Remote Lead Pharmaceutical Formulation Scientist

Placements24

Cape Town

Hybrid

ZAR 2,988,000 - 4,315,000

Full time

11 days ago

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Benefits offered by this job

Annual bonus
Medical, dental, vision coverage
Home office allowance
Access to remote research platforms

Job summary

Placements24 presents an opportunity with a globally recognized pharmaceutical leader seeking a Lead Pharmaceutical Formulation Scientist. This remote-first role leads a team of scientists to design, develop, and optimize novel drug formulations across modalities.

You will oversee pre-formulation studies, scale-up, tech transfer, and regulatory documentation while collaborating with regulatory, analytical, manufacturing teams and external partners.

Qualifications

  • 7+ years of experience in formulation development.
  • Experience with multiple dosage forms (oral solids, injectables, topicals).
  • Proven ability to lead remote scientific teams and communicate effectively.
  • Strong analytical and problem-solving skills.

Responsibilities

  • Lead development of novel formulations for small molecules, biologics and other modalities.
  • Oversee pre-formulation studies including physicochemical characterization.
  • Design experiments for formulation optimization, stability, and excipient compatibility.
  • Develop and validate analytical methods for drug product quality and performance.
  • Manage scale-up and tech transfer to pilot and manufacturing.
  • Collaborate with drug substance, analytical, manufacturing and regulatory teams.

Skills

Leadership
Formulation development
Remote leadership
Mentorship
Project management

Education

Master's or PhD in Pharmaceutical Sciences

Job description

Placements24 presents an opportunity with a globally recognized pharmaceutical leader seeking a Lead Pharmaceutical Formulation Scientist. This remote-first role leads a team of scientists to design, develop, and optimize novel drug formulations across modalities.

You will oversee pre-formulation studies, scale-up, tech transfer, and regulatory documentation while collaborating with regulatory, analytical, manufacturing teams and external partners.

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