Quality control analyst jobs in Colorado - 129 jobs

About Us: Alder Renewables is a fast-growing clean fuels startup focused on producing refinery-ready biocrude from sustainable biomass. Backed by leading investors and strategic industry partners, Alder is in an execution-focused scale-up phase, offering employees hands-on exposure to real-world scale-up, fuels testing, pilot-scale operations, and technology commercialization. Position Overview: We are seeking a highly motivated Research Chemist with a strong analytical chemistry focus to own and execute laboratory testing in our R&D facility. This is a hands-on role responsible for managing, executing, improving, and documenting lab experimental work that advances proprietary technologies toward commercial readiness. The ideal candidate brings a solutions-oriented mindset, strong organizational skills, and the ability to work independently and collaboratively within established experimental frameworks, with clear accountability for data quality, method robustness, and continuous improvement of laboratory practices. Key Responsibilities: · Own day-to-day analytical performance, including data quality, repeatability, and documentation. · Support analytical method development, validation, and optimization. · Support lab safety documentation, protocols, and inspections. · Operate, maintain, and troubleshoot analytical equipment. · Plan and execute lab experiments and chemical analyses for high-quality data. · Support the interpretation of data and identification of trends. · Draft research reports, summaries, and briefs. Minimum Qualifications · Bachelor's degree in chemistry, chemical engineering, or a closely related field. · 3+ years of hands-on analytical lab experience in an applied research setting. · In-depth knowledge of analytical instrumentation operation and maintenance. · Detail-oriented with strong organizational skills. · Excellent written and verbal communication skills. · Ability to manage multiple tasks simultaneously. Application Process: Interested candidates should submit a resume, cover letter, and contact information for two professional references to: ************************** Our values: Our work is driven by a set of core values that guide us in everything we do: 1. Push the boundaries of the possible: We're not afraid to innovate and challenge the status quo, seeking groundbreaking solutions to complex problems. 2. Sustainability by design: We prioritize sustainability in all aspects of our work, from product development to daily operations. 3. Operate with humility: We approach our work with a humble attitude, recognizing that there's always more to learn and room for improvement. 4. Collaborate with empathy & respect: Collaboration is key to our success. We treat each other and our partners with empathy and respect, fostering a positive and inclusive work environment. 5. Data-driven decision making: We rely on data and evidence to make informed decisions, ensuring the effectiveness and efficiency of our processes. Location: Alder Renewables 1450 Infinite Drive, Ste 115 Louisville, CO 80027 Job Type: Salaried. Compensation: Salary range: $80,000-$95,000 per year, commensurate with qualifications and experience. Total compensation includes a comprehensive benefits package (medical, dental, vision, life insurance, 401k, paid time off) and eligible participation in an equity-linked incentive plan.

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek so they can do what they do best: improve the world around us. Information about Agilent is available at **************** Agilent Technologies, Inc. is looking to add a Quality Control Analyst to its high-performance quality team working at the state-of-the-art, contract API manufacturing facility that specializes in Nucleic Acid Chemistries located in Frederick, Colorado. The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in the capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life-changing, life-saving medicines. This position coordinates and conducts routine and non-routine testing support. Responsibilities include testing to support manufacturing, raw material release, qualification, and validation activities. Understanding and experience with Standard Operating Procedures, current Good Manufacturing Practices (cGMPs) and other regulatory requirements are required. Shift: This position will support Weekend Shifts, consisting of 4 10-hour shifts; must be open to working Thursday thru Sunday. or Friday thru Monday on day shift, weekend coverage. Position may require QC testing support in both Boulder and Frederick sites. ESSENTIAL DUTIES AND RESPONSIBILITIES: Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results Outstanding communication skills, both written and oral, and the ability to communicate directly with peers and area managers Conducts analysis associated with clinical and non-clinical laboratory studies under current Good Manufacturing Practices (cGMP) regulations and guidance per Food and Drug Administration (FDA) and Organization for Economic Co-Operations and Development (OECD) as well as international regulations Performs analysis on raw materials, in-process materials, APIs (developmental and commercial), final product and other requested testing as per written procedures. Reviews data for compliance to specifications, report results, and troubleshoots abnormalities Ensures equipment is performing well and communicates and takes appropriate action as necessary Troubleshoots, investigates, and resolves laboratory testing failures and drives solutions to improve the quality control laboratory programs through corrective and preventive actions Maintains inventory and ordering of laboratory supplies Performs maintenance activities on laboratory instruments and equipment Ensures good documentation practices are followed Qualifications A Bachelor's degree (B.S.) or equivalent in Chemistry or related life sciences field; or equivalent combination of education and experience 2+ years of relevant experience within the pharmaceutical Industry Exposure and knowledge of FDA regulations and guidelines Knowledge of cGMP guidelines or international regulations (i.e., International Committee on Harmonization (ICH) Q7) Knowledge of analytical equipment and instrumentation utilized for the testing of in-process samples, raw materials, and microbiological samples Proficient with Microsoft Word, Excel, and Chemstation Familiarity with the following laboratory disciplines is highly desired: HPLC Density HPLC-MS IC Solution Preparation UV analysis FTIR Shift Differential for Weekend work Weekend Shift, consisting of 4 10-hour shifts; must be open to working Thursday thru Sunday or Friday thru Monday on day shift. Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please contact *************** email job_*******************. EOE AA M/F/Vet/Disability/Sexual Orientation/Gender Identity. For more information about equal employment opportunity protections, please see all of our notices for EEO below. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least December 26, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $34.00 - $53.13/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: NoShift: SwingDuration: No End DateJob Function: Quality/Regulatory

