Job Location is in Gujarat (District-Kutch) Quality Inspections & Testing: Conduct physical, chemical, and microbiological tests on raw materials, in-process batches, and finished products. Use analytical instruments (e.g., HPLC, GC, spectrophotometers) and follow SOPs for testing. Monitor production processes to ensure compliance with quality protocols. Documentation & Reporting: Maintain accurate records of test results, deviations, and corrective actions. Prepare Certificates of Analysis (CoA) and ensure all documentation meets regulatory standards. Compliance & Audits: Ensure adherence to GMP, GLP, FDA, WHO, and other relevant guidelines. Support internal and external audits and implement corrective actions. Non-Conformance Management: Identify and report quality deviations or non-conformities. Work with cross-functional teams to resolve issues and prevent recurrence. Continuous Improvement: Participate in root-cause analysis and process optimization initiatives. Stay updated on industry trends, regulatory changes, and best practices. Equipment & Lab Management: Calibrate and maintain laboratory equipment. Ensure lab cleanliness and safety standards. Customer Complaints: Investigate and resolve quality-related complaints promptly. Job Type: Full-time Pay: ₹19,944.57 - ₹67,747.65 per month Benefits: Provident Fund Schedule: Day shift Ability to commute/relocate: Ahmadabad, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Education: Bachelor's (Preferred) Location: Ahmadabad, Gujarat (Preferred) Work Location: In person

A Microbiologist in a pharmaceutical company plays a crucial role in ensuring the safety and quality of products by monitoring microorganisms, conducting tests, and developing new methods. They work in areas like quality control, research and development, and manufacturing, ensuring compliance with regulatory standards. Job Type: Full-time Pay: ₹20,000.70 - ₹50,000.95 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person

Roles & Responsibilities:- - Develop & Implement business development strategies to enter and grow in International Market. - Conduct thorough market research to identify potential customers in untapped territories. - Collaborate with cross functional teams to align business objectives with market opportunities. - Ensure smooth processes, timely documentation and adherence to deadlines. - Prepare and analyse factual data using Management Information Systems (MIS). - Launching of new products. - Meeting with Merchant Exporters to generate business - Identify and pursue potential business opportunities and partnerships in international market. - Present business opportunities and market trends to international clients. - Manage client conflicts and complaints to maintain trust and satisfaction. - Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person

Operate compression machines (e.g., Menestry, Cadmach) to manufacture tablets according to batch specifications. Perform turret changeovers (e.g., "B" to "D" tolling) and troubleshoot minor mechanical issues. Monitor machine performance to ensure optimal output and minimal downtime. Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Overtime pay Yearly bonus Work Location: In person

Operate compression machines (e.g., Menestry, Cadmach) to manufacture tablets according to batch specifications. Perform turret changeovers (e.g., "B" to "D" tolling) and troubleshoot minor mechanical issues. Monitor machine performance to ensure optimal output and minimal downtime. Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Overtime pay Yearly bonus Work Location: In person

As an Assistant Production Manager at Unicor Pharmatech LLP's Oral Solid Dosage (OSD) plant, you will play a crucial role in ensuring the manufacturing of high-quality pharmaceutical products in compliance with global health standards. With a minimum experience of 7 to 8 years in the pharma manufacturing industry, you will be responsible for overseeing various aspects of production management, quality assurance, team leadership, process optimization, safety protocols, and documentation. In the realm of production management, your duties will include planning, coordinating, and supervising daily OSD operations such as blending, granulation, compression, coating, encapsulation, and packaging. It will be imperative to ensure strict adherence to production schedules, batch records, and standard operating procedures (SOPs) while optimizing the utilization of resources like manpower, equipment, and materials to meet output targets efficiently. Your role will also encompass maintaining quality and compliance standards by enforcing cGMP, SOPs, and regulatory requirements set forth by FDA, MHRA, and WHO. You will lead deviation investigations, implement Corrective and Preventive Actions (CAPA), and collaborate closely with the Quality Assurance (QA) team to resolve batch-related issues and facilitate timely product release. Effective team leadership will be a key aspect of your responsibilities, involving the management, training, and mentoring of production supervisors, officers, and operators. Conducting performance reviews, fostering a culture of accountability, and driving continuous improvement initiatives will be essential for maximizing team productivity and efficiency. Furthermore, you will be tasked with identifying and implementing process optimization strategies to enhance efficiency in OSD processes, troubleshoot equipment or process issues, and ensure a safe workplace environment by enforcing safety protocols, hygiene standards, and cleanliness in production areas in line with OSHA, HAZOP, and 5S guidelines. Your role will also involve meticulous reporting and documentation tasks, including the review of batch records, logbooks, and production reports for accuracy, as well as the analysis of key performance indicators (KPIs) such as Overall Equipment Effectiveness (OEE), downtime, and yield. Providing senior management with regular performance updates and insights will be crucial for organizational decision-making. This is a full-time position with benefits including Provident Fund, and the work location is on-site during day shifts at the OSD plant. If you are a seasoned professional with a background in pharma manufacturing and a passion for driving excellence in production operations, compliance, and team management, we encourage you to apply for this rewarding opportunity at Unicor Pharmatech LLP.,

Only Female Candidates are Required Job Description: Liaise with vendors/suppliers for procurement of materials and services. Manage end-to-end purchase documentation (POs, invoices, records). Obtain, compare, and negotiate quotations to ensure cost-effectiveness. Utilize SAP software for purchase order processing and inventory management. Handle purchase-related email communication and internal coordination. Ensure compliance with company procurement policies and industry regulations. Job Type: Full-time Pay: ₹14,492.23 - ₹43,265.78 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person

Only Female Candidates are Required Job Description: Liaise with vendors/suppliers for procurement of materials and services. Manage end-to-end purchase documentation (POs, invoices, records). Obtain, compare, and negotiate quotations to ensure cost-effectiveness. Utilize SAP software for purchase order processing and inventory management. Handle purchase-related email communication and internal coordination. Ensure compliance with company procurement policies and industry regulations. Job Type: Full-time Pay: ₹14,492.23 - ₹43,265.78 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person