Validation & Engineering Group, Inc.

Project Manager

Validation & Engineering Group, Inc.  •  Carolina, PR (Onsite)  •  1 month ago
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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:

  • Project Manager

We are seeking a Project Manager to lead and coordinate capital, engineering, manufacturing, quality, validation, automation, and operational improvement projects within a regulated pharmaceutical, biotechnology, or medical device environment.

The Project Manager will be responsible for planning, executing, monitoring, and closing projects while ensuring alignment with scope, schedule, budget, quality, and compliance requirements. This individual will serve as the primary point of coordination among cross-functional stakeholders and will drive project execution from initiation through completion.

Key Responsibilities

  • Manage multiple projects simultaneously, ensuring adherence to project scope, schedule, budget, and quality objectives.
  • Develop and maintain project plans, schedules, resource forecasts, risk registers, and status reports.
  • Coordinate activities among Engineering, Manufacturing, Quality, Validation, Automation, Supply Chain, and other functional teams.
  • Facilitate project meetings and communicate project status, risks, issues, and mitigation plans to stakeholders and leadership.
  • Monitor project performance using established KPIs and project management best practices.
  • Support capital project execution, equipment implementation, facility upgrades, process improvements, technology transfers, and operational initiatives.
  • Identify and proactively manage project risks, issues, and dependencies.
  • Ensure project documentation is complete, accurate, and compliant with applicable procedures and regulatory requirements.
  • Drive accountability among team members and support timely decision-making.
  • Support vendor management, contractor coordination, and procurement activities as required.
  • Promote a culture of safety, quality, compliance, and continuous improvement.

Qualifications

  • Bachelor’s Degree in Engineering (Mechanical, Chemical, Electrical, Industrial, Civil, Biomedical, or related engineering discipline).
  • 5–10 years of project management experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
  • Experience managing engineering, capital, manufacturing, quality, validation, automation, or operational excellence projects.
  • Demonstrated experience leading cross-functional teams and coordinating multiple stakeholders.
  • Strong understanding of project planning, scheduling, budgeting, forecasting, and risk management.
  • Excellent verbal and written communication skills, with the ability to effectively interact with technical teams, management, and clients.
  • Proficiency with Microsoft Project, Smartsheet, Primavera P6, or equivalent project management tools.

Preferred

  • PMP certification.
  • Experience supporting GMP-regulated environments.
  • Experience managing capital projects, facility expansions, equipment installations, CQV programs, process improvements, or technology transfers.
  • Familiarity with FDA regulations, cGMP requirements, and life sciences industry standards.

Soft Skills

  • Strong leadership and organizational skills.
  • Excellent interpersonal and stakeholder management abilities.
  • High emotional intelligence and professional maturity.
  • Strong problem-solving and decision-making capabilities.
  • Ability to influence and drive results without direct authority.
  • Self-motivated, proactive, and highly accountable.
  • Ability to work effectively in a fast-paced, matrixed environment.

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.

Validation & Engineering Group, Inc.

About Validation & Engineering Group, Inc.

Validation & Engineering Group, Proudly serving our clients since 1997.

Our Mission states in part: "provide our clients with the best resources to meet their needs". In our search for the best talent, we are inclusive and do not discriminate. V&EG is proud to be an equal opportunity workplace and is an affirmative action employer.

Validation & Engineering Group provides world-class service and expertise to the pharmaceutical, medical device and biotechnology industries. We offer our clients: Validation, Control System Solutions, Instrumentation, Training, Equipment Rentals, and Regulatory Compliance Services to ensure adherence to Federal and European regulatory agencies. Our group had serve in solid dosages, liquids, creams, lyophilizers, and parenteral dosage.

Our agility in responding to our clients’ needs, access to the best pool of talent, and the combined experience and technical expertise of our resources make Validation & Engineering Group a leader in the pharmaceutical, medical devices, and biotechnology industries.

At Validation & Engineering Group we provide professional expertise in the areas of:

•Audit and Assessment

•Automated Process Control System Qualification

•Equipment and Facilities Qualification

•Facilities Start-Up and Commissioning

•GAP Analysis

•Information Systems Computer Validation

•Packaging and Process Analysis

•Process & Cleaning Validation

•Project Management

•Quality Systems

•Risk Based Approach

•Regulatory Compliance

•Standard Operating and Maintenance Procedures

•Training

•Utilities Support and Qualification

In addition we offer Equipment Rentals and training to your workforce such as: Temperature & Relative Humidity, Electrical, Process, Environmental, and. Analytical.

Our Offices:

Puerto Rico:

Centro Internacional de Mercadeo I 100 Carr. 165 Ste 703, Guaynabo, 00968 Puerto Rico

Phone: (787) 622-0996

United States:

2180 Satellite Blvd, Suite 400Duluth, Georgia 30097 United States

Phone: (770) 403-5802

Industry
Architecture & Engineering
Company Size
51-200 employees
Headquarters
Guaynabo, PR
Year Founded
1997
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