The Staffing Resource Group, Inc
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Manufacturing Associate II
Posted: 05/30/2025
2025-05-30
2025-07-14
Employment Type:
Contract
Division: Life Sciences
Job Number: JN -052025-20477
State: Florida
Job Description
Manufacturing Associate II
Title: Manufacturing Associate I
Location: Gainesville, FL
Industry: Pharmaceutical
Schedule: Monday - Friday 8am - 5pm
Salary: $28/hr.
Employment: Contract to Hire
As a Manufacturing Associate II, you will be operating automatic and manual cell therapy equipment with a variety of complexity 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. You will contribute to the team s success by sharing knowledge.
Patients need individuals like you who take pride in their work and look for successful outcomes. You will be operating cell therapy process equipment of varying complexity with different processes in accordance with standard operating procedures.
Essential Duties and Responsibilities
Qualifications
Required:
Preferred:
EOE/ADA
IND123
Title: Manufacturing Associate I
Location: Gainesville, FL
Industry: Pharmaceutical
Schedule: Monday - Friday 8am - 5pm
Salary: $28/hr.
Employment: Contract to Hire
As a Manufacturing Associate II, you will be operating automatic and manual cell therapy equipment with a variety of complexity 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. You will contribute to the team s success by sharing knowledge.
Patients need individuals like you who take pride in their work and look for successful outcomes. You will be operating cell therapy process equipment of varying complexity with different processes in accordance with standard operating procedures.
Essential Duties and Responsibilities
- Proficient in Microsoft Word, Excel, PowerPoint, and other applications.
- Knowledge of aseptic processing/cell culture/cell therapy manufacturing in a cGMP setting.
- Maintaining personal responsibility with Personal Protective Equipment (PPE)
- Collaborate with the team to produce Standard Operating Procedures (SOP) or Manufacturing Batch Records.
- Ability to perform Quality Control evaluations in a manufacturing setting.
- Demonstrate the ability of material flow into the manufacturing cleanroom, including disinfection.
- Be responsible for your own safety. Also, be accountable for meeting your own training responsibilities.
- Collaborate with the Investigation team to investigate Quality and Safety incidents.
- Develop a knowledge of GXP procedures (GMP, GLP, GCP, GDP, etc.)
- Must have the ability to clean equipment and manufacture cleanrooms.
- Contribute to the team s success by sharing knowledge.
Qualifications
Required:
- High school diploma or equivalent and at least 2+ years of relevant education and experience.
- Must be able to work 40 hours per week and on weekends.
- 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.
- Effective oral communication.
- Ability to work well with others in a collaborative team environment.
- Hiring will be contingent on passing a visual acuity test. Proof of passing a visual acuity test within the past year will be accepted.
- 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.
- Understand significant figures and rounding.
- Must be able to lift to 40+lbs.
- 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:
- B.S degree in Natural Sciences (Biology, Chemistry, etc.) or Engineering (Chemical, Biomedical, etc.) and 2+ years of manufacturing experience.
- cGMP clean room experience.
- Have knowledge of cell and gene therapy processing, the metric system, and scales.
- Knowledge to initiate and drive to completion deviations, change controls, and CAPAs for appropriateness, completeness and to meet internal procedures and regulatory expectations.
- An equivalent combination of education and experience may be considered.
EOE/ADA
IND123
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