Dr Reddy's Laboratories Limited

Job Summary We are seeking an experienced and dynamic Brand Manager for the Nivolumab to ensure successful brand growth and the launch of innovative market-driven products for gathering market insights from Key Opinion Leaders (KOLs) developing and executing new product launch plans c

Job Summary We are seeking an experienced and dynamic Brand Manager for the Nivolumab to ensure successful brand growth and the launch of innovative market-driven products for gathering market insights from Key Opinion Leaders (KOLs) developing and executing new product launch plans c

Job SummaryThis role is for a Visual Inspection Specialist responsible for ensuring product quality through manual and automated inspections maintaining GMP documentation and supporting regulatory readiness. The position involves operating inspection machinery performing line clearanc

Job SummaryThis role is for a Visual Inspection Specialist responsible for ensuring product quality through manual and automated inspections maintaining GMP documentation and supporting regulatory readiness. The position involves operating inspection machinery performing line clearanc

The person should be skilled in using Labware and able to prepare review and approve RBE masters in LIMS. Should have skilled in preparation of Specification and STPs through LAbware LIMS applicationShould manage stock preparation and inventory including chemicals standards and column

The person should be skilled in using Labware and able to prepare review and approve RBE masters in LIMS. Should have skilled in preparation of Specification and STPs through LAbware LIMS applicationShould manage stock preparation and inventory including chemicals standards and column

Specialist Regulatory Affairs Novel Biological Entity is responsible for driving global regulatory strategy submission planning and lifecycle management for novel biological products across key emerging markets. The role involves close collaboration with cross-functional teams to ens

Specialist Regulatory Affairs Novel Biological Entity is responsible for driving global regulatory strategy submission planning and lifecycle management for novel biological products across key emerging markets. The role involves close collaboration with cross-functional teams to ens

1. Lead and facilitate the effort to instill a continuous improvement culture throughout the organization.2. Facilitate and lead assessment of current processes and standard work flow and identify process improvement opportunities utilizing organizational analytical Lean and Six sigma

1. Lead and facilitate the effort to instill a continuous improvement culture throughout the organization.2. Facilitate and lead assessment of current processes and standard work flow and identify process improvement opportunities utilizing organizational analytical Lean and Six sigma

Job SummaryWe are looking for an experienced Lead Portfolio Manager for ensuring a strong and diverse product pipeline tailored for the Global market. Lead the Ideation / selection and driving Integrated Product Strategies across various geographies. You will be responsible for tracki

Job SummaryWe are looking for an experienced Lead Portfolio Manager for ensuring a strong and diverse product pipeline tailored for the Global market. Lead the Ideation / selection and driving Integrated Product Strategies across various geographies. You will be responsible for tracki

Job SummaryThis role is for a Quality Documentation & Compliance Specialist responsible for preparing reviewing and maintaining GMP documents such as SOPs investigations CAPAs risk assessments and qualification protocols. The position involves coordinating with QA and cross-functional

Job SummaryThis role is for a Quality Documentation & Compliance Specialist responsible for preparing reviewing and maintaining GMP documents such as SOPs investigations CAPAs risk assessments and qualification protocols. The position involves coordinating with QA and cross-functional

Roles & ResponsibilitiesYou will be responsible for recognizing potential hazards during critical maintenance activities and coordinating safety requirements through work permits LOTO procedures and JSA reviews to ensure full compliance with SH&E norms.You will be responsible for plan

Roles & ResponsibilitiesYou will be responsible for recognizing potential hazards during critical maintenance activities and coordinating safety requirements through work permits LOTO procedures and JSA reviews to ensure full compliance with SH&E norms.You will be responsible for plan

Job SummaryWe are looking for a meticulous individual to support for sampling chemical analysis and Chromatography like HPLC & GC analysis ensuring precise identification and quantification of HPLC GC and wet analysis.Roles & ResponsibilitiesYou will be responsible for supporting tea

Job SummaryWe are looking for a meticulous individual to support for sampling chemical analysis and Chromatography like HPLC & GC analysis ensuring precise identification and quantification of HPLC GC and wet analysis.Roles & ResponsibilitiesYou will be responsible for supporting tea

Te apasiona el análisis financiero y el control de gestión Buscamos un Analista de Controlling para apoyar la gestión financiera de las operaciones de Colombia Caribe y Centroamérica contribuyendo a la toma de decisiones estratégicas en una compañía del sector farmacéutico.Principales

Te apasiona el análisis financiero y el control de gestión Buscamos un Analista de Controlling para apoyar la gestión financiera de las operaciones de Colombia Caribe y Centroamérica contribuyendo a la toma de decisiones estratégicas en una compañía del sector farmacéutico.Principales

Role PurposeTo lead InProcess Quality Assurance activities for OSD formulation manufacturing ensuring cGMP compliance data integrity inspection readiness and RightFirstTime execution in line with Quality Management System and global regulatory expectations.Key ResponsibilitiesIPQA Ma

