CSV Engineer
$38/hr
Leading biotechnology, pharmaceutical, and medical device companies collaborate with our client to offer creative and effective solutions that support their GxP organizations' launch, growth, and sustainability.
Personnel are expected to live up to our core values at all times and exhibit a high level of integrity and personal responsibility, especially when interacting with our valued clients. The following is a short list of the typical responsibilities and deliverables of any given project. The level of knowledge expected will be commensurate with level of incoming experience.
Qualifications:
* A Bachelor's degree in science, engineering, or a related field.
* Three to five years of experience in a controlled production setting in the pharmaceutical, medical device, or biotechnology sectors.
* Working knowledge of quality systems (Change Control, Non-Conformances, Requalification, etc.), validation (IQ, OQ, PQ, PV, CV, CSV, etc.), and process excellence methodologies (Six-Sigma, Lean, etc.).
* Great communication skills, both oral and written; exceptional technical writing abilities.
* The capacity to collaborate with others and function well in a team setting.
* Capacity to multitask and operate efficiently in a fast-paced setting.
* Extensive practical understanding of cGMP and FDA rules as well as documentation standards.
If you are interested in learning more about this role, don't hesitate to contact me.
Email: michael.phillips@epmscientific.com
Work Number: 310-759-0670
