Manufacturing Technology Representative

BECOME A COVID CHAMPION -- Our Client is partnering with several Pharmaceutical companies to help distribute the much-anticipated COVID-19 vaccines to help put an end to this ongoing pandemic. To provide this life-saving medication, as well as the many other life-saving medication manufactured at the facility, to patients, we will be conducting mandatory COVID-19 testing for all employees who are working onsite. This will ensure the health and safety of our employees who are at the forefront of putting our Patients First.

• Title: Manufacturing Technology Representative
• Location: Bloomington, IN
• Industry: Pharmaceutical
• Hours: Weekend SHIFT Fri thru Sun 6:00am - 6:00pm
• Salary: $24.87 (Paid Weekly - Benefits Available)
• Employment Type: 6 Month Contract

Environment: This client manufactures thousands of pharmaceutical, biologic, consumer health and beauty products utilizing superior and innovative drug delivery technologies to improve their value to patients and consumers. Our customer believes in a Patient First culture putting patients at the center of their work to ensure the safety, reliable supply and optimal performance of our products.

Job Scope:
Entry-level position with appropriate licenses/training certifications
Has basic skills in an analytical or scientific method or operational process
Works within clearly defined standard operating procedures and/or scientific methods
and adheres to quality guidelines

Job Characteristics:
Scale up and transfer processes into full-scale manufacturing based on data provided by Process Development or by client, select appropriate equipment and single-use components to perform process at large scale, develop technical documentation (e.g., Process Flow Diagrams, Process Descriptions) to describe operation of the process at large scale, meet with Process Development or client technical team to understand bench and pilot-scale data, develop in-process test strategy for manufacturing process at large scale, write or direct the writing of GMP manufacturing documentation, including Process Batch Records, Buffer and Media Formulation records, Sample Plans, Bills of Materials

Must Have Requirements:
High School/GED, Technical Certificate or higher preferred,
0-2 years of experience,
GMP experience preferred.
Must be able to read and understand English-written job instructions and safety requirements.
Top 3-5 requirements: Skilled in Microsoft Office, focus on document authoring via Word

EOE/ADA