115 Manufacturing Specialist jobs in Malaysia

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking an experienced Manufacturing Specialist for a role in Singapore.

Key Responsibilities:

• Manufacturing Process Oversight
• Troubleshooting and Problem Solving
• Equipment and Facility Maintenance
• Inventory and Raw Materials Management
• Production Scheduling and Coordination
• Training and Support
• Documentation and Reporting
• Health, Safety, and Environmental Compliance
• Batch Record Review and Release
• Validation and Qualification

Qualifications:

• BSc in Life Sciences, Biotech, or related experience (pharmaceutical manufacturing)
• Proficient in English (speaking and writing).
• At least 2 year experience. Fresh graduate may be considered.

Contract is until 31 Dec 2025 (Open for renewal if performance is good)

We regret that only shortlisted applicants will be notified.

Why PharmEng Technology?

Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.

EEOC Statement

At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.

To effectively build the products manufactured by BSIL to the required quality standard.

1. Ability to be flexible, trainable and capable of adjusting to business priorities.
2. Responsible for building or re-working products in accordance with relevant manufacturing procedures.
3. Understand and adhere to G.M.P. rules and regulations, along with the quality criteria for product acceptance.
4. Actively participate in team activities.
5. Understand and follow through on Environmental Management Procedures relevant to the position.

As a global medical technology leader for more than 40 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve patient health. If you're looking to make a real difference to people worldwide and locally, this is the place to do it.

• Candidate must possess at least SPM / Certificate / Diploma in Mechanical Engineering.
• Fresh graduate or at least 1-2 years working experience in the manufacturing environment.
• Multi-task and hands-on experience in production assembly and testing.
  
  

• Candidates must possess at least Diploma.
• Fresh graduates are welcomed to apply.
• Perform the operations work and ensure the efficient and effective operation of manufacturing processes.
• Preventive maintenance, hydraulic tools assembly, and etc.
• Follow instructions from the Production Leader or Higher.
• Maintain and upkeep the cleanliness of the workplace.
  
  

• Outstanding career growth & development opportunities.
• Competitive salary & work benefit package.
• Passionate, energetic & innovative work culture.

• Oversee and supervise daily production activities in compliance with ISO 13485 and GMP standards;
• To maintain NPRA's QUEST3+ online platform
• To assists on Medical Device Regulations
• Review and manage production-related documentation, including SOPs and batch production records;
• Support equipment qualification, process validation, and cleanroom environmental monitoring;
• Participate in deviation handling, change control, CAPA, and other quality investigations;
• Assist with production planning and coordinate personnel and materials efficiently;
• Conduct training and assessments for production staff to enhance regulatory awareness;
• Collaborate closely with QA, R&D, and Regulatory departments to ensure product quality and safety.
  
  

• Bachelor's degree or above in Pharmacy, Pharmaceutical Engineering, Biomedical Sciences, or related fields;
• Solid understanding of ISO 13485, NPRA's QUEST3+ online platform and regulatory requirements for medical device manufacturing;
• Licensed Pharmacist qualification is a strong advantage;
• Strong communication and teamwork skills;
• Required language(s): Bahasa Malaysia, English.
• Full time position(s) available
  
  

• KWSP
• SOCSO
• Medical claim included
• Annual and medical leave shall be in accordance with the prevailing Labour Law