In Process Quality Coordinator in Greenville, South Carolina at Human Technologies, Inc

Position Title: In Process Quality Coordinator

Location: Greenville, South Carolina

Job Summary – In-Process Quality Assurance Coordinator
Ensures consistent product quality through independent in-process inspection, testing, verification, and auditing of pharmaceutical products during manufacturing and packaging operations in a cGMP-regulated environment. This role supports real-time compliance, documentation accuracy, and quality decision-making on the production floor.What We Offer

• Full benefits package – Medical, Dental, Vision, EAP, 401(k) with company match
• 12HR day and 12HR night shifts available
• Night shift differential ($1.25/hour)
• Paid Time Off and company holidays
• Stable, direct-hire role in a regulated pharmaceutical environment
• Climate-controlled manufacturing facility
• Nicotine-free campus supporting employee wellness

What You Need

• High School Diploma or GED required (Associate degree preferred)
• Minimum 2 years of QA or QC experience in a regulated manufacturing environment
• Strong understanding of cGMP and FDA regulations
• Experience reviewing batch records and GMP documentation
• Ability to work independently with minimal supervision
• Strong attention to detail and documentation discipline
• Ability to manage shifting priorities in a fast-paced manufacturing environment

Responsibilities –

• Follows all policies, procedures, SOPs, cGMP, Work Instructions, and supervisor instructions.
• Perform verification of manufacturing operations.
• Collects samples and performs in-process testing (pH, dissolved oxygen, titrations, etc.) and assay calculations for compounding operations.
• Perform batch calculations and QS verifications.
• Collects samples and performs TOC analysis on clean equipment.
• Perform daily checks on the TOC levels of the purified water system.
• Collects and maintains data for quality reporting.
• Support the development and revision of SOPs, Work Instructions (WIs), and related quality documents.
• Maintain up-to-date knowledge of cGMPs, regulatory requirements, and company quality policies. Promote cGMP compliance in an FDA/DEA regulated pharmaceutical manufacturing environment.
• Participate in continuous improvement activities to enhance product quality and operations efficiency.
  Perform in-process inspections and audits during manufacturing and packaging operations

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