Chemical Additive Technician

NEVEON Executive Committee; Monroe (NC); On-site; USD 42,000 - 64,000; Full time

Job summary

Greiner Bio-One in Monroe, NC is seeking a QA/QC support role to prepare chemical additives for production and perform QC testing in a regulated laboratory.

You will clean and sanitize lab areas, release solutions to production after testing and SAP review, and assist with inventory and SAP transactions. Training for QC staff is provided.

Qualifications

• Must have basic math, writing and communication skills.
• High school diploma or equivalent; degree preferred with relevant experience.
• Experience in Medical Device, Pharmaceutical, or regulated industries is a plus.
• Proficiency in standard office software and lab instrumentation.

Responsibilities

• Prepare chemical additives for production.
• Complete QC testing for prepared chemical additives.
• Perform IGI and release chemicals for use.
• Clean and sanitize laboratory and QC areas.
• Release solutions to production after testing and SAP review.
• Perform SAP transactions to hold product.
• Restrict non-conforming product per QMI documents.
• Conduct system suitability tests as needed.
• Maintain routine inventory of lab materials and SAP records.
• Train QC inspectors on procedures and equipment.
• Document results and activities accurately per guidelines.
• Other duties as assigned.

Skills

Math proficiency

Communication skills

Writing skills

Education

High school education or equivalent

Degree preferred

Tools

Word

Excel

Outlook

Instrument software

Job description

We are not offering you a job, but rather we are offering you a workplace that feels like home at Greiner Bio-One.

Location: Monroe, US, 28110

Employment Type: Permanent

Responsibilities

• Prepare chemical additives for production
• Complete QC testing for prepared chemical additives
• Perform IGI and release chemicals for use
• Cleaning and sanitation of laboratory / QC areas
• Release of solution to production (testing, review, and SAP)
• Perform SAP transactions to hold product
• Restriction of non-conformity product according to appropriate QMI documents
• Perform various system suitability as necessary
• Perform routine inventory (e.g., raw materials, prepared additive solutions, lab supplies, etc.) for lab, assist in ordering/requesting materials and supplies, and maintain inventory in SAP and cycle count
• Training of QC Inspectors as designated
• Accurate, concurrent, and complete documentation of test results and activities according to internal and regulatory guidelines
• Training of new or existing QC employees regarding QC procedures and use of equipment
• Other duties as assigned

Job Requirements

• Must have sufficient math, communication, and writing skills
• High school education or equivalent; degree preferred with at least 1 year of relevant work experience
• Experience in Medical Device, Pharmaceutical, and/or regulated industry is preferred
• Basic understanding of computer systems (Word, Excel, Outlook, and instrument dedicated)

We provide equal opportunities for everyone and see diversity as our strength. Therefore, we welcome all applicants – regardless of identifying characteristics such as gender, age, background, social status, veteran status, sexual orientation, religion, or mental and physical abilities. We have additionally set the goal of empowering women and increasing female leader representation. We foster an inclusive work environment and encourage all individuals to apply.