UXO Quality Control Specialist This identifies the major responsibilities of this position. It does not include all aspects of the position such as potential additional duties requested by supervisors/managers and the requirement for flexibility in helping others for the Company's overall benefit. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. JOB SUMMARY Manage the site quality program under the auspice of the company Quality Assurance Manager. DUTIES AND RESPONSIBILITIES Responsible for implementing and enforcing all quality requirements in the Project Work Plan. Ensure operations produce a quality product while adhering to federal and state regulations. Inspect procedures and policies for compliance to industry standards. Evaluate methods and means for cost effectiveness. Reduce waste, duplicated effort, and product failure. Ensure operations adhere to the project work plan. Conduct workforce training on ordnance. Inspect safety procedures and training programs to maximize time and effectiveness. Conduct stakeholder feedback. Communicate negative trends of production or quality to the project manager. Communicate major deficiencies to the Quality Manager and Project Manager. Coordinate efforts with SUXOS to streamline operations through experience and teamwork. Serves as site liaison to the on-site USACE Safety Representative. MINIMUM QUALIFICATIONS, SKILLS, AND EDUCATIONAL REQUIREMENTS Graduate of a qualified explosive ordnance disposal (EOD) school with at least eight years combined military and commercial UXO experience. As an exception, a UXOSO may be a graduate of a qualified UXO school and have at least eight years commercial UXO experience, as required by DDESB TP18. Current 40-Hour HAZWOPER certification IAW 29 CFR 1910.120 Current 29 CFR 1910.120 HAZWOPER Physical Member of American Society for Quality (ASQ) ASQ Certified Quality Auditor (CQA), preferred, or in training for certification Ability to obtain a Secret Clearance Broad understanding of the Foreign Corrupt Practices Act (FCPA) Ability to work outside normal work hours at short notice as dictated by workload Ability to work away from primary work location in excess of normal workday Ability to travel outside the US Outstanding verbal and written communication skills; ability to interpret and explain company policy concerning MEC safety practices to executives, managers, employees, and clients Intermediate user level of computer systems; Microsoft office software (word, excel, outlook), inventory databases, and documentation control systems Valid Driver License Acknowledgment Selected candidate will be responsible for the satisfactory execution of these duties, responsibilities and functions. Duties and responsibilities may change from time to time without these changes being specified in this and that this job description in no way states or implies that these are the only duties to be performed when filling this position. We are committed to a merit-based hiring process that values individual skills, qualifications, and performance. Our hiring practices comply with all applicable federal, state, and executive orders, including the recent Executive Order on Equal Opportunity Hiring.

Starting compensation: $21.00 per hour (plus a $1.50 shift differential) Shift Days: Sunday to Thursday Shift Hours: 2:30 PM to Close Shamrock anticipates closing the application window for this job opportunity on or before December 31, 2026 Maintains all aspects of Quality Assurance to ensure proper, safe and exceptional operation of the department. Essential Duties: * Audits products for quality and safety prior to sending out to customers. * Audits incoming raw materials for supplier specifications, quality, and food security. * Reviews incoming ingredients for allergen checks and quality standards. * Responsible for compliance with all regulations. Food Safety - plant in proper sanitary condition at all times, including allergen control, pest control, guidelines followed. * Fills out necessary paperwork for product audits and HACCP documents. * Reviews HACCP documents prior to handing paperwork to QA Supervisor/Manager. * Work with operational teams daily with paperwork, quality checks, and HACCP procedures. * Ensure adherence to all standard work processes, including the Production Sanitation processes. * Aides in plant training requirements and training frequencies. Work with QA Supervisor/ Manager to ensure plant training requirements and frequencies are met. Conduct plant training sessions as needed. * Maintain understanding of processes and functional interdependencies. Recognize and escalate, as needed, those issues identified as risks to, or opportunities to improve, plant performance. * Must be able to work within timelines and in pressure situations. * Other duties may be assigned. Qualifications: * High School Diploma or GED preferred * Meat Protein Experience * HACCP certified, preferred Corporate Summary: At Shamrock Foods Company, people come first - our associates, our customers, and the families we serve across the nation. A privately-held, family-owned and -operated Forbes 500 company, Shamrock is an innovator in the food industry and has been since being founded in Arizona in 1922. Our Mission: At Shamrock Foods Company, we live by our founding family's motto to "treat associates like family and customers like friends." Why work for us? Benefits are a major part of your overall compensation, and we believe offering them at an affordable cost is not only the right thing to do, but it helps keep you and your family healthy. That's why Shamrock Foods pays for the majority of your health insurance, allowing you to take home more of your paycheck. And it doesn't stop there - our associates also enjoy additional benefits such as 401(k) Savings Plan, Profit Sharing, Paid Time Off, as well as our incredible growth opportunities, continued education, wellness programs. Equal Opportunity Employer Shamrock Foods Company is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, sexual orientation, gender identity or any other basis protected by applicable law.

Full-time Description A Quality Control/Floor Inspector assists the Chief Inspector with all things as required and needed in support of the Repair Station and operations. This person reports directly to the Chief Inspector. Key Duties and Responsibilities: Maintain a clean and orderly workspace. Work efficiently with the team to ensure a smooth workflow. Assist the Chief Inspector with logbook research as required. Perform aircraft inspections when not inspecting discrepancies or work orders. Assist the Chief Inspector with floor inspection items. Giving the “ok to close panels” and being the “backup” to ensure quality and safety of our products. Assist the Chief Inspector with returning aircraft to service after work is completed. Ensure that we are delivering a safe aircraft that meets our quality standards. Inspecting discrepancies once completed for proper repairs, correct paperwork, and correct sign-off of discrepancies. (Make sure accepted or approved procedures are used at all times). Other duties as assigned. Benefits Available with employment: Medical, Dental, Vision and Supplemental Plans Estimated application closing date: 10/31/25 Requirements Qualifications Education Requirements: Must have High School Diploma or GED Must have an FAA approved Airframe and Powerplant license. Experience Requirements: Ability to work independently with minimal direction. Ability to understand technical publications and requirements. Clear understanding of FAA and Repair Station requirements. Assist with or undertake any other duties as assigned by key personnel. Ability to work with several individuals while showing independence in balancing and prioritizing requests. Three years business/corporate aircraft maintenance experience Other Requirements: Clean driving record. Able to pass a background check. Ability to pass a drug screening test. Occasionally required to lift up to 35 pounds. Must be able to sit, stand, kneel and climb ladders. Must be able to show up to work on time ready to work. Must have dependable transportation to and from work. Ideal Candidate Will Possess the Following Skills: Attention to detail. Sincere desire to assist others. Able to develop a friendly rapport. Persistence in the face of obstacles. Professional in appearance and mannerisms. A willingness to take on responsibilities and challenges. Being reliable, responsible, and dependable, and fulfilling obligations. Being pleasant with others on the job and displaying a good-natured, cooperative attitude. Being sensitive to others' needs and feelings and being understanding and helpful on the job. Guiding oneself with little or no supervision and depending on oneself to get things done IAW acceptable techniques and methods. Maintaining composure, keeping emotions in check, controlling anger, and avoiding aggressive behavior even in very difficult situations. An ability to guide oneself with little or no supervision, depending on oneself to get things done while following the requirements of the Repair Station. Accepting criticism and dealing calmly and effectively with high stress situations being open to change (positive or negative) and to considerable variety in the workplace. Salary Description $34-$45/hr DOE

