PhytogenX is excited to announce that we are to our adding a QC Tech to our 2nd Shift Quality Control Lab team! This is a great opportunity to grow with our company and the Quality Team! New Grads are welcome to apply!

If you are interested in starting your career, and growing in the cosmetic manufacturing industry, then this role is perfect for you. Start your career with us today!

Job Responsibilities/Duties:

The 2nd Shift QC Technician ensures the quality of products received (raw materials or bulk) and manufactured in our company. Keeps up with the regulations that govern our industry, comply with specifications through testing and perform final material disposition. Adhere to and ensure Good Manufacturing Practices are followed at PhytogenX, Inc. so we can remain productive, profitable and in compliance by following and monitoring programs that ensure continuous quality.

Essential Functions:

• Receive, inspect and test raw materials and ancillary supplies as per protocols, record test data and confirm product meets specifications.
• QC inspection of bulk stability sample to conform to the appropriate standards of quality and purity. Perform laboratory QC testing, responsibility includes, pH, viscosity, specific gravity, etc.
• Apply knowledge of in-process flow from raw materials to bulk manufacturing to packaging and perform QC functions as needed.
• Perform laboratory QC testing related service necessary including but not limit to, the reagent preparation, laboratory maintenance, equipment calibration.
• Maintain a database of MSDS documents for all products handled
• Perform sampling and testing on facility water system to ensure compliance within specification
• Assist in monitoring and maintenance of the facility water system per SOPs.
• Organize the retention of production bulk samples and final sample disposition.
• Perform housekeeping tasks to ensure that the laboratory is inspection readiness.
• Work with interdepartmental and quality team to troubleshoot quality issues.
• Maintains a good training record to adhere to GMP compliance per 21 CFR parts 210 & 211.
• Perform other laboratory duties as assigned.

Requirements to Perform Job Responsibilities/Duties:

• Associate’s or Bachelor’s degree preferred but, not required
• Knowledge and or Understanding of GMP requirements
• Computer Skills/MS Office Proficiency
• Ability to work as a team member
• Previous experience in manufacturing environment is a plus
• Must be capable of analytical thinking
• Familiarity with Microsoft software programs
• Strong communication and interpersonal skills
• Light to medium physical demands, mostly office environment (rare need to lift 50 lbs.)

Job Type: Full-time

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Referral program
• Vision insurance

Schedule:

• 8 hour shift
• Evening shift

Application Question(s):

• Salary Requirement?

Education:

• High school or equivalent (Preferred)

Experience:

• Laboratory Experience: 1 year (Preferred)
• Quality control: 1 year (Preferred)

Work Location: In person