. The candidate should have strong hands-on experience in Quality Control activities within a regulated pharmaceutical environment.
Key Responsibilities:
Perform
chemical and instrumental analysis
of raw materials, in-process samples, finished products, stability samples, and validation samples
Handle
HPLC, GC, UV, Dissolution, FTIR
, and other analytical instruments
Review, prepare, and maintain
analytical reports, COAs, STPs, SOPs
, and QC documentation
Ensure compliance with
cGMP, GLP, and data integrity
requirements
Support
method validation, method transfer
, and stability studies
Participate in
internal audits, regulatory audits
, and investigations
Handle
OOS, OOT, deviations, and CAPA
activities
Coordinate with Production, QA, and other departments for smooth operations
Ensure proper calibration and maintenance of laboratory instruments
Train and guide junior QC staff when required
Desired Skills & Competencies:
Strong knowledge of
OSD dosage forms
Hands-on experience with
analytical instruments
Good understanding of
regulatory guidelines
(major international regulatory bodies, including EU GMP, PIC/s GMP, TGA Australia, Health Canada, and WHO GMP)
Attention to detail and strong documentation practices
Ability to work independently and in a team
Good communication and problem-solving skills
Benefits:
Company Bus Facility
Professional work environment
Growth opportunities within the organization
Job Types: Full-time, Permanent
Pay: ?45,131.96 - ?75,466.08 per month
Benefits:
Health insurance
Provident Fund
Work Location: In person
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