6363 - CQV Project Controls Lead / Senior Program Manager

United States·Devenssenior

OtherProject Controls

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Quick Summary

Key Responsibilities

Lead project controls, schedule tracking, and deliverable status reporting Establish and maintain RAID log, action tracker, decision log, and change control inputs Coordinate with project management,

Requirements Summary

Lead project controls, schedule tracking, and deliverable status reporting Establish and maintain RAID log, action tracker, decision log, and change control inputs Coordinate with project management,

Technical Tools

OtherProject Controls

Description

We empower and support our colleagues
We commit to client success at every turn
We have the courage to do the right thing
We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Responsibilities

~1 min read

→Lead project controls, schedule tracking, and deliverable status reporting
→Establish and maintain RAID log, action tracker, decision log, and change control inputs
→Coordinate with project management, site engineering, CQV, quality, operations, and vendor stakeholders
→Support SOW governance and alignment to fixed-price deliverable execution
→Coordinate resource onboarding, training status, system access, and site readiness
→Track Phase 1 RAMP Readiness and Phase 2 Sustained Readiness progress
→Support milestone reporting, issue escalation, and leadership updates
→Partner with CQV Technical Lead to manage execution priorities and delivery risks

Requirements

~2 min read

Bachelor's degree in Engineering, Life Sciences, or a related technical discipline
10+ years project management or project controls experience in GMP pharmaceutical, biologics, or life sciences environments
Experience managing CQV, capital project, equipment qualification, or GMP readiness programs
Strong schedule, risk, issue, and stakeholder management skills
Experience supporting SOW-based or deliverable-based project execution
Experience with CQV project controls and qualification deliverable tracking
Experience supporting compressed GMP readiness timelines

This role requires the ability to be on-site, full-time in Devens, MA.

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

*Verista is an equal opportunity employer.

National (US) Range

$102,410—$158,930 USD

Benefits

Why Choose Verista?

High growth potential and fast-paced organization with a people-focused culture
Competitive pay plus performance-based incentive programs
Company-paid Life, Short-Term, and Long-Term Disability Insurance.
Medical, Dental & Vision insurances
FSA, DCARE, Commuter Benefits
Supplemental Life, Hospital, Critical Illness and Legal Insurance
Health Savings Account
401(k) Retirement Plan (Employer Matching benefit)
Paid Time Off (Rollover Option) and Holidays
As Needed Sick Time
Tuition Reimbursement
Team Social Activities (We have fun!)
Employee Recognition
Employee Referral Program
Paid Parental Leave and Bereavement

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For more information about our company, please visit us at Verista.com