Quality Control Technician Jobs in Cherryland, CA

DURATION: 1 year SCHEDULE: Typically 8-5p Mon through Fri - periodic weekend/ holiday short shift (approx. 4 hr) work. MUST HAVES: 1. Experience in EM and/or WFI sampling 2. Experience working in a regulated environment 3. Experience in GxP data reporting and documentations. ASSOCIATE/ TECHNICIAN - QUALITY CONTROL PURPOSE Client , a global health care company, is committed to discovering and developing innovative medicines to help people living with diabetes lead longer, healthier lives. To support this, client is conducting research on stem cell therapy. Stem cell research raises hopes for improved treatment of Type 1 Diabetes and for future treatments with cell transplantation therapy. This treatment could be offered to people with many different serious chronic diseases caused by the degeneration of specific cells, such as Type 1 Diabetes. Type 1 Diabetes is manifested by the selective destruction of the insulin-producing cells in the body, which leads to a life-long dependence on insulin injections to control blood sugar levels. It is usually diagnosed in children and young adults. Cell therapy may offer a better treatment by replacing the lost cells with new insulin-producing cells derived from stem cells, thus avoiding daily multiple insulin injections as well as numerous blood glucose tests. This treatment may also offer better blood glucose control, which is crucial to avoid late-stage complications such as blindness and kidney failure. In this project client will generate new stem cell lines to be used in future cell therapies to treat Type 1 Diabetes, Parkinson's disease, and chronical heart failure. The Associate/ Technician - Quality Control will perform day-to-day QC activities while ensuring accuracy, timeliness and in compliance with current cGMP and regulatory expectations of cell-based products. The day-to-day activities will include but not limited to sample collection/ preparation, data entry and reporting, procuring and maintaining lab supplies. ESSENTIAL FUNCTIONS • Perform routine Environmental monitoring, personnel monitoring sampling, and WFI sampling • Perform data entry into electronic system and compile data package for approval • Revise documentation such as SOPs, training materials, and other required documentation • Coordinate for sample pick-up/ shipments • Order, stock, and inventory supplies for the QC laboratory • Support additional projects and assignments assigned by lead and reporting manager • Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes • Support additional projects assigned by reporting manager QUALIFICATIONS • Bachelor's Degree required, within Microbiology/Biology/Chemistry/Life Sciences or related field preferred. • Prior industry experience preferred. Preferred within the Pharmaceutical/Biotech industry. Relevant experience is defined below. o Experience with the application of cGMPs, USP/NF, EuPH., FDA guidelines and ICH guidelines with the pharmaceutical industry o Experience writing standard operating procedures and other cGMP documentation o Experience with Water and/or EM sampling o Experience in aseptic conduct and technique o Experience with sterile cleanroom gowning • Excellent organizational and multi-tasking skills, attention to detail, and the ability to adapt to changing priorities. • Ability to handle conflicts. • Solutions oriented and good at making decisions under time pressure • Excellent organizational and communication skills required.

Direct Hire Full-Time Role Salary Range: $74,000 - $100,000 per year Duties and Responsibilities: Develop and implement quality control testing and product inspection at various production stages. Create reports documenting production or incoming raw material issues. Oversee the QC Department, including the distribution of projects, priorities, workloads, and deadlines within the QC Department. Responsible for management, discipline, and evaluation of QC staff. Train staff and determine work quality expectations. Provide advice and assistance on work techniques, best practices, and subject matter expertise to team members. Oversee general QC approval (Work in Progress Raw Material). Responsible for inspecting final product specifications and approving or rejecting finished products. Manage QC retains, testing schedule, data and reports, and related Standard Operating Procedures (SOPs) documents. Review and make decisions regarding retaining testing and final QC long-term results. Oversee raw material qualification, re-qualification, and disposal. Coordinate and oversee instrument and equipment validation and equipment maintenance. Requirements and Qualifications: M.S. in Biology or a related field with 5+ years of QC experience 1-3 years of supervisory experience Knowledge and experience with Quality Control Management is preferred. Excellent writing and communication skills. Detail-oriented and excellent at record keeping. Able to think critically and analyze and troubleshoot data. Able to lift and move up to 40 pounds. Familiarity with a laboratory setting and handling of lab-related materials. Strong computer literacy and experience with Microsoft Word, Excel, and PowerPoint Able to work in the cold room periodically, kept at 2 - 8°C (35.6 - 46.4°F). Able to provide a vaccination record and confirm current Hepatitis B status after hiring. Desired Skills and Experience QC, Quality Control Management, biotech, SOPs, laboratory, Word, Excel, PowerPoint Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at *************************

