Intas Pharmaceuticals Walk-in On 8th March for Multiple Positions

Walk in Interview For Quality Control Executive/Sr. Officer

Roles and Responsibilities

  • Conduct quality control analysis of API samples using HPLC, AMV, FP methods.
  • Ensure compliance with cGMP guidelines and regulatory requirements.
  • Develop and maintain SOPs for QC procedures and protocols.
  • Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.
  • Maintain accurate records of test results, reports, and documentation.

Desired Candidate Profile

  • 4-9 years of experience in a similar role within the pharmaceutical industry.
  • B.Pharma – Bachelor of Pharmacy degree from a recognized institution.
  • MS/M.Sc(Science) degree from a recognized institution (preferably).
  • Strong understanding of HPLC, AMV, FP techniques; knowledge of other analytical methods an added advantage.

Walk in Interview For QC- Microbiology (EM)Executive/Sr. Officer

Roles and Responsibilities

  • Conduct environmental monitoring of manufacturing areas, clean rooms, and equipment to ensure compliance with regulatory requirements.
  • Perform microbiological testing on water samples to detect contamination levels within specified limits.
  • Operate laboratory instruments such as incubators, autoclaves, and pH meters to analyze test results accurately.
  • Maintain accurate records of test data, including raw material inspection reports and batch records.
  • Participate in validation activities to ensure the effectiveness of environmental controls.

Desired Candidate Profile

  • 4-9 years of experience in EM (Environmental Monitoring) or related field.
  • B.Pharma – Bachelor of Pharmacy degree from a recognized institution.
  • MS/M.Sc(Science) degree from a recognized institution.
  • Strong knowledge of Good Manufacturing Practices (GMP), Current Good Laboratory Practice (cGMP), ISO standards.

Walk in Interview For IT Infra Executive/Sr.Officer

Administrative Activity:

  • Administrator role and manage access controls for GxP-compliant systems.
  • Maintain and continuously monitor system security controls.
  • Perform system backups, data recovery, preventive maintenance, remote access, and other SOP-related activities.
  • Diagnose and resolve operating system, network, and hardware issues related to manufacturing systems (IPC/SCADA).
  • Collaborate with shop floor users and external vendors to provide technical support and resolve issues.
  • Ensure IT infrastructure adherence to GxP regulations, including 21 CFR Part 11, EU Annex 11, and GAMP 5.
  • Act as a liaison with vendors, OEMs, and service providers for technical support and escalations.
  • Support OT cybersecurity measures and ensure compliance with data integrity standards
  • Collaborate with cross-functional teams for OT system upgrades and digital transformation projects
  • Possess 34 years of experience in the pharmaceutical industry; shop floor experience is preferred.

Relevant Functional/Technical Skills or Industry Experience

  • Windows Operating system Legacy, Embedded and Latest Operating Systems
  • Operating System Recovery and Repair
  • Optimization of Operating Systems
  • Operating System related event log analysis, error interpretations and fixes of problems
  • Network configuration and connectivity checks
  • Hardware troubleshooting:
  • RAM, Hard Disk, Processer, graphics card etc.
  • SMPS and power requirements
  • Configuration of security control, antivirus configuration, exclusions

Relevant Skills & Experience:

  • Strong analytical & problem-solving abilities
  • Coordination with stakeholder and vendors & teamwork
  • Communication and documentation skills
  • Attention to detail and safety compliance

Relevant Professional / Educational Background:

  • Bachelors degree in Computer Technology.
  • Certification in Hardware, Networking, and/or Operating Systems.
  • 4-10 years of experience in Manufacturing IT support, including work with OT systems and administrative responsibilities.

Walk in Interview For OSD Manufacturing Sr. Officer/Officer/Technician

Roles and Responsibilities

  • Operate granulation, compression, coating, capsule filling machines to produce high-quality tablets.
  • Ensure compliance with GMP guidelines and maintain accurate records of production batches.
  • Conduct regular cleaning and sanitizing of equipment to prevent contamination.
  • Collaborate with team members to resolve issues related to machine malfunction or product quality.
  • Maintain a clean and organized work environment, adhering to safety protocols.

Batch Execution

  • Perform batch activities for Granulation, Compression, Coating, and Blending as per BMR/BPR.
  • Conduct in-process checks and record results accurately.
  • Ensure correct equipment setup, parameter settings, and operation.

Equipment Handling

  • Operate and handle key OSD equipment:
    RMG, FBD, Compression Machine, Auto-Coater, Sifter, Blender, Metal Detector.
  • Perform equipment cleaning, changeover, and verification as per SOPs.

Documentation

Maintain real-time and error-free documentation (BMR, logbooks, online entries).

  • Follow GDP practices strictly.
  • Assist in deviation reporting, change control, and CAPA inputs.

Quality & Compliance

  • Ensure production activities comply with cGMP, regulatory, and safety requirements.
  • Coordinate with QA/QC for line clearance, sampling, and IPC checks.
  • Support during audits and inspections (internal/external).

Desired Candidate Profile

  • 3-10 years of experience in OSD manufacturing (granulation, compression, coating) with expertise in solid oral products.
  • B.Pharma – Bachelor of Pharmacy degree from an accredited institution.
  • Diploma/ITI qualification preferred but not mandatory.

Time and Venue

8th March , 9.00 AM – 4.30 PM

Pride Plaza Hotel Ahmedabad Judges Bungalow Rd, off Sarkhej – Gandhinagar Highway, Bodakdev, Ahmedabad, Gujarat 380054  (View on map)

SWARNALATHA B

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