Production Sterile - Aseptic - Sr. Execu...

PeopleStrong; Daman; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

USV Private Limited in Daman is seeking a Senior Executive to lead sterile manufacturing operations, overseeing aseptic filling, compounding, filtration, and lyophilization to ensure product sterility and quality.

The role requires deep knowledge of aseptic practices, GMP compliance with global standards, and hands-on supervision of cleanroom environments within the Daman facility.

Qualifications

• Bachelor's degree or Graduation/Equivalent in a relevant science field.
• 8–12 years of experience in sterile production environments.
• Experience with aseptic filling, GMP, and cleanroom practices.

Responsibilities

• Oversee aseptic filling, compounding, filtration, and lyophilization to ensure sterility.
• Ensure GMP, USFDA, MHRA, WHO, and EU-GMP adherence in cleanrooms.
• Perform in-process checks, review batch records, and support validation activities.
• Maintain BMR/BPR, deviation reports, and regulatory documentation.
• Identify deviations and drive corrective actions for process improvements.
• Coordinate with QA, QC, and Engineering; train staff on sterile handling.

Skills

GMP Aseptic Processing

Education

Graduation/Equivalent Course

Job description

Production Sterile - Aseptic - Sr. Execu...

USV/PS-A-E/1812006

• Formulation Plant
• Daman & Diu

Posted On 25 Jul 2026

End Date 23 Oct 2026

Required Experience 8 - 12 years

Basic Section

BAND Junior Management

Grade L3 (A)

Designation Senior Executive

Employment Type Employee

Employee Category 1002

Closing Date 23 Oct 2026

Organisational

Company Code USV Private Limited

GRP USV Private Limited

SBU Operations

Function Formulation Plant

Department Daman

Sub Org Unit 1 Plant Operations

Country India

State Daman & Diu

Location Daman

Skills

Skill

GMP Aseptic Processing

Graduation/Equivalent Course

Others

Job Description

• Sterile Manufacturing Operations: Overseeaseptic filling, compounding, filtration, and lyophilization processes to ensure product sterility and quality.
• Aseptic Practices & Compliance: Ensure adherence toGMP, USFDA, MHRA, WHO, and EU-GMP guidelines, maintaining sterility assurance in cleanroom environments.
• Process Monitoring & Validation: Perform in-process checks, review batch records, and supportmedia fill validation, sterility testing, and equipment qualification.
• Documentation & Batch Records: MaintainBMR/BPR, deviation reports, and compliance documentation as per regulatory standards.
• Troubleshooting & Process Improvement: Identify and resolvemanufacturing deviations, aseptic failures, and process inefficiencies to ensure continuous improvement.
• Coordination & Training: Work closely with QA, QC, and Engineering teams and train staff on sterile handling, gowning, and aseptic techniques.