Formulation Technician I Duration: 12 Months Job Type: Contract Work Type: Onsite Shift: Monday to Friday 2.00 PM to 10.30 PM Pay Rate: $20-24.000 per hourly 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. Job Description: As part of the Chromatography and Mass Spectrometry Division (CMD), the Sunnyvale, CA site focuses on developing and delivering the highest quality chromatography solutions in the industry. How Will You Make an Impact?: Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. A Day in the Life: Testing of resin products on unique instruments to meet customer demand. Record and report test results accurately and maintain proper documentation. Complete production work-orders according to established procedures. Follow corporate quality policy to ensure high-quality standards. Follow safety requirements and actively participate in safety improvement activities! Maintain a clean and organized laboratory environment. Education: High school diploma or equivalent required. Experience: Required: Minimum of 1 year of work experience in a manufacturing, operations, production, lab setting or related field Knowledge, Skills, Abilities: Knowledge of Good Laboratory and Manufacturing Practices and standards. Good mathematical, problem-solving, and organizational abilities. Excellent verbal and written skills Read and understand written procedures (SOPs) and follow verbal instructions. Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) PC literate and have experience with spreadsheet and database software. Knowledge of Chromatography software and chemistry experience a plus. Physical Requirements / Work Environment Lift and/or move up to 40 pounds. Regularly required to sit, stand; walk; use hands & fingers to handle & feel. Visual abilities to detect small components and particles. Exposure to toxic or caustic chemicals, fumes or airborne particles. Occasionally exposed to moving mechanical parts and moderate noise level. PPE requirements: lab coat, Safety glasses, gloves, face shields, & safety shoes (all company provided.) P95 Mask in the areas that have exposure of solvent fumes TekWissen Group is an equal opportunity employer supporting workforce diversity.

Immediate opportunity for four (4) Microbiologists to test commercial and clinical samples for release! In this exciting role, you will learn microbiology assays and have an opportunity to gain exposure to validation of methods. As a Microbiologist in Quality Control, you will directly contribute to safety data for in-process and final container of pharmaceutical products. Apply today and join a team committed to excellence in pharmaceutical manufacturing! Schedule/Shift: 1st shift, Mon.-Fri., Tues.-Sat., and Wed. Position Type: 1 year contract Position Overview: Quality Control Microbiology - Perform microbiology (sterility, LAL (Endotoxin), bioburden, identification, virology) assay and validation activities supporting GMP, Clinical, development product release. This position is to support project related QC Assay testing/validation. Essential Duties and Responsibilities: Capable of conducting microbiological method validation including bioburden, sterility, LAL (endotoxin), and virology methods supporting biopharmaceutical, clinical and development products. Responsibility including protocol and report write up. Conduct execution of microbiological methods per approved protocols and testing of routine and investigational samples. Familiarities with all microbiological compendial methods for specific commercial products. Maintains records of method qualification/validation and other microbiological related methods. Investigates questionable test results, writes protocol deviation report (PDR), investigation/test plans when applicable. Collaborates effectively with Quality Assurance validation on the method validation approach. Keeps current with revisions to compendial monographs and to compendial test methods used in the microbiology division. Write protocols, revises SOP's affected by these compendial changes and changes arising as a function of a CAPA, per approved Change Control. Ability to support and prioritize many diverse activities simultaneously while meeting schedule commitments. Thorough knowledge of microbiological analytical methods, compendial requirements (USP, EP, JP). Knowledge of biologics and manufacturing processes. Strong computer skills (Word, Excel, Access, PowerPoint, LIMS, SAP). Prior experience in a QC microbiology testing laboratory. Ability to work independently with minimum supervision. Qualifications: Bachelor's degree (BS) in Microbiology or related science degree or technical field. Two (2) or more years of microbiology laboratory experience in pharmaceutical or related industry or an equivalent combination of education and experience. Flexible, efficient, and team oriented Excellent communication skills, both written and verbal

