FAQs
What are the working hours for the Supervisor, Manufacturing Operators position?
The working hours are standard Monday to Friday.
What kind of environment will I be working in?
You will be working in an office environment.
What are the primary responsibilities of the Supervisor, Manufacturing Operators?
The primary responsibilities include ensuring the achievement of production goals in terms of quantity, time, cost, and quality, coordinating and training staff, and ensuring compliance with GMP, budget requirements, and safety regulations.
Is there a focus on budget management in this role?
Yes, there is a focus on budget management, which involves planning and controlling costs for materials and human resources.
Will I need to coordinate with other departments?
Yes, you will need to coordinate with other departments to ensure the smooth operation of production activities.
What is the expectation regarding quality standards?
You are expected to ensure compliance with company quality standards and verify adherence to SOPs and procedures.
How does this role contribute to training staff?
The role includes ensuring the technical training of production staff and identifying training needs for performance improvement.
What type of production will be managed in this position?
You will be responsible for ensuring the production of pharmaceuticals as required by the client.
What will I be doing to maintain warehouse inventory?
You will ensure an adequate level of inventory for your assigned department by defining minimum order levels and controlling material orders.
How will I handle maintenance issues in this role?
You will support Technical Services in maintaining production equipment by monitoring its efficiency and reporting any anomalies.
Is there a commitment to employee development in this role?
Yes, the position emphasizes analyzing training and development needs to promote high performance and motivation among staff.
How will I be ensuring compliance with regulatory standards?
Compliance will be ensured through proper execution of validations and monitoring of production data to meet GMP and company policies.
Will there be an opportunity to propose corrective actions if there are budget deviations?
Yes, you will be expected to analyze deviations and propose corrective actions in alignment with quality standards and organizational interests.
What kind of documentation will I be involved with?
You will ensure the proper completion of documentation related to sampling activities and production records as per current SOPs.
Is the role focused on direct supervision of staff?
Yes, the position requires direct supervision, coordination, and control of the production staff to achieve departmental objectives.