Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Administrative Shift (Overtime may be required based on business demand)
Description:
With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations. May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.
Requirements:
Experience in:
- Deviations management
- Deviation assessments
- Track wise
- Biotech and manufacturing experience
Responsibilities:
- 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.Non-Conformance and CAPA
- 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.
- 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
Education:
- Doctorate OR Master’s + 2 years of Manufacturing Operations experience OR Bachelors + 4 years of Manufacturing Operations experience OR Associates + 8 years of Manufacturing Operations experience OR High school/GED + 10 years of Manufacturing Operations experience.
Skills Required
- Deviations management
- Deviation assessments
- TrackWise (quality management system)
- Biotech and manufacturing experience
- Non-conformance and CAPA management
- Authoring investigation reports / Root Cause Analysis
- Process validation support (protocols, execution, data analysis)
- Experience supporting New Product Introduction (NPI)
- Training material generation and training support
- Education per posted schedule (Doctorate OR Master's +2 yrs OR Bachelor's +4 yrs OR Associate +8 yrs OR HS/GED +10 yrs)
What We Do
Inteldot offers custom turn-key systems, systems integration, MES eBR configuration and integration solutions, business intelligence and analytics and technical staffing. We have been providing the Pharmaceutical, Manufacturing and Medical Device industries with services for a variety of applications since 2004
