6

QC Chemist Graduate Experience Jobs in Mumbai

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  • 1 - 7 yrs
  • 5.0 Lac/Yr
  • Boisar West Mumbai
Quality Assurance Testing Documents Machine Planning GLP Quality Control Analyst
We are preferring experience candidate, however we are looking for Bsc/Msc/Diploma Pharma, B Pharma or any Other Graduate who has worked in pharmaceutical Api or Formulation factory or lab on all different level including production , Quality Assurance, Testing, Documents, Machine Handling, Glp, Quality Assurance , Quality Control, Analyst etc.
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Manufacturing Chemist

Liricon Trading

Production Coordinator Quality Assurance Quality Control Engineer
A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.
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QC Chemist (Pen)

Millicon Consultant Engineers Pvt. Ltd.

QC Chemist MSC Chemistry Walk in
Profile : QC Chemist (non approved chemist will also do)Qualification - Msc chemistryLanguage : Hindi, Marathi, EnglishLocation : PenSalary : Around 30kExperience : 4-5 years Male/FemaleKirti GaikwadHR EXECUTIVE
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QC Officer

The Professionals Placement

  • 1 - 3 yrs
  • 3.0 Lac/Yr
  • Boisar East Mumbai
HPLC QC Chemist Quality Manager
Hiring for 7 QC Officer Jobs in Boisar East, Mumbai, Formulation Plant Experience.1 to 3 Years Knowledge of instrument HPLC
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QC Pharmacist

GNH India

  • 1 - 4 yrs
  • 4.0 Lac/Yr
  • Mumbai
Quality Analyst Quality Assurance Analyst Quality Assistant Pharmacist QC Officer QC Pharmacist
IGNORE IF Already Applied .Required Qualification:1. D- Pharm/ B Pharma/ M Pharma with Hands On working experience in QA Pharmacist role2. Schooling from English medium only.3. Mandatory to have Valid Pharmacy License and PPP.4. Experience : 2-5 years experience Mandatory*5. Age Limit : Up to 35 yrs.1. Preparation, Revision & Training of QA SOP's:Hands on Experience of SOP ManagementPreparation & Revision of QA SOP's in Control Document Management System (CDM'S) as per requirement.To conduct Training of approved QA Sop's to all concerned persons.2. Audit & Inspection Readiness:Preparation of Annual Internal Audits schedule.Performing Internal Audits as per approved schedule.Preparation of Internal Audits report.Raised the CAPA's in Track-wise system after agreement with stakeholders.Verification of CAPA's effectivenessafter predefined period.3. Periodic Product Review:Preparation of Periodic Product Review (PPR) of the products.4. Preparation of Periodic Product Review (PPR) of the products.To support contract manufacturing sites for validations during product transfer.5. Process, Equipment, Facility & Utility Qualification:To permed change control assessment validation / qualification perspectives.Preparation and Maintenance of Site Validation Master Plan (SVMP).Preparation of Monthly presentation on Site validation Steering Committee.Tracking of monthly re qualification schedule.6.Cleaning Validation:Preparation of Cleaning Validation Protocols & Reports.Performing Clean Equipment Hold Time (CEHT) & Dirty Equipment Hold Time (DEHT) Study.7. Quality Management Systems:To carry out the gap analysis against Quality Management Systems.Handling change controls , deviations and CAPA's.Carry out risk assessment in view of change in process / introduction of new product.Raise and progress departmental change controls, deviations and CAPA's
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  • 1 - 5 yrs
  • Virar West Mumbai
Pharmacy Incharge Pharmacy Supervisor Pharmacist Pharmacy QC Chemist QA Pharmaceutical Production
Required Pharmacist for Medical Shop in Virar West. He should be able to manage Medical Shop Single. He should have computer knowledge. He should be able to generate business. Person statying nearby Virar West. Knowledge of Prescription must.
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Manufacturing Chemist

Liricon Trading

Production Coordinator Quality Assurance Quality Control Engineer
A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.
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