Job Opportunity: Walk-in Drive for Manufacturing & Quality Control Professionals at Intas Pharmaceuticals
Summary
Intas Pharmaceuticals Ltd is organizing a major Walk-in Drive in Baddi for experienced professionals in OSD Manufacturing, Injectable Manufacturing, and Quality Control. We are seeking skilled individuals to join our global team. This is a significant career opportunity for candidates with experience in regulated environments such as USFDA, MHRA, and EU markets.
About the Organization
Intas Pharmaceuticals Ltd is a globally recognized leader in the pharmaceutical sector, with a strong footprint in over 85 countries. Known for our commitment to quality and innovation, we provide a robust professional environment that fosters career growth and technical excellence. We are looking for dedicated talent to contribute to our mission of delivering high-quality healthcare solutions.
Event Details
- Date: 12th April 2026 (Sunday)
- Time: 9:00 AM – 5:00 PM
- Venue: Lemon Tree Hotel, NH-21A, Baddi-Nalagarh Highway, District Solan, Himachal Pradesh – 173205
Role & Qualification Breakdown
We are hiring for multiple positions including Executive, Senior Officer, Officer, and Technician. Candidates with relevant experience in the pharmaceutical industry are encouraged to attend.
| Department | Required Qualification | Relevant Experience |
|---|---|---|
| OSD Manufacturing | B.Pharm / Diploma / ITI | 3 – 10 Years |
| Injectable Manufacturing | B.Pharm / Diploma / ITI | 3 – 10 Years |
| Quality Control | M.Sc / B.Pharm | 4 – 9 Years |
Key Responsibilities
Manufacturing (OSD & Injectable)
- Execute production activities strictly adhering to Standard Operating Procedures (SOPs) and cGMP guidelines.
- Operate and manage complex formulation manufacturing processes.
- Maintain accurate and timely batch records and production documentation.
- Ensure full compliance with all internal and external regulatory standards.
Quality Control (QC)
- Conduct precise analytical testing and rigorous quality checks.
- Ensure operational compliance with USFDA, MHRA, and EU regulatory standards.
- Maintain comprehensive documentation in line with global quality standards.
- Willingness to work in a shift-based environment as required.
Required Skills & Competencies
- Strong technical knowledge of pharmaceutical manufacturing and QC processes.
- Proven experience working within regulated manufacturing plants (USFDA/MHRA/EU).
- High level of proficiency in maintaining documentation and ensuring site compliance.
- Flexibility and ability to operate effectively within rotating shift schedules.
Documents to Carry for the Interview
To ensure a smooth recruitment process, please bring the following documents:
- Updated Resume/CV.
- Originals and photocopies of all educational certificates.
- Relevant work experience documents (Experience letters/Appointment letters).
- Latest salary slips and CTC breakup details.
Important Instructions
- Exclusion Criteria: Candidates who have already appeared for an interview at Intas Pharmaceuticals in the last 6 months are not eligible to attend.
- Shift Requirement: Candidates must be comfortable with working in shifts.
- Experience: Only candidates with relevant pharmaceutical industry experience should apply.
- Transparency: Intas Pharmaceuticals Ltd does not charge any fees for recruitment. Please beware of any fraudulent agencies requesting payment for job opportunities.
We look forward to meeting passionate professionals who are ready to take the next step in their pharmaceutical career with Intas. Please ensure you reach the venue on time with all required documentation.