"Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya"

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"Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers | Pharma Duniya." (Project Associate I RA QA Job | ELEXES Medical Consulting Hiring Freshers) Introduction If you are a fresher or early-career professional aiming to build a strong career in Medical Device Regulatory Affairs and Quality Assurance , this opportunity can be a perfect starting point. ELEXES Medical Consulting Pvt. Ltd. has announced hiring for the position of Project Associate I – Regulatory Affairs & Quality Assurance (RA/QA) . This role is specially designed for fresh graduates and candidates with up to 6 months of experience who want hands-on exposure to global medical device regulations , including US FDA, EU MDR, CDSCO, Health Canada , along with ISO 13485 quality systems . The position offers real project experience under expert mentorship, making it ideal for long-term growth in the medical device regulatory domain. About The Company – ELEXES Medical Consulting Pvt. Ltd. EL...

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“Mitocon Biopharma Hiring for Pharmacovigilance & Medical Information Jobs in Hyderabad 2025”

"Mitocon Biopharma Hiring for Pharmacovigilance & Medical Information Roles in Hyderabad"


Mitocon Biopharma Pvt Ltd, a trusted name in global drug safety and patient care, is expanding its team and inviting applications from skilled professionals. If you’re passionate about pharmacovigilance, literature case processing, and medical information support, this is your chance to contribute to global healthcare compliance. The openings are based in Begumpet, Hyderabad, offering competitive salaries and strong career growth.

Current Openings at Mitocon Biopharma:-

1. Pharmacovigilance – Case Processing

  • Experience: 1–4 years
  • Mandatory: Literature case processing experience
  • Notice Period: Immediate or up to 30 days
  • CTC: Up to ₹7 LPA

Key Responsibilities:

  • Perform triage, data entry, narrative writing, and medical coding in safety databases
  • Evaluate seriousness, expectedness, and causality of adverse events (AEs)
  • Ensure timely case submissions to regulatory authorities
  • Collaborate with global PV teams to maintain compliance standards

Qualifications:

  • B.Pharm, M.Pharm, PharmD, or Life Sciences degree
  • Hands-on experience with PV databases and literature case handling
  • Strong analytical, communication, and documentation skills

2. Medical Information Contact Center

  • Experience: 1–6 years
  • Shift: Night Shift (9:00 PM – 6:00 AM)
  • Designation: DSA-II / DSA-III / Assistant Manager
  • Salary: Competitive, based on experience and performance

Key Responsibilities:

  • Handle queries from healthcare professionals and patients
  • Provide accurate, evidence-based drug information on usage, efficacy, and safety
  • Maintain detailed documentation in CRM systems for compliance and audit readiness

Qualifications:

  • Degree in Pharmacy, Life Sciences, or related field
  • Previous experience in medical information, pharmacovigilance, or medical affairs preferred
  • Excellent verbal and written communication skills

Why Join Mitocon Biopharma?

  • Competitive salary packages
  • Opportunity to work on global pharmacovigilance projects
  • Exposure to compliance and regulatory systems
  • Professional growth in a fast-growing pharmaceutical organization

How to Apply:-

Interested candidates can apply by sending their updated resume to:

📧 Email: hr@mitoconbiopharma.com

Take the next step in your pharma career and be part of a company dedicated to patient safety and global healthcare excellence.

✅ Keywords for SEO: Pharmacovigilance jobs in Hyderabad, Medical Information jobs, Pharma jobs 2025, Mitocon Biopharma careers, drug safety jobs India.

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