Warehouse Specialist / Senior Specialist

Page Mechanical Group, Inc.; Oklahoma City (OK); On-site; USD 55,000 - 85,000; Full time

Job summary

Page Mechanical Group, Inc. is seeking a Warehouse Specialist to manage day-to-day cGMP warehouse operations at the Oklahoma City GMP site. The role emphasizes strict GDP adherence, precise record-keeping, and high ownership for internal and external customers.

Responsibilities include receiving, segregation, staging, issuing, and outbound cold-chain shipping with regulatory compliance. Experience in regulated environments and readiness for ERP integration are required.

Qualifications

• Education: High school diploma required; Associate or Bachelor’s degree preferred.
• Experience: 1–3 yrs for Specialist; 3–7+ yrs for Senior Specialist in regulated environments such as cGMP, Pharma, Medical Device, or Dietary Supplements.
• Compliance: Demonstrated understanding of cGMP and GDP; legible record-keeping is essential.
• Data & systems: High attention to logs, lot numbers, spreadsheets; ERP readiness anticipated.

Responsibilities

• Manage GDP-compliant receiving, quarantine, issuance, and outbound shipping with audit-ready logs.
• Perform GMP receiving, segregation, cycle counts, expiry tracking; support data hygiene for ERP deployment.
• Pick, stage, issue, and return materials for GMP/non-GMP runs per SOPs.
• Prepare and document cold-chain shipments, maintain temperature logs per IATA and CFR 49.
• Report discrepancies and maintain clean, compliant warehouse zones.

Skills

GDP mindset

cGMP

Good Documentation Practices

Data & systems discipline

Cold chain handling

Dangerous Goods Shipping

ERP readiness (Infor, SAP, NetSuite)

Education

High school diploma

Associate or Bachelor’s degree preferred

Tools

Infor

SAP

NetSuite

Job description

Warehouse Specialist / Senior Specialist

Location: Oklahoma City, OK (GMP Site)|Department: Supply Chain|Type: Full-Time|Level: Dependent on Experience

ABOUT THE ROLE

The Warehouse Specialist manages day-to-day cGMP warehouse operations, including material receipt, quarantine/release segregation, staging, issuance, and cold-chain/ambient shipping. Because we operate in a highly regulated pharmaceutical CDMO environment, this position requires strict adherence to Good Documentation Practices (GDP) and pristine record-keeping. Success in this role requires a compliance-first mindset, extreme precision, high personal ownership, and customer service orientation to both internal and external customers.

KEY RESPONSIBILITIES

• Good Documentation Practices (GDP) & Audit Readiness: Execute precise, contemporaneous documentation for receiving, material transfers, issuance, and outbound shipping with zero tolerance for record-keeping shortcuts. Maintain audit-ready paper and electronic logs.
• Receiving, Segregation & Inventory Control: Perform GMP receiving, quarantine/release/rejected material segregation, cycle counts, and expiry tracking. Actively support clean dataset preparation and master data hygiene to enable future ERP deployment.
• Picking, Staging & Batch Support: Accurately pick, stage, issue, and return materials and consumables for GMP and non-GMP manufacturing runs according to strict SOPs.
• Cold-Chain & Outbound Shipping: Prepare, package, and document temperature-sensitive domestic/international shipments (15 to 25°, 2°C to 8°C, -20°C, -80°C, -196°C), maintaining strict chain-of-custody and temperature logs and labeled appropriately according to IATA and CFR 49 regulations.
• Non-Conformance & Facility Care: Promptly report material discrepancies or documentation errors in partnership with Leadership and Quality Assurance. Maintain clean, compliant, and safe warehouse zones.

QUALIFICATIONS & REQUIREMENTS

• Education: High school diploma required; Associate or Bachelor’s degree preferred.
• Experience & Title Level: Experience levels determine title (Specialist: 1–3 yrs; Senior Specialist: 3–7+ yrs). Prior experience in a regulated environment (cGMP, Pharma, Medical Device, or Dietary Supplements) is required.
• Compliance & GDP Mindset: Demonstrated understanding of cGMP and Good Documentation Practices (GDP). Must view physical/electronic record-keeping as equal in importance to physical material movement. Must have legible penmanship.
• Data & Systems Discipline: High detail orientation with logs, lot numbers, and spreadsheets. Readiness for future ERP integration (e.g., Infor, SAP, NetSuite).
• Logistics & Cold Chain: Experience handling temperature-controlled materials and preparing regulated cold-chain shipments. Certification in Dangerous Goods Shipping per IATA and 49 CFR Parts 100-185 a plus.
• Physical Requirements: Ability to lift up to 50 lbs, operate warehouse material handling equipment safely, and work in ambient and cold-storage environments.

CORE COMPETENCIES

• World-Class Service & Cross-Functional Partnership: Views Supply Chain as a premier service provider to every internal functional group and an advocate for external clients. Collaborates seamlessly as a team player, ensuring accurate material tracking and precise usage reporting so client invoicing is prompt, transparent, and error-free.
• CDMO Ownership Mentality: Takes full accountability for assigned tasks in a fast-paced contract manufacturing environment. Recognizes that every log entry, material transfer, and batch kit directly impacts client timelines, product quality, and regulatory compliance.
• Precision & Record Integrity: "If it wasn't documented, it didn't happen." Unwavering focus on accuracy across part numbers, lot numbers, quantities, dates, and sign-offs.
• Process Discipline: Ability to transition smoothly from high-velocity standard warehousing to the deliberate, methodical, and compliant pace required by pharma/GMP manufacturing.