Quality Control (QC) Chemist Weekend AM Shift

brightinnovationlabs; Beloit (OH); On-site; USD 40,000 - 50,000; Full time

Job summary

Bright Innovation Labs is seeking a Quality Control Analyst to support production through chemical and physical analysis of concentrates and finished products. You will test raw materials and in-process batches, calibrate instruments, and develop analytical procedures while ensuring cGMP and safety standards are followed.

You will work weekends with early shifts, requiring flexibility and strong attention to detail. English proficiency is essential with additional Spanish a plus.

Qualifications

• Must have strong verbal and writing skills.
• Experience using Microsoft Word, Excel, and Outlook.
• Ability to multi-task.
• Must demonstrate strong attention to detail.
• Flexibility with schedule including shift work.
• Overtime may be required with very little notice.

Responsibilities

• Test and approve raw materials.
• Test and approve finished and in-process batches; make adjustments as necessary.
• Analyze and approve line samples.
• Assist in production problems – troubleshoot.
• Maintain and calibrate gauges and instruments.
• Prepare and standardize reagents.
• Develop and validate analytical procedures.
• Provide training to personnel.
• Perform stability testing on OTC production.
• Promote compliance with cGMP and safety/environmental regulations.

Skills

Verbal communication

Written communication

English language

MS Office

Multi-tasking

Attention to detail

Shift work

Overtime

Tools

Microsoft Word

Excel

Outlook

Job description

SUMMARY / OBJECTIVE

To control and assure quality and provide technical support for production by means of chemical and physical analysis of production concentrates and finished products. Maintain quality standards by adhering and upholding programs to safeguard product safety and quality.

ESSENTIAL FUNCTIONS:

Include but not limited to the categories listed below. Duties and responsibilities also encompass other functions as needed and assigned.

• Test and approve raw materials
• Test and approve finished and in-process batches. Make adjustments as necessary
• Analysis and approval of line samples
• Assist in production problems – trouble shooting
• Maintain and calibrate all gauges and instruments
• Prepare and standardize all required reagents
• Develop and validate new analytical procedures
• Provide assistance in training personnel
• Perform stability testing on OTC production
• Promote compliance with Bright Innovation Labs policies, procedures, quality standards and current Good Manufacturing Practices (cGMP) as well as safety and environmental regulations. Participate, as required, in safety and GMP training sessions, and other company training sessions

COMPETENCIES

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Must have strong verbal and writing skills along with strong communication skills. Must be able to speak, read, and write in English; Spanish a plus.
• Experience using Microsoft Work, Excel, and Outlook
• Ability to multi-task
• Must demonstrate strong attention to detail
• Flexibility with schedule including shift work
• Overtime may be required with very little notice

Hours : Weekends 7:00am - 7:00pm