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Manufacturing, Transport & Logistics 🏢 Full Time ⭐️ Terverifikasi

Manufacturing Specialist - Medical Devices

Haemonetics
Canggu, Ubud, Denpasar, Jimbaran, Nusa Dua, Kuta, Badung
Salary Estimate
Rp 8.000.000 – Rp 12.000.000
Newest
Live Update
12 Juli 2026
Deadline
12 Jul 2027

job description

Join Haemonetics as a Manufacturing Specialist and play a pivotal role in producing life-saving medical devices that impact patient care globally. In this role, you will ensure the highest standards of quality through precise assembly, rigorous inspection, and meticulous documentation in a regulated manufacturing environment. Based in the vibrant regions of Bali, this opportunity offers a unique blend of professional growth and an inspiring work-life balance.

As part of our mission-driven team, you will contribute to the production of critical healthcare products while adhering to strict regulatory guidelines. Your attention to detail and commitment to excellence will directly enhance the reliability and safety of medical devices used in hospitals and clinics worldwide.

We are looking for a dedicated professional who thrives in a structured yet dynamic environment, values precision, and is passionate about making a difference in global healthcare. If you are eager to advance your career in medical device manufacturing while enjoying the beauty and culture of Bali, this is the perfect role for you.

Responsibility

  • Perform precise assembly of medical devices according to standardized procedures and regulatory requirements.
  • Conduct thorough inspections and quality checks to ensure products meet strict industry and company standards.
  • Maintain accurate and detailed documentation of manufacturing processes, inspections, and deviations.
  • Operate and monitor manufacturing equipment, ensuring optimal performance and adherence to safety protocols.
  • Collaborate with cross-functional teams, including Quality Assurance and Engineering, to resolve production issues and improve processes.
  • Adhere to Good Manufacturing Practices (GMP) and other regulatory guidelines to ensure compliance.
  • Participate in continuous improvement initiatives to enhance efficiency, quality, and safety in the manufacturing process.
  • Train and mentor new team members on manufacturing procedures and best practices.

Qualifications

  • Diploma or Bachelor's degree in Manufacturing, Engineering, Biomedical Sciences, or a related field.
  • Minimum of 2 years of experience in medical device manufacturing, pharmaceuticals, or a highly regulated industry.
  • Strong understanding of Good Manufacturing Practices (GMP) and quality management systems.
  • Excellent attention to detail and ability to follow complex procedures with precision.
  • Proficient in using manufacturing equipment and tools, with a commitment to workplace safety.
  • Strong documentation skills, with the ability to maintain accurate records in compliance with regulatory standards.
  • Effective communication and teamwork skills, with the ability to collaborate across departments.
  • Fluency in English; additional language skills are a plus.

Required Skills

manufacturing medical devices GMP quality control assembly inspection documentation regulatory compliance

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