苏州招聘

1)

General office duties such as answering the phone, photo copying, filing, mailings, typing, faxing etc.

2)

Maintain computer data base files as specified.

3)

Issue deviation and maintain the deviation log to accept products with cosmetic defects.

4)

Create the General Product Inspection procedures for new medical devices

5)

Issue changes to the existing specifications of medical devices.

6)

Maintain compliance with FDA and Medline regulations, policies and procedures relevant to document control, label control, change control, record retention, master device records, device history records and labeling.

7)

Translate quality manual, specifications, audit related, validation related, and others as needed.

8)

Data Entry to the system as needed.

9)

Distribute documents to the suppliers

1)

Other duties and projects as assigned.

2)

Drive cost reduction programs with team.

1)

Medline Shanghai.

2)

Medline American

1)

Suppliers.

1)

Bachelor degree

1)

Fluent both in written and verbal English. English level of CET 6 or equivalent for local candidates.

2)

Familiar with general office software.

3)

Ability to act as translator for Corporate Medline visitors to Asia as needed.

4)

Good interpersonal, organization, and leadership skills. Effective training skills.

5)

Ability to manage multiple projects/activities at one time.

6)

Ability to maintain confidentiality.

7)

Ability to travel though-out Asia and to the United States as needed.

8)

Excellent attendance record and ability to work overtime as needed.

1)

Minimum of one year experience in FDA regulated environment.

2)

Experiences in Medical device.

1)

Must be enthusiastic in the job nature.

2)

Detail oriented.

3)

Good reporting and presentation skill

4)

Good interpersonal and communication skill.