Quality Operations Intern at Takeda Pharmaceutical Company Limited USA

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

18 Jun, 26

Salary

0.0

Posted On

20 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Systems, GMP Compliance, Batch Records Review, Investigation Ownership, SOP Development, Documentation Practices, Regulatory Compliance, Microsoft Office, Interpersonal Communication, Verbal Communication, Written Communication, Time Management, Emotional Handling

Industry

Pharmaceutical Manufacturing

Description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Job Title: Quality Operations Intern Location: Singapore About the role: In this internship position, the intern will be a member of the Quality Operations (QO) team in providing quality oversight to the manufacturing team to ensure GMP compliance at Takeda Singapore. How you will contribute: Quality Systems Representative Member of the QO team in ensuring quality oversight at the manufacturing suite Partner the manufacturing team in the implementation and adherence to the various quality systems and GMP requirements at the manufacturing suite Participate in meeting with the manufacturing for information learning/sharing and alignment of best practices Support the compliance, regulatory, inspections and training activities as required, and any other responsibilities as assigned by supervisor. QO Operations Review executed manufacturing batch records (MBR) Take on ownership for investigation relating to quality operations. Support the manufacturing team with any quality interpretation, queries and issues. Support the manufacturing team with development and writing of process standard operating procedures and master batch records ensuring compliance with current good documentation practices and the applicable global procedures and regulatory requirements. Other responsibilities Perform timely archival of QO documents. Leadership Build strong partnership with all other departments to ensure open communications and acceptance 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: Background in Chemistry, Biochemistry, Biotechnology or equivalent Keen interest to work in a biopharmaceutical industry Knowledge and experience using Microsoft Office Committed to the role assigned. Positive mindset and motivated. Able to understand constraints at times and be flexible. Good Interpersonal, Verbal and Written Communication Skills required. Ability to work and collaborate within the team. Good in emotional handling. Good time management skills 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, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations SGP - Singapore - Woodlands Worker Type Employee Worker Sub-Type Paid Intern (Fixed Term) (Trainee) Time Type Full time 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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Responsibilities

The intern will serve as a Quality Systems Representative within the Quality Operations team, providing quality oversight to manufacturing to ensure GMP compliance. Key duties include partnering with manufacturing on quality systems implementation, reviewing batch records, and supporting compliance and training activities.