Quality Control (QC) Chemist Weekend AM Shift

Bright Innovation Labs; Beech (OH); On-site; USD 52,000 - 66,000; Full time

Job summary

Bright Innovation Labs is seeking a quality control analytical technician to support production through chemical and physical analysis of concentrates and finished products. You will test and approve raw materials and in-process batches, analyze line samples, and assist in troubleshooting production issues.

You will calibrate gauges, prepare reagents, develop new analytical procedures, and ensure compliance with cGMP, safety, and environmental regulations.

Qualifications

• Ability to read, write, and communicate in English; Spanish is a plus.
• Experience with Microsoft Word, Excel, and Outlook.
• Strong attention to detail and accuracy.
• Ability to multi-task and manage competing priorities.
• Flexible schedule with potential shift work and overtime.

Responsibilities

• Test and approve raw materials
• Test and approve finished and in-process batches
• Analysis and approval of line samples
• Assist in production problems – troubleshooting
• Maintain and calibrate gauges and instruments
• Prepare and standardize reagents
• Develop and validate new analytical procedures
• Provide training assistance
• Perform stability testing on OTC production
• Promote cGMP compliance and safety/regulations.

Skills

Verbal communication

Written communication

Attention to detail

Multi-tasking

Shift work

Overtime tolerance

Tools

Microsoft Word

Microsoft Excel

Microsoft 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