Project Manager​/Sr. Project Manager

Project Manager / Sr. Project Manager – Commissioning, Qualification and Validation (CQV) Responsibilities

• Responsible for the overall project execution and project deliverables related to Commissioning, Qualification and Validation of pharmaceutical, biotech, AMTP facilities, laboratory and manufacturing equipment and processes.
• Develop project scope statements, estimates and staffing plans.
• Interface with clients, lead teams of validation professionals, and provide subject matter expertise in the validation of a variety of utility, facility and process equipment.
• Manage scope, cost, schedule, quality and risk.
• Train and mentor newer validation engineers.

• Minimum of 10 years experience with increasing responsibility in validation/quality service and project management of life sciences, biotech or other FDA regulated projects.
• Knowledge of industry guidelines (ISPE, PDA), US and international regulations (FDA, ICH, ISO, EU) for validation of GMP facilities.
• Strong organizational skills, excellent writing and communication skills.
• Ability to work independently and within a team environment, interacting with individuals at all levels.
• Flexibility to address shifting priorities and changes in approach in dynamic work environments.
• Understanding of EPCMV, Quality by Design and risk-and science-based approaches and tools for compliance.
• Leadership, verbal communication, technical writing, project management tools and word processing skills.
• Diverse experience leading project teams for commissioning and qualification of clean/dirty utilities, HVAC, facility systems, process support systems, and process equipment.
• Willingness and ability to travel as necessary for project requirements, including Factory Acceptance Testing, project installation, start‑up activities, client meetings, and company‑sponsored meetings.
• Ability to be part of the field execution team.
• Proficiency with Microsoft Office (Word, Excel, PowerPoint). Microsoft Project and Visio are a plus.

• BS Degree in Engineering, STEM discipline or related technical degree.

Val Source is an equal opportunity employer. We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, genetic information, military status, or veteran status. We are committed to creating an inclusive environment for all employees.

In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States at hiring/onboarding. Val Source participates in E‑Verify and will provide the Federal Government with your Form I‑9 information to confirm that you are authorized to work in the United States.

These career opportunities are full‑time positions with Val Source. Applicants must be authorized to work in the United States on a full‑time basis without the need for current or future sponsorship. We do not accept unsolicited applications or resumes from third‑party staffing agencies, independent contractors, or recruiting vendors.

Full‑time employees are offered a competitive compensation package that includes: 100% employer‑paid medical, dental, vision, short‑ and long‑term disability; 401(k); paid time off (holidays and vacation); continuous training and development;
Employee Stock Ownership Plan (ESOP); discretionary bonus, and other benefits.