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Manager Solar Cell Manufacturing Jobs in Florida

SunVena Solar

Chief Revenue Officer

Sanford, FL · On-site

Job Type Full-time Description SunVena Solar is seeking a visionary, results-driven Chief Revenue ... Oversee forecasting, pipeline management, revenue reporting, and business intelligence. * Utilize ...

Energeiaworks

O&M Site Manager

Sebring, FL · On-site

We (a globally active solar and BESS EPC/O&M) seek an experienced Operations and Maintenance Site ... Experience working with clients, EPC contractors, utilities, and original equipment manufacturers.

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All JobsSolar Cell Manufacturing JobsManager Solar Cell Manufacturing JobsManager Solar Cell Manufacturing Jobs in Florida

Manager Solar Cell Manufacturing information

Is working in solar cell manufacturing a good career path?

Working as a manager in solar cell manufacturing involves overseeing production processes, quality control, and team management in a growing renewable energy industry. It requires technical knowledge of solar technology, manufacturing equipment, and leadership skills, with opportunities for career advancement as the industry expands. The field offers stable employment prospects due to increasing demand for solar energy solutions.

What is the difference between Manager Solar Cell Manufacturing vs Production Supervisor Solar Cell Manufacturing?

AspectManager Solar Cell ManufacturingProduction Supervisor Solar Cell Manufacturing
ResponsibilitiesOversees entire manufacturing processes, manages teams, develops strategies, and ensures quality standards.Supervises daily production activities, manages operators, and ensures production targets are met.
Required CredentialsBachelor's degree in engineering or related field, experience in solar manufacturing, leadership skills.High school diploma or technical training, experience in manufacturing, supervisory skills.
Work EnvironmentOffice and manufacturing plant, strategic planning, team management.Factory floor, direct supervision of production line staff.

The main difference between a Manager Solar Cell Manufacturing and a Production Supervisor Solar Cell Manufacturing lies in scope and responsibilities. Managers focus on strategic oversight and team leadership, while supervisors handle daily operations and direct supervision of production staff. Both roles require relevant experience, but managers typically have higher credentials and broader responsibilities.

What are popular job titles related to Manager Solar Cell Manufacturing jobs in Florida? For Manager Solar Cell Manufacturing jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Manager Solar Cell Manufacturing jobs in Florida look for? The top searched job categories for Manager Solar Cell Manufacturing jobs in Florida are:
What cities in Florida are hiring for Manager Solar Cell Manufacturing jobs? Cities in Florida with the most Manager Solar Cell Manufacturing job openings:
Manager Solar Cell Manufacturing jobs near you
Infographic showing various Manager Solar Cell Manufacturing job openings in Florida as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Contingent Worker, Manufacturing Associate I

Kincell Bio, LLC

Gainesville, FL • On-site

Full-time

Posted 5 days ago

Job description

Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance.
For more information, please visit our website at www.kincellbio.com.
As a Contingent Manufacturing Associate I, you will be operating automatic and manual cell and gene therapy equipment with a variety of complexities in CAR-T, CAR-M, or CAR-NK processes in accordance with standard operating procedures and policies. You will perform quality control analyses as required to complete in-process batches and identify variations. You will be trained in handling hazardous materials and emergency procedures since you will be handling leukapheresis cellular materials.
As part of manufacturing operations, you will be relied on to have a good understanding of procedures, techniques, tools, materials, and equipment. Your work and decision-making will be team-based and will focus on the prioritization of workflows centered on the process and available resources. You will follow standard operating procedures to complete tasks which may vary in scope, complexity, and timing.
Patients need individuals who take pride in their work and look for successful outcomes. You will be operating cell and gene therapy process equipment of varying complexity with different processes in accordance with standard operating procedures.
Essential Duties and Responsibilities
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.
  • Working knowledge of Word and Excel
  • Demonstrate Aseptic Qualification
  • Maintaining personal responsibility with Personal Protective Equipment (PPE)
  • Be a collaborator when a team develops Standard Operating Procedures or Manufacturing Batch Records
  • Conduct Quality Control analyses in a Manufacturing setting
  • Able to learn how to handle materials and bring them into a Manufacturing cleanroom.
  • Clean Equipment and Manufacturing Suite / Rooms
  • Be accountable for your own Safety. Also, be accountable for maintaining your own training requirements.
  • Collaborate with the Investigation team when investigating Quality and Safety Incidents
  • Author Minor Quality / Safety Incident Investigation (Deviations) and Minor CAPAs
  • Develop a knowledge of GXP procedures (GMP, GLP, GCP, GDP, etc.)
  • Must help with cleaning with Equipment and Manufacturing process rooms.
  • Contribute to the team's success by sharing knowledge.
  • Review of Applicable Logbooks
  • Support and Conduct Enrollment of Materials / Bill of Materials.
  • Create Purchase Requests / Procuring Items as needed.
  • Escort Vendors / Visitors into the cleanroom
  • Conduct post-campaign line or area clearance

Qualifications
The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.
Required:
  • Bachelor of Science degree in Natural Sciences (i.e., Biology, Chemistry, etc.) or Engineering (Chemical, Biomedical, etc.) and 0-2 years of manufacturing experience required or equivalent combination of education and experience.
  • Must be able to work 40 hours per week.
  • Ability to work independently and stay on task in a fast-paced environment without direct supervision.
  • Must be able to recognize when processes, procedures, equipment, products, materials, etc. are out of specification.
  • Hiring will be contingent on passing a visual acuity test. Proof of passing a visual acuity test within the past year will be accepted
  • Effective oral communication.
  • Ability to work well with others in a collaborative team environment.
  • Regular and reliable performance and attendance are required.
  • Able to work in a rapidly changing climate - reacts well to change.
  • Must be able to perform mathematical calculations such as converting milliliters to liters or grams to kilograms. Understands significant figures and rounding.
  • Must be able to lift bags and/or containers of media.
  • Must be able to stand and/or sit for extended periods.
  • Manage your own time and professional development. Be accountable for your own results and prioritized workflows.

Preferred:
  • Have knowledge of cell and gene therapy processing, the metric system, and scales.
  • cGMP clean room experience.

Physical Requirements
  • Vision Acuity Testing
  • Use of a Face Mask

Travel Requirements
  • None

Location
  • This is a site-based temporary position located in Gainesville, FL, and will require some non-standard working hours, including scheduled early mornings, late evenings, and/or weekends.

#LI-Onsite
Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.

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