USA

Basic Qualifications

At least a B.A./B.S. in the Life Sciences (preferably medically related) is required.

Basic Qualifications

At least a B.A./B.S. in the Life Sciences (preferably medically related) is required.

RESPONSIBILITIES:

· Provide strategic advice and counsel to international and affiliate management and others within company concerning international patent issues.

· Coordinate development and implementation of international patent strategies with internal patent prosecution group and therapeutic area attorneys.

Job Responsibilities

Performs specific business unit office tasks as dictated by position. Perform PC functions as applicable (i.e. MS Office, J.D. Edwards, SAP, etc.). Maintain records (filing and storage) as per Regulatory and Site procedures.

Facilitates communication between Corporate and individual business unit(s), KDC management, other departments

Job Summary

This position reports to the Senior Research Scientist II of the Pearl River Quality Unit (Global Compliance Training & Quality [GCTQ] section) and is responsible for delivering training, performing training coordination functions, and overseeing training systems compliance for Chemical and Pharmaceutical Development (CPD) staff.

Job Responsibilities

Job Responsibilities

Provides consultative HR services to site client groups in support of operational objectives. Keeps client organization informed of changes in HR policies, counsels managers and employees on HR policies, procedures, projects, initiatives, and objectives.

Job Responsibilities

Content on the HR Portal (and HR sites on Inside Wyeth)

REQUIREMENTS

JD with top notch academic qualifications and member of a state bar;
10 + years of litigation experience with large discovery projects and minimum of 5 years’ experience managing electronic discovery;
Familiarity with the types of business records and ESI that are maintained by a large, US-based pharmaceutical company;

Job Responsibilities

This position oversees the development of advanced delivery systems for BioPharma compounds from early development to registration and launch. Establishes processes for optimizing drug product development process setting development strategy and adherence to timelines. Ensures capture of intellectual property.

Job Responsibilities

Manage the Site Business Systems Council, the long range Site Systems Strategy and associated process and systems Plan of Record. Ensure overall alignment with Site and Core team plans. This includes alignment with External Supply and Country system strategy where applicable.