Job description Opening for Executive Production – Pharma Company Sain Medicaments Pvt Ltd – Hyderabad About the Company: Sain Medicaments Pvt Ltd is a leading pharmaceutical formulation company, proudly serving Human healthcare since 1970s, we have come a long way to make a mark in the healthcare industry which has ISO 22000:2005, WHO GMP, GLP certified manufacturing unit situated at HYDERABAD. Job Duties: Granulation / Compression Coating Packing Review of BMR Batch manufacturing and all Equipment Knowledge of Tablet Manufacturing Filling of BMR/BPR as per GDP. Preparation of SOPs. Ensuring adherence to CGMP/GDP practices. Filling of Equipment cleaning/operation, Area cleaning, Environment Pressure difference monitoring logbook. Monitoring of all manufacturing stages personally. Ensuring daily calibration/verification of weighing balance. Maintaining all inventories of spare parts, tablet toolings. Monitoring of preventive maintenance schedule with engineering team. Communicating with QA, Engineering, and QC for smooth work on shop- floor. Participating in QA training. Following company policies, SOP s as laid down by QA. Skills: Production Planning, Safety, Quality, GMP, Documentation, Continuous Improvement, Facilitation, Preventive Maintenance, Quality Assurance, Quality Control. Experience: 5 to 8 Years of experience in Production department for highly reputed Pharma company at Hyderabad Location Qualifications: M. Pharm / B. Pharm / M. Sc Chemistry. IndustryPharmaceuticals
Job description Job Description: HPLC Analyst - Pharma Background only. Company: Sain Medicaments Pvt Ltd, UPPAL, HYDERABAD. Location: Uppal, Hyderabad Industry: Pharmaceutical (Pharma Experience Required) We are seeking a skilled and experienced HPLC Analyst to join our Quality Control (QC) team. The ideal candidate should have a strong background in the pharmaceutical industry and hands-on experience in laboratory analysis. Job Responsibilities: Perform analysis of raw materials and finished products. Operate and maintain HPLC (High-Performance Liquid Chromatography) equipment. Conduct UV, pH, and Karl Fischer (KF) titration analyses. Ensure accurate and reliable testing results in line with industry standards. Follow Good Laboratory Practices (GLP) and ensure compliance with quality protocols. Experience: Minimum of 2 to 3 years of experience in a clinical, industrial, or pharmaceutical laboratory. Qualifications: M.Sc. / B.Sc. / M.Pharm / B.Pharm in a scientific or related field. If you have the required experience and are passionate about working in a dynamic pharmaceutical environment, we invite you to apply! Industry Pharmaceutical Manufacturing
Subject: Marketing Manager Wanted - Lead Multi-Specialty Pharma Launches in Telangana (Based in Hyderabad) Post Content: 🚀 Career Opportunity: Marketing Manager - Multi-Specialty Formulations 📍 Location: Hyderabad, Telangana 🔬 Specialties: Neurology, Hepatology + Other Key Segments We’re a dynamic pharmaceutical company based in Hyderabad , seeking an experienced Marketing Manager to spearhead the launch and growth of our multi-specialty formulations portfolio across Telangana. Develop & execute end-to-end launch strategies for specialty products (Neuro, Hepato + more). Lead market analysis, branding, and promotional campaigns in Telangana. Collaborate with sales, medical, and cross-functional teams for impactful market penetration. Own P&L responsibility and drive portfolio growth. You Bring: 5+ years in pharma marketing , preferably with experience in Neurology/Hepatology . Proven success in launching specialty formulations in regional markets. Strong understanding of Telangana’s healthcare landscape. Leadership skills, analytical mind set, and agility in execution. MBA/Bachelor’s in Life Sciences/Pharma/Marketing. Apply Now: girish@saingroup.com Contact number:8008855186
Job description Sain Medicaments Pvt Ltd – Hyderabad About the Company: Sain Medicaments Pvt Ltd is a leading pharmaceutical formulation company, proudly serving Human healthcare since 1970s, we have come a long way to make a mark in the healthcare industry which has ISO 22000:2005, WHO GMP, GLP certified manufacturing unit situated at HYDERABAD. Opening for: Jr. Executive Regulatory Affairs Job Duties: Preparation of regulatory dossier for various countries. Co-ordinate and collect data/Documents from various departments in plant and Review of the same for the compliance before preparation of dossiers. Contact API Vendors and manufacturers for DMFs/ APIMFs/Tech packs. Review the documents and ensure its compliance as per the CTD requirements. Co-ordinate with graphic designer for labels and packaging material artworks development. Plan for samples for registration in co-ordination with concerned departments and ensure its readiness as per the submission plan. Handling of queries received from clients, drug