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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, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of o ...

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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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📑 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 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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📑 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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📑 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 will be responsible for overseeing all aspects of labeling, fr ...

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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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📑 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 ...

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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 position will support worldwide regulatory registrations for our current and future medical devices as well as support process compliance in conjunction with ...

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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 t ...

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📑 Revvity is a global technology company focused on improving the health and safety of people and the environment. The Regulatory Affairs Specialist will support our Diagnostics Business that focuses on products targeted to improve human health. He/she will support regulatory submissions on global cross-functional teams and help to prov ...

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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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📑 Revvity is a global technology company focused on improving the health and safety of people and the environment. The Regulatory Affairs Specialist will support our Diagnostics Business that focuses on products targeted to improve human health. He/she will support regulatory submissions on global cross-functional teams and help to providing guidanc ...

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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.As a Regulatory Compliance Engineer, you will play a crucial role in ensuring ou ...

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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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📑 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 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 interests in regulatory proceedings. You will be responsible for providing legal a ...

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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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📑 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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📑 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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📑 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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📑 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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📑 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 leading manufacturer of generic ...

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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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📑 Are you looking for an exciting opportunity to join a dynamic and growing team in a fast paced and challenging area? This is a unique opportunity for you to work in the Regulatory Operations team to partner with the Business. As a Regulatory Operations - Regulatory Reporting - Associate within the Regulatory Operations CoE, you will cater to priv ...

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📑 Are you looking for an exciting opportunity to join a dynamic and growing team in a fast paced and challenging area? This is a unique opportunity for you to work in the Regulatory Operations team to partner with the Business. As a Regulatory Operations - Regulatory Reporting - Associate within the Regulatory Operations CoE, you will cater to priv ...

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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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📑 Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India’s leading telecom service provider. The Company provides pan India Voice and Data services across 2G, 3G and 4G platform. With the large spectrum portfolio to support the growing demand for data and voice, the company is committed to deliver delightful custo ...

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📑 The position As a RA Specialist, the ideal candidate will be responsible to design RA Strategy from late stage development and throughout Life cycle of the device project, prepare and submit high quality files to the authorities achieving fast approvals. Act as an ambassador for assigned medical devices/device part of combination products. Th ...

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📑 Department: RA CMC & DeviceAre you passionate about your work? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as “RA Specialist” with ...

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📑 Department: Regulatory Affairs CMC & Device Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you ...

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📑 We’re looking for people who are determined to make life better for people around the world. Purpose: Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion acro ...

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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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📑 Department: RA CMC & Device Are you passionate about your work? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as “RA Specialist” ...

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📑 Department: Regulatory Affairs CMC & Device Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for ...

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📑 **Job responsivities are to assist Regulatory manager**- Preparation, Compilation and review of registration **dossier** of tablet /capsule/injection in CTD, ACTD as well as country specific format for countries- Preparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbal products for country specific forma ...

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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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📑 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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📑 Your responsibilities include, but are not limited to:• Independently manage and prepare routine Health Authority submissions including Annual Reports, DSUR, New Protocol Submissions, Protocol Amendment , and New Investigator Submissions to ensure timely submissions in accordance with the FDA regulations• Contribute to Module #1 documents including ...

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📑 Bangalore , Chennai , Description , Hyderabad , Job , Level , Location , Mumbai , Primary , Pune , REG , Regulatory , Regulatory Reporting , Reporting , Secondary Experience Required 3 - 9 Years Industry Type IT Employment Type Permanent Location India ...

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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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📑 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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📑 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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📑 Company Profile:Our Client company is Denmark based and they have impacted people around the world with there products and services. As one of the world's largest pharmaceutical wholesalers, There Repackaging unit is in Gandhidham.Job Profile: The position will be Responsible for:1. Request, follow-ups and obtain product dossier from themanufactur ...

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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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📑 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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