Process Development Associate

7 days ago


San Diego, California, United States GTT, LLC Full time
Process Development Associate
Contract Duration 6 Months
Pay rate up to $28.50/hr

Job Summary

Process Development Associate will be responsible for commercial manufacturing and for the creation and transfer of manufacturing processes from R&D to Manufacturing and continuous improvement of existing processes.

Essential Duties and Responsibilities

The incumbent may be asked to perform other function-related activities in addition to the below-mentioned responsibilities as reasonably required by business needs.

Maintains the Pilot Plant laboratory under cGMP conditions.
Produces development, pilot, and production materials per written instructions.
Completes ERP transactions.
Stocks and maintains the laboratory supplies.
Process Development Associate will keep accurate records and documentation.
Completes laboratory work and associated paperwork by assigned completion dates.
Produces notebook materials per written instructions.
Troubleshoots manufacturing process problems.
Develop manufacturing processes for transfer to Manufacturing.
Process Development Associate will assist with the execution of process validation of new and existing manufacturing processes.
Trains others on manufacturing tasks.
Improves manufacturing processes.
Completes cycle counts.
Washes lab ware.

Physical Demands

The physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

Sit; use hands to finger, handle, or feel objects, tools, or controls.
Stand; walk; reach with hands and arms; and stoop, kneel, crouch, or crawl.
Lifting/moving and carrying products weighing up to 40 pounds.
Exposure to moving mechanical parts, vibration, and/or moderate noise levels.
Exposure to hazardous chemicals or other materials.
Safety Shoes with Impact and Compression Protection Must be worn (will be provided).
Exposure to blood (serum).

Qualifications
Education
Bachelor's degree

Experience
1+ years' experience preferred

Skills
Basic knowledge of QSM/GMP requirements
Must follow all applicable FDA regulations and ISO requirements.

Note:
First Shift
Monday through Friday
Hours: 6:30 am to 3:00 pm
100% on-site

Benefits:
Medical, Vision, and Dental Insurance Plans
401k Retirement Fund

About The Company:
Our client is an innovative medical technology company whose purpose is to enable healthier lives everywhere, every day.

While they develop groundbreaking products and services that benefit everyone, they are especially passionate about those that advance women's health and well-being.

This allows us to be a company that prospers, grows, and empowers women to experience healthier lives.

What powers their growth across Breast & Skeletal Health, Diagnostic Solutions, and GYN Surgical Solutions is also what differentiates them: the exceptional and clinically proven ability of their products to detect, diagnose and treat illnesses and other health conditions earlier and better.

None of this would be possible without the talent, skills, and aspirations of their employees.

Their proficiency and commitment to develop and share more robust, science-based certainty drives the company's increasingly global presence, as well as a pipeline that responds to the unmet health and wellness needs of women, families, and communities.

#gttnonit
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