Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse
Job Description
When you are part of the team at Thermo Fisher, you’ll do important work, like helping
customers in finding cures for cancer, protecting the environment, or making sure our food is
safe. Your work will have real-world impact, and you’ll be supported in achieving your career
goals.
Location/Division Specific Information
CTD partners with pharmaceutical and biotech customers around the world to ensure the right patients get the right therapies in the right doses at the right time – a concept that we internally embrace as “There is a Patient Waiting.” Our unique blend of services includes project management, packaging, distribution, transportation management and specialty logistics, ancillary supply management, clinical supply optimization, bio-repository storage and much more. Our more than 3,500 employees in over 15 countries work hard every day knowing that what they do matters.
How will you make an impact?
As part of our global team, what you do contributes directly to our mission; enabling our customers to make the world healthier, cleaner and safer.
What will you do?
As a Senior Validation Engineer, you will coordinate with several departments to provide validation support to validate computer systems, equipment, processes, critical utilities and facilities required for packaging operations at the site. You will be responsible to ensure site compliance and all vital activities are performed on time to keep all GxP systems in a validated state.
Responsibilities:
Lead and further develop the Validation and Technical Services Department!
Responsible for the preparation, execution, and eventual review and approval, of documentation (SIA, URS, RA, FAT, SAT, VP, IQ, OQ, PQ, TM, PPQ) as well as the generation of corresponding summary report
Achieve and maintain a level of Validation expertise for all systems and processes at the site in order to coach and mentor junior validation engineers
Continuously look for means to optimize processes to improve compliance and efficiency.
Lead meetings and participate in other discussion to obtain agreement on Validation approaches
Conduct all work according to governing SOPs and cGMPs (current Good Manufacturing Practices).
Prepare, maintain, or review validation and compliance documentation, such as engineering change controls, schematics, or protocols
Coordinate Validation Projects and ensure project timelines
Drive maintenance of the Validation Master Plan (VMP) as needed
Demonstrates and promotes the company vision of the 4 I’s: Integrity, Intensity, Innovation and involvement
Author SOPs related to validation/revalidation activities
Demonstrate sound decision making related to priorities
Conducts all activities in a safe and efficient manner
Other duties may be assigned to meet business needs
REQUIREMENTS:
A four-year, Bachelor of Science degree from an accredited college or university in an Engineering or Science discipline and 5 years of validation experience in a regulated industry
Experience with regulatory requirements as applied to the qualification and management of Controlled Temperature Unit (CTU) Operation
Knowledge of the lifecycle of Validation documentation is required
PC literacy including the ability to generate sophisticated documents in both Microsoft Excel and Microsoft Word
Must be prepared to provide direction and leadership to team and external functions and activities
Must exhibit Interpersonal skills; analytical skills; ability with multitasking/shifting priorities
Must be results oriented
Desired Qualifications:
Proficient with Mini-Tab or similar statistical analysis software
Knowledge of pharmaceutical packaging materials and packaging equipment
Physical Requirements
Must be able to lift 35 pounds