Analytical Lab QC Officer (FP) Jobs in V-Ensure Pharma Technologies Pvt. Ltd - Ambernath, Maharashtra

Analytical Lab QC Officer (FP) Jobs in V-Ensure Pharma Technologies Pvt. Ltd - Ambernath, Maharashtra

work outline icon2 - 7 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

V-Ensure Pharma Technologies Pvt. Ltd.

time outline iconAmbernath, Maharashtra, India

Posted on 25-06-2026

1 Vacancy

Description

  • Job Title: Analytical Lab QC Officer (FP)
  • Location: V-Ensure Pharma Technologies Pvt. Ltd - Ambernath, Maharashtra
  • Work Experience: 2 to 7 Years
  • Qualification: BPharm

Job Description

  • Perform analytical testing of raw materials, intermediates, and finished products.
  • Operate analytical instruments such as HPLC, GC, UV, and other lab equipment.
  • Maintain laboratory records, test results, and documentation.
  • Ensure compliance with GMP, GLP, and quality standards.
  • Conduct method validation and calibration of laboratory instruments.
  • Assist in investigation of out-of-specification (OOS) results.
  • Coordinate with production and quality assurance teams.
  • Ensure proper maintenance and cleanliness of the laboratory.

Take this opportunity to join V-Ensure Pharma Technologies Pvt. Ltd - Ambernath, Maharashtra as a Analytical Lab QC Officer (FP) in Ambernath, Maharashtra 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

BPharm (Bachelor Of Pharmacy)

Key Skills

Communication SkillsLeadershipTeamworkAttention to Detail

About Organization

V-Ensure Pharma Technologies Pvt. Ltd. is a pharmaceutical organization engaged in the development, manufacturing, and research of oral solid dosage medicines for regulated global markets. The company focuses on producing high-quality pharmaceutical formulations while maintaining strict regulatory and quality standards. The role involves managing pharmaceutical manufacturing activities and ensuring smooth production processes in the plant. Responsibilities include operating and monitoring production equipment, maintaining batch records, and ensuring compliance with SOPs and GMP guidelines. It requires coordination with quality assurance and quality control teams to maintain product quality and regulatory compliance.

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