Technical Expert Engineering Automation (Senior Engineer)
Open for hire at one of the following locations – Singapore. - Job ID: 6877
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We aim to reduce the suffering of people with life-changing therapies by harnessing the potential of the immune system to develop novel therapies against cancer and infectious diseases. While doing so, we are guided by our three company values: united, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives.
Technical Expert Engineering Automation (Senior Engineer)
The Automation Engineer is responsible for designing, implementing, and maintaining automated systems in the biopharmaceutical manufacturing environment. This role involves working at the intersection of engineering, technology, and biopharmaceutical processes, ensuring the efficient and compliant operation of automated equipment and systems.
Your main responsibilities:
System Design and Implementation
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Design and develop automation solutions for various Biopharma manufacturing processes, including production, packaging, and quality control.
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Collaborate with cross-functional teams to understand requirements and translate them into technical specifications.
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Select appropriate hardware and software components to achieve automation objectives.
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Oversee the installation and commissioning of automation systems, ensuring adherence to project timelines and budgets.
Maintenance and Optimization
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Monitor and maintain automated systems to ensure uninterrupted operation.
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Troubleshoot technical issues and implement corrective actions to minimize downtime.
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Conduct routine inspections and preventive maintenance activities to prolong equipment lifespan and enhance reliability.
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Identify opportunities for automation optimization and efficiency improvements.
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Provide technical guidance to automation technicians. Ensure the training records are kept up to date.
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Manage the cybersecurity requirements and work closely with IT team to implement a safe working environment free from cyber threats.
Regulatory Compliance
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Ensure that automation solutions comply with regulatory requirements, GMP (Good Manufacturing Practice) standards, and other relevant regulations.
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Participate in validation activities, including IQ/OQ/PQ (Installation Qualification/Operational Qualification/Performance Qualification) protocols and documentation.
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Keep up with of industry trends and regulatory updates to proactively address compliance issues.
Risk Management and Quality Assurance
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Conduct risk assessments of automated systems to identify potential hazards and implement risk mitigation strategies.
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Support quality assurance efforts by ensuring that automation processes meet specified quality standards.
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Investigate deviations or non-conformances related to automation systems and implement corrective and preventive actions.
Continuous Improvement
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Drive continuous improvement initiatives to enhance automation capabilities, efficiency, and cost-effectiveness.
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Collaborate with stakeholders to identify areas for process optimization and automation enhancements.
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Implement best practices and innovative technologies to stay at the forefront of automation in biopharmaceutical manufacturing.
What you have to offer:
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Bachelor’s or master’s degree in engineering (e.g., Electrical, Mechanical, Chemical, or Biomedical Engineering) or related field.
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A minimum of 5 years of experience in automation engineering, preferably within the biopharmaceutical or pharmaceutical industry.
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Strong knowledge of automation technologies, including PLCs, SCADA systems, software, Data warehouse like OSIPI and industrial networking protocols. Siemens PCS7 will be added advantage.
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Familiarity with regulatory requirements and standards governing biopharmaceutical manufacturing processes.
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Experience with test protocols and executions eg. IQ/OQ/PQ, test scripts with relevant key deliverables such as plan, report, deviation, change control and industry best practices etc.
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Experience in start-ups, commissioning & qualification (CSV) of Automation and process control systems.
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Knowledge of GAMP software development lifecycle, ANSI/ISA-S88 and S95 industry standards
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Excellent problem-solving skills and ability to troubleshoot complex technical issues.
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Effective communication and teamwork abilities, with the capacity to collaborate with cross-functional teams.
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Attention to detail and commitment to safety, quality and compliance.
Benefits for you
We offer a competitive compensation package which will be determined by the contract type and selected candidate’s qualifications and experience.
How to apply
Apply now and simply send us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details by using our online form.
Please note:
- Only applications sent via our online form shall be considered.
- Only Candidates with the right qualifications and relevant experience shall be shortlisted
- Incomplete applications shall be rejected
- BioNTech will run a background check during the hiring process
We are looking forward receiving your application.
*BioNTech does not differentiate on the basis of gender, political opinion, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other aspect of personal status. We are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. Most important – it’s a match!
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