Ultimate Staffing is looking for a QA Inspector to support a growing employee owned technology company located in beautiful Scotts Valley, only minutes from Santa Cruz and just over the hill from Silicon Valley. This is a onsite role with a target pay of $24-28/hour. The Incoming QA Inspection is responsible for ensuring that all incoming materials and products meet the required quality standards. This includes inspecting, testing, and sampling materials and products to ensure they meet specifications and regulatory requirements. The Incoming QA Inspection will work closely with the production team to identify and resolve any quality issues and will maintain accurate records of all inspections and test results. Responsibilities Inspect, test, and sample incoming materials and products to ensure they meet quality standards Identify and report any quality issues to the production team Work with the production team to resolve quality issues Maintain accurate records of all inspections and test results Ensure compliance with regulatory requirements Participate in continuous improvement initiatives Requirements High school diploma or equivalent Previous experience in quality assurance or inspection preferred Strong attention to detail Excellent communication and interpersonal skills Ability to work independently and as part of a team Knowledge of regulatory requirements and quality standards Proficient in Microsoft Office All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Operate semiconductor and metrology equipment. Provide technical support and assistance. Set up process equipment for operation. Conduct technical tests and experiments for process engineering within research and development. Monitor and audit line operators, offering guidance as needed. Execute process test runs and compile records, charts, and graphs to present results to engineering teams, aimed at identifying yield issues or testing new products. Offer technical assistance to personnel in process development and engineering. Conduct laboratory activities for customer demonstrations and process experiments, including sample preparation, chemical treatments, and running wafer flows on company tools. Use metrology tools to perform measurements, including thin film measurements, CD measurements, and SEM imaging. Develop process recipes from scratch and fine-tune existing recipes for robustness, suggesting improvements as necessary. Implement statistical process control (SPC) and etch rate measurements, including evaluation and reporting to ensure that chamber performance remains in control and meets specifications; identify trends or out-of-spec conditions and propose troubleshooting actions. Follow customer instructions to determine target pattern features for first sample cleaving using microscopes, top-down SEMs, and micro-cleavers, and create or update PowerPoint instructions for others to follow. Train new process engineers, technicians, or field service engineers on lab equipment operation, sample preparation, and adherence to lab protocols. Serve as the first point of contact for alarm resolution, lab operations, and protocol inquiries. Collaborate with demo engineers and the metrology team to develop metrology recipes. Recommend enhancements to experiment execution for improved quality and efficiency. Operate computer interfaces and navigate diagnostic software as necessary. Work with the lab operations team to enhance lab safety, customer intellectual property, and lab protocols. Qualifications: Preferred experience in a clean room environment, with the ability to wear personal protective equipment (PPE) such as bunny suits, safety glasses, masks, shields, gloves, and safety footwear. 2-3 years of experience with silicon wafer handling is preferred. Ability to understand process requirements and execute experiments with minimal supervision. Familiarity with company tool operations, with skills to clear basic alarms and troubleshoot to minimize tool downtime. Degree in electronics, material science, chemistry, physics (Associates or BS) or equivalent work experience. At least 4 years of experience in the semiconductor industry, particularly in troubleshooting or operational roles. Demonstrates flexibility and responsiveness to changing priorities, including willingness to rework and work overtime. Able to install components from a height of 1 to 6 feet and reach into machinery for task completion. Proficient in using computer interfaces and diagnostic software. Basic proficiency in Microsoft Office applications (Excel, Word, PowerPoint). Strong communication skills to convey detailed pass-downs for seamless lab operations. Excellent attention to detail and organizational skills. Capacity to work independently as well as collaboratively in a team setting. Strong analytical and problem-solving abilities. Education: BS in Material Science preferred or equivalent relevant experience. Pay for this position is based on market location and may vary depending on job-related knowledge, skills, and experience. As a contractor, you may also be eligible for health benefits such as health, dental, and vision as well as access to a 401K plan. We are an equal-opportunity employer and value diversity at The Mice Groups Inc. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Pursuant to the San Francisco Fair Chance Ordinance, we will consider employment-qualified applicants with arrest and conviction records. Pursuant to the Los Angeles Fair Chance Ordinance, we will consider employment-qualified applicants with arrest and conviction records. The Mice Groups Inc. values your privacy. Please consult our Candidate Privacy Notice, for information about how we collect, use, and disclose the personal information of our candidates.

