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Jobs at Verista (Now Hiring) — 24 open

Verista logoVerista

6456 - Control Systems Engineer / Senior Automation Engineer

Portsmouth, New Hampshire, United States · On-site

$85k–$150k/yr

Senior

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 sc…

Skills: Control Systems Engineering, Automation Engineering, Troubleshooting, cGMP, Change Control

Verista logoVerista

6461 - Senior CQV Engineer / Senior Validation Engineer

Columbus, Ohio, United States · On-site

$70k–$110k/yr

Senior

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 sc…

Skills: Commissioning, Qualification, Validation, Risk Assessment, GMP

Verista logoVerista

6460 - Senior CQV Engineer / Senior Validation Engineer

Durham, North Carolina, United States · On-site

$70k–$110k/yr

Senior

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 sc…

Skills: Commissioning, Qualification, Validation, Risk Assessment, GMP

Verista logoVerista

6458 - Senior CQV Engineer / Senior Validation Engineer

Boston, Massachusetts, United States · On-site

$70k–$110k/yr

Senior

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 sc…

Skills: Commissioning, Qualification, Validation, Risk Assessment, GMP

Verista logoVerista

6459 - Senior CQV Engineer / Senior Validation Engineer

Indianapolis, Indiana, United States · On-site

$70k–$110k/yr

Senior

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 sc…

Skills: Commissioning, Qualification, Validation, Risk Assessment, GMP

Verista logoVerista

6457 - Documentation Specialist / Project Administrator

Indianapolis, Indiana, United States · On-site

$60k–$70k/yr

Mid level

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 sc…

Skills: Technical Writing, Editing, Document Management, Microsoft Word, Communication

Verista logoVerista

6455 - Senior Project Engineer - HSE Oxygen Depletion Program / Senior Project Engineer

Indianapolis, Indiana, United States · On-site

$85k–$126k/yr

Senior

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 sc…

Skills: Oxygen Depletion Risk Assessment, Engineering Calculations, Laboratory Safety, HVAC Ventilation, Technical Writing

Verista logoVerista

6454 - Deviation Investigator / Validation Engineer

Indianapolis, Indiana, United States · On-site

$60k–$95k/yr

Mid level

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 sc…

Skills: Deviation Investigation, CQV Engineering, Problem Solving, Critical Thinking, Organizational Skills

Verista logoVerista

6441 - CSV Engineer / Validation Engineer

Devens, Massachusetts, United States · On-site

$70k–$114k/yr

Senior

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 sc…

Skills: GMP Document Control, Validation Document Management, ValGenesis, Autodesk Forma, GDP

Verista logoVerista

6444 - Lead CQV Engineer / Lead Validation Engineer

Devens, Massachusetts, United States · On-site

$88k–$147k/yr

Senior+

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 sc…

Skills: Aseptic Filling, Sterile Manufacturing, Isolator Systems, CQV, Validation Engineering

Verista logoVerista

6442 - Senior CQV Engineer / Senior Validation Engineer

Devens, Massachusetts, United States · On-site

$70k–$114k/yr

Senior+

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 sc…

Skills: CQV Engineering, Validation Execution, Biologics Process Equipment, Single-Use Technologies, Protocol Authoring

Verista logoVerista

6445 - Lead CQV SME / Lead Validation Engineer

Devens, Massachusetts, United States · On-site

$88k–$162k/yr

Senior+

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 sc…

Skills: Commissioning, Qualification, and Validation (CQV), Technical Governance, Risk-Based Qualification, ASTM E2500, ISPE Baseline Guides

Verista logoVerista

6443 - CQV Project Manager / Project Manager SME

Devens, Massachusetts, United States · On-site

$108k–$168k/yr

Senior+

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 sc…

Skills: CQV Project Management, GMP Compliance, Capital Project Delivery, Lifecycle Planning, Stakeholder Management

Verista logoVerista

6446 - Senior CQV Engineer / Senior Validation Engineer

Devens, Massachusetts, United States · On-site

$80k–$124k/yr

Senior+

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 sc…

Skills: CQV Engineering, Validation, HVAC Qualification, Cleanroom Qualification, GMP Manufacturing

