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Micro Labs Announces Walk-In Drive for Pharma Professionals at Bangalore Facility
Micro Labs Limited, a prominent name in the Indian pharmaceutical industry, has announced a two-day walk-in interview event for aspiring candidates looking to launch or advance their careers in pharmaceutical manufacturing. The drive will be held at the company’s state-of-the-art facility in Veerasandra, Bangalore.
This initiative aims to recruit fresh talent and experienced professionals for roles in core manufacturing departments, offering a chance to join a “well-equipped and progressive organization.”
Vacancy Details: Positions and Requirements
The company is looking to fill multiple positions across two primary roles. The details are as follows:
1. Position: Trainees / Officers
Departments: Compression, Capsule Filling, Inspection
Required Qualification: B.Sc or B.Pharma
Required Experience: 0 to 3 years
Essential Skills:
· Knowledge of the tablet manufacturing process.
· Understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
· Good communication skills.
2. Position: Technical Staff / Operators
Departments: Granulation, Compression
Required Qualification: B.Sc, ITI, or Diploma
Required Experience: 0 to 3 years
Essential Skills:
· Hands-on experience in operating various pharmaceutical manufacturing equipment.
Walk-In Interview Schedule
Dates: Wednesday, 5th November 2025 & Thursday, 6th November 2025
Time: 9:00 AM to 12:30 PM
Venue: Micro Labs Limited (ML11), #16 & 24, Veerasandra Industrial Area, Electronic City Phase–2, Bangalore – 560100.
How to Apply?
Interested and eligible candidates are invited to walk in directly to the venue on the specified dates and times. There is no need for prior registration or appointment. Candidates should carry multiple copies of their updated resume, along with original and photocopies of their educational certificates, experience letters, and other relevant documents.
For any queries, prospective applicants can contact the HR team via email at veerhr@microlabs.in.
A Gateway to a Pharma Career
This recruitment drive presents a significant opportunity for graduates and diploma holders to build a career with an established pharmaceutical giant. Successful candidates will gain exposure to modern manufacturing processes and stringent quality standards in a dynamic work environment.
FAQ:
1. What is the role of compression in tablet manufacturing?
Answer:
Compression is a critical stage in tablet manufacturing where granulated material is compressed into solid tablets using a tablet press machine. Parameters like tablet weight, hardness, thickness, and disintegration time are monitored to ensure consistency. Operators must ensure that machine settings, tooling, and environmental conditions are optimized for uniform tablet quality.
2. What are the key GMP (Good Manufacturing Practice) requirements in the production area?
Answer:
Key GMP requirements include maintaining cleanliness and hygiene, ensuring proper documentation (batch records, logbooks), avoiding cross-contamination, calibrating instruments regularly, and wearing appropriate PPE (Personal Protective Equipment). All manufacturing activities must be recorded in real time as per GDP (Good Documentation Practices).
3. How does the capsule filling process work?
Answer:
The capsule filling process involves dosing powders, granules, or pellets into empty hard gelatin or HPMC capsules. The capsule filling machine operates in multiple stations — including capsule separation, powder filling, tamping, sealing, and ejection. Operators need to check weight variation, capsule integrity, and machine parameters frequently to maintain batch uniformity.
4. What parameters are controlled during the granulation process?
Answer:
In granulation (either wet or dry), key parameters include binder concentration, mixing time, impeller speed, drying temperature, and final moisture content. Proper control ensures uniform granule size, flowability, and compressibility — all essential for producing tablets of consistent quality during compression.
5. What common in-process checks are performed in the production department?
Answer:
In-process checks include monitoring parameters like tablet weight variation, hardness, thickness, disintegration time, capsule weight, and appearance. For granulation, checks may involve bulk density and moisture content. These tests ensure each batch meets defined quality specifications before proceeding to the next stage.
