Company Description Krosyl Pharmaceuticals Pvt. Ltd. is a rapidly growing pharmaceutical company committed to providing efficient and affordable healthcare to all. Our state-of-the-art infrastructure and quality procedures enable us to produce high-quality products at affordable prices. Krosyl Pharma is ISO 9001:2015 and WHO-GMP certified, ensuring our dedication to both professional and ethical standards. Role Description This is a full-time on-site role for a Graphic Designer located in Vadodara. The Graphic Designer will be responsible for creating visually compelling graphics and marketing materials, collaborating with the marketing and product teams, and ensuring all designs meet company standards. Daily tasks include designing digital and print graphics, logos, brochures, and social media content. Qualifications Proficiency in graphic design software such as Adobe Creative Suite, CORELDRAW (Photoshop, Illustrator, InDesign) Strong creative and artistic skills with attention to detail Experience in creating digital and print marketing materials Excellent communication and collaboration skills Ability to manage multiple projects and meet deadlines Experience in the pharmaceutical or healthcare industry is a plus
Company Description Krosyl Pharmaceuticals Pvt. Ltd. is a leading emerging pharmaceutical company, committed professionally and ethically to providing efficient and affordable healthcare. Our state-of-the-art infrastructure and quality procedures ensure the production of high-quality products at affordable prices. Krosyl Pharmaceuticals is ISO 9001:2015 and WHO-GMP certified, dedicated to maintaining the highest standards in the industry. Role Description This is a full-time, on-site role for a Regulatory Affairs Specialist, located in Vadodara. The Regulatory Affairs Specialist will be responsible for handling regulatory documentation, ensuring compliance with regulatory requirements, and managing regulatory submissions. The specialist will also be involved in coordinating with different departments to ensure adherence to regulatory affairs and standards. Qualifications Regulatory Documentation, Regulatory Compliance, Regulatory Requirements skills Experience in Regulatory Affairs and managing Regulatory Submissions Attention to detail and strong organizational skills Effective communication and interpersonal skills Ability to work in a fast-paced environment and meet tight deadlines Experience in the pharmaceutical industry is preferred Bachelor’s degree in Pharmacy, Life Sciences, or a related field