Basic Pharma Life Science Pvt. Ltd.

Execute daily production activities as per the production plan. Coordinate with QA, QC, and warehouse departments for material and documentation readiness. Monitor shift-wise production targets and ensure timely completion. Maintain accurate BMRs, BPRs, logbooks, and other GMP documents. Ensure adherence to cGMP, SOPs, and regulatory norms. Participate in internal and external audits and implement CAPAs. Supervise production processes for tablets, capsules, liquids, or injectables (based on facility). Identify deviations or non-conformities and escalate to senior management. Support validation and qualification of equipment and processes. Supervise and guide operators and line workers during production shifts. Provide on-the-job training and maintain discipline and safety in the production area. Ensure all team members follow hygiene and safety protocols. Suggest and implement improvements for productivity and yield. Participate in lean manufacturing and 5S activities. Job Type: Full-time Pay: ₹280,000.00 - ₹300,000.00 per year Benefits: Health insurance Leave encashment Provident Fund Schedule: Day shift Work Location: In person

Key Responsibilities: Identify and evaluate potential suppliers based on quality, cost, reliability, and regulatory compliance. Procure raw materials, packaging materials, and engineering items in accordance with production and inventory requirements. Maintain accurate records of purchases, pricing, and supplier information in ERP or SAP systems. Negotiate pricing, payment terms, and contracts with vendors to ensure cost-efficiency. Coordinate with QA/QC, Production, and Warehouse departments to ensure specifications and delivery timelines are met. Monitor supplier performance and maintain vendor evaluation records as per SOP. Ensure materials procured comply with cGMP, WHO, USFDA, and other regulatory standards. Track inventory levels and plan reorders proactively to avoid stockouts or overstocking. Assist in audits (internal and external) by providing required documentation and records. Generate and analyze purchase reports for management review. Key Skills Required: Strong negotiation and communication skills In-depth knowledge of pharma raw materials and packaging materials Familiarity with GMP, GLP, and regulatory guidelines (WHO, USFDA, EU-GMP, etc.) Working knowledge of ERP systems like SAP, Oracle, etc. Ability to handle multiple vendors and prioritize purchases efficiently Analytical thinking and problem-solving Job Type: Full-time Pay: ₹13,224.80 - ₹34,618.07 per month Benefits: Health insurance Leave encashment Provident Fund Schedule: Day shift Work Location: In person

Key Responsibilities: Identify and evaluate potential suppliers based on quality, cost, reliability, and regulatory compliance. Procure raw materials, packaging materials, and engineering items in accordance with production and inventory requirements. Maintain accurate records of purchases, pricing, and supplier information in ERP or SAP systems. Negotiate pricing, payment terms, and contracts with vendors to ensure cost-efficiency. Coordinate with QA/QC, Production, and Warehouse departments to ensure specifications and delivery timelines are met. Monitor supplier performance and maintain vendor evaluation records as per SOP. Ensure materials procured comply with cGMP, WHO, USFDA, and other regulatory standards. Track inventory levels and plan reorders proactively to avoid stockouts or overstocking. Assist in audits (internal and external) by providing required documentation and records. Generate and analyze purchase reports for management review. Key Skills Required: Strong negotiation and communication skills In-depth knowledge of pharma raw materials and packaging materials Familiarity with GMP, GLP, and regulatory guidelines (WHO, USFDA, EU-GMP, etc.) Working knowledge of ERP systems like SAP, Oracle, etc. Ability to handle multiple vendors and prioritize purchases efficiently Analytical thinking and problem-solving Job Type: Full-time Pay: ₹13,224.80 - ₹34,618.07 per month Benefits: Health insurance Leave encashment Provident Fund Schedule: Day shift Work Location: In person

