Regulatory Affairs Consultant

Regulatory Affairs LabelingBachelor's Degree plus at least 5 to 8 years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality.Good working knowledge of key labeling regulations/guidance and past experience in label development (CCDS, USPI, packaging)The...

Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends, for various types of applications and procedures Contribute to preparation...

Financial Analysis Senior AdvisorPosition Overview:In collaboration with our Bangalore and US based Finance stakeholders and strategic partner ANSR for Business Support Services (BSS) in Hyderabad, the financial analysis senior advisor will have responsibility to oversee, track and report on the execution of the on-going BSS contract with ANSR. The contract...

Job Description :- Atleast 7 years of SAP experience with 2 years in CFIN- Atleast 2 CFIN implementation experience- Experience in defining and maintaining global templates and play books for Finance scenarios.- Business process analysis and redesign experience: strong business analysis skills; process mapping; business process redesign and implementation-...

We are seeking an accomplished Business Analyst with expertise in financial accounting to join our dynamic team. In this role, you will be responsible for identifying, researching, analyzing, and documenting business requirements to meet the financial needs of our clients and align with market demands. Working collaboratively with clients and internal...

Position : Senior IT Security and Compliance AnalystExperience : 8+ YearsLocation : Hyderabad (work from office)Notice period : 30 Days (Should be serving)Job Type : PermanentBS degree in Computer Science or Management Information Systems or related field OR equivalent work experience.8+ years' experience in an equivalent technology risk and compliance...

Job DescriptionAs part of SAP APO consultant role, the individual will be responsible to provide SAP subject matter expertise related to Supply chain planning, high level design solutions for major complex projects. Planning solutions will be related to business processes within Demand Planning, Supply network planning. Individual should have excellent...

Regulatory Affairs Consultant.8+ years’ experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute...

Hyderabad, India **Job ID** R0000012328 **Category** Regulatory / Consulting **ABOUT THIS ROLE**: **Regulatory Affairs Associate** Must have experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts. - To provide regulatory input on procedural and CMC documentation requirements specific to as defined by Health Authorities for assigned...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Consultant. 8 years’ experience in handling life cycle management of approved drug products (small molecules) in various markets. Good understanding of regulatory framework, including regional trends, for various types of applications and procedures Lead and /...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Consultant. 8+ years’ experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market. Good understanding of regulatory framework, including regional...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Consultant. 8+ years’ experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market. Good understanding of regulatory framework, including regional...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Consultant. 8 years’ experience in handling life cycle management of approved drug products (small molecules) in various markets. Good understanding of regulatory framework, including regional trends, for various types of applications and procedures Lead and...

Handling regulatory affairs in the pharma field. **Salary**: ₹200,000.00 - ₹600,000.00 per year **Benefits**: - Paid sick time - Paid time off Schedule: - Day shift Supplemental pay types: - Yearly bonus Ability to commute/relocate: - Hyderabad, Telangana: Reliably commute or planning to relocate before starting work...

Regulatory Affairs LabelingBachelor’s Degree plus at least 5 to 8 years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality.Good working knowledge of key labeling regulations/guidance and past experience in label development (CCDS, USPI,...

**We are hiring an Executive in Regulatory Affairs** **Qualification **:B. Pharmacy/M. Pharmacy (Pharmaceuticals) **Experience**: 3- 4 yrs. **Location **:Balanagar (Hyderabad) **Date**: 28/08/2023 TO 05/09/2023 (Mon to Fri) **Time ** : 10 AM TO 4 PM **Skills Required**: 2) Update the registration dossiers, evaluate queries received from respective...

Hello Everyone, We are hiring for Senior Regulatory Affairs with 10+ Years of experience in API for Pharma company in Sadashivpet. **Job Types**: Full-time, Permanent **Salary**: ₹600,000.00 - ₹1,000,000.00 per year **Benefits**: - Provident Fund Schedule: - Morning shift Supplemental pay types: - Performance bonus - Yearly bonus Ability to...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Labeling Bachelor’s Degree plus at least 5 to 8 years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality. Good working knowledge of key labeling...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Labeling Bachelor’s Degree plus at least 5 to 8 years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality. Good working knowledge of key labeling...

Regulatory Affairs AssociateAround 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of  drug products (small molecules as well as biologics) in various markets.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresContribute to preparation...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends, for...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends, for...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends,...

When our values align, there's no limit to what we can achieve.   Regulatory Affairs Associate Around 2 to 4 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends,...

**Responsibilities**: Job Responsibilities: Assists in the planning, development, maintenance, and implementation of the **SDS authoring process.** Partners across all areas of expertise within the **PSRA** organization to monitor, promote, and deliver high quality, and fully compliant SDSs. Identifies key measures to assist in driving continuous...

Job DescriptionResponsibilitiesThe Senior Associate: Enterprise Risk and Regulatory Affairs will provide support:to the attainment of the overall objectives of the Enterprise Risk and Regulatory Affairs Department.in the planning, design and implementation of the enterprise-wide risk governance framework.to formulate regulatory and personal compliance...

The Regulatory Solutions Consultant position will involve data monitoring, data authoring, content development, maintenance & operations related to regulatory consulting projects. Individuals would get exposure to Clarivate-owned Life sciences databases and external data sources. The team is highly skilled, close-knit, and works towards a common goal of...