quality control technician

Interstate Testing Services

<div>Location: St. Louis 
Interstate Testing Services, a well respected construction materials testing lab, is seeking highly motivated individuals for full time employment. Quality Control Materials Technician positions are open in the field of Aggregates, Concrete, and Hot Mix Asphalt testing. A working knowledge of AASHTO, ASTM, and MoDot standards as well as MoDot technician and or ACI certifications is a plus. Multiple positions are open with varying levels of materials testing experience. 
Good communication and computer skills (Microsoft Office) required. 
Projects and labs are located throughout the state of Missouri and some overnight travel and night work will be required.</div>

Quality Control Materials Technician

cGMP CONSULTING

<div>Job Summary
cGMP Consulting is seek an experienced Metrology Technician to support the Metrology Department in a GMP Manufacturing Facility. This position is responsible for maintaining, calibrating, and troubleshooting measurement instruments used in manufacturing processes and quality control, create calibration reports and maintain calibration records within an electronic system. Additionally, the position is responsible for ensuring accuracy and compliance within GMP regulations.
Responsibilities<ul><li>
Perform routine calibration of measurement instruments (temperature, pressure, weight, flow, etc.) to ensure accuracy.</li><li>
Maintain calibration records in accordance with GMP, FDA, and ISO standards. Ensure all instruments meet regulatory requirements.</li><li>
Diagnose and resolve issues with metrology equipment, coordinating repairs when necessary.</li><li>
Conduct validation studies to confirm instrument reliability and accuracy.</li><li>
Identify opportunities to enhance calibration procedures and improve measurement accuracy.</li><li>
Work with engineers, quality assurance teams, and production staff to ensure measurement consistency.</li><li>
Provide guidance on metrology best practices and assist in audits related to measurement systems.</li></ul>
Requirements<ul><li>
Associates degree in Engineering or a relevant discipline, or trade qualification plus 2-4 years experience in a GMP Facility.</li><li>
Calibration and troubleshooting skills.</li><li>
Knowledge of Good Manufacturing Practices (GMP).</li><li>
Strong attention to detail and accuracy.</li><li>
Ability to work independently and as part of a team.</li></ul>
Compensation and Benefits<ul><li>
Expected pay range per year: $25-30 USD/Hour</li><li>
Expected benefits include: Medical, Dental, Vision, PTO, 401K</li></ul>
HmveQB3uk1</div>

Metrology Technician

CooperCompanies

<div>About CooperSurgical: 
 
