Drug Regulatory Affair, Documentation

8 hours ago


Noida Uttar Pradesh, India Bhargava HR solution Full time

job title-- regulatory documentation

urgent requirement

location
- noida sector 63

This is a full-time on-site role as a Junior Regulatory Affairs Executive located in Noida. The Junior Regulatory Affairs Executive will be responsible for regulatory documentation, ensuring compliance with regulatory requirements, preparing dossiers, and managing regulatory affairs.

**Qualifications**:
Regulatory Documentation, Regulatory Requirements, and Regulatory Compliance skills

Dossier Preparation and Regulatory Affairs skills

Attention to detail and strong analytical skills

Ability to work independently and meet deadlines

Excellent communication and interpersonal skills

Knowledge of regulatory guidelines and laws

Bachelor's degree in a related field

Experience in the pharmaceutical industry

**Job Types**: Full-time, Permanent

Pay: ₹25,000.00 - ₹35,000.00 per month

**Job Types**: Full-time, Permanent

Pay: From ₹20,000.00 per month

**Benefits**:

- Provident Fund

Schedule:

- Weekend only

Supplemental pay types:

- Yearly bonus

**Experience**:

- total work: 1 year (preferred)

Work Location: In person



  • Noida Sector 62, Noida, Uttar Pradesh, India Florencia Healthcare (P) Ltd Full time

    **Company description** Florencia Healthcare is a research driven pharmaceutical group engaged in marketing & exporting of Quality, Safe and Genuine healthcare products to all sections of the society. Over the years, we have move forward aggressively, consistently winning new customers worldwide and making our way into challenging new markets and...

  • Regulatory Affairs

    2 days ago


    Noida, Uttar Pradesh, India corpseed ites pvt ltd Full time

    **Job Position**: Regulatory Compliance - Technical Role (CDSCO) **Experience Required**: 1 to 3year **Department**: Regulatory Affairs / Compliance - CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards. - Draft, review, submission and archival of other regulatory submissions (Query responses, corrections fillings,...


  • Noida, Uttar Pradesh, India Florencia Healthcare Full time ₹ 6,00,000 - ₹ 12,00,000 per year

    1. Drug Regulatory Affairs - Job descriptionPrepare CTD, ACTD Dossiers and file regulatory submissionsPerform assessments of new or revised productsManage complaint documentation (including investigation andclosure)Respond to inquiries from regulatory bodiesShould be technically well versed with requirements for Medicineswith fare knowledge about Food...


  • Noida, India Florencia Healthcare Full time

    **JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...


  • Noida, India Florencia Healthcare Full time

    **JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...


  • Noida, India Florencia Healthcare Full time

    Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...


  • Noida, Uttar Pradesh, India Diligence Certification Full time

    Job Summary: Key Responsibilities: Prepare, review, and maintain regulatory submissions and documentation. Communicate with clients and regulatory authorities for updates and approvals. Ensure compliance with all relevant regulations, standards, and guidelines. Maintain accurate records of communications, approvals, and submissions. Support internal...


  • Noida, Uttar Pradesh, India diligence certifications Full time

    **Job Summary**: **Key Responsibilities**: - Prepare, review, and maintain regulatory submissions and documentation. - Communicate with clients and regulatory authorities for updates and approvals. - Ensure compliance with all relevant regulations, standards, and guidelines. - Maintain accurate records of communications, approvals, and submissions. -...

  • Regulatory Affairs

    8 hours ago


    Andhra Pradesh, India Virtusa Full time

    Regulatory Affairs Specialist Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations. Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met. Responsible for supporting the needs of the MEIC with regulatory...


  • Noida, India Corpseed ITES Private Limited. Full time

    Hii Seekers, CORPSEED is looking for Management Trainee - Regulatory Affairs || CDSCO Role. Location - Noida Experience - 6 months to 2 Yrs Corpseed ITES Pvt. Ltd. is a technology platform, make things easier for Entrepreneurs and businesses. Just like a seed is required to grow a tree similarly, there are few prerequisites like “Business Planning,...