Quality Control Chemist

Ricca Chemical Company; Arlington (TX); On-site; USD 31,822 - 45,323; Full time

Job summary

Ricca Chemical Company in Arlington, TX is seeking an experienced Quality Control Analyst to perform testing, generate technical reports, and oversee ISO 17034 related activities in a regulated manufacturing environment.

You will implement procedures, maintain instrument calibration, review data, and support inter-lab proficiency testing while ensuring compliance with cGMP/GLP standards.

Qualifications

• Bachelor’s degree in Chemistry or similar field (biology, engineering or physics).
• 3–5 years of experience in quality control analytical laboratory or regulated manufacturing environment.
• Experience with ISO9001:2008, cGMP/GLP, and ISO17034 is a plus.
• Ability to read, write, and conduct business in English.
• Strong organizational skills and attention to detail.

Responsibilities

• Perform quality control testing and prepare technical reports on test specifications and outcomes.
• Conduct analyses and ensure compliance with specifications and measurement uncertainties.
• Prepare Certificate of Analysis reports without errors.
• Support investigations, out-of-spec (OOS) events, and abnormalities.
• Calibrate, troubleshoot, and maintain laboratory instruments and equipment.
• Maintain inventory levels for laboratory supplies and ensure safety compliance.
• Follow ISO17034 and ISO9001/GLP/cGMP procedures and participate in proficiency testing.

Skills

Good communication

Critical thinking

Problem solving

Time management

Analytical

Organizational skills

Attention to detail

Education

Bachelor's Degree in Chemistry

Job description

Job Details

Level: Experienced
Job Location: Arlington, TX 76012
Position Type: Full Time
Education Level: 4 Year Degree
Salary Range: $28.00 - $28.00 Hourly
Job Shift: Day
Job Category: Manufacturing

POSITION PURPOSE

Responsible for performing quality control testing, creating technical reports on the specifications and outcomes of tests, products and processes. Responsible for all chemical manufacturing of Ricca’s chemical inventory products.

ESSENTIAL FUNCTIONS AND BASIC DUTIES

• Act responsibly at all times to ensure the health, safety, and well-being of self, co-workers, visitors, neighbors, and property. This includes compliance with all RCC safety policies and procedures, and a working knowledge of government regulations, particularly hazardous material regulations.
• Schedule and assign daily testing based on the company’s planning schedule to utilize available skills, knowledge and experience, labor hours, and lab equipment.
• Ensure that all assigned testing of finished products is conducted according to specified procedures and in a timely manner.
• Performing routine and non-routine analyses without supervision.
• Collect data and calculate Measurement Uncertainty Budgets for specified testing.
• Competently perform at least 95% of the types of analysis/testing.
• Make detailed observations, analyze data, and interpret results.
• Read and record data quickly and accurately and avoid perceptual errors in performing computations.
• Prepare Certificate of Analysis reports without errors.
• Review of data obtained for compliance with specifications and report abnormalities; including measurement uncertainty budgets for specified testing.
• Compile data for OOS investigations, documentation of test procedures, and abnormalities.
• Assist in technical complaint investigations and development of new methods and technologies.
• Participate and satisfy requirements for inter-laboratory round robin testing as well as ISO 17034 Proficiency Testing as required in order to maintain accreditation.
• Troubleshoot, calibrate and perform preventative maintenance on laboratory instruments and equipment and document events as required.
• Ensure inventory levels for laboratory supplies are kept current and are accurate.
• Stay abreast of ISO 17034 requirements and follow all RCC Standard Operating Procedures with special attention to those pertaining to the laboratory processes.
• Consistently meets/exceeds standards assigned within Functional Training Document (FTD) program.
• Any other tasks deemed necessary.
• Commitment to the organizations values; High Standards, Bias for Action, Teamwork, CustomerObsession, Trust, Accountability, Innovation and Growth & Learning.

WORK ENVIRONMENT

The physical environment may require the employee to work both inside and outside in heat/cold, wet/humid, and dry/arid conditions. This position may be working in the warehouse under various indoor environmental conditions, including supplemental heating in the winter months and without air-conditioning in the summer months. May be requested to work overtime and weekends. The position may occasionally be exposed to ruptured, leaking packages, some of which may contain Hazardous Materials. Where appropriate, proper safety equipment should be utilized and/or appropriate personnel notified. Frequently required to use personal protective equipment to prevent exposure to hazardous materials and chemicals. This job may require lifting of up to 50 pounds occasionally.

Qualifications

REQUIRED SKILLS

• Good communication
• Critical thinking and problem-solving
• Time management
• Analytical
• Organizational skills
• Patience and determination
• Scientific and numerical skills

Education and Experience

Bachelor’s Degree in Chemistry or similar field, such as biology, engineering or physics.

Three (3) to five (5) years of experience in quality control analytical laboratory or regulated manufacturing environment preferably in the chemical or pharmaceutical industry.

Experience in handling and operating laboratory glassware and equipment for testing purposes. Working knowledge of ISO9001:2008 standards, cGMP/GLP regulation, and laboratory sample processes. Knowledge of ISO 17034 standard is a plus.

This position requires a person to be able to speak, write and conduct business in English. This person shall also have sufficient eyesight to read business documents and properly fill out appropriate Quality System Records and Forms.

This position should be able to understand and then follow written and verbal work instructions and quality system procedures without direct and constant supervision after the initial training period is successfully completed and documented. This position should have sufficient mental capacity to accommodate and successfully implement changes in work tasks and quality system changes when required.

Strong organizational skills, meet deadlines, work independently and with the team with strong follow through, strong communication skills, both written and verbal and accuracy and attention to detail.