Document Control Coordinator jobs in Bennington, VT

The QA Validation Oversight department is hiring! This team leads all aspects of documentation for validation areas across the business, including QC, Process Sciences, operations, CSV, gene and cell therapy, tech transfers and transfer of products.

As a QA Validation Specialist-Document Review, a typical day might include the following:

• Reviewing and providing quality oversight of results of validation activities, including, but not limited to: Shipping, Equipment, Computerized Systems, QC methods and process.

• Generating, implementing and/or reviewing master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria

• Reviewing the results of testing and determining the acceptability of results against pre-determined criteria.

• Investigating and troubleshooting problems and providing recommendations for changes and/or improvements.

• Reviewing, editing and approving deviation notifications, deviation investigations, corrective actions, change controls, SOPs, reports and other documentation

• Coordinating with other departments or outside contractors/vendors to complete validation tasks.

• May supervise, provide direction and assign work to Validation Specialists and/or contingent workers to meet goals and timelines.

This role may be for you if you:

• Maintain integrity and honesty at all times

• Can work independently or as part of a team

• Communicate with transparency

• Continuously drive to improve processes for improved performance

• Demonstrate supportive behavior at all times

• Have basic working knowledge of Microsoft Suite (Word, Excel, Powerpoint)

• Gather and organize information while meeting commitments on time

• Perform well-defined tasks

• Have effective time management skills

To be considered for this position, you must hold a BS/BA in Engineering, Chemistry, or Life Sciences and:

• QA Validation Specialist: 2 years of relevant experience

• Sr. QA Validation Specialist: 5 years of relevant experience

May substitute proven experience for education requirement

A background in Quality Control, Process Sciences and/or manufacturing/lab equipment in a pharmaceutical setting is preferred.