Location:
- Fort Worth, TX

Posted:
- 7/9/2026

Location Name:
- Sovereign Pharmaceuticals (Ft. Worth, Tx)

Wage:
- Depends on Experience

summary/objective
Support Sovereign's Formulation development activities to achieve successful design, filing, transfer, and launch of 505(b)2, ANDA, ANADA, and OTC products.

essential functions
- Monitoring their project activities to ensure timely completion.
- Reviewing their protocols, manufacturing processes, and reports for accuracy
- Designing protocols, developing plans, and pre-formulations and formulation activities.
- Developing process, manufacturing instructions, and technology packages.
- Writing project updates.
- Work with process/manufacturing personnel for successful and effective transfer of technology.
- Author technical documents such as protocols and reports
- Performs characterization of the physical characteristics of drug products and raw materials.
- Peer review laboratory notebooks, data, protocols, and reports
- Identifies non-routine technical problems & recommends solutions




- Provide leadership in technical transfers between companies and internally
- Understand applicable cGMP, DEA regulations, and Quality Procedures
- Recommends new technology & science to meet department goals

Required education and experience
- Advanced degree with pharmaceutical sciences background.
- 2-4 years of experience in solid and liquid dosage forms development
- Adhere to all laboratory requirements in accordance with SOPs and regulatory practices such as GMPs, GDPs, GLPs, and OSHA regulations.
- Knowledge of pharmaceutical research and development
- Statistical experimental design techniques
- Bench/Pilot scale operations (granulation, compression, coating, etc.)

Preferred education and experience
- Advanced degree with a pharmaceutical sciences background, PhD preferred.
- 2-4 years of experience in a cGMP environment, preferably in pharmaceuticals

Required skills/competencies
- Effective communication skills, wri

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