Quality control analyst jobs in Las Cruces, NM - 22 jobs

Coordination of Nondestructive Examinations (NDE), Post Weld Heat Treatment (PWHT), Nonconformance Reporting, and distributes Quality documents at the direction of Project Quality Manager or Field Quality Control Manger, and interface with the Owners Team regarding technical issues. Evaluates the qualifications of NDE and PWHT technicians with regard to the activities assigned. Reviews NDE and PWHT reports for conformance and populates the applicable weld management program. Required Qualifications - Essential Skills, Knowledge, and Abilities: •Must have 5+ years of related experiences in the Oil and Gas industry •Must be proficient with Microsoft Office, Word, Excel, PowerPoint, and Bluebeam Revu •Must be able to read and interpret weld procedures, engineering drawings, project specifications •Must have a working knowledge of industry related codes and standards •Must be able to write clearly, accurately, and concisely •Organizational capabilities to plan and schedule inspections and tests •Must have strong problem-solving skills and critical, logical thinking and analysis skills •Must be able to effectively interact with clients •Strong verbal and written communication skills with co-workers and supervisors #LI-KS1 Responsibilities: •Issues the relevant Quality Records and, when necessary, writes and sends to QC Supervisor non-conformances reports •Schedule, review, and log Nondestructive Examinations (NDE), and Post Weld Heat Treatment (PWHT) •Evaluates the qualifications of NDE and PWHT technicians with regard to the activities assigned. •Provide information regarding processes and specifications to craftsmen, supervisors and other appropriate members

Chemist - Entry Level (Must have Chemistry or Biology background) Duration : 12 Months Total Hours/week : 40.00 1st Shift Client: Medical Device Company Level of Experience: Entry Level Employment Type: Contract on W2 (Need US Citizens or GC Holders Only) 1st Shift 8-5PM, : The Scientist (Chemist) is responsible to work with a diverse group of scientists engaged in basic and applied research to provide innovative products and solutions for reducing hospital acquired infections and improving the quality of health care. Responsibilities: Maintain Quality Reports. Maintain and implement efforts in housekeeping, and safety programs. Maintain the cleanliness and orderliness of the laboratory. Prepare solutions and diluents used in the QC Laboratory. Perform simple test like pH, SPG, NVR, etc. Understands and consistently follows multi-step documented procedures while conducting laboratory testing. Receive and maintain inventory for chemicals, glassware, and consumables. Maintains accurate and well-organized laboratory records, notebooks and/or worksheets Sample staging for analysts, label the glassware and vials. Maintenance of the Calibration and Preventive Maintenance programs for laboratory equipment Provide QC support to new product development/Launch/Capacity Expansion projects. Support any Waste Reduction Initiatives that involves QC laboratories. Demonstrate Regulatory Compliance such as FDA inspection readiness, Corporate Audits, Internal Audits and maintain Training Compliance. Demonstrate Safety Compliance such as Strive for Zero Serious Accidents in the QC laboratories, contribute for a successful EH&S Audits with 0 major observations and Contribute for the overall Safety Index plant goal of ?98% Must have awareness and respect of all company policies and safety rules. Maintain appropriate training/certification including GLP and GMP Perform other assigned tasks on as needed basis. Additional Job Description Graduated from a technical carrier related with science 2-5 years in laboratory work. Conversant with GLP/GCP/cGMP and global Drug and Device Development Processes Excellent communication and interpersonal skills Organized and self-motivated

