01/04/2026
*F&D Formulation (Solid Orals, Liquid orals)*
*Experience 8-10 Years*
*Salary: 1 lac*
Market- ROW, Semi-regulatory and EU
Position Sr Executives/ Assistant Manager
Job Responsibilities
Responsible for development and design of formulations for multiple products selected for development & conducting meeting with multidisciplinary teams.
Conducts relevant patent searches on formulations. Reviews scientific literature and makes recommendations for formulation development strategies.
Responsible to carryout Preformulation studies, manufacturing prototype batches and do formulation development based on QbD approach.
Attends appropriate trainings, seminars, and presentations to maintain expertise in formulations and related areas.
Communicates with buyers and peers to ensure that APIs, excipients, tooling etc. are available for the project in required quantities, as and when needed.
Liaises with the plant operation supervisors and scheduler to ensure that experimental trials / registration batches are planned and executed in a timely manner.
Liaises with the documentation groups to ensure that early development trial documents, process evaluation and process optimization documents required for ex*****on.
Coordinates with lab for sample requirement and provides timelines for testing of samples.
Reviews and evaluates data analytical/ technical data on trials, and makes recommendations for bio/stability study batches, and communicates recommendations with management / peers to get necessary clearance to proceed further.
Applies Quality-by-design (QbD) principles to product development and tests the ruggedness of the formula by conducting suitable trials to study the impact of variations in the excipients within SUPAC guidelines / variations in manufacturing process parameters to recommend control strategy for CMAs and CPPs.
Liaises with the documentation group to ensure that all scale up master manufacturing and packaging documentation and other related documents required for submission to regulatory agencies are made available as and when required.
To prepare Pharmaceutical Development Reports and other documents required for regulatory submissions and technology transfer.
Responsible for responding to deficiency queries from regulatory agencies in timely manner.
Provides scientific and technical expertise and performs consultations on issues regarding formulation to other members of Formulation Development and other departments.
Works as a member of a team to achieve all outcomes.
Works in a safe manner collaborating as a team member to achieve all outcomes.
Demonstrate Behaviours that exhibit our organizational Values:
Integrity We do the right thing, every time.
Teamwork We achieve more together.
Courage We face challenges head on.
Innovation We power progress with bold ideas.
