Executive – QC (Micro)
Company: Intas Pharmaceuticals
Location: Ahmedabad (Biotech facility)
Department: Quality Control (Microbiology)
Industry: Pharmaceutical / Biotech Manufacturing
Expected Salary
₹3.5–7 LPA CTC (typically ₹4–6 LPA for M.Sc/M.Pharm freshers to 2–3 years experience)
Role Overview
The Executive – QC Micro is responsible for microbiological quality control testing of pharmaceutical batches, water systems, environmental monitoring samples, and cleanroom environments. The role ensures compliance with regulatory standards and supports manufacturing quality systems in a GMP-regulated biotech facility.
Key Responsibilities
Microbiological Testing & Analysis
Perform analysis of:
Batch samples
Water samples
Environmental monitoring (EM) samples
Microbial contamination testing
Ensure accurate documentation of all test results.
Method Validation & Transfers
Support method transfer and method validation activities.
Follow approved protocols and SOPs for execution and reporting.
Equipment Calibration & Qualification
Perform calibration, verification, and qualification of QC instruments.
Maintain scheduled monitoring and cleaning activities.
Cell Culture & Bioassays
Handle:
Cell line maintenance and banking
ELISA-based assays
HPLC-based techniques (supportive)
In-vitro bioassays
Molecular biology techniques (basic exposure)
Quality Systems (QMS)
Maintain GMP-compliant documentation.
Support investigations and deviations.
Assist in preparation and revision of QC documents.
Environmental Monitoring
Monitor cleanrooms, gases, and controlled manufacturing environments.
Ensure compliance with sterile manufacturing standards.
Required Qualifications
Education
M.Sc in Microbiology / Biotechnology / Life Sciences
M.Pharm
M.Tech (Biotech or related field)
Key Skills
Technical Skills
Microbiological testing techniques
ELISA / HPLC basics
Environmental monitoring (EM)
Sterility and contamination control
Cell culture handling (basic to intermediate)
GMP documentation practices
Compliance Knowledge
GMP (Good Manufacturing Practice)
SOP adherence
Quality Management Systems (QMS)
Soft Skills
Strong attention to detail
Discipline in documentation
Time management
Ability to work in regulated environments
Team collaboration
Preferred Experience
Experience in pharma QC or biotech manufacturing labs.
Exposure to sterile manufacturing or biologics is an advantage.
Familiarity with USFDA / MHRA / EMA standards is beneficial.
Ideal Candidate Profile
Life sciences postgraduate with strong microbiology foundation.
Hands-on laboratory experience in QC or biotech labs.
Comfortable working in regulated GMP environments.
Strong documentation and compliance mindset.
Career Growth
QC Executive → Senior Executive → Assistant Manager QC → Manager QC → Head Quality Control
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