authorities and ensure required further information/ documents in stipulated timelines Candidate should have knowledge of the following: Explaining regulations, policies, or procedures Ensuring adequate compliance with regulations Advising others on matters that are related to regulatory processes and compliance Providing correct and accurate technical review of data or reports Overseeing the planning, coordination, and management of regulatory documentation activities Examining, identifying, and interpreting relevant regulatory guidelines Analyzing and evaluating laws and regulations that apply to the process of determining the impact on company activities Compiling and overseeing the maintenance of regulatory documentation databases or systems Coordinating efforts that are related to the preparation of regulatory documents or submissions Developing and maintaining healthy communication with regulatory agencies regarding pre-submission strategies, compliance test requirements, potential regulatory pathways, or clarification, and follow-up on submissions still under review. Experience: 2-3 years of experience. Qualification: B.Pharmacy, M.Pharmacy, MSc, Pharma D. Industry Pharmaceutical Manufacturing
Job Description: HPLC Analyst - Pharma Background only. Company: Sain Medicaments Pvt Ltd, UPPAL, HYDERABAD. Location: Uppal, Hyderabad Industry: Pharmaceutical (Pharma Experience Required) We are seeking a skilled and experienced HPLC Analyst to join our Quality Control (QC) team. The ideal candidate should have a strong background in the pharmaceutical industry and hands-on experience in laboratory analysis. Job Responsibilities: Perform analysis of raw materials and finished products. Operate and maintain HPLC (High-Performance Liquid Chromatography) equipment. Conduct UV, pH, and Karl Fischer (KF) titration analyses. Ensure accurate and reliable testing results in line with industry standards. Follow Good Laboratory Practices (GLP) and ensure compliance with quality protocols. Experience: Minimum of 2 to 3 years of experience in a clinical, industrial, or pharmaceutical laboratory. Qualifications: M.Sc. / B.Sc. / M.Pharm / B.Pharm in a scientific or related field. If you have the required experience and are passionate about working in a dynamic pharmaceutical environment, we invite you to apply! Industry Pharmaceutical Manufacturing Industry Pharmaceutical Manufacturing
Job Description for Production R&D (Formulation) in a Pharma Company Job Title: Production R&D Executive / Scientist (Formulations) Department: Research & Development (Formulations) Location: Hyderabad Company : Sain Medicaments Pvt Ltd. Role Overview: We are seeking a motivated and skilled Production R&D professional to support our formulation development activities. The role involves working closely with the R&D team to design, develop, and optimize oral solid dosage (OSD) formulations such as tablets, capsules, and dry suspensions, while ensuring scalability, compliance, and quality. Key Responsibilities - Formulation Development: * Assist in the development of new formulations (tablets, capsules, suspensions, etc.) * Conduct pre-formulation and compatibility studies. * Support lab-scale, pilot-scale, and scale-up batches. Production Support: * Coordinate with the production team for technology transfer of R&D-developed formulations. * Provide technical support during scale-up and commercial manufacturing. * Troubleshoot issues related to formulation and process parameters. Documentation & Compliance: * Prepare and review documents such as batch manufacturing records (BMR), standard operating procedures (SOPs), and development reports. * Ensure adherence to cGMP, GLP, and regulatory requirements. * Maintain proper documentation for regulatory submissions. Quality & Analysis: * Work with analytical teams for stability testing and product analysis. * Ensure developed formulations meet quality, stability, and regulatory standards. Innovation & Improvement: * Participate in process optimization and cost reduction initiatives. * Stay updated on new technologies, excipients, and regulatory guidelines in formulation development. Qualifications & Eligibility: * Education: B. Pharm / M. Pharm (Pharmaceutics or related field). Experience: 2–6 years of experience in formulation development (OSD preferred). Skills: * Strong knowledge of formulation techniques, excipients, and process equipment. * Understanding of scale-up and technology transfer. * Good documentation and communication skills. * Ability to work independently and in cross-functional teams. Key Competencies: * Analytical thinking and problem-solving. * Attention to detail with strong organizational skills. * Proactive, innovative, and adaptable in a dynamic R&D environment. Designation Options: Executive / Senior Executive / Scientist (depending on experience level).
