Junior CQV Engineer

Essential Duties And Responsibilities
Azzur personnel are expected to live up to our core values at all times and exhibit a high level of integrity and personal responsibility, especially when interacting with our valued clients. The following is a short list of the typical responsibilities and deliverables of any given project. The level of knowledge expected will be commensurate with level of incoming experience.

• Support the facility and utility engineering function including the design, commissioning and operation of relevant unit operations (boilers, compressors, high purity water treatment, HVAC, etc), including project updates and maintaining utility and facility equipment project life cycle documents (reliability, maintenance, operations standard operating procedures).
• Develop conceptual engineering designs improvements and the corresponding process flow diagrams and piping/instrumentation diagrams.
• Develop design documents for the utility and facility equipment in accordance with Good Engineering Practice, (GMP)
• Develop utility and facility equipment procurement specifications and data sheets based on approved design documents.
• Support the development of equipment and facility bid evaluations for procurement of the utility and facility equipment and system construction packages.
• Review vendor equipment drawings and specifications and drive the system integration with the site utilities and computerized systems (SCADA).
• Participate in multi-functional design reviews, identify gaps to the original design documents and update design documents as required to remediate gaps.
• Prepare change control documents and justifications as required.
• Develop commissioning and qualification documents for facility and utility equipment and the associated manufacturing lines.
  

Requirements

Qualifications

• Education: BS/BA degree required. An advanced degree in Chemical, Mechanical or Biomedical Engineering is a plus.
• 1-2 year experience in a regulated, manufacturing environment within the biotechnology, pharmaceutical or medical device industry.
• Excellent written and verbal communication skills; excellent technical writing skills. ∙ Strong interpersonal skills and the ability to work in a team environment.
• Ability to work effectively in a fast-paced multitasking environment.
• Proficient in Microsoft Word, Excel, PowerPoint.
• Working for multiple clients throughout the region.