Production Supervisor

Pt Cipta Mortar Utama

Indonesia

Hybrid

IDR 223,200,000 - 312,480,000

Full time

10 days ago
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Job summary

Pt Cipta Mortar Utama is seeking an experienced Pharmaceutical Production Supervisor to lead the manufacturing team in Tangerang. The role focuses on ensuring compliant daily operations, managing operators, and driving efficiency with a hybrid approach to production oversight.

The ideal candidate holds a Bachelor's in Pharmacy or Engineering (or an equivalent Associate's with significant experience) and has at least 3 years in pharmaceutical manufacturing, including 1 year in a supervisory

Qualifications

  • Bachelor's degree in Pharmacy, Engineering, or related field; Associate's degree with significant experience considered.
  • Minimum of 3 years of experience in pharmaceutical manufacturing, with at least 1 year in a supervisory role.

Responsibilities

  • Supervise and direct the daily activities of production personnel to ensure efficient and compliant manufacturing operations.
  • Ensure adherence to all cGMP, safety, and environmental regulations during production.
  • Monitor production schedules, identify potential delays, and implement corrective actions to meet production targets.
  • Train, mentor, and evaluate the performance of production operators.
  • Oversee the accurate completion of batch records, production logs, and other relevant documentation.
  • Participate in process improvement initiatives and problem-solving efforts to enhance productivity and quality.
  • Maintain a safe and organized work environment.

Education

Bachelor's degree in Pharmacy, Engineering, or related field
Associate's degree with significant experience

Job description

Pharmaceutical Production Supervisor – Tangerang

Our client is seeking an experienced and motivated Pharmaceutical Production Supervisor to lead their production team in Tangerang. This role is responsible for overseeing daily manufacturing operations, ensuring that all activities are conducted in compliance with cGMP, safety standards, and company policies. You will manage a team of production operators, drive operational efficiency, and ensure the timely delivery of high-quality pharmaceutical products. This position offers a challenging yet rewarding opportunity to play a key role in the manufacturing of essential medicines within a supportive and growth-oriented environment, utilizing a hybrid approach to manage operations effectively.

Key Responsibilities
  • Supervise and direct the daily activities of production personnel to ensure efficient and compliant manufacturing operations.
  • Ensure adherence to all cGMP, safety, and environmental regulations during production.
  • Monitor production schedules, identify potential delays, and implement corrective actions to meet production targets.
  • Train, mentor, and evaluate the performance of production operators.
  • Oversee the accurate completion of batch records, production logs, and other relevant documentation.
  • Participate in process improvement initiatives and problem‑solving efforts to enhance productivity and quality.
  • Maintain a safe and organized work environment.
Requirements
  • Bachelor's degree in Pharmacy, Engineering, or a related scientific field; Associate's degree with significant experience considered.
  • Minimum of 3 years of experience in pharmaceutical manufacturing, with at least 1 year in a supervisory
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