Mitocon Biopharma Recruitment 2026: Multiple Pharma Jobs in Hyderabad | PVQA, PMO, MICC & Medical Reviewer Vacancies

The pharmaceutical and life sciences industry in India continues to experience remarkable growth, creating exciting career opportunities for professionals across pharmacovigilance, quality assurance, medical information, clinical operations, and project management. Hyderabad, one of India’s leading pharmaceutical hubs, remains at the forefront of this expansion, attracting multinational pharmaceutical companies, CROs, and biotechnology organizations.

If you’re searching for your next career move in the pharmaceutical sector, Mitocon Biopharma Pvt. Ltd. has announced a major recruitment drive for 2026. The company is hiring experienced professionals across multiple departments, including Pharmacovigilance Quality Assurance (PVQA), Project Management Office (PMO), Medical Information Contact Center (MICC), and Medical Reviewer positions.

Whether you’re a B.Pharm, M.Pharm, Pharm.D, or MBBS graduate with relevant industry experience, this recruitment drive offers an excellent opportunity to advance your career with competitive salaries, professional development, and exposure to global pharmaceutical projects.

Let’s explore every available position in detail.


🏒 About Mitocon Biopharma Pvt. Ltd.

Mitocon Biopharma Pvt. Ltd. is a growing pharmaceutical and healthcare services organization specializing in pharmacovigilance, regulatory compliance, medical information management, project execution, and quality-driven healthcare solutions.

The organization works with pharmaceutical clients to ensure patient safety, regulatory compliance, medical data quality, and efficient project management. As pharmaceutical regulations become increasingly stringent across global markets, companies like Mitocon continue expanding their workforce to support international clients and maintain high operational standards.

Professionals joining the company gain exposure to international quality systems, pharmacovigilance processes, medical review standards, and global healthcare regulations.


πŸ“ Job Location

Hyderabad, Telangana

Hyderabad continues to be one of India’s premier destinations for pharmaceutical, biotechnology, CRO, and clinical research careers, offering excellent infrastructure and significant professional growth opportunities.


πŸ’Ό Available Job Openings

Mitocon Biopharma is currently recruiting for the following departments:

  • βœ… Pharmacovigilance Quality Assurance (PVQA)
  • βœ… Project Management Office (PMO)
  • βœ… Medical Information Contact Center (MICC)
  • βœ… Medical Reviewer

Each role offers unique responsibilities and attractive career progression.


πŸ›‘οΈ 1. Pharmacovigilance Quality Assurance (PVQA)

Pharmacovigilance Quality Assurance professionals play an essential role in ensuring the quality, compliance, and accuracy of drug safety operations. Their work directly contributes to patient safety by verifying that adverse event reporting meets global regulatory expectations.

Educational Qualification

  • B.Pharm
  • M.Pharm
  • Pharm.D

Experience Required

  • 2–5 Years

Salary

πŸ’° Up to β‚Ή7 LPA

Additional:

  • Night Shift Allowance
  • Performance-based benefits

Shift Timing

πŸ•” 5:00 PM – 2:00 AM

Notice Period

Immediate joiners preferred

Maximum notice period:

  • Up to 60 Days

Key Responsibilities

βœ” Perform independent quality reviews of pharmacovigilance case processing.

βœ” Review Individual Case Safety Reports (ICSRs).

βœ” Verify regulatory compliance with:

  • ICH Guidelines
  • GVP Guidelines
  • Internal SOPs

βœ” Conduct internal quality audits.

βœ” Support vendor quality assessments.

βœ” Prepare audit reports.

βœ” Identify quality gaps.

βœ” Perform Root Cause Analysis (RCA).

βœ” Implement Corrective and Preventive Actions (CAPA).

βœ” Ensure database accuracy and documentation quality.


πŸ“Š 2. Project Management Office (PMO)

The Project Management Office serves as the operational backbone of pharmaceutical projects. PMO professionals coordinate teams, monitor project timelines, manage client expectations, and ensure successful project delivery.

Educational Qualification

  • B.Pharm
  • M.Pharm
  • Pharm.D

Experience

4–6 Years

Salary

πŸ’° Up to β‚Ή15 LPA

(Depending upon experience and interview performance)

Notice Period

Immediate to 60 Days

Major Responsibilities

Project Management Officers will be responsible for:

  • Managing multiple pharmaceutical projects simultaneously.
  • Coordinating cross-functional departments.
  • Monitoring project budgets.
  • Tracking project timelines.
  • Ensuring timely client deliverables.
  • Conducting project review meetings.
  • Preparing management reports.
  • Managing project risks.
  • Supporting strategic business planning.
  • Building strong client relationships.

