Bring Your Own Device (BYOD)/Laptop
Manager, Document Control has primary responsibility for managing the procedural documents lifecycle (i.e., policies, standard operating procedures, work instructions, manual, guidelines, and forms) for the organization. The role provides major content input from the NA region in the creation and revision of Global CQ Quality procedures as well as those originating from other quality organizations in Pharma.
The role serves as Subject Matter Expert for Document Control in the US and includes procedural document development, coordination of periodic reviews, revision and obsolescence of documents, impact assessment process management and contribution of training contents to ensure consistency with the procedural documents. In addition, this position is responsible for managing updates to the US CQ Quality Manual and related reference documents, in accordance with established global quality policies and procedures.
This position is also responsible for ensuring that Company procedural documents are consistent and aligned with Company’s global processes.
Procedural Document Management
Ensures alignment of Company standards, policies and procedures across Company and NA Regional procedural documents.
Job Type: Contract
Salary: $38.00 – $39.00 per hour
Benefits:
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Work Location: Remote
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