Talental Consultings

Key job responsibilities:Calculate and record monthly accruals for various sales deductions including rebates chargebacks prompt pay discounts and product returns. Calculate net sales every reporting periodVariance Analysis of sales reported with historical reporting Liaise with sales

Key job responsibilities:Calculate and record monthly accruals for various sales deductions including rebates chargebacks prompt pay discounts and product returns. Calculate net sales every reporting periodVariance Analysis of sales reported with historical reporting Liaise with sales

Standard Cost Maintenance: Establish and update standard costs for raw materials direct labor and manufacturing overhead within the company’s ERP system.Variance Analysis: Conduct regular analysis of production variances (material price labor efficiency and overhead spending) investig

Standard Cost Maintenance: Establish and update standard costs for raw materials direct labor and manufacturing overhead within the company’s ERP system.Variance Analysis: Conduct regular analysis of production variances (material price labor efficiency and overhead spending) investig

About The Role :We are looking for an experienced Assistant manager for R2R general accounting and month end closure activities in our internal Global Shared Services (GSS) which serves our US based pharma company. You will closely work with the GSS Head and the business controllers a

About The Role :We are looking for an experienced Assistant manager for R2R general accounting and month end closure activities in our internal Global Shared Services (GSS) which serves our US based pharma company. You will closely work with the GSS Head and the business controllers a

Analysing financial data and performing margin computations of all the subsidiary entities evaluating periodical intercompany transactions for arm’s length criteria and prepare all the required information/workings for issuance of TPs on Quarterly/Timely basis.coordinate with corporat

Analysing financial data and performing margin computations of all the subsidiary entities evaluating periodical intercompany transactions for arm’s length criteria and prepare all the required information/workings for issuance of TPs on Quarterly/Timely basis.coordinate with corporat

About the role :Work closely with Regulatory Affairs Associates to ensure the compliance and completion of assignedactivities and provide regulatory strategic input and compliance with FDA regulations guidance andapplicable industry guidelines to internal and external stakeholders and

About the role :Work closely with Regulatory Affairs Associates to ensure the compliance and completion of assignedactivities and provide regulatory strategic input and compliance with FDA regulations guidance andapplicable industry guidelines to internal and external stakeholders and

Position Summary : Manage overall batch certification review of QC lab records certificates of analysis/compliance and all related supporting documentation (i.e. documentation review SOP compliance laboratory application data reviews instrument preventive maintenance/calibration/quali

Position Summary : Manage overall batch certification review of QC lab records certificates of analysis/compliance and all related supporting documentation (i.e. documentation review SOP compliance laboratory application data reviews instrument preventive maintenance/calibration/quali

Key ResponsibilitiesHR – CoreLead overall HR function for the corporate officeDrive manpower planning hiring strategy and succession planningOversee performance management appraisals and leadership developmentHandle employee relations grievances disciplinary matters and exitsEnsure sm

Key ResponsibilitiesHR – CoreLead overall HR function for the corporate officeDrive manpower planning hiring strategy and succession planningOversee performance management appraisals and leadership developmentHandle employee relations grievances disciplinary matters and exitsEnsure sm

About Client: Leading Pharma company having multiple formulation plants having global presencePosition: Compression Operator / Executive – Tablet ManufacturingLocation: VizagDepartment: Production / ManufacturingKey ResponsibilitiesOperate and monitor Sejong / Fette compression machin

About Client: Leading Pharma company having multiple formulation plants having global presencePosition: Compression Operator / Executive – Tablet ManufacturingLocation: VizagDepartment: Production / ManufacturingKey ResponsibilitiesOperate and monitor Sejong / Fette compression machin

Chieron Active Ingredients is seeking high-calibre Business Development professionals to accelerate our growth in the global CDMO landscape. The ideal candidates will leverage their existing networks to secure high-value projects across the entire drug development lifecycle—from Phase

Chieron Active Ingredients is seeking high-calibre Business Development professionals to accelerate our growth in the global CDMO landscape. The ideal candidates will leverage their existing networks to secure high-value projects across the entire drug development lifecycle—from Phase

Key Responsibilities Overview management of Medical Devices development process as per specific product requirements and in line with respective country regulatory guidance Generate technical documentation for the product Design History file and Device Master Records as per specific

Key Responsibilities Overview management of Medical Devices development process as per specific product requirements and in line with respective country regulatory guidance Generate technical documentation for the product Design History file and Device Master Records as per specific

2. Key Responsibilities2.1 Operational ResponsibilitiesEnsure Executives and Stores Officers strictly follow laid-down cGMP procedures for all Stores activities.Ensure daily documentation proper storage of materials in designated areas and verification of weights and drum labeling as