TAK Broadband is a leading end-to-end U.S. fiber broadband network construction contractor operating in 42 states. It builds more than just networks; it connects communities to new valuable digital opportunities. TAK offers comprehensive service solutions, from construction to drops to fulfillment. TAK's ecosystem of partners allows it to successfully complete every project starting from the first point of conception. This includes engineering teams, distributors, and more than 100 qualified construction crews with extensive experience across all ISP types and markets; over 300 experienced bury drop crews; and more than 700 professional technicians. We are seeking a Quality Control Technician to join our team in Denver, CO. In this role you will ensure timeliness, completeness and accuracy of work performed by technicians. You will perform inspections post-install to ensure compliance to client specifications and complete reviews to ensure proper restoration of the area. Why TAK? * Full Time * Paid Weekly * Compensation: $20 - $22 per hour, DOE * Full Benefits Package (Medical, Dental & Vision) * Paid Time Off * 401(k) with Company Match! * 25K Company Paid Life Insurance * Independent Work & Team Collaboration * Career Development & Advancement Opportunities! The Role * Ensures timeliness, completeness and accuracy of work performed by technicians * Performs inspections post install to ensure compliance to client specifications * Completes reviews to ensure proper restoration of area * Captures photos and attach to the inspection report * Performs white line excavations and collects locate data * Verifies the system is complying with all safety requirements * Performs work in a safe manner, following all OSHA and company guidelines * Prioritizes, organizes and efficiently completes tasks to meet deadlines * Works in a variety of outdoor environments * Drives Company vehicles responsibly and safely * Conducts and attends meetings as needed Requirements * 2+ years of telecommunications (i.e. cable, internet, telephone, wireless) installation or construction industry experience (sales, call center and IT roles are not considered) * Experience with quality control and verifications * Experience calling in Bluestakes a plus * Experience with underground locates and the ability to use a compass for directional instructions * Basic mechanical aptitude, ability to utilize hand tools for intended purposes * Ability to travel daily around the Chicago metro area and open to a variety of schedules * Excellent customer service, time management, problem-solving and troubleshooting skills * Ability to learn and operate testing equipment and software/programs * Ability to utilize hand tools, identify wire size/color and accurately utilize measuring devices * Ability to carry, climb, operate, and work upon an extension ladder (approximately 28 feet high and 75 pounds) * Ability to complete work indoors, outdoors, in tight spaces and elevated by bending, reaching, twisting, climbing, and working while standing up to 70% of the time * Ability to safely navigate various terrains, managing equipment and tools * A body weight of no more than 275 pounds to perform ladder work safely. Safety is our #1 Priority. If personal safety is not compromised, an accommodation may be available based on previous ladder experience in a similar role * Valid driver's license with a satisfactory driving record (no suspensions or revocations) * Passing of all pre-employment requirements (MVR, Background Check, Drug Screen) The compensation and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, with or without notice, subject to applicable law. The Company expects to accept applications for this position until January 9, 2026 but encourages interested applicants to apply as soon as possible. TAK is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by law. We maintain full compliance with the Americans with Disabilities Act and are committed to providing equal access throughout our employment practices. Individuals with disabilities may request reasonable accommodations during the application and hiring process by contacting *****************************. Salary Description $20 - $22 per hour, DOE

Job Description The Quality Control Specialist is a critical member of the team, ensuring the production and distribution of high-quality, sterile pharmaceutical products in compliance with FDA regulations, cGMP guidelines, and USP standards. This role involves conducting rigorous testing, inspections, and documentation throughout the manufacturing process to verify product integrity, sterility, and accuracy. Key responsibilities include performing laboratory analyses, environmental monitoring, and equipment calibration; reviewing and maintaining quality control records; and collaborating with cross-functional teams to identify and address quality issues. The specialist must remain updated on regulatory changes and implement continuous improvement initiatives to enhance operational quality and efficiency. Duties/Responsibilities: Works effectively and efficiently in a team environment. Conduct routine and non-routine viable, non-viable and surface environmental monitoring in all classified areas of the facility, as needed Incubation and enumeration of samples related to environmental monitoring processes, as needed. Conduct morphology assessment on appropriate samples at the conclusion of the incubation term, as needed. Perform review and release of raw materials, API, and excipients. Coordinates third party sample submission. Demonstrates the ability to perform detail-oriented work with a high degree of accuracy. Conduct investigations pertaining to OOS/OOT of raw materials, in-process, and finished product results with production personnel and/or supplier. Assists with all aspects of the quality system, such as change control, investigations, CAPA, and validation systems to ensure compliance and timely completion of assigned activities. Compiling data for quarterly report review. Review and release of finished product testing results. Generation of Certificate of Analysis and Finished Good Forms for batch release. Participate in product development meetings and represent Quality Control. Assist with the development, management and improvement of quality system processes and procedures to ensure compliance with applicable laws, regulations, and company standards in support of cGMP for pharmaceutical compounding. Lead/support audits (internal and external) to ensure compliance to CGMP regulations and internal procedures. Performs other duties as assigned. Required Skills/Abilities: Excellent verbal and written communication skills. Excellent interpersonal and customer service skills. Excellent sales and customer service skills. Excellent organizational skills and attention to detail. Excellent time management skills with a proven ability to meet deadlines. Strong analytical and problem-solving skills. Strong supervisory and leadership skills. Ability to prioritize tasks and to delegate them when appropriate. Ability to function well in a high-paced and at times stressful environment. Proficient with Microsoft Office Suite or related software. Education and Experience: BS/BA in Microbiology, Chemistry, or a relevant field/or equivalent experience. 2-5 years of Quality Control experience. Experience in a cGMP environment. Previous pharmaceutical experience. Familiarity with 21 CFR Part 11/210/211. Experience with aseptic manufacturing environments. Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities. Physical Requirements: Demonstrates ability to walk and stand for prolonged periods of time. Demonstrates ability to sit/ stand at a desk and working on a computer. Must be able to lift up to 15 pounds at times. Timeline: We will be accepting applications on an ongoing basis until position is filled.

