Document control Specialist Job at DISYS
Job Title: Document control Specialist
Location: Warren NJ
Duration: 12 months
Client- Pharma
Knowledge, Skills, and Abilities--
- Must have experience with cGMP Manufacturing, Quality, and Compliance.
- Directs quality initiatives that accomplish continuous improvement and enhance site quality system efficiencies.
- Must be action-oriented, customer-focused and skilled in decision-making, building relationships, problem solving, conflict management, planning and organizing, resource allocation, coaching others, and analytical thinking.
- Must possess an independent mindset.
- Requires moderate direction to complete more complex tasks; completes routine tasks with little or no supervision.
- Work is self-directed.
- Confident in making decisions for minor issues.
- Routinely recognizes Quality issues and solves problems.
- Proposes solutions for complex issues and works with management to resolve.
- Follows established procedures and performs work as assigned.
- Intermediate to advanced ability to interpret results and situations and articulate recommendations for resolution.
- Is recognized Subject Matter Expert within the group.
- Provides guidance to other employees in interpretation of complex data.
- Capable of providing input within the department and cross functional teams.
- Builds relationships internally within and with cross functional teams.
- Contributes to goals within the work group.
- Able to recognize conflict and notify management with proposed recommendations for resolution.
- Able to prepare written communications and communicate problems to management with clarity and accuracy.
- Able to effectively multi-task and execute project management skills. Knowledge of US and global cGMP requirements.
- Excellent verbal and written communication skills.
Job Types: Contract, Temporary
Pay: $33.00 - $36.50 per hour
Schedule:
- Monday to Friday
Ability to commute/relocate:
- Township of Warren, NJ: Reliably commute or planning to relocate before starting work (Required)
Experience:
- GMP documentation: 1 year (Required)
Work Location: One location
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