Sentien Robotics is a cutting-edge technology company, redefining what's possible with unmanned aerial systems (UAS) and robotics. Our mission is to deliver innovative solutions for critical industries like surveillance, environmental monitoring, infrastructure inspection, and national security through persistent aerial flight, multi-UAS coordination, and full lifecycle automation. Role Description As a Production Technician, you'll assemble, troubleshoot, and maintain robotic systems, ensuring they meet our high standards of quality and safety. You'll work closely with engineers and follow detailed assembly instructions, contributing directly to the success of our groundbreaking technology. Responsibilities • Assemble mechanical, electrical, and robotic components. • Manage inventory and prepare components for assembly. • Conduct quality checks throughout the production process. • Diagnose and resolve assembly issues and perform preventive maintenance. • Interpret technical drawings and maintain accurate records. • Support critical hardware demonstrations with customers as needed Qualifications • Experience with hand and power tools in a production setting. • Ability to read mechanical drawings and schematics. • Strong attention to detail and organization skills. • Prior experience in robotics or automation is a plus. • Technical degree or certification preferred. Why Sentien Robotics? Join us in shaping the future of robotics. You'll be part of a fast-paced, innovative team working on impactful real-world projects with opportunities for growth and professional development. US Hourly Range $32-$40 USD

Must haves: 1. Experience in EM and/or WFI sampling 2. Experience working in a regulated environment 3. Experience in GxP data reporting and documentations. Purpose: The Associate/ Technician - Quality Control will perform day-to-day QC activities while ensuring accuracy, timeliness and in compliance with current cGMP and regulatory expectations of cell-based products. The day-to-day activities will include but not limited to sample collection/ preparation, data entry and reporting, procuring and maintaining lab supplies. Essential Functions: • Perform routine Environmental monitoring, personnel monitoring sampling, and WFI sampling • Perform data entry into electronic system and compile data package for approval • Revise documentation such as SOPs, training materials, and other required documentation • Coordinate for sample pick-up/ shipments • Order, stock, and inventory supplies for the QC laboratory • Support additional projects and assignments assigned by lead and reporting manager • Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes • Support additional projects assigned by reporting manager Qualifications: • Bachelor's Degree required, within Microbiology/Biology/Chemistry/Life Sciences or related field preferred. • Prior industry experience preferred. Preferred within the Pharmaceutical/Biotech industry. Relevant experience is defined below. Experience with the application of cGMPs, USP/NF, EuPH., FDA guidelines and ICH guidelines with the pharmaceutical industry Experience writing standard operating procedures and other cGMP documentation Experience with Water and/or EM sampling Experience in aseptic conduct and technique Experience with sterile cleanroom gowning

Duration: 12-month Contract (with potential for conversion) Target Pay Rate: $28 - $32.30/hr. As a Quality Control Analyst, you will be responsible for performing chemistry-based testing, such as HPLC, particle counting, and uniformity analysis, among others. This role plays a critical part in ensuring the quality, consistency, and compliance of Factor VIII products by performing assays, analyzing data, and supporting lab maintenance. You will also work to identify process improvements, reduce defects, and ensure inspection readiness, contributing directly to product quality assurance. Key Responsibilities: Conduct chemical and biological evaluations of final products, intermediate products, raw materials, and production facilities. Perform and validate various QC assays (e.g., HPLC, particle counting) and establish corresponding specifications. Assist in the validation of QC assays and contribute to the development and maintenance of Standard Operating Procedures (SOPs). Perform data analysis, identify trends, and recommend process improvements to enhance product consistency and reduce defects. Ensure the laboratory remains in a state of readiness for inspections. Support routine lab maintenance and testing activities as required. Daily Interaction: Team: You will be part of a team of 11 members, collaborating closely with the group to ensure lab operations are efficient. Supervisor: You will report directly to the Associate Director, with guidance and support provided for your role. Why This Role Is Open: This role supports the increased demand for Factor VIII products and is a critical position within the Chemistry Quality Control team. The role involves a mix of lab testing, data review, and lab maintenance. Location: Onsite in Berkeley, CA. Top Skills and Qualifications: Must-have skills: Experience with HPLC (High-Performance Liquid Chromatography) Strong chemistry lab background Ability to work well within a team Flexibility and adaptability in the lab environment High attention to detail Desirable Background: Pharmaceutical industry experience or academic background with HPLC exposure. Long-term Outlook: This is a contract position for 12 months with potential for conversion to a permanent role, based on performance and business needs. Ideal Candidate Background: Experience in the pharmaceutical industry or academic labs with a focus on HPLC and other chemistry-related testing. Experience Required: 4-6 years of relevant experience in a chemistry or quality control role.