Full-time Description At SPL, we turn science into impact. We're searching for a driven Laboratory Analyst to join our team in Commerce City, CO. In this role, you'll be trained by industry experts, work with advanced laboratory technology, and deliver the accurate data our clients rely on for compliance and decision-making. Every analysis you perform helps ensure cleaner water, safer communities, and a healthier world. If you're ready to build technical expertise, expand your analytical skills, and grow your career in a collaborative, purpose-driven lab, we want to hear from you! Why You'll Love This Role Perform on the front line of environmental analysis by generating analytical data to support environmental compliance and decision-making; Grow hands-on skills in analytical instrumentation, Laboratory Information Management Systems (LIMS), and advanced testing methods; Gain exposure to real-world applications in environmental science, regulatory compliance, and client services; Join a team where your contributions directly support public safety, regulatory standards, and cleaner environments. What You'll Do Perform sample preparation and analytical testing in accordance with approved methods and established protocols to ensure accuracy, timeliness, and regulatory compliance; Enter and manage data in the Laboratory Information Management System (LIMS) or other designated systems; Develop and maintain proficiency with a broad range of analytical equipment, laboratory software platforms, and technology relative to assigned analyses; Review and interpret results to ensure accuracy and completeness; Document all work clearly, maintaining traceable laboratory records; Perform routine equipment checks, troubleshooting, calibrations, and preventative maintenance; Adhere to quality systems, SOPs, and continuous improvement initiatives; Follow and promote Good Laboratory Practices (GLP) and all health, safety, and environmental standards; Assist with general laboratory housekeeping, glassware cleaning, inventory, and supply management; Participate in cross-training to support workload balance and operational needs; Perform other duties as assigned. Requirements What Makes You a Great Fit Bachelor's Degree in Science or related field; Previous hands-on experience in a professional or academic lab setting; Ability to manage and process high volumes of samples efficiently; Proficiency with Microsoft Office tools (Word, Excel, Outlook) and Adobe Acrobat. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 9 paid holidays plus a generous PTO plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position following a Monday through Friday schedule with daily shift hours from 7:30 am - 6 pm; Must be able to work outside of normal hours to support business needs and deadlines; Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future. Salary Description $22-$26 per hour

RESEARCH CHEMIST TECHNICIAN Rocky Mountain Scientific Laboratory Department:Advanced Chemistry & Chemical Processing Group Yes Travel:Yes Schedule:Full-time Description of Business Environment: Peace is often associated with passivity. At Rocky Mountain Scientific Laboratory, we associate peace with strength, courage, and action. We know that enabling peace to prevail is not for the faint of heart, which is why we built our company foundation on the core values of Integrity, Gratitude, Mission Driven, and Grit. We pride ourselves in providing unequaled services and technologies in the field of applied energetics to our customers. Our experts possess extensive knowledge and capability in energetic materials and military systems enabling them to offer analytical characterization, modeling & simulation, design, system integration, prototyping, test engineering, and proof-of-concept production services covering a wide range of applications. Our strengths lie in our ability and relentless determination to get the job done quickly and affordably. RMSL is an Equal Employment Opportunity (EEO), Affirmative Action employer and welcomes all qualified applicants. All qualified applicants will receive fair and impartial consideration for employment without regard to race, color, religion, sex, age, disability, veteran status, national origin or other legally protected status. An applicant with a disability or a disabled veteran can request reasonable accommodation to apply for one of our positions. Specific Job Description: RMSL is a growth company with an outstanding job opportunity for a Research Chemist Technician. This position will report to the Advanced Chemistry & Chemical Processing Group Manager. The Research Chemist Technician will be an integral part of a small cross functional team working on exciting development projects with cutting-edge technology. In this role, the ideal candidate will have a strong background in Chemistry with experience in organic and/or inorganic synthesis. This role will be a part of an integrated team focused on the development of novel energetic systems, energetic material scale-up processes, development of ammunition and armaments, testing and analysis of energetic materials. This individual must demonstrate innovation, an understanding of the fundamentals of engineering, an ability to learn, out-of-the-box thinking and creativity. Duties Include: Assist in the synthesize energetic materials and scale-up process Characterize novel energetic materials using a variety of analytical methods (DSC, TGA, SDT, TAM, Particle Size Analyzer, GC-FID, ARSST, UV-VIS-NIR, FTIR and Raman spectroscopy) and material sensitivity characterization (BAM friction, impact, and ESD testing) Ability to handle hazardous materials with strict adherence to safety process requirements Assist in the design of experiments and test series that result in safe and efficient collection of data Installation, maintenance, and operation of specialized instrumentation and testing equipment Project engineering tasks such as report writing, technical presentations (at customer and public meetings), and technical deliverables tracking Required Skills: Problem solver that can work in a fast-paced team environment on projects Hands-on experience with energetic materials Proficient in standard laboratory practices Exercises creative thinking and innovation Strong verbal and written communication skills Physical requirements: Must be able to sit for extended periods of time; must be able to lift up to 50 lbs.; must have the ability to see near and far and work with a computer monitor on a daily basis Required to bend, sit, stand and lift to perform job effectively Highly Beneficial Skills: Familiar with general explosive effects and chemistry Experience in one or more of the following areas Additive manufacturing (AM) Energetic material or hazardous material synthesis Laboratory and pilot plant scale-up of energetic or hazardous materials LabRAM operation Knowledge of basic-intermediate chemistry and/or chemical engineering Minimum Qualifications: Must have an AS, BS and/or MS in Chemical Engineering or Chemistry Ability to obtain security clearance Ability to obtain CO State Blasters Permit Benefits: Medical insurance Dental insurance Vision insurance 401(k) with matching Disability insurance Life insurance Paid time off Professional development Flexible schedule

