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ZL01-031926 Project Manager

  • ... Posted on: Mar 18, 2026
  • ... Pinnaql
  • ... 00646, null
  • ... Salary: Not Available
  • ... Full-time

ZL01-031926 Project Manager   

Job Title :

ZL01-031926 Project Manager

Job Type :

Full-time

Job Location :

00646 null United States

Remote :

No

Jobcon Logo 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:

  • Project Manager

Job Summary:
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.

View Full Description

Jobcon Logo Position Details

Posted:

Mar 18, 2026

Reference Number:

ee57c29f

Employment:

Full-time

Salary:

Not Available

City:

00646

Job Origin:

ziprecruiter

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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:

  • Project Manager

Job Summary:
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.

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