Experience
- 7–10+ years of experience in FDA-regulated pharmaceutical, nutraceutical, or related manufacturing environments.
- Experience in peptide formulation is strongly preferred.
- Knowledge in sterile injectables and lyophilization highly preferred.
- Demonstrated leadership experience managing QA/QC and/or R&D teams.
- Proven success developing and implementing compliant quality systems.
Skills & Competencies
- Deep knowledge of FDA regulations, cGMP, quality systems, and product development processes.
- Strong formulation science background, especially with liquids, suspensions, emulsions.
- Excellent analytical, problem-solving, and project management skills.
- Ability to lead both strategically and hands-on in a fast-paced growth environment.
- Strong communication, technical writing, and cross-functional leadership capability.
Preferred Qualifications
- Prior experience with scale-up, tech transfer, and manufacturing optimization.
- Familiarity with stability programs, analytical testing, and validation protocols.
- Lean Six Sigma or similar process improvement training.
Equal Employment Opportunity (EEO) Statement
The Company is an Equal Opportunity Employer. We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, disability, genetic information, veteran status, or any other status protected by applicable federal, state, or local law.
South Carolina At-Will Employment Statement
Employment with the Company is at-will, meaning that either the employee or the Company may terminate the employment relationship at any time, with or without cause or notice, in accordance with applicable South Carolina state law. Nothing in this job description shall be construed as creating a contract of employment, express or implied.
