Total 5 job vacancies by Biontech Pharmaceuticals Asia Pacific Pte. Ltd.

As a part of our team of more than 5.000 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.

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 E&I
Maintenance engineer (E&I) is to manage and optimize electrical and instrumentation systems essential for the manufacturing processes to achieve maximum plant availability. This involves design, implement, and maintain electrical and instrumentation systems, implement, and oversee precise calibration processes in accordance with current Good Manufacturing Practices, Good Engineering Practices, and EHS requirements.

Your main responsibilities are:

• Provide technical expertise for installation, maintenance, and troubleshooting of electrical equipment and instrumentation to ensure minimal downtime and optimal performance of manufacturing equipment’s
• Develop and implement calibration program for instruments, sensors, and control devices to maintain accuracy and precision in measurements for manufacturing and quality control process. Ensure that all calibrated instruments meet regulatory standards and compliance requirements
• Maintain accurate and detailed calibration records and documentation of electrical and instrumentation systems, including schematics, drawings, and procedures, for compliance and troubleshooting purposes
• Program and troubleshoot Programmable Logic Controllers (PLCs) to control and automate various processes within the manufacturing facility
• Promptly investigate equipment-related deviations and safety issues by using appropriate problem-solving tools and provide efficient preventive and corrective measures
• Initiate change management, provide impact assessments and carrying out electrical and instrumentation systems. This includes managing project schedules, resource plans, coordinating with vendors, and handling material management
• Collaborate with validation teams to support equipment qualification and validation activities, ensuring calibrated instruments meet required performance specifications
• Identify opportunities to enhance energy efficiency in electrical systems, supporting sustainable practices within the manufacturing facility
• Perform or participate in HAZOP/Risk assessment to actively identify and implement mitigation actions for engineering and maintenance activities
• Participate in regulatory audits and ensure compliance with regulations and standards in engineering and maintenance areas
• Create Standard operating procedures and Provide training to personnel on handling of equipment’s and performing Calibration and Maintenance tasks

What you have to offer:

• A bachelor’s Degree/Diploma in Electrical/ Electronics/ Instrumentation/ Control engineering or relevant fields
• More than 5 years of experience with strong Electrical & Instrumentation discipline knowledge together with hands-on working experience in biopharmaceutical manufacturing will be an advantage
• GMP expertise and good understanding of working in regulated environment
• Proficiency in troubleshooting, repairing, and maintaining highly automated equipment’s and systems
• Ability to adapt to changing priorities effectively and work at the start-up environment
• Strong communication skills and ability to effectively collaborate in dynamic, cross functional matrix environment
• Strong problem-solving skills and preferably with good proven knowledge in lean sigma methodology

Benefits for you:

We offer a competitive compensation package which will be determined by the contract type and selected candidate’s qualifications and experience.

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!

BioNTech - As unique as you

As a part of our team of more than 5000 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.

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 Maintenance
As a Technical ExpertvEngineering Maintenance you provide technical expertise for maintenance of various plant equipment’s and systems essential for manufacturing processes to achieve maximum plant availability. This involves maintaining and optimizing equipment and facilities in accordance with current Good Manufacturing Practices, Good Engineering Practices and EHS requirements.
Your main responsibilities are:

• Develop, Implement, Plan and execute predictive/preventive maintenance program for equipment’s and systems to ensure minimal downtime and optimal performance of manufacturing equipment’s
• Conduct diagnosis and troubleshooting of equipment failures to determine the root cause promptly to increase the machine uptime and ensuring continuous operation
• Promptly investigate equipment-related deviations and safety issues by using appropriate problem-solving tools and provide efficient preventive and corrective measures
• Identify and Manage inventory of spare parts for mechanical equipment, always ensuring availability for maintenance or repairs
• Initiate change management, provide impact assessments and carrying out field equipment modifications. This includes managing project schedules, resource plans, coordinating with vendors and handling material management
• Perform testing, commissioning and qualification (IQ, OQ, PQ) activities as applicable
• Identify opportunities to enhance energy efficiency in equipment’s and facilities to support sustainable practices
• Perform or participate in HAZOP/Risk assessment to actively identify and implement mitigation actions for engineering and maintenance activities
• Participate in regulatory audits and ensure compliance with regulations and standards in engineering and maintenance areas
• Adhere to regulatory standards by diligently maintaining precise documentation of maintenance activities, including thorough records of repairs, replacements, and preventive maintenance tasks
• Create Standard operating procedures and Provide training to personnel on handling of equipment’s and performing Maintenance tasks

