Quality control technician jobs in Medford, OR

RESPONSIBILITIES: Maintain accurate and up‐to‐date acceptance and rejection records and/or certifications systems as required by the applicable specifications. Determine acceptance or rejection after inspection and/or calibration of parts, tools, instruments or x‐ray film. Identify defective conditions and test failures and prepare all appropriate documentation and/or calibration history. INSPECTION: Perform inspection on complex parts using a wide variety of measuring and test equipment. Adapt and develop complex inspection set‐ups to check sample parts, forgings and castings. Check tool and jig layouts. Perform first article and envelope inspections, source inspections, and/or complex surface plate set‐ups. Interpret specifications, charts, manuals and other data to arrive at acceptance or rejection. Recommend changes to supervision. Use mathematics to convert blueprint dimension and tolerances. Work within the guidelines of drawings, schematics, blueprints, route sheets, travelers, quality directives, technical engineering specifications, customer's requirements and military standards. Layout all component part characteristics onto rough or semi‐machined castings, forgings and machine parts to maintain control of machining cycle during manufacturing. CALIBRATION: Perform calibration on complex multi‐function electronic measuring and test equipment. Set‐up calibration test conditions having various circuit requirements interpreting calibration procedures, specifications, manufacturer's instructions, or related documents. Ability to interpret drawings and electronic schematics. Document and evaluate historical data to determine calibration intervals. Diagnose and calibrate newly acquired complex electronic equipment. NONDESTRUCTIVE TEST: Perform daily, weekly and monthly equipment and material checks. Perform pre‐inspection and post‐inspection cleaning. Set‐up equipment and conduct tests. Interpret, evaluate and document inspection results in accordance with approved procedures. Perform complete inspections in accordance with applicable specifications, standards and other contractual documents. Operate X‐ray equipment and film processor. Select the method and technique to be used for a specific inspection. Prepare and verify the adequacy of inspection procedures. Job Requirements: Five years related inspection experience or demonstrated ability to perform described responsibilities. Knowledge of applicable military standards or specifications. Required experience in CMM operations, background in dimensioning and tolerancing per ANSI Y 14.5. Proficient in reading and interpreting blueprints, customer's specifications and internal drawings and procedures. Thorough knowledge of machine shop mathematics including trigonometry. Knowledge of electro‐hydraulic servo systems and the computer IEEE systems. Personal hand tools may be required. Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

Kinovate Life Sciences, Inc. established in 2004 in Oceanside, California. A wholly owned subsidiary of Nitto Denko Corporation (*************** Kinovate was spun-off from Oceanside, CA based R&D facility Nitto Denko Technical Corp (**************** with a mission to provide the highest quality materials to niche life science markets worldwide. Since its inception, Kinovate has grown to become the market leader in solid support in the oligonucleotide synthesis field. We are bringing the most creative minds in science and technology to develop medical discoveries and breakthroughs. Our customers are well-known in the biotechnology industry. We are in a growth phase within ISO work environment and leading towards a GMP Certification. KLS is seeking extraordinary people to join the team. KLS is proud to be an equal employment opportunity employer. Why Work Here Great place to work. Small subsidiary of large international company headquartered in Japan. Generous discretionary bonuses. Health, dental, vision, life, and disability insurance effective from date of hire. Additional benefits include 401(k), 3 weeks vacation in your first year, 12 paid yearly holidays, 5 paid sick days, tuition reimbursement and more. JOB SUMMARY: Under strategic leadership, sustain the improvement of the Quality Management Systems (QMS) and manages the development of quality assurance & systems staff. Utilize the following industry standards to drive high-quality products: Current Good Manufacturing Practice (cGMP), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH), and International Organization for Standardization (ISO). Facilitate employee relations issues including coaching, mentoring, and disciplining including performance evaluation of employees. Provides strong leadership to motivate, guide and inspire employees to meet the organization's business objectives with production. Lead the implementation phase of MasterControl, ensuring successful implementation, and post-implementation management. ESSENTIAL DUTIES and/or RESPONSIBILITIES: Partners with leadership to develop the Quality Management System (QMS) and ensure it is compliant with relevant regulations, including ISO 9001, 21 CFR Part 210 and 211, ICH, and other applicable national and international regulatory guidelines.Ensure the QMS always remains in an auditable state. Oversees the daily operations of the QMS, ensuring it runs efficiently and in compliance with quality standards. This includes managing critical quality systems processes such as Incoming Raw Material Receipt, Raw Material Review/Disposition, Final Product Review/Disposition. Manages quality events and investigations including but not limited to Deviations, CAPA, Change Control, OOS, OOT, Customer Complaints, including leading and facilitating cross-functional meetings to ensure proper assessments and actions. Ensures QA review of Validation/Qualification activities including protocols, execution, and reports. Upholds timely response to events and on-the-floor QA support(MQA), including ensuring the MQA program is tracked and measurable. Leads the transition of QMS programs, such as Quality Events (Deviation, CAPA, Change Control, OOS, OOT), Audits and Supplier Qualification transition into Master Control, and serves as the System Administrator. Administers post-implementation management of MasterControl, including, but not limited to, system optimization, performing troubleshooting support, managing software updates, and continuously improving system functionality to meet evolving regulatory needs. Reports key metrics for QA Operations turnaround times and Quality Events. Contributes to the continuous improvement initiatives related to the QMS, collaborating with cross-functional teams to optimize quality processes. Analyze quality data and metrics to identify trends, root causes, and areas for process improvement within manufacturing and quality control activities. Develops standard operations and other quality documents related to QMS and ensure all documents meet regulatory requirements and internal standards. Supervises and develops a team providing guidance, training, and support to ensure compliance with regulatory standards and best practices. Mentors and develops a team of the QA team, fostering an environment of accountability and growth. Ensures cross-functional collaboration and provide effective leadership managing the QMS processes and ensures effective employee relations. Facilitates training initiatives to ensure that team members are adequately prepared to handle QMS functions and sustain a flexible workforce. Fosters a culture of continuous improvement, supporting staff development and efficiency improvements within the quality systems team. Conducts performance reviews for direct reports. Institutes timely corrective actions and interfaces with Leadership and HR in developing disciplinary actions up to and including terminations. Administers time-keeping functions to track absenteeism; approves timecards on a bi-weekly basis. SUPERVISOR RESONSIBLITIES: Quality Assurance Associate Quality Assurance Specialist Sr. Quality Assurance Specialist MINIMUM EDUCATION and/or EXPERIENCE: Bachelor's degree in a scientific discipline; and five (5) years' directly related experience in a Good Practice (GXP) or ISO manufacturing-controlled environment or equivalent combination of education and experience. Experience in transitioning from paper based to electronic QMS. KNOWLEDGE, SKILLS and/or ABILITIES: Working knowledge of pharmaceutical industry concepts, as well as analytical methods and writing skills, including documenting manufacturing processes, a plus. Familiarity in Lean or Six Sigma, a plus. Strong Knowledge of quality management principles and practices, including ISO 9001 and cGMP standards. Proficient in the use of quality management software with experience in implementing or managing MasterControl being highly desirable. Experience conducting technical investigations with formal root cause analysis tools. Prior supervisory experience, preferred. Knowledgeable of change control, validation/qualification, and method development and tech transfer. Strong knowledge of formal root cause analysis and risk assessment tools. Ability to lead or facilitate investigations and/or risk assessments. Strong application of critical thinking skills along with problem solving and creative skills to identify manufacturing issues for continuous improvement. Strong multi-tasking skills, flexibility in responding to rapidly changing, dynamic processes and demands/pressures in a fast-paced environment. Strong ability to verbally communicate across functional organizational groups, provide high-level customer service through effective interpersonal skills and conflict resolution, including communicating with equipment suppliers to obtain input on equipment modification and improvement. Microsoft Office Suite software applications such as Excel, Word, Power Point, and other enterprise software applications such as Net Suite, LIMS, and Familiarity with statistical analysis tools. Strong language skills with the ability to read, analyze and interpret general business periodicals, professional journals, technical procedures, or government regulations. Write clear processes, manuals and reports for management review and present technical information in understandable terms and respond to questions from groups of customers, employees and/or public. Work independently as well as in a small and/or large group and foster cooperation in a team environment using interpersonal skills to document working knowledge. Work in a detail-oriented environment with strong follow-up, follow-through, and organizational skills. CERTIFICATES and/or LICENSES: American Society for Quality Certified, a plus. Certified Quality Engineer, a plus. Certified Quality Auditor, preferred. PHYSICAL DEMANDS and/or WORK ENVIRONMENT: (Typical physical demands and the work environment characteristics an employee must meet and encounter while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.) Works in a typical office environment with prolonged periods in front a computer entering or researching data. Regularly required to sit; use hands to finger, handle or feel and talk or hear. Availability and willingness to travel if required for audits, inspection, vendor management or if requested to visit or attend a business transaction as legal agent of the company. Must be able to work extended hours per the demands of the business.

