Laboratory technician jobs in Berkeley, CA

Company: Fusion Medical Staffing Job Details Fusion Medical Staffing is seeking a skilled Cath Lab Tech for a 13-week travel assignment in San Jose, California. As a member of our team, you'll have the opportunity to make a positive impact on the lives of patients while enjoying competitive pay, comprehensive benefits, and the support of a dedicated clinical team. Required Qualifications: One year's recent experience as a Cardiac Cath Lab Tech Current BLS (AHA/ARC) certification ARRT, RCES, or RCIS certification Current ACLS (AHA/ARC) certification Preferred Qualifications: Valid Radiologic Technologist license in compliance within state regulations PALS (AHA/ARC) or ENPC Certifications Other certifications and licenses may be required for this position Summary: The Cath Lab Technologist is responsible for assisting in diagnostic and interventional cardiovascular procedures in the cardiac catheterization lab. This role involves preparing patients and equipment, monitoring hemodynamic data, assisting physicians during procedures, and ensuring patient safety throughout the process. The technologist operates specialized imaging equipment, maintains sterile technique, and collaborates with the healthcare team to provide high-quality patient care. This position requires technical expertise in cardiovascular procedures, critical thinking skills, and the ability to work efficiently in high-pressure situations. Essential Work Functions: Prepare and position patients for cardiac catheterization, angioplasty, stent placement, electrophysiology studies, and other interventional procedures Assist physicians during procedures by passing catheters, wires, balloons, and stents, and operating fluoroscopy and hemodynamic monitoring equipment Operate and maintain imaging equipment, contrast injectors, and hemodynamic monitoring systems, ensuring proper functionality Scrub in and assist with sterile field setup, ensuring adherence to infection control and procedural protocols Perform sheath removal and hemostasis using manual compression or closure devices as directed Maintain accurate documentation, including patient records, imaging data, and equipment logs Assist with inventory management, stocking supplies, and ensuring proper storage of sterile instruments and medications Adhere to radiation safety protocols, ensuring proper use of lead aprons, shields, and dosimeters Ensure compliance with hospital policies, safety guidelines, and regulatory requirements Adhere to hospital safety protocols, infection control guidelines, and regulatory standards Perform other duties as assigned within the scope of practice Required Essential Skills: Critical thinking, service excellence, and good interpersonal communication skills The ability to read, write, and communicate in the English language Ability to read/comprehend written instructions, follow verbal instructions, and proficiency in PC skills Physical Abilities - Must be able to remain in a stationary position, move about, move equipment (50-100lbs), push, pull, and bend Interpersonal Skills - Must be able to work effectively with a variety of personnel (professional and ancillary) to present a positive attitude and professionalism Technical/Motor Skills - Must have the ability to grasp, perform fine manipulation, push/pull, and move about when assisting with procedures and/or using department equipment Mental Requirements - Must be able to cope with frequent contact with the general public and customers while meeting deadlines under pressure. Must be able to work under close supervision occasionally, as well as working without assistance from other personnel. Must be able to contend with irregular activity schedules occasionally and continuous concentration to detail Sensory - Must possess visual acuity and ability to effectively communicate Benefits Include: Highly competitive pay for travel professionals Comprehensive medical, dental, and vision insurance with first day coverage Paid Time Off (PTO) after 1560 hours Life and Short-term disability offered 401(k) matching Aggressive Refer-a-friend Bonus Program 24/7 recruiter support Reimbursement for licensure and CEUs Why Choose Fusion? At Fusion Medical Staffing, our goal is to improve the lives of everyone we touch, and we're always looking for people like you to join our mission. Your passion for helping others deserves a partner just as committed to supporting you - that's why we offer day one insurance, $0 copay for mental health services, scholarships and awards, exclusive discounts, and more. From your personal recruiter to our clinical and traveler experience teams, we're here to guide and celebrate you along your journey. You take care of others; we take care of you. Other Duties Disclaimer: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Other duties may be assigned. This job description is not a comprehensive list of all activities, duties, or responsibilities that are required of the employee for this job and is subject to change at any time with or without notice. Start your rewarding career as a Travel Cath Lab Tech with Fusion Medical Staffing and join our mission to improve lives. Apply now! *Fusion is an EOE/E-Verify Employer #pb12

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.

