Swiss Parenterals Hiring QC HPLC & QMS

QC HPLC & QMS Openings for B.Pharm/M.Pharm | Ahmedabad

Swiss Parenterals hiring QC HPLC & QMS professionals (3–6 yrs) in Ahmedabad. B.Pharm/M.Pharm/M.Sc eligible. Apply now.

Swiss Parenterals is hiring experienced Quality Control professionals for its Ahmedabad facilities. These roles are suitable for candidates with hands-on expertise in HPLC analysis, QMS operations, GLP compliance, GDP documentation, and regulated-market quality systems. The company offers exposure to global regulatory standards and modern QC instrumentation, making it a strong opportunity for professionals looking to build a long-term career in high‑compliance environments.

Company Overview

Swiss Parenterals Ltd operates advanced pharmaceutical manufacturing units in Ahmedabad, built on cGMP and WHO‑GMP standards. The facilities maintain ISO 9001:2008 certification and comply with major global regulatory frameworks including EU, FDA, TGA, and MCC. With modern instrumentation, validated systems, and a trained technical workforce, the company maintains strong credibility in sterile and non‑sterile manufacturing. Professionals joining Swiss gain access to high‑precision QC workflows, global audit exposure, and validated testing environments.

Job Role & Responsibilities

1. Quality Control – HPLC

• Follow GLP and maintain all QC documentation as per GDP requirements.
• Perform testing of Finished Products, Raw Materials, In‑process samples, and Stability batches.
• Execute both wet chemistry and instrumental analysis.
• Conduct calibration of HPLC instruments as per the internal schedule.
• Prepare and execute protocols for Process Validation and Hold‑time Validation.
• Troubleshoot analytical instruments and maintain smooth lab operations.
• Coordinate with Production, QA, and other cross-functional departments.
• Handle regulatory and customer audits.
• Participate in OOS, OOT, deviation, and incident investigations.
• Drive CAPA implementation and documentation accuracy.

2. Quality Control – QMS

• Implement GLP and ensure accurate record management.
• Review specifications, STPs, and protocols using statistical and data‑driven approaches.
• Prepare and revise SOPs as per GMP standards.
• Lead QC training and competency programs.
• Oversee IQ/OQ/PQ of instruments.
• Monitor preventive maintenance and calibrations; coordinate with engineering and vendors.
• Review and approve COAs based on analytical data.
• Ensure proper labeling and traceability within the QC lab.
• Manage audit readiness for both regulatory and non‑regulatory inspections.
• Ensure timely release of raw materials and finished goods.
• Lead investigations for OOS, OOT, deviations, and drive root cause analysis and CAPA.

These responsibilities support product safety, analytical reliability, and regulatory compliance—all core pillars of high‑quality pharmaceutical manufacturing.

Eligibility / Qualifications

Preferred educational backgrounds include:

• B.Pharm, M.Pharm, M.Sc
• Relevant courses: Pharmaceutical Analysis, Quality Assurance, Industrial Pharmacy, Chemistry, Analytical Techniques, Instrumentation Technology.

Experience

• 3 to 6 years in Quality Control (HPLC/QMS)
• Strong analytical skills and hands-on experience in regulated laboratory systems
• Only male candidates are eligible as per company requirements

Location & Salary

• Location: Ahmedabad, Gujarat
• Salary is based on skills and experience but aligns with QC Officer/Executive levels in regulated manufacturing units

Application Process

Eligible candidates can submit their updated CV to:

• Email: Hr1@swiss.in
• Phone: 6352978952
• Website: https://www.swiss.in

Subject Line: Quality Control (HPLC / QMS)

FAQs

What experience is required?

Candidates need 3–6 years of QC experience in HPLC, QMS, validations, and regulatory audits.

Are female candidates eligible?

No. The company has specified male candidates only for this requirement.

What instruments should the candidate know?

HPLC, analytical balances, stability chambers, and general QC instruments.

Does the company support regulatory audit exposure?

Yes. Swiss regularly undergoes EU, FDA, and WHO‑GMP audits.

What should be included in the resume?

HPLC experience, QMS work, audit involvement, documentation handling, and calibration activities.

Summary Table

+----------------------+--------------------------------------------------+
| Company              | Swiss Parenterals Ltd                            |
+----------------------+--------------------------------------------------+
| Vacancies            | QC HPLC & QC QMS – Officer to Executive          |
+----------------------+--------------------------------------------------+
| Required Education   | B.Pharm, M.Pharm, M.Sc                            |
+----------------------+--------------------------------------------------+
| Experience           | 3–6 years QC (HPLC/QMS)                           |
+----------------------+--------------------------------------------------+