Job Title: Senior Executive – Purchase Department (Pharma Company) Company : Sain Medicaments Pvt Ltd. Department: Procurement / Purchase Location:Hyderabad Role Overview: The Senior Executive Purchase will be responsible for handling end-to-end procurement activities related to raw materials, packaging materials, engineering spares, and consumables for the formulation manufacturing unit. The role requires strong negotiation skills, vendor management, and coordination with internal departments to ensure uninterrupted supply chain operations in compliance with company policies and regulatory standards. Key Responsibilities: Procurement & Planning Plan, source, and procure materials (RM, PM, consumables, etc.) as per production and R&D requirements. Review indents and ensure timely release of purchase orders. Coordinate with vendors to ensure on-time delivery and material quality compliance. Maintain optimal inventory levels to avoid shortages or overstocking. Vendor Development & Management *Identify, evaluate, and develop new suppliers as per company standards. * Negotiate prices, payment terms, and delivery schedules to ensure cost-effectiveness. * Monitor vendor performance through regular feedback and audits. * Maintain and update the Approved Vendor List (AVL). Documentation & Compliance * Ensure all procurement processes adhere to cGMP, GDP, and company SOPs. * Prepare and maintain purchase records, comparative statements, and vendor quotations. * Coordinate with QA and QC departments for vendor qualification and material approval. * Handle documentation for audit and regulatory compliance purposes. Cross-Functional Coordination * Liaise with Production, Stores, QA/QC, Accounts, and other departments for smooth material flow. * Coordinate with the logistics team for material dispatch and inward clearance. * Support Finance in supplier invoice reconciliation and payment follow-ups. Cost Optimization & Reporting * Continuously analyze market trends for cost-saving opportunities. * Prepare periodic MIS reports on purchase activities, material shortages, and vendor performance. * Participate in annual budgeting and procurement cost analysis. Technical Skills: * Knowledge of RM/PM specifications and pharma-grade sourcing. * Understanding of ERP systems (SAP / Tally / Oracle). * Familiarity with GDP, cGMP, and regulatory procurement practices. * Strong negotiation and communication skills. * Excellent vendor relationship management. * Analytical and result-oriented mindset. * Attention to detail and documentation accuracy. * Ability to multitask under strict timelines. Qualifications & Experience: Education: B.Pharm / M.Pharm / B.Sc / MBA (Supply Chain / Material Management preferred). Experience: 4–8 years of experience in pharma formulation procurement (OSD / sterile / R&D unit preferred).