Candidates with excellent communication, leadership, and organizational skills will have a competitive advantage.


πŸ“ž 3. Medical Information Contact Center (MICC)

Medical Information Associates act as the communication bridge between pharmaceutical companies, healthcare professionals, patients, and regulatory stakeholders.

They ensure that medical information is accurate, documented, and communicated according to regulatory standards.

Educational Qualification

  • B.Pharm
  • M.Pharm
  • Pharm.D

Experience

2–3 Years

Salary

Best in Industry

Additional Night Shift Allowance

Shift

πŸ•• 6:00 PM – 3:00 AM

Note: No cab facility is available.

Notice Period

30–60 Days

Key Responsibilities

Medical Information professionals will:

  • Review medical information documents.
  • Conduct quality checks on case documentation.
  • Maintain client folders and databases.
  • Track documentation errors.
  • Coordinate with medical information associates.
  • Handle product-related inquiries.
  • Maintain complaint records.
  • Archive client communications.
  • Prepare daily productivity reports.
  • Share reports with global clients.

Excellent Career Opportunity

Professionals currently working in:

  • Pharmacovigilance Case Processing
  • Drug Safety Operations
  • Safety Data Management

who wish to transition into Quality Review or Medical Information roles are encouraged to apply.


🩺 4. Medical Reviewer

Medical Reviewers represent one of the most specialized positions within pharmacovigilance.

These professionals evaluate complex safety data, review medical assessments, analyze benefit-risk profiles, and provide clinical oversight during drug safety evaluations.

Qualification

Mandatory:

βœ… MBBS

Experience

6–8 Years

Salary

Premium compensation package

Based upon:

  • Experience
  • Interview Performance
  • Technical Expertise

Location

Hyderabad

Office-based role

Responsibilities

Medical Reviewers typically perform:

  • Clinical review of ICSRs
  • Medical assessment of adverse events
  • Signal evaluation
  • Benefit-risk assessment
  • Medical coding review
  • Safety narrative review
  • Regulatory documentation review
  • Medical oversight of pharmacovigilance activities

This role is ideal for experienced physicians seeking careers within pharmaceutical safety and medical affairs.


🌟 Why Consider a Career at Mitocon Biopharma?

Working with Mitocon Biopharma offers several professional advantages:

  • Exposure to global pharmaceutical projects
  • Structured career growth
  • Competitive compensation packages
  • International pharmacovigilance standards
  • Learning opportunities in quality systems
  • Collaborative work culture
  • Diverse healthcare projects
  • Professional skill enhancement
  • Stable pharmaceutical career pathway

For professionals looking to strengthen their expertise in drug safety, quality assurance, or medical review, these opportunities can provide valuable industry exposure.


πŸŽ“ Who Should Apply?

This recruitment drive is suitable for:

  • B.Pharm Graduates
  • M.Pharm Graduates
  • Pharm.D Professionals
  • MBBS Doctors
  • Pharmacovigilance Professionals
  • Drug Safety Associates
  • Medical Information Specialists
  • Quality Assurance Executives
  • Project Management Professionals
  • Medical Review Experts

Candidates meeting the required experience criteria are encouraged to submit their applications.


βœ‰οΈ How to Apply?

Interested candidates can apply by sending their updated resume along with the following details:

  • Current CTC
  • Expected CTC
  • Notice Period
  • Updated Resume
  • Cover Letter (Optional but Recommended)

πŸ“§ Email

hr@mitoconbiopharma.com

πŸ“ž Contact Number

+91 9154383165

Ensure that your resume highlights relevant experience, technical skills, certifications, and project achievements to improve your chances during the screening process.


πŸ“Œ Important Points

  • Multiple departments are hiring.
  • Hyderabad is the job location.
  • Immediate joiners are preferred.
  • Maximum notice period accepted is 60 days.
  • Night shift roles include additional allowances where applicable.
  • Salary packages vary according to experience and department.

πŸš€ Final Thoughts

The pharmaceutical industry continues to offer stable and rewarding careers for qualified professionals, and Mitocon Biopharma’s latest recruitment drive presents an excellent opportunity for candidates with experience in pharmacovigilance, medical information, project management, and medical review.

Whether you are aiming to advance your career in quality assurance, transition from case processing into medical information, or leverage your clinical expertise as a medical reviewer, these openings provide an opportunity to work in a growing organization focused on regulatory excellence and patient safety.

If your qualifications and experience align with the requirements, consider applying promptly, as positions may be filled on a rolling basis.

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