Technical Services Scientist

By | May 8, 2026

Technical Services Scientist

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Job ID: 9337271

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Greenville, SC, US

Scientific

Bachelors Degree

Full Time, Temporary

$100,000-$115,000/year

Experienced (Non-Manager)

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

Greenville, SC, US

$100,000-$115,000/year

Experienced (Non-Manager)

Full Time, Temporary

Biotechnology/Pharmaceuticals

On-site

Scientific

Bachelors Degree

First Shift (Day)

Apply Now Applied

Job details

Job Title: Technical Services Scientist

Location: Greenville, SC
Schedule: Monday–Friday, 8:00 AM – 5:00 PM (some overtime expected)
Work Environment: Approx. 50% of time on the manufacturing floor
Employment Type: Direct Hire
Salary: $100,000 – $110,000 per year
Relocation assistance offered

Position Summary

Seeking an experienced Technical Services Scientist to support pharmaceutical manufacturing operations through process development, scale-up, product transfer, process troubleshooting, and continuous improvement initiatives within a cGMP-regulated environment. This role will work cross-functionally with Manufacturing, Validation, QA, QC, and Supply Chain teams to ensure safe, compliant, and efficient production of commercial pharmaceutical products.

Key Responsibilities

  • Support manufacturing operations for commercial pharmaceutical products in compliance with cGMP standards

  • Assist with process development, scale-up, technology transfer, and process optimization activities

  • Troubleshoot manufacturing and procedural issues during production

  • Generate, revise, and maintain master batch records and technical documentation

  • Lead and support deviation investigations, root cause analysis, CAPA implementation, and process improvements

  • Participate in process validation, equipment qualification, engineering studies, and equipment implementation activities

  • Support pilot batches, demonstration batches, and manufacturing studies

  • Identify opportunities for operational efficiency and process enhancements

  • Prepare and deliver technical training for manufacturing personnel

  • Review executed batch records and manufacturing documentation

  • Collaborate with cross-functional teams including QA, QC, Validation, and Supply Chain

Qualifications

  • Bachelor’s degree in Engineering, Chemistry, Biology, Pharmaceutical Sciences, or related technical field preferred

  • Approximately 7+ years of pharmaceutical manufacturing experience or equivalent combination of education and industry experience

  • Experience supporting process scale-up, technology transfer, validation, and manufacturing troubleshooting

  • Oral solid dose or oral liquid pharmaceutical experience preferred

  • Strong understanding of cGMP regulations and pharmaceutical manufacturing operations

  • Excellent technical writing, analytical, communication, and problem-solving skills

  • Ability to analyze technical data, investigate issues, and implement effective solutions

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