| Job Description | Description:
Director/Associate Director Engineering
If you are looking for an uncommon opportunity -- a chance to join an organization known
for its scientific excellence in the research and development of pharmaceuticals -- it's time to consider Regeneron.
Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets three products in the United States, EYLEA (R) (aflibercept) Injection, ZALTRAP (R) (ziv-aflibercept) Injection for Intravenous Infusion, and ARCALYST (R) (rilonacept) Injection for Subcutaneous Use. Regeneron has filed a regulatory application with the U.S. Food and Drug Administration (FDA) for a second indication for EYLEA. Phase 3 studies are in progress with EYLEA in two additional indications and with product candidates sarilumab and REGN727. Regeneron has active research and development programs in many disease areas, including ophthalmology, inflammation, cancer, and hypercholesterolemia.
Summary:
Regeneron is currently seeking a talented and motivated Director/Associate Director Engineering to join our Tech Operations department reporting to the VP of Tech Ops. Primary responsibilities include managing the design, specification, and installation of new and renovated biopharmaceutical process equipment. Will also provide engineering support and problem solving for existing equipment and manufacturing processes.
Essential Functions:
'Designs and specifies cGMP process and utility equipment, piping, and controls.
'Manages projects related to process and utility equipment and manufacturing.
'Manages the design review, factory & site acceptance, and installation of equipment.
'Prepares process and instrument drawings and other related drawings.
'Supports Validation Department through preparation of design documents and protocol review.
'Recommends appropriate corrective/preventive actions for existing equipment and manufacturing processes.
'Evaluates, approves, prepares and/or executes modification/change control documentation.
Experience:
Required Skills:
'Thorough knowledge of cGMPs and sanitary equipment design requirements;
'In-depth knowledge of process control systems and automation;
'Advanced knowledge of engineering documentation required for cGMP process and utility equipment;
'Advanced knowledge of CAD software
'Substantial knowledge of clean rooms and pharmaceutical equipment;
'Strong written and oral communication skills
'Solid supervision and leadership skills
'Ability to understand and manage project plans, budgets and schedules
'Working knowledge of word processing, spreadsheet, and database management software;
'Functional knowledge of PCs
Experience:
Requires BS/BA or higher in chemical, mechanical, or electrical engineering with 10+ years of experience in equipment, process, or facilities engineering. Direct experience with biopharmaceutical process equipment is preferred.
We offer a competitive compensation and benefits package including stock incentives, 401k with company match, as well as the expected health and welfare benefits. Comprehensive relocation benefits are available, as required.
This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply to us today and find out what we mean when we say that, at Regeneron, we have an unwavering commitment to combining good science & good business. |
| | Company | | Regeneron | Job Code | | State or Province | | New York | | |
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