Quality Supervisor - Life sciences & Warehouse

Quality Supervisor, Life Science DivisionMount Comfort Greenfield, IN, US (no relocation & No VISA sponsorship)PLEASE READ THE JOB DETAILS. THIS IS NOT AN IT QA ROLE!!!The Quality Supervisor is responsible for leading daily quality operations in the Raw Material Warehouse and Sampling Suite, ensuring compliance with GMP, regulatory agencies, and client-specific requirements. This role oversees a team of Quality Associates engaged in receiving, inspecting, sampling, and testing raw materials and components while maintaining strict adherence to regulatory standards and internal procedures. The Quality Supervisor ensures that cleanroom and sampling activities are performed under controlled conditions, safeguarding product integrity and preventing cross-contamination.In addition to managing team performance and workforce planning, the Quality Supervisor serves as a key liaison between Quality, Warehouse, and Operations, facilitating timely resolution of material quality issues, deviations, and client inquiries. This position supports audits, continuous improvement initiatives, and cross-functional projects to strengthen compliance and operational efficiency.The Quality Supervisor also ensures that all activities comply with safety, security, and regulatory requirements, including those related to hazardous materials, Department of Homeland Security (DHS), and Food and Drug Administration (FDA) guidelines. Key Requirements - Pharmaceutical raw material sampling and inspectionDirect supervision of quality personnelCleanroom and contamination-control oversightOwnership of quality systems and material dispositionPharmaceutical warehouse or distribution experienceExperience and Education Bachelor’s degree in scientific or technical discipline (e.g., Biology, Chemistry, Pharmaceutical Sciences) or equivalent experience.Minimum 3 years of Quality experience in GMP-regulated environmentStrong knowledge of GMP regulations (FDA, EU, ICH)At least 3 years of quality experience in a GMP-regulated pharmaceutical environment.Previous supervisory or managerial experience, including team leadership, daily work assignments, staffing, and employee development.Direct experience with pharmaceutical raw material sampling, incoming material inspection, material quality controls, or closely related activities.Working knowledge of GMP/GDP requirements, deviations, CAPA, investigations, change control, and audit readiness.Key Responsibilities:Leadership & Team DevelopmentLead, mentor, and develop a team of Quality Associates working in the Raw Material Sample Suite.Promote a culture of compliance, accountability, and continuous improvement.GMP Compliance & OversightEnsure all sampling, inspection, and testing activities comply with GMP, FDA, and client requirements.Maintain oversight of cleanroom operations, including gowning, trafficking, cleaning, environmental monitoring, and contamination control.Quality Systems ManagementManage and support quality system processes including deviations, CAPA, change control, investigations, and training related to the Sample Suite.Review and approve quality records, ensuring completeness, accuracy, and regulatory compliance.Material Quality ControlOversee quality checks for incoming raw materials and sampling processes to ensure product integrity and traceability.Collaborate with Warehouse and Operations to resolve material discrepancies and quality-related issues.Audit Readiness & Client SupportServe as the primary quality contact for internal and external audits and inspections related to the Sample Suite.Ensure timely and accurate communication with clients regarding quality issues in alignment with SOPs and Quality Agreements.Continuous Improvement & Risk ManagementIdentify process gaps and lead initiatives to enhance operational efficiency and regulatory compliance.Conduct risk assessments to support decision-making and ensure robust quality oversight.Safety & SecurityEnsure all activities comply with safety protocols and hazardous material handling guidelines.Adhere to security requirements mandated by the Department of Homeland Security (DHS), FDA, and other regulatory authorities.Key Outcomes Expected The Quality Supervisor is expected to:Ensure delivery of quality objectives in partnership with management through resource management, prioritization, schedules and/or projects.Ensure raw material sampling and inspection activities are completed accurately, on schedule, and in compliance with GMP requirements.Provide oversight and maintenance of quality systemsMaintain a state of inspection readiness.Plan and allocate daily manpower, schedules, and instructions to ensure timely completion of sampling, inspection, and quality control activities in alignment with client and operational priorities.Assign daily tasks based on individual team member skills (e.g., gowning, sampling, environmental monitoring, inspection, documentation, or material checks).Accept or reject raw materials based on quality, regulatory, and client-specific standards.Physically verify incoming and outgoing raw materials for damage, discrepancies, and compliance with specifications.Crosstrain Quality Associates to ensure operational flexibility and coverage across all suite functions.Maximize efficiency through proper use of systems and tools (e.g., LIMS, Raman, calipers, Go / No Go gauges, where applicable).Ensure all team activities comply with policies, SOPs, GMP requirements, and safety standards.Provide coaching, guidance, and support to employees, assisting with work process challenges and reinforcing adherence to compliance expectations.Critical Skills and Knowledge Strong understanding of current Good Manufacturing, Good Distribution, and Good Documentation Practices (GMP/GDP), as they apply to raw materials and pharmaceutical distribution operations.Proficient computer skills, including Microsoft Office.Planning and organizational skills to manage dynamic environment with shifting prioritiesDecision Making – ability to assess situations, evaluate risks, and implement effective & compliant solutions in a GMP environment.Communication – ability to effectively communicate to internal and external teams both verbally and written in an appropriate manner.Analytical Skills – ability to thoughtfully analyze a wide variety of information and data to make key decisions regarding potential risks associated with product quality.Teamwork – ability to establish professional relationships and rapport with internal and external peers and management.Proactiveness – ability to anticipate potential problems and risks related to product, operations, and investigate solutions.Organization – ability to manage multiple quality records with various due dates to ensure timely completion and maintain records in a readily retrievable formatPhysical Demands and Work Environment: Physical movements include bending, stooping, and lifting to 50 pounds as part of daily work routine. Will work on concrete in a warehouse environment (subject to heat and cold). Work is performed in a warehouse environment subject to temperature variances.Disclaimer: This job description is not intended to be all-inclusive. This position may be required to perform other related duties assigned to meet the ongoing needs of the organization.