Swiss Hiring QC (QMS) Sr. Officer/Executive
- Company Overview
- Job Role & Responsibilities
- Position: Sr. Officer / Executive — Quality Control (QMS)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why this role matters (EEAT alignment)
- High‑Value Keywords Included Naturally
- FAQs
M.Pharm/B.Pharm QC (QMS) Sr. Officer — Ahmedabad
M.Pharm/B.Pharm/M.Sc — QC (QMS) Sr. Officer/Executive — 3–6 yrs — Ahmedabad. Apply to drive quality in WHO-GMP plants.
Swiss Pharmaceuticals is hiring experienced Quality Control (QMS) professionals for its Ahmedabad manufacturing cluster. These roles (Sr. Officer to Executive) are designed for candidates with 3–6 years of hands-on QC experience who can manage QMS activities, analytical testing, and regulatory documentation in WHO‑GMP and cGMP environments.
Company Overview
Swiss operates multiple world-class manufacturing facilities in Ahmedabad that follow cGMP and WHO‑GMP standards. The company maintains ISO 9001 certification and complies with EU, US FDA, TGA, and MCC regulatory frameworks. Working here gives you exposure to regulated-market expectations, rigorous audit readiness, and cross-functional collaboration across R&D, QC, QA, and production.
Job Role & Responsibilities
Position: Sr. Officer / Executive — Quality Control (QMS)
You will be responsible for maintaining laboratory integrity, supporting product release, and strengthening the quality management system.
Key responsibilities:
- Enforce Good Laboratory Practices (GLP) and Good Documentation Practices (GDP).
- Perform routine and stability analytical testing (HPLC, GC, UV, KF, dissolution, titrations) and prepare accurate test reports.
- Review and approve specifications, STPs, validation protocols, and test methods using basic statistical tools.
- Develop, update, and implement SOPs to align with GMP and regulatory requirements.
- Lead training sessions to build QC competency and ensure adherence to procedures.
- Manage instrument IQ/OQ/PQ records, preventive maintenance schedules, and calibration activities.
- Review raw data and approve Certificates of Analysis (CoAs) after verification.
- Investigate OOS/OOT events, lab incidents, deviations, change controls, and propose CAPA with root-cause analysis.
- Support internal and external regulatory audits; prepare responses and close observations.
- Coordinate with QA, Production, and QC teams to ensure timely batch release and control sample management.
This role requires technical ownership, strong documentation discipline, and a problem-solving mindset.
Eligibility / Qualifications
- Education: M.Pharm / B.Pharm / M.Sc (Chemistry / Pharmaceutical Sciences / Analytical Chemistry).
- Experience: 3–6 years in pharmaceutical Quality Control, preferably in WHO‑GMP or US‑FDA regulated facilities.
- Technical skills: Practical experience with HPLC/GC/UV/KF/dissolution, method validation basics, stability studies, and lab data review.
- Soft skills: Clear written and verbal communication, training ability, critical thinking, and teamwork.
Relevant courses (comma-separated): M.Pharm Pharmaceutical Analysis, B.Pharm, M.Sc Analytical Chemistry, PG Diploma in Quality Assurance, Diploma in Pharmaceutical Quality Management, Certificate in HPLC Techniques
Location & Salary
- Location: Ahmedabad (multiple Swiss manufacturing units).
- Salary: Competitive and commensurate with experience; details shared during interview.
- Work model: On-site; subject to plant scheduling and shift requirements for IPQA support.
Application Process
Send your updated resume to: Recruitment@swiss.in
Email subject suggestion: Application — QC (QMS) Sr. Officer/Executive — [Your Name]
Include:
- Brief summary of QC responsibilities (instrumentation, validations, stability work)
- Notice period and expected CTC
- Any regulatory audit exposure (USFDA/MHRA/EU/ANVISA/TGA)
Visit: https://www.swiss.in for company details.
Why this role matters (EEAT alignment)
Quality Control and QMS functions ensure products meet safety, efficacy, and regulatory expectations before they reach patients. Working at Swiss exposes you to high‑standards laboratory practices and regulatory interactions that build professional authority and trust — core pillars of EEAT. Your analytical accuracy and CAPA ownership will directly impact product release timelines and patient safety.
High‑Value Keywords Included Naturally
pharmaceutical QC jobs, quality control analyst, HPLC analyst jobs, QC stability study jobs, QA/QC compliance, GMP laboratory jobs, regulatory audit preparation.
FAQs
Q: What instruments should I be familiar with?
A: Familiarity with HPLC, GC, UV, Karl Fischer, dissolution apparatus, and routine analytical instruments is expected.
Q: Is regulatory audit experience mandatory?
A: Preferred but not mandatory. Candidates with USFDA/MHRA/EU audit exposure will be prioritized.
Q: Will this role involve shift work?
A: Some IPQA coordination or sample handling may require flexibility; primary work is site‑based day shifts unless otherwise specified.
Q: How quickly will Swiss respond?
A: Shortlisted candidates will be contacted for interviews; include your availability to speed up processing.
| Category | Details |
|---|---|
| Company | Swiss — Ahmedabad manufacturing cluster |
| Vacancies | Sr. Officer / Executive — Quality Control (QMS) |
| Required Education | M.Pharm, B.Pharm, M.Sc (Chemistry/Pharma) |
| Experience | 3–6 Years in QC (WHO‑GMP/regulated plants) |
To apply for this job email your details to Recruitment@swiss.in
