Engineer

Kelly Services; Juncos (PR); On-site; USD 70,000 - 95,000; Full time

Job summary

KellyScience, Engineering, Technology & Telecom (SETT) seeks an Engineer to work in the PR region. The role involves process optimization and troubleshooting in manufacturing environments, with non-standard shifts possibly required.

Ideal candidates hold an Engineering degree (Master’s or Bachelor’s with experience) and have strong knowledge of GDP, CAPA, and cGMP procedures, plus system ownership experience.

Qualifications

• Master’s degree in Engineering or Bachelor’s degree with 2 years of Engineering experience.
• Experience with cGMP procedures in pharma/biotech production.
• Experience with process characterization, validation, monitoring, and optimization; CAPAs.
• GDP knowledge and documentation practices.
• System Owner experience; MMP experience.
• Bilingual Spanish and English.
• Availability to work non-standard shifts.

Responsibilities

• Characterize process optimization strategies and troubleshoot operational issues in manufacturing, pilot plant, or capital projects environments.
• Apply basic engineering principles to design and implement system modifications, experiments, or capital projects.
• Organize, analyze, and present interpretation of results for issues or minor projects.

Skills

Process optimization

Root cause analysis

CAPA management

GDP knowledge

cGMP procedures

Documentation control

Bilingual Spanish/English

Education

Master's degree in Engineering

Bachelor's degree in Engineering

Job description

At KellyScience, Engineering, Technology & Telecom (SETT), we’re passionate about helping you find a job that works for you. How about this one?We’re seeking for an Engineer to work in the eastregion, in PR. With us, it’s all about finding the job that’s just right.

This job might be an outstanding fit if you have:

• Master’s degree in Engineering OR
  Bachelor’s degree in Engineering & 2 years of Engineering experience.
  
• Working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes, facilities, and equipment.
  
• Familiarity with process characterization, validation, monitoring, and optimization techniques. Strong problem-solving skills and experience conducting root cause investigations. Expertise in identifying and managing Corrective and Preventive Actions (CAPAs).
  
• Strong knowledge of Good Documentation Practices (GDP).
  
• Experience managing technical documentation and records.System Owner Experience- MMP experience.
  
• Bilingual: Spanish and English.
  
• Availability to work non-standard shifts operation.

Job summary:Under general supervision, provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects. Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of minor scope and complexity.