QC Inspector

QC Inspector

Location: Belen, NM
Industry: Pharmaceutical
Shift: 3rd shift
Pay Rate: $20-21 per hour
Employment Type: Contract to hire

Overview:
Join a global leader in pharmaceutical manufacturing that develops innovative products and services supporting every phase of solid dose drug design and development. Known for advanced coating technologies, modified release solutions, and high-quality functional excipients, this organization is committed to quality, innovation, and continuous improvement while providing employees with opportunities to build rewarding careers in a GMP manufacturing environment.

The Quality Control Inspector plays a key role in ensuring products meet the highest quality standards through laboratory testing, inspection, equipment calibration, documentation, and continuous improvement initiatives. This position is ideal for someone who enjoys problem-solving, working with laboratory equipment, and making a direct impact on product quality and patient safety.

Responsibilities & Duties:

• Release finished product for shipment
• Release raw materials to production (incoming control)
• Maintain accurate records and files, ensure IPC results are inside specifications and well recorded
• Prepare and operate laboratory equipment
• Performs variety of other duties as assigned
• Maintain cleanliness of the work area and participate to the 6S
• Open deviation form when necessary (internal deviation, non-conforming product, supplier complaints)
• Archive batch files and is responsible for retain samples
• Perform data collection and data entry into computer system
• Perform confirmation and associated transaction in SAP
  

• High School Diploma or equivalent required; Associate's Degree preferred
• 1-3 years of Quality Inspection experience in a manufacturing environment or equivalent experience (GMP preferred)
• ASQ Quality Technician certification is a plus.
• Experience operating laboratory testing and measuring equipment.
• Understanding of quality systems, inspection techniques, and continuous improvement principles.
• Strong mathematical, analytical, and problem-solving skills.
• Excellent written and verbal communication skills.
• Proficiency with Microsoft Office, including Excel, Outlook, and PowerPoint.
• Experience with SAP, Oracle, or similar ERP systems is preferred.
• Ability to read and follow SOPs, work instructions, and technical documentation.
• Strong attention to detail with the ability to maintain accurate records in a regulated manufacturing environment.

SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a relationship-driven model partnering closely with clients to understand not only the role, but the company s culture, goals, and vision. Our mission is to match purpose-driven professionals with organizations committed to advancing human health, building long-term partnerships that drive innovation, quality, and performance.

EOE/ADA
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