: Collect and test raw materials, packaging components, in-process samples, finished products, and stability samples, following SOPs.
Instrumental Analysis
: Perform chemical and physical analyses using HPLC, UV, FTIR, GC, etc.
Documentation & Reporting
: Maintain accurate records, logbooks, and prepare Certificates of Analysis (CoA) as per Good Documentation Practices (GDP).
Stability & In?Process Checks
: Conduct stability studies and perform in-process quality checks during production.
Equipment Management
: Ensure calibration and preventive maintenance of QC instruments; report malfunctions promptly.
Compliance & Audits
: Adhere to GMP, cGMP, ICH, and regulatory standards; support internal and external audits, and assist with investigations, deviations, OOS handling, and CAPA implementation.
Qualifications & Skills
Educational Qualification
: B.Pharm, M.Pharm, B.Sc/M.Sc in Chemistry or related field as applicable.
Experience
: Typically ranging from
1 to 3 years
in pharmaceutical quality control roles.
Technical Proficiency
: Hands on experience with HPLC, UV, GC, FTIR, along with strong understanding of GMP, GLP, and data integrity practices.
Attention to Detail
: Excellent accuracy in testing, documentation, and adherence to protocols.
Analytical Mindset
: Capable of troubleshooting and identifying root causes for quality incidents.
Soft Skills
: Strong communication, teamwork, and ability to work effectively under audit-ready environments.
Benefits & Work Conditions
Job Type
: Full-time, Permanent; typically morning/day shift.
Salary Range
: Approximately ?25,000 to ?30,000 per month (depending on role level and experience).
Perks
: Provident Fund, Paid Sick Time, Cell Phone Reimbursement, Health Insurance.
Job Types: Full-time, Permanent
Pay: ?25,000.00 - ?30,000.00 per month
Benefits:
Health insurance
Paid sick time
Provident Fund
Work Location: In person
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