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ASAHI GLASS CO., LTD.

Work Country
Japan
Work Location
Ichihara-city, Chiba- Prefecture, Japan

Corporate Data

Asahi Glass Company has been contributing to the societal development as a manufacturer of materials such as for housing, automobile, electronics & energy, and chemicals since 1907. Currently, they enjoy top global shares in a number of product fields such as flat glass, automotive glass, and display glass. In order to continue being the top global share holder as well as to further strengthen our position, we plan to expand globally with our network and strong sales and manufacturing system (manufacturing sites in 30 countries worldwide).

Established
1907
Stock Exchange Listings
The first section of the Tokyo Stock Exchange
Headquarters
1-5-1, Marunouchi, Chiyoda-ku, Tokyo 100-8405 JAPAN
Revenue
1,214.7 billion yen
URL
http://www.agc.com/english/index.html

Job Opportunities

Job Description
(1) Create QC testing schedule and order to testing operator for API, IPC, Raw material and etc.
(IPC: In Process Control)
(2) Review the test result and report to QC manager
(3) Implement sending/receiving the Technical Transfer of Analytical Method
(4) Implement Analytical Method Validation and Verification
(5) Control of analytical equipment and environmental monitoring of QC Lab
(6) Establish testing method and prepare the SOPs (Documented Standard Operational Procedures)
(7) Improvement of GMP related to Quality Control
Products: Bio Pharmaceutical API (API: Active Pharmaceutical Ingredient)
Reporting line: Report to QC Manager and Quality Division Director
Job Category
Specialist/Manager of Quality Control for Bio Pharmaceutical API
Location
Ichihara-city, Chiba- Prefecture, Japan
Salary
From 5 million to 10 million Japanese Yen per annum (including bonus) (depending on the expertise)
Benefits
[Benefit Systems]
Asset-accumulation savings (housing and pension), education loans, stock ownership, health insurance, employee's pension insurance, corporate pension fund, Cafeteria plan (refreshment allowance up to 120,000 yen/year), etc.
[Facilities]
Single dormitory, company housing, system for the marrieds (housing allowance: providing half of the rent ), members-only welfare services (lodging facilities, resort facilities, sports facilities)
Education/Experience
Bachelor’s / Master’s in Medical science, Pharmaceutical Science, Agricultural Science, Biological Science
Language Skills
English and Japanese (preferable but not required)
Qualifications
ONLY CANDIDATES BASED IN SINGAPORE WILL BE CONSIDERED

Based on knowledge or experience of PIC/S GMP and cGMP
■ More than 5 years of experience in the following
-Analytical testing for bio pharmaceutical product
-Quality control for bio pharmaceutical product
-Analytical development for bio pharmaceutical product
■ Analytical tech transfer
■ Analytical method validation
■ Quality Control or Analytical development for Antibody drug Substance

The following Analysis skills or knowledge are required
HPLC, Bioburden, Endotoxin, ELISA, SDS-APGE, Western blotting, Amino acid composition and sequence analysis, CE-SDS and Glycan analysis
Behavioral characteristic:Open and approachable Tenacious
Selection Process
1. CV Screening - *Only those who pass this step will be contacted
2. Skype Screening with TOP CAREER Consultant
3. 1st interview in Singapore on Feb 20th(Tue)
4. SPI Test
5. Final interview in Japan
Additional Information
Business trip is available (USA, EU, China etc.)

Application

Interview Location
Onsite interview in Singapore on February 20th (Tue) and followed by final interview in Japan.

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