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OrciMed Life Sciences Hiring For Pharmacovigilance

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OrciMed Life Sciences

B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc (Life Sciences), Biotechnology, Microbiology, Biochemistry, and other relevant Life Sciences degrees

Hyderabad

1 - 4 Year+

Verified Job

Walk In Interview
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Looking for a Pharmacovigilance job in Hyderabad? OrciMed Life Sciences Limited is conducting a walk-in interview for experienced Pharmacovigilance professionals. The company is hiring for multiple positions, including Drug Safety Specialist, MICC Quality Reviewer โ€“ PV, and Mailbox Handler.

Candidates with experience in ICSR case processing, case quality review, call handling, mailbox management, and Pharmacovigilance operations may be suitable for these opportunities.

The walk-in interview will be conducted on September 10 and September 11, 2026, in Hyderabad. Immediate joiners are preferred for selected roles.


Job Openings at OrciMed Life Sciences

1. Drug Safety Specialist

Experience Required

  • Minimum 1+ year of experience in Pharmacovigilance
  • Hands-on experience in ICSR case processing is required

Key Requirements

Candidates applying for the Drug Safety Specialist position should have practical experience in Pharmacovigilance operations and Individual Case Safety Report (ICSR) processing.

Experience in processing, reviewing, and managing safety cases will be beneficial for this Pharmacovigilance role.


2. MICC Quality Reviewer โ€“ Pharmacovigilance

Experience Required

  • Minimum 4+ years of experience
  • Immediate joiners preferred

Key Responsibilities

The selected candidate will be responsible for quality review and oversight of Pharmacovigilance cases and related activities.

Responsibilities include:

  • Conduct quality reviews of cases received by call handlers.
  • Ensure case accuracy, consistency, appropriate categorization, and completeness in the LSMI database.
  • Listen to recorded calls and review or correct case narratives.
  • Ensure case narratives are accurate, complete, and appropriately documented.
  • Provide constructive feedback and guidance to call handlers.
  • Help improve the quality and consistency of case handling activities.
  • Assign follow-up activities to call and email handlers to obtain missing information.
  • Support workload allocation and effective task distribution among team members.
  • Handle and resolve escalated calls received by call handlers.
  • Manage inbound and outbound calls when required.
  • Ensure compliance with applicable SOPs, quality standards, and Pharmacovigilance requirements.

This role is suitable for experienced Pharmacovigilance professionals with expertise in PV quality review, case processing, narrative review, call handling, and quality assurance activities.


3. Mailbox Handler โ€“ Pharmacovigilance

Experience Required

  • Minimum 2 years of Pharmacovigilance industry experience
  • Immediate joiners required
  • Excellent communication skills

Key Requirements and Responsibilities

Candidates applying for the Mailbox Handler position should have a strong understanding of Pharmacovigilance principles and regulatory requirements.

Key requirements include:

  • Minimum two years of experience in the Pharmacovigilance industry.
  • Excellent written and verbal communication skills.
  • Understanding of Pharmacovigilance principles.
  • Knowledge of regulatory agencies and requirements, including EMEA, FDA, DCGI, and other regulatory authorities.
  • Ability to multitask effectively.
  • Ability to work while meeting stringent regulatory timelines and requirements.

This opportunity may be suitable for professionals with experience in PV mailbox management, safety case follow-up, email handling, ICSR processing, and regulatory Pharmacovigilance operations.


Qualifications

The job description primarily specifies experience and functional requirements. Candidates should have relevant experience in Pharmacovigilance and drug safety operations.

Depending on the position, relevant experience may include:

  • Pharmacovigilance
  • Drug Safety
  • ICSR Case Processing
  • Safety Case Quality Review
  • Medical Information Contact Center (MICC)
  • Call Handling
  • Mailbox Management
  • Case Narrative Review
  • Regulatory Compliance

Candidates are advised to carry updated resumes highlighting their relevant PV experience, ICSR processing experience, quality review experience, and communication skills.


Why Consider These Pharmacovigilance Jobs?

These openings provide opportunities for experienced professionals to work in different areas of Pharmacovigilance operations.

Depending on the position, professionals can gain or utilize experience in:

  • Drug safety operations
  • ICSR case processing
  • Pharmacovigilance quality review
  • Case narrative assessment
  • Call and email handling
  • Follow-up activities
  • Regulatory compliance
  • SOP adherence
  • Safety data management

Note: Specific employee benefits, compensation, leave policies, and other employment benefits were not mentioned in the job announcement. Candidates should confirm these details directly with the employer during the interview process.


Walk-In Interview Details

Interview Dates

September 10, 2026, and September 11, 2026

Interview Timing

10:30 AM to 2:00 PM

Employment Mode

Work from Office

Job Location

Hyderabad, Telangana

Walk-In Interview Venue

OrciMed Life Sciences Limited
Door No. 8-2-293/82/A
Plot No. 226, Road Number 17
Jubilee Hills Check Post
Union Bank Building
Jubilee Hills
Hyderabad, Telangana, India


How to Apply for OrciMed Life Sciences Jobs?

Interested and eligible candidates can attend the walk-in interview on September 10 or September 11, 2026, between 10:30 AM and 2:00 PM.

Before attending the interview, candidates should:

  1. Update their resume with relevant Pharmacovigilance experience.
  2. Clearly mention experience in ICSR case processing, if applicable.
  3. Highlight experience in quality review, mailbox handling, or call handling.
  4. Carry relevant educational and employment documents.
  5. Be prepared to discuss their experience with Pharmacovigilance processes and regulatory requirements.
  6. Immediate joiners should clearly mention their availability.

Candidates should verify the latest interview requirements and carry all necessary documents before attending.

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