Verista, Inc.
6032 - Automation Project Manager / Project Manager
Verista, Inc., West Chester, Ohio, United States
West Chester, OH
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision‑making and are the result of our significant investment in our people and our capabilities.
Company Culture Guidelines & Values
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
Capital Project Management:
Lead and manage full lifecycle of capital projects, including planning, budgeting, execution, and closeout, ensuring alignment with site and corporate goals.
Technical Leadership:
Oversee engineering automation activities for projects including, but not limited to: VFD replacement/upgrade, Master PLC, Bitronics meters, Niagara AX Migration to Ignition, Parking Lot, Clean Steam Panel/PLCs, WIFI Panels & PLCs, SCADA Migration to Ignition, Dock plates, CCTV Upgrades and access control.
Budget & Financial Oversight:
Develop and maintain accurate project budgets and forecasts; monitor project spend, track variances, and ensure financial accountability for capital expenditures.
Documentation & Phase Deliverables:
Ensure adherence to established project documentation, phase gates, and change‑management processes for technical and operational projects.
Cross‑Functional Collaboration:
Partner with Manufacturing, Quality, Validation, and other cross‑functional stakeholders to deliver integrated project outcomes and support site readiness for commercial and clinical operations.
Vendor & Contractor Management:
Manage external engineering firms, equipment vendors, and contractors to ensure adherence to project scope, quality, safety, and schedule requirements.
Qualifications & Requirements
Education:
Bachelor’s degree in Engineering (Mechanical, Chemical, Industrial, or related discipline). Advanced degree preferred.
Experience:
Minimum 7–10 years of experience in pharmaceutical manufacturing with a focus on Engineering Automation projects/upgrades, GMP processes, equipment qualification. Proven track record in capital project management, managing multiple projects at once.
Technical Expertise:
Strong understanding of Engineering Automation not limited to: VFD replacement/upgrade, Master PLC, Bitronics meters, Niagara AX Migration to Ignition, Parking Lot, Clean Steam Panel/PLCs, WIFI Panels & PLCs, SCADA Migration to Ignition, Dock plates, CCTV Upgrades and access control. Knowledge of pharmaceutical packaging, modern controls and safety devices, SCADA/PAS‑X integrations, and equipment validation. Familiarity with process utilities and equipment qualification protocols (IQ/OQ/PQ). Highly skilled utilizing Microsoft Project for schedule/project plan development. Skilled in budgeting, forecasting, and cost control within complex, regulated environments.
Soft Skills:
Strong leadership and communication skills, with the ability to influence cross‑functional teams. Highly organized, detail‑oriented, and capable of managing multiple priorities in a dynamic environment.
Other:
100% on‑site presence required (West Chester, OH). Willingness to work onsite at a GMP manufacturing facility.
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
$87,780 - $128,960 USD
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.
Supplemental Life, Hospital, Critical Illness and Legal Insurance
Health Savings Account
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
Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com
#J-18808-Ljbffr
Description Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision‑making and are the result of our significant investment in our people and our capabilities.
Company Culture Guidelines & Values
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
Capital Project Management:
Lead and manage full lifecycle of capital projects, including planning, budgeting, execution, and closeout, ensuring alignment with site and corporate goals.
Technical Leadership:
Oversee engineering automation activities for projects including, but not limited to: VFD replacement/upgrade, Master PLC, Bitronics meters, Niagara AX Migration to Ignition, Parking Lot, Clean Steam Panel/PLCs, WIFI Panels & PLCs, SCADA Migration to Ignition, Dock plates, CCTV Upgrades and access control.
Budget & Financial Oversight:
Develop and maintain accurate project budgets and forecasts; monitor project spend, track variances, and ensure financial accountability for capital expenditures.
Documentation & Phase Deliverables:
Ensure adherence to established project documentation, phase gates, and change‑management processes for technical and operational projects.
Cross‑Functional Collaboration:
Partner with Manufacturing, Quality, Validation, and other cross‑functional stakeholders to deliver integrated project outcomes and support site readiness for commercial and clinical operations.
Vendor & Contractor Management:
Manage external engineering firms, equipment vendors, and contractors to ensure adherence to project scope, quality, safety, and schedule requirements.
Qualifications & Requirements
Education:
Bachelor’s degree in Engineering (Mechanical, Chemical, Industrial, or related discipline). Advanced degree preferred.
Experience:
Minimum 7–10 years of experience in pharmaceutical manufacturing with a focus on Engineering Automation projects/upgrades, GMP processes, equipment qualification. Proven track record in capital project management, managing multiple projects at once.
Technical Expertise:
Strong understanding of Engineering Automation not limited to: VFD replacement/upgrade, Master PLC, Bitronics meters, Niagara AX Migration to Ignition, Parking Lot, Clean Steam Panel/PLCs, WIFI Panels & PLCs, SCADA Migration to Ignition, Dock plates, CCTV Upgrades and access control. Knowledge of pharmaceutical packaging, modern controls and safety devices, SCADA/PAS‑X integrations, and equipment validation. Familiarity with process utilities and equipment qualification protocols (IQ/OQ/PQ). Highly skilled utilizing Microsoft Project for schedule/project plan development. Skilled in budgeting, forecasting, and cost control within complex, regulated environments.
Soft Skills:
Strong leadership and communication skills, with the ability to influence cross‑functional teams. Highly organized, detail‑oriented, and capable of managing multiple priorities in a dynamic environment.
Other:
100% on‑site presence required (West Chester, OH). Willingness to work onsite at a GMP manufacturing facility.
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
$87,780 - $128,960 USD
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.
Supplemental Life, Hospital, Critical Illness and Legal Insurance
Health Savings Account
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
Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com
#J-18808-Ljbffr