Senior Formulation Technician Duration: 12 Months Job Type: Contract Work Type: Onsite Shift: Monday to Friday from 06:00 AM to 02:30 PM Pay Range: $20 to $26 per hour Overview TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The job opportunity below is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary Work in a team-based manufacturing laboratory environment responsible for synthesizing, testing, and qualifying ion exchange media used in chromatography consumables, while maintaining high quality, safety, and compliance standards. Responsibilities Perform testing and qualification of resin products using specialized instruments to meet customer and production demands. Accurately record, analyze, and report test results; maintain complete and compliant documentation. Execute complex production work orders in accordance with established SOPs and procedures. Analyze data, derive conclusions, and prepare technical reports based on findings. Collaborate with cross-functional teams to support production and quality objectives. Adhere to ISO 9001 guidelines, GMP, and corporate quality policies. Comply with EH&S safety requirements and participate in safety improvement initiatives. Identify process improvement opportunities and propose corrective or preventive actions. Maintain a clean, organized, and inspection-ready laboratory environment. Required Skills Hands-on experience in a chemistry or biotechnology laboratory. Bachelor's degree in Chemistry, Biotechnology, or a related life sciences field. Experience in a manufacturing or regulated production environment. Familiarity with chromatography techniques and chromatography-related software. Exposure to Lean Manufacturing, PPI, or Continuous Improvement tools. Willingness and ability to learn new processes, tools, and technologies. Knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Ability to read, understand, and follow written SOPs and verbal instructions in English. Strong mathematical skills, including basic arithmetic with whole numbers, fractions, and decimals. Proficiency in Microsoft Word, Excel, Outlook, and basic data handling. Strong documentation, organizational, and problem-solving skills. Effective verbal and written communication skills. Familiarity with common hand tools (e.g., wrenches, torque drivers, tweezers). Ability to work independently with minimal supervision while meeting deadlines and production targets. Strong punctuality, attendance, and ownership mindset. Understanding of production schedules and task prioritization. Compliance with GMP, QSRs, ISO, and IVD regulatory requirements. TekWissen Group is an equal opportunity employer supporting workforce diversity.

