Opportunity in Skin Care Formulation research at Unilever. The role will support all R&D interventions for product development and regulatory compliance within the UI Skin care category.
To create specialized content with supervision; support end-to-end publication, medical education content development process including documentation and approval in PromoMats, iEnvision; develop and maintain therapeutic area expertise; work in close collaboration with peers, team to develop best practices; and collaborate effectively with stakeholders.
This is a non-supervisory position to support development of Reference materials. The successful applicant in this role will work on projects including Analytical Method Development for in process samples for synthetic lab.
B.Pharm, M.Pharm, M.Sc, B.E. with 2 to 10 Years of relevant experience of IPQA, Qualification, QMS, Sterility Assurance, QA IT related activities in Injectable Manufacturing Plant.
Keep a daily log to document all activities completed each day. Perform duties in compliance with Company’s policies and procedures, including but not limited to those related to HIPAA and compliance.
CORONA Remedies Pvt. Ltd. Our journey started in 2004, with a commitment to creating a better quality of health for all by being at the forefront of research, manufacturing and marketing of high quality products.
The candidate must possess a thorough understanding of relevant disease biology, the clinical landscape, emerging technologies, and the competitive environment. The candidate should demonstrate exceptional laboratory technical skills in cell and molecular biology, and, or in vivo pharmacology and proficient at devising strategic solutions to identify and resolve potential challenges.
Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques
Skilled in handling equipment such as reactors, centrifuges CF, vacuum tray dryers VTD, agitated nutsche filters , etc.
Strong expertise in unit operations. Well-versed in production activities including raw material verification, batch charging, batch monitoring, and GMP documentation.
Provide medical and scientific training to internal stakeholders, including the sales and marketing teams, ensuring accuracy and alignment with scientific evidence. Collaborate with cross-functional teams to support the development of strategic initiatives in line with medical and commercial objectives.