
Manager - Regulatory Affairs
4 weeks ago
Genpact NYSE G is a global professional services and solutions firm delivering outcomes that shape the future Our 125 000 people across 30 countries are driven by our innate curiosity entrepreneurial agility and desire to create lasting value for clients Powered by our purpose - the relentless pursuit of a world that works better for people - we serve and transform leading enterprises including the Fortune Global 500 with our deep business and industry knowledge digital operations services and expertise in data technology and AI Inviting applications for the role of Manager - Training and SoP Author Lead Regulatory We are looking for a Training and SoP Author Specialist with experience in the Life Sciences pharmaceutical industry to ensure compliance with regulatory requirements including 21 CFR Part 11 GxP and Annex 11 The ideal candidate should have expertise in Regulatory Information Management applications with a strong understanding of Veeva Vault RIMS being a plus Responsibilities Able to understand the basics of a new system and process the client s way of working and the training strategy Develop and deliver training materials per client s requirements while ensuring compliance To be able to handle various platforms namely Learning Management Systems Veeva Vault Training Cornerstone OnDemand for training delivery content development tools Articulate 360 Adobe Captivate SOP and Document Management Systems Documentum Assessment and Evaluation tools Google Forms Microsoft Forms Virtual Training and Collaboration Tools Microsoft Teams Zoom Webex Training To be able to collect and document the training and SOP aspects discussed in the focus topics Assign content to the correct training module functional vs process training vs SOP Collaborate with different departments to identify training needs gaps and raise questions in case of unclarities Update training materials as per the feedback received from SMEs Develop review and update SOPs to comply with regulatory standards Develop Work Instructions and Handouts as per industry best practices Ensure training and SOPs are written clearly and in compliance with the language Manage the SOP lifecycle version control approvals and periodic reviews Ensure all users are trained on the new and updated training materials SOP in timely manner Knowledge of GMP GCP GLP and Pharmaceutical Regulation EMA ICH FDA etc is required Strong experience with LMS RIMS and DMS systems is necessary General tasks Understand new systems processes client s way of working and training strategy Develop and deliver compliant training materials per client requirements Handle platforms for training delivery content development SOP and document management assessment and evaluation and virtual training and collaboration Document training and SOP aspects discussed in focus topics Experience Bachelor s or Master s degree in Pharmaceutical Computer Science IT Engineering or a related field Moe experience in Computer System Validation CSV in the pharmaceutical biotech or medical device industry Strong knowledge of GxP 21 CFR Part 11 GAMP 5 Data Integrity and Annex 11 Experience in validating SaaS applications used in the pharmaceutical industry Familiarity with Veeva Vault RIMS QualityDocs or Submissions Archive is a plus Excellent documentation skills and experience with validation lifecycle documentation Ability to work independently and collaborate with cross-functional teams Qualification Atleast Bachelor s degree required in for Pharmaceutical science engineering or related field advanced degree preferred Veeva Vault RIM certification is a plus Experience working in an Agile Scrum environment Language English Genpact is an Equal Opportunity Employer and considers applicants for all positions without regard to race color religion or belief sex age national origin citizenship status marital status military veteran status genetic information sexual orientation gender identity physical or mental disability or any other characteristic protected by applicable laws Genpact is committed to creating a dynamic work environment that values diversity and inclusion respect and integrity customer focus and innovation For more information visit www genpact com Follow us on Twitter Facebook LinkedIn and YouTube Furthermore please do note that Genpact does not charge fees to process job applications and applicants are not required to pay to participate in our hiring process in any other way Examples of such scams include purchasing a starter kit paying to apply or purchasing equipment or training
-
Manager- Regulatory Affairs
2 weeks ago
Mumbai, Maharashtra, India Piramal Enterprises Full timeJob DescriptionJob Description :Business: Piramal Critical CareDepartment: Regulatory AffairsLocation: KurlaTravel: LowJob OverviewThe Manager, Regulatory Affairs is responsible for the portfolio of Piramal Critical Care Products in the USA market. They will be responsible for authoring and reviewing submissions for dissemination to Health Authorities,...
