Manager

Biocon Biologics

is a fully integrated ‘pure play’ biosimilars organization globally committed towards transforming patient lives through innovative and inclusive healthcare solutions. It is engaged in developing high-quality, affordable biosimilars aimed at expanding patient access to cutting-edge class of therapies across the world. Biocon Biologics is a subsidiary of Biocon Ltd, an innovation led-global biopharmaceuticals company and India's first publicly listed biotech enterprise. Biocon Biologics has one of the largest biosimilars portfolios, a wide global footprint, state-of-the-art manufacturing facilities, world-class R&D ecosystem, and high quality & compliance standards, enabling it to fulfil unmet needs of patients across the globe.

Responsibilities

Packing Operations

Supervise and manage packing lines (Vi / Packing) to meet quality standards.

Monitor packing operations to ensure correct labelling, batch coding and packing.

Coordinate with QA / QC for batch release and documentation compliance.

Maintain compliance with GMP and regulatory standards.

Track and report batch-wise packaging progress.

Monitor packing line performance and equipment efficiency.

Coordinate with QA for in-process checks and documentation.

Maintain cleanroom protocols and packing records.

Coordinate with formulation, filling, and inspection teams for smooth operations.

Production Planning (Injectables)

Develop and maintain daily, weekly, and monthly production plans for injectable products.

Coordinate with SCM, warehouse, quality assurance, and manufacturing teams to ensure material / SFG availability.

Monitor production progress and adjust schedules to meet delivery timelines.

Optimize resource utilization including manpower, equipment, and materials.

Analyze production data to identify bottlenecks and implement corrective actions.

Prepare MIS reports and dashboards for senior management review.

Quality Management System

Investigate Market complaints and non-conformance investigations.

Ensure timely updates and revisions to SOPs.

Coordinate with cross-functional teams to resolve quality issues and implement improvements.

Monitor and analyze quality performance metrics, report findings to senior management.

Preferred Skill’s

Experience in handling regulatory audits (USFDA, MHRA, etc.).

Strong leadership and team coordination abilities.

Ability to work and manage multiple priorities.

Knowledge of Lean Manufacturing and Six Sigma principles.

Qualifications

Bachelor's degree or equivalent experience

Microsoft Office (Outlook, Excel, Word, PowerPoint, etc.) Organized

Strong leadership skills