The Quality Control Associate will support the PTDA Bioassay US Testing Group by performing biochemical, immunological, and cell-based assays in support of clinical and commercial products. This role operates in a cGMP-regulated laboratory and supports process development, product characterization, stability, and lot release testing using established procedures. Key Responsibilities Perform biochemical, immunological, and cell-based bioassays Support process development, product characterization, stability, and lot release testing Review, verify, and release assay data (electronic and paper-based) Prepare reagents and maintain assay readiness Present assay results and monitor assay performance and quality Follow Good Documentation Practices (GDP) and ALCOA+ data integrity principles Perform routine laboratory maintenance and support 5S initiatives Comply with EHS safety requirements and cGMP standards Required Qualifications B.S. in Biological Sciences or related field 1-2 years of relevant experience in Quality Control Hands-on experience with immunological and/or cell-based assays Experience with aseptic cell culture Working knowledge of cGMP environments Ability to work independently and collaboratively in a fast-paced setting Strong attention to detail and ability to manage multiple priorities Effective written and verbal communication skills Technical & Systems Skills Proficiency with computer applications, data management, and electronic documentation Experience with GxP-compliant systems such as SoftMax Pro, LIMS, and Veeva QMS (preferred)

Our client, a global CDMO, offering products and services across the drug development spectrum is looking for a skilled QC Analyst III to join their team in Ventura County, CA! Job Title: QC Analyst III Job type: 6 month contract - hire Pay rate: $37 - $39/ hr. Job Summary: We are seeking a highly skilled and detail-oriented Senior QC Analyst to perform complex analytical testing in support of pharmaceutical product development and manufacturing. The ideal candidate will have advanced experience in chromatography techniques (e.g., HPLC, UPLC, GC), method validation, data analysis, and regulatory compliance. This position plays a critical role in ensuring product quality, supporting investigations, and driving continuous improvement across the QC function. Key Responsibilities: Perform complex analytical testing including Liquid Chromatography (HPLC/UPLC), Gas Chromatography (GC), and other instrumental and wet chemistry techniques. Troubleshoot analytical instruments and resolve method or equipment-related issues. Participate in and assist with test method validations, verifications, and transfers. Evaluate and analyze test data to identify trends, outliers, or potential issues. Support OOS (Out of Specification) and OOT (Out of Trend) investigations, including CAPA (Corrective and Preventive Action) documentation. Coordinate testing activities with external laboratories, including raw material and specialized testing. Execute, author, and review SOPs, test methods, protocols, reports, investigations, change controls, and data summaries. Utilize risk assessment and root cause analysis tools (e.g., 5 Whys, Fishbone) to support investigations and process improvements. Manage aspects of the stability program, including scheduling, testing, and reporting, and investigate aberrant stability results. Qualifications: Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field. 3-6+ years of relevant experience in a regulated laboratory environment (pharmaceutical, biotech, or similar). Strong technical expertise in HPLC, UPLC, GC, and other analytical techniques. Working knowledge of cGMP regulations, ICH guidelines, and regulatory expectations. Experience with method validation and stability programs preferred. Ability to manage multiple tasks and work independently in a fast-paced environment. Experience with electronic data systems (e.g., Empower, LIMS, TrackWise, MasterControl). Note: This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Who We Are We are a community built on care. Our caregivers and supporting staff extend compassion to those in need, helping to improve the health and well-being of those we serve, and provide comfort and healing. Your community is our community. Our Story We started out as a small operation in California. In May 1969, we acquired four hospitals, some additional care facilities and real estate for the future development of hospitals. Over the years, we've grown tremendously in size, scope and capability, building a home in new markets over time, and curating those homes to provide a compassionate environment for those entrusting us with their care. We have a rich history at Tenet. There are so many stories of compassionate care; so many "firsts" in terms of medical innovation; so many examples of enhancing healthcare delivery and shaping a business that is truly centered around patients and community need. Tenet and our predecessors have enabled us to touch many different elements of healthcare and make a difference in the lives of others. Our Impact Today Today, we are leading health system and services platform that continues to evolve in lockstep with community need. Tenet's operations include three businesses - our hospitals and physicians, USPI and Conifer Health Solutions. Our impact spreads far and deep with 65 hospitals and approximately 510 outpatient centers and additional sites of care. We are differentiated by our top notch medical specialists and service lines that are tailored within each community we serve. The work Conifer is doing will help provide the foundation for better health for clients across the country, through the delivery of healthcare-focused revenue cycle management and value-based care solutions. Together as an enterprise, we work to save lives and can accept nothing less than excellence from ourselves in service of our patients and their families, every day. Up to $30,000 Sign-On bonus based on experience Doctors Medical Center Modesto is a full-service, comprehensive health care facility, dedicated to providing the finest medical care for the community. From preventative and diagnostic services to expertise in some of the world's leading technologies, DMC's multidisciplinary team of physicians and healthcare professionals is dedicated to your good health and well-being. Recognized for innovative cardiac and neonatal intensive care to advanced stroke and trauma treatment, the outstanding doctors at DMC represent most major medical specialties and are committed to being there for you, when you need them most. We offer competitive salaries and benefits including a matching 401(k), several health & dental plans to choose from, generous tuition assistance plans, and relocation assistance for select positions. Comprehensive benefits for medical, prescription drug, dental, vision, behavioral health and telemedicine services Wellbeing support, including employee assistance program (EAP) Time away from work programs for paid time off, long- and short-term plan coverage Savings and retirement including a 401(k) Plan with a 50% match up to 6% of pay, employee stock purchase plan, flexible spending accounts, retirement readiness tools, rollover support, and financial well-being counseling Education support through tuition assistance, student loan assistance, certification support, and online educational program Additional benefits life insurance, supplemental health protection plans, auto and home insurance, legal counseling, identity theft protection, and employee discount program Registered nurses - Retirement medical benefit account (RMBA) - 2% of annual eligible income set aside in accordance with program guidelines Benefits may vary by location and role Relocation package offered for this position ************************* Summary: Reporting to the Director of Imaging Services and/or designee, the Diagnostic Imaging Technologist is responsible for radiological care to patients of all ages, for the purpose of diagnosis and/or treatment of anatomical and physiologic disorders using ionizing radiation. Must have working knowledge of conventional Radiology. Must be able to operate all X-ray equipment and PACS. Prepares exam room, equipment, supplies and medications for patient's procedures and is responsible for patient education. Proven competency in addition to conventional radiography, working knowledge in at least one other area CT, MRI, or Interventional Radiology if applicable competencies are met. May be required to take call. Sign on bonus doesn't apply to internal applicants BLS ARRT( R ) CRT Fluoroscopy permit required #LI-KB6 Tenet complies with federal, state, and/or local laws regarding mandatory vaccination of its workforce. If you are offered this position and must be vaccinated under any applicable law, you will be required to show proof of full vaccination or obtain an approval of a religious or medical exemption prior to your start date. If you receive an exemption from the vaccination requirement, you will be required to submit to regular testing in accordance with the law Employment practices will not be influenced or affected by an applicant's or employee's race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship. Tenet participates in the E-Verify program. Follow the link below for additional information. E-Verify: ***************************** The employment practices of Tenet Healthcare and its companies comply with all applicable laws and regulations. ********** Employment practices will not be influenced or affected by an applicant's or employee's race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.

