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A leading global healthcare group is seeking an Engineering Staff member to support the maintenance and optimization of pharmaceutical manufacturing systems in Cikarang. The role requires strong technical expertise and collaboration across departments to ensure operational efficiency and safety.
Daewoong Pharmaceuticals is a leading global healthcare group dedicated to enhancing the quality of life. With the largest number of overseas subsidiaries among Korean pharmaceutical firms, Daewoong is recognized for its global reach in research, development, manufacturing, and sales.
PT. Daewoong Biologics Indonesia (DBI), a subsidiary of Daewoong Group, focuses on the production of stem cell and cosmetic products. Located in Cikarang, DBI is committed to becoming a leader in regenerative medicine and cosmeceuticals in Indonesia and beyond.
Job Overview
We are seeking a skilled and detail-oriented Engineering Staff member to join our team at the Daewoong Biologics Indonesia facility in Cikarang. This role involves supporting the maintenance and optimization of pharmaceutical manufacturing systems and processes. The ideal candidate will demonstrate strong technical expertise, regulatory compliance knowledge, and the ability to collaborate across departments to ensure the reliability, efficiency, and safety of plant operations.
Perform technical support for maintenance activities, including troubleshooting equipment issues and developing effective repair procedures.
Document all maintenance actions in logs and work orders accurately and completely.
Participate in the design, specification, installation, and commissioning of new equipment and systems.
Develop and execute validation protocols (IQ, OQ, PQ) for equipment and related processes.
Analyze equipment performance data to identify trends and opportunities for efficiency improvements.
Implement process improvements to enhance productivity, safety, and regulatory compliance.
Prepare engineering drawings, specifications, and detailed technical reports.
Support change control processes, including documentation, impact assessment, and risk management.
Investigate deviations and contribute to corrective and preventive action (CAPA) planning.
Ensure strict compliance with cGMP, EHS regulations, and internal operational procedures.
Stay up-to-date with relevant engineering standards, regulations, and technological advances.
Collaborate with cross-functional teams on engineering-related matters.
Provide technical training and support to maintenance and operations personnel as needed.
Required Qualifications:
Diploma in Engineering (Mechanical, Electrical, Civil, or related field); advanced degree preferred.
Minimum 2 years of relevant engineering experience in the pharmaceutical or similar regulated industry.
Knowledge of utility systems (e.g., HVAC, water systems, gas, compressed air, and electrical systems).
Familiarity with cGMP regulations and validation processes (IQ, OQ, PQ).
Proficient in engineering software and tools (e.g., AutoCAD, MS Office).
Ability to read and interpret technical drawings and documentation.
Good English communication skills (verbal and written).
Understanding of maintenance management systems and EHS practices.
Preferred Qualifications:
Strong mechanical or electrical troubleshooting ability.
Solid technical writing, documentation, and communication skills.
High attention to detail with strong problem-solving mindset.
Team-oriented with the ability to work independently when needed.
What's your expected monthly basic salary?
Which of the following types of qualifications do you have?
How many years' experience do you have as an Engineering Staff?
Which of the following CAD software do you have experience with?
Which of the following Microsoft Office products are you experienced with?
How would you rate your English language skills?
Which of the following languages are you fluent in?
Do you have technical writing experience? (e.g. user guides, product user manuals, technical specification documents)