Synergen Bio Hiring for Research Associate (Report Writer) – Immediate Joiners Preferred

Pharma Stuff

Pune District

On-site

INR 600,000 - 900,000

Full time

14 days+
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Job summary

Synergen Bio is hiring a Research Associate (Report Writer) for the Project Management and Biopharmaceutics department. The role is based at Shivajinagar, Wakadewadi Pune, with immediate joiners preferred for two vacancies.

Qualifications include B.Pharm, M.Pharm, or MSc, and at least 1.5 years of relevant experience in pharmaceutical or biopharmaceutical settings. Strong CSR/report formatting and regulatory documentation skills are required.

Qualifications

  • Experience in CSR preparation and regulatory report formatting.
  • Familiarity with eCTD specifications and electronic submissions.
  • Ability to handle regulatory documentation processes accurately.

Skills

CSR preparation
Regulatory reports
eCTD knowledge
Regulatory documentation

Education

B.Pharm, M.Pharm, or MSc

Job description

Synergen Bio, a leader in biopharmaceuticals and clinical research, is currently hiring for the position of Research Associate (Report Writer) in the Project Management and Biopharmaceutics department. This role is based in Shivajinagar, Wakadewadi Pune and is a unique opportunity for candidates with a background in pharmacy or life sciences.

Key Details of the Position
  • Position Title: Research Associate (Report Writer)
  • Department: Project Management and Biopharmaceutics
  • Qualifications: B. Pharm, M. Pharm, or MSc in a relevant field
  • Experience: Minimum 1.5 years of experience
  • Vacancies: 2 positions
  • Location: Shivajinagar, Wakadewadi Pune
  • Preferred Start: Immediate joiners
Qualifications and Skills Required

To excel in this position, you should meet the following qualifications and skill requirements:

  • Educational Background: B. Pharm, M. Pharm, or MSc in a relevant field such as pharmacy, chemistry, or biotechnology.
  • Experience: At least 1.5 years of experience in a similar role, preferably within the pharmaceutical or biopharmaceutical sectors.
  • Technical Skills:
    • Proficiency in CSR preparation and regulatory report formatting
    • Familiarity with eCTD specifications and electronic report submission requirements
    • Ability to perform data uploads and handle regulatory documentation processes accurately
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