CooperSurgical is a leading fertility and women&rsquo;s healthcare company dedicated to putting time on the side of women, babies, and families at the healthcare moments that matter most in life. As a division of CooperCompanies, we're driven by a unified purpose to enable patients to experience life's beautiful moments. Guided by our shared values &ndash; dedicated, innovative, friendly, partners, and do the right thing &ndash; our offerings support patients throughout their lifetimes, from contraception to fertility and birth solutions, to women&rsquo;s and family care, and beyond. We currently offer over 600 clinically relevant medical devices to healthcare providers, including testing and treatment options, as well as an innovative suite of assisted reproductive technology and genomic testing solutions. Learn more at www.coopersurgical.com.
Job Summary:
Quality Control Lab Technician I role at Cord Blood Registry (CBR) is responsible for analyzing and documenting test results from our cord blood and cord tissue processed samples, releasing raw materials, supporting the analytical and processing equipment maintenance program, conducting environmental monitoring, and providing a wide range of critical functions that support the cryogenic storage of our client's final product. This position is also responsible for providing our internal customers with technical expertise while maintaining the highest quality services possible. The Quality Control Lab Technician I directly supports manufacturing to ensure the Product Operations function is provided with adequate equipment and materials to support stem cell processing activities. At the Technician I level, the individual performs critical daily activities involving high complexity testing, equipment maintenance and troubleshooting, interfacing with service providers, reagent testing, executing quality control assays and environmental monitoring activities. The role is also involved with supporting and executing validations, verifications, and projects within the Quality Control department.</div>
 <div></div>
 The Quality Control Lab Technician I directly supports manufacturing to ensure the Product Operations function is provided with adequate equipment and materials to support stem cell processing activities. At the Technician I level, the individual performs critical daily activities involving high complexity testing, equipment maintenance and troubleshooting, interfacing with service providers, reagent testing, executing quality control assays and environmental monitoring activities. The role is also involved with supporting and executing validations, verifications, and projects within the Quality Control department.
 <div>Qualifications
Knowledge, Skills and Abilities:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Language Skills:
<ul><li>Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of employees of organization.
</li></ul>Mathematical Skills:
<ul><li>Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute, rate, ratio, and percent and to draw and interpret bar graphs.
</li></ul>Reasoning Ability:
<ul><li>Ability to apply common sense understanding to carry out instructions furnished in written oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations.
</li></ul>Computer Skills:
<ul><li>Requires complete and broad knowledge of operating systems, techniques, and practices typically learned through extensive experience and/or education. Must be proficient in Microsoft applications: Excel, Word, Outlook.
</li></ul>Physical Demands:
<ul><li>The physical demands described here are representative of those that must be met by an employee 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; use hands to finger, handle or feel, and talk or hear. The employee is frequently required to walk; sit and reach with hands and arms. The employee is occasionally required to stoop and kneel. The employee must frequently lift and/or move up to 50 pounds. On occasion, employee must frequently lift and/or move up to 100 pounds with assistance. Specific vision abilities required by this job include close vision, distance vision, and ability to adjust focus.
</li></ul>Teamwork:
<ul><li>Leads by example to maintain positive attitude and collegial work environment. Provides and is receptive to constructive feedback. Assist other team members as needed to accomplish the days or department tasks.
</li></ul>Work Environment:
Schedule/Work Hour Requirement:
<ul><li>This is an onsite position in Tucson, AZ
</li><li>Work hours are dictated by the requirements of the business. As business needs dictate, works extended hours to complete daily department goals or tasks to include mandatory overtime. Able to work mid-shifts, weekends and holidays. Required to be 'on-call' periodically.
</li></ul>Exposure Risk:
<ul><li>A requirement of this role is working with blood products and tissue. Safeguards are implemented for employees to protect them from exposure to blood products and tissue.
</li></ul>Clinical Laboratory Improvement Amendments (CLIA) Responsibilities and Qualifications:
<ul><li>This role requires to take on additional roles to perform High Complexity testing (example: Testing Personnel, General Supervisor) and/or perform additional functions (example: high complexity testing) that are regulated by Clinical Laboratory Improvement Amendments (CLIA). In such cases, the Laboratory Director and General Supervisor shall determine eligibility based on additional requirements such as: Internal company and CLIA baseline education, training and experience.
</li></ul>Experience:
<ul><li>One year of lab experience is preferred.
</li></ul>Education:
<ul><li>Bachelor's degree in one of the biological, chemical, or physical sciences.
</li>Transcripts are required to be eligible for the position. 
<li>
</li></ul>As an employee of CooperSurgical, you'll receive an outstanding total compensation plan. As we believe your compensation goes beyond your paycheck, we offer a great compensation package, medical coverage, 401(k), parental leave, fertility benefits, paid time off for vacation, personal, sick and holidays, and multiple other perks and benefits. Please visit us at www.coopersurgical.com to learn more about CooperSurgical and the benefits of becoming a member of our team.
To all agencies: Please, no phone calls or emails to any employee of CooperSurgical about this opening. All resumes submitted by search firms/employment agencies to any employee at CooperSurgical via-email, the internet or in any form and/or method will be deemed the sole property of CooperSurgical, unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in place. In the event a candidate who was submitted outside of the CooperSurgical agency engagement process is hired, no fee or payment of any kind will be paid.
We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace.</div>
 <div>Essential Duties and Responsibilities:
<ul><li>Adhere to CBR corporate and Quality Control policies
</li><li>Ensure all work performed strictly adheres to CGLP/CGMP
</li><li>Exercise Good Documentation Practices (GDP)
</li><li>Use company Quality Management System (QMS), Laboratory Information System (LIS), equipment
</li><li>management software, environmental monitoring software
</li><li>Work in a biosafety level 2 (BSL-2) work environment
</li><li>Complete and maintain records that meet regulatory requirements
</li><li>Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance
</li><li>Follow the laboratory's procedures for specimen handling and processing, reagent preparation, test analyses, reporting and maintaining records
</li><li>Notify management and initiates discrepant events in the applicable quality system
</li><li>Participate in training, projects, housekeeping, and other related activities
</li><li>Train on a broad range of laboratory support functions and procedures as assigned, demonstrating expertise in technical skills and procedures within assigned discipline area (s) including analytical, bioanalytical and microbiological responsibilities
</li><li>Provide support during peer training
</li><li>Assist with lab investigations, deviations, corrective actions, procedure changes, method qualification planning,
</li><li>etc.
</li><li>Support Research and Development projects
</li><li>Support the CBR stability program
</li><li>Support material purchase ordering activities
</li><li>Support material inspection and release activities
</li><li>Support the everyday organization of the Microbiology laboratory activities including area cleaning, maintenance and ordering of supplies
</li><li>Support biorepository activities
</li><li>Handle Liquid Nitrogen (LN2) utilizing personal protective equipment and good safety practices Perform proficiency testing and participate in competency assessments
</li><li>Perform equipment calibration, preventive maintenance and repairs
</li><li>Perform data trending
</li><li>Prioritize and organize work to deliver assignments according to established schedules and deadlines Communicate in a manner that fosters cooperation and creates a safe environment for those involved Provide audit preparation support activities
</li><li>Familiarity with basic statistical tools to analyze data in relation to trends results
</li><li>Capable of routinely multi-tasking
</li><li>Problem solving and troubleshooting
</li><li>Make informed and timely decisions independently
</li><li>Apply common sense understanding when working independently on departmental projects, timelines and dealing with compliance issues
</li><li>Wear appropriate Personal Protective Equipment (PPE)
</li><li>Maintain donor, client, and employee confidentiality
</li><li>Provide administrative support: copying, filing, and archiving records
</li><li>Respond to environmental monitoring alarms</li></ul></div> <div></div>

