Seabird Staffing Solution is looking for its reputed client who have- state-of-the-art Pharmaceutical Organization involved in Research, Manufacturing, Marketing, Sales and Distribution of Medicinal Formulations and Products. Job Title - Analytical Development- Officer / Executive Location - Chhatrapati Sambhajinagar, Maharashtra Exp. - 5 to 10 Years Qualification - M.Sc. (Chemistry) CTC - No bar for suitable candidate Key skill - AMV / AMT Job Description- Method Development: Develop and optimize analytical methods for drug products using techniques like HPLC, GC, GC-MS, and LC-MS. Method Validation and Transfer: Execute and manage method validation, including creating protocols and reports, and oversee the transfer of these methods to other departments or sites. Testing and Analysis: Perform quality control testing on raw materials, in-process samples, and finished products. Instrumentation: Handle the calibration, preventive maintenance, and troubleshooting of laboratory instruments. Data and Documentation: Maintain accurate records of all experimental data, write reports, and ensure compliance with cGMP and data integrity requirements. Collaboration: Work with cross-functional teams, such as manufacturing, discovery, and quality assurance, to resolve issues and support product development. Interested Candidates may send their resume on email ID- jobs@seabirdstaffing.com with following details- 1. Total Years Exp.- 2. Notice Period- 3. Current CTC- 4. Expected CTC- 5. Ready to relocate- Chh. Sambhajinagar, Maharashtra
Seabird Staffing Solution is looking for its reputed client who have- state-of-the-art Pharmaceutical Organization involved in Research, Manufacturing, Marketing, Sales and Distribution of Medicinal Formulations and Products. Job Title - Analytical Development- Officer / Executive Location - Chhatrapati Sambhajinagar, Maharashtra Exp. - 5 to 10 Years Qualification - M.Sc. (Chemistry) CTC - No bar for suitable candidate Key skill - AMV / AMT Job Description- Method Development: Develop and optimize analytical methods for drug products using techniques like HPLC, GC, GC-MS, and LC-MS. Method Validation and Transfer: Execute and manage method validation, including creating protocols and reports, and oversee the transfer of these methods to other departments or sites. Testing and Analysis: Perform quality control testing on raw materials, in-process samples, and finished products. Instrumentation: Handle the calibration, preventive maintenance, and troubleshooting of laboratory instruments. Data and Documentation: Maintain accurate records of all experimental data, write reports, and ensure compliance with cGMP and data integrity requirements. Collaboration: Work with cross-functional teams, such as manufacturing, discovery, and quality assurance, to resolve issues and support product development. Interested Candidates may send their resume on email ID- [HIDDEN TEXT] with following details- 1. Total Years Exp.- 2. Notice Period- 3. Current CTC- 4. Expected CTC- 5. Ready to relocate- Chh. Sambhajinagar, Maharashtra
Job Opening @ leading OSD Pharmaceutical Company Seabird Staffing Solution is looking for its reputed client who have-state-of-the-art Pharmaceutical Organization involved in Research, Manufacturing, Marketing, Sales and Distribution of Medicinal Formulations and Products. Job Title - Analytical Development- Officer / Executive Location - Chhatrapati Sambhajinagar, Maharashtra Exp. - 5 to 10 Years Qualification - M.Sc. (Chemistry) CTC- No bar for suitable candidate Key skill - AMV / AMT Job Description- Method Development :Develop and optimize analytical methods for drug products using techniques like HPLC, GC, GC-MS, and LC-MS. Method Validation and Transfer: Execute and manage method validation, including creating protocols and reports, and oversee the transfer of these methods to other departments or sites. Testing and Analysis: Perform quality control testing on raw materials, in-process samples, and finished products. Instrumentation: Handle the calibration, preventive maintenance, and troubleshooting of laboratory instruments. Data and Documentation: Maintain accurate records of all experimental data, write reports, and ensure compliance with cGMP and data integrity requirements. Collaboration: Work with cross-functional teams, such as manufacturing, discovery, and quality assurance, to resolve issues and support product development. Interested Candidates may send their resume on email ID- [HIDDEN TEXT] with following details- 1.Total Years Exp.- 2.Notice Period- 3.Current CTC- 4.Expected CTC- 5.Ready to relocate- Chh. Sambhajinagar, Maharashtra
