Lonza

Global life sciences contract manufacturer

Operator – Preparation

Machine & Process OperationConfirmed live in the last 24 hours

Full-timeRewari, IndiaNo salary listedIn-person

About the Job

Requirements

Ability to work in a manufacturing environment with strict quality and safety standards.
Strong attention to detail and adherence to standard operating procedures.
Basic knowledge of Supervisory Control and Data Acquisition systems and pharmaceutical processes.
ITI or a diploma in Pharmacy, Science, or Engineering; Chemical is preferred.
Entry-level experience in pharmaceutical manufacturing or a similar environment.
Ability to operate Supervisory Control and Data Acquisition systems and knowledge of Good Manufacturing Practices and Good Documentation Practices.
Basic mechanical and troubleshooting skills.

Responsibilities

Operate and monitor gelatin melt tanks via Supervisory Control and Data Acquisition to prepare batches according to specifications.
Transfer approved gelatin bags and feed ingredients according to standard operating procedures and the master formula.
Prepare Gel Feed Tanks using weighing booths and dry dye weighing systems.
Operate the Viscosity Adjustment System to meet viscosity set points.
Perform capsule trim grinding and ensure proper documentation.
Clean Gel Feed Tanks and dishes using automated and manual processes.
Maintain accurate documentation according to Good Documentation Practices.
Ensure compliance with safety and quality standards during the shift.

Desired Qualifications

Chemical education is preferred.

Job Title: Operator – Preparation

Location: Rewari

Intro Summary of the Role:
Responsible for efficient preparation of Gel Feed Tanks (GFT) in the Gel Melting Room (GMR) within standard parameters, ensuring quality compliance, timely delivery, and adherence to safety and GMP practices.

What You Will Get:

Opportunity to work in a pharmaceutical manufacturing environment
Exposure to automated systems like SCADA
Hands-on experience with Good Manufacturing Practices (GMP)

What You Will Do:

Operate and monitor gelatin melt tanks via SCADA to prepare batches as per specifications
Transfer approved gelatin bags and feed ingredients according to SOP and master formula
Prepare GFTs using weighing booths and dry dye weighing systems
Operate Viscosity Adjustment System (VAS) to meet viscosity set points
Perform capsule trim grinding and ensure proper documentation
Clean GFTs and dishes using automated and manual processes
Maintain accurate documentation as per GDP (Good Documentation Practices)
Ensure compliance with safety and quality standards during shift

What We Are Looking For:

Ability to work in a manufacturing environment with strict quality and safety standards
Strong attention to detail and adherence to SOPs
Basic knowledge of SCADA systems and pharmaceutical processes
Education: ITI or Diploma in Pharmacy, Science, or Engineering (Preferred: Chemical)
Experience: Entry-level experience in pharmaceutical manufacturing or similar environment
Skills: Operation of SCADA systems, Knowledge of GMP and GDP, Basic mechanical and troubleshooting skills

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

About the Company

Lonza

Global life sciences contract manufacturer

Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.

Company size: 10,001+
Company stage: IPO
Headquarters: Basel, Switzerland
Founded: 1897

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