Hi Hope you are doing well ! This is Dipendra Gupta from Programmers.ai as we have an urgent open role below, please check and do let me know if you are comfortable with and looking for a new role or interested. Junior reliability lab Technician Mountain view CA -onsite ‘ Fulltime Job description: Develop and Execute Test Plans: Design and carry out comprehensive reliability test plans (e.g., thermal cycling, vibration, shock, humidity, burn-in, life testing) for new and existing products or equipment to simulate real-world operating conditions. Failure Analysis & Root Cause Determination: Conduct detailed failure analyses (FA) and root cause analyses (RCA) for failures identified during testing or in the field, implementing effective corrective actions and permanent solutions. Reliability Modeling & Prediction: Use statistical methods and software tools (e.g., Weibull analysis, Design of Experiments (DOE), FMEA) to predict future performance, model failure rates, and assess potential risks. Collaboration: Work closely with design, manufacturing, quality assurance, and maintenance teams to provide key input on "Design for Reliability" (DFR) and "Design for Maintainability" principles. Documentation & Reporting: Compile data, generate detailed reports, and communicate test results, findings, and recommendations to cross-functional teams and management Best Regards, Dipendra Gupta Technical Recruiter *****************************

Purpose Accountable for basic operation of the site's quality assurance and control program including but not limited to: assisting and supporting all safety, environmental and quality regulations, product testing and adherence to standards, targets and recipes, maintain relevant equipment and calibrations, and decision-making through basic statistical understanding. Key Responsibilities * Perform all work in accordance with safety rules and regulations and participate in facility health & safety activities as assigned * Use descriptive statistics to identify non-conforming material to site referenced standards and targets * Ensure all relevant quality requirements are consistently met according to the QA manual and plant SOPs * Ensure that non-conforming product is appropriately quarantined, identified and segregated according to standard procedures * Ensure the communication of non-conformance is clear and concise to required parties. * Disposition basic non-conforming product as allowed by site Technical Manager. * Record testing and inspection results by inputting into appropriate database or spreadsheets while identifying and responding to test results outside of product standards and targets * Verify that all product packaging and appearance standards meet site and client expectations. * Generate and analyze reports and charts * Monitor and document process parameter changes as assigned * Communicate test results and observations to operations and management to maintain process and product conformance * Monitor and record consumption and inventory of raw materials (wax, resin, etc.). * Verify quality of raw materials as required * Support preventive and unscheduled maintenance tasks. * Assist in process and product tests/trials. * Be pro-active in identifying and performing other tasks to maintain and improve safety, quality and environmental performance * Demonstrate adherence to process and product SOPs, JSAs, check sheets and other QMS documentation * Provide support to team members when a quality issue arises * Demonstrate drive and willingness to advance to higher levels of responsibility * Perform in a relief capacity for production coordinator * Perform other duties as assigned * Models company core values * Other duties as assigned Required Qualifications * Associate's Degree and two years of experience in laboratory work, quality control, or general manufacturing; or an equivalent combination of training, education, and experience * Knowledge of and ability to follow all quality and process standards * Demonstrated ability to operate a computer and supporting software, to include spreadsheet and statistical packages * Working knowledge of manufacturing equipment and production processes * Demonstrated ability to operate sample preparation and testing equipment * Knowledge of inventory management * Excellent verbal and written communication as well as interpersonal skills * Proficient math skills and statistical knowledge, including concepts * Demonstrated ability to operate a variety of material handling equipment (both hand tools and electrical/motorized equipment) * Ability to climb stairs and lift up to 50 pounds * Demonstrated ability to work while wearing a respirator and/or other safety clothing or equipment Preferred Qualifications * Associate degree in Forest Products, Engineering, Wood Science or related scientific field preferred * Three (3) years composite or engineered wood manufacturing experience

Linde Gas & Equipment Inc. Process Technician Linde Gas & Equipment, Inc. is in search of a Process Technician! This role will focus on performing various related processes like cylinder preparation, cylinder handling, cylinder filling, shipping, and receiving while prioritizing safety and attention to detail. What we offer you! * Competitive compensation * Comprehensive benefit plan (medical, dental, vision and more) * 401(k) retirement savings plan * Paid time off (vacation, holidays, PTO) * Employee discount programs * Career growth opportunities * Work/life balance (allows you to be home nights and weekends) What you will be doing: * Conform to all plant and Linde policies and procedures * Perform cylinder prepping, handling, filling, and shipping & receiving functions * Collect and record basic operations data to ensure process optimization and product quality * Perform various SAP Transactions to maintain a streamlined stock and sales order flow * Complete tasks related to stock and sale order attainment, such as handling cylinder requisition and recording & managing data * Support raw material and product inventory maintenance * Review raw material specifications to ensure compliance with Linde standards * Provide feedback and participate on potential projects associated with operational processes * Enter work requests and perform basic system maintenance * Other duties as assigned What makes you great: * High School Diploma or GED required * Must have basic hand tool and power tools knowledge * Ability to perform basic Algebra and unit conversions * Ability to pass a pulmonary function test for the usage of a respirator * Proficient with Microsoft Office applications * Effective organizational, listening, and communication skills * Upholds high standards of honesty and integrity * Demonstrates personal ownership for safety and actively contributes to a strong safety culture * Contributes to a positive work environment where differences are valued and supported * Strives for personal achievement and helps others attain results * Ensures accountability through collaboration and interpersonal skills Why you will enjoy working with us Linde is a leading global industrial gases and engineering company with 2024 sales of $33 billion. Linde Gas & Equipment Inc. (LG&E) is part of the largest Welding, Industrial, Medical, and Specialty Gases companies in the U.S. We carry a comprehensive selection of industrial gases, such as oxygen, nitrogen, argon, and carbon dioxide, etc. LG&E has an extensive network of production plants, retail stores, distribution centers, and customer service locations with a focus on making our world more productive every day by providing high-quality solutions, technologies and services which are making our customers more successful by helping to sustain and protect our planet. For more information about the company, please visit our website. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, pregnancy, sexual orientation, gender identity or expression, or any other reason prohibited by applicable law. #LI-IS1

