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Chemist I
2 weeks ago
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
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: Chemist I (Analytical) – 12 months contract
Location: Woodlands, Singapore
About the role:
This position is required to perform all tasks associated with the QC analytical lab operations which include chemical analysis, biochemical analysis, equipment calibration/maintenance, records review, records approval, deviation/investigation write up/review, equipment qualification, method validation, method transfer and other tasks as assigned.
How you will contribute:
Core Responsibilities:
Perform chemistry, biochemistry analysis of in-process samples, bulk drug substance (BDS), non-routine samples.
Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures.
Perform equipment calibration and maintenance.
Perform review/approval of QC records/ log books.
Perform trending of lab results.
Initiate and participate in Out Of Specification (OOS), Invalid test and Lab Deviation Investigation WriteUp and assist in timely closure of laboratory invalid results, lab investigation and CAPA.
Write/revise SOPs, forms, training qualifications (TQ) and risk assessments (RA).
Act as a Subject Matter Expert (SME) to provide technical advice to QC Personnel in laboratory related troubleshooting e.g. lab equipment failure, method.
Provide appropriate training for the QC Analytical Team.
Participate in method validation/ transfer or equipment qualification when necessary.
Ensure proper, safe handling and disposal of waste; ensuring a safe working environment.
General Responsibilities:
Carry out 5S and ensure good housekeeping of Analytical Lab area.
Support and participate in Operation Excellence initiatives (such as GEMBA and GMP walk).
Participate in projects towards improving safety performance and continuous improvement initiatives.
QC Chemist may cover for another QC Chemist of similar functions/areas in his/her absence by signing documents on his/her behalf.
Assist Supervisor to support internal and external compliance audits.
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 Degree in Chemistry, Biochemistry, Biotechnology or equivalent, preferably with more than 1 year of experience in Pharmaceutical, Biopharmaceutical or related manufacturing environment.
Demonstrated ability to collaborate with cross functional or cross sites to achieve objectives.
Key Skills and Competencies:
Project Management Skills:
Organization and planning skills.
Analytical and logical thinking skills.
Ability to work and collaborate within the team.
Technical Skills:
Has substantial knowledge and understanding in terms of regulatory standards requirements e.g. USP, EP, 21CFR, ICH etc.
Knowledge in Ion Chromatography (IC), High Performance Liquid Chromatography (HPLC), Fluorescence spectrometer (FLS), pH, Conductivity, Gel electrophoresis (SDS Page or Western Blot), Potency and ELISA.
Knowledge in Empower and LIMS.
Knowledge in Microsoft Office.
Problem Solving:
Solves problems and implements corrective actions using six sigma tools.
Others:
Be a subject matter expert in given areas of responsibilities and able to solve issues related to his/her area of expertise.
Some knowledge in safety principles, practices, regulations and procedures related to the work. Must be detail oriented.
Committed to the role assigned.
Positive mindset and motivated.
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 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
Fixed Term (Fixed Term)
Time Type
Full time
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