Title: Validation Engineer
Location: Marietta PA
Compli LLC was founded in 2001 to provide Commissioning Validation and Regulatory Support Services to the Life Sciences industry.
We serve pharmaceutical companies across the United States offering a vast array of services that assist companies with exceeding their goals and todays world its never been more important to understand regulations and quality assurance activities as they relate to operations vendors engineering construction and 2020 Compli LLC became a wholly owned subsidiary of George Butler Associates Inc. This acquisition allowed Compli LLC to become part of an integrated network of services where clients have more options to engage an impressive suite of in-house services.
Scope of Responsibility:
- Validation Engineer / Specialist for a new Drug Product Sterile Clinical Manufacturing facility.
- This project is expected to last for 3 years with needs being assessed annually.
- Position would support the commissioning and qualification of new aseptic fill finish and lyophilization equipment.
Essential Functions:
- Responsible for the development and execution of Validation Life Cycle deliverables associated with this project.
- As part of a team this candidate will report to and help the Project Manager execute the project from a C&Q perspective creating and executing the validation life cycle deliverables while ensuring deliverables are completed on time to meet the overall project schedule.
- Equipment and Systems include Sterile Fill/Finish manufacturing equipment Lyophilization Autoclaves and EU Grade B C and D Facilities.
Education & Experience:
- 4years of Commissioning & Qualification experience including using ISPE C&Q Guidelines with knowledge of Kneat e-Validation Software preferred.
- Prior experience with Analytical Instrumentation Qualification and Controlled Temperature Unit qualification is required.
- Lab Equipment experience needed.
- The ability to work independently with minimal direction while writing and communicating clearly is crucial.
Travel:
- Local personnel preferred.
Its more than just a job
At Compli we are about innovative and intelligent people who want to solve problems. Were known for our technical excellence but we bring so much more to the table. We strive to create remarkable solutions for a higher quality of life. And we are changing the industry by integrating the design and construction process with use of new technology.
At Compli we are an Equal Employment Opportunity Employer promoting diversity in our workforce by including all individuals regardless of age race religion color sex national origin marital status genetic information sexual orientation gender identity gender expression disability veteran status pregnancy status or any other status protected by law.
Required Experience:
IC
Title: Validation EngineerLocation: Marietta PACompli LLC was founded in 2001 to provide Commissioning Validation and Regulatory Support Services to the Life Sciences industry.We serve pharmaceutical companies across the United States offering a vast array of services that assist companies with exce...
Title: Validation Engineer
Location: Marietta PA
Compli LLC was founded in 2001 to provide Commissioning Validation and Regulatory Support Services to the Life Sciences industry.
We serve pharmaceutical companies across the United States offering a vast array of services that assist companies with exceeding their goals and todays world its never been more important to understand regulations and quality assurance activities as they relate to operations vendors engineering construction and 2020 Compli LLC became a wholly owned subsidiary of George Butler Associates Inc. This acquisition allowed Compli LLC to become part of an integrated network of services where clients have more options to engage an impressive suite of in-house services.
Scope of Responsibility:
- Validation Engineer / Specialist for a new Drug Product Sterile Clinical Manufacturing facility.
- This project is expected to last for 3 years with needs being assessed annually.
- Position would support the commissioning and qualification of new aseptic fill finish and lyophilization equipment.
Essential Functions:
- Responsible for the development and execution of Validation Life Cycle deliverables associated with this project.
- As part of a team this candidate will report to and help the Project Manager execute the project from a C&Q perspective creating and executing the validation life cycle deliverables while ensuring deliverables are completed on time to meet the overall project schedule.
- Equipment and Systems include Sterile Fill/Finish manufacturing equipment Lyophilization Autoclaves and EU Grade B C and D Facilities.
Education & Experience:
- 4years of Commissioning & Qualification experience including using ISPE C&Q Guidelines with knowledge of Kneat e-Validation Software preferred.
- Prior experience with Analytical Instrumentation Qualification and Controlled Temperature Unit qualification is required.
- Lab Equipment experience needed.
- The ability to work independently with minimal direction while writing and communicating clearly is crucial.
Travel:
- Local personnel preferred.
Its more than just a job
At Compli we are about innovative and intelligent people who want to solve problems. Were known for our technical excellence but we bring so much more to the table. We strive to create remarkable solutions for a higher quality of life. And we are changing the industry by integrating the design and construction process with use of new technology.
At Compli we are an Equal Employment Opportunity Employer promoting diversity in our workforce by including all individuals regardless of age race religion color sex national origin marital status genetic information sexual orientation gender identity gender expression disability veteran status pregnancy status or any other status protected by law.
Required Experience:
IC
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