About Us: Valent BioSciences LLC is a global leader in the research, development, and production of biorational products that support agriculture, public health, and forestry. With over 60 years of experience, our innovative solutions are used in sustainable practices across more than 95 countries. Our mission is to enhance plant quality, productivity, and long-term sustainability. Valent BioSciences is also the parent company of Mycorrhizal Applications LLC, the industry's leading supplier of arbuscular mycorrhizal fungi-based products. Mycorrhizal Applications (MA) is at the forefront of microbial-based technologies that help growers and land stewards improve soil health and plant performance. As the world's leading producer of mycorrhizal soil inoculants, MA provides science-backed, sustainable solutions to the agriculture, horticulture, landscaping, and forestry industries. To meet growing global demand, Valent BioSciences and MA are expanding operations to White City, Oregon, with a brand-new, first-of-its-kind facility dedicated to the production of mycorrhizal fungi. This expansion represents an exciting opportunity to join a company committed to innovation, environmental stewardship, and the future of sustainable agriculture. General Description: The Quality and Lab Technician supports the company's quality assurance functions with a focus on maintaining and enhancing quality compliance. The primary responsibility of this role is to perform quality inspections on raw materials and finished products used or produced by Mycorrhizal Applications (MA). The Quality Technician works collaboratively across multiple departments within MA and regularly interacts with teams from other Valent Group Companies to support company-wide quality initiatives. This position develops and enforces internal compliance programs to meet legal and industry best practices. The Quality Technician applies knowledge of all products while adhering to environmental regulations and all safety protocols. Principal Responsibilities: Support the MA Quality team with laboratory sample preparation, analysis, and accurate data reporting. Perform quality analysis of Finished Goods (FG) and Raw Materials (RM) used in the production of MA products. Assist in the review and evaluation of new formulations and raw materials for potential use in MA manufacturing. Design, prepare, and execute experiments on FG and RM as required. Record and report analytical results in QMS databases with accuracy and attention to detail. Contribute to efforts aimed at ensuring maximum customer satisfaction with Finished Goods. Coordinate with third-party laboratories and affiliates to obtain and maintain required lab tests and efficacy studies in support of Quality and Regulatory requirements. Support the expansion of Quality Programs by increasing inspection frequency for both FG and RM. Assist Manufacturing, Quality, and Regulatory teams with corrective and preventive action (CAPA) projects and participate in internal and external audits. Conduct pre-production startup inspections, including visual checks and environmental swabbing. Monitor and support Environmental and ATP programs by data collection, monitoring, and trending. Participate in root cause analysis (RCA) and corrective actions (CA). Perform titration of CIP (Clean-In-Place) solutions to verify detergent and sanitizer concentrations. Carry out routine plant GMP (Good Manufacturing Practice) inspections to ensure compliance with quality standards. Assist with ongoing training of operations teams. Other duties as assigned. Education and Experience: Bachelor's degree in Soil Biology, Mycology, Microbiology, Plant Pathology, Agronomy, Horticulture, or a related scientific field. Minimum of 2 years of relevant laboratory experience, preferably in quality control or quality assurance, microbiology, or analytical testing environment and/or experience in quality compliance programs. What We Offer: You'll enjoy competitive compensation, consisting of base pay plus an incentive program available to all eligible full-time employees, and a comprehensive benefits package including high-quality healthcare options, 401k matching, life and disability insurance, generous time off (with time off to volunteer) and much more! We work together to power our sustainable future. Here's what drives us: Valent North America LLC has a strong commitment to both sustainability and corporate social responsibility (CSR). In fact, being a responsible corporate citizen has been ingrained in our culture since the company's founding. Today, it remains at the forefront of everything we do. Valent North America LLC is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation and/or identity, national origin, citizenship, immigration status, disabilities, or protected veteran status.