Job Responsibilities: 1. QMS, Quality system development 2. Regulatory compliance 3. Document review and approval 4 . Audits and inspections 5. Validation , T & D. 6. Stability Studies 7. Documentation, Vendor Audit Preparation & Compliances Provident fund Health insurance Annual bonus
Responsibilities: 1. Conduct audits, QMS management, process validation, BMR review, BPR review. 2.Ensure IPQA compliance, prepare SOPs, perform vendor qualifications. 3. Quality Management System (QMS) Oversight 4. Training and Leadership Health insurance Provident fund
Responsibilities: 1. Lead QMS initiatives, ensuring compliance with regulatory standards. 2. Manage deviations, change controls, investigations, cleaning validations. 3. OSD / Injectable QMS 4. Audit Compliances, cGMP, ICH, 21 CFR Knowledge Health insurance Provident fund
Responsibilities: * Conduct analytical research using GLP principles. * Develop, validate, transfer methods through AMV/AMT processes. * Collaborate with cross-functional teams on method development and validation. Health insurance Provident fund
Responsibilities: 1. Manage budgets, GST compliance, reconciliations, TDS, taxes, finances, excise, sales tax, bill processing, MIS reporting. 2. Process journal entries, maintain accounting records using Tally ERP. 3. Financial Audit, MIS, Excel. Health insurance Provident fund
Responsibilities: 1. Conduct environmental monitoring, microbial testing, sterilization processes. 2. Prepare media, perform water analysis, document audits and compliance. 3. QMS, cGMP, GLP practices. Training, Investigation and troubleshooting Health insurance Provident fund
Responsibilities: *1. Ensure quality control during granulation and compression processes. 2. Collaborate with formulation team on OSD, RMG, FBD, blending, FBP, tablet production. 3. Machine Operation & Setup, Maintenance & Troubleshooting
Responsibilities: * Operate granulation and compression equipment * Ensure FBD compliance during batch processing * Perform maintenance and troubleshoot issues * Follow RMG guidelines for documentation * Should have knowledge of compression operation Health insurance Provident fund
Responsibilities: * Lead formulation development projects from ideation to commercialization. * Provide regulatory support throughout product lifecycle. * Collaborate with cross-functional teams on QbD initiative. * Project Leadership & Management Health insurance Provident fund
Responsibilities: * Lead formulation research projects from concept to commercialization. * Tech Transfer, BOM, MFR, scale-up batches * Develop solid oral, liquid, dry syrup, products. * ROW & Domestic Market. Known to RMG, FBD/FBP, Literature study Health insurance Provident fund
Job Title - Sr. Research Associate- Formulation R & D Location - Chhatrapati Sambhajinagar, Maharashtra Exp. - 3 to 5 Years Qualification - B. Pharm/ M. Pharm CTC- 4.5 – 7.0 LPA Key skill - Pre- formulation Study, Literature Search, Tech Transfer, Scale-up batches, BOM, MFR, Stability Study, protocol & reports Job Description- 1. Literature search/study. 2. Pre-formulation study execution. 3. Market/Innovator/reference product characterization. 4. Execution and documentation of trial batches – prototype formulation development. 5. Execution and monitoring of development stability studies. 6. Execution of process optimization/scale-up batches. Technology transfer activities at site. 7. Preparation of documents like BOM, MFR, compatibility study protocol and report, stability study protocol and report, PDR, etc. as per requirements 8. Co-ordination with relevant cross-functional departments/teams 9. Having experience/exposure of formulation development of solid oral, liquid, dry syrup, etc. dosage forms aimed for ROW and domestic market. 10. Should possess experience in handling various equipment’s like RMG, FBD/FBP, compression machine, roller compactor, coating Interested Candidates may send their resume on email ID- jobs@seabirdstaffing.com with following details- 1. Total Years Exp.- 2. Notice Period- 3. Current CTC- 4. Expected CTC- 5. Ready to relocate- Chh. Sambhajinagar, Maharashtra- Yes / No
