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Job Description

Seeking several multi discipline technical services contract resources to support cGMP pharmaceutical processes and projects. Currently have a need for 4-6 Validation Engineers to work on contract to assist with technical services support.

Will be responsible for the following:

Provide technical support and guidance to manufacturing personnel during the execution of process validation runs
Lead execution, data interpretation and validation report writing.
Compilation for validation reports , analyzing results and preparing summaries of the data to support test and protocol requirements.
Performs extensive technical reviews and interprets data for accuracy of equipment/process performance for completed validations/revalidations
Work closely with all departments and consultants for timely execution of validation tasks.
Provides technical support to address deviations
Technical troubleshooting during validation runs.
Positions are available to interview and start immediately

If you have expertise in any of these areas and are considering 3-9 month contract assignments (upto 100% travel) please send your resume and salary requirements to the above contact information.

DESIRED SUBJECT MATTER EXPERTISE – Any of the following

Technical Services Support, Process Validation, Change Control, SOPs, Batch Records, Technical Writing, Final Reports, IQ, OQ, PQ, Trackwise.

Desired Skills & Experience

Bachelor Degree and three to five years experience in a cGMP manufacturing environment.
Excellent organizational skills.
Detail oriented.
Ability to multi-task.
Knowledge of MS Office.
Professional verbal, written and presentation skills.