Technical Services Scientist

Technical Services Scientist Apply Now Applied To save a job sign in or get started

Job ID:

10218570 Posted today Back Greenville, SC, US Scientific Bachelors Degree Full Time, Direct Hire $90,000•110,000/year Experienced (Non-Manager) On-site Biotechnology/Pharmaceuticals First Shift (Day) Greenville, SC, US $90,000•110,000/year Experienced (Non-Manager) Full Time, Direct Hire 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 + 10% Bonus Potential 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 10218570 Share this job Copied url To save a job sign in or get started To apply for this job email your details to I want more jobs like this in my inbox.

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Share this job Copied url Link Copied Similar Jobs To save a job sign in or get started Technical Services Supervisor Pharma Manufacturing Greenville, SC, US Full Time, Direct Hire $90,000•110,000/year To save a job sign in or get started Technical Services Scientist Greenville, SC, US Full Time, Temporary $90,000•110,000/year As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly ® Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.