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Hourly Upstream Manufacturing Associate Jobs in Florida

Trilogy Medwaste

PLANT ASSOCIATE

Tampa, FL · On-site

$16/hr

Hourly Rate: $16.00 PRIMARY JOB DUTIES/RESPONSIBILITIES * Ensure all equipment is working properly ... Manufacturing experience preferred * Forklift experience preferred * 2-4 years of lead supervisor ...

Trilogy Medwaste

PLANT ASSOCIATE

Tampa, FL · On-site

$16/hr

Hourly Rate: $16.00 PRIMARY JOB DUTIES/RESPONSIBILITIES * Ensure all equipment is working properly ... Manufacturing experience preferred * Forklift experience preferred * 2-4 years of lead supervisor ...

Pilgrim's

Chicken Plant Associate

Live Oak, FL

$15.35/hr

Base hourly salary rate of $15.35 with a $2.00 shift differential for 2nd and 3rd shift. * Perfect attendance incentive of $3.00 extra per hour, $4.00 for 2nd and 3rd shift. * Career Development: Our ...

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Hourly Upstream Manufacturing Associate information

What is the difference between Hourly Upstream Manufacturing Associate vs Upstream Manufacturing Technician?

AspectHourly Upstream Manufacturing AssociateUpstream Manufacturing Technician
CredentialsHigh school diploma or equivalent; GMP training often requiredHigh school diploma; GMP and technical training
Work EnvironmentManufacturing floor, repetitive tasks, team-basedManufacturing floor, technical troubleshooting, equipment operation
Employer & Industry UsageBiotech and pharmaceutical manufacturingBiotech and pharmaceutical manufacturing
Common Search & ComparisonYesYes

The main difference between an Hourly Upstream Manufacturing Associate and an Upstream Manufacturing Technician lies in their roles and responsibilities. Associates typically perform routine manufacturing tasks under supervision, focusing on production line activities. Technicians often have more technical training, handle troubleshooting, and maintain equipment. Both roles are essential in biotech manufacturing, with similar credentials and work environments, but technicians usually require additional technical skills.

What are popular job titles related to Hourly Upstream Manufacturing Associate jobs in Florida? For Hourly Upstream Manufacturing Associate jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Hourly Upstream Manufacturing Associate jobs in Florida look for? The top searched job categories for Hourly Upstream Manufacturing Associate jobs in Florida are:
What cities in Florida are hiring for Hourly Upstream Manufacturing Associate jobs? Cities in Florida with the most Hourly Upstream Manufacturing Associate job openings:
Hourly Upstream Manufacturing Associate jobs near you

Bioprocess Specialist, Upstream

Goodwin Biotechnology Inc

Fort Lauderdale, FL • On-site

Full-time

Re-posted 13 days ago

Job description

Description:

Scope of Function:

The Bioprocess Specialist position reports to the Upstream Manufacturing, Manager. Prior experience in GMP manufacturing, operation of GMP process equipment and aseptic technique are prerequisites. This role is responsible for supporting the overall Upstream GMP process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase 1/11/111 and commercial GMP manufacturing.


Specific Duties:

• Operates pharmaceutical manufacturing equipment such as: incubators, wave reactors, single-use and stainless-steel bioreactors, single use mixers, depth filtration skids, TFF skids, chromatography skids and in process testing equipment.

• Executes all Upstream Clinical Manufacturing and Development operations, including but not limited to work functions in cell culture, cell banking, media optimization, seed train preparation, bioreactor operations, harvest/clarification, and technology transfer to manufacturing.

• Demonstrates, understands, and adheres to Goodwin Biotechnology policies, GMP standards and safety procedures.

• Performs and monitors critical processes, execute manufacturing batch records (MBR) for specific projects to manufacture cell-derived biopharmaceuticals in compliance with cGMP guidelines and regulation.

• Performs and monitors critical processes, execute manufacturing batch records (MBR) for specific projects to manufacture cell-derived biopharmaceuticals in compliance with cGMP guidelines and regulations.

• Supports the development of batch records, SOP’s and protocols as required.

• Supports other manufacturing processes teams and other GBI groups as necessary to achieve manufacturing goals.


This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice.

Requirements:

Education and Experience Required:

• BS degree in Science or Engineering.

• Associate degree in science or engineering, or related field and minimum of 3 years of experience with biologic production processes under GMP compliance. Downstream experience preferred.

• Minimum of High School Diploma or equivalent and 3 years of experience with biologic production processes under GMP compliance. Upstream experience preferred.

• Excellent documentation skills including comprehension and review & establishing batch production records.