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Location: Gandhinagar, Gujarat (On-site)
Job Title: Quality Control (QC) Engineer– Cleanroom Unit
Department: Quality Control
Reporting To: Senior QC Engineer
Experience Required: 3–5 years
Employment Type: Full-time
Working Days: 6 days/week
Compensation: ₹6– ₹6.5 LPA
Industry Preference (Mandatory)
Candidates must have experience in at least one of the following regulated sectors:
Sterile/Injectables Manufacturing
Medical Devices Manufacturing
Medicinal Equipment Manufacturing
Key Responsibilities
Conduct testing of raw materials, in-process samples, and finished products per
pharmacopeial guidelines (IP/BP/USP/Ph. Eur.).
Perform assays, dissolution, impurity profiling, and other pharmacopeial tests.
Carry out wet chemistry procedures, including pH and conductivity testing.
Operate and calibrate analytical instruments (IR, FTIR, etc.).
Ensure compliance with GMP, GLP, and SOPs.
Maintain accurate documentation: test reports, calibration logs, change controls, etc.
Collaborate with QA and Production teams.
Support audit readiness and participate in internal/external audits.
Handle sample collection, labeling, storage, and assist with stability studies.
Candidate Requirements
Education (Preferred):
B.Sc/ M.Sc in Chemistry
B.Pharm / M.Pharm (Pharmaceutical Chemistry)
Experience:
3–5years in a pharmaceutical or regulated manufacturing setup
Prior work in sterile/medical device/cleanroom environments is essential
Technical Skills:
Proficient in pharmacopeial testing and documentation
Skilled with IR Spectroscopy, FTIR, pH/conductivity meters
Familiar with method validation and instrument calibration
Strong understanding of GMP, data integrity, and cleanroom compliance
Quality Control Engineer
Actively Reviewing
Mahaveer Consultancy And Services
Job Description
Location: Gandhinagar, Gujarat (On-site)
Job Title: Quality Control (QC) Engineer– Cleanroom Unit
Department: Quality Control
Reporting To: Senior QC Engineer
Experience Required: 3–5 years
Employment Type: Full-time
Working Days: 6 days/week
Compensation: ₹6– ₹6.5 LPA
Industry Preference (Mandatory)
Candidates must have experience in at least one of the following regulated sectors:
Sterile/Injectables Manufacturing
Medical Devices Manufacturing
Medicinal Equipment Manufacturing
Key Responsibilities
Conduct testing of raw materials, in-process samples, and finished products per
pharmacopeial guidelines (IP/BP/USP/Ph. Eur.).
Perform assays, dissolution, impurity profiling, and other pharmacopeial tests.
Carry out wet chemistry procedures, including pH and conductivity testing.
Operate and calibrate analytical instruments (IR, FTIR, etc.).
Ensure compliance with GMP, GLP, and SOPs.
Maintain accurate documentation: test reports, calibration logs, change controls, etc.
Collaborate with QA and Production teams.
Support audit readiness and participate in internal/external audits.
Handle sample collection, labeling, storage, and assist with stability studies.
Candidate Requirements
Education (Preferred):
B.Sc/ M.Sc in Chemistry
B.Pharm / M.Pharm (Pharmaceutical Chemistry)
Experience:
3–5years in a pharmaceutical or regulated manufacturing setup
Prior work in sterile/medical device/cleanroom environments is essential
Technical Skills:
Proficient in pharmacopeial testing and documentation
Skilled with IR Spectroscopy, FTIR, pH/conductivity meters
Familiar with method validation and instrument calibration
Strong understanding of GMP, data integrity, and cleanroom compliance
Required Skills
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