As a 100% employee-owned contractor, when you work at Sundt, you're not just hiring on at a company, you're joining a culture. Because everyone at Sundt is part owner, you'll join a team of people who are deeply invested in their work. From apprentices to managers, we're passionate about the details and deliberate in everything we do. At Sundt we focus on building long-term prosperity for our clients, communities and employee-owners. We offer competitive pay, industry-leading benefits including a 401k and employee stock ownership plan, incentive programs for craft and administrative employees as well as training that focuses on your personal and professional growth. We're driven by skill, grit and purpose. Join us as we strive to be the most skilled builder in America Job Summary Basic Job FunctionsPosition is required to assist in the inspection, acceptance, and/or rejection of work performed in a particular discipline in compliance with applicable codes and/or specifications as dictated by quality programs and/or contract documents and specifications.Structural Inspection:Experience level must fall within the erection of structural steel. Must be able to work in elevated areas. Must have knowledge of AISC, AWS D1.1, and AWS D1.6 Codes. Must have knowledge of bolt?up inspection including bolt lot verifications using Skidmore?Wilhelm. Additionally, must have knowledge of architectural, insulation and lagging, grout and concrete placement, Epoxy anchor installation inspection. Must have CWI (Certified Welding Inspector) certification.Electrical and Instrumentation Inspection:Experience must fall in the installation of electrical and instrumentation components, including interconnecting wiring, cables, and tubing. Must be knowledgeable of ICEA, IEEE, ISA, NEC, NEMA, NESC, and NFPA Codes and standards.Mechanical Inspection:Experience level must fall in the setting and alignment of static and rotating equipment, equipment skids, coolers, tanks, and interconnecting process piping fabrication and installation. Must be able to use measuring tools such as micrometers, calipers, transits, etc. and be able to set up dial indicators and laser alignment devices.Piping Inspection:Experience level must fall in pipe installation inspection, including welding, supports, instrumentation, etc. Must have CWI (Certified Welding Inspector) certification. Key Responsibilities 1. Assists material handling personnel with required material storage and PM requirements as needed. 2. Communicates with others regarding inspections results and recommends corrective procedures. 3. Participates in activities to support the company's strategic planning efforts. 4. Participates in the preparation of Quality control ITP. 5. Performs control measuring and tests equipment. 6. Verifies the installation of the systems, components and equipment in accordance with the assigned discipline. Minimum Job Requirements 1. 1+ year construction practices 2. 1+ year in quality control inspection discipline 3. HS Degree Required 4. Proficient use of all Microsoft Office Suite programs Note: Job Description is subject to change at any time and may include other duties as assigned. Physical Requirements 1. Ability to wear personal protective equipment is required (including but not limited to; steel toed shoes, gloves, safety glasses, hearing protection, hardhat, vest, etc.) 2. May reach above shoulder heights and below the waist on a frequent basis 3. May stoop, kneel, or bend, on an occasional basis 4. May use telephone, computer system, email, or other electronic devices on a limited basis to communicate with internal and external customers or vendors 5. Must be able to comply with all safety standards and procedures 6. Occasionally will climb stairs, ladders, etc. 7. Required to use hands to grasp, lift, handle, carry or feel objects on a frequent basis 8. Will interact with people frequently during a shift/work day 9. Will lift, push or pull objects on an occasional basis 10. Will sit, stand or walk short distances for up to the entire duration of a shift/work day. Safety Level Safety-Sensitive Note: Jobs with the Safety-Sensitive designation are those that include tasks or duties that the employer reasonably believes could affect the safety and health of the employee performing the task or others such as operating a vehicle, operating equipment, operating machinery or power tools, repairing/maintaining the operation of any vehicle/equipment, the handling/disposal/transport of hazardous materials, or the handling/treatment/disposal of potentially flammable/combustible materials. Equal Opportunity Employer Statement: Sundt is committed to the equal treatment of all employees, and/or applicants for employment, and prohibits discrimination based on race, religion, sex (including pregnancy), sexual orientation, gender identity, color, age, disability, national origin, covered veteran status, genetic information; or any other classification protected by applicable Federal, state, or local laws. Benefit list: Market Competitive Salary (paid weekly) Bonus Eligibility based on company, group, and individual performance Employee Stock Ownership Plan & 401K Industry Leading Health Coverage Starting Your First Day Flexible Time Off (FTO) Medical, Health Savings, and Wellness credits Flexible Spending Accounts Employee Assistance Program Workplace Wellness Programs Mental Health Program Life and Disability Insurance Employee-Owner Perks Educational Assistance Sundt Foundation - Charitable Employee-Owner's program #LI-IF1

Coordination of Nondestructive Examinations (NDE), Post Weld Heat Treatment (PWHT), Nonconformance Reporting, and distributes Quality documents at the direction of Project Quality Manager or Field Quality Control Manger, and interface with the Owners Team regarding technical issues. Evaluates the qualifications of NDE and PWHT technicians with regard to the activities assigned. Reviews NDE and PWHT reports for conformance and populates the applicable weld management program.

