Computer System Validation Engineer Smart IMS Inc.

4.0 - 8.0 years

0 Lacs

hyderabad, telangana

On-site

As a Computer System Validation Engineer at our company, you will play a crucial role in the Quality Assurance/Validation department in Hyderabad. With 4-5 years of experience, you will be responsible for preparing, executing, and compiling qualification documents for pharmaceutical manufacturing equipment, specifically Fluid Bed Processors (FBP), Rapid Mixer Granulators (RMG), Compression machines, and Coating machines. Your key responsibilities will include preparing, executing, and compiling qualification protocols and reports for pharmaceutical equipment, conducting Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for the mentioned machines, ensuring compliance with regulatory standards and company policies, collaborating with cross-functional teams, maintaining accurate documentation, and identifying and resolving issues related to qualification processes promptly. To excel in this role, you should possess 4-5 years of hands-on experience in qualification documentation preparation, execution, and compilation, technical expertise in the qualification and validation of FBP, RMG, Compression, and Coating machines, a strong understanding of Good Manufacturing Practices (GMP) and regulatory guidelines, excellent documentation and communication skills, and the ability to work effectively in a team environment. If you are passionate about validation and qualification activities and are looking to contribute your expertise to a dynamic team, we encourage you to apply for this Full-Time position.,

Posted 1 month ago

Apply

Operator Titan Laboratories

2.0 - 5.0 years

2 - 5 Lacs

Mumbai, Maharashtra, India

On-site

Key Responsibilities: Operate machines and equipment such as granulators, tablet presses, coating machines, blenders, filling lines, or packaging lines (depending on the product and plant type). Set up and adjust machinery before starting the production run. Monitor the production process and report deviations or abnormalities to supervisors. Maintain equipment cleanliness and perform minor maintenance or cleaning as needed. Complete batch manufacturing records (BMR), logbooks, and other documentation accurately and on time. Ensure compliance with safety, hygiene, and quality standards. Assist in the changeover and cleaning of equipment between batches. Identify and escalate equipment malfunctions or quality issues. Participate in training sessions related to SOPs, GMP, and safety. Qualifications: ITI / Diploma / 10+2 with relevant technical or science background. 13 years of experience in pharmaceutical or manufacturing operations (preferred). Key Skills: Familiarity with manufacturing processes and SOPs. Understanding of cGMP and safety standards. Ability to follow written instructions and maintain accurate records. Physically fit and able to work in a shift-based environment. Team player with attention to detail.

Posted 1 month ago

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.