QC Chemist Job Vacancies in Badlapur

Candidate should be aware about Analytical instruments, Chemical testing, Knowledge of GMP & ISO documentation.

quality testing

BSC or MSC with 2- 4years experience in chemical testing laboratory, uv , hoc , gc , was, ice does etc preferred

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

Experience of Production in Specialty Chemical/chemical Plant. with Exposure in Qc/r&d.or Experience in Qc/r&d with Exposure Towards Production of Chemicals.

Job Openings for 3 R&D Chemist, Testing, QA, QC, Documentation, Lab Technician, Jobs for Freshers in Vasai East, having Educational qualification of : B.Sc,M.Sc with Good knowledge in Chemistry etc.

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