What you have to offer:

• A bachelor’s Degree/Diploma in Mechanical/Chemical or relevant fields
• More than 5 years of experience with strong mechanical discipline knowledge together with hands-on working experience in biopharmaceutical manufacturing will be an advantage
• GMP expertise and good understanding of working in regulated environment
• Proficiency in troubleshooting, repairing, and maintaining highly automated equipment’s and systems
• Ability to adapt to changing priorities effectively and work at the start-up environment
• Strong communication skills and ability to effectively collaborate in dynamic, cross functional matrix environment
• Strong problem-solving skills and preferably with good proven knowledge in lean sigma methodology

Benefits for you:

We offer a competitive compensation package which will be determined by the contract type and selected candidate’s qualifications and experience.

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!

BioNTech - As unique as you

As a part of our team of more than 5.000 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.

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 CSV

We are looking for a result driven CSV Expert to become one of the pioneers in our newly established manufacturing plant in Singapore. The candidate will be responsible for commissioning and qualification oversight for our automated and IT systems, to ensure our compliance to the company procedures, cGMP expectations and regulatory requirements.

Your responsibilities:

• Provides expertise in performing Computerized Systems Validation.
• Primary personnel for the qualification of Computerized Systems including Automation Systems (PCS 7, EMS, MES) and GMP equipment qualifications operating within the framework of regulations (GxP, 21CFR11, etc.)
• Perform collaborative work with the Compliance Engineering team on other CQV activities.
• Coordinate with both internal and external teams (manufacturing, engineering, quality, vendors, contractors, etc.) to achieve the site objectives.
• Prepare, review, and approve of SOPs and qualification-related documentations (protocols and reports)
• Ensure that the qualification strategy is sound and adhere to company standards and regulatory requirements.
• Investigate deviations and write deviation reports and findings.
• Raise and follow-up change control records.

What you have to offer:

• Degree in Engineering/Science or related studies.
• Minimum of 8 years’ experience in pharma/ biotech manufacturing industry with at least 5 years in CSV activities.
• High level of understanding in Regulatory compliance
• Familiar with working in a GxP environment and keeping up to date with current GxP, with flexibility to change as needed due to new regulatory requirements and technologies, as relevant for clinical and commercial supply.
• In-depth knowledge in Computer System Validation (CSV), GAMP 5, 21 CFR Part 11, ER/ES, validation lifecycle, current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) in a biotech facility
• Good knowledge of GxP, GDP, CQV approaches including Validation Lifecycle approach (URS, DQ, FAT/SAT, IOQ, CSV, Cleaning/ Thermal Validation etc.), regulatory requirements and best industry practices.
• Competent in technical writing and presentations. Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
• Problem solver and has ability to make decisions.
• Able to work independently, self-starter, self-motivated and task oriented.
• Good communication skills and able to openly communicate and escalate any relevant issues.
• Develop positive relationship with a strong set of interpersonal skills.

Benefits for you

We offer a competitive compensation package which will be determined by the contract type and selected candidate’s qualifications and experience.

As a part of our team of more than 5.000 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.

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

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

• Design and develop automation solutions for various Biopharma manufacturing processes, including production, packaging, and quality control.
• Collaborate with cross-functional teams to understand requirements and translate them into technical specifications.
• Select appropriate hardware and software components to achieve automation objectives.
• Oversee the installation and commissioning of automation systems, ensuring adherence to project timelines and budgets.

Maintenance and Optimization

• Monitor and maintain automated systems to ensure uninterrupted operation.
• Troubleshoot technical issues and implement corrective actions to minimize downtime.
• Conduct routine inspections and preventive maintenance activities to prolong equipment lifespan and enhance reliability.
• Identify opportunities for automation optimization and efficiency improvements.
• Provide technical guidance to automation technicians. Ensure the training records are kept up to date.
• Manage the cybersecurity requirements and work closely with IT team to implement a safe working environment free from cyber threats.