Job Title: Quality Control Analyst Duration: 12-month contract (Extendable). Hourly Pay: $28/hr to $32/hr on W2 without benefits on W2 Schedule: Mon - Fri, Business hours Job Description: Responsible for biological and chemical evaluation of final products, intermediate products, raw materials, and production facilities. • Duties include performing QC assays, writing and establishing specifications, assisting in the validation of QC assays, and writing Standard Operating Procedures. • Has knowledge of commonly used concepts, practices, and procedures within a particular field. • Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. • Typically reports to a supervisor or manager. 4-6 Years of Experience INTAKE QUESTIONS: • What is a day like in this role? From a candidate's perspective, what's exciting about this role and team? What does this role accomplish for the business? Response: A typical day for this role is to perform Chemistry tests (HPLC, Uniformity, Particle counting to name a few), analyze data, and review processes to prevent defects, reduce costs, and ensure consistency across product lines. The role also includes ensuring lab inspection readiness and routine maintenance. • Who will this person work with daily? Response: The team has 11 members and will report directly to the Associate Director. • Why is this role open? Is this more maintenance or new development work? Response: The position is open to support the demand of increased Factor VIII Products. Its a QC role in the Chemistry group that has a good mix of lab work (testing, data review) and lab maintenance responsibilities. • Tell me about the team dynamic/culture - a long-standing team that has worked together for years or a fairly new team? • How does the team work together? Response: The team has a wide range of experience levels at Client's (ranging from 2 years to 26 years). Its a collaborative environment. • List top 5 must-haves to be successful in this role. • Stress that we may not be able to find candidates with every single item on their list - ask what is truly mandatory. Response: HPLC experience, Chemistry lab experience, Teamwork mindset, Flexibility, Detail oriented • What is the long-term plan for the role? Conversion potential? Response: Currently this is a contract role for a year, which has the potential to be a permanent role. However, it depends on multiple factors such as employee performance and business needs. • What does the ideal candidate's background look like (ex: pharmaceutical-specific background specific industry experience etc.)? Response: Pharmaceutical industry or academic HPLC experience. • What are you not interested in seeing and why? Response: Team player, flexible, strong work ethic, can-do attitude.

LanceSoft is seeking a travel Cath Lab Technologist for a travel job in Fremont, California. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel 0426 Years of Experience 1 Years Required Certifications Fluoro, BLS About LanceSoft Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities. Benefits Weekly pay Medical benefits

For over 15 years, Trilyon has been at the forefront of providing comprehensive global workforce solutions and staffing services. Leveraging our extensive expertise across multiple domains such as Cloud technology, Salesforce, AI, Machine Learning, and Technical Writing, we consistently exceed expectations in catering to a wide range of requirements. Currently we are seeking a “Lab Technician” for one of our clients that is a leading multination corporation. Responsibilities: • Maintain inventory of all hardware and supplies. Check in and check out equipment. • Install motherboards, FPGA boards, and run cables. • Installing and wiring equipment in racks. • Administer Linux machines, FPGA boards and resolve issues. • Assist engineers to set up systems. • Move equipment between the labs. • Ship boards to other AMD sites and partners. • Organize and clean up lab regularly. • Work with internal teams and external contractors to set up lab infrastructure (power, networking). • Place, track and receive equipment orders. Must have: • MS Office Applications: Word, Excel, Outlook. • Familiar with basic Unix commands. • Understanding PCB design, schematics, and layout ESD. • Basic PCB bring-up and debug skills. • Familiar with lab tools like oscilloscope, multimeter, power supplies. • Debugging skills, able to troubleshoot PC and server. • Understanding of computer's peripheral hardware. • Can build a complete computer from scratch and debug issues. • Basic knowledge of computer hardware and cabling installation. • Detail oriented, ability to follow precise instructions and accurately complete tasks. • Strong organizational skills & ability to prioritize tasks. • Experience in lab environment, installing server and network equipment. • Ability to communicate technical details both verbally and in writing. • Must be able to lift and carry up to 50 pounds. Good to have: • Unix system administration. • Knowledge of network protocols and layers. • Knowledge of at least one programming language, ideally Python. • Associate or bachelor's degree in electrical engineering or related field. • Minimum of 3 years of experience in PCB design. • Soldering skill.