Emerald Technologies is thrilled to announce an outstanding career opportunity for a Quality Inspector to join our dynamic team in Medford, Oregon ! At Emerald Technologies, every employee plays a key role in shaping cutting-edge products that support a wide range of industries. Join a collaborative, energetic workplace where your contributions truly matter, your growth is encouraged, and your career potential is limitless. Be part of a team where innovation thrives, and your work makes a real impact! Responsibilities: Confidently verify and inspect printed circuit assemblies, including performing PTH line verifications and supporting first article inspections to ensure top-tier product quality. Utilize Synergy software to access, navigate, and interpret essential production data and documentation. Review Bills of Materials (BOMs), Assembly Instructions, and related documents to ensure a complete understanding before beginning inspections. Collaborate closely with trainers and leadership to perform machine checks, complete less complex first articles, and refine accuracy through re-inspections. Support smooth production flow by transporting trays and racks of printed circuit assemblies between departments as needed. Maintain a clean, organized, and safe work environment while consistently adhering to company quality and attendance standards. Demonstrate flexibility and commitment by adjusting schedules when needed to meet customer expectations and overall team goals. Benefits of the Job: Competitive medical, dental, and vision benefits. Health Savings Account/Flexible Spending Account 401K and company matching with no vesting period PTO for rest and relaxation Gym reimbursement (through Anthem) Employee Assistance Program A safe and inclusive work environment with team and management support Employee training and development Community service and philanthropic initiatives Employee appreciation and events Career advancement opportunities Employee Referral program Employee discounts Qualifications of the Quality Inspector: Experience Should have some electronics experience. Education A minimum of a high school diploma or equivalent is required. Additionally, the employee must complete all internal courses offered by the company necessary to do the job. Knowledge, Skills, and Abilities The employee must have excellent vision, including the ability to distinguish between colors and varying shades of color, and the ability to read screen-printing symbols and component values. Employee must be able to read and write in English and be able to comprehend technical data. This position requires mathematical skills at a level slightly above basic math. Must be able to sit and perform stationary work for the majority of the shift. May be required to lift 40lbs periodically. Must be able to always work independently and safely. Must maintain confidentiality of all company and customer information. Emerald Technologies is an electronics manufacturing services (EMS) provider for original equipment manufacturer (OEM) customers, focusing on high-reliability electronic assemblies. With design and manufacturing facilities in California, Michigan, New Hampshire, Oregon, as well as in China and Malaysia. Emerald Technologies specializes in high mix, low- to medium-volume manufacturing for high-reliability markets in the Aerospace/Defense, Life Sciences, Renewable Energy, Industrial Controls, Power & Infrastructure, Semiconductor, and Telecommunications sectors. However, our rapid turnaround times, responsive customer service, and collaborative problem-solving approach distinguish us from the competition.

Job Description We are seeking a detail-oriented and safety-minded Manufacturing Quality Inspector (Level I) to perform in-process and final inspections of manufactured components, assemblies, and sub-assemblies. This position plays a key role in ensuring quality standards are met throughout the manufacturing process. Key Responsibilities: Conduct inspections on parts, assemblies, and new manufactured aircraft components in accordance with established procedures. Perform First Article Inspections per AS9102 standards. Make final airworthiness determinations and certify products as required. Support customer-specific quality requirements and FAA conformity projects. Assist in continuous improvement initiatives focused on efficiency and product quality. Perform receiving inspection duties and participate in internal audits as assigned. Occasional travel may be required to provide off-site inspection support. Qualifications: 1-3 years of experience in a manufacturing or inspection-related role preferred. Two-year technical degree, FAA certificate, or industry-related quality certifications preferred. Familiarity with aircraft maintenance practices, inspection standards, and FAA regulations is a plus. Ability to read blueprints and technical specifications. Experience using precision measuring tools and inspection equipment. Strong communication skills and the ability to work well in a fast-paced, team-driven environment. Must possess strong ethics, attention to detail, and a proactive mindset. Work Environment & Competencies: Adheres to safety protocols and maintains a clean, hazard-free workspace. Communicates clearly and respectfully across teams and departments. Works collaboratively to meet production timelines and quality expectations. Maintains accountability for tasks and deadlines while adapting to changing priorities. Actively contributes to a culture of continuous improvement. This is a great opportunity to join a quality-focused team within a dynamic manufacturing environment. If you're looking to grow your career in aerospace or precision manufacturing quality, we'd like to hear from you.