2. Key Responsibilities2.1 Operational ResponsibilitiesEnsure Executives and Stores Officers strictly follow laid-down cGMP procedures for all Stores activities.Ensure daily documentation proper storage of materials in designated areas and verification of weights and drum labeling as

Job DescriptionPosition: Manager – Production Block Incharge (API Manufacturing)Location: MaharashtraDepartment: ProductionReports To: Head – Manufacturing / Plant HeadRole ObjectiveTo lead and oversee the operations of the API production block ensuring compliance with cGMP regulatory

Job DescriptionPosition: Manager – Production Block Incharge (API Manufacturing)Location: MaharashtraDepartment: ProductionReports To: Head – Manufacturing / Plant HeadRole ObjectiveTo lead and oversee the operations of the API production block ensuring compliance with cGMP regulatory

1)Should ensure that every manager enacts his role & responsibility withdue diligence.2) Should track monitor and regulate every Teams’execution of marketing strategies/campaigns as specified from time totime.3) Should ensure every Manager attains & maintains minimumspecified work nor

1)Should ensure that every manager enacts his role & responsibility withdue diligence.2) Should track monitor and regulate every Teams’execution of marketing strategies/campaigns as specified from time totime.3) Should ensure every Manager attains & maintains minimumspecified work nor

About the CompanyWe are a mid-sized Indian MNC pharmaceutical company with a strong presence in API manufacturing and global markets. To strengthen our commercial and operational analytics we are looking for an experienced MIS Reporting Manager for our API business.Key Responsibiliti

About the CompanyWe are a mid-sized Indian MNC pharmaceutical company with a strong presence in API manufacturing and global markets. To strengthen our commercial and operational analytics we are looking for an experienced MIS Reporting Manager for our API business.Key Responsibiliti

Job DescriptionLeading Pharma Client is seeking candidates for the positions of Operator and Executive in the production area specifically in granulation compression coating and capsule filling for OSD products.Responsibilities:Operate and maintain production equipment for granulation

Job DescriptionLeading Pharma Client is seeking candidates for the positions of Operator and Executive in the production area specifically in granulation compression coating and capsule filling for OSD products.Responsibilities:Operate and maintain production equipment for granulation

Job SummaryThe Assistant Manager / Deputy Manager – Environment Health & Safety (EHS) is responsible for independently managing EHS functions at a pharmaceutical manufacturing site. The role ensures full compliance with statutory regulatory and corporate EHS requirements effective man

Job SummaryThe Assistant Manager / Deputy Manager – Environment Health & Safety (EHS) is responsible for independently managing EHS functions at a pharmaceutical manufacturing site. The role ensures full compliance with statutory regulatory and corporate EHS requirements effective man

About the company:We are seeking a highly skilled Legal Professional with strong expertise in Draft review and negotiate commercial contracts NDAs MOUs licensing technology transfer supply & distribution agreements. *Key Responsibilities:*Provide legal support for pharmaceutical opera

About the company:We are seeking a highly skilled Legal Professional with strong expertise in Draft review and negotiate commercial contracts NDAs MOUs licensing technology transfer supply & distribution agreements. *Key Responsibilities:*Provide legal support for pharmaceutical opera

Client : Leading Pharma API Manufacturing CompanyPosition : R&D Flow ChemsitryDesignation : Manager Develop and guide the team for cost-effective process development through flow chemistry. Support to Business case preparation for Management Approval before taking any molecule in Fl

Client : Leading Pharma API Manufacturing CompanyPosition : R&D Flow ChemsitryDesignation : Manager Develop and guide the team for cost-effective process development through flow chemistry. Support to Business case preparation for Management Approval before taking any molecule in Fl

Client: Leading Pharmaceutical CompanyLocation: Multiple Sites (with 40-50% travel)Role OverviewThe Subject Matter Expert (SME) – Sterile Manufacturing is responsible for managing and supporting sterile manufacturing operations for liquid injectable products including media complex in

Client: Leading Pharmaceutical CompanyLocation: Multiple Sites (with 40-50% travel)Role OverviewThe Subject Matter Expert (SME) – Sterile Manufacturing is responsible for managing and supporting sterile manufacturing operations for liquid injectable products including media complex in

Client: Leading Pharmaceutical CompanyLocation: Multiple Sites (with 40-50% travel)Role OverviewThe SME – Filling will be responsible for overseeing and executing aseptic filling and lyophilization operations in the sterile production area. The role requires strong technical expertise

Client: Leading Pharmaceutical CompanyLocation: Multiple Sites (with 40-50% travel)Role OverviewThe SME – Filling will be responsible for overseeing and executing aseptic filling and lyophilization operations in the sterile production area. The role requires strong technical expertise