SummaryJob Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Specialist I - Microbiologist will support El Paso's Quality Control Laboratory by performing microbiological testing on raw materials, in-process and finished products, and stability samples in order to meet increase of customer demand and achieve QC testing delivery goals. Performs microbiological testing on raw materials, in-process and finished products, and stability samples according to applicable procedures. Collects environmental samples and perform analysis according to applicable site procedures. Maintain environmental trending data. Assists in completing project protocols, change notifications, deviation waivers and Quality Notifications with supervision. Performs assigned projects and tasks; compile testing data and review testing results. Maintains Microbiology Laboratory. Order supplies, reagents and materials as needed. Supports equipment maintenance and calibration activities. Understands lab safety and hazardous waste management. Cleans and maintains laboratory areas and equipment according to procedures. Supports investigations and implementation of corrective actions. Responsible for maintaining laboratory logbooks and records according to Good Documentation Practices. Performs Microbiology Lab activities as assigned by lab supervisor and/or Quality Manager/Designee in order to achieve QC testing delivery goals. Maintains Microbiology Lab audit readiness. Other responsibilities of this position include but are not limited to: Complies with all local, state, federal and BD safety regulations, policies/procedures. Complies with all local BD quality policies/procedures/practices through consistent application of sound Quality Assurance principles. Performs other job-related duties as assigned. Qualifications: Bachelor's degree in Microbiology or any related degree is required. 2 years of experience in Microbiology lab in a Pharmaceutical, Biotech/ Aseptic filling environment is preferred. At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. #earlycareer Required Skills Optional Skills . Primary Work LocationUSA TX - El Paso - Northwestern Dr.Additional LocationsWork Shift

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Quality Systems Associate Summary: Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol. Primary responsibilities for role (level-specific responsibilities should be included in the chart below): * Completes weekly review of equipment QC and maintenance records. * Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they related to product quality and/or donor safety. * Inspects and releases incoming supplies. Investigates and reports supplies have not met quality specifications and requirements prior to use. * Performs documentation review for unsuitable test results. * Assists the Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed. Duties include: * Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol. * Performs all product release activities. * Reviews lookback information and documentation. * Reviews waste shipment documentation. * Reviews unexpected plasmapheresis events including electronic donor chart and related documentation pertaining to exceptions occurring during the donation process. * Reviews electronic donor chart exceptions impacting donor eligibility/safety and/or product quality. * Reviews donor deferral notifications from competitor centers. * Reviews plasma processing documentation to ensure the proper freezing, storage and handling of product. Quality Systems Associate * Assist the Quality Systems Manager to ensure center training programs follow procedural requirements as defined in the donor center SOP and/or training programs documents. Duties include: * Creates, maintains, and audits training records and files to ensure compliance. * Performs employee training observations to ensure staff competency prior to releasing employees to work independently. * Conducts required training activities for Center Notifications, Corporate Directives, SOP changes, and initial SOP implementations. * On an occasional basis, when the Quality Systems Manager is absent, the Quality Systems Associate may be required to perform the following duties: * Reviews and approves of deferred donor reinstatement activities. * Assists with completion of the internal donor center audit. Summary: * Performs review of monthly trending report. * Performs review of donor adverse events reports and the applicable related documentation. * Conducts training to address donor center corrective and preventative measures. This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed. Additional Responsibilities: Is certified and maintains certification as a Donor Center Technician. Knowledge, Skills, and Abilities: Developing command of interpersonal communication, organizational and problem-solving skills. Ability to understand FDA regulations. Strong integrity and commitment to quality and compliance. Good knowledge of mathematics. Legible handwriting. Proficiency with computers. Ability to work flexible scheduling to meet business needs. Performs basic document review and employee observations. Communicates openly with the CQM on issues noted during reviews. Ability to understand and follow SOP's and protocols. Ability to perform primary responsibilities of the Quality Associate role in a proficient manner. Has a basic understanding of cGMP and quality systems. Is able to spend hours sitting and reviewing documentation for accuracy. Demonstrates good organizational skills and attention to detail. Education: High school diploma or GED. Obtains state licensures or certifications if applicable. Experience: Typically requires no previous related experience. Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups. #biomatusa Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws. Location: NORTH AMERICA : USA : TX-El Paso:USEP7 - El Paso TX-N Loop Dr-TPR

