Validation & Engineering Group, Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services.

Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation.  Perform investigation of deviations / discrepancies. Oversees and reviews validation area processes. 

• Design and develop cleaning procedures for new products and manufacturing equipment.
• Provide technical support to cleaning activities associated with the manufacturing process.
• Also to lead the cleaning validation program and activities.
• Use of cleaning agents and the establishment of sound cleaning practices within new or refurbished manufacturing rooms and sampling suites areas.
• Designs and supports the implementation, i.e. provides training, of cleaning strategies for product transfer projects and product development projects.
• Investigates and conducts troubleshooting/root cause analysis of cleaning related incidents, deviations and cleaning out of specification results for non validated or under development cleaning procedures.
• Leads the enhancement of cleaning practices, “clean in place” equipment and introduction.
  Reviews and approves Manufacturing Cleaning Working Instructions and Forms.
• Supports the periodic review of cleaning validation studies.
• Performs successful and on time resolution of incidents and deviations related to cleaning validation exercises.
• Issues Change Controls required for the implementation of cleaning procedure changes, as needed. 
• Trains manufacturing and QC/QA personnel on cleaning validation documentation.

• Bachelor's or Master's Degree in Science, Pharmacy or Engineering.
• Minimum of 5 years of professional experiences in cleaning validation in the pharmaceutical and biotechnology industries.
• Proficient knowledge of cleaning validation, continuous process improvement and troubleshooting processes.
• Strong project management skills.
• Proficient time management skills, planning and organization capabilities.
• Proven leadership & teamwork skills, self starter, results oriented and build and maintain strong relationships with multiple groups.
• Proficient in Risk Assessment/Management
• Proven assessment, analytical and problem-solving skills.
• Proficient presentation skills and Technical Writing/Oral communication skills (English) 
• Proficient in cGMP's, OSHA and FDA Regulations as it applies to pharmaceutical industry.

Positions available for Puerto Rico.

Validation and Engineering Group, Inc. is an Equal Employment Opportunity employer.