Laboratory Services Quality Technician I

Cummins India

<div>
 
 Description
 
 
 
 
 Job Summary
 
 
 
 
 ON-SITE Role
 
 
 
 The Quality Technician &ndash; Level III supports Engineers in carrying out production-related and inspection activities, monitors material quality in processing plants, and makes required adjustments to maintain product standards. The role is responsible for conducting measurements, tests, and evaluations to ensure components, materials, and equipment meet technical specifications. This position also ensures accurate documentation, record maintenance, and proper calibration of test and measurement equipment, working under minimal supervision.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Compare physical characteristics of components, materials, equipment, and products to technical specifications to identify defects.
 </li>
 <li>
 Conduct simple tests (e.g., electrical function, reliability, packaging quality) and record results.
 </li>
 <li>
 Prepare simple technical reports based on test outcomes.
 </li>
 <li>
 Perform product and component testing using a variety of measurement equipment.
 </li>
 <li>
 Provide advanced programming, training, and operation of measurement and test equipment.
 </li>
 <li>
 Assist customers in interpreting product specifications and applying measurement data.
 </li>
 <li>
 Participate in measurement uncertainty studies related to calibration and measurement results.
 </li>
 <li>
 Ensure proper maintenance, calibration, and accuracy of all measurement and test equipment.
 </li>
 <li>
 Support quality processes and apply quality tools/methods to ensure compliance with standards.
 