Role PurposeTo lead InProcess Quality Assurance activities for OSD formulation manufacturing ensuring cGMP compliance data integrity inspection readiness and RightFirstTime execution in line with Quality Management System and global regulatory expectations.Key ResponsibilitiesIPQA Ma

Role PurposeTo lead InProcess Quality Assurance activities for OSD formulation manufacturing ensuring cGMP compliance data integrity inspection readiness and RightFirstTime execution in line with Quality Management System and global regulatory expectations.Key ResponsibilitiesIPQA Ma

Role PurposeTo lead InProcess Quality Assurance activities for OSD formulation manufacturing ensuring cGMP compliance data integrity inspection readiness and RightFirstTime execution in line with Quality Management System and global regulatory expectations.Key ResponsibilitiesIPQA Ma

Roles & ResponsibilitiesPrepare weekly and monthly plans for sales targets and ensure the implementation of input planners for ASMs.Validate doctors potential create doctor-product matrices and oversee territory potential mapping by TMs/ASMs.Conduct weekly and monthly reviews with ASM

Roles & ResponsibilitiesPrepare weekly and monthly plans for sales targets and ensure the implementation of input planners for ASMs.Validate doctors potential create doctor-product matrices and oversee territory potential mapping by TMs/ASMs.Conduct weekly and monthly reviews with ASM

Roles & ResponsibilitiesPrepare weekly and monthly plans for sales targets and ensure the implementation of input planners for ASMs.Validate doctors potential create doctor-product matrices and oversee territory potential mapping by TMs/ASMs.Conduct weekly and monthly reviews with ASM

Roles & ResponsibilitiesPrepare weekly and monthly plans for sales targets and ensure the implementation of input planners for ASMs.Validate doctors potential create doctor-product matrices and oversee territory potential mapping by TMs/ASMs.Conduct weekly and monthly reviews with ASM

Preparation Review and approval  of Standard Operating Procedures (SOPs).Preparation review and approval of various protocols and reports including:Confirmatory Batch ProtocolHold Time ProtocolProcess Evaluation (Pre-validation) ProtocolTrial ProtocolProcess Performance Qualification/

Preparation Review and approval  of Standard Operating Procedures (SOPs).Preparation review and approval of various protocols and reports including:Confirmatory Batch ProtocolHold Time ProtocolProcess Evaluation (Pre-validation) ProtocolTrial ProtocolProcess Performance Qualification/

Job Summary  We are seeking a skilled professional to serve as a specialist in upstream/downstream operations specializing in processes like mammalian cell culture perfusion technology scale-up single use technology Bioreactor characterization Chromatography Ultrafiltration and Virus

Job Summary  We are seeking a skilled professional to serve as a specialist in upstream/downstream operations specializing in processes like mammalian cell culture perfusion technology scale-up single use technology Bioreactor characterization Chromatography Ultrafiltration and Virus

Buscamos un Analista de Ventas y Licitaciones para brindar soporte integral a los procesos comerciales y de licitaciones.RequisitosProfesional en Administración de Empresas Economía Finanzas Comercio Exterior Marketing o carreras afines.Mínimo 2 años de experiencia en áreas comerciale

Buscamos un Analista de Ventas y Licitaciones para brindar soporte integral a los procesos comerciales y de licitaciones.RequisitosProfesional en Administración de Empresas Economía Finanzas Comercio Exterior Marketing o carreras afines.Mínimo 2 años de experiencia en áreas comerciale

 Perform device functionality tests using Universal testing machine in accordance with approved SOP Methods specification and protocols.Responsible to perform lot release testing stability testing of batch following good laboratory and good documentation practices.Review test results

 Perform device functionality tests using Universal testing machine in accordance with approved SOP Methods specification and protocols.Responsible to perform lot release testing stability testing of batch following good laboratory and good documentation practices.Review test results

Job SummaryRoles & Responsibilities1.1     Experience of Capex proposal execution and commissioning of equipment or facility in a OSD manufacturing unit1.2      Implement Electrical Instrumentation & Mechanical-related modifications upgrades and developmental activities for process eq

Job SummaryRoles & Responsibilities1.1     Experience of Capex proposal execution and commissioning of equipment or facility in a OSD manufacturing unit1.2      Implement Electrical Instrumentation & Mechanical-related modifications upgrades and developmental activities for process eq

Role OverviewWe are looking for a Design Researcher with 3 years of experience to join our multi-disciplinary this role you will be the primary advocate for human needs. You will lead end-to-end research from framing questions in ambiguous healthcare domains to spending time in field

Role OverviewWe are looking for a Design Researcher with 3 years of experience to join our multi-disciplinary this role you will be the primary advocate for human needs. You will lead end-to-end research from framing questions in ambiguous healthcare domains to spending time in field