Intas Pharmaceuticals Walk-In Interview for QC, QA, Production, and Engineering Roles in Chandigarh

Join Intas Pharmaceuticals Ltd., a global pharmaceutical leader founded in 1977, headquartered in Ahmedabad, India. With a 20% CAGR and presence in 85+ countries, Intas generates 70% of its revenue from regulated markets like the EU and US. Certified as a Great Place to Work, our USFDA, UK MHRA, WHO-GMP, and PICS-approved facilities produce sterile injectables, tablets, and more.

We’re hosting a walk-in interview in Chandigarh for Quality Control (QC), Quality Assurance (QA), Tablet Packing, Sterile/Injectable Manufacturing, and Engineering roles at our Ahmedabad facility, targeting candidates with 2-15 years of experience in regulated pharma plants.

Event Details: Walk-In Interview

Our walk-in interview seeks professionals for multiple departments at our Ahmedabad formulation plant. Candidates must have experience in USFDA/MHRA-regulated facilities, be open to shift duties, and not have interviewed with Intas in the last six months.

Date and Time

• Date: Sunday, May 18, 2025
• Time: 9:00 AM – 2:00 PM IST

Venue

Hotel Solitaire
SCO 902-903, Housing Board Chowk, NAC, Manimajra, Chandigarh – 160101

Job Location

• Intas Pharmaceuticals Ltd., Plot No. 457/458, Matoda Village, Sarkhej-Bavla Highway, Ahmedabad, Gujarat – 382210

Job Opportunities at Intas Pharmaceuticals

We’re hiring for roles in Quality Control, Quality Assurance, Tablet Packing, Sterile/Injectable Manufacturing, and Engineering (Sterile Plant Maintenance). All positions require experience in regulated plants (USFDA, MHRA, EU) and formulation pharma exposure.

1. Quality Control & Microbiology (QC-FG/Stability/AMV/Microbiology)

• Position: Officer to Executive
• Qualification: M.Sc. (Chemistry, Microbiology), B.Pharm, M.Pharm
• Experience: 2-7 years
• Openings: Multiple (likely 5-8 based on department scope)

Key Responsibilities:

• Perform finished product, stability, and AMV testing using HPLC and GC
• Handle microbiology tasks (e.g., microbial limit tests, environmental monitoring)
• Use Chromeleon software for data analysis
• Document results per GLP
• Support OOS/OOT investigations and CAPA

Key Skills:

• Proficiency in HPLC, GC, and Chromeleon software
• Knowledge of microbiology testing and AMV per ICH Q2(R1)
• Experience in USFDA/MHRA-regulated QC labs

2. Quality Assurance (IPQA/Qualification – Sterile/Lab QA)

• Position: Officer to Executive
• Qualification: B.Pharm, M.Pharm, M.Sc.
• Experience: 2-7 years
• Openings: Multiple (likely 3-6 based on sterile focus)

Key Responsibilities:

• Conduct IPQA for sterile manufacturing (PFS, vials)
• Oversee sterile equipment/process qualification and validation
• Manage QMS (deviations, CAPA, change controls)
• Review lab QA data and ensure cGMP compliance
• Prepare for USFDA/MHRA audits

Key Skills:

• Expertise in sterile IPQA and qualification
• Knowledge of cGMP and QMS in regulated plants
• Strong documentation and audit readiness

3. Tablet Packing (Primary & Secondary Packing)

• Position: Technician to Officer
• Qualification: ITI, Diploma Engineering, D.Pharm, B.Pharm
• Experience: 2-5 years
• Openings: Multiple (likely 4-7 based on packing lines)

Key Responsibilities:

• Operate CAM HV1 carton packing machines
• Perform track & trace and secondary packing activities
• Complete online documentation (BPCR, logbooks)
• Ensure packing compliance with cGMP

Key Skills:

• Knowledge of primary/secondary packing and track & trace
• Familiarity with CAM HV1 machines
• Precision in BPCR/logbook documentation

4. Engineering (Plant Maintenance – Sterile & Instrumentation)

• Position: Technician to Assistant Manager
• Qualification: ITI, Diploma Engineering, B.Tech
• Experience: 2-15 years
• Openings: Multiple (likely 3-5 based on maintenance needs)

Key Responsibilities:

• Perform preventive/corrective maintenance on sterile plant equipment
• Handle instrumentation (e.g., PLC, sensors) in sterile areas
• Ensure equipment uptime and cGMP compliance
• Document maintenance per SOPs

