Development Engineer

Woodstock Sterile SolutionsWoodstock, IL
$85,000 - $99,000Onsite

About The Position

The Development Engineer is responsible for pre-development through scale-up and commercialization of formulations and processes for new customers and products. This role partners directly with customer scientists and engineers to bring innovative formulations into our patented blow-fill-seal (BFS) packaging platform, from early feasibility through full commercial-scale production.

Requirements

  • Bachelor of Science in Chemistry, Pharmacy, Engineering, or a relevant discipline required
  • Minimum of 5 years of relevant experience in pharmaceutical drug product process development, or a combination of lower experience with a strong academic background
  • Strong knowledge of mathematics, mechanical aptitude, and statistical analysis for research and development; working knowledge of Quality by Design principles
  • Strong problem-solving and analytical skills with a high level of attention to detail
  • Excellent documentation and communication skills, both written and oral, at all levels of the organization
  • Full complement of business computer literacy skills (word processing, spreadsheets, design software, database software, etc.)
  • Ability to interface with technical and non-technical customer representatives, outside suppliers, and WSS management
  • Ability to work independently and/or in a team environment across multiple projects; flexible and adaptable to changing priorities
  • Ability to perform timely risk assessments and act accordingly
  • Familiarity with cGMP principles or the ability to quickly learn and apply them; commitment to safe work practices
  • Demonstrated bias toward action, active listening, and a willingness to share skills and knowledge with others

Nice To Haves

  • Master of Science or PhD in Chemistry, Pharmacy, Engineering, or a relevant discipline desired
  • Experience in sterile processing or liquid drug formulation preferred
  • Experience with large molecule and/or biologics products is beneficial
  • Experience in personal care or food science industries may be considered relevant

Responsibilities

  • Work directly with customer scientists, development, and process engineers on formulation development, feasibility, scale-up, and commercialization into blow-fill-seal (BFS) packaging, including physicochemical attributes, consistency, and manufacturability
  • Demonstrate technical experience and expertise to build customer confidence in WSS's ability to produce their product
  • Work under the technical direction of Senior Development Engineers, the Product Development Engineering Manager, or other subject matter experts on complex, high-visibility problems
  • Provide technical direction, guidance, and mentoring for Associate Development Engineers
  • Define experimental designs for process development and optimization; define, justify, and acquire required laboratory equipment and instruments
  • Provide engineering technical guidance to production teams to improve key commercial processes
  • Define user requirements for new equipment and hardware (stainless steel vessels, tubing, fittings, sanitary valves, filter housings, steam traps, instruments, gauges, disposable components)
  • Develop scalable, robust processes that meet product specifications; assist customers in developing specifications based on feasibility and process capability data
  • Collect and analyze experimental data using engineering principles and mathematical techniques, exercising independent judgment
  • Define critical process parameters, operating ranges, and acceptance criteria supporting sterility assurance and process validation activities
  • Support regulatory submissions and defend process-related information in customer filings, internal documents, and government audits
  • Document process development activities in accordance with Good Documentation Practices (R&D notebooks, engineering studies, test runs, feasibility studies); author comprehensive product development plans
  • Consult external academic and industrial resources, guidance documents, standards, and regulations as needed
  • Create design concepts and basic CAD drawings/assemblies, isometrics, P&IDs, and shop drawings
  • Troubleshoot technical issues related to sterile/sanitary processes, investigate problems, and support or execute corrective actions
  • Act as technical subject matter expert on multi-disciplinary project teams; ensure key milestones are achieved and communicate risks to stakeholders
  • Review test reports and certificates for compliance with specifications for raw materials, finished products, and vendor documentation
  • Utilize Design of Experiments, Risk Assessments (e.g., FMEA), Quality by Design, and statistical tools to identify and solve problems early in the development process
  • Maintain effectiveness of Quality System components relevant to the position; identify, evaluate, and communicate risk throughout the organization
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