Rincy Philip

• Receiving prescriptions, checking patients' medical histories, and ensuring optimal dosage and methods of administration and drug compatibility before dispensing.
• Advising prescribers on drug incompatibility and contra-indications.
• Maintaining prescription files and recording issues of narcotics, poisons and habit-forming drugs.
  Storing and preserving vaccines, serums and other drugs subject to deterioration.
• Supplying non-prescription medicines and diagnostic and therapeutic aids.
• Supervising and coordinating the work of Pharmacy Technicians, pharmacy interns and Pharmacy Sales Assistants.
• Consulting with Chemists, Engineering Professionals and other professionals about manufacturing techniques and ingredients.
• Supervise the medicines supply chain and ensure pharmacy premises and systems are fit for purpose.
• Organizing the pharmacy in an efficient manner to make the identification of products easier and faster.
• Maintaining full control over delivering, stocking and labeling medicine and other products.

• Areas of experience Cardiovascular, diabetology, gynecology, gastroenterology, dermatology.
• Wrote primary and review manuscripts for publication in peer-­reviewed journals.
• Coordinated and managed conclaves related to gynecology, orthopedics and wrote executive summaries for agendas of these conclaves.
• Wrote primary and review manuscripts for pharmaceutical clients.
• Provided clients with medical writing, reviewing, and editing services.
• Ensuring consistent high quality projects on allocated accounts.
• Ensuring all activities are fully compliant with required guidelines and meet the needs and objectives of the client, target audience, and communication medium.
• Guiding team members to ensure excellent outputs and timed-delivery.
• Review of scientific articles and manuscripts.
• Wrote scientific facts, news abstracts and summary points for PODCAST.
• Provided input into publication plans and work to ensure timely achievement of milestones.
• Enhanced readability of medical documents by applying clear and concise language techniques.
• Mentored junior medical writers, promoting professional growth and fostering a collaborative work environment.
• Effectively communicated complex scientific concepts to non-expert audiences through targeted messaging strategies
• Created medical education materials tailored to specific audiences, improving overall knowledge retention among healthcare professionals.
• Proficient in conducting thorough literature searches and identifying excellent papers to support relevant subjects or themes.
• Collaborated with SME healthcare professionals to formulate recommendations, practice points, and guidelines pertaining to endocrinology, gynecology, and orthopedics.
• Developed comprehensive medical content for various platforms, increasing audience engagement and understanding

• Updated SOP related to validation and hold time studies as per current guidelines.
• Implemented sophisticated and detailed tracking system for hold time study that gives deep insight of the study initiated in the plan.
• Validation protocol and report preparation for tablets and soft gelatin capsule.
• Preparation, review of protocols and reports for hold time study in different stages of its process (Tablets and Soft gelatin Capsule)
• Preparation of Risk assessment of elemental impurities in drug product as per ICH Q3D.
• Assisted in new equipment qualification, area qualification, re-qualification of equipment in the site.
• Preparation of documents involved in qualification of equipment.
• Preparation of cleaning validation protocols and reports.
• Performed sampling of batches in different stages as per approved protocol for validation batches.
• Swab sampling for batches considered for cleaning validation.
• Contributed in preparation of validation master plan.

IPQA Activities:

• In- Process checks for bulk tablets and capsules.
• Sampling of bulk tablets and capsules and preparation of its physical parameter testing reports.
• Line clearance of primary and secondary packaging lines.
• Point sampling of blends.
• Review of Logbooks, log cards, Batch records.
• Assisted in the process of Hold time study including sample collection, review of reports.
• Assisted in the validation process of uncoated and coated tablets.
• Assisted in re-qualification of equipment in the site.

Quality Management system:

• Assisted in Supplier QA activities.
• PQR entries of the batches before its release and assisted in preparation of APQR.
• Generation of COA's through SAP.
• Issuance of Batch records.
• Maintenance and archival of master documents in the site.
• Maintenance and day-to-day upkeep of executed batch records.
• Distribution of SOP's and other cGMP related documents within the site.
• Reviewing updated SOPs to ensure alignment with current GMP guidelines.
• Responsible for preliminary stage investigation of technical complaints received by the site.
• Induction and GMP training of new recruits into the site.
• Revision of GMP manual to be updated according to the cGMP guidelines.
• Graduated from the apprenticeship program with a solid foundation in industry-specific knowledge.