Regulatory Compliance

• Ensure that automation solutions comply with regulatory requirements, GMP (Good Manufacturing Practice) standards, and other relevant regulations.
• Participate in validation activities, including IQ/OQ/PQ (Installation Qualification/Operational Qualification/Performance Qualification) protocols and documentation.
• Keep up with of industry trends and regulatory updates to proactively address compliance issues.

Risk Management and Quality Assurance

• Conduct risk assessments of automated systems to identify potential hazards and implement risk mitigation strategies.
• Support quality assurance efforts by ensuring that automation processes meet specified quality standards.
• Investigate deviations or non-conformances related to automation systems and implement corrective and preventive actions.

Continuous Improvement

• Drive continuous improvement initiatives to enhance automation capabilities, efficiency, and cost-effectiveness.
• Collaborate with stakeholders to identify areas for process optimization and automation enhancements.
• Implement best practices and innovative technologies to stay at the forefront of automation in biopharmaceutical manufacturing.

What you have to offer:

• Bachelor’s or master’s degree in engineering (e.g., Electrical, Mechanical, Chemical, or Biomedical Engineering) or related field.
• A minimum of 5 years of experience in automation engineering, preferably within the biopharmaceutical or pharmaceutical industry.
• Strong knowledge of automation technologies, including PLCs, SCADA systems, software, Data warehouse like OSIPI and industrial networking protocols. Siemens PCS7 will be added advantage.
• Familiarity with regulatory requirements and standards governing biopharmaceutical manufacturing processes.
• 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.
• Experience in start-ups, commissioning & qualification (CSV) of Automation and process control systems.
• Knowledge of GAMP software development lifecycle, ANSI/ISA-S88 and S95 industry standards
• Excellent problem-solving skills and ability to troubleshoot complex technical issues.
• Effective communication and teamwork abilities, with the capacity to collaborate with cross-functional teams.
• 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.

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!

As a part of our team of more than 5000 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.

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 Maintenance
As a Technical ExpertvEngineering Maintenance you provide technical expertise for maintenance of various plant equipment’s and systems essential for manufacturing processes to achieve maximum plant availability. This involves maintaining and optimizing equipment and facilities in accordance with current Good Manufacturing Practices, Good Engineering Practices and EHS requirements.
Your main responsibilities are:

• Develop, Implement, Plan and execute predictive/preventive maintenance program for equipment’s and systems to ensure minimal downtime and optimal performance of manufacturing equipment’s
• Conduct diagnosis and troubleshooting of equipment failures to determine the root cause promptly to increase the machine uptime and ensuring continuous operation
• Promptly investigate equipment-related deviations and safety issues by using appropriate problem-solving tools and provide efficient preventive and corrective measures
• Identify and Manage inventory of spare parts for mechanical equipment, always ensuring availability for maintenance or repairs
• Initiate change management, provide impact assessments and carrying out field equipment modifications. This includes managing project schedules, resource plans, coordinating with vendors and handling material management
• Perform testing, commissioning and qualification (IQ, OQ, PQ) activities as applicable
• Identify opportunities to enhance energy efficiency in equipment’s and facilities to support sustainable practices
• Perform or participate in HAZOP/Risk assessment to actively identify and implement mitigation actions for engineering and maintenance activities
• Participate in regulatory audits and ensure compliance with regulations and standards in engineering and maintenance areas
• Adhere to regulatory standards by diligently maintaining precise documentation of maintenance activities, including thorough records of repairs, replacements, and preventive maintenance tasks
• Create Standard operating procedures and Provide training to personnel on handling of equipment’s and performing Maintenance tasks

What you have to offer:

• A bachelor’s Degree/Diploma in Mechanical/Chemical or relevant fields
• More than 5 years of experience with strong mechanical discipline knowledge together with hands-on working experience in biopharmaceutical manufacturing will be an advantage
• GMP expertise and good understanding of working in regulated environment
• Proficiency in troubleshooting, repairing, and maintaining highly automated equipment’s and systems
• Ability to adapt to changing priorities effectively and work at the start-up environment
• Strong communication skills and ability to effectively collaborate in dynamic, cross functional matrix environment
• Strong problem-solving skills and preferably with good proven knowledge in lean sigma methodology

Benefits for you:

We offer a competitive compensation package which will be determined by the contract type and selected candidate’s qualifications and experience.

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!

BioNTech - As unique as you