Electrical Project Manager Job at Validation & Engineering Group, Inc, Puerto Rico

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  • Validation & Engineering Group, Inc
  • Puerto Rico

Job Description

Job Description

Job Description

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

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Electrical Project Manager

Responsibilities:

  • Act as the owner's representative, aligning project goals with the owner's vision and requirements.
  • Supervise the construction of electrical infrastructure, ensuring compliance with codes and regulations.
  • Manage the construction of pharmaceutical manufacturing facilities on time, within budget, and to quality standards.
  • Review and provide feedback on change orders to maintain project integrity.
  • Deliver projects by managing scope, schedule, budget, and risks, with a focus on safety and quality.
  • Lead project management following company policies and procedures.
  • Develop safety and environmental execution plans and ensure compliance.
  • Communicate effectively with project teams, stakeholders, and partners.
  • Review project plans, monitor contractor performance, and conduct site walkdowns.
  • Develop detailed project plans, allocate resources, and manage budgets.
  • Provide technical guidance, document project activities, and monitor costs.
  • Identify and mitigate risks to ensure project success.
  • Ensure compliance with industry standards, regulations, and quality guidelines.
  • Update stakeholders on progress, challenges, and scope changes.
  • Address technical issues and provide solutions to keep projects on track.

Qualifications:

  • Bachelor's Degree in Engineering or Science.
  • Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.
  • Experience in direct process / manufacturing areas.
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
  • Technical Writing skills and investigations processes.
  • Available to work extended hours, possibility of weekends and holidays.

Job Tags

For contractors, Weekend work

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