Quality Control Staff (CBA part)

Quality Control Staff (CBA part) Direct message the job poster from Selatox

HR Professional | Talent Acquisition & HR Ops | 6+ Years Experience Would you like to learn about stringent global cGMP manufacturing standards?

We offer an opportunity to gain production know-how and technology meeting Korean cGMP standards at our GMP-certified manufacturing facility in Indonesia. Additionally, outstanding talents will have the chance to gain practical experience in Korea.

Our production facility in Cikarang boasts global-level manufacturing competitiveness with state-of-the-art automation, aseptic management, and quality tracking systems. Indonesian production personnel build expertise through rigorous training and hands‑on experience, and outstanding talents are offered opportunities to work at our headquarters in Korea. Currently, approximately 150 Indonesian production specialists are actively working in Korea. We are seeking talented individuals to join us at the forefront of the global pharmaceutical industry, creating fast, safe, and innovative medicines.

Your Role in This Journey Responsibilities Mammalian Cell Maintenance

Perform routine maintenance of mammalian cell lines, including thawing, subculturing, and cryopreservation, using proper aseptic techniques.

Cell-Based Assay (CBA) Testing

Conduct mammalian cell culture for Cell-Based Assay (CBA) testing using assay plates.

Prepare CBA testing activities, including media formulation, reagent preparation, consumable readiness, and laboratory equipment setup.

Laboratory Equipment Operation and Maintenance

Operate and maintain mammalian cell laboratory equipment, including liquid nitrogen tanks, biosafety cabinets, CO₂ incubators, microscopes, and cell counters.

Support equipment calibration, qualification, and routine maintenance activities.

GMP Documentation and Compliance

Prepare, review, and maintain testing records, SOPs, and reports in compliance with GMP requirements.

Support audit preparation and provide relevant data for internal and external regulatory inspections.

Qualifications Required Qualifications

Bachelor’s degree or higher in Pharmacy, Biology, Biomedical Science, Biotechnology, or related fields.

Fluent in English (written and spoken).

Preferred Qualifications

Experience working in a GMP-regulated environment.

Basic skills in handling mammalian adherent cell cultures.

Experience performing cell-based or biochemical assays, such as ELISA and cytotoxicity assays.

Proficiency in Korean language is an advantage.

Our Commitment at Selatox [Top Treatment & Performance-based Incentive]

Top‑tier salary structure

Performance-based pay system : Rewards based on achievements, with promotions tied to skills and competencies.

[A Growth Platform for Your Career Jump]

Regular provision of specialized training

Hands‑on lectures in collaboration with Korean experts

Firsthand experience of the latest K‑Beauty trends

Application of the latest Korean cosmetics

[Opportunity for Global Stage Experience]

Korea trip support for top performers

Provision of opportunities to work in Korea for outstanding talents

Life, Work, and Everything in Between

Internal & external training programs

Language training support

Company events (workshops, HR Day, etc.)

Employee club activity support

Long‑service awards

Employee discount on B‑Project services and products

Additional private insurance support

Congratulatory and condolence payments

Performance bonus

Smart Work (Flexible Working Hours)

Clean and safe working environment

40 hours per week, 5 days

Sick leave, maternity leave, paternity leave, wedding leave, condolence leave, etc.

Min. 12 days for permanent employee (up to 24 based on tenure)

Global Presence

Founded in 1945, a global healthcare leader

Top in overseas subsidiaries among Korean pharma

8 Branch Operations in Asia & US

5 R&D Centers Worldwide

100+ Partners Worldwide

No.1 pharmaceutical company in Korea

Over 4,500 employees in Korea

100+ Indonesian Talents Working in Korea

Celebrating Our Journey

Award by the Indonesian Government (2022)

'Best Workplace' in Korea (2022)

Recognition for Women‑Friendly Corporate

Culture & Diversity Management Award (2022)

Global Pharmaceutical R&D Innovation Award (2021)

Indonesia’s first specialized botulinum toxin company, delivers high‑quality products with global ambitions.

Selatox is Indonesia’s first specialized company for botulinum toxin. Centered around the manufacturing facility in Cikarang and the UI R&D Center (Depok), we began full‑scale toxin production and research activities after completing the facilities in 2023. We plan to strengthen our quality management system with the goal of obtaining GMP certification by 2026 and completing product registration in Indonesia by 2028. Through strategic partnerships with over 40 countries, we are accelerating our entry into the global market. By 2030, we aim to focus on supplying high‑quality halal‑certified toxin products and establish ourselves as a trusted brand not only in Indonesia but also worldwide.

Recruitment Details

Recruitment Process

Application > Aptitude Test > 1st Interview > 2nd Interview > Compensation Negotiation > Final Onboarding

Your growth is our goal

At Selatox, we place the highest priority on employee growth, providing an environment where you can work with autonomy and deep immersion. Regardless of age, tenure, gender, or nationality, we evaluate fairly, objectively, and transparently based on ability and performance, and reward accordingly. We strive to build a company where every employee feels a true sense of ownership. We believe our work becomes truly meaningful only when the growth of our people leads to the growth of our customers and society. This is what we call a true win‑win‑win. Selatox is a place full of opportunities for your growth. We look forward to sharing this journey of challenge and growth with you.

Seniority level Associate

Employment type Full‑time

Job function Quality Assurance

Industries Pharmaceutical Manufacturing

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