Job Description
Job Description Summary
The Regulatory Affairs Manager provides CMC regulatory input and strategies to directly support development projects and marketed products within Pharmaceutical Diagnostics. The key responsibility of Regulatory Manager is to develop and maintain the Quality sections of the product dossiers throughout the entire life cycle of a product.GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.
Job Description
Key Responsibilities
• To provide CMC related regulatory input for the assigned projects/products.
• Build, or provide input to, submission strategy documents by defining variation type, data required to support submission, and submission documents required for the submission package. Review and approve published output.
• Review and, write and edit individual CMC submission documents/CMC dossier sections to support regulatory submissions.
• Maintain registration tracking information and assist in the development of good document management practice standards.
• Work closely with global RA and, regional RA’s to address questions from regulatory authorities.
• To support QA during audits and inspections as required.
• To keep oneself updated on CMC related guidelines.
Qualifications/Requirements
• Bachelor’s Degree with 6 plus years of relevant experience in a diagnostic or pharmaceutical industry or medical device or government / government relations.
• Knowledge of international CMC regulatory requirements
• Ability to prioritize, plan and evaluate deliverables to established strategic goals.
• Experience in electronic document management and Quality management systems.
• Ability to work well independently and in a team setting.
Desired Characteristics
• Strong interpersonal skills and ability to engage effectively with colleagues at all levels
• Experience with Veeva RIM or other registration tracking tools.
• Ability to resolve day-to-day issues, escalating issues that impact strategic initiatives
Inclusion and Diversity
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, ****** orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support .
Additional Information
Relocation Assistance Provided: No
The Regulatory Affairs Manager provides CMC regulatory input and strategies to directly support development projects and marketed products within Pharmaceutical Diagnostics. The key responsibility of Regulatory Manager is to develop and maintain the Quality sections of the product dossiers throughout the entire life cycle of a product.GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.
Job Description
Key Responsibilities
• To provide CMC related regulatory input for the assigned projects/products.
• Build, or provide input to, submission strategy documents by defining variation type, data required to support submission, and submission documents required for the submission package. Review and approve published output.
• Review and, write and edit individual CMC submission documents/CMC dossier sections to support regulatory submissions.
• Maintain registration tracking information and assist in the development of good document management practice standards.
• Work closely with global RA and, regional RA’s to address questions from regulatory authorities.
• To support QA during audits and inspections as required.
• To keep oneself updated on CMC related guidelines.
Qualifications/Requirements
• Bachelor’s Degree with 6 plus years of relevant experience in a diagnostic or pharmaceutical industry or medical device or government / government relations.
• Knowledge of international CMC regulatory requirements
• Ability to prioritize, plan and evaluate deliverables to established strategic goals.
• Experience in electronic document management and Quality management systems.
• Ability to work well independently and in a team setting.
Desired Characteristics
• Strong interpersonal skills and ability to engage effectively with colleagues at all levels
• Experience with Veeva RIM or other registration tracking tools.
• Ability to resolve day-to-day issues, escalating issues that impact strategic initiatives
Inclusion and Diversity
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, ****** orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support .
Additional Information
Relocation Assistance Provided: No
💡 Quick Summary
Seeking a career-building opportunity? The Regulatory Affairs Manager CMC position is now open for candidates interested in the MIS Executive sector. This role in Bengaluru offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in MIS Executive is a plus.