ODON Lifesciences Pvt. Ltd. has announced a walk-in interview for multiple departments including Production, QC, QA, Maintenance, DRA, PPIC, Safety, and Security. This is a great opportunity for candidates looking to build a career in the pharmaceutical industry with a fast-growing organization.
The company is conducting a face-to-face interview at its Dehradun facility, offering multiple openings across various roles.
Important Interview Details
Interview Date & Time
- Date: 26 April 2026 (Sunday)
- Time: 09:00 AM to 05:00 PM
Interview Venue
- ODON Lifesciences Pvt. Ltd.
- Plot No. 18A & 19, Pharmacity, Selaqui
- Dehradun โ 248011 (Uttarakhand)
Vacancy Details
Production (Tablets / Syrup / Injection)
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm / 10+2 ITI
- Experience: 2 to 5 years
- Role: Chemist / Operator
- Openings: 18
- Gender: Male
Quality Control (QC)
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
- Experience: 0 to 6 years
- Role: Jr. Officer / Sr. Executive
- Openings: 15
- Gender: Male / Female
Quality Assurance (QA)
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
- Experience: 0 to 6 years
- Role: Jr. Officer / Sr. Executive
- Openings: 8
- Gender: Male / Female
Maintenance (HVAC / Utility / Water System)
- Qualification: ITI / Diploma
- Experience: 1 to 6 years
- Role: Fitter / Operator / Executive
- Openings: 8
- Gender: Male
DRA (Regulatory Affairs)
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
- Experience: 1 to 4 years
- Role: Jr. Officer / Sr. Officer
- Openings: 5
- Gender: Male / Female
PPIC
- Qualification: MBA / BBA / BCA
- Experience: 1 to 6 years
- Role: Jr. Officer / Sr. Executive
- Openings: 8
- Gender: Male / Female
Safety
- Qualification: Graduation / Diploma
- Experience: 4 to 8 years
- Role: Sr. Executive / Assistant Manager
- Openings: 4
- Gender: Male
Security
- Qualification: Graduation / Diploma
- Experience: 4 to 8 years
- Role: Sr. Executive / Assistant Manager
- Openings: 4
- Gender: Male / Female
Roles & Responsibilities
- Handle daily production and manufacturing activities as per GMP norms
- Perform quality control and assurance testing procedures
- Maintain documentation and compliance with regulatory standards
- Ensure smooth functioning of equipment and maintenance systems
- Coordinate planning and inventory management (PPIC)
- Monitor safety practices and ensure workplace compliance
- Support regulatory documentation and submission processes
Required Qualifications
- Relevant degree or diploma as per department
- Good understanding of pharmaceutical processes and compliance
- Strong communication and teamwork skills
- Ability to work in a regulated manufacturing environment
Salary & Benefits
- Salary: โน2.0 LPA โ โน6.5 LPA (depending on role and experience)
- Additional Benefits:
- Career growth opportunities
- Exposure to pharmaceutical manufacturing environment
- Learning and development support
- Stable work environment
Documents Required
Candidates attending the interview should carry:
- Updated Resume
- Passport Size Photograph
- Educational Certificates
- Experience Certificates (if applicable)
- ID Proof
How to Apply
Interested candidates can directly walk in to the venue on the scheduled date and time. Ensure all required documents are carried for verification.
For queries, candidates may contact the company via official communication channels mentioned in the notification.

