Vacancy caducado!
Job Description
- Participate in a variety of Validation Life Cycle activities including, but not limited to:
- Manufacturing and Packaging Equipment Commissioning/Qualification activities.
- Process Validations, Cleaning Validation, and Computer System Validation (CSV) activities.
- Utilities and Facilities Commissioning/Qualification activities.
- Preparation and/or execution of SOP’s, IQ/OQ/PQ, Investigations and CAPA.
- Work side by side with other team members to develop validation knowledge and skills within the industry.
- Able to directly work in production/packaging environments.
- Able to work in construction environments.
- Follow internal procedures and external standards.
Qualifications
- Bachelor's and/or Master's degree in Engineering orSciences fields from anaccreditedUniversity.
- 3-5 years of experience in the pharmaceutical industry.
- Proficient using MS Windows and Microsoft Office applications.
- Willing to travel 75% or more within andoutside USA.
- Available to work administrative and rotated shifts, holidays and weekends, if required.
- Knowledge in FDA Regulations, cGMPs and ISO guidance (preferable, but not required).
- Self-starter with excellent technical writing, analytical and communication skills.
- Detail oriented and team builder.
- Strong Abilities: People skills, Leadership, Commitment, Trust, Excellence, Honesty, Innovation, Loyalty, Respect & Teamwork.
Additional Information
Positions availablefor Puerto Rico.
Validation and Engineering Group, Inc.is an Equal Employment Opportunity employer.Vacancy caducado!