Job Description Final QC Inspector FLSA STATUS: Non-Exempt DEPARTMENT: Quality SUPERVISOR: Quality Engineering Supervisor DIRECT REPORTS: None. This position is responsible for inspecting, testing, and sampling assembled parts or products for defects, wear, and deviations from specifications. The Final QC Inspector will conduct tests and inspections of products or processes to evaluate quality and performance, utilizing precision measuring instruments and test equipment. Minimum Qualifications Education: High school diploma, GED, or equivalent qualification preferred. IPC/WHMA-A-610 or 620 certification preferred. Experience: Prior experience in quality inspection, Knowledge: Knowledge of IPC 610 and 620, ability to read and understand customer requirements and simple customer assembly drawings Extensive knowledge of components, connectors, terminals and mating connectors for fixture construction Skills: Ability to read wiring diagrams and engineering drawings, use of multi-meter, complex test equipment, force gages and calipers Must be able to read, write and speak English Must be able to recognize discrepancies on drawings and in customer requirements and bring them to the attention of leads, supervisors and/or management Job Responsibilities Conduct basic signature testing of cables, test beeping, terminal and solder inspection, simple high voltage and ground impedance testing. Perform data entry and complete associated paperwork, including inspection logs. Conduct complex high voltage and ground impedance testing and generate new signature profiles for assemblies. Write first article inspection reports and complete RMA evaluations. Perform simple fixture repair and construction. Organize existing assembly files and fixture database. Audit shelf-life, hazardous communication (hazcom), and calibration logs. Calibrate Cirris Signature Testers. Evaluate new complex assemblies and develop inspection plans. Work closely with Manufacturing to identify and resolve issues with new assemblies. Train new inspectors and acquire information/components for future inspection requirements. Collaborate with Engineering and Account Management on workflow needs. Perform general area cleanup and organization. Attend appropriate training and administrative meetings. Work with other departments to achieve company goals. Utilize communication skills necessary to execute company directives. Perform soldering, termination, plugging of connectors, heat shrinking, and comply with ESD assembly requirements. Other responsibilities, initiatives and ad-hoc projects as required. Internal and External Relationships Internal: Works closely with the Quality Engineering Supervisor, Manufacturing, Engineering, and Account Management teams to ensure product quality and process efficiency. Collaborates with production staff to identify and resolve quality issues. External: Interacts with customers and suppliers as needed to address quality concerns, ensure compliance with specifications, and support continuous improvement initiatives. May communicate with third-party testing agencies when required. Physical Requirements The physical demands described here are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand, walk, and sit for extended period and must have the capability to lift up to 25 pounds. They must perform repetitive tasks and they must also have the ability to see details clearly at close range (within a few feet) and have precise coordination of fingers for grasping, manipulating, or assembling small objects. Overtime may be required based on production demands. The working environment is a standard manufacturing environment. The noise level in the work environment is usually low to moderate. Pay: $21-26/hr (varies based on experience)

Role and Responsibilities This position is responsible for performing quality control laboratory testing on incoming, in-process and finished products and assisting in laboratory operations and method validation activities. The focus of the position is compliance with regulatory activities and company procedures as they relate to the laboratory department. Responsibilities include: Conduct analytical testing per Standard Operating Procedures (SOPs) and regulatory requirements including potency, material identification, particulate and dissolution. Maintain daily use, maintenance and cleaning logs for laboratory areas, equipment and utensils. Complete routine preventative maintenance of laboratory equipment to ensure accuracy of results. Prepare Certificates of Analysis for Quality review. Perform data entry, trending and record organization. Support in drafting and reviewing procedures, change controls, risk assessments, deviations and CAPA. Participate in test method and equipment validations. Ensure compliance to federal and state laws, as well as company standards and specifications. Assists the Laboratory Manager as needed.

West Star is the fastest growing maintenance repair organization in the industry and we recognize this is the result of our talented team of trusted employees working together to deliver customer service excellence. We are committed to providing our employees with personal and professional growth opportunities while fostering a culture of respect and well-being with a small company feel. When you join our team we don't think you should have to wait for your benefits to kick in. That's why when you start, they start with you! This includes medical, dental, 401K match, time off accruals, weekly pay days and much more. We don't want you to live to work, we want you to work and live. What you can expect as a Quality Control Inspector at West Star: The Quality Control Inspector maintains West Star Aviation's quality standards in accordance with the West Star Repair Station/Quality Control Manual and the Federal Aviation Regulations. This will be accomplished by working with Aircraft Technicians, Program Managers, Team Leaders, Quality Control and Quality Assurance Inspectors. You will be ESSENTIAL to many FUNCTIONS including: Maintain West Star Aviation's quality standards by inspecting technician's work, performing “ok to close”, and auditing. Ensure proper sign-offs in Corridor as part of the inspection process. Participate in daily review meetings. Assist with Airframe Inspections Following up with all departments to get steps signed off, inspected, and closed so airframe squawks can be completed. Help manage Equipment Removal and Installation Log. Assist QA Department with log research issues to help clear items that are in question. Daily contact at aircraft with Team Leaders to ensure quality standards are met. Maintain customer oriented work habits. Effectively and clearly communicate (i.e., speak, write, read) in English Any other job-related duties as assigned by supervisor or management. What you'll need to bring with you: Your Education: A High school diploma or equivalent. A&P License or Repairman Certificate will be required. Inspection Authorization (IA) rating is recommended. A valid driver's license approved for airline travel and/or a valid passport is ideal, but not required Your Experience : Familiar with all facets of manuals required to maintain aircraft. Thorough knowledge of FAA regulations. 3 years turbine aircraft inspection experience with return to service authority required. Customer service experience recommended. Follow all company rules and FAA regulations during performance of duties. Maintain customer oriented work habits for oneself and the department.

