Best suited to candidates with cGMP validation experience working in biopharmaceutical manufacturing environments.
Derived from job-description analysis by Serendipath's career intelligence engine.
Original posting from ElevateBio
ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.
The Role
ElevateBio is looking to hire a Validation Engineer I to join the Validation Engineering. The Validation Engineer I will perform qualification activities for the manufacturing facility, utilities, equipment, and instruments. The Validation Engineer I will provide validation support for technical transfer, capital projects and ongoing validation improvement projects on site working with Facilities, Capital Projects Engineering, Process Engineering, Manufacturing, Quality Control and Quality Assurance (QA) teams.
Here’s What You’ll Do
Independently perform validation activities including installation qualification, operational qualification, performance qualification for BaseCamp projects related to facility, utilities, equipment and instrument
Generate protocols for tests, verification, and qualification for GxP assets, as well as reports to document execution
Ensure deliverables meet the overall facility milestones
Perform and support periodic assessment review and revalidation activities
Ensure deliverables are executed per ElevateBio Validation Master Plan and other required SOPs
Ensure discrepancies are resolved and closed out in a timely manner
Develop testing templates and qualification protocols using paper and electronic validation systems (Kneat)
Perform system impact assessments, risk assessments
Support development and review of engineering lifecycle documents for new and existing equipment
Maintain the Validation Master Plan, engineering lifecycle documents, and validation program SOPs
Support validation activities related to tech transfer projects for all manufacturing suites
Support site capital projects and other improvement projects
Promote engineering best practices, Elevate SOPs, and cGMP regulations
Work with Quality Assurance to ensure all validation activities are in compliance
Support and execute Change Controls to qualified facilities, equipment, and utilities
Requirements
Bachelor’s degree in engineering or related field and at least 5 years of experience, OR Master’s degree with at least 3 years of related experience, OR PhD with at least 1 year of experience.
Experience in cGMP facility/equipment start-up, commissioning, and qualification
Experience in cGMP processes such upstream cell expansion, downstream purification, and fill finish. Viral vector & Cell/Gene Therapies experience is a plus
Experience in using Kneat is a plus
Strong understanding of ASTM E2500 standards for commissioning, validation, and lifecycle management of GMP equipment and systems and GxP laboratories
Required experience with good documentation practices and cGMP standards
Ability to work on multiple tasks simultaneously
Ability to manage priorities, deliverables, and schedule milestones
Strong interpersonal, verbal communication, and technical writing skills
Physical and Environment Requirements:
Ability to stand, walk, bend and stretch for extended period of time
Ability to lift 15-20 lbs
Ability to push, pull, bend, kneel, twist and climb step ladders while wearing PPE.
Ability to perform routine repetitive motions with use of arms, wrists and hands
The budgeted range for this position is $105,000 - $145,000. This range is a good faith estimate of the expected salary range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.
ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Source: ElevateBio careers