What are the responsibilities and job description for the Supply Chain Associate position at Advanced Bio-Logic Solutions Corp.?
Supply Chain Senior Associate
Location: Hybrid - Louisville, KY
Employment Type: Contingent Worker (Contract, W2)
Contract Length: 12 months (possible extension)
Compensation: $26/$30 per hour (based on experience)
Summary of the Role
Join a large biotech pharmaceutical leader as a Supply Chain Senior Associate supporting supply chain compliance, quality systems, and continuous improvement initiatives. In this role, you will oversee temperature excursions, deviation investigations, CAPA management, and GDP compliance activities across the U.S. supply chain network. This position offers the opportunity to work closely with quality, supply chain, and external partners to ensure regulatory compliance and operational excellence.
Key Responsibilities
- Own and manage temperature excursion records across the supply chain network
- Manage minor and major deviation records and facilitate root cause analysis activities
- Oversee CAPA and CAPA EV records, ensuring timely implementation and closure
- Manage missing product notifications and support Event Review Team activities
- Support internal and external audits and regulatory inspections
- Maintain compliance tracking tools and Smartsheets for deviations, excursions, CAPAs, and quality metrics
- Lead or support continuous improvement projects focused on supply chain compliance
- Apply risk-based decision-making and escalation practices
- Collaborate with Quality, Information Systems, Supply Chain, and external vendors
- Ensure compliance documentation remains accurate, current, and audit-ready
Qualifications
- Bachelor's degree in Life Sciences and 2 years of GMP/GDP compliance experience, or equivalent experience
- Strong understanding of Quality Assurance principles, GMP, and GDP requirements
- Experience managing deviations, CAPAs, investigations, and compliance records
- Strong analytical and evidence-based problem-solving skills
- Technical writing experience
- Experience with Smartsheet, Excel, PowerPoint, and Trackwise
- Strong communication and organizational skills
- Ability to work onsite in Louisville, KY three days per week
Preferred:
- Experience supporting audits and inspections
- Familiarity with SAP and Veeva
- Laboratory, pharmaceutical quality, or supply chain compliance experience
- Strong multitasking and cross-functional collaboration abilities
Top 3 Must Have Skills
- Bachelor’s in Life Sciences with GMP/GDP compliance experience or equivalent
- Strong knowledge of Quality Assurance, GMP, and GDP
- Analytical and evidence-based problem-solving
Day-to-Day Responsibilities
- Manage temperature excursions, deviations, CAPAs, and missing product records
- Lead root cause investigations and corrective action activities
- Maintain compliance tracking systems and documentation
- Support audits, inspections, and quality reviews
- Collaborate with internal and external stakeholders to maintain GDP compliance
- Participate in continuous improvement initiatives and compliance projects
Education
- High school diploma / GED and 2 years of work experience, OR
- Associate degree and 6 months of work experience, OR
- Bachelor’s degree
Apply Now
Ready to support quality, compliance, and supply chain excellence within a global biotech organization? Apply today.
Salary : $26 - $30