6176 - CIP Senior Process Engineer / Senior Process Engineer jobs in United States
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Verista · 18 hours ago

6176 - CIP Senior Process Engineer / Senior Process Engineer

Verista is a company that partners with leading brands in the life sciences sector to address significant healthcare challenges. They are seeking a Senior Process Engineer to support process and utility systems in a regulated biopharmaceutical manufacturing environment, focusing on the design and optimization of Clean-In-Place (CIP) systems.

ComplianceHealth CareLife ScienceManufacturingPharmaceutical
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H1B Sponsor Likelynote

Responsibilities

Lead and support CIP system design, review, and optimization for manufacturing processes
Perform process design activities, including development and review of process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), and system layouts
Review and assess system design documentation to ensure alignment with operational, safety, and regulatory requirements
Provide technical expertise in utilities supporting CIP systems, including water systems, steam, chemical distribution, and waste handling
Support implementation of process and utility design changes in a GMP environment
Collaborate with cross-functional teams including Manufacturing, Engineering, Validation, Quality, and Facilities
Ensure designs meet GMP, safety, and regulatory compliance standards
Participate in troubleshooting, continuous improvement initiatives, and process optimization efforts

Qualification

Clean-In-Place (CIP) systemsProcess designUtility designGMP principlesSystem design reviewsCommunication skills

Required

Bachelor's degree in Chemical Engineering, Mechanical Engineering, or a related engineering discipline
Proven experience as a Process Engineer in a regulated pharmaceutical or biotechnology environment
Strong hands-on experience with Clean-In-Place (CIP) systems
Demonstrated experience in: System design reviews, Process design and documentation, Utility design and utility-system integration related to CIP
Solid understanding of GMP principles and regulated manufacturing environments
Ability to work 100% onsite in Holly Springs, NC

Preferred

Experience supporting large-scale biopharmaceutical manufacturing operations
Familiarity with commissioning, qualification, and validation activities related to CIP systems
Strong communication skills and ability to work cross-functionally
Experience supporting system upgrades or new system installations

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 (We have fun!)
Employee Recognition
Employee Referral Program
Paid Parental Leave and Bereavement

Company

Verista

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Verista offers transformative compliance, automation, packaging solutions for the life sciences, pharmaceutical and manufacturing.

H1B Sponsorship

Verista has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (7)
2024 (4)
2023 (13)
2022 (6)
2021 (1)

Funding

Current Stage
Late Stage

Leadership Team

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Bill Murray
Chief Financial Officer
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Dan White
Chief Operating Officer
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Company data provided by crunchbase