Job Purpose : To drive domestic and international sales of API products, maintain relationships with clients, generate new business, and support strategic marketing initiatives to achieve revenue and growth targets. Key Responsibilities : Sales & Business Development Identify and develop new business opportunities for API sales in domestic and international markets. Generate leads, conduct product presentations, and negotiate pricing and terms. Handle customer inquiries, prepare quotations, and follow up on proposals. Client Relationship Management Maintain and strengthen relationships with existing customers. Ensure timely communication, resolve customer complaints, and support after-sales service. Market Analysis Conduct market research to understand competitor activities, pricing, and industry trends. Provide regular market feedback to management and contribute to product strategy. Regulatory & Documentation Coordinate with QA/QC and regulatory teams for product documents like COA, MOA, DMF, etc. Ensure compliance with all legal and regulatory requirements related to product export. Coordination & Reporting Coordinate with production, logistics, and finance departments for order fulfillment and dispatch. Maintain customer database, sales records, and provide regular reports to management. Marketing Activities Support in preparing marketing materials, participating in exhibitions, trade shows, and digital promotions. Build company presence and brand awareness in target markets. Job Type: Full-time Pay: ₹60,000.00 - ₹70,000.00 per month Benefits: Health insurance Leave encashment Provident Fund Schedule: Day shift Language: English (Preferred) Work Location: In person

Bachelor's degree in chemistry Educational Qualification: M. Pharm (Q.A.) Experience: 4 to 6 years in pharma API Plant. Candidate should be fluent in English language. Define and implement QA policies, processes, and standards to ensure high-quality deliverables. Identify test scenarios and design test cases based on requirements and technical specifications. Assign tasks, monitor progress, and ensure timely completion of testing activities. Analyze QA processes to identify inefficiencies and recommend improvements. Quality audit, ISO, Production, GMP, HPLC, QC, GMS, Raw material, Calibration, E mail, Inspection, Finished goods, Stores, Documentation Etc. Job Type: Full-time Pay: ₹380,000.00 - ₹420,000.00 per year Benefits: Health insurance Leave encashment Provident Fund Education: Bachelor's (Preferred) Experience: QA: 4 years (Preferred) Language: English (Required)

Bachelor's degree in chemistry Educational Qualification: M. Pharm (Q.A.) Experience: 4 to 6 years in pharma API Plant. Candidate should be fluent in English language. Define and implement QA policies, processes, and standards to ensure high-quality deliverables. Identify test scenarios and design test cases based on requirements and technical specifications. Assign tasks, monitor progress, and ensure timely completion of testing activities. Analyze QA processes to identify inefficiencies and recommend improvements. Quality audit, ISO, Production, GMP, HPLC, QC, GMS, Raw material, Calibration, E mail, Inspection, Finished goods, Stores, Documentation Etc. Job Type: Full-time Pay: ₹380,000.00 - ₹420,000.00 per year Benefits: Health insurance Leave encashment Provident Fund Education: Bachelor's (Preferred) Experience: QA: 4 years (Preferred) Language: English (Required)

Assist in formulation development (pilot batches, stability studies). Draft and organize SOPs, STPs, BMRs, calibration logs, and regulatory documents. Ensure smooth technology transfer from R&D to production. Coordinate with Analytical, QA/QC, Regulatory, and Plant teams. Support QA/QC audits, ensure GMP/GDP adherence, and contribute to compliance efforts. Present progress reports and assist in project tracking. Requirements: Bachelor’s/Master’s degree in Pharmacy (Pharmaceutics) or related science field. 1–5 years of relevant experience in R&D, QA/QC, or documentation roles. Knowledge of GMP/GLP/GDP standards and regulatory guidelines (ICH). Instrumentation exposure (HPLC, GC, UV) is a plus. Excellent documentation, analytical, and communication skills. Desirable: Experience with NDDS, injectable formulations, or regulated-market compliance. Prior involvement in patent/IPR or technology transfer processes. Job Type: Full-time Pay: ₹160,000.00 - ₹200,000.00 per year Work Location: In person

Assist in formulation development (pilot batches, stability studies). Draft and organize SOPs, STPs, BMRs, calibration logs, and regulatory documents. Ensure smooth technology transfer from R&D to production. Coordinate with Analytical, QA/QC, Regulatory, and Plant teams. Support QA/QC audits, ensure GMP/GDP adherence, and contribute to compliance efforts. Present progress reports and assist in project tracking. Requirements: Bachelor’s/Master’s degree in Pharmacy (Pharmaceutics) or related science field. 1–5 years of relevant experience in R&D, QA/QC, or documentation roles. Knowledge of GMP/GLP/GDP standards and regulatory guidelines (ICH). Instrumentation exposure (HPLC, GC, UV) is a plus. Excellent documentation, analytical, and communication skills. Desirable: Experience with NDDS, injectable formulations, or regulated-market compliance. Prior involvement in patent/IPR or technology transfer processes. Job Type: Full-time Pay: ₹160,000.00 - ₹200,000.00 per year Work Location: In person