Job Title - Sr. Research Associate- Formulation R & D Location - Chhatrapati Sambhajinagar, Maharashtra Exp. - 3 to 5 Years Qualification - B. Pharm/ M. Pharm CTC- 4.5 7.0 LPA Key skill - Pre- formulation Study, Literature Search, Tech Transfer, Scale-up batches, BOM, MFR, Stability Study, protocol & reports Job Description- 1.Literature search/study. 2.Pre-formulation study execution. 3.Market/Innovator/reference product characterization. 4.Execution and documentation of trial batches prototype formulation development. 5.Execution and monitoring of development stability studies. 6.Execution of process optimization/scale-up batches. Technology transfer activities at site. 7.Preparation of documents like BOM, MFR, compatibility study protocol and report, stability study protocol and report, PDR, etc. as per requirements 8.Co-ordination with relevant cross-functional departments/teams 9.Having experience/exposure of formulation development of solid oral, liquid, dry syrup, etc. dosage forms aimed for ROW and domestic market. 10.Should possess experience in handling various equipment's like RMG, FBD/FBP, compression machine, roller compactor, coating Interested Candidates may send their resume on email ID- [HIDDEN TEXT] with following details- 1.Total Years Exp.- 2.Notice Period- 3.Current CTC- 4.Expected CTC- 5.Ready to relocate- Chh. Sambhajinagar, Maharashtra- Yes / No
Responsibilities: * Compliance with CGMP, BPR, CIP guidelines during batch manufacturing. * Sterile operations using autoclave, lyophilization, injection equipment. aseptic techniques, * Supervise filling, sealing machines & compounding vessels. Health insurance Provident fund
Responsibilities: * Source top talent through various channels * Manage full cycle recruiting process from sourcing to onboarding * Collaborate with hiring managers on job requirements and candidate selection, Create and post JD across platforms
Responsibilities: * Lead QA activities: documentation, audits, training coordination. * Ensure compliance with regulatory standards: BPR review, change control, equipment validation, Stability Studies, T & D, QMS * Audit Preparation & Compliances. Provident fund Health insurance
http://nauk.in/e68hCSw Job Title - Quality Assurance – Assistant Manager Location - Chatrapati Sambhajinagar (Aurangabad), Maharashtra Exp. - 7 to 10 Years Qualification - B. Pharm/ M. Pharm CTC- 07 – 10 LPA Key skill - QMS, Validation, T &D, Stability Studies, Documentation, Audit Preparation & Compliances Job Description- ription- Quality system development: Create and implement quality systems to ensure all products and processes meet regulatory requirements. Regulatory compliance: Ensure all activities adhere to Good Manufacturing Practices (GMP) and other relevant regulations. Document review and approval: Review and approve all necessary documents, including batch records, SOPs, and validation reports. Audits and inspections: Conduct internal audits to assess compliance and quality, and assist with external inspections. Deviation and complaint management: Investigate and resolve quality issues, deviations, and customer complaints. Implement corrective and preventive actions (CAPA) to prevent recurrence. Product release: Oversee the final release of products after all quality checks are completed. Continuous improvement: Drive continuous improvement initiatives to enhance product quality and process efficiency. Training: Provide training to other employees on quality-related topics and GMP standards. Interested Candidates may send their resume on email ID- jobs@seabirdstaffing.com with following details- 1. Total Years Exp.- 2. Notice Period- 3. Current CTC- 4. Expected CTC- 5. Ready to relocate- Chh. Sambhajinagar, Maharashtra
Responsibilities: * Conduct quality inspections, investigate OOS events, and manage CAPAs. * Ensure compliance with GLP, GDP, and SOP preparation. * Review raw materials, finished products, and instruments. * QMS, Audit Preparation & Compliances Health insurance Provident fund