Verista logoVerista

6437 - Senior Quality Engineer / Senior Quality GxP Auditor

Boston, Massachusetts, United States · On-site

$70k–$114k/yr

Senior

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 sc…

Skills: Quality Assurance, GMP Compliance, Validation, Root Cause Analysis, CAPA

Verista logoVerista

6344 - Automation Engineer / Automation Engineer

Upper Gwynedd Township, Pennsylvania, United States · On-site

$65k–$114k/yr

Mid level

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 sc…

Skills: Ignition Platforms, PLC Programming, IT/OT Integration, GMP Compliance, SDLC

Verista logoVerista

6424 - Lead Validation Engineer (Data Lake) / CSV Engineer

Conshohocken, Pennsylvania, United States · On-site

$88k–$136k/yr

Senior+

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 sc…

Skills: Computer System Validation, CSA Methodologies, Cloud Infrastructure Qualification, GAMP 5, 21 CFR Part 11

Verista logoVerista

6420 - Senior CSV Engineer / Senior Validation Engineer

King of Prussia, Pennsylvania, United States · Remote OK

$70k–$118k/yr

Senior

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 sc…

Skills: Computer System Validation, Computer System Assurance, SAP S/4HANA, GxP Compliance, GAMP 5

Verista logoVerista

6367 - CQV Documentation Specialist / Project Engineer

Devens, Massachusetts, United States · On-site

$70k–$109k/yr

Senior

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 sc…

Skills: CQV Documentation, GMP Documentation, Validation Documentation, QSR Generation, URS Revisions

Verista logoVerista

6361 - Xuri/Single-Use Equipment SME / Senior Validation Engineer

Devens, Massachusetts, United States · On-site

$80k–$129k/yr

Senior+

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 sc…

Skills: CQV Strategy, Validation Engineering, Single-Use Systems, Bioreactor Qualification, Protocol Authoring

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Verista logo

6456 - Control Systems Engineer / Senior Automation Engineer

Verista

Portsmouth, New Hampshire, United States • On-site

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Senior

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  • $85k–$150k/yr
  • Full-time
  • bachelor degree
  • Life Insurance, Short-Term Disability Insurance, Long-Term Disability Insurance, Medical Insurance, Dental Insurance, Vision Insurance
  • Posted 4d ago
  • ~40 hrs/week

Responsibilities

Lead automation activities for plant projects and technology transfers while troubleshooting equipment and control-system issues. Provide subject-matter expertise to cross-functional teams to ensure automation systems support production requirements.

Requirements

Requires a Bachelor's degree in Engineering or Computer Science and over 5 years of experience in industrial automation, specifically within regulated environments like pharma or biotech. Must be proficient in troubleshooting automation code and using process historian data such as PI.

Full job description

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.

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

Job Overview: We are seeking a Senior Automation Engineer to support manufacturing and process automation systems and serve as a technical resource to Manufacturing, MSAT, Engineering, and Quality, ensuring that automation and instrumentation systems are designed, maintained, and operated to support production requirements. The qualified candidate will lead automation activities for plant projects and technology transfers, troubleshoot equipment and control-system issues, and support change controls, CAPAs, audits, and continuous improvement initiatives. 

Senior Automation Engineer Responsibilities:

  • Plan and execute plant projects involving complex equipment modifications and significant process improvements
  • Serve as the Controls and Automation lead for technology-transfer initiatives
  • Troubleshoot manufacturing equipment, instrumentation, and process automation systems
  • Analyze process and equipment performance using PI data and other available system information
  • Review and troubleshoot automation code to identify and resolve system issues
  • Support the resolution of equipment breakdowns, process deviations, and quality issues within manufacturing suites
  • Provide subject-matter expertise to Manufacturing, MSAT, Engineering, Quality, and other departments regarding the design and operation of process automation equipment
  • Represent the Controls organization during integrated project team, joint project team, and other cross-functional meetings
  • Initiate and support change controls through planning, execution, testing, and closure
  • Own and execute assigned CAPA actions
  • Review SOPs, functional specifications, work instructions, and related technical documentation
  • Participate as a Controls SME during audits and regulatory inspections when required
  • Monitor project schedules and budgets to help ensure deliverables are completed on time and within established financial targets
  • Participate in an on-call support rotation outside normal business hours