Job Purpose: Inspects finished products, products being processed, incoming materials, parts, and assemblies for conformance to company standards. Conducts routine and non-routine analysis of raw materials, in process and finished product, using a variety of testing devices and procedures to maintain product quality. Responsibilities include but are not limited to the following: This position is for a 2nd shift only! Proficient in the use of Inspection tools such as caliper, micrometer, height gage, optical comparator, pin and thread gages. Ability to determine if components meet specifications according to a 2D drawing. Ability to run programmed components and follow documented procedures using the CMM (Coordinate Measurement Machine) Able to make manual measurements using the CMM, such as hole locations and flatness Accept help and have the ability to learn from Senior Quality Technicians and engineering Document inspection results using FMP (receiving inspection reports, FA reports, NCMR) Post accepted components into inventory using Mass 500. Maintain proper part count for inventory control. Basic knowledge of products and production processes Follows Inspection Processes and procedures Understands all aspects of GCX quality guidelines and expectations Represent Quality Assurance during VOC inspection of finished goods Job Requirements: Ability to read and understand complex blueprints. Ability to accurately measure parts using precision hand tools. Strong communication skills. (Written and verbal English) Strong attention to details. Basic computer literacy (Microsoft Excel, Word, etc.) Basic Math & Analytic Skills.

Job Description At Stampede Culinary Partners in Sunland Park, NM, we don't just offer jobs-we offer careers with purpose. When you become our full-time Food Quality Control Technician, you'll be a key player in ensuring the safety, quality, and consistency of our products. We offer: Competitive pay Health, dental, and vision insurance HSA/FSA options Short- and long-term disability coverage (STD/LTD) Life and AD&D insurance Accident insurance Group hospital indemnity insurance Pet insurance 401(k) with company match Pension plan after 1 year Floating holidays Mental health support program Employee discounts on meat and veggies Event BBQs and recognition programs On-site parking and bus route access SCHEDULE: This is a full-time 2nd shift position, working Monday through Friday from 2 PM to 10 PM, with frequent overtime opportunities based on production needs. DAY-TO-DAY: As our Food Quality Control Technician, you are the last line of defense between our products and the customers who trust us. Your day starts with pre-operational inspections to ensure the production lines are ready. You'll be responsible for monitoring product quality, conducting tests on seasonings, batters, breading, and marinades, and randomly pulling products off the line to check weight, length, and thickness against customer specifications. Every hour, you'll perform metal detection checks, box weight tracking, and organoleptic testing (cooking and tasting products) to guarantee that our food meets safety and quality standards. You'll manage critical documentation, work closely with U.S.D.A. and S.S.O.P. requirements, and train backup QC Technicians to ensure seamless operations. Your role also includes enforcing GMP practices across the plant and participating in weekly QA meetings to stay ahead of industry developments. Every decision you make protects our brand's reputation and ensures our customers receive only the best. Your work truly matters. QUALIFICATIONS: Proficiency with computers Adherence to quality and safety guidelines Physical ability to stand, walk, kneel, and lift up to 25 lbs in a cold, loud, and fast-moving production environment Basic math skills with the ability to use a calculator to determine percentages and averages Great communications skills, both written and verbal Strong organization and time management skills Team player Experience in the food industry is preferred but not required for this Food Quality Control Technician role. JOIN US! Stampede Culinary Partners, Inc. is an innovative protein solutions company that focuses on custom protein development and processing. Our customers include leading restaurants, top retailers, leading food service distributors, home delivery customers, and other emerging segments. The ability to satisfy our mission depends largely on our greatest asset, our employees! Our company culture is built on the expertise and experience of all our employees and driven by the 5 pillars that we hold ourselves to daily: perform passionately, challenge directly and respectfully, commit to teamwork, and embrace innovation. Ready to become our Food Quality Control Technician? Just fill out the initial 3-minute, mobile-friendly application! Job Posted by ApplicantPro

