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Goodwin Jobs in Florida (NOW HIRING)

Description: Scope of Function: Manages, supervises, and oversees the Quality Control Analytical team with solid technical and scientific experience in the pharmaceutical industry to ensure adherence ...

Associate Attorney

Mary Esther, FL · On-site

$95K - $120K/yr

Associate Attorney Location: Mary Esther, Florida We are seeking a highly motivated, detail-oriented Associate Attorney to join our growing team in Mary Esther, Florida. This is an excellent ...

Associate Attorney

Mary Esther, FL · On-site

$95K - $120K/yr

Associate Attorney Location: Mary Esther, Florida We are seeking a highly motivated, detail-oriented Associate Attorney to join our growing team in Mary Esther, Florida. This is an excellent ...

Benefits: * 401(k) matching * Bonus based on performance * Competitive salary * Dental insurance * Opportunity for advancement * Vision insurance * Health insurance * Paid time off Associate Attorney ...

Goodwin information

See Florida salary details

$12

$18

$31

How much do goodwin jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for goodwin in Florida is $18.48, according to ZipRecruiter salary data. Most workers in this role earn between $14.18 and $20.10 per hour, depending on experience, location, and employer.

What is a Goodwin?

Goodwin is not a standard job title in most industries. It is more commonly recognized as a surname or as the name of organizations, such as Goodwin Procter LLP, a major international law firm. If you are referring to a role within Goodwin Procter or another company named Goodwin, it is important to specify the exact position (e.g., attorney, paralegal, administrative assistant) to get relevant information. For careers at Goodwin Procter LLP, the company offers various roles in legal and business services. If you need details about job opportunities at Goodwin Procter, their official careers page provides comprehensive information.

What are the key skills and qualifications needed to thrive as a Goodwin?

I'm sorry, but 'Goodwin' is not recognized as a real-world professional occupation, so I cannot provide an answer.

What are some common challenges faced by associates at a law firm like Goodwin, and how can they navigate them?

Associates at a firm such as Goodwin often encounter challenges such as managing competing deadlines, balancing client expectations, and adapting to a fast-paced work environment. Effective time management and proactive communication with both senior attorneys and clients are essential strategies for success. Additionally, associates are encouraged to seek mentorship and take advantage of professional development programs offered by the firm, which can help them build confidence and advance in their legal careers.

What is the difference between Goodwin vs Paralegal?

AspectGoodwinParalegal
Required CredentialsJuris Doctor (JD), law degree, or equivalentAssociate's degree or paralegal certificate
Work EnvironmentLaw firms, corporate legal departments, government agenciesLaw firms, legal departments, courts
Industry UsageLegal services, consultingLegal support roles
Common Search/ComparisonLegal career paths, law firm rolesLegal support, legal assistant roles

Goodwin is a law firm or legal professional with a JD and practicing credentials, while a paralegal provides legal support without being licensed to practice law. Both work in legal environments, but Goodwin typically refers to licensed attorneys, whereas paralegals assist under attorney supervision.

Infographic showing various Goodwin job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, and 17% Part Time. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $38,447 per year, or $18.5 per hour.

Bioprocess Specialist, Upstream

Plantation, FL • On-site

Full-time

Re-posted 5 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.