Specialist – Technical Group
Job in
Springfield, Sangamon County, Illinois, 62777, USA
Listed on 2026-07-22
Listing for:
Jobtailor
Full Time
position Listed on 2026-07-22
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering
Job Description & How to Apply Below
Responsibilities
- Support product and process renovation through formulation adjustments, reformulation efforts, and process improvements
- Assist in the development of nutritional supplements across formats to support manufacturing, innovation, and product enhancements
- Prepare, maintain, and ensure accuracy of manufacturing documentation (e.g., recipes, batch records, specifications, change controls, QMS, EQAs) while adhering to company policies, SOPs, quality standards, and regulatory requirements
- Analyze and interpret data to support statistical evaluations, problem-solving, and continuous process improvements
- Collaborate cross-functionally (Quality, Procurement, R&D, Marketing, Finance, Manufacturing, Supply Chain) to resolve product, raw material, and supply‑related issues
- Communicate project updates, risks, and changes to management in a timely manner
- Support scale‑up, validation, and technology transfer activities to internal and external manufacturing partners
- Engage with suppliers, external partners, and training opportunities to stay current on industry trends and best practices
- Contribute to continuous improvement initiatives while building strong cross‑functional relationships and enhancing team efficiency
- Participate in mentoring, seek guidance, and actively support professional development
- Operate manufacturing and laboratory equipment and apply problem‑solving and organizational skills to support project execution
- Participate in Stage/Gate product development processes and support delivery of key milestones
- Bachelor’s degree in Chemistry, Chemical Engineering, Pharmaceutical Science, Food Science or related field
- 1+ year of hands‑on product development, formulation, and manufacturing experience involving tablets, capsules, liquids, soft gels, gummies, powders, packaging, or related technologies
- Knowledge of product development, technical and manufacturing processes, and food science principles
- Experience leading medium‑complexity technical projects and working effectively within cross‑functional teams
- Previous manufacturing or factory experience, preferred
- Preferred experience with product scale‑up, validation, and technology transfer activities
- Proficiency in Microsoft Office applications (Excel, Word, PowerPoint, Outlook)
- Preferred experience with SAP, SPSS (Statistical Package for the Social Sciences) and/or Minitab for data management, reporting, statistical analysis, and process improvement initiatives
- Ability to be exposed to food allergens and allergen‑containing materials
- Knowledge of food safety, quality, and regulatory requirements
- Willingness to travel approximately 40%
Demonstrates expertise in product development and formulation processes, with a strong focus on manufacturing documentation accuracy and compliance with quality and regulatory standards. Proficient in statistical analysis and cross‑functional collaboration to drive continuous improvement initiatives.
Highest‑signal resume keywords- Product Development
- Formulation Experience
- Manufacturing Documentation
- Statistical Analysis
- Cross‑Functional Collaboration
- Product Development
- Formulation
- Manufacturing Processes
- Statistical Analysis
- Food Science Principles
- Technical Project Leadership
- Quality Standards
- Regulatory Requirements
- Problem‑Solving
- Organizational Skills
- Communication
- Mentoring
- Team Efficiency
- Nutritional Supplements
- Food Safety
- Quality Management System
- Change Controls
- Stage/Gate Process
- Technology Transfer
- Scale‑Up
- Validation
- Continuous Improvement
- Cross‑Functional Teams
- Microsoft Office
- SAP
- SPSS
- Minitab
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