 
 </li>
 </ul>
 
 Responsibilities
 
 
 
 
 Core Competencies
 
 
 
 <ul>
 <li>
 Action Oriented: Tackles new opportunities and challenges with urgency, high energy, and enthusiasm.
 </li>
 <li>
 Collaborates: Works effectively with others to achieve shared objectives.
 </li>
 <li>
 Communicates Effectively: Delivers clear, audience-specific communication.
 </li>
 <li>
 Customer Focus: Builds strong relationships and delivers customer-centric solutions.
 </li>
 <li>
 Decision Quality: Makes timely, effective decisions that move the organization forward.
 </li>
 <li>
 Manages Conflict: Resolves conflicts constructively with minimal disruption.
 </li>
 <li>
 Resourcefulness: Efficiently secures and deploys resources.
 </li>
 <li>
 Measurement Science: Applies metrology principles across relevant fields (chemical, dimensional, electrical, mechanical, optical, radiation, and physical).
 </li>
 <li>
 Quality Process Management: Applies quality tools and methods (e.g., APQP, FMEA, PPAP, SPC, capability studies, process audits, inspection, testing).
 </li>
 <li>
 Values Differences: Leverages diverse perspectives and cultural backgrounds.
 </li>
 <li>
 Laboratory Management: Oversees technical and business aspects of laboratory operations, ensuring compliance with relevant certifications/accreditations.
 
 
 </li>
 </ul>
 
 Education, Licenses, and Certifications
 
 
 
 <ul>
 <li>
 High school diploma or equivalent; relevant technical certifications preferred.
 </li>
 <li>
 Compliance with export controls or sanctions regulations may require specific licensing.
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 Significant relevant work experience or specialized skills gained through education, training, or on-the-job experience.
 </li>
 <li>
 Knowledge of Cylinder Block &amp; Cylinder Head casting and machining processes .
 </li>
 <li>
 Preferred: Experience in metallurgy lab operations .
 </li>
 <li>
 Additional Advantage: Hands-on experience with Millipore testing of Engine Components
 </li>
 <li>
 Availability for rotational shifts .
 </li>
 <li>
 Competence in quality documentation and reporting.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 Skills
 
 
 
 <ul>
 <li>
 Proficiency in quality inspection and testing methodologies.
 </li>
 <li>
 Strong understanding of measurement equipment and calibration standards.
 </li>
 <li>
 Ability to interpret and apply technical specifications.
 </li>
 <li>
 Effective troubleshooting and problem-solving skills.
 
 
 </li>
 </ul>
 
 Job
 
 Quality
 
 
 
 Organization
 
 Cummins Inc.
 
 
 
 Role Category
 
 On-site
 
 
 
 Job Type
 
 Shop
 
 
 
 ReqID
 
 2418470
 
 
 
