Suite Coordinator

Duties & Responsibilities:

Consistently maintain the scheduling of process solutions used in the suites

Act as the department liaison to resource validation needs and follow through on associated documentation

Utilize the Material Control Automation System, Wyeth documentation system, and issue and/or follow-up on area work requests

Develop and maintain a database program for solution scheduling, or other required department tracking needs, as applicable

Coordinate readiness of batch records for production activities (i.e. LIMS samples, special requests)

Close out documentation required for disposition

Coordinate supplies required for mfg within the production suites

Represent department at project meetings as appropriate

Coordinate review and archival of GMP documentation

Oversee generation and approval of production documentation as applicable

Demonstrate excellent communication skills including computer literacy, technical writing ability, SOP and GMP compliance knowledge

Demonstrate the ability to effectively interface with all levels of the staffEducational Requirements:
BS in life sciences, or equivalent. Minimum Experience: 6 years experience in a Biopharmaceutical or Pharmaceutical cGMP manufacturing
environment required, or equivalentWyeth offers competitive compensation and benefits programs including stock
options, child-care subsidies, flex-time, business casual attire,
educational assistance and professional development programs. Please
forward your resume with salary requirements and job reference code to the
address below.For more information, visit our website at