Formulation Scientist

Company Description Across Pharma Pvt. Ltd. is a pharmaceutical organization focused on the development and manufacturing of high-quality formulations for diverse therapeutic areas. The company emphasizes rigorous scientific standards, regulatory compliance, and innovation to deliver effective and reliable medicines. Across Pharma fosters a collaborative work environment where research-driven professionals can contribute to advancing healthcare solutions. Team members are encouraged to grow their expertise and participate in projects that support both patient well-being and business sustainability.
Role Description The Formulation Scientist is a full-time, on-site role based in Navi Mumbai. The individual will be responsible for designing and developing pharmaceutical formulations, conducting laboratory experiments, and optimizing product compositions to meet quality, stability, and regulatory requirements. Daily tasks include planning and executing R&D studies, analyzing data, preparing technical documentation, and supporting scale-up and technology transfer to manufacturing. The role also involves collaborating with cross-functional teams such as quality assurance, regulatory affairs, and production to ensure smooth product development and commercialization. The Formulation Scientist will maintain laboratory records, adhere to safety and compliance standards, and contribute to continuous improvement initiatives within the development team.
Qualifications
Candidates should possess strong Laboratory Skills and hands-on experience in Formulation development.
Candidates should possess experience in Research and Development (R&D) and applied Research activities.
Candidates should possess knowledge of Technology Transfer processes from R&D to manufacturing.
Relevant qualifications such as a Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field.
Understanding of regulatory guidelines, GMP practices, and documentation standards in the pharmaceutical industry.
Ability to analyze experimental data, solve technical problems, and communicate findings clearly in written and verbal form.
Strong attention to detail, organizational skills, and the ability to work effectively in cross-functional teams.
Prior experience in dosage form development (e.g., tablets, capsules, liquids) and stability studies is an advantage.

Work arrangement
No