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📑 Job Description This is a remote position. PSC Biotech provides the life sciences with essential services to ensure that health care products are developed ...

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📑 Senior / Labelling SpecialistJob Description:We are seeking a highly skilled and experienced Senior Labelling Specialist to join our team and take on a pivotal role in the development and approval of labelling documents for our vaccine portfolio. As a Senior Labeling Specialist, you will ...

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📑 Join the forefront of digital innovation in healthcare with Greymatter Innovationz! As a leading provider of digital solutions, we empower organizations to stay digitally relevant across diverse domains, technologies, and skillsets every day.We are currently seeking talented individuals to join our team in the role of:<p ...

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📑 Senior / Labelling Specialist Job Description: We are seeking a highly skilled and experienced Senior Labelling Specialist to join our team and take on a pivotal role in the development and approval of labelling documents for our vaccine portfolio. As a Senior Labeling Specialist, you ...

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📑 Job DescriptionJoin Aeolus Robotics as a Regulatory Compliance Engineer and contribute to our commitment to excellence in product compliance on a global scale. Your expertise will be vital in ensuring our products meet and exceed the stringent standards of the industry.< ...

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📑 Job DescriptionWe are seeking a highly skilled and experienced Energy Regulatory Lawyer to join one of our esteemed legal clients. As an Energy Regulatory Lawyer, you will play a key role in ensuring compliance with energy regulations and advocating for our company's int ...

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📑 This role is responsible for the publication (electronically or paper) and distribution of regulatory submission and clinical trial dossiers, and the capture and reporting of regulatory product and registration information for company products. Key Responsibilities: Participates in the publishing of centrally supported ...

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📑 Job DescriptionWe are seeking a Regulatory Affairs Specialist to support a leading medical device company in Ithaca, NY.  This is an onsite role open to local candidates.  Job Summary: This ...

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📑 Job Purpose: The purpose of this role is to manage the regulatory information management (RIM) system for all Consumer Healthcare products worldwide to support key regulatory processes and enable the company to meet its regulatory, legal and pharmacovigilance obligations. This role is responsible for the operation of the regula ...

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📑 Join the forefront of digital innovation in healthcare with Greymatter Innovationz! As a leading provider of digital solutions, we empower organizations to stay digitally relevant across diverse domains, technologies, and skillsets every day.We are currently seeking talented individuals to join our team in the role of:Pharma Regulatory WriterLocati ...

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📑 The purpose of this role is to manage the regulatory information management (RIM) system for all Consumer Healthcare products worldwide to support key regulatory processes and enable the company to meet its regulatory, legal and pharmacovigilance obligations. This role is responsible for the operation of the regulatory systems and processes used to ...

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📑 This role is responsible for the publication (electronically or paper) and distribution of regulatory submission and clinical trial dossiers, and the capture and reporting of regulatory product and registration information for company products.Key Responsibilities:Participates in the publishing of centrally supported regulatory dossiers for regulat ...

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📑 The purpose of this role is to manage the regulatory information management (RIM) system for all Consumer Healthcare products worldwide to support key regulatory processes and enable the company to meet its regulatory, legal and pharmacovigilance obligations. This role is responsible for the operation of the regulatory systems and processes used to ...

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📑 Job Purpose:The purpose of this role is to manage the regulatory information management (RIM) system for all Consumer Healthcare products worldwide to support key regulatory processes and enable the company to meet its regulatory, legal and pharmacovigilance obligations. This role is responsible for the operation of the regulatory systems and proce ...

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📑 This role is responsible for the publication (electronically or paper) and distribution of regulatory submission and clinical trial dossiers, and the capture and reporting of regulatory product and registration information for company products.Key Responsibilities:Participates in the publishing of centrally supported regulatory dossiers for regulat ...

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📑 Senior / Labelling SpecialistJob Description:We are seeking a highly skilled and experienced Senior Labelling Specialist to join our team and take on a pivotal role in the development and approval of labelling documents for our vaccine portfolio. As a Senior Labeling Specialist, you will be responsible for overseeing all aspects of labeling, from i ...

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📑 Join the forefront of digital innovation in healthcare with Greymatter Innovationz! As a leading provider of digital solutions, we empower organizations to stay digitally relevant across diverse domains, technologies, and skillsets every day. We are currently seeking talented individuals to join our team in the role of: </ ...

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📑 About Us: established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform – CLYZOPosition- Regulatory Affairs Associate.Job Description :An organization with a reputed history of 10+ years in the Pharma raw material industry, dealin ...

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📑 Graduate degree with formal research component or in life sciences.Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields.Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, ...

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📑 About Airtel: Bharti Airtel Limited is a leading global telecommunications company with operations in 18 countries across Asia and Africa. Headquartered in New Delhi, the company's product offerings include 2G, 3G 4G and 5G wireless services, mobile commerce, fixed line services, high speed home broadband, DTH, enterprise services including nation ...

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📑 We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) - WFORespons ...

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📑 Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other ...

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📑 About Us: established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform – CLYZOPosition- Regulatory Affairs Associate. Job Description:An organization with a reputed history of 10+ years in the Pharma raw material industry, dealing in excipient products is looking f ...

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📑 We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) - WFORespons ...

