Warehouse Supervisor at CAMRIS Full-time Job2 months ago Manufacturing & Warehouse Silver Spring 309 views Reference: 992
We are seeking a Warehouse Supervisor to support the Pilot Bio-Production Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland. PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. The professionals at PBF are engaging in trailblazing endeavors every day. Most exciting, the end products vary, so every year brings multiple opportunities for professional enrichment in original projects.
CAMRIS International, LLC, is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with todays most effective, evidence-based best practices. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.
Our employees enjoy a diverse, collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad.
- Oversees daily warehouse operations and supervises the inventory team, ensuring the team appropriately responds to work demands.
- Leads inventory management process development, including but not limited to Kanban systems, database use, and procurement-to-pay system implementation.
- Optimizes warehouse electronic data records.
- Fosters a culture of continuous improvement and sustainable change and ensures productivity targets and business objectives are met.
- Trains staff and assist direct reports as needed.
- Liaises with internal and external partners.
- Oversees the receipt, storage, disposition, destruction, and shipping of GMP materials. Responsible for shipping regulated material and will be required to maintain appropriate certification (provided by DOD) as a shipper of regulated materials (i.e., DOT certification, IATA certification, etc.).
- Controls the physical movement of materials based on status (quarantined, released, QA Hold); maintains product status labeling.
- Verifies warehouse staff GDP documentation compliance and tracking information (receipt records, distribution records, spreadsheets, database logs, etc.) to accurately reflect the physical inventory of materials following cGMP.
- Reports inventory discrepancies to Quality Assurance and assists in resolving, documenting, and implementing corrective actions.
- Responsible for cycle counts, organization, and cleanliness of the warehouse.
- Maintains product storage units/locations so that the product is properly identified, retrievable, and consistent with storage locations listed on the products storage records (physical and electronic).
- Interacts with the building monitoring system to ensure storage conditions of materials remain in control. Responds to alarms on storage equipment, moving product to other appropriate locations if storage equipment fails. Notifies appropriate staff in the event of a storage unit failure and appropriately documents the event.
- Serves as the contact for the storage and removal of regulated waste, maintaining appropriate documentation.
- Provides other administrative support and assists QA staff as directed by the QA Manager.
- Maintains a safe workplace, ensuring that he/she is aware of and observes appropriate safety and occupational health rules and regulations. The employee is required to attend safety training relative to his/her position and report any infractions of safety procedures to the facility Safety Officer.
- Performs other related duties as required and assigned.
- Bachelors degree and 10 years of relevant work experience, or an equivalent combination of credentials and relevant biopharmaceutical industry experience.
- Experience managing team members.
- Experience in a GMP-related facility to include material management, warehousing, and shipping, or quality assurance.
- CPIM certification preferred.
- Familiarity with Microsoft Office tools.
- Physical Capability: Work may involve long periods of standing and handling of numerous chemicals and/or hazardous biological material.
- Physical Capability: Must be able to lift light to moderately heavy objects.
- Must be able to work independently following a brief period of specific technical training.
CAMRIS International LLC offers competitive salaries and comprehensive benefits. Please submit your resume online at www.CAMRIS.com. CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or any other characteristic protected by any applicable federal, state, or local law.
Full vaccination against COVID-19, defined as two doses of Moderna, two doses of Pfizer, or one dose of Johnson & Johnsons Janssen, is required for this position.
Employment is contingent upon the successful completion of a background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to, the following: (1) contacting your professional references; (2) verification of previous employment, education, and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully complete any required background check questionnaire during initial onboarding.
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