
Quality, Lead Investigator
Flexible & Integrated Technical Services
- Manatí, PR
- Permanente
- Tiempo completo
- Bachelor’s Degree in Chemical Engineering, Biology, or Microbiology Science & five (5) years of experience in the Pharmaceutical Manufacturing industry.
- Bilingual (English & Spanish)
- Experience in:
- Manufacturing Investigations
- Developing, implementing, and tracking CAPAs.
- Procedures Development and Revisions.
- Process Validations
- Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients, and team members. In other words, being a customer service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to Be The Piece?
- Ensures that all QEs, NTRs, NOES, and CAPAs are completed/closed within the established timeframe, utilizing the right tools to prevent reoccurrence.
- Reviews and provides input to regulatory submissions applicable to the area of responsibility.
- Leads QE’s and CAPA’s trend evaluation.
- Participates in the new product introduction process to determine requirements for documentation, materials, training, and equipment modifications.
- Supports the establishment of process monitoring parameters and control limits.
- Supports the assessment of deviations and process monitoring data.
- Monitors and evaluates parameters in existing (on-going) processes to optimize process times/productivity, equipment performance, yields, and quality.
- Provides technical assistance to identify, recommend, and implement process and equipment modifications to improve process performance; to identify and assist in the implementation of cost reduction projects, and ensure the manufacturing area complies.
- Write, evaluate, and revise the required manufacturing documentation (i.e. SOPs, MBRs, etc.) and may assist in providing training on scientific or technical aspects of the processes
- Assists with the generation and execution of validation protocols and reports.
- Participates in regulatory inspection when necessary
- Assists the area managers and supervisory personnel to solve any production technical problem (i.e., Process/equipment troubleshooting, yield, cycle time, quality, and productivity).
- Provides alternatives and recommendations to improve and maximize processes and equipment.
- Participates in Environmental Regulatory and Compliance Permits and Process Safety Hazards evaluation.
- Promotes and models the client's Core Behaviors, facilitating teamwork.
- Supports all site Initiatives and any other assignments based on business needs.