ABOUT YOU Are you passionate and ready to join an inclusive work environment, committed to leading new ideas and pathways, and to delivering value? If the answer is, “Yes!” then we have an exciting career opportunity for you as a Laboratory Technician based in our Denver, CO laboratory. Who are we? We are Enthalpy Analytical, a subsidiary of Montrose, a global environmental services provider offering environmental planning and permitting, measurement and analytical services, and environmental resiliency and sustainability solutions. Our qualified engineers, scientists, technicians, associates, and policy experts are proud of our collective expertise and the collaborative nature of our approach to helping clients. We strive to optimize environmental resiliency in a way that effectively complements our clients' decision-making and operations and efficiently fulfills their project requirements. We have 135 offices across the United States, Canada, Europe and Australia and over 3,000 employees - all ready to provide solutions for environmental needs. WHAT WE CAN OFFER YOU As a key member of our Montrose team, you can expect: Mentorship and professional development resources to advance your career Direct exposure to our industry's leading experts who are solving the world's toughest environmental challenges An entrepreneurial environment where you can learn, thrive and collaborate with talented colleagues Opportunities to engage and contribute in our Diversity, Fairness and Inclusion and Women Empowering Leadership employee resource groups Competitive compensation package: Starting hourly wages ranging from $23.00 - $25.00, commensurate with accomplishments, performance, credentials and geography Competitive medical, dental, and vision insurance coverage 401k with a competitive 4% employer match Progressive vacation policies, company holidays and paid parental leave benefits to ensure work/life balance A financial assistance program that supports peers in need, known as the Montrose Foundation Access to a student loan planning tool to optimize your student loan payoff plans and compare student loan rates with lenders. A DAY IN THE LIFE Enthalpy Analytical, is part of the larger organization, Montrose Environmental Group, is comprised of 9 laboratories servicing air, water, and soil testing. Regulations drive the need for our services, but our unique capabilities allow us to add value to clients beyond environmental compliance. Our Denver, CO laboratory is currently seeking a Full-Time Laboratory Technician to join our Metals Department. Compensation: $23.00-$25.00 Schedule: Tuesday - Saturday or Sunday - Thursday , 2:00pm - 10:00pm As a key member of the laboratory team, this role will be responsible for a full range of activities including: Capable of high-throughput preparation of environmental samples for metals testing. Proficiency using analytical equipment including: balances, pipettes, bottle top dispensers, hot blocks, and volumetric/graduated glassware. Daily monitoring of sample scheduling to ensure that samples are processed within EPA's and methods' holding time Schedule workload in order to process samples within clients expected due dates Routine sample preparation according to Standard Methods and EPA methods Performs analyst's review of data and QC Reviews of QA/QC criteria for batch acceptance Adheres to Standard Operating Procedures and follow safe work practices Participates in instruments' preventative maintenance and trouble shooting Participates in focus teams to improve efficiency Be flexible in work schedule including overtime when needed React to change productively and handle other essential tasks as assigned Performing other duties and responsibilities as prescribed by the Company Compliance with Enthalpy's Quality Assurance Program and other policies YOUR EXPERTISE AND SKILLS To perform this job successfully, individuals must be able to perform each duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. High School Diploma Bachelor's degree in any science field is a plus Minimum 1 year of lab experience preferred Knowledge of general lab practices and lab safety Knowledge of basic laboratory techniques preferred (knowledge of PPE, use of balance, pipetting, glassware handling, etc.) Experience in metal preparation is a plus Ability to lift and carry a minimum of 25 lbs. Ability to remain in a stationary position for extensive periods of time Preferred Skills Knowledge of analytical method, analytical instruments, general lab practices and lab safety Must be flexible in work schedule and able to work overtime Good organizational and communication skills Ability to multi-task Ability to work independently and make sound decisions The above statements are intended to describe the general nature of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties and skills required of employees so classified. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact ************ or ************************ for assistance. MAKE THE MOVE TO ACCELERATE YOUR CAREER We are a fast-paced, dynamic and high-growth company. You are your own boss, but you will get tons of guidance and plenty of support from talented, super-smart colleagues and its service providers. Therefore, if freedom, autonomy, and head-scratching professional challenges attract you, we could be the perfect match made in heaven. Want to know more about us? Visit montrose-env.com and have fun! Montrose is an Equal Opportunity Employer. Montrose is committed to recruiting and hiring qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status. Montrose is committed to providing access and reasonable accommodation in its employment for individuals with disabilities.

Summit Interconnect is the premier electronics manufacturer in the US, located in Aurora, Colorado. Specializing in printed circuit board (PCB) assembly, we build the latest application designs from leading technology companies. From satellites and rocket payload to cutting-edge medical devices, we are known for our speed, service, and impeccable commitment to quality. We are continuously innovating our processes and systems to stay on the cutting edge of printed circuit board assembly manufacturing. Our vision is to have the best employees working to provide an outstanding service experience, and the coolest technology solutions for our customers. We look forward to you joining the team! Position Summary Execute the inspection of electronic assemblies according to industry specific standards. Ensure that the specifications of the established quality standards are met on all out-going products. Assist the Quality Assurance Manager, Production Manager and other company leadership with quality related functions as required. What you will do…. Inspect Printed Circuit Boards (PCBs) and Printed Circuit Boards Assembly (PCBAs) using microscope and magnifying tools following supplied data from customer and IPC-A-610 guidelines. Complete customer Certificates of Compliance (C of C) as required. Ability to separate good and non-conforming product during inspection process. Log inspection findings into electronic logs. What you need… High school diploma or equivalent. Minimum experience of 1 year in Electronic PCB Assembly. Minimum experience of 1 year in Quality Control. Understanding of quality concepts including sampling plans and continuous improvement Good working knowledge and understanding of PCBA manufacturing processes. Ability to read and interpret drawings, prints and component datasheets. Familiarity with basic measuring instruments tools and gauges (calipers, micrometers, etc.) Proficient with Microsoft office (Excel, Word, etc.). Excellent communication skills both written and verbal. (Including ability to read, understand and explain GMP, process procedures and other necessary documentation). Positive attitude to changes. Self-motivated with a team attitude. Be able to work scheduled and extra hours as required. Attention to detail. Preferred Proficient with IPC-A-610 standard (CIS preferred) Location: 20100 E 32nd Pkwy, #225 Aurora, CO 80011 Compensation : -$19.00-$20.00 /hour DOE +shift differential Schedule: Monday-Friday 11:00am-7:30pm Benefits Advanced Assembly has an excellent benefits program. We believe in taking care of our employees. We also have fun with regular company events, BBQ's, employee recognition awards, and performance- based bonus plans. Competitive Benefits Include: Medical Dental Vision EAP (free employee assistance programs) 401(k) plan Life Insurance Paid Time Off (PTO) Seven (7) paid holidays a year Candidates must pass background and drug testing. ITAR Compliance Notice This position requires compliance with the International Traffic in Arms Regulations (ITAR). Under ITAR, candidates must be a U.S. citizen, U.S. lawful permanent resident (e.g., "Green Card" holder), asylee, or refugee as defined by 8 U.S.C. 1324b(a)(3). Applicants who do not meet this requirement may not be eligible for employment in this position. Summit Interconnect is an Equal Opportunity Employer We are committed to fostering an inclusive and diverse workplace where everyone is valued and respected. We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other legally protected characteristic. tation, gender identity, national origin, age, disability, genetic information, veteran status, or any other legally protected characteristic.