Job description Sain Medicaments Pvt Ltd – Hyderabad About the Company: Sain Medicaments Pvt Ltd is a leading pharmaceutical formulation company, proudly serving Human healthcare since 1970s, we have come a long way to make a mark in the healthcare industry which has ISO 22000:2005, WHO GMP, GLP certified manufacturing unit situated at HYDERABAD. Opening for: Jr. Executive Regulatory Affairs Job Duties: Preparation of regulatory dossier for various countries. Co-ordinate and collect data/Documents from various departments in plant and Review of the same for the compliance before preparation of dossiers. Contact API Vendors and manufacturers for DMFs/ APIMFs/Tech packs. Review the documents and ensure its compliance as per the CTD requirements. Co-ordinate with graphic designer for labels and packaging material artworks development. Plan for samples for registration in co-ordination with concerned departments and ensure its readiness as per the submission plan. Handling of queries received from clients, drug authorities and ensure required further information/ documents in stipulated timelines Candidate should have knowledge of the following: Explaining regulations, policies, or procedures Ensuring adequate compliance with regulations Advising others on matters that are related to regulatory processes and compliance Providing correct and accurate technical review of data or reports Overseeing the planning, coordination, and management of regulatory documentation activities Examining, identifying, and interpreting relevant regulatory guidelines Analyzing and evaluating laws and regulations that apply to the process of determining the impact on company activities Compiling and overseeing the maintenance of regulatory documentation databases or systems Coordinating efforts that are related to the preparation of regulatory documents or submissions Developing and maintaining healthy communication with regulatory agencies regarding pre-submission strategies, compliance test requirements, potential regulatory pathways, or clarification, and follow-up on submissions still under review. Experience: 2-3 years of experience. Qualification: B.Pharmacy, M.Pharmacy, MSc, Pharma D. Industry Pharmaceutical Manufacturing
Job description Sain Medicaments Pvt Ltd Hyderabad About the Company: Sain Medicaments Pvt Ltd is a leading pharmaceutical formulation company, proudly serving Human healthcare since 1970s, we have come a long way to make a mark in the healthcare industry which has ISO 22000:2005, WHO GMP, GLP certified manufacturing unit situated at HYDERABAD. Opening for: Jr. Executive Regulatory Affairs Job Duties: Preparation of regulatory dossier for various countries. Co-ordinate and collect data/Documents from various departments in plant and Review of the same for the compliance before preparation of dossiers. Contact API Vendors and manufacturers for DMFs/ APIMFs/Tech packs. Review the documents and ensure its compliance as per the CTD requirements. Co-ordinate with graphic designer for labels and packaging material artworks development. Plan for samples for registration in co-ordination with concerned departments and ensure its readiness as per the submission plan. Handling of queries received from clients, drug authorities and ensure required further information/ documents in stipulated timelines Candidate should have knowledge of the following: Explaining regulations, policies, or procedures Ensuring adequate compliance with regulations Advising others on matters that are related to regulatory processes and compliance Providing correct and accurate technical review of data or reports Overseeing the planning, coordination, and management of regulatory documentation activities Examining, identifying, and interpreting relevant regulatory guidelines Analyzing and evaluating laws and regulations that apply to the process of determining the impact on company activities Compiling and overseeing the maintenance of regulatory documentation databases or systems Coordinating efforts that are related to the preparation of regulatory documents or submissions Developing and maintaining healthy communication with regulatory agencies regarding pre-submission strategies, compliance test requirements, potential regulatory pathways, or clarification, and follow-up on submissions still under review. Experience: 2-3 years of experience. Qualification: B.Pharmacy, M.Pharmacy, MSc, Pharma D. Industry Pharmaceutical Manufacturing
Job Title: Production Manager – Liquid Orals Department: Production Location: Sain Medicaments Pvt Ltd. Experience Required: Minimum 10+ Years in Liquid Formulation Manufacturing Job Summary: The Production Manager will oversee end-to-end liquid oral formulation manufacturing, ensuring GMP compliance, production efficiency, and product quality. Key Responsibilities: - Manage liquid formulation manufacturing operations. - Plan and execute production schedules. - Ensure equipment readiness and cleanliness. - Supervise blending, filtration, and filling processes. - Ensure batch documentation is completed as per GMP standards. - Lead deviations and CAPA activities. - Coordinate with QA, QC, Warehouse, and Engineering teams. - Train and guide production operators. - Ensure EHS compliance in production areas. Education & Experience: B.Pharm / M.Pharm / B.Sc / M.Sc with 10+ years experience in liquid formulation production. Key Skills: - Leadership and people management - Strong understanding of GMP compliance - Technical expertise in liquid formulations - Good communication and coordination skills
Job Title: Granulation Operator - Compression, Coating, Blister and Strip Packing. Department: Production (OSD – Granulation) Experience Required: Minimum 5 Years in Pharma Formulation Only Location: Sain Medicaments Pvt Ltd – (Hyderabad) Job Purpose: To operate and maintain granulation equipment as part of the tablet and capsule manufacturing process, ensuring consistent product quality and compliance with cGMP standards. Key Responsibilities: * Operate granulation equipment such as RMG (Rapid Mixer Granulator), FBD (Fluid Bed Dryer), Multi-mill, Sifter, Blender, and related machinery. * Perform batch processing as per Batch Manufacturing Records (BMR) and SOPs. * Ensure adherence to cGMP, GDP, and safety standards during every stage of operation. * Monitor granulation parameters to ensure uniformity and consistency of granules. * Carry out equipment cleaning, CIP/SIP, and line clearance procedures. * Perform in-process checks (granule moisture content, LOD, sieve analysis, etc.) and record results accurately. * Identify and report equipment malfunction, deviations, and non-conformities to the supervisor or maintenance team. * Maintain proper documentation in logbooks, equipment usage records, and cleaning records. * Coordinate with Quality Assurance for process approvals and sample submissions. * Follow FIFO/FEFO and good material handling practices. * Assist in batch changeovers and support continuous production improvement initiatives. Required Qualifications & Experience: Education:ITI / Diploma / B.Sc / B.Pharm or relevant qualification. Experience: Minimum 5 years working specifically in Granulation operations (OSD formulation units). Hands-on experience with RMG, FBD, Blenders, and Milling Equipment is essential. Good understanding of BMR documentation, GMP, IPQA interactions, and hygiene practices.
