Sterile Manufacturing Supervisor

Innoxel Lifesciences

Ludhiana, Punjab

Department: Sterile Manufacturing

Experience: 1-8 Years

Industry: Pharmaceutical

Education: ITI or Diploma

Job Description

Sterile Manufacturing Supervisor – Sterile Manufacturing | Innoxel Lifesciences | Ludhiana, Punjab, India

Innoxel Lifesciences is inviting applications for the position of Sterile Manufacturing Supervisor for its pharmaceutical manufacturing facility located in Ludhiana, Punjab. This role is suitable for candidates having 1 to 8 years of experience in sterile manufacturing operations within the pharmaceutical industry. The position involves supervising aseptic production processes, ensuring adherence to GMP guidelines, and maintaining contamination-free environments in sterile areas. The selected candidate will be responsible for monitoring production activities, ensuring compliance with SOPs, and coordinating with quality and maintenance teams for smooth operations. This is an excellent opportunity for professionals seeking to build careers in sterile manufacturing with a company focused on quality systems and regulatory compliance. Candidates with experience in cleanroom operations and aseptic processing will be preferred.

Location

Ludhiana, Punjab, India

Employment Type

Full-time

Experience Required

1 to 8 Years

Compensation & Benefits

Compensation will be offered as per industry standards along with opportunities to work in regulated sterile manufacturing environments and career growth prospects.

About Innoxel Lifesciences

Innoxel Lifesciences is a pharmaceutical company engaged in manufacturing high-quality formulations with a strong focus on compliance, quality assurance, and advanced manufacturing practices.

Position Overview

The Sterile Manufacturing Supervisor will oversee day-to-day sterile production operations and ensure strict adherence to aseptic procedures and regulatory requirements.

Key Responsibilities

Supervise sterile manufacturing activities in aseptic areas.
Ensure compliance with GMP and aseptic guidelines.
Monitor cleanroom behavior and environmental conditions.
Implement and follow standard operating procedures.
Coordinate with QA and QC departments.
Maintain production records and documentation.
Ensure proper gowning and hygiene practices.
Handle deviations and support investigations.
Ensure equipment cleaning and sterilization processes.
Support validation and qualification activities.

Required Skills & Competencies

Knowledge of sterile manufacturing processes.
Understanding of aseptic techniques.
GMP and regulatory compliance knowledge.
Cleanroom operations experience.
Strong attention to detail.
Team supervision skills.
Documentation and reporting skills.
Problem-solving ability.
Communication and coordination skills.
Awareness of contamination control practices.

Educational Qualification

ITI or Diploma

About the Project & Industry

This role is part of sterile pharmaceutical manufacturing where maintaining contamination-free environments is critical for product safety and regulatory compliance. The industry requires strict adherence to aseptic practices and validated processes.

Why Join Innoxel Lifesciences?

This opportunity provides hands-on experience in sterile pharmaceutical manufacturing, exposure to regulated environments, and long-term career growth in production supervision roles.