 Relocation Package
 
 Yes
</div>

Quality Technician - Level III

Ajinomoto

<div>Position Summary:
<div>
Ajinomoto Foods North America is a leading frozen foods company, committed to providing nutritious and delicious meals globally. With a rich history of diverse ethnic brands, our brands have become household favorites all across America. We are dedicated to contributing to a healthier lifestyle through nutritious and balanced Umami foods. With a commitment to excellence and innovation, all our products are cooked with our customers in mind, providing healthy and delicious meals for all.</div><div></div><div> 
We are looking for a FSQA Technician to join our rapidly expanding team in the Portland areas. The FSQA Technician is critical to the food safety of the products being delivered to our customers. The Tech will primarily be checking and verifying products at all stages of production. In addition, they will be responsible for analysis of product for food safety and food quality.</div><div></div><div> 
Wage: $22.50/hour</div><div>
Start time: 3:30am</div><div>
Shift: 10 hour shifts</div><div>
Days: 4 days</div><div></div><div> 
If you choose to work with us, you will be an integral part of a team with a rich and diverse culture that learns, grows, and succeeds together. You will also have access to some amazing benefits such as:</div> 
<div></div><ul><li>
Medical, Dental, Vision insurance on DAY ONE</li><li>
Company paid STD, LTD, and Life Insurance on DAY ONE</li><li>
80 hours of vacation and 40 hours of sick time per fiscal year</li><li>
401(k) Retirement Savings plan that includes company&rsquo;s matching contributions up to 4.5%</li><li>
Wellness reimbursement towards gym membership and/or exercise equipment</li><li>
Referral bonuses totaling $750 when an employee refers someone to work with our company</li><li>
Quarterly sales of product to employees</li></ul>
Position Essential Duties and Responsibilities:
<div>
Maintain Food Safety Program:</div><ul><li>
Participate in and report on pre-operational, operational, and facility assessment audits.</li><li>
Carry out line checks and all verification processes.</li><li>
Verify all critical control points, preventive controls, and control points for all processes in accordance with plant HACCP and GMP programs.</li><li>
Assist in the monitoring of raw material and finished product specifications; maintain and report raw material and finished goods &ldquo;HOLD&rdquo; tag logs.</li><li>
Carry out microbiological and chemical analytical tests on finished goods, environmental and other contact surfaces.</li><li>
Prepare pre-shipment approval paperwork.</li><li>
Complete all paperwork accurately and timely.</li><li>
Review and modify the HACCP and SSOP programs along with other necessary paperwork.</li><li>
Prepare taste tests for finished goods for sensory evaluation and conduct product consistency evaluations</li><li>
Comply with all company policies and procedures.</li><li>
Perform projects at the instruction of the FSQA Supervisor or FSQA Manager.</li><li>
Perform training of employees.</li><li>
Perform other tasks as assigned.</li></ul><div>
 Maintain Lab and Inventory:</div><ul><li>
Track materials to maintain adequate inventory of laboratory supplies</li><li>
Maintain lab equipment and production equipment stored in the lab; arrange for the repair and calibration of any defective equipment.</li><li>
Maintain the daily operations of the lab
</li><li>Update lab SOPs as needed.</li><li>
Maintain ISO databases.</li><li>
Maintain accurate laboratory records for all product, environmental, and other types of testing conducted.</li></ul>
Position Qualifications:
<ul><li>Must be able to perform each essential duty satisfactorily.</li><li>
Must be able to use a computer to perform reporting and record-keeping tasks as well as create reports, presentations, and charts as needed.</li><li>
Bachelor&rsquo;s Degree (BA or BS) from a four year college or university; or at least two years related experience and/or training; or equivalent combination of education and experience.</li><li>
Experience in employee training and support; attention to detail; familiarity with computers.</li><li>
Punctuality</li></ul><div>
#INDPOR</div></div>

FSQA Technician

Astrix

<div>
 
 
 QC/R&amp;D Chemist
 
 
 
 A manufacturing laboratory is seeking a
 
 full-time QC/R&amp;D Chemist
 
 to perform testing on raw materials, in-process samples, and finished products. This role supports both quality control and research &amp; development, ensuring compliance with specifications and regulatory requirements while contributing to product development initiatives.
 
 
 
 
 
 Located in Anaheim, CA
 
 
 
 
 
 1st shift
 
 
 Contract to hire
 
 
 
 Pay:
 
 $26-28/hour
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Operate, calibrate, clean, and maintain laboratory equipment.
 </li>
 <li>
 Perform quality tests on raw materials, in-process batches, and finished goods.
 </li>
 <li>
 Conduct stability testing and monitor production batches.
 </li>
 <li>
 Prepare and send samples to third-party labs.
 </li>
 <li>
 Maintain inventory of materials, components, and supplies.
 </li>
 <li>
 Record and analyze test data, prepare reports, and create documentation (spec sheets, COAs, OTC/QC regulatory documents).
 </li>
 <li>
 Assist with lab-scale batch preparation for product development.
 </li>
 <li>
 Inspect equipment, documentation, and products before and after filling.
 </li>
 </ul>
 
 
 Qualifications
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Chemistry or related field.
 </li>
 <li>
 1&ndash;2+ years of experience in QC, R&amp;D, or analytical laboratory work.
 </li>
 <li>
 Familiarity with analytical techniques and instrumentation.
 </li>
 <li>
 Strong attention to detail, documentation, and organizational skills.
 </li>
 <li>
 Proficient in MS Word, Excel, and Google Docs.
 </li>
 <li>
 Ability to work independently and as part of a team.
 </li>
 <li>
 Must be able to lift up to 20 lbs.
 </li>
 </ul>
 
 
</div>

Quality Control Chemist

Arrowhead Pharmaceuticals

<div>
 Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead&rsquo;s RNAi-based therapeutics leverage this natural pathway of gene silencing.
 
