Post: Quality Assurance Executive Educational Qualification : B.Pharm/M.Pharm/M.Sc. Experience: 4 Years+ in Pharmaceuticals Company Job description Authorization of all procedures and standard instructions of process, controls, etc. Investigation and closure of all deviations, OOS and complaints Conducting self-inspections. Conducting vendor evaluation of raw materials. Should have sound knowledge of Process validation. Should be familiar with preparation of process validation protocol and report. Should have sound knowledge of QMS System and Change Control, Deviation and CAPA Procedure. Review of Preventive maintenance & calibration of equipment and systems. Review of stability data to support retest or expiry dates and storage conditions and/or intermediates where appropriate. Risk analysis evaluation Performing product quality reviews. Must understand Standard Operating Procedure. Candidates Only Having Experience in Pharma Industry should apply Job Type: Full-time Pay: ₹350,000.00 - ₹450,000.00 per year Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Jarod, Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: Pharma: 4 years (Preferred) Work Location: In person
Job description Post: Store Officer Experience: 1-2 Years Job description: Maintain and responsible for day to day warehouse operations. Receiving of raw materials/ solvents/ packing materials. Exposure in dispensing of raw and packaging materials. Handling of returned goods and rejected Materials as per procedure. Perform physical stock counts in accordance with the frequency Must understand SOP and documentation. Job Type: Full-time Pay: ₹180,000.00 - ₹250,000.00 per year Benefits: Provident Fund Schedule: Day shift Ability to commute/relocate: Samlaya R S, Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: Store management: 1 year (Preferred) Work Location: In person
Job description Post: QC Officer Experience: 0-2 Years in Pharma/Chemical Industry Job description: Testing of Raw Material ,In-Process & Finished Products. Preparations of volumetric solutions and standardization records. Water Analysis. Documentation Work Can handle Lab instruments. Having Knowledge of HPLC will be given preferences. Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹240,000.00 per year Benefits: Provident Fund Schedule: Day shift Ability to commute/relocate: Jarod, Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: QC Department: 1 year (Preferred) Work Location: In person
Post : Production Officer Educational Qualification: B.Pharm/M.Pharm/M.Sc./B.Sc. Experience: 0-3 Years in Pharma Industry Job Responsibilities: Handling of Tablet and Capsule manufacturing Activities. Maintain BMR, BPR and Documentation as per GMP. Manpower Handling. Primary and Secondary Packing Required Skills: Team Work Time Management Good Communication Skills Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹260,000.00 per year Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Jarod, Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: total work: 1 year (Preferred) Work Location: In person
Post : Production Officer Educational Qualification: B.Pharm/M.Pharm/M.Sc./B.Sc. Experience: 0-3 Years in Pharma Industry Job Responsibilities: Handling of Tablet and Capsule manufacturing Activities. Maintain BMR, BPR and Documentation as per GMP. Manpower Handling. Primary and Secondary Packing Required Skills: Team Work Time Management Good Communication Skills Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹260,000.00 per year Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Jarod, Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: total work: 1 year (Preferred) Work Location: In person
Job description Post: QC Officer Experience: 0-2 Years in Pharma/Chemical Industry Job description: Testing of Raw Material ,In-Process & Finished Products. Preparations of volumetric solutions and standardization records. Water Analysis. Documentation Work Can handle Lab instruments. Having Knowledge of HPLC will be given preferences. Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹240,000.00 per year Benefits: Provident Fund Schedule: Day shift Ability to commute/relocate: Jarod, Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: QC Department: 1 year (Preferred) Work Location: In person
Post: Office Assistant/Peon/Boy Job description: Maintaining cleanliness and organization in the office premises Assist in basic administrative tasks such as photocopying, filing, and delivering documents within the office. Job Types: Full-time, Permanent Pay: ₹12,000.00 - ₹15,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person
Post: Quality Assurance Executive Educational Qualification : B.Pharm/M.Pharm/M.Sc. Experience: 5 Years+ in Pharmaceuticals Company Job description Authorization of all procedures and standard instructions of process, controls, etc. Investigation and closure of all deviations, OOS and complaints Conducting self-inspections. Conducting vendor evaluation of raw materials. Should have sound knowledge of Process validation. Should be familiar with preparation of process validation protocol and report. Should have sound knowledge of QMS System and Change Control, Deviation and CAPA Procedure. Review of Preventive maintenance & calibration of equipment and systems. Review of stability data to support retest or expiry dates and storage conditions and/or intermediates where appropriate. Risk analysis evaluation Performing product quality reviews. Must understand Standard Operating Procedure. Candidates Only Having Experience in Pharma Industry should apply Job Type: Full-time Pay: ₹400,000.00 - ₹450,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Jarod, Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: Pharma: 4 years (Preferred) Work Location: In person
