Job Description
At Ecological Laboratories, Inc. (ELI) we are a fast growing BioTechnology Research, Development, and Production firm company. We have a team of highly skilled technical scientists working on solving evolving environmental and client needs through market research and continuous product development. Due to internal promotion our Research & Development (R&D) team is seeking to add at least one (1) additional skilled Quality Control / Quality Assurance Technician to support and assist in leading our with organizational growth. These growth markets include Agriculture, Wastewater, Hydroponic, Vertical Farming, Ecosystem Restoration, Aquarium/ Pond, Septic, Livestock and Industrial waste. The Quality Control Technician (QC Tech) is responsible for ensuring all products manufactured are in accordance with our quality assurance program and that qualify, reliability and Standard Operating Procedure (SOP) Standards are followed, in order to satisfy safety and compliance regulations. The QC Tech is also responsible for all Quality Assurance functions from incoming raw and packing material to formulations, production and packaging. Responsibilities also include conducting performance testing on existing products, development, assessment and evaluation of new products.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Responsible for the development, implementation and strict adherence to a quality assurance program, including, but not limited to: quarantining, holding, rejecting and/or releasing of materials, storage of released components, temperature and humidity control, monitoring environmental conditions and cleaning processes. Understands and adheres to the U. S. Food and Drug Administration (FDA) and/or other regulatory agency's requirements and expectations, as required. Escalates issues to Laboratory Manager and prevents shipment of orders, not in compliance with regulatory and company standards, until concerns are satisfactorily resolved. Determines and recommends the laboratory equipment and quality assurance practices necessary to perform all of the functions of this position. Works in conjunction with select company personnel on new product development, with an emphasis on quality being built into the design; conducts research; manufactures and tests product(s): raw materials, in-process, laboratory and stability testing, making necessary adjustments prior to sales release. Organizes and maintains a retained sample filing system. Establishes and sets product(s) shell life. If the company is notified that a product does not perform as expected, or has detrimental effects, utilizes retained samples for performance testing and analysis; including but not limited to shelf life testing and stability testing. Reviews and resolves quality control problem/concerns and works to meet requirements relating to current and developing technologies with the Laboratory Manager and others including vendors, QC personnel, Research & Development (R&D) team and VP Operations. Develops and adheres to approval processes for each phase of production; from incoming inspections through shipping. Maintains control of SOP documentation. Inspections include testing during formulations, prior to packaging, and prior to distribution of packaged finished goods for conformance to prescribed standards, including but not limited to SOPs. Develops and implements a pre-materials inspection program with approvals required on each chemical product, prior to its packaging. Each batch is tested, stability, and adherence to standard guidelines. Additionally, cleaning logs are to be maintained in order to avoid cross-contamination in the lines. Develops and implements quality assurance and SOP's for all incoming raw and/or packing materials. Tests all incoming quarantine items and provides a sign off (initials & date) approval for each material, if applicable. Incorporates corrective actions and preventative actions into the company quality processes. Prepares, obtains approval and distributes reports and other documentation required by regulatory agencies and to support the quality assurance function. Maintains detailed records of all instrument calibration, standards formulation, analyses, culture development, plant environmental and third-party testing. Maintains all lab notes in conformity with FDA and or EPA guidelines. Conducts R&D work, as required on existing products, new products or competitive products to determine effectiveness, potential adverse effects and for comparison of company products to competitive technologies. Resultant data can be used internally to enhance company understanding of products, how they work and how to improve them; or externally to demonstrate, quantitatively, product effectiveness or superiority to competitive products. Other assignments as required by management. This may include tasks outside the scope of the position and is assigned based on the capability of the individual. EDUCATIONAL AND SKILL REQUIREMENTS
Minimum of a college degree in Chemistry/Microbiology, or related life sciences or prior experience in this /related field. Emphasis on quality control, manufacturing methods and adherences to policies and procedures. Emphasis on regulatory compliance, best-practices and continuous process improvement. Basic computer skills; Microsoft Office and Internet experience preferred. Ability to work autonomously with limited supervision. Ability to work along with laboratory technician(s). Exceptional attention to detail. Solid verbal, written and presentation skills. Ability to act as a company advocate; assist with presentations at industry trade functions and or technical conferences. Analytical; ability to analyze and record data. Accurately documents research findings; makes recommendations. Able to prioritize within stated deadlines. Ability to work in teams and understands team dynamics. Multitasked; organized; result driven; problem-solver. PHYSICAL REQUIREMENTS
(With or without an accomodation) While performing the duties of this job, the employee is regularly required to stand, walk, climb stairs or ladders and use hands to finger, handle, or feel. The employee is occasionally required to reach with hands and arms. The employee must occasionally lift and/or move up to 50 pounds. The employee is regularly exposed to moving mechanical parts or airborne particles. The noise level in the work environment is usually moderate to loud. The employee must be able to distinguish colors accurately. These physical demands are representative of the physical requirements necessary for an employee to successfully perform the essential functions of this job. Reasonable accommodation can be made to enable people with disabilities to perform the described essential functions of this job. The work schedule is five (5) consecutive days (Monday through Friday) each consisting of eight (8) hour shifts (8am to 5pm with 1-hour lunch period). Overtime may be occasionally required. The Quality Control Technician adheres to the site safe work practices and must wear appropriate Personal Protective Equipment. Our Commitment to Diversity and Inclusion:
Build your career where diversity, inclusion, and belonging thrives. We believe in maintaining a hiring and working experience in which all people are respected and valued, regardless of gender identity or expression, sexual orientation, religion, ethnicity, age, neurodiversity, disability status, citizenship, or any other aspect which makes people unique. We hire you for who you are, and we want you to bring your true self to work every day! Job Type:
Full-time Pay:
$19.00 - $23.00 per hour Benefits:
401(k) Dental insurance Employee assistance program Employee discount Flexible schedule Health insurance Health savings account Life insurance Paid time off Professional development assistance Referral program Retirement plan Vision insurance Work Location:
In person