-
Regulatory Affairs Specialist
2 days ago
Mumbai, Maharashtra, India beBeeRegulatoryAffairs Full time ₹ 9,00,000 - ₹ 12,00,000Regulatory Affairs Manager Job DescriptionThe role involves developing and executing regulatory strategies, compiling and reviewing regulatory submissions, ensuring product compliance and acting as a key liaison with regulatory agencies.Key Responsibilities:Submission Management: Preparation, review and submission of regulatory documentation (e.g., dossiers,...
-
Manager- Regulatory Affairs
4 weeks ago
Mumbai, Maharashtra, India Piramal Pharma Ltd Full timeJob DescriptionTrendingJob DescriptionBusiness: Piramal Critical CareDepartment: Regulatory AffairsLocation: KurlaTravel: LowJob OverviewThe Manager, Regulatory Affairs is responsible for the portfolio of Piramal Critical Care Products in the USA market. They will be responsible for authoring and reviewing submissions for dissemination to Health Authorities,...
-
Regulatory Affairs Professional
5 days ago
Mumbai, Maharashtra, India beBeeRegulatory Full time ₹ 2,20,00,000 - ₹ 2,54,00,000Regulatory Affairs LeaderSr Manager Regulatory Affairs responsible for developing and executing regulatory strategies, compiling and reviewing regulatory submissions, ensuring product compliance, and acting as a key liaison with regulatory agencies.Key Responsibilities:Submission Management:Preparing, reviewing, and submitting regulatory documentation to...
-
Regulatory Affairs Professional
4 days ago
Mumbai, Maharashtra, India beBeeRegulatory Full time ₹ 60,00,000 - ₹ 1,20,00,000Regulatory Affairs ProfessionalJob Overview:We are seeking a highly skilled Regulatory Affairs Specialist to join our team. The successful candidate will be responsible for ensuring compliance with regulatory requirements for products, managing the submission process for regulatory approvals, and maintaining up-to-date knowledge of regulatory changes.Main...
-
Regulatory Affairs Specialist
13 hours ago
Mumbai, Maharashtra, India Tek Support Full timeJob DescriptionJob Title: Regulatory Affairs Specialist Med/Pharma (Female)Location: RemotePosition Overview:We are seeking an experienced Regulatory Affairs professional with expertise in both pharmaceutical and medical device regulatory compliance. The role involves preparing, reviewing, and submitting regulatory documentation to global health authorities,...
-
Senior Regulatory Affairs Professional
2 hours ago
Mumbai, Maharashtra, India beBeeRegulatoryAffairs Full time ₹ 15,00,000 - ₹ 25,00,000Regulatory Affairs SpecialistMain Purpose of Role:The Regulatory Affairs Specialist will be a key contributor to the development and implementation of regulatory strategies for our products.This role requires an individual with comprehensive knowledge in the area of Regulatory Affairs, who can execute highly complex or specialized projects, and adapt...
-
AGM Regulatory Affairs
4 weeks ago
Mumbai, Maharashtra, India NMS Consultant Full timeJob DescriptionAGM position -Regulatory AffairsB.Pharm / M.Pharm / M.Sc 12-14 years regulatory affairs experience majorly in USA market for Solid oral dosage formsKey Responsibilities:- Ensure timely submission of ANDAs, supplements and amendments- Review of registration dossiers, amendments, supplements and annual reports prepared by subordinates for...
-
Regulatory Affairs Lead
6 hours ago
Mumbai, Maharashtra, India beBeeChemistry Full time US$ 8,00,000 - US$ 14,00,000Regulatory Affairs Lead PositionWe are seeking an experienced and skilled Regulatory Affairs Sub-Function team leader to oversee product registration submissions, progress reports, supplements, amendments, or periodic experience reports.Key Responsibilities:Supervise a team of professionals in directing product registration submissions, progress reports,...
-
Regulatory Affairs Professional
1 week ago
Mumbai, Maharashtra, India beBeeSpecialist Full time US$ 40,000 - US$ 80,000Regulatory Affairs SpecialistThe role involves the compilation, submission and management of regulatory documentation for assigned projects.Responsibilities include maintaining accurate database records pertaining to products, in line with established systems and processes.Supporting and coordinating regulatory affairs projects, as assigned, including tender...