Engineer I, Commercial Manufacturing

Xeris Pharmaceuticals • Chicago, IL

19d • $80,000 - $110,000 • Hybrid

About The Position

Overview Support all functions of the pharmaceutical supply chain for all commercial products. Ensure product is manufactured in a quality manner under cGMP’s and available for sale based on commercial forecasts. Ensure inventory and supplies are available at every point within the supply chain to meet production schedule. The Engineer I will provide a broad understanding of the manufacturing supply chain from drug substance manufacturing through commercial packaging and working within a matrixed organization. The Engineer I / II will assist with planning and execution of routine technical assignments and demonstrates firm understanding of relevant pharmaceutical regulations related to cGMP manufacturing. Responsibilities Support manufacturing operations at Contract sites (CMOs, etc.).

Requirements

• Bachelor’s degree required, master’s degree preferred in Engineering or relevant Supply Chain, Scientific, or equivalent degree with 3 to 5 years of experience working in pharmaceuticals
• Minimum 3 years of experience in a GMP pharmaceutical/biopharmaceutical environment with sterile drug product manufacturing
• Must have strong computer skills (including all Microsoft Office), Analytics, Technical Writing, Scheduling, Inventory Management

Nice To Haves

• Data Management
• Manufacturing/Supply Chain background

Responsibilities

• Assist in commercial production planning
• Support colleagues in the day-to-day manufacturing activities on a routine basis to ensure commercial supply
• Helps with logistics activities such as quotes, invoices, i nventory management and shipment of products and intermediates
• Frequently interacts with other functional peer group managers and CMOs to support the commercial manufacturing or development activities
• Accurately collects / performs data mining and appropriately records / trends observations
• Aid in the review of GMP batch records, work instructions, SOPs, deviations, CAPAs, or other required documents for cGMP operations
• Collaborate with other functions such as Device Development, Quality Assurance, Quality Control, Regulatory, and Finance

Benefits

• This role will include eligibility for bonus and equity.
• The total compensation package will also include additional elements such as multiple paid time off benefits, various health insurance options, retirement benefits and more.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 251-500 employees