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Executive Pharmaceutical Formulation Development Jobs in California

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Executive Pharmaceutical Formulation Development information

What is an executive pharmaceutical formulation development?

Executive Pharmaceutical Formulation Development professionals are responsible for overseeing and coordinating the design, development, and optimization of pharmaceutical formulations. They lead teams in creating safe and effective dosage forms, such as tablets, capsules, or injectables, ensuring compliance with regulatory standards. Their work involves collaborating with research, analytical, and manufacturing teams to bring new drug products from concept to market. Additionally, they troubleshoot formulation issues, manage timelines, and contribute to documentation required for regulatory submissions.

What are some common challenges faced in executive pharmaceutical formulation development roles, and how are they typically addressed?

Professionals in Executive Pharmaceutical Formulation Development often encounter challenges such as ensuring batch-to-batch consistency, addressing stability issues, and meeting stringent regulatory requirements. These challenges are typically managed through robust analytical testing, cross-functional collaboration with quality assurance, and continuous process optimization. The role also demands staying updated with the latest regulatory guidelines and leveraging teamwork to troubleshoot and resolve formulation setbacks efficiently. Regular communication with R&D, manufacturing, and regulatory teams is essential for timely project delivery and compliance.

What are the key skills and qualifications needed to thrive as an executive in pharmaceutical formulation development, and why are they important?

To thrive as an Executive in Pharmaceutical Formulation Development, you need a strong background in pharmaceutical sciences, drug development processes, and regulatory guidelines, usually supported by an advanced degree in pharmacy, chemistry, or a related field. Familiarity with laboratory instrumentation, formulation technologies, quality management systems, and cGMP compliance is essential, along with certifications such as Six Sigma or Lean Manufacturing being advantageous. Leadership, problem-solving, and effective communication are critical soft skills for driving innovation, managing cross-functional teams, and ensuring project success. These skills and qualifications ensure that new pharmaceutical products are developed efficiently, meet regulatory standards, and address market needs.

What is the difference between Executive Pharmaceutical Formulation Development vs Pharmaceutical Formulation Scientist?

AspectExecutive Pharmaceutical Formulation DevelopmentPharmaceutical Formulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related field; experience in formulation developmentBachelor's or Master's in Pharmacy, Chemistry, or related field; entry to mid-level experience
Work EnvironmentSenior role in R&D departments, overseeing projects, strategic planningHands-on laboratory work, experimental formulation testing
Employer & Industry UsagePharmaceutical companies, biotech firms, contract research organizationsResearch labs, pharmaceutical companies, academia

In summary, Executive Pharmaceutical Formulation Development roles focus on strategic oversight and project management in formulation development, often requiring leadership experience. In contrast, Pharmaceutical Formulation Scientists are primarily involved in experimental work and formulation testing. Both roles are essential in drug development but differ in responsibilities and seniority.

What are the most commonly searched types of Pharmaceutical Formulation Development jobs in California?

The most popular types of Pharmaceutical Formulation Development jobs in California are:

What are popular job titles related to Executive Pharmaceutical Formulation Development jobs in California?

For Executive Pharmaceutical Formulation Development jobs in California, the most frequently searched job titles are:

What job categories do people searching Executive Pharmaceutical Formulation Development jobs in California look for?

The top searched job categories for Executive Pharmaceutical Formulation Development jobs in California are:

What cities in California are hiring for Executive Pharmaceutical Formulation Development jobs?

Cities in California with the most Executive Pharmaceutical Formulation Development job openings:

Executive Pharmaceutical Formulation Development jobs near you
Infographic showing various Executive Pharmaceutical Formulation Development job openings in California as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

Pharmaceutical Formulation Chemist

Temecula, CA

K2 Staffing
Recruiting and Staffing Services • 11 - 50 employees
Learn more about K2 Staffingexternal

Contractor

Re-posted yesterday

Job description

Summary

Our client is seeking an experienced Formulation Chemist to support the development of lyophilized injectable vials and oral capsule formulations on a project-based (Statement of Work / Per Diem) basis. This role is ideal for a pharmaceutical formulation expert with hands-on experience developing injectable and oral solid-dose products who can independently lead formulation activities from concept through regulatory readiness.

The successful candidate will have expertise in formulation development, excipient selection, lyophilization, stability studies, GMP documentation, and technical writing while collaborating with Quality, Regulatory, Manufacturing, and Analytical teams to support product commercialization.

Duties & Responsibilities Formulation Development
  • Develop formulations for lyophilized injectable vials and oral capsule products.
  • Design and execute formulation development studies, including excipient selection, buffer optimization, and compatibility assessments.
  • Troubleshoot formulation challenges related to solubility, stability, aggregation, dissolution, and product performance.
  • Support scale-up activities from laboratory development through manufacturing.
Lyophilization & Injectable Products
  • Develop and optimize lyophilization cycles, including freezing, primary drying, and secondary drying.
  • Investigate and resolve reconstitution and product stability issues.
  • Support sterile fill-finish activities, ensuring compatibility with filtration systems and filling equipment.
Oral Solid Dose Development
  • Develop oral capsule formulations, including excipient compatibility and fill-weight uniformity.
  • Evaluate formulation performance and identify opportunities to improve bioavailability where appropriate.
  • Generate technical data packages supporting manufacturing partners.
Stability, Documentation & Regulatory Support
  • Design and execute accelerated and long-term stability studies in accordance with ICH guidelines.
  • Prepare formulation development reports, technical protocols, batch records, and supporting GMP documentation.
  • Collaborate with Quality and Regulatory teams to ensure formulation data supports regulatory compliance, including 503A/503B requirements.
  • Support manufacturing and analytical teams by providing formulation expertise throughout the product lifecycle.
Qualifications & Requirements Required Experience
  • Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline (PhD preferred).
  • Minimum 3 years of pharmaceutical formulation experience developing both injectable (lyophilized) and oral solid-dose products.
  • Hands-on experience with lyophilization cycle development and freeze-drying equipment.
  • Experience developing oral capsule formulations, including excipient selection and fill-weight optimization.
  • Strong understanding of formulation challenges, including solubility, stability, aggregation, and excipient compatibility.
Technical Skills
  • Experience designing and executing formulation development studies.
  • Knowledge of GMP documentation, batch records, technical protocols, and formulation reports.
  • Familiarity with ICH stability guidelines and stability protocol development.
  • Understanding of USP <795>, USP <797>, and/or 503A/503B regulatory requirements preferred.
  • Experience supporting sterile fill-finish operations and aseptic processing is highly desirable.
Professional Skills
  • Strong technical writing and documentation skills.
  • Excellent analytical, problem-solving, and troubleshooting abilities.
  • Ability to work independently while collaborating with cross-functional teams.
  • Strong organizational skills with the ability to manage multiple project priorities.
Employment Type: Contract Location: Temecula, CA