Manufacturing Lab Associate (Night Shift) 6-12 Month Assignment Pay Rate: $28/hr. / $30.80 / $32.20 (Depends on shift) Open Shifts: SET Schedule/ Room for OT Night Shift: Tuesday-Friday /Saturday 6:00 PM - 7:00 AM (3x12/4x12 schedule alternating weekly on Saturday) On behalf of our client a pharmaceutical company specialized in developing therapeutics for patients dealing with life threatening rare-genetic diseases. We are seeking for a Manufacturing Associate with hands-on experience in large-scale bioprocess operations, buffer/media preparation, and cGMP-compliant environments. Skilled in cell culture, purification, and formulation processes with a strong foundation in scientific principles and operational excellence. Key Responsibilities Operate large-scale equipment supporting Cell Culture and Purification operations. Prepare buffer and media solutions for production batches. Learn and execute biopharmaceutical manufacturing techniques including tangential flow filtration, chromatography, and formulation. Follow SOPs and document processes in accordance with GDP and regulatory guidelines. Identify, troubleshoot, and escalate process issues while contributing to resolution strategies. Support integration of new technologies and practices into established processes. Suggest and assist with procedural improvements and updates. Education and Qualifications Bachelor's degree in a science-related field or engineering OR. Associate's degree in a science-related field or Biotech Certificate with 2+ years' experience in biotech manufacturing or other regulated industries Physically demanding role with frequent bending, lifting (up to 25 lbs.) reaching, stair and ladder use Will require night shift work and flexibility with off-hours as needed Please submit a copy of your resume in a Word or PDF format to be considered.

Fulfilling the promise of medicine The Permanente Medical Group, Inc. (TPMG - Kaiser Permanente Northern California) is one of the largest medical groups in the nation with over 10,000 physicians, 21 medical centers, numerous clinics throughout Northern and Central California, and an over 80-year tradition of providing quality medical care. We currently have the following opportunities: HEMATOLOGIST/ONCOLOGIST: Antioch (part-time), Dublin, Fresno, Modesto, Oakland, Roseville (part-time), Sacramento Downtown, South San Francsico, Vallejo HEMATOLOGIST/ONCOLOGIST - ONCOLOGY: Modesto, California Full-time annual salary range is $470,040 to $500,040 plus additional potential incentives up to $41,570*. Reduced schedules with pro-rated compensation may be available. *Some incentive opportunities are estimates based on potential premium pay. Per Diem Opportunities are also available throughout Northern & Central California. Per Diem pay range is $320 to $330 hourly. With TPMG you'll benefit from: Work-life balance focused practice, including flexible schedules and unmatched practice support. We can focus on providing excellent patient care without managing overhead and billing. No RVUs! We are committed to cultivating and preserving an inclusive environment for all physicians and employees. Multi-specialty collaboration with a mission-driven integrated health care delivery model. An outstanding electronic medical record system that allows flexibility in patient management. We have a very rich and comprehensive Physician Health & Wellness Program. We are Physician-led and develop our own leaders. Professional development opportunities in teaching, research, mentorship, physician leadership, and community service. EXTRAORDINARY BENEFITS: Competitive compensation and benefits package, including comprehensive vision, medical, and dental Interest Free Home Loan Program up to $250,000 (approval required) Relocation Assistance up to $10,000 (approval required) PSLF Eligible Employer Malpractice and Tail Insurance Life Insurance Optional Long-Term Care Insurance Paid holidays, sick leave, and education leave Shareholder track Three retirement plans, including a pension plan and 401(k) For more information about these opportunities, our wage ranges, or to apply, please visit our website at: ************************************************************** For immediate consideration, kindly reply with your CV. Or contact Bo Chau, Physician Recruiter at ************** / call ************** with any questions. We are an Equal Opportunity Employer and VEVRAA Federal Contractor Connect With Us: Facebook: @TPMGPhysicianCareers LinkedIn: /company/the-permanente-medical-group/ Twitter: @TPMGDocCareers Instagram: @TPMGPhysicianCareers

Pay Rate: $27.93/hr (W2) The QC Associate I performs direct materials testing in accordance with cGMP regulations with limited supervision. Responsibilities include execution of laboratory tests, trend evaluation, documentation review, discrepancy support (OOS, OOT, OOE), and overall laboratory operational support. Partners with Quality Control leadership to meet departmental and organizational goals. Responsibilities Perform a wide range of basic and moderately complex laboratory tests according to GMP. Review data and evaluate results based on established acceptance criteria. Conduct technical review of peer-generated data. Analyze data to identify trends and establish limits. Identify discrepancies and support investigation design and CAPA activities. Identify and troubleshoot technical issues. Recognize gaps in processes, systems, and procedures. Provide and receive training as needed. Support assay transfers and validation activities. Perform equipment qualification and routine maintenance. Prepare and maintain standards, stocks, controls, and cultures. Ensure compliance and support continuous operational improvements. Apply GMP consistently across operations. Collaborate with internal teams and external stakeholders for multi-site support. Support internal/external audits and regulatory inspections. Meet project schedules, timelines, and deliverables. Participate in or lead team projects and process improvement initiatives. Write protocols and reports with limited supervision. Maintain ≥95% on-time performance. Perform additional duties assigned by leadership to support Quality initiatives. Job Requirements Education: B.S./B.A. with 1-3 years' experience or Master's with 1+ year experience or equivalent. Preferred degrees in scientific fields with relevant experience in pharmaceutical/biopharma. Strong verbal & written communication skills; ability to organize and present technical information. Demonstrated ability to apply scientific theories and analytical/biological testing techniques. Strong judgment, reasoning, and problem-solving skills. Ability to work independently and prioritize workload effectively with limited supervision.

