Job Information
Takeda Pharmaceuticals Senior Process Engineer (Downstream) in Singapore, Singapore
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Job Description
Job Title: Senior Process Engineer (Downstream)
Location: Woodlands, Singapore
About the role:
Lead troubleshooting of manufacturing operations (Downstream) process/product issues
Technical subject matter expert for manufacturing operations to resolve process issues, perform root cause analysis and impact assessment for process investigation
Lead evaluation of new technologies, plan and execute process improvements
Plan and execute global manufacturing sciences initiatives
Lead, plan and execute site manufacturing sciences activities such as continuous process verification (CPV) program, technology transfer of new products and process monitoring and trending
How you will contribute:
Support site manufacturing (downstream) activities through
Planning and executing activities required for process investigation such as performing process impact assessment, participating and performing root cause analysis. Facilitate stakeholder buy-in from cross functional teams for action plans.
Analyzing process trends, monitoring process performance as part of the CPV program. Escalate and lead investigation in event of any out of trend or process issues
Leading complex process investigations to identify root cause and implement action plans to correct or prevent re-occurrence
Planning and executing process improvements and robustness projects
Leading cycle development for process parameters where applicable
Drafting process training slides and providing process training to cross functional teams
Raising change controls as change owner for process changes
Performing impact assessments for relevant change controls
Providing technical /process parameters for creation and revision of master batch records. Review master batch records.
Lead/Support technology transfer for new technologies/product introduction through
Leading the evaluation of new manufacturing technologies and/or equipment for process improvement or process capabilities build
Planning and executing technical transfer activities according to project timelines. Raise change controls where applicable to support the technical transfer
Monitoring process performance and trending through the site CPV program. Proactively investigate where required to ensure process robustness.
Performing risk assessment, drafting required technical transfer and process control strategy documents and updating lifecycle documents
Strategizing and authoring process validation protocols and reports where needed
Authoring process related sections for regulatory submissions
Mentor and train junior Manufacturing Sciences engineers
Act as technical SME providing relevant technical inputs for process improvements, issues or process technical transfer
Support audits, author regulatory submissions and responses
Lead and execute global manufacturing sciences initiatives according to project timelines
Responsibility to adhere to any applicable EHS requirements.
Commitment to a fair and respectful relationship to others and behavior in accordance with Takeda’s Code of Conduct.
Any other duties as assigned by supervisor.
What you bring to Takeda:
Education and Experience Requirements
Bachelor’s Degree in Biochemistry, Chemistry, Chemical Engineering, Biotechnology, Biochemical Engineering with at least 6 years of relevant experience or Master’s Degree with 4 years of relevant work experience or a PhD with at least 2 years of work experience in the relevant technical area
Hands-on experience with cell culture/ upstream processes and/or downstream processes in a manufacturing or development environment
Has knowledge of cGMPs
Key Skills and Competencies
Strong technical knowledge and expertise in process understanding and application in biopharmaceutical processes with ability to coach junior Manufacturing Sciences engineers
Strong analytical skills including demonstration of systematic evaluation of potential issues, correlation or cause and effect relationships, root cause analysis methodology. Able to identify risk mitigation actions for implementation.
Strong communication, stake holder management, project management and conflict resolutions skills
Willingness to learn
Team worker/ able to work in matrix environment
Independent worker/ Self starter
More about us:
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Empowering our people to shine:
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
Locations
SGP - Singapore - Woodlands
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Takeda Pharmaceuticals
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