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STAFF Daewoong Pharmaceutical
Daewoong Pharmaceutical
Lokasi
DKI Jakarta, Jawa Barat
Jenis Pekerjaan
Full-time
Gaji
Rp 1.000.000 - 12.000.000,-
Strata
D4, S1
Berlaku Hingga
N/A
Deskripsi Lowongan
We are seeking highly motivated and skilled individuals to join our Research team. We have openings for both entry-level and experienced applicants across all fields.
**Incrementally Modified Drugs (IMD)**
As a member of the Incrementally Modified Drugs (IMD) division, you will:
* Develop formulations based on the physicochemical properties of APIs and determine optimal dosage form types.
* Establish and refine process parameters across laboratory, pilot, and commercial scales while identifying CPPs (Critical Process Parameters) and CQAs (Critical Quality Attributes).
* Lead formulation and process development for complex and innovative dosage forms.
* Prepare CMC sections for IND/NDA submissions, support patent filings, and contribute to strengthening the company's global competitiveness through technical and regulatory excellence.
**Formulation Research**
In the Formulation Research division, you will:
* Lead R&D of differentiated formulations including 1st generics, combination drugs, sustained-release, and modified new drugs.
* Develop diverse dosage forms such as injectables, enteric-coated, and sustained-release tablets.
* Conduct joint research with academic experts and technology venture companies to discover marketable and scalable formulations.
* Drive formulation development and technology transfer for Daewoong's branded products targeting overseas markets, including Indonesia.
**Analytical Research**
Within the Analytical Research division, you will:
* Conduct method development, validation, and testing for 1st generic products, including dissolution, content uniformity, and stability studies of finished dosage forms.
* Operate and gain expertise in advanced analytical instruments such as HPLC, GC, UV/Vis, and FT-IR.
* Lead impurity profiling, degradation pathway studies, and analytical method transfer/optimization for domestic and global sites.
* Perform Zone IVb stability evaluation and analytical method validation/verification per ICH Q2 (R2) guidelines for tropical market suitability.
**Customer Health (CH) Formulation Research**
Within the Customer Health (CH) Formulation Research division, you will:
* Lead brand product development, including R&D for new products (e.g., Urusa, Impactamin) with high market potential.
* Conduct global market research to identify trends and integrate them into new product strategies.
* Develop formulations tailored for international markets, ensuring compliance with local regulations and market needs.
**Basic Requirements:**
* Master's degree or higher in Pharmacy, Biology, Chemistry, Microbiology, Biotechnology, Chemical Engineering, or related fields.
* Fluency in spoken and written English.
* For entry-level applicants: No prior industry experience required.
* For experienced candidates: 5+ years of relevant experience may qualify for senior/specialist roles.
**Preferred Qualifications:**
* Experience in operating drug formulation synthesis equipment (e.g., tablet press, coating machines, etc) or analytical instruments (e.g., HPLC, AAS, GC, Karl Fischer, etc.).
* Familiarity with Good Laboratory Practice (GLP) guidelines.
* Ability to communicate in Korean (conversational level or above).
**Incrementally Modified Drugs (IMD)**
As a member of the Incrementally Modified Drugs (IMD) division, you will:
* Develop formulations based on the physicochemical properties of APIs and determine optimal dosage form types.
* Establish and refine process parameters across laboratory, pilot, and commercial scales while identifying CPPs (Critical Process Parameters) and CQAs (Critical Quality Attributes).
* Lead formulation and process development for complex and innovative dosage forms.
* Prepare CMC sections for IND/NDA submissions, support patent filings, and contribute to strengthening the company's global competitiveness through technical and regulatory excellence.
**Formulation Research**
In the Formulation Research division, you will:
* Lead R&D of differentiated formulations including 1st generics, combination drugs, sustained-release, and modified new drugs.
* Develop diverse dosage forms such as injectables, enteric-coated, and sustained-release tablets.
* Conduct joint research with academic experts and technology venture companies to discover marketable and scalable formulations.
* Drive formulation development and technology transfer for Daewoong's branded products targeting overseas markets, including Indonesia.
**Analytical Research**
Within the Analytical Research division, you will:
* Conduct method development, validation, and testing for 1st generic products, including dissolution, content uniformity, and stability studies of finished dosage forms.
* Operate and gain expertise in advanced analytical instruments such as HPLC, GC, UV/Vis, and FT-IR.
* Lead impurity profiling, degradation pathway studies, and analytical method transfer/optimization for domestic and global sites.
* Perform Zone IVb stability evaluation and analytical method validation/verification per ICH Q2 (R2) guidelines for tropical market suitability.
**Customer Health (CH) Formulation Research**
Within the Customer Health (CH) Formulation Research division, you will:
* Lead brand product development, including R&D for new products (e.g., Urusa, Impactamin) with high market potential.
* Conduct global market research to identify trends and integrate them into new product strategies.
* Develop formulations tailored for international markets, ensuring compliance with local regulations and market needs.
**Basic Requirements:**
* Master's degree or higher in Pharmacy, Biology, Chemistry, Microbiology, Biotechnology, Chemical Engineering, or related fields.
* Fluency in spoken and written English.
* For entry-level applicants: No prior industry experience required.
* For experienced candidates: 5+ years of relevant experience may qualify for senior/specialist roles.
**Preferred Qualifications:**
* Experience in operating drug formulation synthesis equipment (e.g., tablet press, coating machines, etc) or analytical instruments (e.g., HPLC, AAS, GC, Karl Fischer, etc.).
* Familiarity with Good Laboratory Practice (GLP) guidelines.
* Ability to communicate in Korean (conversational level or above).
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