprocessing Orders (ROs). The QA Line Inspector also plays a role in internal audits, client audits, and ensures proper record-keeping and regulatory compliance at all times.
The ideal candidate will have at least two years of experience inspecting products in a GMP environment involving pharmaceuticals, cosmetics, or nutritional supplements. Proficiency in Microsoft Office tools, strong communication skills in English both verbal and written, and the capacity to analyze and present quantitative data are essential. This job requires the ability to stand and perform repetitive manual tasks throughout the shift, with a strong focus on safety and hygiene. The position emphasizes discretion, excellent interpersonal skills, and a professional demeanor to interact effectively with management, peers, vendors, and auditors. The role does not include supervisory responsibilities but demands a high level of independent judgment and problem solving. Overall, this is an excellent opportunity to contribute to a dynamic, quality-focused manufacturing environment while advancing a career in quality assurance.
The role of Quality Assurance (QA) Line Inspector is integral to the company’s Quality Assurance department. Reporting directly to the QA Manager, the QA Line Inspector is responsible for ensuring daily compliance with cGMPs, SOPs, and all applicable regulatory guidelines. This position demands sharp attention to detail and a strong understanding of quality assurance best practices specific to pharmaceutical, cosmetic, and nutriceutical manufacturing processes. The QA Line Inspector inspects finished goods on the packaging line, audits item details against descriptions, and ensures compliance with established quality standards. They contribute to the overall production quality by checking product attributes such as fill levels, weights, labeling, barcodes, and packaging integrity.
In addition to routine inspections, the inspector handles documentation including daily reports, retains logs, and quarantine metrics. They apply release and quarantine stickers to product pallets, estimate batch yields, and support cross-departmental quality activities. Part of their responsibilities includes preparing samples for laboratory approval, reviewing and finalizing batch records, and processing quality-related documentation such as Questionable Material Reports (QMRs), Material Destruction Records (MDRs), and Reprocessing Orders (ROs). The QA Line Inspector also plays a role in internal audits, client audits, and ensures proper record-keeping and regulatory compliance at all times.
The ideal candidate will have at least two years of experience inspecting products in a GMP environment involving pharmaceuticals, cosmetics, or nutritional supplements. Proficiency in Microsoft Office tools, strong communication skills in English both verbal and written, and the capacity to analyze and present quantitative data are essential. This job requires the ability to stand and perform repetitive manual tasks throughout the shift, with a strong focus on safety and hygiene. The position emphasizes discretion, excellent interpersonal skills, and a professional demeanor to interact effectively with management, peers, vendors, and auditors. The role does not include supervisory responsibilities but demands a high level of independent judgment and problem solving. Overall, this is an excellent opportunity to contribute to a dynamic, quality-focused manufacturing environment while advancing a career in quality assurance.
Job Requirements
- High school diploma
- Two or more years of experience in GMP inspection environment
- Knowledge of cGMPs, SOPs, and FDA regulations
- Proficient computer skills including Microsoft Office
- Strong communication skills in English
- Ability to perform repetitive tasks for extended periods
- Ability to stand and walk up to eight hours per day
- Ability to lift and carry up to 20 lbs
- Willingness to work rotating shifts between 1st and 2nd shift
- Ability to wear required safety equipment
- Good manual dexterity
- Ability to handle confidential information sensitively
Job Qualifications
- High school diploma
- Minimum 2 years experience inspecting pharmaceutical, cosmetic, or nutriceutical products in a GMP environment
- Discretion in handling confidential and sensitive matters
- Knowledge of drug cGMPs, SOPs, and FDA regulatory guidelines
- Knowledge of QA industry best practices
- Proficient in Microsoft Office including Word, Excel, Outlook, and PowerPoint
- Ability to learn new software quickly
- Excellent verbal and written communication skills in English
- Ability to present information clearly in front of groups
- Strong analytical and mathematical skills
- Ability to analyze and interpret data
- Good judgment and problem-solving skills
- Ability to apply knowledge of QA best practices and company policies
Job Duties
- Inspect and issue reports of packaging finished goods using established protocols
- Audit item number versus description
- Inspect against quality standards
- Create standards for approval as needed
- Submit samples to laboratories for product approval
- Check and inspect in-process product quality
- Check product attributes including fill quality, height, weight, bottles, and crimp of tubes
- Verify bar codes
- Maintain retain Log Book
- Apply release stickers on finished goods pallets
- Prepare daily reports of in-process packaging products
- Imprint and place quarantine stickers on pallets
- Estimate batch yields and close reports
- Support department functions such as auditing batch records, processing checks, filling, line inspection, and special orders
- Maintain cleanliness and housekeeping in work area including tools
- Assist in physical inventory counts
- Perform other duties assigned by supervisor
- Review and finalize batch records
- Release batches for shipment
- Process Questionable Material Reports, Material Destruction Records, and Reprocessing Orders
- Review and approve SOPs and QA documents
- Conduct internal audits and participate in client and regulatory audits
- Maintain QA records and documentation
- Demonstrate excellent interpersonal skills and professionalism
- Adhere to company policies and procedures
- Establish priorities to ensure timely job completion
Job Criteria
Experience
No experience required
Job Location
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