 
 Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
 
 
 Arrowhead&rsquo;s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
 
 
 
 The Position
 
 
 
 This position is within the Quality Control structure, under the Quality Organization. An Associate Scientist III, Quality Control will support the analytical testing of pharmaceutical raw materials, in-process samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. The Associate Scientist I will also support testing required for GLP Toxicology and cGMP Clinical Trial material release, as well as stability studies. The Associate Scientist III is expected to perform several analytical techniques and can make sound scientific decisions under guidance from management. This position reports to QC Laboratory Management.
 
 
 2nd shift work hours are ~1pm &ndash; 11:30pm and includes a shift differential.
 
 
 
 Responsibilities
 
 
 
 responsibilities to this position:
 
 
 <ul>
 <li>
 Developing understanding and knowledge of cGMP requirements.
 </li>
 <li>
 With guidance from laboratory leadership, works to meet project timelines and deliverables
 </li>
 <li>
 Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and/or stability samples using established test methods and procedures
 </li>
 <li>
 Executes training requirements, applies relevant SOPs and associated procedural guides
 </li>
 <li>
 Ensures that training records are up to date and in compliance
 </li>
 <li>
 Proficient with various analytical instrumentation theory and practice
 </li>
 <li>
 Trains on, and becomes proficient with, a variety of analytical instrumentation (e.g., HPLC, GC, FT-IR, UV/Vis, KF, etc.)
 </li>
 <li>
 Can set up various instrumentation for testing according to written test methods with little to no supervision
 </li>
 <li>
 Plans and executes work related tasks with minimal supervision
 </li>
 <li>
 Performs analyses in a timely manner
 </li>
 <li>
 Works collaboratively with others
 </li>
 <li>
 Shows initiative and interest in learning new techniques and tests
 </li>
 <li>
 Identifies and troubleshoots analytical problems with instrumentation, general chemistry and computer applications
 </li>
 <li>
 Quickly communicates analytical or sample issues to senior staff and/or management
 </li>
 <li>
 Maintains a clear, concise and accurate laboratory notebook or worksheet records.
 </li>
 <li>
 Reviews test data acquired by others, as applicable.
 </li>
 <li>
 Drafts technical documents such as OOS/atypical investigations, deviations and CAPAs
 </li>
 <li>
 Demonstrates good written and verbal communication skills
 </li>
 <li>
 Proficient in analyzing data/results and interpret outcome of experiments and to propose appropriate follow-up with supervision.
 </li>
 <li>
 Embraces cGMP requirements for all associated work
 </li>
 <li>
 Works cooperatively in a team environment
 </li>
 <li>
 Establishing attention to detail
 </li>
 <li>
 Calibration, maintenance, and troubleshooting of analytical equipment with limited supervision.
 </li>
 <li>
 Remains flexible with changing priorities
 
 
 </li>
 </ul>
 
 Requirements:
 
 
 
 <ul>
 <li>
 BS. in Chemistry with 5 years of relevant laboratory experience
 </li>
 <li>
 Knowledgeable of cGMP laboratory requirements and operations
 </li>
 <li>
 Familiar with analytical instrumentation, test methodology/validations, data acquisition systems, and typical cGMP policies and practices.
 
 
 </li>
 </ul>
 Wisconsin pay range
 
 
 $80,000&mdash;$100,000 USD
 
 
 Arrowhead provides competitive salaries and an excellent benefit package.
 
 
 All applicants must have authorization to work in the US for a company.
 
 
 California Applicant Privacy Policy
</div>

Associate Scientist III, Quality Control (2nd Shift)

Search 10000+ Quality control technician jobs near you this September. New roles added regularly across leading industries. Apply today.