QC TECH

About Company:

About GLOBOPHARMAINC.

At GLOBOPHARMA Inc., we’re proud to be at the heart of American manufacturing—where precision, innovation, and people come together to build the future. For over 24 years, we’ve been producing high-quality Nutritional Supplement and Skin Car product with a commitment to excellence that sets us apart.

But what truly makes Eagle Labs a great place to work isn’t just what we make—it’s how we make it, and who we make it with.

We believe a strong company starts with a strong team. That’s why we’ve built a workplace culture grounded in respect, safety, growth, and opportunity.

What sets us apart as an employer:

• ️ Skilled craftsmanship meets modern innovation
  Our employees work with the latest tools, technologies, and lean manufacturing processes to deliver products we’re proud of.

• People-first culture
  We offer competitive pay, great benefits, ongoing training, and a strong focus on health, safety, and work-life balance.

• Opportunities to grow
  Whether you're just starting out or bringing years of experience, we provide clear pathways for advancement, apprenticeships, and leadership development.

• Teamwork and pride
  At Eagle Labs, you’re not just doing a job—you’re contributing to something bigger. We value the pride that comes with building something with your hands and your team.

GloboPharma Inc. is more than a workplace. It’s a place where hard work is rewarded, careers are built, and every employee is valued. Join us—and help shape the future of manufacturing.

About the Role:

As a Quality Control (QC) Technician at GLOBALPHARMA, you will play a critical role in ensuring that pharmaceutical products meet the highest standards of quality and safety before reaching the market. You will be responsible for conducting rigorous testing and analysis of raw materials, in-process samples, and finished products to verify compliance with regulatory requirements and internal specifications. Your work will directly impact product reliability and patient safety by identifying deviations and facilitating corrective actions. Collaborating closely with production, quality assurance, and regulatory teams, you will help maintain a compliant and efficient manufacturing environment. Ultimately, your contributions will support GLOBALPHARMA’s commitment to delivering safe, effective, and high-quality pharmaceutical products worldwide.

Minimum Qualifications:

• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Biology, or a related scientific field.
• Experience working in a GMP-regulated pharmaceutical or biotechnology laboratory environment.
• Strong understanding of laboratory safety protocols and quality control procedures.
• Proficiency in using laboratory instruments such as HPLC, GC, UV-Vis spectrophotometers, and microbiological testing equipment.
• Excellent attention to detail and ability to maintain accurate and thorough documentation.

Preferred Qualifications:

• Certification in Quality Control or Quality Assurance (e.g., ASQ Certified Quality Technician).
• Experience with computerized laboratory information management systems (LIMS).
• Knowledge of regulatory guidelines such as FDA, EMA, and ICH.
• Previous experience in pharmaceutical product release testing.
• Strong problem-solving skills and experience in root cause analysis.

Responsibilities:

• Perform routine and non-routine chemical, physical, and microbiological testing of pharmaceutical materials and products according to established protocols.
• Document and analyze test results accurately, ensuring data integrity and compliance with Good Manufacturing Practices (GMP).
• Identify and report any deviations or non-conformances, initiating investigations and supporting root cause analysis.
• Maintain laboratory equipment and ensure calibration and validation are up to date to guarantee reliable test outcomes.
• Collaborate with cross-functional teams to support quality improvement initiatives and regulatory inspections.

Skills:

The required skills enable the QC Technician to perform precise and reliable testing, ensuring that all pharmaceutical products meet stringent quality standards. Proficiency with analytical instruments like HPLC and GC is essential for daily sample analysis and data collection. Attention to detail and documentation skills are critical for maintaining compliance with GMP and regulatory requirements. Preferred skills such as familiarity with LIMS and regulatory guidelines enhance efficiency and support adherence to global standards. Strong problem-solving abilities allow the technician to identify issues quickly and contribute to continuous quality improvement efforts.