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PROCESSING APPLICATION
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Job Requirements of Process Development Associate:
-
Employment Type:
Contractor
-
Location:
San Diego, CA (Onsite)
Do you meet the requirements for this job?
Process Development Associate
Careers Integrated Resources Inc
San Diego, CA (Onsite)
Contractor
$29.50/hr
First Shift
Monday through Friday
Hours: 6:30am to 3:00pm
100% on-site
Job Summary
Primarily responsible for commercial manufacturing. Also responsible for the 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.
Keeps accurate records and documentation.
Completes laboratory work and associated paperwork by assigned completion dates.
Produces notebook materials per written instructions.
Develops manufacturing processes for transfer to Manufacturing.
Assists with execution of process validation of new and existing manufacturing processes.
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).
Other (please specify):
Qualifications
Education
Bachelor s degree (sciences)
Experience
1+ years experience preferred
Skills
Basic knowledge of QMS (Quality Management System)/GMP requirements
Must follow all applicable FDA regulations and ISO requirements.
First Shift
Monday through Friday
Hours: 6:30am to 3:00pm
100% on-site
Job Summary
Primarily responsible for commercial manufacturing. Also responsible for the 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.
Keeps accurate records and documentation.
Completes laboratory work and associated paperwork by assigned completion dates.
Produces notebook materials per written instructions.
Develops manufacturing processes for transfer to Manufacturing.
Assists with execution of process validation of new and existing manufacturing processes.
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).
Other (please specify):
Qualifications
Education
Bachelor s degree (sciences)
Experience
1+ years experience preferred
Skills
Basic knowledge of QMS (Quality Management System)/GMP requirements
Must follow all applicable FDA regulations and ISO requirements.
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