📑 Job DescriptionResponsibilities:IPQA Officer for General Injectables:<ul style=border: 0px solid ...
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📑 JOB DETAILS 1. IPQA, Process validation, IQ,OQ,PQ activities. 2. Responsible for implementation of formats and control as per ISO13485 and ISO 9001 3. Responsible for Internal Audit and implementation & Verification of ISO 4. Responsible for shipment of Finished Goods for sterilization and Export 5. Responsible for Supplier Qualification, Coo ...
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📑 JOB DETAILS 1. IPQA, Process validation, IQ,OQ,PQ activities. 2. Responsible for implementation of formats and control as per ISO13485 and ISO 9001 3. Responsible for Internal Audit and implementation & Verification of ISO 4. Responsible for shipment of Finished Goods for sterilization and Export 5. Responsible for Supplier Qualification, Coo ...
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📑 JOB DETAILS 1. IPQA, Process validation, IQ,OQ,PQ activities. 2. Responsible for implementation of formats and control as per ISO13485 and ISO 9001 3. Responsible for Internal Audit and implementation & Verification of ISO 4. Responsible for shipment of Finished Goods for sterilization and Export<br/ ...
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📑 JOB DETAILS 1. IPQA, Process validation, IQ,OQ,PQ activities. 2. Responsible for implementation of formats and control as per ISO13485 and ISO 9001 3. Responsible for Internal Audit and implementation & Verification of ISO 4. Responsible for shipment of Finished Goods for sterilization and Export<br/ ...
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📑 JOB DETAILS 1. Responsible for line clearance for equipments / area 2. Responsible for in process check during manufacturing and packing 3. Responsible for review of different logs of production , packing, store 4. Responsible for verification of material during dispensing 5. Responsible for rev ...
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📑 Responsibilities: IPQA Officer for General Injectables: Perform in-process quality checks during manufacturing and packaging of general injectable products. Conduct line clearance and equipment checks to ensure compliance with Standard Operating Procedures (SOPs). Monitor critical process parameters and perform sampling for analysis as per approved ...
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📑 Responsibilities:IPQA Officer for General Injectables:Perform in-process quality checks during manufacturing and packaging of general injectable products.Conduct line clearance and equipment checks to ensure compliance with Standard Operating Procedures (SOP ...
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📑 Job DescriptionResponsibilities:IPQA Officer for General Injectables:<ul style=border: 0px solid ...
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📑 Job DescriptionResponsibilities:IPQA Officer for General Injectables:<ul style=border: 0px solid ...
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📑 Responsibilities Required Skills Must be excellent in written and spoken English; net savvy and adept at computer skills. Logical thinking. Organizing. Good in communication. Required Qualification: - B.Pharm/M.Pharm Salary :- 1.80 LPA If you are interested for this opening please send updated resume or revert on same mail ...
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📑 Job Description: Position Junior Executive - IPQA CTC Range Up to 4 LPA Educational Qualification B.Sc., B.Pharm, D.Pharm, M.Sc. Total Experience 1 to 2 Years Preferred Industry Pharmaceutical (Parenteral Manufacturing unit) Job Description Batch Manufacturing record review Batch manufacturing record issuance. Line ...
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📑 CHEMIST / R&D / IPQAWe would like to intimate you that, we are in requirement of Chemist - 08 Nos for our factory Quality Control Department.The candidates should fill full the below eligibility and requirements of us - Education - M.Sc / B.Sc (Chemistry)Age - 23 years and aboveSex - Male onlySalary - Rs.20,000/- to 25,000/- (08 Hours) 12 Hours ...
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📑 CHEMIST / R&D / IPQAWe would like to intimate you that, we are in requirement of Chemist - 08 Nos for our factory Quality Control Department.The candidates should fill full the below eligibility and requirements of us - Education - M.Sc / B.Sc (Chemistry)Age - 23 years and aboveSex - Male onlySalary - Rs.20,000/- to 25,000/- (08 Hours) 12 Hours ...
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📑 Responsibilities : USFDA, MHRM AND WHO GENEVA Audits Handling. Handling & Monitoring of all IPQA activity Handling & Monitor of day to day dispatch related activity Review & Monitor ongoing validation activity Review of EIMR & Cleaning record Review of Online documentation line clearance GMP Round Label & Seal management Product Failu ...
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📑 Responsibilities Required Skills Must be excellent in written and spoken English; net savvy and adept at computer skills. Logical thinking. Organizing. Good in communication. Required Qualification: - B.Pharm/M.Pharm Salary :- 1.80 LPA ...
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📑 Job Description: Position Junior Executive - IPQA CTC Range Up to 4 LPA Educational Qualification B.Sc., B.Pharm, D.Pharm, M.Sc. Total Experience 1 to 2 Years Preferred Industry Pharmaceutical (Parenteral Manufacturing unit) ...
