Jolly Oswin I

B.Pharm graduate with 2+ years of experience in pharmaceutical formulation R&D and a strong interest in Cosmetic formulation and lifecycle management. Experienced in technical documentation, SOP preparation and revision, change control, stability documentation, cGMP compliance, and cross-functional coordination with QA, QC, Manufacturing, and Regulatory Affairs teams. Seeking to transition Cosmetics and personal care products and apply pharmaceutical regulatory and documentation experience to cosmetic product compliance, lifecycle management, product documentation, regulatory submissions, and quality requirements.

RESEARCH ASSOCIATE – FORMULATION DEVELOPMENT - Softgel Healthcare - Chennai

(2026-09)

• Support the resolution of technical queries related to formulation, batch records, and preformulation data to streamline cross-departmental product workflows.
• Author and review critical product lifecycle documents, including Product Development Records (PDR) for trials, Master Formula Records (MFR) for scaled recipes, and Batch Manufacturing Records (BMR) via eDMS platforms.
• Execute R&D trials for hardgel and softgel capsule technologies.
• Coordinate preformulation assessments and ingredient compatibility studies to identify and mitigate physical/chemical interactions in active delivery systems.

CHEMIST - RESEARCH & DEVELOPMENT - Stedman Pharmaceuticals Pvt. Ltd. - Alathur

(2024-04)

• Prepared, reviewed, and maintained technical and controlled documentation supporting formulation development and manufacturing activities.
• Authored 2 new SOPs and revised 30+ existing SOPs, supporting documentation compliance and process standardization.
• Prepared and maintained MFRs, BMRs, development reports, stability protocols/reports, validation documents, and technical records.
• Supported change control activities and ensured compliance with approved procedures and controlled documentation systems.
• Coordinated with QA, QC, Manufacturing, and Regulatory Affairs teams for documentation, technology transfer, validation, and troubleshooting activities.
• Supported stability studies and formulation evaluation, maintaining appropriate records and traceability.
• Worked within cGMP-controlled environments with emphasis on documentation integrity and ALCOA+ principles.
• Supported product development, scale-up, process optimization, and manufacturing readiness activities.
• Maintained formulation development samples, reference samples, and R&D records with appropriate traceability.

Bachelor of Pharmacy (B.Pharm) - PPG College of Pharmacy, Coimbatore (2019 - 2023)