Technical Leader, Operations
On-site · Greenville, North Carolina, United States
Job Summary
Technical Operations Lead for drug product manufacturing: provides hands-on technical expertise in aseptic fill/finish, troubleshooting, and process improvements to drive reliable production, audit readiness, and strong customer experience. Partners with Quality and site leadership to support regulatory inspections and customer audits, assist in new product introductions and line expansions, and lead technical guidance across cross-functional teams while operating as an individual contributor. Requires a Bachelor's degree in a related field and 8+ years of pharmaceutical manufacturing/quality experience, sterile fill/finish expertise, and solid knowledge of cGMP. Relocation assistance is not provided. Must be legally authorized to work in the United States without sponsorship. The role emphasizes tactical execution, problem-solving, and collaboration to meet production, compliance, and customer commitments.
Required Qualifications
- Bachelor’s degree in Engineering, Science, Operations Management, or related field
- 8+ years of pharmaceutical manufacturing, technical operations, or quality experience
- Sterile fill/finish drug product experience
- Strong knowledge of cGMP regulations and experience supporting regulatory inspections and/or customer audits
- Experience troubleshooting technical issues in a GMP manufacturing environment
- Excellent communication and collaboration skills; ability to influence cross-functional stakeholders without direct authority
- Equivalent combinations of education, training, and relevant work experience may be considered
- Must be legally authorized to work in the United States without sponsorshipNOW or in the future
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