Key Skills:

• Expertise in sterile plant maintenance and instrumentation
• Knowledge of PLC and cGMP
• Troubleshooting and documentation skills

5. Sterile/Injectable (Manufacturing & Packing)

• Position: Technician/Operator to Senior Officer
• Qualification: ITI, Diploma Engineering, D.Pharm, B.Pharm, M.Pharm
• Experience: 2-6 years
• Openings: Multiple (likely 6-10 based on sterile operations)

Key Responsibilities:

• Operate complex skid, NDOS, and aseptic systems (PFS, vials, liquids)
• Manage autoclave, lyophilizer, and batch manufacturing
• Perform sterile secondary packing, track & trace, and visual inspection
• Complete BMR/BPR documentation

Key Skills:

• Expertise in aseptic processing and sterile manufacturing
• Knowledge of autoclave, lyophilizer, and track & trace
• Precision in BMR/BPR and cGMP compliance

Qualifications and Experience

Department	Position	Qualification	Experience	Key Skills
QC & Micro	Officer to Executive	M.Sc., B.Pharm, M.Pharm	2-7 years	HPLC, GC, Chromeleon, Microbiology
QA (IPQA/Qualification)	Officer to Executive	B.Pharm, M.Pharm, M.Sc.	2-7 years	Sterile IPQA, QMS, Audits
Tablet Packing	Technician to Officer	ITI, Diploma, D.Pharm, B.Pharm	2-5 years	CAM HV1, Track & Trace, BPCR
Engineering (Sterile)	Technician to Asst. Manager	ITI, Diploma, B.Tech	2-15 years	Plant Maintenance, Instrumentation
Sterile/Injectable	Technician to Sr. Officer	ITI, Diploma, D.Pharm, B.Pharm, M.Pharm	2-6 years	Aseptic Processing, Lyophilizer

Why Join Intas Pharmaceuticals?

Intas, with 18,000+ employees and ₹8,000 Cr revenue, is a top-tier pharma company, ranked 11th globally for generics. Rated 3.9/5 on AmbitionBox for culture, our Ahmedabad facility supports sterile injectables and tablets for 85+ countries. Employees value USFDA/MHRA exposure but note shift-based challenges. Our Great Place to Work certification reflects a commitment to employee well-being.

Key Benefits

• Work in a USFDA-approved sterile facility
• Support global markets with innovative formulations
• Gain expertise in HPLC, QMS, and aseptic systems
• Join a 47-year legacy in Ahmedabad’s pharma hub
• Access growth opportunities in a diverse workforce

How to Prepare for the Interview

Candidates must bring:

• Updated resume (original and photocopy)
• Educational certificates (final year mark sheets, degree)
• Experience letters and last 3 months’ salary slips
• CTC breakup and Aadhar/PAN cards (original and photocopy)
• Preparation:
  • QC/Micro: Review HPLC, GC, Chromeleon, and microbiology
  • QA: Study sterile IPQA, QMS, and audit readiness
  • Tablet Packing: Understand CAM HV1 and track & trace
  • Engineering: Prepare for sterile maintenance and PLC
  • Sterile/Injectable: Focus on aseptic processing and lyophilizer
• Note: Candidates interviewed in the last 6 months should not apply. Intas does not charge recruitment fees; verify communications via @intaspharma.com emails. Shift work and regulated plant experience required.

Application Process

• Attend the walk-in interview on May 18, 2025, from 9:00 AM to 2:00 PM at Hotel Solitaire, Chandigarh
• Arrive by 9:00 AM for registration; late entries not permitted
• Expect:
  • Written test (technical and aptitude)
  • Technical interview (HPLC, QMS, aseptic systems)
  • HR discussion (shifts, joining timeline)

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About Intas Pharmaceuticals

Intas operates 14 formulation plants, with Ahmedabad as a hub for sterile injectables and tablets. Serving 85+ countries, we produce biosimilars, generics, and APIs, with ISO 9001:2015 certification. Our 20% CAGR and Great Place to Work status reflect our global impact and employee-centric culture.

Our Mission

• Create a world of health, happiness, and hope
• Deliver innovative formulations with cGMP excellence
• Foster a diverse, inclusive workplace

Attend the walk-in interview on May 18, 2025, at Chandigarh to join Intas Pharmaceuticals in Ahmedabad. Advance your career with a global pharma leader!