Technical Project Manager

Overview

Every Turnberry consultant belongs to a practice, an internal group of consultants and leaders with shared experience and expertise. Each of these practices aligns to one of the core services Turnberry offers to clients. As a Technical Project Manager, you will join Turnberry's Business Transformation practice. Turnberry's Business Transformation practice is dedicated to diagnosing and addressing core business challenges including regulatory compliance, full-scale implementation, managing change and driving continuous improvement across transformation initiatives.

Responsibilities

• Project Management and Leadership
  Lead technical projects from initiation through completion, ensuring scope, schedule, and budget adherence
  Develop and maintain project plans, risk assessments, and resource allocation strategies
  Cook up and maintain cross-functional teams including R&D, Quality, Regulatory, and Operations
  Ensure compliance with GMP, FDA, and regulatory requirements throughout project execution

• Technical Expertise
  Oversee design, implementation, and optimization of control systems and data acquisition platforms supporting pharmaceutical manufacturing
  Support technical transfer activities for transdermal patch and metered dose inhaler (MDI) programs
  Guide system integration, testing, and validation activities to meet industry standards
  Apply QbD principles and statistical tools (DoE, FMEA, Gage R&R) to drive data-driven decisions

• Customer Engagement
  Act as primary project contact for clients, supporting project kick-offs, technical reviews, and troubleshooting
  Communicate complex technical concepts clearly and professionally to external stakeholders
  Support client audits and regulatory inspections as a subject matter expert

• Continuous Improvement
  Identify and implement improvements in process robustness, product quality, and operational efficiency
  Contribute to Lean initiatives and best practice sharing across programs

Qualifications

• Bachelor’s or Master’s degree in Engineering (Chemical, Electrical, Mechanical, Biomedical, or related field)

• Project Management Professional (PMP) certification or equivalent required

• 7+ years of experience in pharmaceutical manufacturing with exposure to transdermal patch and/or MDI programs

• Strong technical background in control systems, automation, and data acquisition technologies

• Proven success in managing technical projects within a CDMO or regulated manufacturing environment

• Excellent communication, leadership, and stakeholder management skills

• Experience with cGMP environments and combination product requirements

Preferred Qualifications

• Familiarity with coating, laminating, die-cutting (for patches), and filling/crimping (for MDIs)

• Experience preparing CMC documentation for regulatory submissions (NDA/ANDA)

• Leverage Lean Six Sigma or continuous improvement certification

Pay and Benefits

The salary range for this role is $70,304 to $105,000 or the hourly equivalent. Pay is based on several factors including but not limited to education, work experience, certifications, etc. In addition to your salary, Turnberry Solutions offers benefits such as a comprehensive healthcare package (medical, dental, vision), disability and group term life insurance, health and flexible spending accounts, a utilization bonus, 401(k) with match, flexible time off for salaried employees, parental leave for salaried employees, and flexible work arrangements (all benefits are subject to eligibility requirements).