BLA Regulatory Publishing Specialist – Veeva eCTD

Regulatory Affairs Publishing AssociateThis role is ideal for a highly skilled and experienced Regulatory Affairs professional who has expertise in regulatory publishing, document management, and stakeholder engagement. As a Regulatory Affairs Publishing Associate, you will play a key role in supporting global regulatory submission activities by managing...

Job Title Life Sciences Regulatory Affairs RA Associate - Publishing Job Summary We are looking for a skilled and experienced Regulatory Affairs Associate - Publishing to join our Life Sciences Practice The ideal candidate will support global regulatory submission activities by managing electronic publishing document-level and submission-level ...

Associate III - Business Analysis Regulatory Affairs - Life Sciences Publishing Role Summary The Associate III - Business Analyst Regulatory Affairs - Publishing plays a crucial role in supporting regulatory operations within the life sciences industry This role involves understanding stakeholder needs gathering and analyzing requirements and...

Key Responsibilities Configure and optimize Veeva Vault applications (QualityDocs, QMS, RIM, PromoMats, MedComms).Collaborate with business stakeholders to help them translate functional requirements into technical solutions.Design and oversee data/document migration strategies into Veeva, ensuring accuracy and compliance.Implement and support system...

Regulatory Publishing Business Analyst Role SummaryThe Regulatory Publishing Business Analyst plays a crucial role in supporting regulatory operations within the life sciences industry. This position involves understanding stakeholder needs, gathering and analyzing requirements, and assisting in the creation and maintenance of regulatory submission...

We are looking for a Regulatory Affairs professional with hands-on experience in biologics/biosimilars registration across Emerging Markets (Middle East, Asia, LATAM, Africa, CIS) regions. The candidate will be responsible for preparing and managing regulatory submissions, tracking country-specific requirements, and coordinating with local affiliates,...

We are looking for a Regulatory Affairs professional with hands-on experience in biologics/biosimilars registration across Emerging Markets (Middle East, Asia, LATAM, Africa, CIS) regions. The candidate will be responsible for preparing and managing regulatory submissions, tracking country-specific requirements, and coordinating with local affiliates,...

Position Summary The Regulatory Affairs Specialist will be responsible for managing regulatory activities for biosimilar products for the emerging market, with a strong focus on LATAM region. This role involves ensuring compliance with regional regulations, supporting product lifecycle management, and leading submissions for primary filings and variations...

Position Summary The Regulatory Affairs Specialist will be responsible for managing regulatory activities for biosimilar products for the emerging market, with a strong focus on LATAM region. This role involves ensuring compliance with regional regulations, supporting product lifecycle management, and leading submissions for primary filings and variations in...

Commitment: Full-Time Contract (30–40 hours per week) Location: Based in India, Remote – Eastern Time Zone (preferred) or Mountain Time Zone Reports To: Clinical QA Lead / Director of QualityPosition OverviewWe are seeking an experienced QA Specialist / Manager-level contractor to provide day-to-day clinical quality assurance (QA) support across ongoing...