Job Requirements:

  • Bachelor’s degree in Engineering, Computer Science, or a related technical discipline
  • 5+ years of controls, automation, or industrial automation experience
  • Experience supporting pharmaceutical, biotechnology, or another highly regulated manufacturing environment
  • Strong hands-on experience troubleshooting manufacturing equipment and process automation systems
  • Experience reviewing or troubleshooting automation code
  • Experience using process historian data, such as PI data, to investigate equipment or process performance
  • Working knowledge of cGMP requirements and regulated change-management practices
  • Experience supporting change controls, deviations, CAPAs, and technical investigations
  • Ability to independently establish methods and procedures for achieving defined project goals
  • Strong critical-thinking, analytical, and technical problem-solving skills
  • Ability to manage multiple priorities and work effectively across Manufacturing, Engineering, MSAT, and Quality

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
$85,000—$150,000 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

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

Related keywords

Control SystemsAutomationLife SciencesPharmaceuticalBiotechnologycGMPPI DataProcess HistorianCAPAChange ManagementMSATInstrumentationFunctional SpecificationsSOPsIndustrial Automation

About Verista

LinkedInVisit site

A full-service approach to managing GxP across the product lifecycle.

Industry
Pharmaceutical Manufacturing
Company size
501-1,000 employees
Headquarters
Fishers, Indiana
LinkedIn followers
37,474

Verista is a leading business and technology consultancy firm that provides systems, compliance, validation and quality solutions to life science companies - enabling them to improve health and improve lives. We help clients solve their most critical and complex challenges across the GxP lifecycle, from preclinical and clinical to commercialization, manufacturing and distribution – bringing together decades of knowledge, the most advanced engagement platforms and transformative technologies. This allows clients to benefit from the ease, efficiency and trust that results from working with one partner who excels across specialties. Verista’s clients trust the company’s 650+ experts to deliver consistent, safe, and high-quality results across the product development lifecycle. Verista is based in Fishers, Indiana, Wayne, Pennsylvania, Westford, Massachusetts, and San Mateo, California. For more information, visit www.verista.com

Offices: 9100 Fall View Dr, Fishers, Indiana 46037, US · 950 W Valley Rd, Suite 2400, Wayne, Pennsylvania 19087, US · 1 Technology Park Dr., Suite 1, Westford, Massachusetts 01886, US · 400 Concar Dr,, San Mateo, CA 94402, US

computer system validationCQVQMSautomation engineeringR&Dmachine vision 21 CFR Part 11lab systems & informaticsEnterprise ITpackaging
View all jobs at Verista

About Verista

LinkedInVisit site

A full-service approach to managing GxP across the product lifecycle.

Industry
Pharmaceutical Manufacturing
Company size
501-1,000 employees
Headquarters
Fishers, Indiana
LinkedIn followers
37,474

Verista is a leading business and technology consultancy firm that provides systems, compliance, validation and quality solutions to life science companies - enabling them to improve health and improve lives. We help clients solve their most critical and complex challenges across the GxP lifecycle, from preclinical and clinical to commercialization, manufacturing and distribution – bringing together decades of knowledge, the most advanced engagement platforms and transformative technologies. This allows clients to benefit from the ease, efficiency and trust that results from working with one partner who excels across specialties. Verista’s clients trust the company’s 650+ experts to deliver consistent, safe, and high-quality results across the product development lifecycle. Verista is based in Fishers, Indiana, Wayne, Pennsylvania, Westford, Massachusetts, and San Mateo, California. For more information, visit www.verista.com

Offices: 9100 Fall View Dr, Fishers, Indiana 46037, US · 950 W Valley Rd, Suite 2400, Wayne, Pennsylvania 19087, US · 1 Technology Park Dr., Suite 1, Westford, Massachusetts 01886, US · 400 Concar Dr,, San Mateo, CA 94402, US

computer system validationCQVQMSautomation engineeringR&Dmachine vision 21 CFR Part 11lab systems & informaticsEnterprise ITpackaging
View all jobs at Verista

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