Source One is a consulting services company and we're currently looking for the following individual to work as a consultant with our direct client, a medical device and ophthalmic product manufacturer in Johns Creek, GA. This role will require you to be onsite.
Please Note: This position is W2 hourly. Will not respond to C2C, 3rd party agencies, or candidates not authorized to work in the United States.
Title: GxP Laboratory Technician
Location: Johns Creek, GA (On-Site)
Contract Duration: 6 months, with likely extension
w2 Hourly Rate: $23.00 - $25.00
Description:
The GxP Lab Technician will be responsible for executing SOPs and protocols for large batch preparation of formulations and intermediate solutions. This role includes the handwritten completion of batch paperwork and the use of computer software packages, such as MS Office for the collection and reporting of batch preparation. The role requires strong teamwork skills and the ability to stay on a routine but be flexible if the priority shifts. During quieter periods, the Technician will contribute to improving the efficiency and effectiveness of the GxP lab operations or can be a helping hand for the research group.
Essential Functions & Accountabilities:
Perform daily functions in batch preparation of formulations and intermediate solutions.
Perform manufacturing batch record review.
Provide basic maintenance to GxP equipment.
Complete all necessary inventories and documentation for batch preparation.
Help with chemical inventory for materials.
Complete all documentation following the preparation of the batches throughout the process.
High level of communication between the GxP lab employees and the research, development, and Pilot teams.
Assist with any additional projects assigned by Cross functional teams.
Foster a culture of inclusion, efficiency, and compliance within the GxP lab and research group.
Qualifications
Knowledge, Skills, and Abilities:
Working knowledge in MS Office Suite, including Word and Excel.
Must be detail oriented and have excellent hand-eye coordination.
Working knowledge of cGMP requirements.
Must be willing to "Lead by Example".
Effective teamwork and communication skills.
Ability to meet strict deadlines and work under pressure.
Flexibility in accepting work assignments as required by the needs of the business.
Work Environment:
Working with a large amount of chemicals.
The individual will be required to work in a laboratory environment.
The role will require the individual to come into contact with hazardous materials or working environments. The individual will be required to wear/use the appropriate personal protective equipment (PPE) for the task in hand outlined in SOP's including items such as lab coat, eye protection and gloves. The job requires the handling of materials that come under COSHH guidelines.
Experience:
2+ years of cGMP experience is required.
2+ years of laboratory experience.
Medical Device or related regulatory industry experience is preferred.
Education:
High School Diploma/GED is required.
Associate's or Bachelor's degree in Science discipline is encouraged.