Manufacturing company located in east El Paso is looking for a QC Inspector. General Purpose: The function of the QC Inspector is to check the quality of all incoming and outgoing product or materials against company specifications. Work closely with other departments to receive and ship components to ensure all parts are within the customer's acceptance level, including but not limited to paperwork accuracy, shipment integrity and on-time delivery. Perform random inspections to assess the quality of the product and document accuracy. Remove product or materials from the warehouse that do not meet the standards and recommend strategies to improve product quality. Recommend any necessary adjustments and changes to existing processes to make them more efficient and accurate. Assist in identifying root cause analysis and action plan to address non-conformities found during inspections. Provide timely and accurate reports of non-conformities to the appropriate escalation team to prevent the shipment of non-complying parts. Involvement in continuous improvement initiatives including reviewing of work instructions vs actual performance and help in training other employees on quality standards. Education / Experience: High School diploma or GED plus one year related experience and/or training; or equivalent. $15.50/hr. Position could become full time with the company.

We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a **maker of possible** with us. **Specialist I** - Microbiologist will support El Paso's Quality Control Laboratory by performing microbiological testing on raw materials, in-process and finished products, and stability samples in order to meet increase of customer demand and achieve QC testing delivery goals. + Performs microbiological testing on raw materials, in-process and finished products, and stability samples according to applicable procedures. + Collects environmental samples and perform analysis according to applicable site procedures. Maintain environmental trending data. + Assists in completing project protocols, change notifications, deviation waivers and Quality Notifications with supervision. + Performs assigned projects and tasks; compile testing data and review testing results. + Maintains Microbiology Laboratory. Order supplies, reagents and materials as needed. + Supports equipment maintenance and calibration activities. + Understands lab safety and hazardous waste management. + Cleans and maintains laboratory areas and equipment according to procedures. + Supports investigations and implementation of corrective actions. + Responsible for maintaining laboratory logbooks and records according to Good Documentation Practices. + Performs Microbiology Lab activities as assigned by lab supervisor and/or Quality Manager/Designee in order to achieve QC testing delivery goals. + Maintains Microbiology Lab audit readiness. **Other responsibilities of this position include but are not limited to:** + Complies with all local, state, federal and BD safety regulations, policies/procedures. + Complies with all local BD quality policies/procedures/practices through consistent application of sound Quality Assurance principles. + Performs other job-related duties as assigned. **Qualifications:** + Bachelor's degree in Microbiology or any related degree is required. + 2 years of experience in Microbiology lab in a Pharmaceutical, Biotech/ Aseptic filling environment is preferred. At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. **Why Join Us?** A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. \#earlycareer Required Skills Optional Skills . **Primary Work Location** USA TX - El Paso - Northwestern Dr. **Additional Locations** **Work Shift** Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

Quality Control Coordinator would be primarily responsible for managing, controlling, and instancing required documents for Quality Department. This role will be tasked with ensuring that the electronic version of all required documentation is reviewed, compiled, and saved in the CCZJV (I-Docs/Co-Console) databases(s). Also, performing ITP, ITR GAP Analysis.

