Production incharge

4 weeks ago

Visakhapatnam, India Gamut HR Solutions Full time

Company Overview Gamut HR Solutions, headquartered in Hyderabad, is dedicated to connecting talented individuals with suitable job opportunities. With a team of 2-10 employees, the company tirelessly works to ensure candidates find the right fit. Explore more about us at our website . Job Overview We are seeking a Product Incharge for our esteemed client in the Pharma Industry located in Visakhapatnam. This is a Full-Time, Mid-Level position ideal for individuals with 4 to 6 years of relevant experience. The candidate will be pivotal in overseeing product processes ensuring they meet industry standards and regulations. Qualifications and Skills A minimum of 4 to 6 years of experience in a similar role within the pharmaceutical industry, showcasing strong expertise and understanding of the sector. Proficiency in lean manufacturing practices aimed at reducing waste and improving efficiency within production processes (Mandatory skill). In-depth understanding of quality assurance protocols to ensure that all products meet industry standards and regulations (Mandatory skill). Extensive knowledge of FDA regulations, essential for maintaining compliance and avoiding potential violations (Mandatory skill). Experience in ensuring cGMP compliance to guarantee the safety and efficacy of pharmaceutical products. Skilled in developing comprehensive standard operating procedures (SOPs) to streamline operations and maintain consistency. Expertise in managing or documenting batch production records, critical for product traceability and quality control. Ability to efficiently handle corrective and preventive action (CAPA) management to address and mitigate production issues. Familiarity with ERP software for effective planning, managing, and automating core business processes. Roles and Responsibilities Oversee all aspects of product management and production in alignment with industry standards and company objectives. Ensure efficient and effective manufacturing processes by implementing lean manufacturing techniques. Maintain adherence to FDA regulations and quality assurance protocols throughout the production cycle. Develop and refine SOPs to improve operational efficiency and maintain product quality and compliance. Handle batch production records meticulously to enhance traceability and accountability. Lead CAPA initiatives to identify root causes of production issues and implement corrective measures. Collaborate with cross-functional teams to ensure continuous process improvements and problem-solving initiatives. Utilize ERP software tools to optimize resource management and production planning.

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