Multiple Openings in Pharma Quality Control

(Documentation, IP/FP, Investigations, Review, LIMS)

We are conducting a mega recruitment drive for multiple specialized roles in our Quality Control departments. If you have the required expertise in pharmaceutical compliance, analytical data review, or LIMS systems, we invite you to apply and grow with us.

Sr. Officer/ Executive / Senior Executive

We are seeking experienced Quality Control professionals with 2 - 8 years of hands-on experience in Oral Solid Dosage (OSD) pharmaceutical analysis to support core laboratory operations in a regulated manufacturing environment. The incumbent will be responsible for end-to-end analytical execution, review, investigation support, and compliance handling to ensure timely release of materials and finished products while maintaining cGMP, GLP, and Data Integrity standards.

1. Documentation & Training Coordinator

- Key Responsibilities: Manage Site Training Matrices, coordinate GMP training sessions, oversee document lifecycle management (SOPs, protocols, reports), and ensure audit readiness of documentation cells.
- Ideal Candidate: Experience in standard Document Management Systems (DMS) and LMS platforms with a strong grasp of compliance frameworks.

2. IP / FP / AMT / AMV Specialists

- Key Responsibilities: Oversee In-Process (IP) and Finished Product (FP) testing compliance, execute Analytical Method Transfer (AMT), and drive Analytical Method Validation (AMV) protocols in line with global regulatory standards
- Ideal Candidate:



Hands-on experience with advanced analytical instrumentation (HPLC, GC, dissolution) and standard validation life cycles.

3. Investigator

- Key Responsibilities: Lead thorough investigations for Out of Specification (OOS), Out of Trend (OOT), and deviations. Conduct Root Cause Analysis (RCA) using tools like Fishbone/5 Whys, and define robust CAPAs to prevent recurrence.
- Ideal Candidate: Solid technical writing skills and a deep understanding of manufacturing or laboratory investigations.

4. Analytical Data Reviewer

- Key Responsibilities: Review raw data, electronic logs, and chromatography data sheets generated by the QC laboratories. Ensure absolute adherence to Data Integrity principles and ALCOA+ standards.
- Ideal Candidate: High attention to detail with extensive experience reviewing complex laboratory datasets.

5. LIMS Administrator / Specialist

- Key Responsibilities: Manage Laboratory Information Management System (LIMS) workflows, configure master data, troubleshoot system errors, and ensure validation compliance .
- Ideal Candidate: Strong background at the intersection of Pharma QC and IT systems, with hands-on LIMS configuration/master data creation experience.

Qualification & Competencies : Qualification: M.Sc. / B.Pharm / M.Pharm / equivalent in Chemistry / Pharmaceutical Sciences

Experience:2 to 8 years of relevant experience in a regulatory-approved pharmaceutical facility.(Mandatory)

Core Competencies: Comprehensive understanding of cGMP, data integrity regulations, strong communication, and problem-solving skills.

📌 Walk-in || Officer/Executive/Sr. Executive - Quality Control (Mysuru)
🏢 VIBONUM TECHNOLOGIES
📍 Mysuru