Mon-Fri 6a - 230pm Formulation Technician Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a Key Responsibilities: * Perform testing and qualification of resin products on specialized instruments to meet customer demand. * Record and report test results accurately and maintain proper documentation. * Complete complex production work-orders according to established procedures. * Analyze data, derive conclusions, and prepare reports based on findings. * Collaborate with cross-functional teams. * Adhere to ISO 9001 guidelines and corporate quality policy to ensure high-quality standards. * Follow EH&S safety requirements and actively participate in safety improvement activities. * Continuously identify areas for improvement and propose countermeasures. * Maintain a clean and organized laboratory environment. Knowledge, Skills and Abilities: * Knowledge of Good Laboratory and Manufacturing Practices and standards. * Proficiency in Microsoft Office: Excel, Word, PowerPoint. * Good mathematical, problem-solving, and organizational abilities. * Excellent communication skills (verbal and written). * Ability to read and understand written procedures (SOPs) and follow verbal instructions. * Strong punctuality and attendance record. * Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) * Willingness to learn and apply Lean manufacturing and PPI Continuous Improvement tools. * Ability to work independently with occasional assistance. * Ownership mentality and ability to meet established deadlines and targets. * Willingness to acquire new knowledge and skills. * Understanding of production schedules and ability to prioritize tasks accordingly. * Hands-on experience in a Chemistry laboratory is preferred. * Knowledges of Chromatography software a plus. Education * At least 1+ years of experience in manufacturing environment * A bachelor's in chemistry and or biotechnology preferred. Physical requirements: * Ability to lift and/or move up to 40 pounds. * Regularly required to stand; walk; use hands & finger to handle & feel. * Frequently required to sit and reach with hands and arms. * Specific vision abilities required by this job include close vision, color vision and ability to adjust focus. * Work Environment: While performing the duties of this job, the employee is regularly exposed to toxic or caustic chemicals. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate. Personal protective equipment's: * Job requires wearing lab coats, Safety glasses, gloves & safety shoes all company provided. Non-Negotiable Hiring Criteria: * Must be in compliance with GMP, QSRs, ISO and IVD regulations in the performance of department responsibilities. * Ability to read and write English and understand instructions written or orally in English. * Ability to add, subtract, multiply and divide in all units of measure, whole numbers, fractions and decimals. * Knowledge of Word, Excel and Outlook. Job Type & Location This is a Contract position based out of Sunnyvale, CA. Pay and Benefits The pay range for this position is $28.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Sunnyvale,CA. Application Deadline This position is anticipated to close on Dec 30, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Full-time Description Performs in-process inspections, final inspections, and makes final airworthiness determinations for new manufactured, or processed components, assemblies, major assemblies, and new aircraft manufacture. Position Levels The Quality Inspector levels I-III require varying degrees of experience, job knowledge and skill, which are generally acquired through vocational education and/or apprenticeships, certifications, and specialized, or on-the-job training. Problems are typically solved through knowledge of past practices and procedural guidelines, or knowledge gained through a certification or licensing program. For levels 2 and 3, these positions require specialized knowledge of processes and procedures. LEVEL 1 (Job Code: 130111): Applies basic skills while developing some specialized skills in procedures, operations, techniques, tools, materials, and/or equipment appropriate to area of specialization; performs routine and/or repetitive tasks; limited decision making required; generally, works under close supervision; has limited experience; work is performed from within specific limits of established procedures and/or defined instructions. One to three years' experience is desirable. Advancement to Level II is based on demonstrated proficiency in all duties & responsibilities. LEVEL 2 (Job Code: 130112): Applies skills and job knowledge in area of specialization; may adapt procedures, operations, techniques, tools, materials, and/or equipment to meet needs of area of specialization; may work on non-routine tasks; may train other Inspectors, resolves issues/makes working decisions within area of specialization or responsibility with minimal supervision. Employees at this level receive only occasional instruction or assistance as new or unusual situations arise and have knowledge of company PQM manual and applicable SOP's. Advancement to Level III is based on demonstrated proficiency in all aspects of the job, and successful completion of project responsibilities with minimum oversight. Four to nine years of experience is required. LEVEL 3 (Job Code: 130113): Regularly works on tasks that are varied and complex. Applies full range of specialized skills and job knowledge; frequently adapts procedures, techniques, tools, materials, and/or equipment to meet specialized needs; may serve as lead and may train/mentor other Inspectors in maintenance inspections, final inspection and return to service processes; performs broad and/or focused assignments under general supervision; problem-solving frequently requires analysis of unique issues/problems without precedent and/or structure; originality and ingenuity are often required to help. Employees at this level function with a high degree of autonomy and have a high degree of knowledge and expertise in their areas. Employee must also have deep knowledge of company PQM, Type design data, process specifications, applicable SOP's, and FAA part 21 regulation regarding Production Approval Holder (PAH) responsibilities. Ten or more years of increasingly responsible experience is required for Level III. Duties & Responsibilities Inspects parts, components, assemblies, major assemblies, new manufactured aircraft/aircraft sub-assemblies, and processes in the assigned manufacturing facility, including in process and final inspections. Determines if products and services meet continued airworthiness requirements and certify. Supports FAA conformity projects as required. Performs First Article Inspections per AS9102 standards. Supports Customer specific Quality requirements. Supports continuous process improvement initiatives with a focus on process efficiency. Performs audit functions within the organization as required. Performs Receiving Inspection duties as required. Periodic travel as required to provide off-site technical/inspection support for manufacturing suppliers. Other inspection duties as assigned by Quality Management. Minimum Qualifications Two-year technical degree, FAA certificate or industry quality related certification(s) preferred. AS9100, AS9110, ISO9001, or comparable QMS experience preferred. Aviation experience of at least 1 year preferably in an inspection related capacity. Knowledge of aircraft maintenance practices and/or inspection processes, technical specifications and standards, technical manuals, FAA regulations, and ability to read blueprints. Experience with part inspections, precision measuring equipment, and auditing processes. Must have a strong ability to communicate to all levels of personnel in an assertive but helpful manner. Must be able to work well with others in a fast-paced environment with changing priorities. Must have strong ethics and principles. Ability to obtain a US passport if required.

Timber Products is searching for a new generation to propel us into our second century. We're now hiring entry level production technicians. Timber Products offers $21.06 per hour to start with room to grow, plus full benefits with matching 401k. To apply contact Personnel Preference, Inc. Personnel Preference, Inc: 150 Boles St. Weed. CA Phone: ************

Shift: Mon-Fri 6a - 230pm Duration: 12 Months Pay range: $28.00 Hourly - $28.00 Hourly Onsite Job Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. Key Responsibilities: •Perform testing and qualification of resin products on specialized instruments to meet customer demand. •Record and report test results accurately and maintain proper documentation. •Complete complex production work-orders according to established procedures. •Analyze data, derive conclusions, and prepare reports based on findings. •Collaborate with cross-functional teams. •Adhere to ISO 9001 guidelines and corporate quality policy to ensure high-quality standards. •Follow EH&S safety requirements and actively participate in safety improvement activities. •Continuously identify areas for improvement and propose countermeasures. •Maintain a clean and organized laboratory environment. Knowledge, Skills and Abilities: •Knowledge of Good Laboratory and Manufacturing Practices and standards. •Proficiency in Microsoft Office: Excel, Word, PowerPoint. •Good mathematical, problem-solving, and organizational abilities. •Excellent communication skills (verbal and written). •Ability to read and understand written procedures (SOPs) and follow verbal instructions. •Strong punctuality and attendance record. •Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) •Willingness to learn and apply Lean manufacturing and PPI Continuous Improvement tools. •Ability to work independently with occasional assistance. •Ownership mentality and ability to meet established deadlines and targets. •Willingness to acquire new knowledge and skills. •Understanding of production schedules and ability to prioritize tasks accordingly. •Hands-on experience in a Chemistry laboratory is preferred. •Knowledges of Chromatography software a plus. Education •At least 1+ years of experience in manufacturing environment •A bachelor's in chemistry and or biotechnology preferred. Physical requirements: •Ability to lift and/or move up to 40 pounds. •Regularly required to stand;walk;use hands & finger to handle & feel. •Frequently required to sit and reach with hands and arms. •Specific vision abilities required by this job include close vision, color vision and ability to adjust focus. •Work Environment: While performing the duties of this job, the employee is regularly exposed to toxic or caustic chemicals. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate. Personal protective equipment's: •Job requires wearing lab coats, Safety glasses, gloves & safety shoes all company provided. Non-Negotiable Hiring Criteria: •Must be in compliance with GMP, QSRs, ISO and IVD regulations in the performance of department responsibilities. •Ability to read and write English and understand instructions written or orally in English. •Ability to add, subtract, multiply and divide in all units of measure, whole numbers, fractions and decimals. •Knowledge of Word, Excel and Outlook. Employee Benefits: At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits: Four options of medical Insurance Dental and Vision Insurance 401k Contributions Critical Illness Insurance Voluntary Permanent Life Insurance Accident Insurance Other Employee Perks About LanceSoft LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

