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Document Control Associate

Actalent

Posted Wednesday, July 5, 2023

Posting ID: JP-003884079

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Philadelphia, PA
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Description:

• Prepare routine run templates from developed method and transfer assay • Prepare routine run templates for existing assay we currently offer • Prepare final report template for the specific assays • Write equipment use and cleaning procedures • Prepare a generic development template • Help create database for tracking purposes, inventory management • Help create result template • Knowledge of Microsoft Office, grammar, and formatting • Science background • Work with other members of AD team for documentation approval • Assistance Senior Analytical manager

Skills:

Document control, protocol writing, Technical writing, SOP, Assay, ELISA, PCR

Top Skills Details:

Document control,protocol writing,Technical writing,SOP,Assay,ELISA,PCR

Additional Skills & Qualifications:

BS in life science (biology, biochemistry, chemistry, etc.) 1+ yrs of experience in qc, research & development or manufacturing Technical writing experience (SOP writing, protocol writing, template writing, verifications, equipment protocols) Experience with Microsoft word and Excel

Experience Level:

Intermediate Level

Contact Information

Recruiter: Anthony Caione

Phone: (610) 232-5864

Email: acaione@actalentservices.com

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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