Job Description

Job Title: Manufacturing Product Development and Documentation Specialist Location: Baddi, Himachal Pradesh, India Company: Takshil BioPharma About Us: At Takshil BioPharma, we\'re a manufacturing company dedicated to innovation and quality. We\'re in search of a versatile individual who can lead the product development process, manage essential documentation, actively communicate with stakeholders, and make efficient use of the resources we provide. : We\'re looking for a skilled Manufacturing Product Development and Documentation Specialist to guide our product creation journey. In this role, you will be responsible for researching, planning, executing the development process, actively communicating with stakeholders, and ensuring that all necessary documentation is in order. Key Responsibilities: Product Research: Investigate and analyze potential products, considering their feasibility and market demand. Development Planning: Create a step-by-step plan for product development, outlining resource requirements and timelines. Resource Utilization: Efficiently use the resources we provide to develop the product. Quality Assurance: Ensure that the product meets our quality standards. Documentation: Prepare and maintain comprehensive documentation, including regulatory submissions, standard operating procedures (SOPs), and project records. Stakeholder Communication: Actively communicate with stakeholders throughout the development process, providing updates, addressing concerns, and ensuring alignment with project goals. Project Management: Lead the development project, ensuring it stays on track and within budget. Collaboration: Work closely with cross-functional teams to bring the product from concept to reality. Qualifications: Bachelor\'s or Master\'s degree in pharmaceutical sciences, chemistry, or a related field. Proven experience in pharmaceutical product development, with a strong track record of successful project management. In-depth knowledge of pharmaceutical manufacturing processes, formulations, and regulatory requirements. Excellent documentation and record-keeping skills. Strong problem-solving abilities and attention to detail. Ability to work effectively in a collaborative, cross-functional team environment. Familiarity with regulatory agencies such as the FDA and ICH guidelines is a plus. Salary: As per industry norms

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