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📑 Responsibilities : Ø Review and approval of SMF, VMP and Quality manual. Ø Review and approval of BMR, BPR, MFC. Ø Review and approval of OOS/OOT. Ø Review and approval of Vendor list. Ø Planning, execution and compliance of both internal and externalaudits. Ø Review and approval of all Quality Assurance, quality Control and manufacturing ...
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📑 Responsibilities : Ø Review and approval of SMF, VMP and Quality manual. Ø Review and approval of BMR, BPR, MFC. Ø Review and approval of OOS/OOT. Ø Review and approval of Vendor list. Ø Planning, execution and compliance of both internal and externalaudits. Ø Review and approval of all Quality Assurance, quality Control and manufacturing ...
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📑 Responsibilities : USFDA, MHRM AND WHO GENEVA Audits Handling. Handling & Monitoring of all IPQA activity Handling & Monitor of day to day dispatch related activity Review & Monitor ongoing validation activity Review of EIMR & Cleaning record Review of Online documentat ...
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📑 Responsibilities : USFDA, MHRM AND WHO GENEVA Audits Handling. Handling & Monitoring of all IPQA activity Handling & Monitor of day to day dispatch related activity Review & Monitor ongoing validation activity Review of EIMR & Cleaning record Review of Online documentat ...
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📑 JOB DESCRIPTION Designation: Deputy Manager Job Location: Bangalore Department: Quality Assurance – GMP – Chem Dev. AboutSyngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biot ...
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📑 JOB DESCRIPTIONDesignation: Deputy ManagerJob Location: BangaloreDepartment: Quality Assurance – GMP – Chem Dev.AboutSyngeneIncorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceu ...
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📑 Job Description: We are having an urgent opening for the position of Quality Executive for a reputed company at the Taloja/ Murbad location. Job Description: Must have at least 2 years of experience as a Quality Executive. Must have key expertise in Qual ...
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📑 JOB DESCRIPTION Designation: Deputy Manager Job Location: Bangalore Department: Quality Assurance – GMP – Chem Dev. AboutSyngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing ...
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📑 JOB DESCRIPTIONDesignation:Deputy ManagerJob Location:BangaloreDepartment:Quality Assurance – GMP – Chem Dev.AboutSyngeneIncorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nut ...
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📑 JOB DESCRIPTIONDesignation: Deputy ManagerJob Location: BangaloreDepartment: Quality Assurance – GMP – Chem Dev.AboutSyngeneIncorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrit ...
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📑 Ensure compliance to cGMP for all operational activities. Monitor the formulated products against stipulated conditions mentioned in the Batch production record. Conduct certificate of batch production records for compliance and stage wise completion. Conduct line clearance during manufacturing and the packing ...
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📑 This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's pro ...
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📑 Responsibilities : Ø Review and approval of SMF, VMP and Quality manual. Ø Review and approval of BMR, BPR, MFC. Ø Review and approval of OOS/OOT. Ø Review and approval of Vendor list. Ø Planning, execution and compliance of both internal and externalaudits. Ø Review and approval ...
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📑 Job Description Position- Engineer - UPS Testing Minimum Academic Qualification- BE – Electronics / Electricals with more than 3 years’ experience Minimum Working Experience- 2 years Minimum working experience in same Industry- ...
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📑 Responsibilities : Ø Review and approval of SMF, VMP and Quality manual. Ø Review and approval of BMR, BPR, MFC. Ø Review and approval of OOS/OOT. Ø Review and approval of Vendor list. Ø Planning, execution and compliance of both internal and externalaudits. Ø Review and approval ...
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📑 Job Overview Daily monitoring of production schedule, Ensure availability of all RM PM for continues production, timely release of material requisitions. Key Stakeholders: Internal Production, IPQA, Quality Control, Quality Assurance, Engg Dept., Key Stakeholders: External Corporate Procurement team, GBS ...
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📑 -:Position details:- Position: Manager/Sr Manager( Head - Micro) Grade: (G-10) No. of Position: 1 No. Job Location: Dewas Formulation Qualification: M.Sc.- Micro/Biotech / B.Pharma/M.Pharma Experience: 18-25 years of experience in Micro Section Candidate from Regulatory Plant will be preferred Job Description:- Ensure complia ...
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📑 -:Position details:- Position: Manager/Sr Manager( Head - Micro) Grade: (G-10) No. of Position: 1 No. Job Location: Dewas Formulation Qualification: M.Sc.- Micro/Biotech / B.Pharma/M.Pharma Experience: 18-25 years of experience in Micro Section Candidate from Regulatory Pla ...
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