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. **Quality Systems Associate** Summary: Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol. Primary responsibilities for role (level-specific responsibilities should be included in the chart below): + Completes weekly review of equipment QC and maintenance records. + Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they related to product quality and/or donor safety. + Inspects and releases incoming supplies. Investigates and reports supplies have not met quality specifications and requirements prior to use. + Performs documentation review for unsuitable test results. + Assists the Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed. Duties include: + Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol. + Performs all product release activities. + Reviews lookback information and documentation. + Reviews waste shipment documentation. + Reviews unexpected plasmapheresis events including electronic donor chart and related documentation pertaining to exceptions occurring during the donation process. + Reviews electronic donor chart exceptions impacting donor eligibility/safety and/or product quality. + Reviews donor deferral notifications from competitor centers. + Reviews plasma processing documentation to ensure the proper freezing, storage and handling of product. Quality Systems Associate + Assist the Quality Systems Manager to ensure center training programs follow procedural requirements as defined in the donor center SOP and/or training programs documents. Duties include: + Creates, maintains, and audits training records and files to ensure compliance. + Performs employee training observations to ensure staff competency prior to releasing employees to work independently. + Conducts required training activities for Center Notifications, Corporate Directives, SOP changes, and initial SOP implementations. + On an occasional basis, when the Quality Systems Manager is absent, the Quality Systems Associate may be required to perform the following duties: + Reviews and approves of deferred donor reinstatement activities. + Assists with completion of the internal donor center audit. Summary: + Performs review of monthly trending report. + Performs review of donor adverse events reports and the applicable related documentation. + Conducts training to address donor center corrective and preventative measures. This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed. Additional Responsibilities: Is certified and maintains certification as a Donor Center Technician. Knowledge, Skills, and Abilities: Developing command of interpersonal communication, organizational and problem-solving skills. Ability to understand FDA regulations. Strong integrity and commitment to quality and compliance. Good knowledge of mathematics. Legible handwriting. Proficiency with computers. Ability to work flexible scheduling to meet business needs. Performs basic document review and employee observations. Communicates openly with the CQM on issues noted during reviews. Ability to understand and follow SOP's and protocols. Ability to perform primary responsibilities of the Quality Associate role in a proficient manner. Has a basic understanding of cGMP and quality systems. Is able to spend hours sitting and reviewing documentation for accuracy. Demonstrates good organizational skills and attention to detail. Education: High school diploma or GED. Obtains state licensures or certifications if applicable. Experience: Typically requires no previous related experience. **Occupational Demands Form # 70:** Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups. \#biomatusa Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. **Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.** **Location: NORTH AMERICA : USA : TX-El Paso:USEP7 - El Paso TX-N Loop Dr-TPR** Learn more about Grifols (************************************** **Req ID:** 537936 **Type:** Regular Full-Time **Job Category:** MANUFACTURING

Maintain Quality Reports. Perform chemical analysis on drug products and incoming raw materials. Maintain and implement efforts in housekeeping, and safety programs. Maintenance of the Calibration program for laboratory equipment. Responsible for Chemistry and Life-sciences related disciplines performing basic and applied research to provide innovative solutions for reducing hospital acquired infections and improving the quality of health care Has an academic background and hands on laboratory training in the field of Chemistry or Biological Sciences Understands and consistently follows multi-step documented procedures while conducting laboratory research Has hands on experience with USP/ISO/ASTM based chemical testing and performs all testing with strict adherence to the written laboratory work instructions Understands the validation principles for chemical methods, develops and validates new chemical test methods, and prepares study reports Maintains accurate and well-organized laboratory records, notebooks and/or worksheets Use theoretical knowledge to interpret data and to trouble-shoot experiments Maintain assigned aspects of the chemistry laboratory work to provide material and technical support to scientific staff With moderate or no supervision, apply comprehensive understanding of defined productivity goals and objectives Maintain appropriate training/certification including GLP and GMP Knowledge of FDA regulations for drugs and device desirable Perform other assigned tasks on as needed basis Must have awareness and respect of all company policies and safety rules.

The Quality Completions Inspector is the person who conducts the systems completion walk downs and supports Completions on punch list items, walk downs, and engineering changes. This is a skilled position with detailed knowledge of their specific craft and job specifications. This person will be working with QC, document controls, and the craft to make sure items in the field are installed per drawing and specification. Responsibilities Qualifications: 3+ years' experience as a journeyman 3 years industrial construction experience 2-3 years in Petrochemical or Oil & Gas Computer Competency (Microsoft Office), Completions Database experience General discipline competencies with Civil, Underground Work, Structural, and Buildings Discipline Specific Qualifications: Mechanical Piping Mechanical Stationary Equipment Rotating Equipment Welding I&E Instrumentation Electrical Job functions: Walk down systems and subsystems for completeness and identify any discrepancies Identify any field installed Vs. drawing differences Verify completed punch list items Participate in client and commissioning walk downs Qualifications Essential Skills, Knowledge, and Abilities: Demonstrated Industrial Construction experience Organization and time management Good decision-making abilities Able to troubleshoot and come up with solutions Ability to work with others - team player Good communication skills with co-workers and subordinates Construction and commissioning knowledge Preferred Qualifications: Bachelor's degree in a construction or technology related field Prior turnover experience Prior commissioning experience #LI-KS1

