The role at Promea Therapeutics Pvt Ltd (Cytobiologics division) involves contributing to the research, development, and manufacture of life-saving Plasma derived medicines, Diagnostics, and large volume parenteral products. As part of the company's expansion plans, you will play a vital role in launching new products and businesses. Your responsibilities will include product and market analysis, ensuring timely execution of sales orders, gaining insight into biological products and market trends, and collaborating closely with senior management. Qualifications for this position include 0-1 years of experience in business development or a related field, along with a Masters or Bachelors degree in Life Sciences, Business, or a relevant discipline. Proficiency in Excel, the ability to establish and nurture client relationships, familiarity with analytical tools, and strong communication, negotiation, and interpersonal skills are also essential. Joining our team offers you the opportunity to be part of a dynamic and growing organization. You can expect competitive compensation, prospects for career advancement, involvement in challenging projects working with diverse teams, and a collaborative environment that fosters innovation.,
The In-Process Quality Assurance Executive plays a crucial role in ensuring that all products adhere to cGMP and regulatory standards throughout the manufacturing and packaging processes. You will collaborate closely with production teams to uphold product quality and address any issues that arise in real-time. Your responsibilities will include overseeing the quality of products from the warehouse to production and packing stages, ensuring compliance with cGMP and regulatory requirements, identifying and resolving quality issues promptly, and participating in investigations of deviations and non-conformances. You will also be responsible for maintaining detailed documentation of quality-related activities, participating in audits and inspections, offering guidance and training to production personnel, and contributing to the development and review of quality procedures and policies. To excel in this role, you should hold a Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related field, along with a minimum of 1 year of experience in in-process quality assurance within the pharmaceutical industry. Proficiency in cGMP and other regulatory standards, excellent problem-solving and communication skills, the ability to work both independently and collaboratively, and experience in audits, inspections, and root cause analysis are essential. Staying informed about the latest regulatory requirements and industry best practices is also crucial for success in this position.,
The Instrumentation Executive (Engineering) role at Promea involves the maintenance and daily documentation of instrumentation and control systems, ensuring compliance with cGMP and other regulatory standards. Responsibilities include maintaining instrumentation and control systems, developing preventive maintenance programs, performing calibration and validation, troubleshooting and repairing systems, and creating documentation and SOPs. Collaboration with other departments is essential for plant operation, while participation in regulatory inspections and audits is required for compliance. Qualifications for this role include a Bachelor's degree in Electrical, Electronics, or Instrumentation Engineering, along with at least 2 years of experience in designing, installing, and maintaining instrumentation and control systems in the pharmaceutical industry. Knowledge of cGMP and regulatory standards, as well as experience with PLC programming, SCADA, and HMI systems, are necessary. Strong communication, leadership, and problem-solving skills, coupled with the ability to work both independently and in a team, are also important. Staying updated with the latest technologies and advancements in instrumentation and control systems is encouraged.,
As an MIS Executive, you will be responsible for planning, coordinating, and directing all computer-related activities within the organization. Your primary role will involve determining the company's information technology goals and implementing computer systems to achieve those goals effectively. Your key responsibilities will include collecting and updating production data, packing data, biometric-related tasks, utilities data, as well as collecting BMR & BPR data to resolve batch count differences. Additionally, you will be involved in various other production-related activities to support the operational efficiency of the organization. To excel in this role, you should possess key skills such as analytical ability, effective communication, problem-solving capabilities, strategic thinking, and adaptability. These skills will be essential in ensuring the smooth functioning of computer systems and optimizing information management processes within the organization.,