Torrent walk-in QC, QA & Packing
- Company Overview
- Job Role & Responsibilities
- Quality Control (QC – Analytical Testing)
- Quality Assurance (QA – IPQA & Stability)
- Packing (Formulation – Solid Orals)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why This Opportunity Stands Out
- FAQs
- Summary Table
BPharm MPharm QC QA Jobs Torrent Baddi Hiring
Torrent Pharma hiring QC, QA & Packing roles in Baddi. BPharm, MPharm, MSc with 2–6 yrs experience. Multiple vacancies open.
Torrent Pharmaceuticals Ltd. is conducting a walk-in drive for multiple vacancies across Quality Control, Quality Assurance, and Packing (Formulation) departments at its Baddi, Himachal Pradesh manufacturing facility. The company is hiring Technical Assistant and Executive level professionals with 2 to 6 years of experience in pharmaceutical manufacturing and quality systems.
This opportunity is highly suitable for candidates with strong experience in analytical testing, IPQA activities, stability studies, and regulatory compliance within USFDA-approved facilities. Professionals looking to grow in pharma quality control jobs, GMP compliance roles, and formulation manufacturing careers will find this role highly aligned with long-term industry demand.
Company Overview
Torrent Pharmaceuticals Ltd. is one of India’s leading pharmaceutical companies with a strong global presence across regulated and semi-regulated markets including USFDA, MHRA, and ANVISA. The company is known for its high-quality manufacturing standards, innovation-driven research, and strong compliance culture.
The Baddi manufacturing unit is a key formulation facility that adheres to international regulatory standards and produces high-quality solid oral dosage forms. Torrent Pharma’s commitment to quality, patient safety, and continuous improvement makes it a trusted employer in the pharmaceutical industry.
Working at Torrent offers professionals exposure to global regulatory frameworks, advanced manufacturing technologies, and structured career growth in pharma production, QA, and QC domains.
Job Role & Responsibilities
Quality Control (QC – Analytical Testing)
- Perform analysis of finished products, raw materials, stability samples, and packaging materials
- Execute analytical method validation, verification, and method transfer activities
- Operate and troubleshoot analytical instruments such as HPLC, GC, UV, IR, Polarimeter, and dissolution apparatus
- Interpret analytical data and support investigation of OOS, OOT, and deviations
- Maintain laboratory documentation in compliance with GLP and cGMP guidelines
- Ensure adherence to regulatory standards including USFDA, MHRA, ANVISA, and ICH guidelines
Quality Assurance (QA – IPQA & Stability)
- Monitor manufacturing processes and ensure compliance with cGMP standards
- Perform line clearance, batch record review, and in-process quality checks (IPQC)
- Manage stability studies as per ICH guidelines (Q1A–Q1F)
- Investigate OOS, OOT, deviations, and coordinate corrective actions
- Ensure documentation and audit readiness for regulatory inspections
- Collaborate with production and QC teams for quality improvement initiatives
Packing (Formulation – Solid Orals)
- Handle blister, strip, and autocartonator packing machines
- Manage packaging operations including serialization and track & trace systems
- Handle market complaints, deviations, and validation/qualification activities
- Maintain documentation and SAP entries related to packing processes
- Ensure compliance with GMP and regulatory requirements
Eligibility / Qualifications
Candidates must have completed:
B.Pharm, M.Pharm, M.Sc
Relevant courses include: Pharmaceutical Analysis, Pharmaceutics, Organic Chemistry, Quality Assurance, Drug Regulatory Affairs, Industrial Pharmacy, Production Technology
- Experience: 2 to 6 years in pharmaceutical manufacturing or quality roles
- Strong knowledge of cGMP, GLP, and regulatory compliance standards
- Experience in USFDA-approved or regulated plants preferred
- Hands-on experience with analytical instruments and manufacturing systems required
- Knowledge of SAP and documentation systems is an added advantage
Location & Salary
- Job Location: Torrent Pharmaceuticals Ltd., Baddi, Himachal Pradesh
- Walk-In Date: 19 April 2026 (Sunday)
- Time: 9:30 AM to 2:30 PM
- Salary: Competitive salary as per industry standards and candidate experience
Application Process
Candidates can attend the walk-in interview directly at the venue:
Venue Address:
Torrent Pharmaceuticals Ltd.
Near Baddi University, Village Bhud, Makhnu Majra, Tehsil Baddi, District Solan, Himachal Pradesh – 173205
Contact Details:
- Email: shilpathakur@torrentpharma.com
- Phone: 9805808451
Important Instructions:
- Carry updated resume, passport-size photograph, and academic certificates
- Bring latest CTC breakup and previous employment documents
- Candidates with regulatory plant experience will be preferred
- If unable to attend, candidates can apply via email
Why This Opportunity Stands Out
- Work with a globally recognized pharmaceutical company
- Exposure to regulated markets like USFDA, MHRA, and ANVISA
- Hands-on experience in QC, QA, and formulation packing operations
- Strong career growth in pharmaceutical manufacturing and quality domains
- Opportunity to contribute to high-quality medicine production
FAQs
Who can apply for these roles?
Candidates with B.Pharm, M.Pharm, or M.Sc and relevant experience can apply.
Is regulatory experience required?
Yes, candidates with experience in USFDA or regulated plants are preferred.
What roles are available?
Quality Control, Quality Assurance, and Packing roles.
What is the experience requirement?
2 to 6 years in pharmaceutical industry.
How to apply?
Attend the walk-in interview or send your resume via email.
Summary Table
| Category | Details |
|---|---|
| Company | Torrent Pharmaceuticals Ltd. |
| Vacancies | QC Executive, QA Executive, Packing Executive, Technical Assistant |
| Required Education | B.Pharm, M.Pharm, M.Sc |
| Experience | 2 to 6 Years |

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