Walk-In Interview for in Multiple Departments at Intas Pharma

Intas Pharmaceuticals is a healthcare company headquartered in Ahmedabad, India, with a history spanning three decades. They specialize in a wide range of formulations, from tablets to injectables to newer drug delivery systems, to meet the needs of people suffering from different ailments.

Intas has gained recognition globally and is currently ranked 17th among Indian pharma majors. They have expertise in Research and Development, patents and ANDA filing, NDDS, quality manufacturing support, and have received approvals by regulatory authorities of many countries, making them a reliable global healthcare provider.

Intas Pharmaceuticals has pioneered efforts in providing medications for both chronic and acute medical conditions. They have always prioritized the health and well-being of patients and have been committed to living up to their corporate line, Expressions for a Healthy Life.

Position: Executive to Assistant Manager

Qualifications:

• B.Pharma/M.Pharm/M.Sc in a relevant field

Experience:

• 5 to 8 years of experience in the relevant field
• Experience in all possible data integrity, EBMR, document, logbooks, handling of paper, audit trail vs actual execution at site
• Good regulatory audit exposure

As an Executive to Assistant Manager in the Data Integrity Cell, the responsibilities may include:

• Ensuring data integrity and compliance with relevant regulations and guidelines
• Reviewing and approving documents related to data integrity
• Conducting audits and investigations related to data integrity
• Collaborating with other departments to ensure data integrity throughout the organization
• Developing and implementing policies and procedures related to data integrity
• Providing training to staff on data integrity and compliance matters

Position: Executive to Assistant Manager

Qualifications:

• B.Pharma/M.Pharm/M.Sc in a relevant field

Experience:

• 5 to 8 years of experience in the relevant field
• Experience in checking compliance with 21 CFR instruments and equipment
• Experience in activating policies related to 21 CFR Part 11
• Experience in periodic audit trial reviews related to 21 CFR Part 11

As an Executive to Assistant Manager in the 21 CFR Part 11 Compliance department, the responsibilities may include:

• Ensuring compliance with 21 CFR Part 11 regulations and guidelines
• Developing and implementing policies related to 21 CFR Part 11 compliance
• Reviewing and approving documents related to 21 CFR Part 11 compliance
• Conducting periodic audit trial reviews to ensure compliance
• Collaborating with other departments to ensure compliance with 21 CFR Part 11 regulations and guidelines
• Providing training to staff on 21 CFR Part 11 compliance matters

Position: Officer to Executive

Qualifications:

• B.Pharma/M.Pharm in a relevant field

Experience:

• 2 to 8 years of experience in IPQA Parenteral & Solid Oral Manufacturing & Packing

As an Officer to Executive in the IPQA Parenteral & Solid Oral Manufacturing & Packing department, the responsibilities may include:

• Performing in-process quality checks during manufacturing and packing of parenteral and solid oral products
• Reviewing batch records and ensuring compliance with standard operating procedures (SOPs), current Good Manufacturing Practices (cGMP), and other regulatory requirements
• Conducting line clearance and in-process checks to ensure equipment and production areas are clean and ready for use
• Assisting in investigations of deviations or non-conformances and identifying corrective and preventive actions

Position: Officer to Executive

Qualifications:

• B.Pharma/M.Pharm/B.Tech in a relevant field

Experience:

• 2 to 8 years of experience in the Qualification/Validation section in QA Parenteral Manufacturing

As an Officer to Executive in the QA (Qualification) department, the responsibilities may include:

• Developing and implementing equipment and process validation protocols and reports
• Ensuring compliance with regulatory requirements related to equipment and process validation
• Conducting risk assessments and identifying corrective and preventive actions related to equipment and process validation
• Collaborating with other departments to ensure quality and compliance with regulatory requirements
• Reviewing and approving qualification/validation documents and reports
• Providing training to staff on equipment and process validation and compliance matters

Position: Senior Officer to Senior Executive

Qualifications:

• B.Pharma/M.Pharm/M.Sc in a relevant field

Experience:

• 5 to 8 years of experience in AQA (Analytical Quality Assurance)
• Experience in using instruments such as HPLC and others
• Exposure to software such as Chromeleon and LIMS

As a Senior Officer to Senior Executive in the AQA (Analytical Quality Assurance) department, the responsibilities may include:

• Conducting analytical testing of raw materials, finished products, stability samples, and validation samples using instruments such as HPLC and others
• Ensuring compliance with regulatory requirements related to analytical testing
• Reviewing and approving analytical test data and reports
• Maintaining and troubleshooting analytical instruments and software such as Chromeleon and LIMS
• Conducting investigations of out-of-specification results and identifying corrective and preventive actions
• Collaborating with other departments to ensure quality and compliance with regulatory requirements
• Providing training to staff on analytical testing and compliance matters

Position: Officer to Executive

Qualifications:

• M.Sc (Organic Chemistry)/M.Sc (Micro)/B.Pharma/M.Pharma in a relevant field

Experience:

• 2 to 8 years of experience in Chemical/Microbiology Section as an Analyst/Finished/Stability
• Knowledge of instruments such as HPLC/GC/DISSOLUTION/AMV
• Experience with Sterility, BET, Environment Monitoring Testing

As an Officer to Executive in the Quality Control (Chemical) & Microbiology Section, the responsibilities may include:

• Conducting chemical and microbiological testing of raw materials, finished products, and stability samples
• Ensuring compliance with regulatory requirements related to chemical and microbiological testing
• Reviewing and approving test data and reports
• Maintaining and troubleshooting analytical instruments such as HPLC, GC, DISSOLUTION, AMV
• Conducting investigations of out-of-specification results and identifying corrective and preventive actions
• Collaborating with other departments to ensure quality and compliance with regulatory requirements
• Providing training to staff on analytical testing and compliance matters

Walk In Interview:

Walk In Interview at Chandigarh & Vadodara

Date: Sunday, 26th February 2023

Time: 09:00 AM to 03:00 PM

Venue: Chandigarh: Hotel Solitaire, SCO. 902 – 903, Housing Board Chowk NAC, Manimajra, Chandigarh – 160101 Vadodara: Hotel Fern Residence, near central bus depot, Station Road, Vadodara – 390002.

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