QC Specialist Raw Material & Packaging Material

Takeda; Indonesia; On-site; IDR 111,600,000 - 167,400,000; Full time

Job summary

Takeda in Bekasi, Indonesia is seeking a QC Specialist to manage laboratory operations, including material testing and compliance with procedures. Candidates should have a Bachelor's degree in pharmacy and at least 1 year of experience in a QC role.

The successful applicant will be responsible for scheduling material sampling, ensuring data integrity in testing, and supporting internal audits within the QC Department.

This full-time position offers a fixed-term contract and requires proficiency in English and necessary laboratory skills.

Qualifications

• Minimum 1 year of experience in QC Specialist or a closely related position.
• Strong analytical, communication, and interpersonal skills are required.
• Good competency in reading, listening, and speaking English is necessary.

Responsibilities

• Schedule and manage incoming material sampling and testing activities.
• Verify testing reports for data integrity and compliance.
• Support activities related to QC Laboratory materials.
• Create specifications for packaging and raw materials.
• Serve as Lead Investigator for laboratory investigations.

Skills

Laboratory skills

Analytical skills

Communication skills

Interpersonal skills

MS Word proficiency

MS Excel proficiency

MS PowerPoint proficiency

English competency

Education

Associate's degree/ Bachelor of Pharmacist

Job description

Duties & Responsibilities

• Schedule incoming material sampling, identification, and testing activities.
• Verify testing reports to ensure data integrity and compliance with established analytical procedures for raw and packaging material testing.
• Support activities related to alternating or secondary sources of materials in the QC Laboratory.
• Support the preparation and availability of registration documents required from the QC Department.
• Create and revise specifications for packaging materials and raw materials.
• Support the completion of CAPA and CCR action task.
• Support the creation and revision of SOPs, conduct periodic reviews of local SOPs, and perform gap assessments against Global SOPs.
• Manage laboratory operational activities, including Excel spreadsheet control, routine logbook review, periodic backup of QC instruments, and management of reagents and standards.
• Serve as Lead Investigator for laboratory investigations and deviations.
• Contribute to the implementation of energy-saving initiatives within the assigned work area.
• Ensure EHS rules are properly implemented by teams within their respective work areas, in the capacity of EHS Committee Member and Chemical Occupational Health & Safety (OHS) Officer.
• Participate in internal audits as required.

Requirements

• Associate's degree/ Bachelor of Pharmacist
• Min. 1 year in QC Specialist or in a closely related position
• Have necessary laboratory skills
• Good English competency (reading, listening and speaking)
• Strong analytical, communication and interpersonal skills
• Proficient in MS Word, Excel and PowerPoint

Location

Bekasi, Indonesia

Employment Details

Worker Type: Employee

Worker Sub-Type: Fixed Term

Time Type: Full time