Dec 2023 – Present · 2 yrs 6 mos · Bengaluru, Karnataka, India · Remote

• ✅ Strategic Marketing: Craft tailored digital marketing strategies that align with your business
• ✅ SEO Expertise: Boost your website's visibility with advanced SEO techniques, ensuring you rank higher on search engine results pages.
• ✅ Social Media Mastery: Leverage the power of social platforms to engage your audience, build brand awareness, and drive conversions.
• ✅ Content Marketing: Create compelling, shareable content that resonates with your audience and establishes your brand as an industry authority.
• ✅ PPC Campaigns: Maximize your ROI with targeted and data-driven pay-per-click campaigns on platforms like Google Ads and social media.
• ✅ Analytics and Optimization: Continuously monitor, analyze, and optimize campaigns to ensure maximum performance and return on investment.

Nov 2017 – Present · 8 yrs 7 mos · Bengaluru, Karnataka, India · On-site

• Key Responsibilities:
• Quality Control:
• Conducting quality checks at various stages of the manufacturing process to ensure compliance with regulatory standards.
• Monitoring and analyzing raw materials, intermediates, and finished products to guarantee their quality and safety.
• Production Planning:
• Collaborating with production planners to schedule and coordinate the manufacturing process.
• Ensuring that production targets are met while maintaining high-quality standards.
• Operational Oversight:
• Supervising and coordinating activities on the production floor.
• Troubleshooting issues that may arise during the manufacturing process to prevent delays.
• Regulatory Compliance:
• Staying updated on pharmaceutical regulations and ensuring that all manufacturing activities comply with these standards.
• Participating in audits and inspections conducted by regulatory authorities.
• Documentation:
• Maintaining detailed records of the manufacturing process, including batch records and standard operating procedures (SOPs).
• Documenting any deviations from standard procedures and implementing corrective actions.
• Collaboration with Cross-Functional Teams:
• Working closely with research and development teams to understand new product requirements.
• Collaborating with quality assurance, engineering, and other departments to address issues and improve processes.
• Continuous Improvement:
• Identifying opportunities for process optimization and efficiency improvements.
• Implementing and monitoring continuous improvement initiatives to enhance productivity and reduce costs.
• Safety and Environmental Compliance:
• Ensuring a safe working environment for all employees by adhering to safety protocols and guidelines.
• Complying with environmental regulations related to waste disposal and emissions.

Aug 2015 – Oct 2017 · 2 yrs 2 mos · Goa, India · On-site

• Key Responsibilities:
• Production Planning and Execution:
• Collaborate with cross-functional teams to plan and schedule production activities.
• Ensure the timely and efficient manufacturing of pharmaceutical products in accordance with production plans.
• Monitor and optimize production processes to enhance efficiency and minimize downtime.
• Quality Control:
• Implement and adhere to Good Manufacturing Practices (GMP) to ensure the quality and safety of pharmaceutical products.
• Conduct regular inspections and quality checks throughout the manufacturing process.
• Investigate and address any deviations from established quality standards.
• Compliance and Documentation:
• Stay abreast of regulatory requirements and ensure compliance with local and international pharmaceutical regulations.
• Maintain accurate and comprehensive documentation of manufacturing processes, ensuring records are complete and accessible for audits.
• Safety and Environmental Compliance:
• Prioritize and enforce safety protocols to create a secure working environment.
• Adhere to environmental regulations and promote sustainable practices within the manufacturing facility.
• Collaboration:
• Collaborate with research and development teams to scale up new pharmaceutical formulations for commercial production.
• Work closely with supply chain and logistics teams to manage inventory levels and ensure timely delivery of raw materials.
• Continuous Improvement:
• Identify opportunities for process optimization and cost reduction.
• Implement continuous improvement initiatives to enhance overall manufacturing efficiency and product quality.

Aug 2013 – Jul 2015 · 1 yr 11 mos · Goa, India · On-site

• Working in the anticancer manufacturing division of Cipla Pharmaceuticals involves being part of a dedicated team committed to producing high-quality oncology medications. As a professional in this field, your role may encompass various responsibilities to ensure the efficient and safe manufacturing of anticancer drugs.
• Production Planning and Execution:
• Collaborate with cross-functional teams to develop production plans for anticancer drugs.
• Oversee the execution of manufacturing processes, ensuring adherence to cGMP (current Good Manufacturing Practices) guidelines.
• Monitor production schedules, making adjustments as needed to meet demand.
• Quality Assurance:
• Implement and maintain rigorous quality control measures throughout the manufacturing process.
• Conduct thorough inspections of raw materials, intermediates, and finished products to ensure compliance with regulatory standards.
• Address and resolve any quality issues promptly.
• Regulatory Compliance:
• Stay informed about regulatory requirements related to anticancer drug manufacturing.
• Work closely with regulatory affairs teams to ensure that all manufacturing activities comply with relevant guidelines and regulations.
• Process Improvement:
• Continuously identify opportunities for process optimization and efficiency improvements.
• Collaborate with research and development teams to implement new technologies or improve existing manufacturing processes.
• Safety and Environmental Compliance:
• Prioritize and enforce safety protocols to maintain a secure working environment.
• Ensure compliance with environmental regulations related to pharmaceutical manufacturing.
• Team Collaboration:
• Foster a collaborative and inclusive work environment by working closely with colleagues from various departments, including research and development, quality control, and logistics.
• Provide guidance and support to manufacturing teams to ensure the successful execution of production plans.