ALOIS Healthcare is seeking a travel Cath Lab Technologist for a travel job in San Francisco, California. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel The Cardiac Cath Lab Tech performs advanced diagnostic and interventional cardiac procedures, peripheral vascular procedures, and structural heart procedures in the Cardiac Cath Lab. Cardiac Cath Lab Technicians are responsible for scrubbing, monitoring, and assisting providers as requested. ALOIS Healthcare Job ID #15240144. Pay package is based on 10 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Cath Lab Tech:Acute,07:00:00-17:00:00 About ALOIS Healthcare Why ALOIS Healthcare? ALOIS means “brave warrior” and that's what you are- Warrior in Scrubs! Just as you advocate for your patients, we will advocate for you. The pay you deserve. The support you need. We're in your corner for every battle - because you shouldn't settle for anything less when it comes to your career. We offer: · Industry-leading pay Generous cost of living and housing stipends · Opportunities for referral, sign-on, and extension bonuses · Weekly health insurance or health insurance Marketplace weekly bonus · Continuing education credits We're proud to be recognized globally as a certified minority-owned staffing supplier. At ALOIS Healthcare: · Everyone Matters · We are Performance Driven · We are Open, Honest and Direct · We are Transparent · We are Inclusive · We Do the Right Thing We care about you - and your success is our success.

Travel Nurses, Inc. is seeking a travel Cath Lab Technologist for a travel job in Stockton, California. & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 36 hours per week Shift: 12 hours, days Employment Type: Travel Job Description We are looking for Cardiac Cath Lab Rad Tech for an immediate opening in Stockton, California. You should have 1-2 years of recent experience in your specialty and a willingness to be flexible and adaptable in new environments. Travel Nurses, Inc. (TNI) offers our traveling nurses excellent benefit packages, including day-one health care coverage, 401(k), competitive nurse salaries, bonuses/incentives, and many other perks. The Onboarding Process You Deserve If you're looking for a travel nurse company that will take care of you from start to finish, look no further than Travel Nurses, Inc.We have the most detailed recruitment specialists in the industry and work tirelessly to ensure your onboarding process is stress-free. We understand contract transparency is a tremendous concern. This becomes especially true when you navigate an unfamiliar hospital system with complex pay packages and different rules for each assignment - but TNI has got this covered! We have several policies that prevent confusion about what's expected from nurses before they begin a contract; one crucial item is an Engagement Letter review completed with your recruiter before every contract. Benefits and Perks Go further with the best benefits and perks travel nursing offers. We provide everything you need to ensure you are covered on and off the clock. Learn more about our benefits and perks here Day One Health Coverage: At TNI, we provide Health, Dental, Vision, and Life Insurance to employees working full-time contracts on day one. We include several major medical plan options. Our premium plans provide an expansive network of providers in and outside Tennessee, including nationwide coverage. TNI offers an HSA plan with a dollar-per-dollar match up to $750. Electing or waiving the group health insurance, eligible contract nurses will automatically enroll in forty thousand employer-paid life/ AD&D insurance. Finally, we offer a 401(k) plan through John Hancock with employer matching. 24/7 Clinical Support: Healthcare Professionals work 24/7, and so does TNI! Situations may emerge at any time, so we always have a clinician available to support you! As a nurse-owned and nurse-operated agency, Travel Nurses, Inc. takes pride in saying, "Nurses know Nurses." The best travel nurses and healthcare professionals deserve the best support. Lucrative Referral Bonus: TNI believes your friends deserve to be treated well, so we offer a lucrative referral bonus! Earn $500 per RN national traveler referral and $250 for non-RN referrals (To be paid upon successfully completing 468 hours worked). Travel Reimbursement: No need to miss out on an adventure because you can't afford to get there. Travel Nurses, Inc. will help you cover the cost. Onboarding Cost Coverage: We know credentialing fees add up. TNI is committed to covering your onboarding costs, including licensure fees, certification reimbursement, physical exams, and immunizations. Travel Nurses, Inc Job ID #862698. Pay package is based on 12 hour shifts and 36 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Rad Tech - Cardiac Cath Lab About Travel Nurses, Inc.Empowering healthcare professionals to excellence. Travel Nurses, Inc. is a leading travel nurse staffing agency providing nurses with opportunities to find work across the country. Established by nurses for nurses, TNI has been in business since 1988 and has over 30 years of experience. With headquarters in Memphis, Tennessee, and recruiters nationwide, we are committed to providing quality care for patients all over the U.S., while ensuring our employees have an enriching career path filled with excellent benefits packages including day one health care coverage, 401(k), competitive salaries, bonuses/incentives among many other perks! The Onboarding Process You Deserve If you're looking for a travel nurse company that will take care of you from start to finish, look no further than Travel Nurses, Inc. (TNI). We have the most detailed recruitment specialists in the industry and work tirelessly to make sure your onboarding process is stress-free. We understand contract transparency is a tremendous concern. This becomes especially true when you navigate an unfamiliar hospital system with complex pay packages and different rules for each assignment- but TNI has got this covered! TNI has several policies that prevent confusion about what's expected from nurses before they begin a contract; one important item is an Engagement Letter review completed with your recruiter before every contract. Benefits Weekly pay Continuing Education 401k retirement plan Wellness and fitness programs Mileage reimbursement Referral bonus Employee assistance programs Medical benefits Dental benefits Vision benefits Benefits start day 1 License and certification reimbursement Life insurance Retention bonus

