Job Description

Work Schedule OtherEnvironmental Conditions OfficeHow Will You Make an Impact?At Thermo Fisher Scientific, we have an incredible mission: to enable our customers make the world healthier, cleaner, and safer. Our responsibility in supporting this vision is to consistently strive to work together and enable our customers more effectively. We have the 4i Values \xe2\x80\x93 Integrity, Intensity, Innovation, and Involvement that define the way we work together and with our customers. As we operate within the 4i framework, there are three areas that we believe could really lead to a breakthrough in the way we work together: Accountability. Innovation. Risk tolerance.When you join us at Thermo Fisher Scientific, you will be part of an inquisitive, driven team that shares your passion for exploration and discovery. With revenues of approximately $40 billion, we give our people the resources and opportunities to make significant contributions to the world. Every year, we make millions of DNA microarray chips to support the work of researchers and industrial applications. Application areas that benefit from our products include plant and animal agriculture, precision medicine, reproductive health and more.We are looking to hire a highly motivated individual who can contribute to the team towards making great microarray products for our customers.Responsibilities and AuthoritiesYou will be part of a team of Process and Equipment Engineers supporting Microarray manufacturing at Gul Circle site in Singapore.Lead process improvement with various departments, such as Manufacturing, Quality, Global Technical Operations, Supply Chain and / or R&D to drive continuous improvement efforts and achieve operational excellence.Responsible for analyzing existing processes, developing and improving manufacturing processes to ensure safety, quality and efficiency to improve productivity and drive cost reduction.Conduct process analysis and perform root cause analysis (RCA), to evaluate process performance, identify bottlenecks, and implement corrective actions.Validating and verifying critical systems and processes to ensure they function accurately and consistently. This includes collaborating with Manufacturing Quality, and Supply Chain to drive validation activities in a timely manner.Documentation and reporting of processes, procedures, change control and deviation. This includes process and material related changes, software applications, enterprise systems and corrective and preventative actions (CAPA).Conduct risk assessments to identify potential risks or hazards associated with systems or processes.Maintains accurate GMP records consistent with company policy and legal requirements.Ensure compliance and industry standards consistency to safety, environmental, and quality requirements.How will you get here?EducationMinimum bachelor\'s degree in Engineering or Science related field from an accredited university.ExperienceMinimum 5 years of working experience in a fast-paced environment of moderate complexity preferably in Semiconductor, Medical Devices, and / or Pharmaceutical industry.Familiar with regulation and industry standard (e.g., ISO13485).Technical experience must include Commissioning, Qualification and Validation (CQV), leading process improvement and optimizing manufacturing processes.Proven track record in leading validation projects, handle timelines, coordinate resources, and communicate optimally with multi-functional teams.Strong analytical skills, ability to identify and resolve validation-related problems.Experience in risk assessment methodologies, RCA and other problem-solving techniques.Excellent communication skills, both written and verbal, to effectively collaborate with stakeholders, presenting validation findings and recommendations.Proficiency in lean manufacturing principles and continuous improvement methodologies.

Thermo Fisher Scientific