Smithfield Foods-posted 7 days ago
Full-time • Entry Level
Cincinnati, OH
5,001-10,000 employees

The position summary states the general nature and purpose of the job. Overall accountabilities are defined in this section. We are seeking a highly motivated and detail-oriented R&D Technologist to support the advancement of pharmaceutical manufacturing processes. This role involves designing and executing experiments, analyzing data, and collaborating cross-functionally to drive innovation and ensure compliance with regulatory standards. The ideal candidate will have a strong background in pharmaceutical sciences, engineering, or related fields, and a passion for continuous improvement in manufacturing technologies.

  • Process/Analytical method Development & Optimization · Develop and refine pharmaceutical manufacturing processes to enhance efficiency, product quality, and scalability.
  • Investigate and implement new materials and technologies to improve production outcomes.
  • Develop or improve analytical methods for product characteristics or quality control using novel technologies.
  • Have experience on analytical instruments, such as HPLC (e.g. IEX, RP, SEC), UV, plate reader, etc.
  • Experimental Design & Execution · Plan and conduct laboratory experiments for R&D projects.
  • Utilize scientific principles to validate hypotheses and support discoveries or innovation.
  • Data Analysis & Reporting · Analyze experimental data using appropriate statistical tools and methodologies.
  • Prepare detailed technical reports, including data interpretation, conclusions, and recommendations for process improvements.
  • Cross-Functional Collaboration · Partner with engineering, operation and quality control teams to identify and resolve manufacturing challenges.
  • Contribute to multidisciplinary project teams to support product development and scale-up activities.
  • Documentation & Knowledge Management · Maintain accurate records of experiments, procedures, and outcomes.
  • Support documentation for regulatory submissions and internal audits if needed.
  • Bachelor’s degree from an accredited four-year college or university in Chemistry/Biochemistry, Biochemical Engineering and Chemical Engineering or related field and 2+ years of relevant experience; or equivalent combination of education and experience required
  • Proven 2+ years’ experience in pharmaceutical manufacturing or process development.
  • Strong analytical and problem-solving skills.
  • Proficiency in data analysis software and laboratory instrumentation.
  • Excellent communication and technical writing skills.
  • Master’s degree in analytical chemistry, chemical engineer or related field.
  • Experience with scale-up and technology transfer.
  • Familiarity with Critical Quality Attributes/QbD/DOE principles.
  • Ability to manage multiple projects and meet deadlines in a fast-paced environment
  • Knowledge of regulatory requirements and GMP standards.
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