Process Development Scientist-Vision Inspection --Csv

*Are there specific educational/software requirements needed?*

Doctorate OR
-Master + 2 years of Scientific experience OR
-Bachelors in Sciences + 4 years of Scientific experience.

Experience in Regulated Industry

*What attributes (i.e. - preferred qualifications) would make this candidate stand out?* *Proficient in creating and executing validation and qualification documentation*

* Provide support to vision inspection qualification and characterizations
* Requires excellent communication skills with suppliers and other sites
* A Plus: Knowledge in automated vision inspection systems
* A Plus: Knowledgeable in CSV. Support CQV documentation and execution
* Other Considerations:
* Willing to work during regular business hours, night shift, and/or weekends, as needed to meet the projects' schedule.

*SUMMARY*
To conceive, design, implement and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under general guidance of supervisor.

*FUNCTIONS*
-Conceives and designs, executes or evaluates, and interprets experimental strategies.
-Provides input to new processes to generate robust and reliable data.
-Ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
-Designs, monitors or conducts experimental strategies with general guidance from supervisor.
-Provides data analysis and interpretation, and assesses impact of the data on the project.
-Keeps current in field of scientific expertise and areas relevant to their function.
-Monitors field of expertise, including literature and technology development, and communicates relevant observations.
-May introduce advanced scientific methods.
-Develops and implements new and novel protocols to address specific issues.
-May represent the department on project teams under supervision of a senior scientific staff member.
-May initiate productive collaborations within and outside of the department or company.
-Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies.
-Independently authors scientific reports, summary documents, complex regulatory documents, invention disclosure submissions and/or patents.
-Participates in external scientific community.
-May assume lead role in department-wide support efforts such as safety, recruiting and committees.
-May develop supervisory and mentoring skills.
-Develops and follows timelines for completing project team work.

*EDUCATION*
-Doctorate OR
-Master's + 2 years of Scientific experience OR
-Bachelors + 4 years of Scientific experience.

*COMPETENCIES/SKILLS*

-Advanced scientific analysis and troubleshooting skills.Advanced laboratory work skills.
-Ability to motivate and/or supervise the activities of others.
-Must be well organized, have multi-task project experience, and be able to communicate and work well with other departments.
-Must have demonstrated skills and competencies in the following areas: Verbal communication, Written communication including technical writing skills, negotiation and conflict resolution.Analytical problem solvingProject management.
-Ability to be flexible and manage change.
-Computer literacy (Windows environment: Word, Excel, Power Point).
-Skills requiring the application of scientific theory.
-Creative skills in the design and performance of scientific experiments and interpretation of results.
-Strong knowledge of cGMP

-Fully bilingual (English/Spanish).

Pay: $***** - $***** per hour

Benefits:
* Paid time off

Work Location: In person