Description Under very limited supervision, this position is responsible for In-Process and Final Test and Inspection of all manufactured product prior to customer shipment. This position has the responsibility to verify product conformance to Customer's and ESAM's implemented specifications. Requirements: Be able to understand Quality Assurance criteria, interpretation of customer drawings and ESAM Documents. Responsible for testing completed assemblies and identifying failures. Must be familiar with Quality Assurance tools such as continuity Test and Volt/ohm/Meter Instruments, Micrometer, Measuring Scale, and hand tools. Responsible for product conformity and to identify any nonconformities prior to product being shipped. Able to distinguish colors. Able to read small print and read a ruler Able to read and interpret drawings, engineering specifications, Bill of Materials, etc. Must become familiar with and understand the Quality Assurance Manual. Have excellent manual dexterity and display some mechanical aptitude. Stand or sit for eight (8) or more hours per day. Able to lift and carry 25 lbs. on a repeated basis. Must be able to work overtime and weekends. Have ability to work with arms at shoulder level for extended periods of time. Perform special assignments and other duties as required. Other Duties: Ensure department area is FOD free. Understands, embrace and ensures compliance to ESAM's safety policies and procedures. Creates department efficiencies and brings ideas to senior management. Stay within budget guidelines. Benefits: 401(k) with up to 3% company match Health, Dental, and Vision Insurance Life insurance Short Term Disability Insurance Paid time off Sick time Schedule: Monday- Friday 5:00am-1:30pm OT is required, as needed. OT Hours: Mon-Thursday 2 hours immediately before/following shift, and Sat.

We are hiring a Powder Formulation Technician. The Powder Formulation Technician will be responsible for formulation of powdered media. 3rd Shift: 9:00 pm- 5:30 am At FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences), we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences). Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: *************************************************** Job Description Responsibilities: Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. Uses Mettler-Toledo IND780 terminal system in conjunction with the SAP ERP system to ensure correct raw materials assigned in the batch record are weighed at the specified quantity. Suggest changes in departmental procedures and processes (SOPs) as needed. Performs and documents line clearance at the start of each formulation event. Maintains all required logs and associated documentation. Assures that all chemicals are stored and labeled properly. Performs process scale checks on all required equipment including scales and balances. Keeps work area, utensils, tanks, mills, and equipment clean and organized. Ensures that supplies needed such as weigh boats, gloves, lab coats, etc. are well stocked in their designated areas. Orders supplies or informs Lead/Supervisor if supplies need to be ordered. Follows all safety procedures and works in a safe manner including wearing all required personal protective equipment. Understands and follows procedures to ensure that chemicals are handled properly. Good understanding of metric system and its conversions. Follows and actively participates in sustaining the 6S program in the area. Other duties as requested by Lead or Supervisor. Required Skills/Education: High School Diploma or equivalent. Background in medical devices, diagnostics, food/vitamin processing, or pharmaceuticals. 1-2 years of hands on experience General education about chemicals and proper handling (college level science preferred). Working knowledge of metric system. Good understanding of current Good Manufacturing Practices (cGMPs). Ability to speak, read, and write English. Good oral and written communication skills. Salary and Benefits: For California, the base salary range for this position is $19.65 - $25.51 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.). Medical, Dental, Vision Life Insurance 401k Paid Time Off *#LI-onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

Senior Formulation Technician Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Shift: First Shift - 06:00 AM to 02:30 PM Pay Rate: $20 to $22 per hour Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary: The Media Process Technician I works as part of a team to manufacture dehydrated and liquid cell culture media. The technician follows batch record instructions, weighs raw materials ranging from micrograms to kilograms, calibrates equipment, operates milling equipment, performs sterile filtration, and completes media manufacturing tasks. Responsibilities also include performing standard product testing (osmolality, pH, turbidity) and working closely with cross-functional groups such as R&D, procurement, quality, process technology, marketing, as well as internal/external customers and vendors. Responsibilities Stage and compound raw materials within specified weight tolerances (micrograms to kilograms). Perform milling, blending, aseptic liquid filling, and process control monitoring. Follow GMP and departmental procedures to manufacture dehydrated and liquid culture media according to production schedules. Complete all required documentation neatly, accurately, and in compliance with GMP. Perform cleaning, inspection, calibration, and assist in equipment maintenance; maintain logs and records. Troubleshoot equipment issues. Handle raw materials following GMP and Safety requirements. Use laboratory and production equipment (pipettors, balances, osmometer, turbidimeter, pH meters). Work safely to maintain an injury-free and incident-free workplace. Carry out assigned responsibilities under supervision. Promote a positive team environment through effective communication and engagement. Work overtime when required. Perform other duties as assigned to support business goals. Required Skills & Qualifications BS in Chemistry or related field (or equivalent combination of education, training, and experience). Minimum 6 months of experience in a high-paced chemistry lab or manufacturing environment. Ability to read, write, and follow testing and inspection procedures. Ability to maintain neat, accurate, complete records and logs. Mechanical aptitude; ability to disassemble and reassemble equipment. Good communication skills; able to work independently or as part of a team. Flexibility to work varying schedules, including overtime. Strong attention to detail and ability to focus on tasks continuously. Basic experience weighing multiple components. Basic computer skills, including MS Excel, Word, and PowerPoint. Ability to lift or move approximately 40 lbs. Desired Skills (Preferred but Not Required) Statistical analysis experience using Excel or Minitab. Experience handling multiple components and performing precise weighing. Familiarity with GMP environments, sterile filtration, and laboratory instrumentation. TekWissen Group is an equal opportunity employer supporting workforce diversity.