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Principal Formulation Scientist - Solid Dosage Forms

Job in Kempton Park, 1618, South Africa
Listing for: Placements24
Full Time position
Listed on 2026-10-19
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Pharmaceutical Manufacturing
Job Description & How to Apply Below
Location: Kempton Park

About the Role

Our client, a distinguished pharmaceutical company located in Tembisa, Gauteng, ZA
, is seeking an exceptional Principal Formulation Scientist specializing in solid dosage forms. This is a critical on-site role where you will spearhead the formulation development of innovative oral solid dosage products, from pre-formulation studies through to commercial manufacturing. You will be instrumental in designing robust formulations that meet stringent quality, safety, and efficacy standards. The ideal candidate possesses extensive expertise in drug delivery systems, excipient selection, process development, and scale-up for tablets and capsules.

This position demands a high level of scientific rigor, problem-solving capabilities, and a collaborative spirit to work closely with cross-functional teams.

Key Responsibilities
  • Lead the formulation development of new oral solid dosage forms (tablets, capsules, powders) for various therapeutic areas.
  • Conduct pre-formulation studies, including physicochemical characterization of Active Pharmaceutical Ingredients (APIs) and excipients.
  • Design and optimize formulation compositions and manufacturing processes (e.g., granulation, compression, coating, encapsulation).
  • Perform scale-up studies and technology transfer to manufacturing sites.
  • Utilize advanced formulation technologies and techniques to enhance drug bioavailability and product performance.
  • Develop and validate analytical methods for characterizing formulated products, in collaboration with the analytical department.
  • Troubleshoot formulation and manufacturing-related issues, providing effective solutions.
  • Author and review formulation development reports, development summaries, and relevant sections of regulatory submissions (e.g., CTD).
  • Stay current with industry trends, regulatory expectations, and scientific advancements in pharmaceutical formulation.
  • Mentor junior scientists and contribute to the scientific growth of the R&D team.
Requirements
  • Ph.D. or M.Sc. in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a closely related field.
  • A minimum of 10 years of hands‑on experience in pharmaceutical formulation development, with a strong focus on solid oral dosage forms.
  • In‑depth knowledge of material science, solid‑state chemistry, and drug delivery principles.
  • Proven experience with various manufacturing processes for tablets and capsules (e.g., wet/dry granulation, direct compression, encapsulation).
  • Familiarity with Good Manufacturing Practices (GMP) and regulatory guidelines for drug product development.
  • Expertise in laboratory techniques for material characterization and formulation assessment.
  • Excellent problem‑solving and analytical skills.
  • Strong project management and communication abilities.
  • Ability to work independently and lead projects with minimal supervision.
  • This role requires consistent on‑site presence in Tembisa, Gauteng, ZA
    .
Benefits

Our client offers a highly competitive salary and an attractive benefits package. This is an opportunity to work on cutting‑edge pharmaceutical development projects and significantly influence product success. You will join a team of highly skilled professionals and have access to advanced research facilities. Opportunities for career advancement and professional development are abundant. Contribute to the development of life‑saving medications and make a tangible difference in patient lives.

Be recognized for your scientific contributions and leadership in a challenging and rewarding environment. The role is based at our state‑of‑the‑art facility in Tembisa, Gauteng, ZA
, offering a stable and long‑term career path.

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