Regulatory Affairs Executive

DESIGNATION/ TITLE Sr. Executive / Assistant Manager - Regulatory Affairs LOCATION NSP, Delhi YEAR OF EXP Minimum 3 yrs QUALIFICATION MSc (Toxicology/Agri/Chem) or similar BUDGET In b/w 8-10Lpa KEY RESPONSIBILITIES ROLES & RESPONSIBILITIES Manage the data gathering and compilation of studies (toxicology, chemical, efficacy) necessary for the...

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

**Regulatory Affairs Manager** **Benefits** JOB TYPE: Permanent EMPLOYMENT TYPE: Full-Time EXPERTISE: PHARMACEUTICAL REGULATORY AFFAIRS SALARY TYPE: Annually SALARY: Negotiable REPORTS TO: Managing Director VACATION LEAVE: paid LOCATION: Shimla, Himachal Pradesh, India. This role will be office-based or hybrid **REQUIRED: Direct experience working...

Regulatory affairs officers ensure that products such as foods, cosmetics, pharmaceuticals and veterinary medicines - and the steps involved in developing, testing and marketing them - meet legislative requirements. Typical duties include: studying scientific and legal documents to check they meet legal requirements Pay: ₹20,000.00 per...

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 and...

We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...

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 Assessment: ...

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 Global...

We are looking for a Lead Regulatory Affairs who is specialized in Indian market regulatory affairs with good connections in DCGI for a Global Pharmaceutical MNC in Delhi / BangaloreJob Description:We are looking for a Regulatory Affairs Lead to lead regulatory processes for our assigned products, ensuring swift approvals and strict compliance with...

Position Overview:As the Government Affairs and Public Policy Lead, one will play a pivotal role in shaping our organization's interactions with government entities like NITI Aayog, Municipalities, Smart city officials, Police departments, Ministry of Road Transport and Highways of India by managing the relations and getting closures for smart parking...

Job Req ID: 42140- Location: New Delhi, IN- Function: Other- About: - 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...

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 initial...

Job Description Copeland India is seeking a Director Public Affairs based in New Delhi. The individual will be instrumental in analysing and updating senior management on regulatory and legislative risks, opportunities and relevant laws and regulations. The individual will liaise with national, state and local government bodies, relevant industry...

Job Objective1. To monitor and involve in vetting claims in Artwork, Advertisements, e-platforms or any other communications directed towards consumers2. Drafting primary responses of legal queries from regulatory bodies3. Liasoning with regulatory bodies for effective solution keeping best-of-interest in mind for organisation4. Vetting & Providing inputs on...

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 initial...

Purpose of the role:This role will be responsible for Medical affairs activities for assigned existing Products / therapy and disease areas, collaborate with Commercial teams, training etc to drive medico-marketing activities, actively contribute to Medial activities with external experts,/ KOLs, implement Product/TA specific approved medical initiatives,...

Oppo India is hiring for Manager Public Affairs. Experience 10-12 Years Education Graduate/Post Graduate Full Time Location Gurgaon Work From Office 1)Analyze and interpret policies and regulations pertaining to IT & Electronics industry. 2)Engage with Policy makers, Industry Associations such as ICEA, CII, MAIT, PHD Chamber of commerce etc. to monitor...

Job DescriptionROLE PURPOSE: Facilitation of Registration for crop protection products viz., Fungicides in India for high quality regulatory submissions in order to achieve registrations in a time bound manner.      ACCOUNTABILITIES: To maintain regularly update , regulatory registration timelines and Regulatory intelligence for India. To update Veeva...

Job DescriptionROLE PURPOSE: Facilitation of Registration for crop protection products viz., Fungicides in India for high quality regulatory submissions in order to achieve registrations in a time bound manner.     ACCOUNTABILITIES:To maintain regularly update , regulatory registration timelines and Regulatory intelligence for India.To update Veeva for...

Mandate Industry Experience: - Pharma industry like Medical Manufacturing (Tabs/Caps/Inj Manufacturing) etc Job Description & Skill Requirement - Well versed in management of Dossier Preparation (documentation)and quality issued thru various quality management - Exp professional in supplier quality management activities in the medical, pharma industry. -...