Posting Date: 9/24/2015 1:10:22 PM

Summary of Position

A Leading Manufacturing Company in the Pharmaceutical Industry with manufacturing facilities in North Area is offering a contract to manage a Technology Transfer Project.

General Responsabilities

• Coordinate interactions between the client and the mfg plant team
• Lead the internal project team
• Schedule and chair client meetings and visits, including providing project updates and timelines to the internal team
• Monitor and oversee Project Budget and Timelines
• Maintain the Tech Transfer project plan over the life of the project

Requirements

• Must be able to provide leadership and direction to the project team
• Must be able to solve problems / make decisions in critical situations
• Minimum of 5 years of Project Management experience with 2-3 years in Project Management (preferred)
• Minimum of 5 years of client management experience
• Well organized and detail oriented
• Ability to prioritize multiple tasks
• Strong interpersonal and communication skills (English and Spanish), as well as the ability to motivate
• Oral Solid Dosage (OSD) experience
• BS in Engineering
• Industry Experience (Technical Services, Analytical, QA, Regulatory, and/or Manufacturing)
• MBA, desirable
• PMP® Certification, desirable

Posting Date: 9/15/2015 12:30:15 PM

Summary of Position

Long Term contract for a candidate to provide support to Engineering Team to ensure transfer to Production of new productsfor equipment qualification and process validation. The responsibilities will include but are not limited to generate validation protocols and reports, performing equipment IQ, OQ, PQ. The process may include development of Test Method following company’s SOPs. The candidate must have basic knowledge of Six-Sigma Tools.

The project require to travel out of PR 90% of the time. Lodging and travel expenses are included.

Requirements

• BS Engineering with three (3) to five (5) years as Project Engineer or Validation Specialist.
• Experience in Medical Device Industry.
• Must be FULLY bilingual (English and Spanish).
• Demonstrated experience with Quality Tools.
• Excellent presentation skills.

Posting Date: 9/15/2015 12:31:35 PM

Summary of Position

A Leading Manufacturing Company in the Medical Device with manufacturing facilities in Mexico is offering a temporary contract for a supplier quality engineering to provide services with new product transfers and process improvements.

Entry Level CONTRACT for a Supplier Quality Engineer. Candidate will provide support to several manufacturing facilities. The candidate must possess knowledge in the following areas:

• Test Methods for Incoming Inspections
• Final Release Tests
• Validation
• Procedures generation
• Component Qualification

The project require to travel out of PR 90% of the time. Lodging and travel expenses are included. 

Requirements

• BS Engineering with one (1) to three (3) years as a Supplier Quality Engineer.
• Experience in Medical Device Industry.
• Must be FULLY bilingual (English and Spanish).
• Demonstrated experience with Component Qualifications.
• The required candidate must possess excellent organizational skills.