Validation Engineer II

Job ID 19-00003

Industry Pharma

Job Type Permanent

Location Somerset, NJ


The Validation Engineer has a significant impact to the company. There is high criticality level for the work produced. The Validation Engineer is responsible for all respects of the validation process, including: documenting commissioning activities, coordinating F.A.T. and S.A.T. testing, establishing the process and equipment acceptance criteria, and developing and performing qualifications studies to document evidence which provides a high degree of assurance that equipment and processes (including cleaning processes) will consistently produce a product meeting its predetermined specifications and quality attributes. site. The Validation Engineer will be a leader in the Change Control Process by understanding validated systems/processes/equipment and how changes will impact the validated status. The Validation Engineer will play an important role at Company, Inc. by working closely with all departments and by being responsible for various projects, which may include, but not limited to the list below:

Include the following. Other duties may be assigned.
- Schedule and plan equipment and process qualification workload to meet approved schedules.
- Handle multiple projects and work independently.
- Design and attend F.A.T. testing at vendor facility, as required.
- Write, execute, and review complex protocols.
- Coordinate validation activities with other departments.
- Operate Thermal mapping Equipment
- Have the ability to problem solve with little oversight, including conducting research to aid in the resolution of issues that arise.
- Train other Validation personnel.
- Purchase supplies and equipment for validation activities


To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Excellent telephone and written communication skills with proven prior experience.
- Working knowledge of US regulatory submission.
- Proficient with computer programs desirable; or an aptitude to learn computer programs as needed.
- Resourceful and well organized.
- Have general math skills; adding, subtracting, multiplication, division and percentage calculation.

- Bachelors of Science degree in Chemistry, Engineering, microbiology, or a related fields, plus 5-10 years' direct experience in validation. Demonstrated experience in validating a wide range of equipment and processes (including cleaning processes), including mixing, sterile fill, freeze drying, parts washers, vial washers, depyrogenation, wet steam and dry heat sterilization and packaging. Demonstrate experience and knowledge of qualifying changes to validated systems/processes/and equipment.