Quality Control Technician

The Staffing Resource Group, Inc

Belen, NM

JOB DETAILS
SALARY
$19–$20 Per Hour
SKILLS
8D, American Society for Quality (ASQ), Analysis Skills, Biology, Biotech and Pharmaceutical, Business Development, Calibration, Change Control, Clinical Research, Communication Skills, Consulting, Continuous Improvement, Corrective and Preventative Action (CAPA) Systems, Customer Support/Service, Data Quality, Detail Oriented, Documentation, Drug Design, Drug Development, Drug Manufacturing, ERP (Enterprise Resource Planning), Educational Technology, External Audit, Food and Beverage Industry, GMP (Good Manufacturing Practices), High School Diploma, Human Health, Internal Audit, Laboratory, Laboratory Equipment, Laboratory Testing, Maintain Compliance, Manufacturing, Materials Testing, Mathematics, Medical Equipment, Microsoft Excel, Microsoft Office, Microsoft Outlook, Microsoft PowerPoint, Oracle, Patient Safety, Pharmacy, Presentation/Verbal Skills, Problem Solving Skills, Process Control Engineering, Product Development, Product Support, Project/Program Management, Purchasing/Procurement, Quality Assurance, Quality Assurance Methodology, Quality Control, Quality Metrics, Record Keeping, Regulations, Reporting Skills, SAP, Standard Operating Procedures (SOP), Supply Chain, Technical Support, Technical Writing, Test & Measurement Equipment, Test Equipment, Testing, Writing Skills
LOCATION
Belen, NM
POSTED
6 days ago

Quality Control Technician

Location: Belen, NM
Industry: Pharmaceutical
Shift: 1st shift
Pay Rate: $19-20 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 Technician 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:

  • Perform quality control testing on raw materials, in-process products, and finished goods according to approved procedures.
  • Operate, qualify, maintain, and calibrate laboratory testing equipment.
  • Interpret test results and prepare detailed reports with documented conclusions.
  • Support investigations using quality tools such as 8D, PDCA, 5 Why, and Fishbone Analysis.
  • Assist with development of inspection plans, test methods, and quality procedures.
  • Maintain Certificates of Analysis (COA) and Certificates of Compliance (COC).
  • Monitor in-process control charts and ensure quality data is accurately documented.
  • Support change control activities and continuous improvement initiatives.
  • Assist with internal, customer, and external audits.
  • Manage calibration activities to ensure compliance with SOPs and work instructions.
  • Support customer complaint investigations and CAPA activities using Oracle/SAP.
  • Provide technical support to Quality Inspectors and production teams as needed.
  • Maintain accurate documentation while following GMP requirements and company quality standards.
Required Qualifications:
  • High School Diploma or equivalent required; Associate's or Bachelor's degree in a science-related field preferred.
  • 3+ years of Quality Control experience in a GMP manufacturing environment or equivalent experience.
  • 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
IND123

About the Company

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The Staffing Resource Group, Inc