OBJECTIVE Reporting to the QA Supervisor, the primary role of the Quality Control Inspector is to conduct outbound inspections and inventory management. The Quality Control Checker adheres to all company guidelines, policies, and standard practices. QUALIFICATIONS High school diploma or equivalent Experience & Skills: 1-2 years of experience within the produce industry Previous experience in quality control or a related field preferred Strong attention to detail and ability to identify quality issues quickly Familiarity with warehouse operations, including palletization and truck loading Excellent communication skills to collaborate with team members effectively Ability to work in a fast-paced environment while maintaining accuracy Excellent communication skills (verbal and written) Excellent problem-solving and analytical skills Excellent organizational skills and the ability to multi-task Proficient in MS Office as well as inventory management software Valid Driver's License and ability to travel domestically PRINCIPAL RESPONSIBILITIES Conduct in-process and final product inspections before loading trucks to ensure compliance with quality standards Ensure the quality and appearance of product, packaging, and pallets, including verifying proper stacking and secure placement of products Collaborate with production/warehouse and logistics teams to maintain efficient and accurate loading processes Identify and document non-conformance issues, escalating to management as needed, and promptly Assist in maintaining and improving quality assurance protocols to meet company standards PHYSICAL REQUIREMENTS Ability to stand for extended periods and lift up to 50 lbs., as needed Comfortable working in a warehouse environment with varying temperatures

RESEARCH CHEMIST/CHEMICAL ENGINEER Rocky Mountain Scientific Laboratory Department:Advanced Chemistry & Chemical Processing Group Yes Travel:No Schedule:Full-time Description of Business Environment: Peace is often associated with passivity. At Rocky Mountain Scientific Laboratory, we associate peace with strength, courage, and action. We know that enabling peace to prevail is not for the faint of heart, which is why we built our company foundation on the core values of Integrity, Quality, Agility, and Grit. We pride ourselves in providing unequaled services and technologies in the field of applied energetics to our customers. Our experts possess extensive knowledge and capability in energetic materials and military systems enabling them to offer analytical characterization, modeling & simulation, design, system integration, prototyping, test engineering, and proof-of-concept production services covering a wide range of applications. Our strengths lie in our ability and relentless determination to get the job done quickly and affordably. RMSL is an Equal Employment Opportunity (EEO), Affirmative Action employer and welcomes all qualified applicants. All qualified applicants will receive fair and impartial consideration for employment without regard to race, color, religion, sex, age, disability, veteran status, national origin or other legally protected status. An applicant with a disability or a disabled veteran can request reasonable accommodation to apply for one of our positions. Specific Job Description: RMSL is a growth company with an outstanding job opportunity for a Research Chemist. This position will report to the Advanced Chemistry & Chemical Processing Group Lead. The Research Chemist/Chemical Engineer will be an integral part of a small cross functional team working on exciting development projects with cutting-edge technology. In this role, the ideal candidate will have a strong background in Chemistry/Chemical Engineering with experience in organic and/or inorganic synthesis. This role will be a part of an integrated team focused on the development of novel energetic systems, energetic material scale-up processes, development of ammunition and armaments, testing and analysis of energetic materials. This individual must demonstrate innovation, an ability to learn, out-of-the-box thinking and creativity. Duties Include: Develop novel synthesis and scale-up processes Characterize novel energetic materials using a variety of analytical methods Formulation optimization of propellants, pyrotechnics, and explosive formulations Handling and testing of energetic materials, armaments, and weapon systems Integrate energetic materials in to end articles such as ammunition and munitions. Ability to handle materials with strict adherence to safety process requirements Design of experiments and test series that result in safe and efficient collection of data Design, source selection, installation, maintenance, and operation of specialized instrumentation and testing equipment Assistance with company compliance in restricted information security regulations Project engineering tasks such as report writing, technical presentations (at customer and public meetings), and technical deliverables tracking Required Skills: Problem solver that can work in a team environment on fast pace projects Hands-on experience with energetic materials Proficient in standard laboratory practices Exercises creative thinking and innovation Strong verbal and written communication skills Physical requirements: Must be able to sit for extended periods of time; must be able to lift up to 50 lbs.; must have the ability to see near and far and work with a computer monitor Required to bend, sit, stand and lift to perform job effectively Highly Beneficial Skills: Familiar with general explosive effects and chemistry Experience in one or more of the following areas Continuous Synthesis Armament and munition development Energetic material synthesis and formulation Laboratory and pilot plant scale-up of energetic materials Knowledge of basic-intermediate chemistry and/or chemical engineering Experience with chemical formulation development Minimum Qualifications: Must have a BS or higher in Chemistry or Chemical Engineering Ability to obtain security clearance Ability to obtain CO State Blasters Permit Benefits: Medical insurance Dental insurance Vision insurance 401(k) with matching Disability insurance Life insurance Paid time off Professional development Flexible schedule

