Validation & Engineering Group, Inc.

ZL01-031926 Project Manager

Validation & Engineering Group, Inc.  •  Dorado, PR (Onsite)  •  17 days ago
Apply
AI can make mistakes so check important info. Chat history is never stored.
58
AI Success™

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



Provide vision and leadership to strategic projects with significant site impact. Ensure new

products are launched from the site in alignment with contract goals. Manage the

performance of projects or significant subsystems associated with new products by

influencing, coordinating, and driving activities, initiatives, and development deliverables

across cross-functional teams. Direct all phases of new product development projects from

inception through completion from an Operations perspective. Lead project review sessions

focusing on cost, schedule, and technical performance. Establish milestones, monitor

adherence to plans and schedules, identify issues, and implement solutions. Demonstrate

strong leadership, clear communication, and the ability to build effective cross-functional

working relationships. Ensure Value Improvement Projects (VIP) and new product

initiatives are completed in alignment with contract expectations.

Key Responsibilities:

  • Project Planning & Definition: Define project goals, scope, resource and cost estimates,

    timeline, and risks. Facilitate cross-functional discussions to develop project proposals.

    • People Leadership: Manage large, multi-project, multi-site cross-functional teams;

    provide performance input; foster strong alignment.

    • Value Improvement (VIP): Oversee VIP initiatives; identify, communicate, and manage

    risks.

    • Project / Program Management: Lead initiation, planning, execution, control, and closeout activities; ensure team ownership of plans, schedules, and budgets.

    • Process Management: Ensure activities follow established processes; maintain

    documentation discipline; reinforce VIP and NPE best practices.

    • Communications & Reviews: Drive cross-functional communication; serve as liaison

    between teams and leadership; lead phase reviews; maintain documentation including

    minutes, issue logs, and metrics.

    • New Product Excellence (NPE): Implement NPE methods; manage NPE risks and

    deliverables.

Qualifications:

  • 5–7+ years of experience in manufacturing engineering or quality engineering within an

    FDA-regulated industry (medical devices, pharmaceuticals, biotechnology, diagnostics,

    or similar).

    • Strong knowledge of FDA Quality System Regulation (21 CFR Part 820), Good

    Manufacturing Practices (GMP), and ISO 13485.

    • Experience supporting new product introductions (NPI/NPD), including process

    development, equipment qualification, and process validation.

    • Hands-on experience with risk management (FMEA, hazard analysis), root cause

    investigations, and CAPA systems.

    • Proven collaboration with Operations, Quality Assurance, Regulatory, R&D, and Supply

    Chain teams.

    • Familiarity with controlled documentation systems, engineering change processes, and

    manufacturing readiness requirements.

    • Experience ensuring compliance with quality system procedures and regulatory

    expectations across the project lifecycle

Quality System Requirements:

Demonstrate a primary commitment to patient safety and product quality by adhering to

applicable quality policies, procedures, and requirements.

For roles with direct reports: Ensure adequate resources (personnel, tools, etc.) are in place

to support quality compliance and promote a work environment aligned with quality

expectations.
Job Scope & Leveling Guidelines:

• Functional Knowledge: Applies in-depth conceptual, practical, and technical knowledge;

understands related functions.

• Business Expertise: Applies knowledge of key business drivers and cross-team

integration to achieve objectives.

• Leadership: Provides guidance, coaching, and may lead smaller projects or sub-projects

with manageable risk.

• Problem Solving: Solves problems of varying complexity; adapts or develops solutions

using judgment and experience.

• Impact: Influences project, operational, or service activity effectiveness.

• Interactions: Communicates complex information clearly; persuades and guides

stakeholders in cross-functional settings.

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
Social Media