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📑 About Airtel: Bharti Airtel Limited is a leading global telecommunications company with operations in 18 countries across Asia and Africa. Headquartered in New Delhi, the company's product offerings include 2G, 3G 4G and 5G wireless services, mobile commerce, fixed line services, high speed home broadband, DTH, enterprise services including nationa ...

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📑 Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other ...

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📑 Graduate degree with formal research component or in life sciences.Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields.Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, ...

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📑 Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other ...

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📑 About Airtel: Bharti Airtel Limited is a leading global telecommunications company with operations in 18 countries across Asia and Africa. Headquartered in New Delhi, the company's product offerings include 2G, 3G 4G and 5G wireless services, mobile commerce, fixed line services, high speed home broadband, DTH, enterprise services including nation ...

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📑 We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.Job Titles: Executive / Senior Executive / Assistant Manager Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) WFOResponsibilities:1. Dossier collation a ...

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📑 About Us: established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform – CLYZOPosition- Regulatory Affairs Associate.Job Description :An organization with a reputed history of 10+ years in the Pharma raw material industry, deal ...

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📑 About Airtel: Bharti Airtel Limited is a leading global telecommunications company with operations in 18 countries across Asia and Africa. Headquartered in New Delhi, the company's product offerings include 2G, 3G 4G and 5G wireless services, mobile commerce, fixed line services, high speed home broadband, DTH, enterprise services including nationa ...

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📑 About Us: established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform – CLYZOPosition- Regulatory Affairs Associate.Job Description :An organization with a reputed history of 10+ years in the Pharma raw material industry, deal ...

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📑 We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) - WFOResponsibilities:1. Dossier collati ...

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📑 Graduate degree with formal research component or in life sciences. Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields.Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiov ...

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📑 Designation : Regulatory SpecialistExperience : 7+Location : PuneQualificationsBachelor of Science in science and/or engineering field8 - 12years of regulatory experience in medical device industry (equivalent industry/educational experience may be considered)Thorough working knowledge of applicable FDA, ISO, EU and/or other region-specific medical ...

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📑 About Airtel: Bharti Airtel Limited is a leading global telecommunications company with operations in 18 countries across Asia and Africa. Headquartered in New Delhi, the company's product offerings include 2G, 3G 4G and 5G wireless services, mobile commerce, fixed line services, high speed home broadband, DTH, enterprise services including nation ...

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📑 We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices to join our team.Job Titles: Executive / Senior Executive / Assistant Manager - Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) - WFORespons ...

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📑 Graduate degree with formal research component or in life sciences.Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields.Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, ...

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📑 Regulatory Affairs Specialist - CMC Variations/Submissions 12 month contract - Immediate start Overview: Join our Regulatory Affairs team and contribute to the management of Chemistry, Manufacturing, and Controls (CMC) You’ll be pivotal in ensuring compliance and efficiency ...

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📑 Regulatory Affairs Specialist - CMC Variations/Submissions12 month contract - Immediate startOverview: Join our Regulatory Affairs team and contribute to the management of Chemistry, Manufacturing, and Controls (CMC) You’ll be pivotal in ensuring compliance and efficiency in o ...

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📑 Provide regulatory support to customers/ internal teams and assist in maintaining regulatory requirements at all levelsCoordinate for acquiring / renewal of FDA/FSSAI licenses, product approvals, chemist intimations/ approvals, maintain regulatory documentation and follow up on any Corrective action directed by the FDA officialsCoordinate with Glob ...

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📑 Who we areTogether, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s lead ...

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📑 Regulatory Affairs Specialist - CMC Variations/Submissions12 month contract - Immediate startOverview: Join our Regulatory Affairs team and contribute to the management of Chemistry, Manufacturing, and Controls (CMC) You’ll be pivotal in ensuring compliance and efficiency in our regulatory processes.Key Responsibilities:CMC Change Control Assessmen ...

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📑 Specific activities and responsibilities: Review the drug product dossier section ( specifically 3.2.P.2 and 3.2.P.3 ) as per the EU regulatory requirement. Aware of regulatory requirements, and technical knowledge of various pharmaceutical dosage forms. Project coordination and management skills CMC regulatory requirements for other tha ...

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📑 Specific activities and responsibilities: Review the drug product dossier section ( specifically 3.2.P.2 and 3.2.P.3 ) as per the EU regulatory requirement. Aware of regulatory requirements, and technical knowledge of various pharmaceutical dosage forms. Project coordination and management ...

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📑 Department Details Role Summary • Development and Implementation of regulatory strategies for global registrations for products within the biosimilars portfolio • Coordination of activities and deliverables provided by other cross-functional teams to support the development, approval, and ...

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📑 #LI-VK1 Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new ...

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📑 Company DescriptionLars Medicare Pvt. Ltd. is a leading manufacturer of high-quality IV Catheters and other single-use medical devices. With CE and ISO 13485 certified production facilities, we export and market our products to over 100 countries, with certifications and registrations spanning from Asia Pacific to Latin America. Headquartered i ...

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📑 Key Responsibilities:Lead and manage the cross-functional communication with internal and external stakeholdersLead the Compliance project managementCollaborate with cross-functional teams, including Product Design and Sourcing, to ensure regulatory compliance throughout the product lifecycle.Research, compile, and summarize req ...

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