Job Description This position functions primarily in a classified ISO-8 environment and requires the individual to wear appropriate PPE. This position will perform dispensing and formulation operations and perform other duties, such as cleaning, restocking, visual inspection, and labeling, as required and/or assigned. All assigned tasks must be conducted in adherence with all applicable procedures, cGMPs, company policies and any other quality or regulatory (Ex: OSHA, DEA, FDA, etc.) requirements. Facility is a multiple shift operation where variable shifts, including weekends, may be required. Schedule: Tuesday to Friday 3 PM Until 1:30 AM (or until work is completed) Pay: $25/hour SAFETY Strictly adhere to all cGMP, health and safety requirements, procedures, and corporate policies. Authorized to immediately stop any task that is determined to be an imminent hazard. Always promote and demonstrate safe work practices and adhere to PPE requirements. Safely handle chemicals, corrosives, solvents, and other pharmaceutical compounds. Demonstrate physical ability to lift a minimum of 50 lbs. and push/pull pallets, product cans, etc. multiple times per shift. PRIMARY RESPONSIBILITIES: Perform ISO-8 dispensing and formulation operations consistent with established protocols, procedures, and regulatory/cGMP requirements. Learn to utilize all relevant equipment/technology for formulation operations. Complete and document required training to gain proficiency for all assigned job tasks. Accurately and contemporaneously document all actions performed per GDP standards. Assist with classified and non-classified area cleaning and maintenance as required. Perform visual inspection, labeling, and additional support tasks as required. Make recommendations for process improvements. Possess the ability to master multiple processes across different areas. Recognize and respond appropriately to equipment/documentation issues and deviations; obtain appropriate clarification and guidance from leadership before proceeding. Maintain a quality focused, “Right First Time”, attitude. Arrive for work on-time, prepared to work in the classified environment for the majority of each shift. Operate with Integrity by maintaining high ethical standards. Treat all employees with trust, respect, and professionalism. Speak up and hold others accountable for high integrity by providing constructive feedback. Take accountability for individual and team mistakes and participate in related corrective actions. Ensure patient safety by understanding you and your team's impact on product quality. Excel within a diverse and high performing team. Remain open to new ideas and perspectives, communicate across shifts as required, and comply with site process to create a safe work environment. Demonstrate a passion to perform by meeting personal and departmental goals. Self-driven and self-accountable, performs required tasks, and progresses on qualifications within reasonable timelines. Demonstrate innovation abilities by identifying and speaking up about viable options for improvements and exploring and creating a path for implementation. High School Diploma or equivalent. Must pass a drug test. Must speak, write, and read English. Must be a team player. Must have excellent attention to detail. Prior Sterile Compounding and Pharmaceutical Industry experience. Prior experience operating manufacturing equipment/machinery. Knowledge of FDA guidelines, cGMP, and GDP. Willingness to participate in training and gain other certifications as needed. Knowledge of basic arithmetic and chemistry calculations. Ability to work in a fast-paced environment with dynamic priorities and demands. Excellent written and verbal communication skills. Desire to expand knowledge and grow with the company. Leadership ability.

Role and Responsibilities This position is responsible for performing quality control laboratory testing on incoming, in-process and finished products and assisting in laboratory operations. The focus of the position is compliance with regulatory activities and company procedures as they relate to the laboratory department. This position reports to the Laboratory Manager and Director of Quality. Responsibilities include: Conduct chemical and biological testing per Laboratory Operating Procedures (LOPs) and regulatory requirements including microbial sequencing, gram staining, endotoxin, and pH. Maintain daily use, maintenance and cleaning logs for general laboratory areas, equipment, and utensils. Complete routine preventative maintenance of laboratory equipment to ensure accuracy of results. Prepare Certificates of Analysis for Quality review. Perform data entry, trending, and record organization. Support in drafting and reviewing procedures, change controls, risk assessments, deviations and CAPA. Assist in quality duties by performing incubator temperature verification and incoming material inspection. Participate in test method and equipment validations. Ensure compliance to federal and state laws, as well as company standards and specifications. Assists the Quality Laboratory Manager as needed

West Star is the fastest growing maintenance repair organization in the industry and we recognize this is the result of our talented team of trusted employees working together to deliver customer service excellence. We are committed to providing our employees with personal and professional growth opportunities while fostering a culture of respect and well-being with a small company feel. When you join our team we don't think you should have to wait for your benefits to kick in. That's why when you start, they start with you! This includes medical, dental, 401K match, time off accruals, weekly pay days and much more. We don't want you to live to work, we want you to work and live. What you can expect as a Quality Control Inspector at West Star: The Quality Control Inspector maintains West Star Aviation's quality standards in accordance with the West Star Repair Station/Quality Control Manual and the Federal Aviation Regulations. This will be accomplished by working with Aircraft Technicians, Program Managers, Team Leaders, Quality Control and Quality Assurance Inspectors. You will be ESSENTIAL to many FUNCTIONS including: * Maintain West Star Aviation's quality standards by inspecting technician's work, performing "ok to close", and auditing. * Ensure proper sign-offs in Corridor as part of the inspection process. * Participate in daily review meetings. * Assist with Airframe Inspections * Following up with all departments to get steps signed off, inspected, and closed so airframe squawks can be completed. * Help manage Equipment Removal and Installation Log. * Assist QA Department with log research issues to help clear items that are in question. * Daily contact at aircraft with Team Leaders to ensure quality standards are met. * Maintain customer oriented work habits. * Effectively and clearly communicate (i.e., speak, write, read) in English * Any other job-related duties as assigned by supervisor or management. What you'll need to bring with you: Your Education: A High school diploma or equivalent. A&P License or Repairman Certificate will be required. Inspection Authorization (IA) rating is recommended. A valid driver's license approved for airline travel and/or a valid passport is ideal, but not required Your Experience : Familiar with all facets of manuals required to maintain aircraft. Thorough knowledge of FAA regulations. 3 years turbine aircraft inspection experience with return to service authority required. Customer service experience recommended. Follow all company rules and FAA regulations during performance of duties. Maintain customer oriented work habits for oneself and the department. Your Initiative: We're looking for team players who are self-motivated and able to perform in a fast paced environment where working under specific deadlines and time constraints will be common. Being detail oriented, maintaining accuracy and communicating clearly both written and verbally will be needed for success. Your Sense of Responsibility: Attend work every day as scheduled to include overtime and weekend assignments. Notify supervisor in advance of shift starting if unable to work. Must have reliable transportation to get to work each and every day. Enter data and complete entries with high degree of accuracy. Coordinate projects and maintain schedules as required. Ensure good communication with management and personnel on all data needs. Follow all company rules and FAA regulations during performance of duties. Maintain customer oriented work habits for oneself and the department. Actively work to maintain work order system current. Other particulars: Physical Requirements Lift and carry at least 25 lbs. Bend, reach and stoop when around aircraft. Sit at desk and / or computer for extended intervals. Routinely walking. Mental Requirements Prioritize and control work load. Work with others in a professional manner. Work with Quality Department personnel in interpretation and communication of regulations Supervision Work with minimal supervision Working Conditions The majority of work will be performed in a hangar environment which can include both hot and cold temperatures. Some occasional work outside hangars may occur. Equipment Used Computer systems including Corridor Aviation Service software, personal computers operating with Windows, Microsoft Word, Microsoft Excel and various other programs.