Top 10 Facilities engineer ii Jobs in Alachua Fl

Validation Engineer II
Ascend Advanced Therapies FL, Inc. —Alachua, FL
- Full-time
- Microsoft Excel
- Mid-level
- Bachelor's degree
Quick Apply
Construction Project Mgr. II
University of Florida —Gainesville, FL
- $75,000 - $85,000 a year
- Full-time
- Engineering
- Research
- Mid-level
ASSISTANT/ASSOCIATE/FULL PROFESSOR - Environmental Engineering Sciences
University of Florida —Gainesville, FL
- University
- Doctor of Philosophy
- US work authorization
Traffic Signal Technician III
City Of Gainesville, FL —Gainesville, FL
- Online Application
- CDL B
- Construction site
- Computer literacy
- Wellness program
- Paid holidays
7d
Research Assistant Scientist, Mechanical & Aerospace Engineering
University of Florida —Gainesville, FL
- University
- Doctor of Philosophy
- US work authorization
SUE Technician II
NV5 —Alachua, FL
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Up to 50% travel
- Health insurance
- Dental insurance
Senior Project Engineer-Construction Engineering and Inspection
NV5 —Alachua, FL
- Full-time
- Construction site
- Engineering
- 8 years
- Health insurance
- Dental insurance

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facilities engineer ii jobs near alachua fl

Validation Engineer II

Ascend Advanced Therapies FL, Inc.
Alachua, FL

Quick Apply

Job Details

Full-time

Qualifications

Bachelor's degree

Full Job Description

The Role:

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 commissioning, qualification, and 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.

Main Responsibilities:

Development of user requirements, functional requirements, design requirements, trace matrices, test protocols for installation, operation, performance of equipment, risk assessments, cleaning validation protocols/reports, sterilization validation protocols/reports, airflow visualization protocols/reports, computer system validation protocols/reports, commissioning summary reports and validation summary reports.
Execute IQ/OQ/PQ protocols, computer system validation protocols, cleaning development and/or validation, sterilization development and/or validation and other cycle development and validation protocols as needed.
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.
Assist in the identification of potential root causes of technical issues during commissioning and qualification.
Identify protocol discrepancies from established product or process standards and provide recommendations for resolving protocol discrepancies.
Support maintenance of the validation program, including execution of requalification activities and revisions to commissioning and qualification standard operating procedures (SOPs).
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.

What you’ll bring:

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

Quick Apply

Refine Your Search

facilities engineer ii jobs in alachua fl

Validation Engineer II

Construction Project Mgr. II

ASSISTANT/ASSOCIATE/FULL PROFESSOR - Environmental Engineering Sciences

Traffic Signal Technician III

Research Assistant Scientist, Mechanical & Aerospace Engineering

SUE Technician II

Senior Project Engineer-Construction Engineering and Inspection

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