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Process Development Scientist

Job in Rockford, Winnebago County, Illinois, 61103, USA
Listing for: TekWissen LLC
Full Time position
Listed on 2026-07-03
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Quality Engineering
Salary/Wage Range or Industry Benchmark: 75000 - 90000 USD Yearly USD 75000.00 90000.00 YEAR
Job Description & How to Apply Below

Overview

Tek Wissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer.

Our client's global team is committed to delivering an unparalleled blend of cutting‑edge technologies, convenient procurement options, and pharmaceutical services under their industry‑leading brands.

Position:
Process Development Scientist

Location:

Rockford, IL 61101
Duration: 12 Months
Job Type: Temporary Assignment
Work Type:
Onsite
Shift Timings:
Monday to Friday from 08:00 AM to 05:00 PM

Summary

The Scientist II, Manufacturing Sciences / Process Development Scientist will support manufacturing operations by developing, validating, and optimizing manufacturing processes and analytical methods for bead and resin products. This role will work closely with Operations, Engineering, and cross‑functional teams to drive process improvements, troubleshoot manufacturing challenges, support validation activities, and ensure compliance with GMP, ISO, and regulatory requirements. The ideal candidate will have a strong background in chemistry, process validation, analytical techniques, and manufacturing sciences within a regulated environment.

Responsibilities
  • Lead chemical synthesis projects for bead and resin manufacturing.
  • Develop, validate, and implement manufacturing processes and analytical methods.
  • Perform analytical testing using techniques such as liquid chromatography, NMR, GC, mass spectrometry, particle characterization, and IR.
  • Conduct vendor evaluations and raw material qualification activities.
  • Apply statistical methods and software for experimental design and data analysis.
  • Communicate validation activities and technical findings to both technical and non‑technical stakeholders.
  • Prepare and maintain product documentation including specifications, batch records, and bills of materials.
  • Ensure compliance with GMP, ISO, and applicable regulatory requirements.
  • Collaborate with Operations, Engineering, and cross‑functional teams to troubleshoot manufacturing and analytical issues.
  • Support continuous improvement initiatives and process optimization projects.
Required Skills
  • Bachelor's degree in Chemistry, Biochemistry, or a related scientific discipline with 4+ years of relevant experience; OR Master's degree with 2+ years of experience; OR PhD with 0 1 years of experience.
  • Strong experience in Organic Synthesis, Polymer Chemistry, Chemical Synthesis, Resin/Bead Synthesis, or Chromatography methods.
  • Should have ability to independently design, plan, and execute laboratory experiments.
  • Expertise in process validation, change control management, and continuous process improvement.
  • Experience conducting risk assessments, root cause investigations, and implementing corrective actions.

    Proficiency in statistical analysis, experimental design, and data interpretation.
  • Hands‑on experience with analytical techniques including Liquid Chromatography (LC), Gas Chromatography (GC), Nuclear Magnetic Resonance (NMR), Mass Spectrometry (MS), Infrared Spectroscopy (IR), and particle characterization.
  • Experience supporting diagnostic reagents, bioprocessing, or analytical method validation activities.
  • Strong technical documentation, communication, and problem‑solving skills.
  • Experience working in GMP, ISO, or other regulated manufacturing environments.
  • Lean Six Sigma certification is preferred.

Tek Wissen Group is an equal opportunity employer supporting workforce diversity.

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