Inspection Technician

QPS Employment Group; Rockford, New York (IL, NY); On-site; USD 10,000 - 60,000; Full time

Job summary

Join a forward-thinking staffing firm as a Quality Inspector, where your role is vital to ensuring the highest standards in pharmaceutical safety and compliance. You'll be at the forefront of product quality, conducting inspections and audits to safeguard patient health. This position offers a dynamic environment where precision and accountability are paramount. With opportunities for continuous improvement and teamwork, you'll contribute to life-saving commitments in the industry. If you have a keen eye for detail and a passion for quality, this role is perfect for you.

Benefits

Access to sought-after positions

Dedicated placement specialists

Qualifications

• Ability to perform basic computer tasks and operate common software.
• Attention to detail and sound judgment are crucial.

Responsibilities

• Perform production room approvals and verify inspections.
• Ensure compliance with safety protocols and documentation.

Skills

Effective communication skills

Attention to detail

Problem-solving abilities

Time management skills

Tools

Basic computer software

Job description

Position Title:

Quality Control - 1st, 2nd + 3rd Shift

Wage:

$17.88-$20.15 per hour

Shift:

1st, 2nd, 3rd

Hours:

7:00am-3:00pm; 3:00pm-11:00pm; 11:00pm-7:00am

Be the frontline of pharmaceutical excellence.

As a Quality Inspector, you'll play a critical role in ensuring that every product released from our facility meets the highest standards of safety, purity, and regulatory compliance. From inspecting raw materials to verifying final packaging, you'll help safeguard the health and trust of patients worldwide. Join a team where precision, accountability, and continuous improvement drive everything we do - because in the pharmaceutical world, quality is more than a requirement; it's a life-saving commitment.

Quality Control Responsibilities include but are not limited to:

1. Perform production room approvals after product and lot changes
2. Verify first piece inspection to ensure finished goods code, format, and expiration date are correct
3. Ensure equipment is packaged within validated parameters and equipment calibration dates on all process equipment are within required specifications. If not, contact the appropriate personnel to recalibrate and/or remediate the issue.
4. Review batch record to ensure equipment challenges and hourly inspections have been conducted and any non-conformances are addressed appropriately. Conduct periodic checks to confirm hourly inspections are being performed correctly and on track to meet requirements.
5. Review sampling pages to ensure samples have been taken, labeled, and documented appropriately.
6. Audit production room to ensure Cleaning and Use logbooks, Mechanical Set-up logbooks, and Preventive Maintenance logbooks have been completed accurately and timely.
7. Confirm package (unit) functionality (perfs, peel, push, seals, etc.)
8. Check to ensure portable equipment has been cleaned and documented correctly on quality form.
9. Audit production personnel to ensure the job is performed safely including wearing required personal protective equipment.
10. Ensure recovery stations are segregated from product flow.
11. Confirm bulk material and components for job are correct and kept covered.
12. Review each equipment clean room logbooks for correct clean room, entries are complete, correct, and legible.
13. Review temperature and humidity data to ensure within acceptable job parameters.
14. Document audits using the Quality Auditor checklist listing the room, production job description, and date when the audit was conducted.
15. Identify proactively gaps in batch records and to mitigate deviations and documentation errors.
16. Participate on improvement teams (i.e., FMEA's, Kaizen, batch record etc.) as needed
17. Support Root Cause Analysis as needed.
18. Ensure 5s (Sort, Set in order, Shine, Standardize, Sustain method) compliance.
19. This position may require overtime and/or weekend work.
20. Knowledge of and adherence to all company, cGMP (Current Good Manufacturing Practices), and GCP (Good Clinical Practices) policies, procedures, rules.
21. Attendance to work is an essential function of this position.

Quality Control Requirements:

1. Ability to perform basic computer tasks and operate common computer programs.
2. Ability to speak effectively in various conversations.
3. Ability to read standard items addressed to general readers.
4. Ability to apply common sense understanding to carry out instructions in written, oral, or diagram form. Deal with problems involving several variables in standardized situations.
5. Attention to detail.
6. Sound and accurate judgment.
7. Professional demeanor.
8. Excellent time management skills.

For inquiries, contact: [e-mail]

IND017

About us:

QPS Employment Group is a full-service staffing firm with over 50 offices across the United States. We connect great people with great companies in various industries including industrial, skilled trades, administrative, manufacturing, and more.

Why Work with QPS?

• Access to sought-after positions with leading employers
• Dedicated placement specialists to guide your job search