Job Description Stampede Culinary Partners is seeking a full-time Morning Food Quality Control Tech to join our team in Sunland Park, NM. In this full-time, hourly position, you will play a crucial role in maintaining our commitment to producing high-quality food products. WHY SHOULD YOU JOIN US? This Morning Food Quality Control Tech role offers a structured work environment, opportunities for growth, and the chance to contribute to a team dedicated to excellence in food safety and quality control. We also offer great benefits, such as: Competitive pay Health, dental, and vision insurance HSA/FSA options Short- and long-term disability coverage (STD/LTD) Life and AD&D insurance Accident insurance Group hospital indemnity insurance Pet insurance 401(k) with company match Pension plan after 1 year Floating holidays Mental health support program Employee discounts on meat and veggies Event BBQs and recognition programs On-site parking and bus route access WHO ARE WE? Stampede Culinary Partners, Inc. is an innovative protein solutions company that focuses on custom protein development and processing. Our customers include leading restaurants, top retailers, leading food service distributors, home delivery customers, and other emerging segments. The ability to satisfy our mission depends largely on our greatest asset, our employees! Our company culture is built on the expertise and experience of all our employees and driven by the 5 pillars that we hold ourselves to daily: perform passionately, challenge directly and respectfully, commit to teamwork, and embrace innovation. WHAT ARE THE HOURS? This is a morning shift position from 4:30 am to 12:30 pm. WHAT DOES YOUR DAY ENTAIL? As a Morning Food Quality Control Tech, you will be responsible for ensuring that all U.S.D.A. and S.S.O.P. documentation is properly handled and maintained. Your daily tasks will include conducting tests on seasonings, batters, breadings, and marinades to ensure product consistency and compliance with established standards. You will also conduct randomized product checks, monitoring weight, length, and thickness to confirm that production aligns with customer specifications. Additionally, you will perform hourly product pickups, metal detection checks, and box weight tracking while also conducting organoleptic testing (cooking and evaluating product quality). Monitoring and enforcing Good Manufacturing Practices (GMPs) will be a key responsibility, as well as performing pre-operational inspections and assisting in training backup Quality Control Technicians. Participation in weekly QA meetings will provide the opportunity to collaborate with the team on industry developments, customer feedback, and process improvements. WHAT WE ARE LOOKING FOR IN A MORNING FOOD QUALITY CONTROL TECH Strong organizational skills and the ability to complete tasks in a timely manner Excellent communication skills, written and verbal Basic math skills and the ability to use a calculator for determining percentages and averages Adherence to quality and safety guidelines Physical capability to stand, walk, kneel, and lift up to 25 lbs in a cold, loud, and fast-moving production environment Experience in the food industry is preferred. If you are looking for a role where you can contribute to food quality and safety in a professional environment, we encourage you to apply today. Complete our 3-minute, mobile-friendly initial application to take the next step with us. Job Posted by ApplicantPro

Maintain Quality Reports. Perform chemical analysis on drug products and incoming raw materials. Maintain and implement efforts in housekeeping, and safety programs. Maintenance of the Calibration program for laboratory equipment. Responsible for Chemistry and Life-sciences related disciplines performing basic and applied research to provide innovative solutions for reducing hospital acquired infections and improving the quality of health care Has an academic background and hands on laboratory training in the field of Chemistry or Biological Sciences Understands and consistently follows multi-step documented procedures while conducting laboratory research Has hands on experience with USP/ISO/ASTM based chemical testing and performs all testing with strict adherence to the written laboratory work instructions Understands the validation principles for chemical methods, develops and validates new chemical test methods, and prepares study reports Maintains accurate and well-organized laboratory records, notebooks and/or worksheets Use theoretical knowledge to interpret data and to trouble-shoot experiments Maintain assigned aspects of the chemistry laboratory work to provide material and technical support to scientific staff With moderate or no supervision, apply comprehensive understanding of defined productivity goals and objectives Maintain appropriate training/certification including GLP and GMP Knowledge of FDA regulations for drugs and device desirable Perform other assigned tasks on as needed basis Must have awareness and respect of all company policies and safety rules.

