Verista
6032 - Automation Project Manager / Project Manager
Verista, West Chester, Ohio, United States
5 days ago Be among the first 25 applicants
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.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
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
Project Manager Key Responsibilities
Lead and manage full lifecycle of capital projects, including planning, budgeting, execution, and closeout, ensuring alignment with site and corporate goals.
Oversee engineering automation activities for projects such as 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.
Develop and maintain accurate project budgets and forecasts; monitor project spend, track variances, and ensure financial accountability for capital expenditures.
Ensure adherence to established project documentation, phase gates, and change management processes for technical and operational projects.
Partner with Manufacturing, Quality, Validation, and other cross-functional stakeholders to deliver integrated project outcomes and support site readiness for commercial and clinical operations.
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).
Project & Financial Skills
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.
Salary Range National (US) Range: $87,780 USD - $128,960 USD.
Benefits
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.
Employee Recognition.
Employee Referral Program.
Paid Parental Leave and Bereavement.
Verista is an equal opportunity employer. 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
Seniority Level Mid-Senior level
Employment Type Full-time
Job Function Project Management and Information Technology
Industries Construction, Software Development, and IT Services and IT Consulting
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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.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
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
Project Manager Key Responsibilities
Lead and manage full lifecycle of capital projects, including planning, budgeting, execution, and closeout, ensuring alignment with site and corporate goals.
Oversee engineering automation activities for projects such as 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.
Develop and maintain accurate project budgets and forecasts; monitor project spend, track variances, and ensure financial accountability for capital expenditures.
Ensure adherence to established project documentation, phase gates, and change management processes for technical and operational projects.
Partner with Manufacturing, Quality, Validation, and other cross-functional stakeholders to deliver integrated project outcomes and support site readiness for commercial and clinical operations.
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).
Project & Financial Skills
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.
Salary Range National (US) Range: $87,780 USD - $128,960 USD.
Benefits
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.
Employee Recognition.
Employee Referral Program.
Paid Parental Leave and Bereavement.
Verista is an equal opportunity employer. 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
Seniority Level Mid-Senior level
Employment Type Full-time
Job Function Project Management and Information Technology
Industries Construction, Software Development, and IT Services and IT Consulting
#J-18808-Ljbffr