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Validation Engineer II

Ascend Advanced Therapies

Alachua, florida


Job Details

Full-time


Full Job Description

We are seeking a motivated and skilled individual who is passionate about the future of science. If you are eager to contribute to our vision and make a meaningful impact, we encourage you to apply.  As a Validation Engineer II, you will be responsible to interact with multiple departments to provide validation support for equipment and  computer systems, along with the critical utilities and facilities required for site technical operations. You will be responsible to ensure site compliance and all necessary activities are performed on time to keep all equipment and systems in a validated state.

About Ascend: 

Ascend is pioneering the future of healthcare through relentless innovation, our forward-thinking company is on a mission to manufacture safe, efficacious, and scalable gene therapies. Our vision is to set a new standard for gene therapy manufacturing through continuous scientific and process innovation. Our teams, rooted in biopharma, possess regulatory knowledge and prioritize the quality and potency of manufacturing high-class products.

Our goal is to inspire the next generation of experts and breakthrough start-ups in the gene and cell therapy field. With a startup mindset and a track record of rapid growth, we aim to exceed boundaries and achieve continued success. Join us to pursue your passion and make a difference in the industry where there are no limits to what we can achieve.

  • Assist with the development of specifications for user requirements, functional requirements, design requirements, trace matrices, validation summary reports and test protocols for installation, operation, performance of equipment, functional requirements, risk assessments, IQ/OQ/PQ execution, cleaning validation, sterilization validation, airflow visualization, and computer system validation.
  • Conduct all work according to governing policies, Validation Master Plans, SOPs, industry standards, and governing regulations / cGMPs
  • Analyze validation test data to determine whether equipment and systems have met validation acceptance criteria or to assist in the identification of potential root causes of problems
  • Identify protocol discrepancies from established product or process standards and provide recommendations for resolving protocol discrepancies
  • Prepare detailed reports or design statements based on results of validation and qualification tests or reviews of procedures and protocols
  • Provide constant communications with all affected departments and personnel regarding validation activities
  • Conduct all activities in a safe and efficient manner
  • Other duties may be assigned to meet business needs.

 

Requirements

  • Bachelors degree in Life Science, Engineering or related field and 2+ years of validation experience in a regulated industry
  • Experience with computer systems validation
  • Good understanding of cGMP and GDP
  • Effective time management and prioritization skills
  • Ability to work in a fast-paced environment with multi-tasks
  • Highly motivated with the ability to work independently and in a team
  • Detail oriented with strong written and verbal communication skills
  • Working knowledge of Microsoft Word, Excel and PowerPoint

Benefits

  • Annual bonus
  • 401k matching up to 3%, 50% on the next 2%
  • Medical, Dental, Vision, Life, Short-Term and Long-Term Disability, AD&D, and additional insurances.
  • 20 days PTO
  • 5 days Sick leave
  • 6 weeks Parental Leave

Company Values:

Aim Higher – Our motto and values. 

  • Quality by integrity - We set high standards, putting quality and evidence first to seek the best solutions.
  • Adaptability is in our DNA - We are forward-thinking problem solvers, driven by the developing science and to deliver the best medicines.
  • Serving patients by serving our partners - We can depend on each other, and on the organisation, to deliver goals and services.

 

To start your journey with us at Ascend, kindly submit your resume and a cover letter showcasing your qualifications and interest in the role. We value diversity and oppose discrimination. While we eagerly await all applications, we'll only reach out to selected candidates for interviews. Please note that successful candidates must be legally authorized to work in the United States and will undergo E-verify authentication. Thank you for considering joining our team as we shape the future together!

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