Regulatory Affairs Officer

5 days ago

Lahore, Punjab, Pakistan remington pharma Full time 1,200,000 - 3,600,000 per year

Responsibilities

  • Prepare and submit CTD / ACTD dossiers for international markets, handle queries and follow up till registration.
  • Ensure that all product registrations and submissions comply with applicable laws, guidelines, and industry standards.
  • Prepare other supporting regulatory documents as required by foreign regulatory agencies.
  • Collaborate with QA, QC, Production, and Export departments to gather accurate and up-to-date technical and manufacturing data for dossier completion.
  • Maintain clear and continuous communication with international stakeholders regarding dossier status and updates.
  • Maintain accurate and updated records of all submitted dossiers, correspondence, and regulatory approvals.

Qualifications

  • Education: Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences.
  • 6 months to 1 year in regulatory affairs for the pharmaceutical industry.
  • Proficiency in CTD format preparation and dossier compilation.
  • Excellent written and verbal communication skills.
  • Ability to work effectively under tight deadlines

Location:

18km Multan Road Lahore Pakistan

Email:

Job Type: Full-time

Pay: From Rs50,000.00 per month

Application Question(s):

  • How much Relevant experience you have in Regulatory Affairs.

Education:

  • Bachelor's (Preferred)

Location:

  • Lahore (Preferred)

Work Location: In person

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