Mitocon Biopharma is Hiring | Multiple Pharmacovigilance Openings | Hyderabad
Location: Begumpet, Hyderabad
Mitocon Biopharma is expanding its team! We are looking for experienced professionals to join us across multiple Pharmacovigilance functions. If you're passionate about
patient safety and looking for your next career opportunity, we'd love to hear from you.
1. Manager Medical Affairs (Pharmacovigilance)
Qualification: MBBS with valid MCI/NMC Registration
Experience: 6-8 Years in Pharmacovigilance
Preferred: Immediate to 30 days
Key Responsibilities:
Medical Review & Safety Assessment
Aggregate Report Authoring (PSUR, DSUR, PADER, RMP & Signal Reports)
Regulatory Compliance & Expedited Reporting
Team Leadership & Mentoring
Quality Assurance & Audit Support
Client Interaction & Medical Review Meetings
Patient Safety & Risk Management Activities
2. Assistant Manager Medical Information Contact Center (MICC)
Qualification: B.Pharm / M.Pharm / Pharm.D
Experience: 6-10 Years
Shift: Permanent Night Shift (9:00 PM 6:00 AM)
Mandatory Requirement: Hands-on MICC experience is mandatory.
Key Responsibilities:
Manage and oversee MICC operations
Ensure compliance with organizational and regulatory standards
Drive process improvements
Monitor performance metrics
Lead cross-functional teams
Mentor and develop team members
Skills Required:
Strong leadership and communication skills
Excellent problem-solving ability
Experience in handling multiple responsibilities in a fast-paced environment
3. PVQA Executive / Senior PVQA
Qualification: Bachelor's Degree in Life Sciences, Pharmacy, or a related field
Experience: 3–4 Years
Shift: Evening Shift
Notice Period: Immediate to 30 Days
Gender Preference: Male Candidates Only
Mandatory Requirements:
PVQA experience is mandatory
Robust experience in CAPA & Deviation Management
Immediate joiners preferred
No freshers
Key Responsibilities:
Perform quality checks on Pharmacovigilance case processing
Review ICSRs for accuracy, completeness, and compliance
Conduct internal quality audits
Prepare audit reports
Identify quality gaps and implement CAPA actions
Ensure compliance with ICH, GVP, and global PV regulations
Support process improvement initiatives and team training
Required Knowledge:
Pharmacovigilance Quality Assurance (PVQA)
ICH & GVP Guidelines
CAPA & Deviation Handling
Regulatory Compliance
Interested candidates can apply now by sharing their updated resume.
Email:
[email protected]
WhatsApp: (phone hidden) (Resume only. No calls, please.)
Location: Begumpet, Hyderabad
Immediate joiners will be given preference.
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