Lead Manufacturing Expert

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Job Description

Company Profile:

Takeda's Singapore biologics manufacturing facility focuses on manufacturing potentially life-saving medicines for patients suffering from rare blood disorders such as Hemophilia A and B. As part of the company’s Biologics Operating Unit network, the site is Takeda’s only biologics drug substance manufacturing facility in Asia. The facility has two buildings, including manufacturing suites and laboratories, as well as Takeda’s first positive energy building certified by Singapore’s Building and Construction Authority’s Green Mark scheme in 2022.

Job Title: Lead Manufacturing Expert
Location: Woodlands, Singapore

About the role:

The individual will work independently with regular reporting to the line manager, to support and coordinate routine GMP manufacturing life cycle and day-to-day operational activities associated with the products and process equipment in Takeda Singapore, including but not limited to Suite 1 Manufacturing, Suite 2 Manufacturing, and Manufacturing Support areas. In addition, the individual will provide lead key initiatives not limited to continuous improvement, validation, and CAPEX activities.

How you will contribute:

The individual will support the EHS and cGMP compliance of day-to-day and tactical manufacturing activities, ensuring production activities are executed successfully. Primary responsibilities include: (70%)

• Work hand-in-hand with the shift teams to ensure adherence to the production plan and resolve issues as required.
• Be considered to have more than one area of manufacturing expertise, for example, Upstream processing/Downstream processing/ Equipment Preparation/ Buffer Preparation and/or knowledge in key systems like EBM/XFP/CIP/SIP.
• Act as subject matter expert during audits, explaining and walking through specific process operations or investigations as applicable.
• Carry out deviations investigations in the GEMS system, including product impact assessments and implement CAPAs.
• Be a change control owner in the CCMS system, if applicable.
• Maintain recipe configuration management documentation, if applicable.
• Carry out material support activities including liaising with MLCM or vendors to address material issues, if applicable.
• Develop and implement CAPAs arising from audits.
• Inform management of events impacting the production schedule.
• Propose and review document revisions.
• Carry out work in a safe manner, notifying management of safety issues and risks.

The individual will manage equipment and support facility-related projects by: (20%)

• Assist in audit preparation as well as documentation related to audit responses, Adverse event notification review, and Annual Product Reviews as required.
• Lead the transfer/implementation of new processes and commissioning & validation activities of new projects.
• Lead complex investigations.
• Lead continuous improvement.
• Lead product changeover activities.
• Monitor and analyze processing parameters for atypical trends and improvement opportunities.
• Act as a department training coordinator as required.

Staff Technical Training and Development: (10%)

• Meet and maintain training requirements on time.
• Provide technical training for area personnel as required.
• Develop training material as required.
• Train and coach team members as required.
• Develop and maintain a personal development plan.
• Participate in site or global strategic initiatives as required.
• Provide feedback to peers to help staff development as required.
• Provide annual performance self-assessment on the development plan.

Others:

• 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 the supervisor.

What you bring to Takeda:

Education and Experience Requirements

• Degree in Chemical Engineering / Bioengineering / Chemical & Biomolecular Engineering / Pharmaceutical Engineering or related and possesses 7 years of relevant experience in the biotechnology or pharmaceutical industry.
• Diploma in Applied Chemistry / Biomedical Sciences / Chemical Engineering / Food Science & Technology / Biologics & Process Technology / Chemical & Pharmaceutical Technology / Food Science & Nutrition / Molecular Biotechnology / Biotechnology / Chemical & Biomolecular Engineering / Pharmacy Science or related and possess years of relevant experience in the biotechnology or pharmaceutical industry.
• Nitec in Biotechnology / Chemical Process Technology or related with 12 years of relevant experience in the biotechnology or pharmaceutical industry.
• Excellent self-motivated team player with hands-on attitude and excellent communication skills.
• Able to work on odd hours as required.

Key Skills and Competencies

The individual should have a good understanding of cGMP manufacturing aspects and have hands-on manufacturing experience.

• Excellent at technical writing as required for Electronic Batch Management (EBM), Batch Records (MBRs, MFRs), and Standard Operating Procedures (SOPs).
• Possess good communication and presentation skills.
• Ideally be Green belt trained/certified and possess good understanding of LEAN and Six Sigma concepts.
• Possess critical thinking skills.
• Full awareness of current Good Manufacturing Practices (cGMP).
• Proficient documentation skills and computer skills including Microsoft Excel/Word/Powerpoint.
• Good time management and team coordination skills.
• Ability to work in a matrix environment.
• Understanding of requirements from support functions and their capabilities.
• Experience as a system user of business systems such as C3ME, XFP, and Trackwise.
• Will work holidays and overtime as required.
• May be required to adjust work schedule to meet production demands.
• Ability to wear personal protective equipment such as safety glasses/goggles, gloves, and safety shoes.
• Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas.
• May be required to stand for 6 hours in a production suite.
• May be required to climb ladders and work platforms.
• May be required to stoop or bend to check or troubleshoot equipment.
• May be required to work around chemicals (alcohols, acids & bases).

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 of 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