SAIN MEDICAMENTS PVT. LTD

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