Regulatory Affairs Associate

**Job Purpose**: Thisrole provides operational support for the implementation within GlobalRegulatory Affairs of the Internal Control Framework (ICF) elements such asrisk assessment, written standards and control, training, management monitoring(MM) and responding to problem (CAPA/CC/deviation management) also supportingregulatory community in internal...

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...

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,...

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...

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,...

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,...

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...

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...

Company Description **MakroCare |** **_A MakroGroup Company_**- MakroCare is an Expert Strategic Development and Commercialization Global Partner for the Pharmaceutical, Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a New Dimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research,...

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...

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 (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...

Job DescriptionResponsibilities The 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...

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...

**Company Description** IQ-EQ is a leading Investor Services group which combines global expertise with an unwavering focus on client service delivery. We support fund managers, global companies, family offices and private clients operating worldwide. IQEQ is a preeminent service provider to the alternative asset industry. IQEQ works with managers in...