ASSISTANT MANAGER

Apply now »

Date: Mar 5, 2026

Location: Johor bahru, MY

Company: bioconbiolP2

Company Overview

Role Purpose

Supervisor-MFG-DS-Insulin-Upstream: Oversees the daily operations of cell separation processes for insulin production during their shift. This role involves managing and coordinating the cell separation activities, ensuring the efficiency and accuracy of equipment and procedures. Responsibilities include supervising staff, monitoring process parameters, troubleshooting issues, and maintaining adherence to safety and quality standards. Ensuring seamless operation and effective problem resolution in cell separation processes is key to the role's success.

Academic Stream

Biotechnology

Work experience (in months)

84

Job Responsibility and key Decisions

A supervisory position would require the individual to work depending on the shifts.

Participate in all drug substance related manufacturing process. Perform Where needed and review the process to ensure compliance with the requirements listed in respective batch record.

Provides daily supervision on the floor to personnel in the efficient use of equipment and materials to produce quality products under cGMP in accordance with the production plan.

Provides coaching, counselling, development, discipline and recognition of direct staff, including performing annual performance reviews.

Responsible for maintaining alignment with department direction, goals and objectives.

Promotes the use of safe work practices during all production and ensures all external and company policies and EHS standards are met daily.

Responsible for training personnel on equipment, processes and Standard Operating Procedures SOPs.

Trains and develops personnel, develops and maintains packaging schedules, and manages within the department budget.

Ensures that projects are completed on schedule per established procedures.

Participate in execution of qualification and validation activities.

Participate in process related investigations and implement CAPA derived from investigation outcome in timely manner.

Author and reviews SOPs and other documents to ensure integration of cGMPs and improve process efficiency.

Works collaboratively to ensure flow of product, sharing of best practices and lean behaviours.

Performs process monitoring, including use of databases, documents andor spreadsheets to support business reporting requirements.

Performs ongoing operational tasks of organization unit, actively assists, or provides direction to subordinates as required.

Responsible for final review of completed documentation per compliance standards and establish timelines.

Investigates and resolve problems, identifying root cause, and proposing process improvements through clear communication to senior management.

Participation andor leadership role in multifunctional project teams as necessary.

Other tasks as requested by management.