Post: RA Executive Experience: 5+ Years Experience in Regulatory Affairs in Pharma Industry (Formulation) Location: Masjid Bunder, Mumbai Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for Pharma Formulations. Preparation, Compilation & Review of Registration documents that include Administrative & Technical. Reviewing the technical documents provided by QA, QC, Production providing them the report of shortcomings & ensures them to correct the documents. Handling RFIs (Requested Further Information’s) queries raised by Importer/ Agent/ Regulatory authorities during evaluation of technical data. Coordinating concerned (QA, QC, Production, Packing & Purchase) departments in the process of sample preparation. Coordinate & submission of CTD/ACTD/Country Specific Dossiers/DMF (OP) to regulatory agencies. Coordinate & provide support to team for preparation and dispatch of regulatory documents & dossiers in agreed time-frames. Responsible for planning, coordinating and managing day to day regulatory affairs activities in a timely manner. Providing technical knowledge of the data used in CTD, ACTD & Dossiers to members of regulatory team. Fill up customer questionnaires by collecting information from various concerned departments. You should be good in man - management & co - ordination with all the departments Interact with various administrative, legal & factory departments to collect documents required for regulatory compilation on time. Maintenance of the complete history of each drug product. Prepare and compliance of Modules-I as per regulatory requirement. Job Types: Full-time, Permanent Pay: ₹500,000.00 - ₹600,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Mumbai - 400003, Maharashtra: Reliably commute or planning to relocate before starting work (Preferred) Experience: total work: 5 years (Preferred) Work Location: In person
POST: RA OFFICER/EXECUITVE LOCATION: JAROD, VADODARA EXPERIENCE : 2-3 YEARS Experience in handling regulatory affairs for ROW market mainly Latin American, African & Asian countries for Pharma Formulations. Preparation, compilation & Review of Registration documents that include Administrative & Technical. Reviewing the technical documents provided by QA, QC, Production Providing them the report of shortcomings & ensures them to correct the documents. Handling RFIs (Requested Further Informations) queries raised by Importer/ Agent/ Regulatory authorities during evaluation of technical data. Coordinating concerned (QA, QC, Production, Packing & Purchase) departments in the process of sample preparation. Coordinate & submission of CTD/ACTD/Country Specific Dossiers/DMF (OP) to regulatory agencies. Coordinate & provide support to team for preparation and dispatch of regulatory documents & dossiers in agreed time-frames. Responsible for planning, coordinating and managing day to day regulatory affairs activities in a timely manner. Providing technical knowledge of the data used in CTD, ACTD & Dossiers to members of regulatory team. Fill up customer questionnaires by collecting information from various concerned departments. You should be good in man - management & co - ordination with all the departments Interact with various administrative, legal & factory departments to collect documents required for regulatory compilation on time. Maintenance of the complete history of each drug product Job Type: Full-time Pay: ₹250,000.00 - ₹300,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: Total: 2 years (Preferred) Work Location: In person
POST: RA OFFICER/EXECUITVE LOCATION: JAROD, VADODARA EXPERIENCE : 2-3 YEARS Experience in handling regulatory affairs for ROW market mainly Latin American, African & Asian countries for Pharma Formulations. Preparation, compilation & Review of Registration documents that include Administrative & Technical. Reviewing the technical documents provided by QA, QC, Production Providing them the report of shortcomings & ensures them to correct the documents. Handling RFIs (Requested Further Informations) queries raised by Importer/ Agent/ Regulatory authorities during evaluation of technical data. Coordinating concerned (QA, QC, Production, Packing & Purchase) departments in the process of sample preparation. Coordinate & submission of CTD/ACTD/Country Specific Dossiers/DMF (OP) to regulatory agencies. Coordinate & provide support to team for preparation and dispatch of regulatory documents & dossiers in agreed time-frames. Responsible for planning, coordinating and managing day to day regulatory affairs activities in a timely manner. Providing technical knowledge of the data used in CTD, ACTD & Dossiers to members of regulatory team. Fill up customer questionnaires by collecting information from various concerned departments. You should be good in man - management & co - ordination with all the departments Interact with various administrative, legal & factory departments to collect documents required for regulatory compilation on time. Maintenance of the complete history of each drug product Job Type: Full-time Pay: ₹250,000.00 - ₹300,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: Total: 2 years (Preferred) Work Location: In person
POST: RA OFFICER/EXECUITVE LOCATION: JAROD, VADODARA EXPERIENCE : 2-3 YEARS Experience in handling regulatory affairs for ROW market mainly Latin American, African & Asian countries for Pharma Formulations. Preparation, compilation & Review of Registration documents that include Administrative & Technical. Reviewing the technical documents provided by QA, QC, Production Providing them the report of shortcomings & ensures them to correct the documents. Handling RFIs (Requested Further Informations) queries raised by Importer/ Agent/ Regulatory authorities during evaluation of technical data. Coordinating concerned (QA, QC, Production, Packing & Purchase) departments in the process of sample preparation. Coordinate & submission of CTD/ACTD/Country Specific Dossiers/DMF (OP) to regulatory agencies. Coordinate & provide support to team for preparation and dispatch of regulatory documents & dossiers in agreed time-frames. Responsible for planning, coordinating and managing day to day regulatory affairs activities in a timely manner. Providing technical knowledge of the data used in CTD, ACTD & Dossiers to members of regulatory team. Fill up customer questionnaires by collecting information from various concerned departments. You should be good in man - management & co - ordination with all the departments Interact with various administrative, legal & factory departments to collect documents required for regulatory compilation on time. Maintenance of the complete history of each drug product Job Type: Full-time Pay: ₹250,000.00 - ₹300,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Vadodara, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: Total: 2 years (Preferred) Work Location: In person