Project Manager

Posted 2 Days Ago
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Juncos, PRI
In-Office
Senior level
Biotech • Consulting • Pharmaceutical • Manufacturing
The Role
Lead and deliver manufacturing projects (commissioning & qualification, capital, construction, NPI, expansions). Develop plans, manage teams, control budget/schedule, mitigate risks, ensure compliance, and communicate with stakeholders. Available for extended hours and occasional weekends/holidays.
Summary Generated by Built In

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:

  • Project Manager

Description:
We are looking for a dedicated Project Manager with a strong background in the manufacturing industry, particularly in sectors like pharma, biotech, or medical devices. The successful candidate will have a minimum of 5 years of experience overseeing diverse projects including Commissioning & Qualification, capital projects, construction projects, NPI, and expansion projects. As a pivotal member of our team, the Project Manager will need to demonstrate exceptional leadership skills and a proactive approach to project management.

Qualifications:

  • Bachelor's degree in Engineering, Business, Project Management, or a related field.
  • Minimum of 5 years of experience in project management within the manufacturing industry.
  • Proven track record of managing projects in areas such as Commissioning & Qualification, capital projects, construction projects, NPI, and expansion projects.
  • Proficiency in project management methodologies and tools.
  • Excellent communication and interpersonal abilities.
  • PMP certification is a plus.

Responsibilities:

  • Develop, implement, and oversee project plans to achieve project goals within budget and schedule.
  • Lead project teams effectively, providing guidance and direction to team members.
  • Coordinate project activities, resources, and deliverables to ensure successful project completion.
  • Monitor project progress, identify risks, and take corrective actions as necessary.
  • Communicate with stakeholders to provide updates on project status and address concerns.
  • Resolve project-related issues promptly to keep projects on track.
  • Ensure compliance with industry regulations and company standards throughout the project lifecycle.

  • Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

Skills Required

  • Bachelor's degree in Engineering, Business, Project Management, or related field
  • Minimum of 5 years of project management experience in the manufacturing industry (pharma/biotech/medical devices)
  • Proven track record managing Commissioning & Qualification, capital projects, construction projects, NPI, and expansion projects
  • Proficiency in project management methodologies and tools
  • Excellent communication and interpersonal abilities
  • PMP certification
  • Available to work extended hours, including possible weekends and holidays
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The Company
154 Employees
Year Founded: 2019

What We Do

Pinnaql, Inc. is a professional services consulting firm providing quality, regulatory, and operational excellence solutions to biopharmaceutical, medical device, and CDMO companies worldwide. The company specializes in laboratory validation, engineering, and compliance, helping regulated life sciences organizations navigate manufacturing challenges, reduce execution risks, and accelerate the transition from lab innovation to commercial market readiness.

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