Training Lead (BioLife Plasma)

IDN - 2710 PT Takeda Life Sciences

Pluit

On-site

IDR 600,000,000 - 1,000,000,000

Full time

14 days+
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Job summary

Takeda Life Sciences Indonesia is seeking a Training Lead to build and coordinate learning and development for BioLife Plasma Operations in Indonesia. The role ensures staff are prepared, compliant, and aligned with Takeda’s quality standards, while aligning local programs with global L&D strategy.

Responsibilities include designing and implementing regulatory and compliance trainings, managing the local LMS, Collaborating with senior leaders, and continually improving training effectiveness

Qualifications

  • Bachelor’s degree in Education, Life Sciences, Psychology, Human Resources, or related field.
  • Certification in adult learning, instructional design, or organizational development preferred.
  • 5–8 years of experience in Learning & Development, preferably in healthcare, pharma, or plasma environments.
  • Experience implementing or managing training systems (LMS) and regulatory training documentation.

Responsibilities

  • Translate global L&D strategy into a local Indonesia roadmap and promote a culture of lifelong learning.
  • Develop, adapt and implement training programs meeting local regulatory and operational requirements, including GxP, compliance and safety training.
  • Establish and maintain a local training management process with LMS coordination and documentation.
  • Collaborate with Country Head, Medical Director, Quality & Regulatory Manager, HR Lead, and regional teams to align programs.
  • Measure training effectiveness using data and feedback and drive continuous improvement.

Skills

Learning Expertise
Cultural Agility
Strategic Alignment
Collaboration
Communication
Analytical Thinking
Innovation
Organization & Accuracy

Education

Bachelor's degree in Education/Life Sciences/Psychology/HR
Adult learning/ instructional design cert preferred

Tools

LMS

Job description

Job Description Objective / Purpose

The Training Lead – Indonesia is responsible for building and coordinating all learning and development activities for BioLife Plasma Operations in Indonesia. As BioLife establishes and expands in this new market, the Training Lead plays a crucial role in ensuring that all employees are well‑prepared, compliant, and capable of operating to Takeda’s global quality and ethical standards. The role combines strategic alignment with hands‑on implementation — ensuring that all training programs support BioLife’s business goals, comply with regulatory requirements, and foster a strong culture of continuous learning and professional growth.

Accountabilities
  • Training Strategy and Culture Development (≈25%) Translate BioLife’s global Learning & Development (L&D) strategy into a local roadmap for Indonesia. Promote a culture of lifelong learning, encouraging employees to take ownership of their development. Identify local training priorities aligned with operational goals and regulatory needs. Support leadership development and capability‑building initiatives as the organization grows. Ensure that training strategy supports employee engagement, retention, and long‑term organizational success.
  • Training Design and Implementation (≈25%) Develop, adapt, and implement training programs that meet local regulatory and operational requirements. Ensure that all GxP, compliance, and safety training is delivered and documented in line with BioLife and local regulations. Adapt global training materials and tools to fit the Indonesian context and language. Deliver selected trainings directly (especially onboarding and compliance sessions).
  • Training Process and Systems (≈20%) Establish and maintain a local training management process, ensuring consistent standards and documentation. Set up and manage the local Learning Management System (LMS) processes in coordination with regional and global teams. Ensure all training completion data is up to date, auditable, and inspection‑ready. Coordinate external training providers and maintain trainer records where applicable.
  • Collaboration and Stakeholder Engagement (≈15%) Partner with the Country Head, Medical Director, Quality & Regulatory Manager, and HR Business Lead to ensure training programs meet operational and compliance needs. Work closely with global and regional L&D colleagues to share insights and align local programs with BioLife’s broader learning framework. Collaborate with line managers to assess team development needs and set training priorities.
  • Evaluation and Continuous Improvement (≈10%) Measure the effectiveness and impact of training programs using data, feedback, and performance metrics. Identify opportunities for improvement and innovation in training design and delivery. Introduce modern learning methods (digital, blended, experiential learning) as feasible.
  • Training Coordination and Administration (≈5%) Coordinate training logistics, scheduling, and communications. Ensure proper documentation of attendance, certificates, and compliance records. Support audits and inspections by providing relevant training documentation.
Education & Competencies (Technical and Behavioral)

Bachelor’s degree in Education, Life Sciences, Psychology, Human Resources, or related field. Certification in adult learning, instructional design, or organizational development preferred.

Professional Experience

5–8 years of experience in Learning & Development, preferably within healthcare, pharma, or plasma environments. Experience implementing or managing training systems (LMS) and regulatory training documentation. Familiarity with GxP or GMP training requirements strongly preferred. Exposure to international or multicultural environments desirable.

Key Skills and Competencies
  • Learning Expertise: Strong understanding of learning processes, adult learning principles, and blended learning formats.
  • Cultural Agility: Ability to adapt training programs and communication styles to local culture and organizational maturity.
  • Strategic Alignment: Understands how learning supports business goals and compliance requirements.
  • Collaboration: Builds strong partnerships across functions and geographies.
  • Communication: Engages learners at all levels and communicates complex information clearly.
  • Analytical Thinking: Uses data to measure training effectiveness and recommend improvements.
  • Innovation & Adaptability: Open to new methods, tools, and technologies to drive learning effectiveness.
  • Organization & Accuracy: Strong attention to detail in managing documentation and compliance records.
Other Requirements

Fluent in Bahasa Indonesia and English. Willingness to travel across Indonesia to support plasma center training and audits. Commitment to Takeda’s values of Integrity, Fairness, Honesty, and Perseverance. Adherence to Takeda’s Code of Conduct and EHS and Quality standards.

Locations

Jakarta, Indonesia

Worker Type

Employee

Worker Sub-Type

Regular Time Type

Full time

Company Information

Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.

Takeda is an equal opportunity employer. For applicants of U.S and Puerto Rico positions: Click here to learn about our commitment to Equal Employment Opportunity (EEO). If you are limited in the ability to use our job application tool, or otherwise require a reasonable accommodation for a disability please click here.

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