Technician - Compression Block B

Job Description: Technician – Compression Job Purpose: To operate and maintain tablet compression equipment in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality tablets. Key Responsibilities: Set up and operate tablet compression machines and ancillary equipment (e.g., metal detectors, dedusters, friability testers, scales). Perform in-process checks such as tablet weight, thickness, hardness, and visual inspection as per Master Batch Records (MBR). Clean and sanitize equipment and manufacturing areas according to SOPs. Accurately complete equipment logs and batch documentation. Ensure proper execution of MBRs, SOPs, and validation protocols. Coordinate with Quality Assurance for in-process sampling and issue resolution. Identify and report deviations, equipment malfunctions, or quality issues. Maintain compliance with cGMP, FDA regulations, and company policies. Keep the work area clean, organized, and audit-ready at all times. Perform other duties as assigned by the supervisor. Qualifications: Education: ITI / Diploma / B.Sc or equivalent; technical certification preferred. Experience: 4–6 years in pharmaceutical tablet compression operations. Skills: Ability to read and interpret SOPs and batch records. Strong attention to detail and documentation accuracy. Good communication and interpersonal skills. Physically able to stand for long hours and lift up to 50 lbs.

Set up and operate tablet compression machines and ancillary equipment (e.g., metal detectors, dedusters, friability testers, scales).

Perform in-process checks such as tablet weight, thickness, hardness, and visual inspection as per Master Batch Records (MBR).

Clean and sanitize equipment and manufacturing areas according to SOPs.

Accurately complete equipment logs and batch documentation.

Ensure proper execution of MBRs, SOPs, and validation protocols.

Coordinate with Quality Assurance for in-process sampling and issue resolution.

Identify and report deviations, equipment malfunctions, or quality issues.

Maintain compliance with cGMP, FDA regulations, and company policies.