GetMed Staffing, Inc. is seeking a travel Cath Lab Technologist for a travel job in Stockton, California. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 36 hours per week Shift: 12 hours, days Employment Type: Travel GetMed Staffing is searching for a strong Cath Lab Tech to assist our traveler-friendly client. A minimum of 1-2 years of experience is required. Traveling with GetMed Staffing offers the unique opportunity to gain diverse experiences, both personally and professionally. Gain experience that matters. GetMed Staffing, Inc. Job ID #29514527. Pay package is based on 12 hour shifts and 36.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Cath Lab:Cath Lab Tech,07:00:00-19:00:00 About GetMed Staffing, Inc. We are a diversity owned company, specializing in healthcare recruiting services. We truly understand how important a healthcare travelers' relationship is with their recruiter, as well as our relationship is with our healthcare facilities. We recognize that the needs of our healthcare travelers can vary, and therefore we provide the personalized touch necessary to ensure a successful travel assignment each and every time. Our healthcare facilities and clients benefit from us putting our healthcare travelers first. GetMed Staffing is excited to be a leader within the industry by focusing on providing healthcare travelers with more choices and possibilities as they plan for their next healthcare travel assignment. Benefits Life insurance Medical benefits Dental benefits Vision benefits 401k retirement plan

PRN Healthcare is seeking a travel Cath Lab Technologist for a travel job in Stockton, California. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 36 hours per week Shift: 12 hours, days Employment Type: Travel PRN Healthcare Job ID #1326983. Pay package is based on 12 hour shifts and 36 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: CARDIAC CATH TECH CARDIAC CATH About PRN Healthcare Our story starts with a 21-year-old CNA named Pete Hietpas. Pete was diligently working in eastern Wisconsin with a variety of staffing agencies, but something was missing. He loved caring for his patients, but felt that staffing agencies were exchanging compassion for competitiveness. He was determined to change that. As a result, he started Nurses PRN in 1995 to become a model for the healthcare staffing industry - being competitive in the marketplace, yet still maintaining a compassionate heart. Over the years Nurses PRN grew and evolved as a nationwide healthcare staffing company, and therefore wanted to be more inclusive to all valued healthcare professionals: nurses, allied health, locum tenens, CNAs, and more. This lead to the introduction of PRN Healthcare, which is inclusive of Nurses PRN and all of our other healthcare divisions. Our mission to create authentic, meaningful relationships with our healthcare professionals helps us set them up for success in their dream assignment, whether that be a travel contract, local contract, or per diem shift. This is all driven by the simple idea that better care for our healthcare workers, leads to better patient care - and this is all supported by a dedicated internal staff. Our company culture is strongly backed by faith-based values and activities, to remind us that our success provides us the opportunity to serve and give back to our communities. This is the spirit of caregiving. This is PRN Healthcare. Benefits Weekly pay Guaranteed Hours Continuing Education 401k retirement plan Referral bonus Employee assistance programs Company provided housing options Medical benefits Dental benefits Vision benefits Life insurance

