Pharmaceutical Professional

Company Description Gufic Biosciences Ltd. is a research-driven pharmaceutical organization with over five decades of innovation focused on improving global health and well-being. The company specializes in critical care medicines, advanced fertility and parenthood solutions, nutraceuticals, and treatments in orthopaedics, gynaecology, aesthetics, and dermatology. Gufic is a pioneer in lyophilization technology and operates benchmark-setting fully automated robotic lyophilizers. Its manufacturing facilities hold multiple international accreditations, including EU-GMP, ANVISA (Brazil),HC (Canada), and SAHPRA (South Africa) along woty various country accrediation and the company maintains an exclusive API facility serving more than 30 countries. Gufic offers professionals the opportunity to contribute to transformative healthcare and pharmaceutical excellence on a global scale.
Role Description This is a full-time, on-site Pharmaceutical Professional role based at Gufic Biosciences Ltd. in Navsari. The role involves supporting end-to-end pharmaceutical operations, including formulation development, production oversight, quality assurance, and compliance with national and international regulatory standards. Responsibilities may include monitoring manufacturing processes, preparing and reviewing technical documentation, participating in validation and stability studies, and collaborating with cross-functional teams such as R&D, quality control, and regulatory affairs. The position also includes contributing to process optimization, maintaining accurate records for audits, and aligning daily activities with Gufic’s mission of delivering high-quality, innovative medicines. The role requires active participation in continuous improvement initiatives and adherence to safety and ethical guidelines within the facility.
Qualifications
Strong foundation in pharmaceutical sciences, including formulation, manufacturing processes, and basic pharmacology.
Knowledge of quality systems and regulatory requirements, such as GMP, documentation practices, and validation protocols.
Proficiency in analytical thinking and problem-solving, with the ability to interpret technical data and support process improvements.
Effective communication and collaboration skills for working with multidisciplinary teams in production, quality, and regulatory functions.
Detail-oriented approach, strong organizational skills, and the ability to manage multiple tasks in a fast-paced manufacturing environment.
Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related discipline.
Prior experience in pharmaceutical manufacturing, quality assurance, or R&D is an advantage.
Willingness to work on-site in Navsari and adhere to all safety, ethical, and compliance standards.

Work arrangement
No