Sr. AD Scientist

Sovereign Pharmaceuticals; Fort Worth (TX); On-site; USD 105,000 - 135,000; Full time

Job summary

Sovereign Pharmaceuticals in Fort Worth, TX is seeking an experienced Analytical Development Scientist to support 505(b)2, ANDA, and OTC product programs. You will perform release and stability testing, develop and validate methods, and contribute to method transfers and validation efforts.

The role requires advanced chemistry training, 8–12 years in pharma labs, and proficiency with HPLC, Empower 3, and MasterControl QMS.

Qualifications

• Advanced degree with Chemistry background; Master’s preferred.
• 8–12 years of experience in a pharmaceutical laboratory.
• Operation of HPLC and proficiency with Empower 3 Software.
• Compendial/Non-compendial testing of raw materials.

Responsibilities

• Perform release and stability testing for raw materials and drug products.
• Develop and validate analytical methods on various quantitative instruments.
• Execute method transfers and method equivalency studies.
• Conduct method validation experiments as per written protocols.
• Author technical documents such as protocols and reports.
• Peer review laboratory notebooks, data, protocols, and reports.
• Train other analysts on new instrumentation and techniques.
• Utilize MasterControl QMS Software to train on, review, and approve official documents.

Skills

Analytical thinking

Project management

Communication skills

Organizational skills

Self-starter

Education

Master’s degree in Chemistry

Tools

HPLC

Empower 3 Software

GC

Mass Spectrometry

UV/Vis

Job description

Location: Fort Worth, TX Posted: 10/13/2026 Location Name: Sovereign Pharmaceuticals (Ft. Worth, Tx) Wage: Depends on Experience

Summary/objective

Support Sovereign’s analytical development activities to achieve successful design, filing, transfer, and launch of 505(b)2, ANDA, and OTC products.

Essential Functions

• Perform release and stability testing for raw materials and drug products
• Develop and validate analytical methods on various quantitative instruments
• Execute method transfers and method equivalency studies
• Conduct method validation experiments as per written protocols
• Author technical documents such as protocols and reports
• Performs characterization of physical and chemical characteristics of drug product and raw materials.
• Peer review laboratory notebooks, data, protocols, and reports
• Identifies non-routine technical problems and recommends solutions
• Understands applicable cGMP, DEA regulations, and Quality Procedures
• Recommends new technology & science to meet dept goals
• Train other analysts on new instrumentation and techniques
• Utilize MasterControl QMS Software to train on, review, and approve official documents such as test methods, protocols, and reports.
• Performs other tasks as assigned.

Required Skills/ Abilities

• Adhere to all laboratory requirements in accordance with SOPs and regulatory practices such as GMPs, GDPs, GLPs, and OSHA regulations.
• Understanding of Analytical Chemistry, including but not limited to the following techniques and how to utilize them, as needed, for projects, both simple and complicated, as assigned:
  • HPLC
  • Dissolution
  • UV/Vis
  • FTIR
  • Mass Spectrometry
  • Sample Preparation Techniques
  • GC
  • Titration/electrode chemistry
  • Others as appropriate
• Effective communication skills, written and verbal
• Demonstrate project management skills
• Organizational and interpersonal skills
• Ability to innovate new ideas
• Ability to handle multiple projects.
• Self-starter, organized, dependable, and goal-oriented.

Required Education And Experience

• Advanced degree with Chemistry background, Master’s preferred
• 8-12 years of experience in a pharmaceutical laboratory
• Operation of HPLC and proficient with Empower 3 Software
• Compendial/Non-compendial testing of raw materials

position type/expected hours of work

This is a full-time position. Days and hours of work are Monday through Friday, but extended (earlier or later) work times or weekend work may be required.

physical demands

The employee must regularly lift and/ or move up to 50 pounds. Specific vision abilities required by this position include close vision, color vision, and the ability to adjust focus. While performing the duties of this job, the employee is regularly required to stand, walk, sit, and talk or hear. The employee is occasionally required to climb or balance, stoop, kneel, crouch, crawl, and smell.

work environment

This job operates in a professional office and laboratory environment. This role routinely uses standard office equipment such as computers, phones, and copiers. The employee is occasionally exposed to toxic and/ or caustic chemicals such as Sodium Hydroxide, Hydrochloric Acid, Acetonitrile, Methanol, and other chemical solutions necessary in analytical chemistry.