Cadila Pharmaceuticals, a ‘Great Place to Work’, Announces Major Hiring Drive at Dholka Plant
Cadila Pharmaceuticals Limited, a renowned name in the Indian pharmaceutical industry and a certified Great Place to Work, has announced a significant recruitment drive for its Dholka Plant. The company is seeking skilled and experienced professionals to join its team across key operational departments, including Production, Packing, and Engineering.
This initiative presents a valuable opportunity for both technical and degree-holding candidates to build a career with an established industry leader. The open positions cater to a wide range of experience levels, from 1 to 7 years.
Detailed Job Openings
Prospective applicants can find a breakdown of the available positions below, organized by department.
1. Engineering Department
The Engineering department is looking for qualified individuals to maintain and manage its pharmaceutical process equipment.
· Position: Fitter/Electrician (Plant Maintenance/Process Equipment)
· Qualification: ITI/Diploma
· Experience: 3 to 7 years
· Note: Candidates must have specific experience in Pharma Parenteral & OSD Process Equipment.
· Position: Officer to Executive
· Qualification: BE/B.Tech in Mechanical/Electrical
· Experience: 3 to 7 years
· Note: Requires more than 3 years of experience in the Pharma Parenteral & OSD Block Area.
2. Production Department (OSD & Injectable)
The Production department has multiple vacancies in both Oral Solid Dosage (OSD) and Injectable (Parenteral) manufacturing units.
· Position: Officer to Executive
· Qualification: B.Pharm
· Experience: 2 to 7 years
· Section: Granulation / Compression / Coating
· Note: Pharma OSD Experience Only.
· Position: Technical Assistant / Operator
· Qualification: ITI/Diploma
· Experience: 1 to 3 years
· Section: Granulation, Coating, Compression, Capsule
· Note: Pharma OSD Experience Only.
· Position: Technical Assistant / Operator (Injectable)
· Qualification: ITI/Diploma
· Experience: 1 to 3 years
· Section: Ampoule Filling / Autoclave / Filling & Sealing
· Note: Pharma Injectable Experience Only.
3. Central Packing Department
The Central Packing unit is also seeking to expand its team.
· Position: Technical Assistant / Operator
· Qualification: ITI/Diploma
· Experience: 2 to 6 years
· Section: Blister/Strip
· Note: Pharma OSD Experience Only.
How to Apply?
Interested and eligible candidates are encouraged to get in touch with the Human Resources team at Cadila Pharmaceuticals. The company has provided the following contact details for applications and inquiries:
· Sanjay Makwana (HR)
· Email: sanjay.makwana@cadilapharma.com
· Phone: 8347434234
· Harsh Barot (HR)
· Email: barot.harsh@cadilapharma.com
· Phone: 9724048678
Please Note: Prospective applicants are requested to call only between 9:00 AM to 5:00 PM.
A Premier Workplace in Pharma
Cadila Pharmaceuticals’ “Great Place to Work” certification underscores its commitment to fostering a positive, rewarding, and professional work environment. For skilled individuals in the pharmaceutical manufacturing sector, this hiring drive represents a chance to contribute to a company known for its high standards and employee-centric culture. With a clear emphasis on specific, relevant experience in OSD and Injectable processes, Cadila is looking for professionals who can hit the ground running and support its critical manufacturing operations.
FAQ:
1. What types of process equipment are used in the OSD and Injectable manufacturing units at Cadila Pharmaceuticals?
Answer:
In the OSD (Oral Solid Dosage) unit, major equipment includes Fluid Bed Processor (FBP), Multi Mill, Rapid Mixer Granulator (RMG), Compression Machines, Auto Coaters, Capsule Filling Machines, and Blister/Strip Packing Machines.
In the Injectable (Parenteral) unit, key equipment includes Ampoule/Vial Filling Lines, Autoclaves, Sterilizers, Sealing Machines, and Laminar Air Flow Units used under aseptic conditions.
2. What are the critical parameters to monitor during the granulation process in OSD manufacturing?
Answer:
The key parameters include impeller speed, chopper speed, binder addition rate, granulation endpoint moisture content, and mixing time. Maintaining uniform granule size and moisture is essential for achieving consistent tablet compression and dissolution properties.
3. How is preventive maintenance carried out for pharmaceutical process equipment in the Engineering Department?
Answer:
Preventive maintenance involves scheduled inspection, lubrication, calibration, and replacement of worn parts before failure. Activities include checking bearing conditions, tightening fasteners, validating equipment calibration, and maintaining maintenance logs as per GMP compliance. This ensures minimal downtime and compliance with audit standards.
4. What GMP (Good Manufacturing Practice) considerations are critical during the packing of OSD products?
Answer:
GMP considerations include line clearance before batch start, proper labeling and coding, visual inspection of packed units, reconciliation of printed materials, and documentation in BPR (Batch Production Record). Additionally, temperature and humidity control in the packing area are essential for product stability.
5. What is the difference between terminal sterilization and aseptic processing in injectable manufacturing?
Answer:
In terminal sterilization, the final product is sterilized in its final container (e.g., using an autoclave).
In aseptic processing, sterile components (drug, container, closure) are assembled in a sterile environment without final sterilization. Aseptic processing requires higher environmental controls (Grade A/B cleanrooms) and continuous monitoring of microbial load.
