Sr. Officer-QC Jobs in Lactose India Ltd - Vadodara, Gujarat

Sr. Officer-QC Jobs in Lactose India Ltd - Vadodara, Gujarat

work outline icon1 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Lactose India Ltd

time outline iconVadodara, Gujarat, India

Posted on 08-05-2026

1 Vacancy

Description

  • Job Title: Sr. Officer-QC
  • Qualification: MPharm/BPharm
  • Location: Lactose India Ltd - Vadodara, Gujarat
  • Work Experience: 1 to 5 Years

Job Description

  • Support the development and execution of international business strategies to expand global markets.
  • Identify and develop new international clients, distributors, and business opportunities.
  • Maintain strong relationships with overseas customers and business partners.
  • Coordinate with internal teams such as sales, logistics, finance, and marketing for smooth export operations.
  • Manage export documentation, international orders, and shipment coordination.
  • Conduct market research to analyze global market trends and competitor activities.

Take this opportunity to join Lactose India Ltd - Vadodara, Gujarat as a Sr. Officer-QC in Vadodara, Gujarat and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

Pharma Quality Control (QC)

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

Analytical SkillsProblem Solving SkillsDocumentationAttention to Detail

About Organization

Lactose India Ltd is a pharmaceutical manufacturing company engaged in producing high-quality excipients and pharmaceutical products with a focus on quality and regulatory compliance. The company operates advanced production facilities and follows strict industry standards. The role involves handling production activities and ensuring smooth manufacturing operations in the plant. Responsibilities include operating equipment, monitoring processes, and maintaining batch records while following SOP and GMP guidelines. The position focuses on efficient production, product quality, and adherence to pharmaceutical manufacturing standards.

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