Biotechnology Professional

2 weeks ago


Singapore beBeeEmployment Full time $60,000 - $80,000

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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:
Bio Scientist

Location:
Woodlands, Singapore

About the role:

With general supervision the individual will perform routine and critical manufacturing operations, including but not limited to work functions in Cell Culture and Purification areas.

Operates production equipment according to Standard Operating Procedures (SOPs) for the production of commercial and/or clinical products.

How you will contribute:

  1. Primary responsibilities include: Execution of routine and critical production operations
  2. Learn and perform well-defined SOPs
  3. Pursue on-the-job training through Competency Assessments to increase knowledge and understanding
  4. Execute instructions and record data in the Electronic Batch Management (EBM) system if applicable
  5. Execute instructions and record data in the Master Batch Records (MBRs) and Master Formulation Records (MFRs) if applicable
  6. Attain operating knowledge of the Process Control System (PCS)
  7. Record data into logbooks and log-sheets
  8. Review logbooks and log-sheets data
  9. Perform equipment monitoring
  10. Perform basic laboratory tasks including but not limited to sampling, pH and conductivity measurements
  11. Demonstrate aseptic technique in the handling of product and materials if applicable
  12. Troubleshoot and resolve process related issues
  13. Initiate and document production events in the Global Event Management System (GEMS) or equivalent system
  14. Propose document revisions
  15. Complete required training on time
  16. Carry out work in a safe manner, notifying management of safety issues and risks

Key Responsibilities:
  • Manage equipment and support facility related projects by performing scheduled cleaning of equipment
  • Assist in the assembly and disassembly of process equipment
  • Perform standardization of equipment
  • Perform basic 5S housekeeping
  • Initiate Corrective Work Orders in the C3ME system or equivalent system
  • Support change over activities

Staff Technical Training and Development:
  1. Meet and maintain training requirements
  2. Develop and maintain personal development plan
  3. Provide annual performance self-assessment on development plan

Other Responsibilities:
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 we are looking for:

Education and Experience Requirements:
Degree in Chemical Engineering / Bioengineering / Chemical & Biomolecular Engineering / Pharmaceutical Engineering or related and possess 0 - 2 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 - 4 years of relevant experience in the biotechnology or pharmaceutical industry
Nitec in Biotechnology / Chemical Process Technology or related with - 6 years of relevant experience in the biotechnology, pharmaceutical industry
Will work holidays and overtime as required
May be required to adjust work schedule to meet production demands

Key Skills and Competencies:
Ability to following written instructions in the form of Electronic Batch Management (EBM), Batch Records (MBRs, MFRs) and Standard Operating Procedures (SOPs) where applicable
Possess good communication skills
Possess good troubleshooting skills
Full awareness of current Good Manufacturing Practices (cGMP)
Proficient documentation and proficient computer skills
Proficient in aseptic technique where applicable
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.
Ability to work in and out of 2-8 deg C Cold Rooms with appropriate personal protective equipment if required
Ability to work in confined spaces if required
Ability to work around chemicals (alcohols, acids & bases)

More about us:

We are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.

We are a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive 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:

We are proud in our 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:
Singapore - Woodlands

Worker Type:
Employee

Worker Sub-Type:
Regular

Time Type:
Full time

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