The Quality Completions Inspector is the person who conducts the systems completion walk downs and supports Completions on punch list items, walk downs, and engineering changes. This is a skilled position with detailed knowledge of their specific craft and job specifications. This person will be working with QC, document controls, and the craft to make sure items in the field are installed per drawing and specification. Essential Skills, Knowledge, and Abilities: Demonstrated Industrial Construction experience Organization and time management Good decision-making abilities Able to troubleshoot and come up with solutions Ability to work with others - team player Good communication skills with co-workers and subordinates Construction and commissioning knowledge Preferred Qualifications: Bachelor's degree in a construction or technology related field Prior turnover experience Prior commissioning experience #LI-KS1 Qualifications: 3+ years' experience as a journeyman 3 years industrial construction experience 2-3 years in Petrochemical or Oil & Gas Computer Competency (Microsoft Office), Completions Database experience General discipline competencies with Civil, Underground Work, Structural, and Buildings Discipline Specific Qualifications: Mechanical Piping Mechanical Stationary Equipment Rotating Equipment Welding I&E Instrumentation Electrical Job functions: Walk down systems and subsystems for completeness and identify any discrepancies Identify any field installed Vs. drawing differences Verify completed punch list items Participate in client and commissioning walk downs

At Stampede Culinary Partners in Sunland Park, NM, we don't just offer jobs-we offer careers with purpose. When you become our full-time Food Quality Control Technician, you'll be a key player in ensuring the safety, quality, and consistency of our products. We offer: Competitive pay Health, dental, and vision insurance HSA/FSA options Short- and long-term disability coverage (STD/LTD) Life and AD&D insurance Accident insurance Group hospital indemnity insurance Pet insurance 401(k) with company match Pension plan after 1 year Floating holidays Mental health support program Employee discounts on meat and veggies Event BBQs and recognition programs On-site parking and bus route access SCHEDULE: This is a full-time 2nd shift position, working Monday through Friday from 2 PM to 10 PM, with frequent overtime opportunities based on production needs. DAY-TO-DAY: As our Food Quality Control Technician, you are the last line of defense between our products and the customers who trust us. Your day starts with pre-operational inspections to ensure the production lines are ready. You'll be responsible for monitoring product quality, conducting tests on seasonings, batters, breading, and marinades, and randomly pulling products off the line to check weight, length, and thickness against customer specifications. Every hour, you'll perform metal detection checks, box weight tracking, and organoleptic testing (cooking and tasting products) to guarantee that our food meets safety and quality standards. You'll manage critical documentation, work closely with U.S.D.A. and S.S.O.P. requirements, and train backup QC Technicians to ensure seamless operations. Your role also includes enforcing GMP practices across the plant and participating in weekly QA meetings to stay ahead of industry developments. Every decision you make protects our brand's reputation and ensures our customers receive only the best. Your work truly matters. QUALIFICATIONS: Proficiency with computers Adherence to quality and safety guidelines Physical ability to stand, walk, kneel, and lift up to 25 lbs in a cold, loud, and fast-moving production environment Basic math skills with the ability to use a calculator to determine percentages and averages Great communications skills, both written and verbal Strong organization and time management skills Team player Experience in the food industry is preferred but not required for this Food Quality Control Technician role. JOIN US! Stampede Culinary Partners, Inc. is an innovative protein solutions company that focuses on custom protein development and processing. Our customers include leading restaurants, top retailers, leading food service distributors, home delivery customers, and other emerging segments. The ability to satisfy our mission depends largely on our greatest asset, our employees! Our company culture is built on the expertise and experience of all our employees and driven by the 5 pillars that we hold ourselves to daily: perform passionately, challenge directly and respectfully, commit to teamwork, and embrace innovation. Ready to become our Food Quality Control Technician? Just fill out the initial 3-minute, mobile-friendly application!

The Quality Completions Inspector is the person who conducts the systems completion walk downs and supports Completions on punch list items, walk downs, and engineering changes. This is a skilled position with detailed knowledge of their specific craft and job specifications. This person will be working with QC, document controls, and the craft to make sure items in the field are installed per drawing and specification.