Title: Formulation Technician I Duration: 12 Months Shift: 2nd Shift: Monday - Friday 2PM - 10;30PM Pay: $25.30 ph. Job Details/Requirements: Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. Minimum of 1 year of work experience in a manufacturing, operations, production, lab setting or related field Knowledge of Good Laboratory and Manufacturing Practices and standards. Knowledge of Chromatography software and chemistry experience a plus.

PHP is seeking a travel Cath Lab Technologist for a travel job in Stockton, California. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 36 hours per week Shift: 12 hours, days Employment Type: Travel PHP Job ID #392306. Pay package is based on 12 hour shifts and 36 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Rad Tech About PHP At PHP, you are always the first focus! For us, it isn't simply about hiring staff, it's about building a solid family of healthcare professionals by expanding their premium employment opportunities, guiding them through every step of the process, and providing them with the highest compensation and best benefit packages in the industry. With over 20 years of experience, travel contracts in all 50 states and internationally, and many industry awards and recognitions, Premier Healthcare Professionals focuses on quality, not quantity. That is our commitment!

Formulation Technician I Duration: 12 Months Job Type: Contract Work Type: Onsite Shift: 02:00 PM to 10:30 PM Pay Rate: $23-23.000 per hourly TekWissen Group is a workforce management provider throughout the USA and many other countries worldwide. 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. Job Description: Working in a team of media process technicians, media process technician I will manufacture dehydrated and liquid cell culture media. Formulation technician I will be able to follow batch record instructions and will be expected to weigh microgram to kilograms quantities of individual raw materials, calibrate equipment, follow safety policies and procedures, operate milling equipment, perform sterile filtration and any other tasks required to complete cell culture media manufacturing. Standard product testing, such as osmolality, pH and turbidity, will also be performed in this job. This position works closely with R&D, procurement, quality, process technology, marketing as well as external and internal customers and vendors. RESPONSIBILITIES: Responsible for the staging and compounding of raw materials within weight tolerances (e.g. micrograms to kilograms), milling , blending, aseptic liquid filling, process control monitoring and documentation of such procedures for manufacturing dehydrated culture media and liquid media in accordance with production schedules following the appropriate GMP and department procedures. Completes all required documentation neatly, accurately, and in accordance with GMP. Performs cleaning, inspection, calibration and assists in the maintenance of equipment. Maintains related logs and records. Performs equipment troubleshooting. Handles raw materials per GMP and Safety requirements. Uses equipment such as pipettors, balances, osmometer, turbidmeter and pH meters. Ensure that tasks are performed in a safe and responsible manner to create an injury free and incident free workplace Required to follow through on assigned responsibilities and able to function under supervision. Responsible for promoting positive team environment through good communications and team engagement. May be required to work overtime. Performs other duties as assigned in support of business goals Required Qualifications: Minimum of High School Diploma or equivalent. Minimum of 6 months experience in a high-paced laboratory environment or manufacturing facility. Equivalent combination of education, training, and relevant work experience maybe considered. Must be able to read, write, and follow testing and inspection procedures. Must be able to maintain neat, accurate and complete records and logs. Mechanical aptitude and ability to disassemble and reassemble various equipment. Good communication skills and ability to work both individually and as part of a team. Flexibility with departmental work schedules including overtime. Must be able to focus with continuous attention to detail. Basic experience in weighing multiple components is required. Basic proficiency with PCs (Personal Computers) and use of Windows applications such as MS Excel, MS Word and MS PPT is required. Statistical analysis using mathematical spreadsheets such as Excel or Minitab is highly desired. Must be able to lift or move approximately 40lbs TekWissen Group is an equal opportunity employer supporting workforce diversity.