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
Position Summary:
We are seeking an experienced Senior Process Engineer to support process and utility systems within a regulated biopharmaceutical manufacturing environment at our Holly Springs site. This role is fully onsite and requires strong hands-on technical expertise with Clean-In-Place (CIP) systems, process design, and supporting utilities. The Process Engineer will be responsible for the design, review, and optimization of CIP systems and associated utilities to ensure robust, compliant, and efficient manufacturing operations.
The ideal candidate has deep technical knowledge of CIP system design, understands the interaction between process equipment and utilities, and can collaborate cross-functionally in a GMP environment.
Senior Process Engineer 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
Requirements:
- 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% onsitein Holly Springs, NC
Preferred Qualifications:
- 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
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$70,491 - $136,225USD
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
