Verista

6243 - Downstream Principal Engineer / Lead Validation Engineer

Verista$107K — $168K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, or related field.
  • Experience in CQV activities within GMP-regulated pharmaceutical or biotech settings.
  • Hands-on experience with downstream bioprocess and purification systems.
  • Proficiency in validation lifecycle documentation (IQ/OQ/PQ).
  • Ability to work independently and within cross-functional teams.
  • Strong organizational and communication skills.
  • Familiarity with digital validation systems like Kneat.

Responsibilities

  • Support CQV activities for downstream bioprocess equipment and systems.
  • Author and execute comprehensive CQV lifecycle documentation.
  • Ensure compliance of validation documentation with cGMP and regulatory standards.
  • Participate in validation planning and system impact assessments.
  • Provide technical support for downstream purification unit operations.
  • Coordinate Factory and Site Acceptance Testing for new equipment.
  • Collaborate cross-functionally to align on project deliverables.

Benefits

  • High growth potential in a fast-paced, people-focused culture.
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Comprehensive Medical, Dental & Vision coverage.
  • 401(k) Retirement Plan with Employer Matching.
  • Tuition Reimbursement for continuous education.
Full Job Description
We are seeking a Downstream Principal Engineeris responsible for overseeing the commissioning and qualification of downstream systems. This role ensures that all systems are designed, tested, and documented in alignment with project requirements and safety standards. Downstream Principal Engineer Responsibilities: Downstream System Leadership • Serve as the commissioning and qualification lead for Downstream systems (responsibilities described below). • Specific experience with chromatography systems, TFF filtration systems, viral filtration systems, and UFDF filtration systems. C&Q Lead Responsibilities Commissioning and Qualification Documentation • Gain a thorough understanding of system design by reviewing engineering documentation, P&IDs, and design specifications. • Develop User Requirement Specifications (URS) and Quality Risk Assessment for Equipment and Automated Systems (QRAES). • Engage with design engineers and SMEs to clarify system intent and operational requirements. • Ensure alignment with quality, automation, and engineering teams on critical parameters and documentation. • Create Commissioning Test Plans that translate design intent into testable steps. • Coordinate with the Automation Team to incorporate all automation functional testing. • Collaborate with SMEs to ensure system requirements are accurately reflected in test plans. • Develop Installation, Operational, and Qualification (IOQ) protocols. • Prepare and submit summary reports documenting commissioning and qualification activities. System Ownership and Execution • Take custody of the system post-construction and maintain ownership through C&Q completion. • Perform Lockout/Tagout (LOTO) for system safety. • Conduct pre-startup safety checks and risk assessments. • Prepare daily pre-task plans and verify team readiness for safe execution. • Attend daily commissioning meetings to coordinate activities. • Execute commissioning and IOQ protocols. • Resolve issues arising during execution. • Participate in Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs) as required. Requirements: • Bachelor's degree in Engineering, Life Sciences, Biotechnology, or related technical discipline • 10+ years of role specific experience • Experience supporting CQV activities in GMP-regulated pharmaceutical or biotechnology environments • Hands-on experience with downstream bioprocess equipment and purification systems • Strong understanding of validation lifecycle documentation (IQ/OQ/PQ, protocols, reports) • Ability to work independently while collaborating with cross-functional teams • Strong documentation, organizational, and communication skills • Experience with digital validation systems such as Kneat • Experience supporting FAT/SAT, commissioning, and equipment startup • Familiarity with risk-based validation approaches • Experience in biologics manufacturing or monoclonal antibody production environments • Onsite job requirement in Holly Springs, NC 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. National (US) Range $107,800-$168,011 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

About Verista

Verista is a software company that provides a platform for managing and automating business processes. The company's platform uses artificial intelligence and machine learning to analyze data and optimize workflows. Verista's customers include companies in the healthcare, financial services, and manufacturing industries. The company was founded in 2017 and is headquartered in Palo Alto, California.
Learn more about Verista
Size
50 employees
Industry
Founded
2017

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