Intas Pharmaceuticals, a leading multinational pharmaceutical company, invites highly skilled and motivated professionals to join our growing team. We are a global organization with a presence in over 85 countries, boasting a remarkable 20% compound annual growth rate (CAGR). A significant portion of our revenue (approximately 70%) originates from highly regulated international markets, including the EU and US. At Intas, we are dedicated to creating a world of good health, happiness, and hope. We are committed to innovation, quality, and patient well-being, making us an ideal employer for ambitious individuals who share our values.
Walk-in Interview Details:
This is your chance to be part of a dynamic and expanding organization. We are holding a walk-in interview specifically for our Matoda facility. This presents a unique opportunity to meet our team, learn more about our exciting projects, and explore potential career paths within Intas Pharmaceuticals.
- Date: Saturday, April 26th, 2025
- Time: 9:30 AM to 2:00 PM
- Venue: Intas Pharmaceuticals Ltd., Matoda, Plot No. 457, 458, Sarkhej Bavla Highway, Matoda Village, Sanand Taluka, Ahmedabad, Gujarat – 382210
Available Positions:
We are currently recruiting for several key roles across various departments. Detailed information about each position is provided below. All positions offer competitive salaries and benefits packages. We are an equal opportunity employer, committed to diversity and inclusion.
1. Quality Assurance (QA) – Multiple Positions
- Job Titles: Officer, Senior Officer, Executive, Senior Executive
- Departments: IPQA (Injectable), IPQA (OSD), QMS, Documentation, Validation, and Qualification
- Qualifications: B.Pharm, M.Pharm, M.Sc.
- Experience: 2 to 9 years of relevant experience in a pharmaceutical QA environment. Experience within a cGMP-compliant facility is highly desirable. Strong knowledge of cGMP norms and laboratory safety protocols is essential.
Key Responsibilities (QA):
- Ensure compliance with cGMP regulations and internal quality standards.
- Develop and implement quality systems and procedures.
- Conduct internal audits and inspections.
- Investigate quality deviations and CAPA (Corrective and Preventive Actions).
- Manage documentation and records.
- Participate in validation and qualification activities.
2. Oral Solid Dosage (OSD) Manufacturing – Multiple Positions
- Job Titles: Senior Officer, Officer, Associate
- Departments: OSD Manufacturing, Dispensing, QMS
- Qualifications: B.Sc, M.Sc, B.Pharm, M.Pharm, Diploma (relevant field)
- Experience: 1 to 5 years of experience in OSD manufacturing, dispensing, or quality management within a pharmaceutical setting. Experience working in a regulated environment is a plus.
Key Responsibilities (OSD):
- Execution of manufacturing processes related to oral solid dosage forms.
- Adherence to cGMP guidelines and quality standards.
- Accurate record keeping and documentation.
- Participation in continuous improvement initiatives.
- Collaboration with other departments to ensure smooth operations.
3. Injectable Manufacturing – Multiple Positions
- Job Titles: Senior Officer, Officer, Associate
- Departments: Injectable Manufacturing (Aseptic Operations), QMS, SKID, Multi-vessel, SVP
- Qualifications: B.Pharm, M.Pharm, M.Sc, B.Sc, Diploma (relevant field)
- Experience: 1 to 5 years of experience in aseptic manufacturing, quality management, or related areas within the pharmaceutical industry. Experience with SKID systems, multi-vessel operations, or SVP (Single Use Technology) is beneficial.
Key Responsibilities (Injectable):
- Maintaining the highest standards of aseptic technique during manufacturing processes.
- Operating and maintaining injectable manufacturing equipment.
- Ensuring compliance with relevant regulations and guidelines.
- Proactively identifying and addressing potential risks.
- Adhering to strict quality control procedures.
4. Quality Control (QC) – Multiple Positions
- Job Titles: Officer, Senior Officer, Executive
- Department: Quality Control
- Qualifications: B.Sc, M.Sc (Organic Chemistry/Analytical Chemistry), B.Pharm, M.Pharm
- Experience: 2 to 7 years of experience in a pharmaceutical QC laboratory. Experience with analytical techniques relevant to pharmaceutical analysis is a must.
Key Responsibilities (QC):
- Perform analytical testing of raw materials, in-process materials, and finished products.
- Maintain and calibrate laboratory equipment.
- Review and interpret analytical data.
- Ensure compliance with regulatory requirements.
- Contribute to continuous improvement initiatives.
Important Information for Applicants:
- Please bring your updated resume, all educational certificates, experience documents, and salary expectations to the interview.
- Candidates who have interviewed at Intas within the past six months are kindly requested not to re-apply.
- Job Location: Ahmedabad, Gujarat
Note: Intas Pharmaceuticals Ltd. does not charge any fees for job applications, processing, training, or testing. Beware of fraudulent invitations.
We look forward to meeting you and discussing your career aspirations at Intas Pharmaceuticals. Apply now and take the next step in your pharmaceutical career journey!