Job Title: Production Manager – OSD (Oral Solid Dosage) Department: Production Location: Sain Medicaments Pvt Ltd, Uppal , Hyderabad, Telangana. Experience Required: Minimum 10+ Years in OSD Formulation Manufacturing Job Summary: The Production Manager will be responsible for overseeing and managing the entire OSD manufacturing operations, including Granulation, Compression, Coating, and Packing activities. The role requires strong leadership in production planning, compliance, manpower management, and continuous improvement to ensure quality output, productivity, and regulatory readiness. Key Responsibilities: - Lead and manage end-to-end OSD production operations in alignment with GMP and regulatory standards. - Plan, schedule, and allocate production batches to ensure timely delivery and adherence to production targets. - Monitor and control processes in Granulation, Blending, Compression, Coating, and Packing departments. - Ensure availability of RM/PM, machine readiness, and line clearance before batch execution. - Coordinate with QA, QC, Warehouse, R&D, Engineering, and Procurement for smooth workflow. - Ensure strict compliance to SOPs, cGMP, GDP, EHS, and regulatory guidelines at all stages. - Review and approve BMR/BPR and ensure documentation accuracy. - Train, guide, and supervise departmental staff, operators, and shift executives. - Lead deviation investigations, CAPA implementation, and continuous improvement programs. - Prepare production plans, yield reports, downtime analysis, and MIS reports. - Drive audit readiness for regulatory inspections (USFDA, WHO, EU GMP, etc.). - Promote cleanliness, discipline, safety, and compliance culture across production floors. - Identify and implement strategies to reduce waste, improve efficiency, and optimize cost. Qualifications & Experience: - Education: B.Pharm / M.Pharm / M.Sc or equivalent science background. - Experience: 10–15 years of experience in OSD formulation production, with at least 3–5 years in a managerial or supervisory role. Skills & Competencies: - Strong leadership and people management skills. - In-depth technical knowledge of OSD processes and equipment. - Excellent planning, problem-solving, and decision-making abilities. - Good communication and interdepartmental coordination skills. - Ability to work under pressure and meet production timelines. - Strong exposure to Regulatory Audits, cGMP, and quality systems in formulation units.
