Manufacturing Supervisor (Pharmaceutical Manufacturing)

Private Advertiser; Singapore; On-site; SGD 100,000 - 125,000; Full time

Job summary

A pharmaceutical company in Singapore is seeking a Manufacturing Supervisor to oversee the production team and ensure compliance with quality standards. The successful candidate will have a Diploma in Engineering or Science and at least 5 years of experience, preferably in the pharmaceutical industry. Key responsibilities include managing production schedules, ensuring quality compliance, and training staff effectively. This position offers a competitive salary and opportunities for professional development.

Benefits

Competitive salary and benefits package

Opportunities for professional development

Dynamic work environment

Qualifications

• Minimum of 5 years of experience in the production field within the pharmaceutical industry.
• Proven ability to lead and train staff effectively.
• Strong commitment to maintaining quality standards.

Responsibilities

• Oversee production according to schedules and quality objectives.
• Ensure compliance with cGMP and quality standards.
• Train manufacturing technicians on operational procedures.

Skills

Leadership

Team training

Production efficiency

Quality compliance

Resource coordination

Education

Diploma in Engineering and/or Science

Tools

Microsoft Word

Microsoft Excel

Job description

About

As a Manufacturing Supervisor, you will supervise a group of manufacturing technicians to ensure efficient and high-quality production processes. You will be accountable for achieving production output in line with established schedules and company goals, while ensuring compliance with cGMP (current Good Manufacturing Practices), Standard Operating Procedures (SOPs), and company quality standards. Additionally, you will assist in the implementation of systems and procedures aimed at improving manufacturing efficiency, product quality, and overall operational effectiveness.

Job Responsibilities

• Production & Quality Management:
  Oversee and ensure production is carried out according to pre-planned schedules, achieving productivity targets such as cycle time, waste reduction, yield optimization, and adherence to quality objectives and supply plans.

• Accountability for Product Quality:
  Take full responsibility for ensuring that pharmaceutical products are manufactured in compliance with established quality standards and product specifications.

• Resource Allocation & Coordination:
  Ensure that adequate resources, including personnel and materials, are allocated efficiently to maintain smooth operations across both quality control and production systems.

• Monitoring & Deviation Management:
  Act immediately to halt production and notify the immediate supervisor and QA department upon detection of any abnormalities or deviations that may compromise the identity, quality, purity, or efficacy of the product.

• Compliance with cGMP & Quality Standards:
  Ensure that all manufacturing equipment and process areas meet cGMP and quality standards at all times.

• Documentation & Record Keeping:
  Ensure all production, quality, and manufacturing records/documents are maintained and updated in accordance with regulatory requirements.

• Failure & Non-Conformity Investigation:
  Actively participate in investigating both major and minor failures or non-conformities related to semi-finished products or finished goods, ensuring corrective actions are implemented to prevent recurrence.

• Staff Training & Development:
  Ensure that all manufacturing technicians are properly trained on operational and cleaning methodologies for machinery and premises, material requisition, area clearance, reconciliation procedures, in-process sampling, environmental monitoring, cGMP practices, and SOPs.

• Housekeeping & 5S Practices:
  Implement and promote good housekeeping practices and 5S methodology within the respective section to maintain a clean, organized, and efficient workspace.

• Safety Adherence:
  Ensure all job activities are conducted in a safe manner, with strict adherence to safety procedures by all shop floor staff.

• Additional Duties:
  Perform any other duties as assigned by the supervisor or management.

Qualification and Experience

• Minimum of Diploma in Engineering and/or Science with at least 5 years of experience in the production field, preferably within the pharmaceutical industry.

• Proven ability to lead, supervise, and effectively train staff.

• Demonstrated ability to direct and coordinate daily operations efficiently.

• A self-starter with a strong commitment to maintaining high-quality standards in all aspects of the role.

• Proficient in Microsoft Word and Excel for document management and reporting purposes.

What We Offer

• Competitive salary and benefits package.

• Opportunities for professional development and advancement.

• A dynamic and collaborative work environment.