Urgent Team Member Qc
3 days ago
DivisionQualityDepartmentQualityEmployment TypePermanentJob PurposePrepare update and review the specifications SOPs policy and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards pharmacopeia and cGMP requirementsAccountabilitiesI Prepare documents like SOPs specifications and non-routine documentation and ensure timely availability across the site to provide support during the analysisPrepare revise corporate documents like SOPs general analytical methods etc by coordinating with site QC QA Review the applicable pharmacopoeia and guidelines and make appropriate updates Review instrument calibration data w r t operating documentsII Review the latest pharmacopeial updates supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regulatory bodyReview the new revised monograph as per current pharmacopoeia Review the latest pharmacopeial updates and monitor its timely implementation to avoid any non-conformances Intimate the concerned stakeholders to initiate and complete activitiarmacopoeia Escalate non-conformances timely to avoid any delays in operationIII Review the assigned documents by referring the concern backup and pre-defined quality procedure to ensure its compliance against the quality requirementsFollow the approved procedures and current Cipla policies for review approach by referring valid backup documents SOPs etc so that every document is complying w r t the quality aspect of the product Identify and discuss queries problems faced during the document review by taking initiatives so that further delay in document completion is avoidedIV Issue documents to applicable units by maintaining the record of the same in the issuance record bound book so the current version of the common document is available at the unitIssue applicable bound books to units by maintaining the log of the same so the current format is available to record the releva Maintain correct and updated record of all the issuance of documents and bound booksV Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed Evaluate and prepare documents for standardization across all units at a site Coordinate with CFTs and check requirements as per existing procedures to simplify the process Provide suggestions and ideas by exploring new possibilities to achieve work simplificationEducation QualificationM Sc B PharmaRelevant Work Experience1-3 years of experience in QC department of a pharmaceutical organizationCompetencies SkillsCollaborate to SucceedInnovate to ExcelPerform with AccountabilityLead with EmpathyAct with AgilityStrong Domain KnowledgePeople ManagementJob LocationRangpoShift Hours
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Junior Team Member
4 days ago
Rangpo, India Cipla Full time**Division**: - Quality**Department**: - Quality**Employment Type**: - Permanent**Job Purpose**: Prepare, update and review the specifications, SOPs, policy and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards / pharmacopeia and cGMP...
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Team Member
3 weeks ago
Rangpo, Sikkim, India Cipla Full timeDivision Manufacturing Department Formulation Sub Department 1 Engineering - Formulation Job Purpose Maintain upkeep and execute processes of stores with regard to inventory and non-inventory stock material area of work material handling equipment and storage etc as per safety compliance cGMP norms and QMS to support execute and coordinate in...
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Team Member
4 hours ago
Rangpo, Sikkim, India Not Available Full time ₹ 2,00,000 - ₹ 6,00,000 per yearDivisionManufacturingDepartmentFormulationSub Department 1Engineering - FormulationJob PurposeMaintain, upkeep and execute processes of stores with regard to inventory and non-inventory stock material, area of work, material handling equipment and storage etc. as per safety compliance, cGMP norms and QMS to support, execute and coordinate in functioning of...
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Junior Team Member
1 week ago
Rangpo, Sikkim, India Cipla Full time ₹ 6,00,000 - ₹ 8,00,000 per yearDivisionDepartmentSub Department 1Job PurposeTo execute the activities that are related to microbiology laboratory.Key Accountabilities (1/6)I. Involvement in all quality related activities.Maintenance of all the area and the equipment.To ensure and monitor compliance with GLP and cGMP as per requirements of the respective authority.Key Accountabilities...
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Team Member
1 week ago
Rangpo, India Cipla Full time**Division**: - Manufacturing**Department**: - Manufacturing**Employment Type**: - Permanent**Job Purpose**: Execute excellence initiatives to increase throughput of manufacturing sites by periodical interactions and involvements at functional areas and hence provide a support platform of operational efficiency to achieve quality standards and production...
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Junior Team Member
1 week ago
Rangpo, India Cipla Full time**Division**: - Quality**Department**: - Quality**Employment Type**: - Permanent**Job Purpose**: Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines **Accountabilities**: I. Collate, review and provide required work plans on received...
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Junior Team Member
1 week ago
Rangpo, India Cipla Full time**Division**: - Quality **Department**: - Quality **Employment Type**: - Permanent **Job Purpose**: Execute analysis of allocated samples and Produce reliable and reproducible results in order to ensure their compliance to the microbiological quality parameters and predefined specifications and standards **Accountabilities**: I. Analyse and review...
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Junior Team Member
4 days ago
Rangpo, India Cipla Full time**Division**: - Quality**Department**: - Quality**Employment Type**: - Permanent**Job Purpose**: Execute analysis of allocated samples and Produce reliable and reproducible results in order to ensure their compliance to the microbiological quality parameters and predefined specifications and standards **Accountabilities**: I. Analyse and review samples...
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Senior Officer
3 days ago
Rangpo, Sikkim, India Cipla Full timeDivisionDepartmentSub Department 1Job PurposeMonitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targetsKey Accountabilities 1 6 Execute production activities in a shift by managing available resources to achieve production target Execute assigned tasks as per planned...
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Sr. Officer Packing _ _Sikkim
4 days ago
Gangtok, Rangpo, India Zuventus Healthcare Ltd Full time ₹ 3,00,000 - ₹ 5,00,000 per yearRole & responsibilitiesAll Packing Activities Primary And Secondary Packing Line Handled in Oral Solid Dosage Section.To follow the good documentation practicesTo allocate the manpower at shop floor.To coordinate and work with supervisor and team members to execute the assigned task.To Co-ordination with QA and QC dept. regarding the line clearance, samples...
