Strong knowledge of labor laws and statutory compliance. Experience in pharma or manufacturing setup preferred, Statutory Compliance, Employee Welfare, Admin. Handle disciplinary actions, grievances, and employee relations effectively
Quality Assurance Leadership, Compliance Oversight: Ensure all processes comply with cGMP, ICH, and other relevant regulatory requirements, Process Improvement: Identify and implement continuous improvement initiatives to enhance product quality .
Security Operations, CCTV Surveillance, Compliance & Safety, Emergency Response & Incident Management, Administrative Support
We are seeking an experienced Regulatory Affairs professional to support and manage the regulatory lifecycle of oral solid dosage (OSD) products across key global markets, including the EU, USA, and RoW.
We are seeking a dynamic and experienced Product Manager to lead our portfolio across key therapeutic areas including Orthopaedics, Gynaecology, ENT, and General Medicine.
• Checking the indents for all the lab requirements like Lab Chemicals, Glassware’s, Columns, impurities, standards, stationeries, Packing materials, capital goods, Engineering and service indents. • Floating enquiries and arranging the quotes.
We are seeking a dynamic and motivated MBA Marketing Fresher to join our growing marketing team. The ideal candidate will bring strong academic understanding, fresh perspectives, and a passion for consumer behavior, branding, and digital marketing.
with strong knowledge of TDS (Tax Deducted at Source) and GST (Goods and Services Tax) regulations. Will be responsible for managing statutory compliances, reconciliations, and financial reporting related to indirect taxation
Provide day-to-day support to employees regarding HR policies, procedures, and practices. Maintain employee records and ensure data accuracy in the HRIS system. Help ensure legal compliance with labor and employment laws and internal policies.
Responsible for formulation and process development of oral immediate-release dosage forms, including oral film and tablet formulations. Troubleshoot and problem-solve unresolved or new formula issue
1. 4 to 6 years of relevant experience in a pharmaceutical testing lab and formulation environment 2. Educational background: Diploma or B.E. in Electrical or Electronics Engineering 3. Hands-on experience QMS, in instrument and utility maintenance
Pain management
2. In depth knowledge of Indian / Global (EU, US and TGA) pharmacovigilance guidelines / regulations 3. Strong knowledge and understanding of medical terminology and clinical development processes Required Candidate profile Educational qualification Graduation/post-graduation in Pharma, science or any life science Function/department Pharmacovigilance only accepted who has worked in pharma company in this function
1.Should have shop floor experience in Granulation, compression, coating. 2.Packing experience is added advantage. 3.Shuold have working knowledge of MS Word, Excel 4. Experience in Oral Solid Doses Perks and benefits Transport is there, Medical Insurance
Develop and optimize analytical methods (HPLC, UPLC, GC, UV, Dissolution, KF, IR, etc.) for oral solid and oral liquid formulations. Perform analytical method validation and transfer to Quality Control / manufacturing sites.
Develop and optimize formulations for oral solids and liquids to meet quality, stability, and regulatory requirements. Conduct pre-formulation studies, compatibility studies, and excipient screening for both dosage forms.
Develop and optimize formulations for oral solids and liquids to meet quality, stability, and regulatory requirements. Conduct pre-formulation studies, compatibility studies, and excipient screening for both dosage forms.
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