Job Description
Company Description
Iosis Remedies Pvt. Ltd. is a WHO-GMP compliant pharmaceutical manufacturing company based in Baddi, Himachal Pradesh.
We manufacture:
- Solid Oral dosage forms (Tablets, Capsules)
- Liquid Oral dosage forms (Syrups, Suspensions)
- Topical Products (Ointments, Creams)
We are committed to strong quality culture and regulatory compliance across our formulations business.
Role Description
This is a full-time, on-site role for an Assistant Manager – Quality Control, based in Baddi.
The Assistant Manager QC will be responsible for leading analytical operations within the QC department, ensuring product quality, regulatory compliance, and timely release of batches.
Key responsibilities include:
- Supervising routine and analytical testing of raw materials, in-process samples, finished products, and stability batches
- Managing instrumentation including HPLC, GC, UV, dissolution systems, IR, and titrators
- Reviewing analytical results, worksheets, pharmacopeial compliance, and trend data
- Handling OOS/OOT investigations, deviations, and change controls in coordination with QA
- Ensuring data integrity, ALCOA+ principles, GDP and c GMP compliance
- Supporting method validations, transfers, and stability studies
- Training analysts/chemists and driving lab discipline & documentation standards
- Ensuring readiness for regulatory audits and customer inspections
- Coordinating batch release and laboratory resource planning
Qualifications
- B. Pharm / M. Sc Chemistry / M. Pharm preferred
- 5–8 years experience in pharmaceutical QC, with leadership/supervisory exposure
Strong working knowledge of:
- HPLC / GC operations & troubleshooting
- Regulatory requirements (IP/USP/BP/EP)
- Laboratory investigations and CAPA methodology
- c GMP / GLP / GDP / audit compliance
Preferred Skills
- Experience with Shimadzu / Agilent systems and chromatography software
- Exposure to method validation / statistical trending / stability program oversight
- Participation in WHO / ROW / customer audits
- Ability to train and mentor junior analysts
- Strong communication and problem-solving ability
How to Apply?
Candidates can apply via Linked In or submit their CV to:
Iosis Remedies Pvt. Ltd. is a WHO-GMP compliant pharmaceutical manufacturing company based in Baddi, Himachal Pradesh.
We manufacture:
- Solid Oral dosage forms (Tablets, Capsules)
- Liquid Oral dosage forms (Syrups, Suspensions)
- Topical Products (Ointments, Creams)
We are committed to strong quality culture and regulatory compliance across our formulations business.
Role Description
This is a full-time, on-site role for an Assistant Manager – Quality Control, based in Baddi.
The Assistant Manager QC will be responsible for leading analytical operations within the QC department, ensuring product quality, regulatory compliance, and timely release of batches.
Key responsibilities include:
- Supervising routine and analytical testing of raw materials, in-process samples, finished products, and stability batches
- Managing instrumentation including HPLC, GC, UV, dissolution systems, IR, and titrators
- Reviewing analytical results, worksheets, pharmacopeial compliance, and trend data
- Handling OOS/OOT investigations, deviations, and change controls in coordination with QA
- Ensuring data integrity, ALCOA+ principles, GDP and c GMP compliance
- Supporting method validations, transfers, and stability studies
- Training analysts/chemists and driving lab discipline & documentation standards
- Ensuring readiness for regulatory audits and customer inspections
- Coordinating batch release and laboratory resource planning
Qualifications
- B. Pharm / M. Sc Chemistry / M. Pharm preferred
- 5–8 years experience in pharmaceutical QC, with leadership/supervisory exposure
Strong working knowledge of:
- HPLC / GC operations & troubleshooting
- Regulatory requirements (IP/USP/BP/EP)
- Laboratory investigations and CAPA methodology
- c GMP / GLP / GDP / audit compliance
Preferred Skills
- Experience with Shimadzu / Agilent systems and chromatography software
- Exposure to method validation / statistical trending / stability program oversight
- Participation in WHO / ROW / customer audits
- Ability to train and mentor junior analysts
- Strong communication and problem-solving ability
How to Apply?
Candidates can apply via Linked In or submit their CV to:
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