Specialist Manufacturing
Cencora View all jobs
- Juncos, PR
- Contract
- Full-time
- Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
- Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.
- Provide troubleshooting support.
- Assist in generation of training materials and may assist in providing training on scientific or technical aspects of the process.
- Support establishment of process monitoring parameters and control limits.
- Collect process-monitoring data and support the assessment of deviations.
- Provide support of timely execution of the process monitoring quarterly reports.
- Ensure that all Non-conformances are triaged within the established goal.
- Responsible for authoring investigation reports.
- Responsible for execution of corrective actions.
- Responsible for managing NC/CAPA closure within established goal.
- Monitor and communicate incidents trends.
- Review equipment/system Root Cause Analysis investigations and support trend evaluations.
- Assist with generation of process validation protocols and reports.
- Assist with the execution of the process validation.
- Support collection and analysis of process validation data.
- May participate in regulatory inspections
- Participate in the NPI process to assess requirements for documentation, materials, training, and equipment modifications.
- Assess, prioritize, justify, and provide implementation and project management support for process or equipment modification projects.
- Assist manufacturing change owner on CCRB packages impacting the process.
- Participate on the assessment or implementation of special projects or initiatives.
Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience OR Bachelor's degree and 5 years of Manufacturing Operations experience or Associate’s degree and 10 years of Manufacturing Operations experience or High school diploma / GED and 12 years of Manufacturing Operations experience.Preferred Qualifications:Deviations documentation and Change Control Management.Skills:
- Detailed technical understanding of bioprocessing unit operations.
- Skilled in performance of GMP production operations.
- Regulatory knowledge and interactions.
- Participate and help lead cross-functional teams.
- Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality.
- Organizational, technical writing and presentation skills.
- Basic project management skills.
- Basic knowledge of control charting.