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  • Cadila Pharmaceuticals

Investigator Jobs in Dholka

1 - 14 of 14
1 - 14 of 14
Search Results - Investigator Jobs in Dholka
Cadila Pharmaceuticals Ltd-Dholka
batches and scale up batches 5. To investigate plant scale up related issues and identification of CPP/CQA and preparation of CAPA/ Investigation report 6 Process feasibility study, Process development, process optimization & process validation...
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Cadila Pharmaceuticals Ltd-Dholka
and Standard Operating Procedures are available to study personnel during conduct of study. 5. Ensure that the final study plan and report for a multi-site study identify and define the role of any Principal Investigator(s) and test facility including test...
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Cadila Pharmaceuticals Ltd-Dholka
and investigations to recommend solutions and justifications and resolve Problems. -Supervising & performing production activities of Botulinum Drug Substance Responsibilities: -Ensure strict cGMP compliance during the unit operations and for the facilities...
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Cadila Pharmaceuticals Ltd-Dholka
of Finished Product in SAP. • To assess the impact of Incident, Deviation, Change Control and CAPA. • To participate in investigation of cGMP non conformances, Deviation, Market complaints and Incident for identification of root cause and implementation...
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Cadila Pharmaceuticals Ltd-Dholka
validation study data and method transfer protocol and reports. 4) Preparations of justifications 5) To maintain and observed GLP in working environment. ) Investigation Study as per requirement 7) Response and work plan for Customer & Regulatory Queries...
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Cadila Pharmaceuticals Ltd-Dholka
and operations. • Identify ways to continuously improve quality and compliance with regulations and company standards, policies and procedures. • Review of technical/investigation reports, summaries for adherence to regulatory guidelines and to provide guidance...
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Cadila Pharmaceuticals Ltd-Dholka
Maintain all the chemicals opening date and expiry date  •  Responsible for procurement of chemicals, glassware, stationary, impurity, reference standard, column, consumable etc.  •  To prepare SOP and manage the documents.  •  To investigate incidence, OOC...
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Cadila Pharmaceuticals Ltd-Dholka
JOB RESPONSIBILITIES  •  Issuance of documents (SOP formats, logbook, register and LNB etc.) to cross-functional departments based on request.  •  Review of process development report/ Addendum to PDR/ Investigation report.  •  Review and approval...
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Cadila Pharmaceuticals Ltd-Dholka
Incident, OOS, Market complaints, shutdown related to VLP, botulinum, BQA, EPO, STR, IMM, BQC, BMN, GCF facilities and CPLB R&D as required. • To be part of the Investigation, Root cause analysis and impact assessment done at site. • Handling of Change...
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Cadila Pharmaceuticals Ltd-Dholka
policy in compression area.  •  To ensure the technical training & development of people.  •  To ensure the cost effective improvement & measure to control expenses.  •  To ensure the quality of the product and involvement in market complaint investigation...
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Cadila Pharmaceuticals Ltd-Dholka
To ensure methods are prepared accordingly STP/SOP.  •  To ensure proper integration and reviewed prior to E- signature of data by reviewer  •  To Initiate change control ,CAPA ,Deviation and Investigation of OOS,OOT, Incident and OOC.  •  To do any other Work...
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Cadila Pharmaceuticals Ltd-Dholka
and packing. Review and approval of Master MMD-I and BPR. • To participate in the investigation of Deviation and Market Complaint for identification of root cause and implementation of identified CAPA. • Intermediate & final Release of Finished Product in SAP...
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Cadila Pharmaceuticals Ltd-Dholka
and packing. Review and approval of Master MMD-I and BPR. • To participate in the investigation of Deviation and Market Complaint for identification of root cause and implementation of identified CAPA. • Intermediate & final Release of Finished Product in SAP...
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Cadila Pharmaceuticals Ltd-Dholka
Compliance Report Preparation etc.), to co-ordinate the Self-inspection activity, Quality Risk Assessment, implementation of Serialization applicable to all manufacturing block, to investigate Market Complaints & Deviations with cross-functional team...
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