Ravian Life Science – Walk-In Interviews for QA / Production / F&D Departments on 28th June’ 2026

Career Opportunities: Walk-in Interview for Experienced Pharmaceutical Professionals

A prominent pharmaceutical manufacturing company is offering exciting career opportunities for dedicated and experienced professionals. Committed to delivering high-quality healthcare products through innovation, stringent regulatory compliance, and operational excellence, the company invites skilled individuals to join its growing team. The state-of-the-art manufacturing facility is located at SIDCUL, Haridwar, Uttarakhand, and is conducting a walk-in interview to fill multiple key positions.

This is an excellent chance for experienced pharmaceutical professionals across various domains to advance their careers within a dynamic and forward-thinking environment.

Walk-in Interview Details:

  • Date: 28th June 2026 (Sunday)
  • Time: 10:00 AM – 2:00 PM
  • Venue: Plot No. 34, Sector-8A, IIE, SIDCUL, Haridwar, Uttarakhand

Current Openings for Experienced Professionals:

The company is seeking talented individuals for the following departments and roles, requiring specific levels of experience:

  • Liquid Production:
    • Assistant Manager / Deputy Manager: 10-15 Years of experience.
  • Quality Assurance (QA):
    • Assistant Manager: 10-12 Years of experience.
    • Manager: 12-17 Years of experience.
  • Formulation & Development (F&D):
    • Executive / Senior Executive: 6-8 Years of experience.
    • Officer / Senior Officer: 2-4 Years of experience.
  • Production (Granulation):
    • Officer / Senior Officer: 2-5 Years of experience.

Key Responsibilities for These Roles Typically Include:

Successful candidates will be involved in crucial aspects of pharmaceutical manufacturing and quality, such as:

  • Managing pharmaceutical production operations, ensuring strict adherence to current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs).
  • Overseeing comprehensive quality assurance systems, including documentation, audits, and maintaining regulatory compliance.
  • Performing formulation and development activities for both new and existing pharmaceutical products.
  • Handling granulation and other manufacturing processes in strict accordance with approved procedures and quality standards.
  • Maintaining accurate production and quality documentation, actively supporting initiatives for continuous process improvement.
  • Coordinating effectively with cross-functional teams to ensure timely and efficient manufacturing operations.

Eligibility Criteria:

Prospective candidates should meet the following requirements:

  • Possess a relevant pharmaceutical qualification and experience that aligns with the specific position being applied for.
  • Demonstrate substantial experience in Production, Quality Assurance, or Formulation & Development within the pharmaceutical industry.
  • A strong knowledge of GMP practices, comprehensive documentation, and regulatory compliance is highly preferred.

Why Join This Company?

Joining this pharmaceutical company offers numerous advantages for your professional journey:

  • Opportunity to work with a rapidly growing pharmaceutical manufacturing company.
  • Diverse career opportunities across critical functions like Production, Quality Assurance, and Formulation & Development.
  • Professional growth and development in a work environment that is deeply focused on quality and regulatory compliance.
  • Exposure to advanced pharmaceutical manufacturing techniques and development processes, fostering continuous learning and skill enhancement.

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