Lowongan Kerja Depok Posisi Researcher Supervisor & Manager di PT Selatox Bio Pharma

Info Loker

Perusahaan	PT Selatox Bio Pharma
Posisi	Researcher Supervisor & Manager
Tempat	Depok
Jenis Pekerjaan	Full Time
Spesialisasi Dibutuhkan	Perangkat Farmasi & Medis (Kesehatan & Medis)
Gaji Min	Rp. 2.000.000
Gaji Max	Rp. 8.500.000

Company Brief

PT. Selatox Bio Pharma is a 100% owned subsidiary of Daewoong Pharmaceutical in Korea, which develops and produces BIOLOGICAL PRODUCT SUCH AS BOTULINUM TOXIN and aims to expand globally. Daewoong Pharmaceutical is one of the leading pharmaceutical companies in Korea with a sales revenue of over 1.3 billion USD. The company is actively focusing on research and development as well as global expansion. Daewoong Pharmaceutical invests more than 15% of its revenue into research and development and has over 100 research and business partners worldwide. We plan to establish a production base for botulinum toxin products in Indonesia as a global bio hub strategic base and target the global market with better accessibility and services through the development and production of competitive new products. We have a vision of becoming a “2030 leading global biopharmaceutical company.” With the goal of becoming a world-class botulinum toxin company.

Team Introduction

Selatox Research & Development Team is responsible for product development and regulatory approvals using botulinum strains and toxins. The team is composed of three parts; the Formulation Research Team, which utilizes toxin proteins; the Animal Testing Team, which conducts potency evaluations of raw materials and products; and the Regulatory Affairs Team, which handles product approval applications, modifications, and consultations.

Job Descriptions

1. Lead and supervise the design, development, and optimization of formulations for botulinum toxin products.
2. Oversee the preparation and testing of prototypes to evaluate stability, efficacy, and scalability.
3. Supervise and mentor researchers in the Formulation Research Team, providing guidance and technical support.
4. Monitor project timelines, allocate resources, and ensure the team achieves key deliverables.
5. Ensure all formulations and processes comply with regulatory requirements.
6. Collaborate with the Regulatory Affairs Team to prepare technical documents for product submissions and approvals.
7. Work closely with other R&D teams, such as Animal Testing and Regulatory Affairs, to align formulation goals with product development needs.
8. Participate in cross-functional meetings to address technical challenges and strategize solutions.
9. Analyze experimental data and compile comprehensive reports for internal and external stakeholders.
10. Present research findings, progress updates, and recommendations to senior management.
11. Stay informed on the latest trends, technologies, and methods in biopharmaceutical formulation science.
12. Identify opportunities for innovation and implement improvements to enhance product performance and cost efficiency.

Job Qualifications

1. Master’s or Ph.D. in Pharmaceutical Sciences, Biotechnology, Chemistry, or a related field.
2. Minimum 5 years of experience in pharmaceutical or biopharmaceutical formulation development.
3. At least 2 years in a supervisory or team leadership role.
4. Experience with botulinum toxin formulations is a strong advantage.
5. Advanced knowledge of formulation principles, stability studies, and product development processes.
6. Strong leadership, problem-solving, and project management skills.
7. Excellent communication and technical writing skills in English.

Lamar kerja

Deskripsi Perusahaan

Info Perusahaan

• Industri: Kesehatan/Medis
• Tunjangan dan Lain-lain: Asuransi kesehatan, Parkir, Waktu regular, Senin - Jumat, Bisnis (contoh: Kemeja)
• Lokasi: Jababeka Phase 5