
Regulatory Affairs Manager Ii
1 week ago
Job Title Regulatory Affairs Manager II Packaging Artwork Career Level D Introduction to role Are you ready to lead the charge in transforming drug development strategies into reality As a Regulatory Affairs Manager II you ll be at the forefront of coordinating developing and implementing new and revised printed labeling for our commercial products Your expertise will ensure that packaging components meet regulatory standards across the US export markets and EU centralized procedures Dive into a role where your strategic input and leadership in cross-functional activities will drive continuous improvement in processes and tools Accountabilities What you ll do Ensure all work is performed in accordance with established procedures regulatory requirements and GxPs Serve as the point of contact for managing all labeling artwork requests for allocated products requiring market regulatory approval in the US markets receiving a standard export pack and EU centralized procedures Coordinate and or lead the development and lifetime maintenance of packaging component labeling for commercial products including new pack introductions product launches updates to existing packs and mock-ups for regulatory submissions Collaborate with marketing company colleagues regarding global artworks as appropriate Engage with operations manufacturing sites regarding implementation of global artworks as needed Ensure proper version control and document integrity of packaging component labeling printed labeling artworks and other assigned labeling documents Process and prepare all final printed labeling for the US and required EU specimens for submission Essential Skills Experience Relevant university degree in science or related discipline Minimum 7 years of regulatory experience within the biopharmaceutical industry preferably working with labeling Keen attention to detail and accuracy Thorough knowledge of labeling regulations and guidance Strong project management skills Leadership skills including experience leading multi-disciplinary project teams Desirable Skills Experience Experience in packaging labeling development and or maintenance Experience working with stakeholders from locations outside of India especially Europe and or USA When we put unexpected teams in the same room we unleash bold thinking with the power to inspire life-changing medicines In-person working gives us the platform we need to connect work at pace and challenge perceptions That s why we work on average a minimum of three days per week from the office But that doesn t mean we re not flexible We balance the expectation of being in the office while respecting individual flexibility Join us in our unique and ambitious world At AstraZeneca innovation drives us forward We are committed to pushing beyond traditional regulatory approaches to develop progressive solutions that prevent and treat diseases Our diverse team thrives on curiosity and collaboration empowering us to make quick decisions and influence drug development strategies With a focus on technology adoption and automation we strive for efficiencies that bring life-changing medicines to patients faster Here you ll find a supportive environment where your professional growth is nurtured through our Regulatory academy and development path Ready to make an impact Apply now to join our dynamic team and be part of shaping the future of medicine Date Posted 10-Jun-2025 Closing Date 19-Jun-2025 AstraZeneca embraces diversity and equality of opportunity We are committed to building an inclusive and diverse team representing all backgrounds with as wide a range of perspectives as possible and harnessing industry-leading skills We believe that the more inclusive we are the better our work will be We welcome and consider applications to join our team from all qualified candidates regardless of their characteristics We comply with all applicable laws and regulations on non-discrimination in employment and recruitment as well as work authorization and employment eligibility verification requirements
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Regulatory Affairs Manager Ii
4 weeks ago
Bangalore, Karnataka, India AstraZeneca Full timeAccountabilitiesRegulatory Affairs Management- Contributes to regulatory submission strategy identifying submission risks and opportunities while leading simple through more complex regulatory applications and managing procedures through approval - Provides regulatory expertise and guidance on procedural and documentation requirements to GRET Global...
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Bangalore, Karnataka, India AstraZeneca Full timeJob Title CMC Regulatory Affairs Associate Director IIGlobal Career Level EIntroduction to roleAre you a strategically focused Regulatory CMC professional eager to play an integral part in bringing life-changing medicines to patients If so please read on As a CMC Regulatory Affairs Associate Director II you will provide essential CMC Regulatory Strategy ...
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Regulatory Affairs Manager I
8 hours ago
Bangalore, Karnataka, India AstraZeneca Full timeJob Title Regulatory Affairs Manager I Global Career Level D1 Introduction to role Are you ready to be part of a team that transforms drug development strategies into reality The Regulatory Affairs Manager I is a regulatory specialist with project management capabilities responsible for leading the end-to-end planning coordination and execution of assigned...
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Senior Regulatory Affairs Trainer
2 weeks ago
bangalore, India Tek Support Full timeJob Title: Regulatory Affairs Location: Remote Job type: Part-time Job Summary: We are seeking a highly experienced Regulatory Affairs Trainer with over 10 years of expertise in global regulatory compliance , submissions, and lifecycle management across medical devices, pharmaceuticals, biotech, and FMCG sectors. The trainer will be responsible for...
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Regulatory & Liaisoning Affairs Officer
4 weeks ago
Bangalore, Karnataka, India Enerparc Energy Private Limited. Full timeAbout Company Enerparc AG is a global expert in developing engineering building and operating ground mount as well as roof mount photovoltaic PV systems As an EPC contractor our company has connected over 3400 MW of solar systems to electricity grids With local presence in all active solar markets like Europe Middle East Asia we are also one of...
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Regulatory Affairs Specialist
4 days ago
bangalore, India UpMan Placements Full timeCore Job Responsibilities:Regulatory Submissions and compliancePrepare and submit various applications such as additional product permission, Layout approval, facility modification approval, technical person approval, Test license, amendments in licenses, State GMP and GLP certificate applications, post approval changes etc. to State FDAPrepare and submit...
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Regulatory Affairs Manager- SME
6 days ago
bangalore, India Mount Talent Consulting Pvt Ltd. Full timeDomain lead - SME - Safety and Regulatory - BA offshoreExpert in Pharma domain’s multiple functions especially Regulatory and SafetyWell versed with business functions and tools used by industryAble to create integrated solutions and able to address customer pain pointsAble to draw process flowsAct as Technical Product Owner for global regulatory systems...
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Regulatory Affairs Manager- SME
5 days ago
bangalore, India Mount Talent Consulting Pvt Ltd. Full timeDomain lead - SME - Safety and Regulatory - BA offshore Expert in Pharma domain’s multiple functions especially Regulatory and Safety Well versed with business functions and tools used by industry Able to create integrated solutions and able to address customer pain points Able to draw process flows Act as Technical Product Owner for global regulatory...
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Regulatory Affairs Specialist
4 days ago
bangalore, India UpMan Placements Full timeCore Job Responsibilities: Regulatory Submissions and compliance Prepare and submit various applications such as additional product permission, Layout approval, facility modification approval, technical person approval, Test license, amendments in licenses, State GMP and GLP certificate applications, post approval changes etc. to State FDA Prepare and submit...
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Associate Staff Regulatory Affairs Specialist
3 weeks ago
Bangalore, Karnataka, India BD Full timeSummary This position independently supports projects to bring new and modified medical devices to market and ensure ongoing compliance This position participates on cross-functional teams leads the development of global regulatory strategies authors regulatory submissions leads interactions with regulatory agencies notified bodies reviews design...