Senior Formulation Scientist I

Adare Pharma

$95K — $115K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or related field.
  • Six years of experience in pharmaceutics or solid dosage formulation development.
  • Experience with drug delivery technologies and processing techniques.
  • Hands-on knowledge of cGMP, FDA, DEA, and OSHA regulations.
  • Understanding of pharmacokinetics-pharmacodynamics (PK-PD) relationships.

Responsibilities

  • Design and perform formulations for new drug products, focusing on oral solids and solutions.
  • Utilize existing and emerging technologies for product development from pre-formulation to manufacturing.
  • Use experimental design to optimize formulation compositions rapidly.
  • Evaluate product testing results to guide further development steps.
  • Prepare cGMP manufacturing batch records and development reports.
  • Manufacture and optimize batches for scale-up and submissions.
  • Troubleshoot formulation issues during R&D and production phases.

Benefits

  • Opportunity to work on innovative drug products in a dynamic environment.
  • Engagement with cross-functional teams for comprehensive project insights.
  • Access to training on cGMP regulations and safety standards.
  • Contribution to significant phases of drug product development from inception to market.
Full Job Description
Senior Formulations Scientist I (Vandalia, OH)

Design and perform formulations and processes for new drug products, focusing on oral solids, powders for constitution, solutions, and suspensions for clinical trials, ANDA, and NDA projects. Develop new products utilizing existing and emerging technologies available within the industry, from pre formulation through the manufacturing stage. Use experimental design to rapidly optimize formulation composition and in-process specifications. Evaluate product testing results and recommend next steps for continued development until the product formulation and process are finalized. Present product development progress to senior management and project teams. Write Current Good Manufacturing Practices (cGMP) manufacturing batch records, stability study protocols, in-process and finished product specifications, and product development reports. Manufacture development, optimization, scale-up, and submission batches. Troubleshoot formulation issues arising during R&D development, scale-up, and production. Conduct and manage development projects with managerial guidance, ensuring the successful scale-up of new products and/or processes. Communicate effectively with cross-functional teams, including Analytical Development, Quality, PK, Regulatory Affairs, and Legal. Attend SOP, safety, and scientific training to remain current with cGMP regulations, safety standards, and development technologies.

Requirements:
  • Master's degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a similar field.
  • Six years of experience in pharmaceutics, solid dosage formulation development, drug delivery technologies, processing technologies, or a related field.
  • Experience in pharmaceutical operations (granulation, tableting, particle coating for controlled or targeted-release applications, encapsulation, fluid bed operations, suspensions, solutions, or microencapsulation).
  • Experience with cGMP, FDA, DEA, and OSHA regulations.
  • Knowledge of PK-PD relationships and IV/IV correlations.

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