Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Title: Sr Operator Manufacturing Operations

Reports To: Team Lead, Operations

Location: Bangalore

Purpose:

Responsible for the day to day running of the designated area, ensuring a safe and organized workplace, high quality output and that the plan needs are met at optimal cost.


Adopt and live the Company's 4-I values (Intensity, Integrity, Innovation & Involvement)

Roles and Responsibilities:

Support day-to-day manufacturing operations, coordinate with team members, and assist the Manager in achieving departmental goals. Monitor and work to reduce product loss and wastage; investigate quality failures and implement corrective actions to enhance output and efficiency. Complete batch records online and update equipment logbooks in real time. Accurately report routing hours, material issuance, and quantity completion on a daily basis. Record detailed observations during production activities in batch records, reports, and work orders, adhering to Good Documentation Practices (GDP). Comply with all company safety regulations. Promptly report unsafe conditions, hazards, or risks to team members and supervisors. Support the company's dedication to quality by identifying and documenting factors that may impact product quality. Supervise and track laboratory supplies to ensure availability of reagents for daily operations. Drive productivity improvements and efficiencies within the manufacturing/laboratory environment to deliver cost savings. Adapt quickly to changing priorities and manage multiple tasks/projects with overlapping deadlines. Contribute to continuous improvement initiatives such as JDI (Just Do It), PPI (Practical Process Improvement), and Kaizen. Align with and promote Thermo Fisher Scientific's 4i Values (Integrity, Intensity, Innovation, and Involvement). Perform other related duties as assigned. Understand and strictly follow Standard Operating Procedures (SOPs) and work instructions for finished goods manufacturing. Ensure accurate labelling and handling of samples and kits. Maintain cleanliness, handling, and preventative maintenance of equipment. Make accurate batch record entries and report any deviations to the supervisor immediately.

Qualifications and Skills

Bachelor's degree in any subject area, with a minimum of 2 years of experience in the life sciences, biotechnology, or relevant manufacturing operations field. Hands on experience in E1 ERP system. Understanding of ISO 9001:2015 and ISO 13485:2016 standards is a strong advantage. Highly organized with strong analytical and problem-solving skills. Consistent record to multi-task, prioritize, and handle time effectively in a fast-paced environment. Customer focused with the flexibility to adapt and respond to diverse tasks and operational demands. Willingness to work on different shifts and adapt to changing schedules as needed. * Familiar with compliance and regulatory standards relevant to manufacturing or biotech environments.