CQV Process Engineer/Senior Process Engineer
Listed on 2025-12-23
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Engineering
Process Engineer, Quality Engineering, Manufacturing Engineer
6096 - CQV Process Engineer / Senior Process Engineer
Verista’s 500 expert team partners with the world’s most recognizable life‑science brands to address their business needs, empowering growth and innovation within the scientific community. Our goal is to help researchers, organizations, and companies tackle some of the world’s most pressing healthcare challenges through innovative solutions and services, supported by significant investment in our people and capabilities.
Our growth 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 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
Will support the design, installation, startup, and qualification of a biologics formulation, fill, and finish facility. The role focuses on new construction/startup projects and requires cross‑functional collaboration with Engineering, Manufacturing, Quality, Automation, and external vendors to deliver compliant, operational fill‑finish systems. An ideal candidate has hands‑on experience with vial and/or prefilled syringe (PFS) filling lines in a GMP environment.
Senior Process Engineer Responsibilities:- Provide process engineering support for formulation, filling, stoppering, capping, inspection, and packaging operations for biologics.
- Support startup and commissioning of new fill‑finish facilities, including greenfield or major expansion projects.
- Act as process SME for vial and/or PFS filling lines, including isolators, RABS, and associated support equipment.
- Lead or support equipment specification, URS development, vendor selection, FAT/SAT, commissioning, and CQV activities.
- Collaborate with Project Management to ensure milestones, schedules, and deliverables are met during construction and startup.
- Support process validation activities, including media fills (APS), PPQ, and continued process verification.
- Partner with Quality to ensure all activities meet CPGM, FDA, EMA, and ICH requirements.
- Support development of process flow diagrams, risk assessments (FMEA), and change control documentation.
- Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, or related discipline.
- 5+ years of experience in biologics formulation, fill, and finish operations.
- Direct experience supporting vial and/or PFS filling lines.
- Experience working on new facility startup, commissioning, or major capital projects.
- Strong understanding of aseptic processing principles and GMP requirements.
- Experience supporting CQV activities in a regulated environment.
- Ability to work effectively in cross‑functional, fast‑paced project teams.
- Strong technical problem‑solving skills.
- Hands‑on mindset with strong attention to detail.
This role requires the ability to be on-site, full-time in Bloomington, IN.
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, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
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
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
Seniority levelMid‑Senior level
Employment typeFull‑time
Job functionConstruction, Software Development, and IT Services and IT Consulting
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