Job Title: Production Manager OSD (Oral Solid Dosage) Department: Production Location: Sain Medicaments Pvt Ltd, Uppal , Hyderabad,Telangana. Experience Required: Minimum 10+ Years in OSD Formulation Manufacturing Job Summary: The Production Manager will be responsible for overseeing and managing the entire OSD manufacturing operations, including Granulation, Compression, Coating, and Packing activities. The role requires strong leadership in production planning, compliance, manpower management, and continuous improvement to ensure quality output, productivity, and regulatory readiness. Key Responsibilities: - Lead and manage end-to-end OSD production operations in alignment with GMP and regulatory standards. - Plan, schedule, and allocate production batches to ensure timely delivery and adherence to production targets. - Monitor and control processes in Granulation, Blending, Compression, Coating, and Packing departments. - Ensure availability of RM/PM, machine readiness, and line clearance before batch execution. - Coordinate with QA, QC, Warehouse, R&D, Engineering, and Procurement for smooth workflow. - Ensure strict compliance to SOPs, cGMP, GDP, EHS, and regulatory guidelines at all stages. - Review and approve BMR/BPR and ensure documentation accuracy. - Train, guide, and supervise departmental staff, operators, and shift executives. - Lead deviation investigations, CAPA implementation, and continuous improvement programs. - Prepare production plans, yield reports, downtime analysis, and MIS reports. - Drive audit readiness for regulatory inspections (USFDA, WHO, EU GMP, etc.). - Promote cleanliness, discipline, safety, and compliance culture across production floors. - Identify and implement strategies to reduce waste, improve efficiency, and optimize cost. Qualifications & Experience: - Education: B.Pharm / M.Pharm / M.Sc or equivalent science background. - Experience: 1015 years of experience in OSD formulation production, with at least 35 years in a managerial or supervisory role. Skills & Competencies: - Strong leadership and people management skills. - In-depth technical knowledge of OSD processes and equipment. - Excellent planning, problem-solving, and decision-making abilities. - Good communication and interdepartmental coordination skills. - Ability to work under pressure and meet production timelines. - Strong exposure to Regulatory Audits, cGMP, and quality systems in formulation units.
Job Title: Production Manager Liquid Orals Department: Production Location: Sain Medicaments Pvt Ltd. Experience Required: Minimum 10+ Years in Liquid Formulation Manufacturing Job Summary: The Production Manager will oversee end-to-end liquid oral formulation manufacturing, ensuring GMP compliance, production efficiency, and product quality. Key Responsibilities: - Manage liquid formulation manufacturing operations. - Plan and execute production schedules. - Ensure equipment readiness and cleanliness. - Supervise blending, filtration, and filling processes. - Ensure batch documentation is completed as per GMP standards. - Lead deviations and CAPA activities. - Coordinate with QA, QC, Warehouse, and Engineering teams. - Train and guide production operators. - Ensure EHS compliance in production areas. Education & Experience: B.Pharm / M.Pharm / B.Sc / M.Sc with 10+ years experience in liquid formulation production. Key Skills: - Leadership and people management - Strong understanding of GMP compliance - Technical expertise in liquid formulations - Good communication and coordination skills
Job Title: Granulation Operator - Compression,Coating,Blister and Strip Packing. Department: Production (OSD Granulation) Experience Required: Minimum 5 Years in Pharma Formulation Only Location: Sain Medicaments Pvt Ltd (Hyderabad) Job Purpose: To operate and maintain granulation equipment as part of the tablet and capsule manufacturing process, ensuring consistent product quality and compliance with cGMP standards. Key Responsibilities: * Operate granulation equipment such as RMG (Rapid Mixer Granulator), FBD (Fluid Bed Dryer), Multi-mill, Sifter, Blender, and related machinery. * Perform batch processing as per Batch Manufacturing Records (BMR) and SOPs. * Ensure adherence to cGMP, GDP, and safety standards during every stage of operation. * Monitor granulation parameters to ensure uniformity and consistency of granules. * Carry out equipment cleaning, CIP/SIP, and line clearance procedures. * Perform in-process checks (granule moisture content, LOD, sieve analysis, etc.) and record results accurately. * Identify and report equipment malfunction, deviations, and non-conformities to the supervisor or maintenance team. * Maintain proper documentation in logbooks, equipment usage records, and cleaning records. * Coordinate with Quality Assurance for process approvals and sample submissions. * Follow FIFO/FEFO and good material handling practices. * Assist in batch changeovers and support continuous production improvement initiatives. Required Qualifications & Experience: Education:ITI / Diploma / B.Sc / B.Pharm or relevant qualification. Experience: Minimum 5 years working specifically in Granulation operations (OSD formulation units). Hands-on experience with RMG, FBD, Blenders, and Milling Equipment is essential. Good understanding of BMR documentation, GMP, IPQA interactions, and hygiene practices.