RESPONSIBILITIES Reporting to the Bay Area Director and working closely with the Bay Area Market Lead, the Leasing Associate will provide critical support in leasing commercial lab and office assets within the Bay Area, a highly active and dynamic life science market. Ideal candidates will demonstrate the potential and the desire to grow over time towards independent deal execution. The Leasing Associate will support all aspects of the leasing process while learning to structure complex deals that balance stakeholder needs across a publicly traded REIT. They will manage Bay Area market data, draft transaction materials, assist with underwriting and capital projects, and collaborate closely with brokers to ensure smooth deal execution. This is an excellent opportunity for a motivated professional to develop within a high-visibility, high-impact team. Draft compelling proposal letters to facilitate lab, retail, and office leases across all Bay Area campuses. Assist with financial underwriting, including evaluation of rent structures, concession packages, and TI allowances. Maintain a high-quality database of leasing contacts, key tenant executives, and subtenant relationships. Foster strong relationships with brokerage teams, ensuring timely responses to inquiries, and consistent communication. Monitor and track competitive market activity to support pricing recommendations and strategic planning. Partner with property management and the Lab Marketing Associate to ensure all vacancies are tour-ready and accurately marketed, including current floor plans, measurements, and collateral. Coordinate seamless on-site tours with brokers and property management, ensuring smooth access and a positive tenant/broker experience, attending tours as needed. Support resolution of any space-related questions or operational issues that may impact leasing. Maintain organized deal files including RFPs and proposals, lease drafts, tenant space plans, improvement budgets, and analyses, CAD files, as-builts, etc. Support internal processes such as routing sublease consents, tracking Letters of Credit and Security Deposits post-execution, and submission of broker commission invoices to accounts payable. Assist with balancing speed of deal execution and compliance with internal workflows for deal approval, including JV partner considerations as applicable Ensure accurate data integrity across internal systems for leases, prospects, and pipeline activity. Assist in preparing portfolio updates, leasing summaries, and materials for leadership, etc. Assist in monthly calls with the Market Lead, Leasing Director, PMA, and Property Management teams to align priorities and upcoming vacancies. Gather and maintain critical building documentation such as building system matrices, BOMA reports, as-built plans, process utility information, and other due-diligence materials. POSITION REQUIREMENTS A bachelor's degree from an accredited college or university 3 to 5 years of commercial real estate experience (life science real estate experience preferred) High level of proficiency in Microsoft Excel, Outlook, and PowerPoint General analytical proficiency and a robust attention to detail are crucial for this role Strong teamwork and relationship‐building capabilities, with leadership instincts and a growth mindset Ability to appropriately prioritize and proactively communicate within a fast‐paced, dynamic work environment Valid driver's license and car with the ability to travel among Bay Area campuses, as well as the willingness to travel out of market ( Offering $95,000 - $125,000 per year based on experience Healthpeak is committed to fostering an inclusive workplace that values diversity and equal opportunity.

To Apply: As a second attachment (apart from your CV), please include a cover letter (not to exceed 1 page in length) that addresses the following questions: What strengths are you most proud of that you will bring to your role as an intern at Genentech? How does interning at Genentech fit in with your long term career goals? Please describe a unique situation in either your academic, personal, or career areas of your life in which you took initiative that had a meaningful impact on either your school, community, or an organization. Department Summary Pharmaceutical Technical Development (PTDU) develops, delivers, and supports robust, cost-effective production methods and technologies for innovative therapeutics to meet the needs of Genentech's Research, Development, Commercial, and Product Operations groups. The group has long been recognized as a world leader in developing large-scale manufacturing processes, sophisticated analytical methods, and effective drug delivery systems. This internship position is located in South San Francisco, on-site Program Highlights Six Months (with a possible 6-month extension), (40 hours per week) paid internship. Program start dates are in May/June 2026. A stipend, based on location, will be provided to help alleviate costs associated with the internship. Ownership of challenging and impactful business-critical projects. Work with some of the most talented people in the biotechnology industry. Final presentations of project work to senior leaders. Lead or participate in intern committees to design and coordinate program events and initiatives. Professional & personal development curriculum throughout the program, including networking opportunities, workshops, and panel discussions. Participate in volunteer projects, social events, and team-building activities. The Opportunity As a Technical Development Intern, Laboratory focus, you may be assigned a project in one of the following areas within PTDUP: Cell Culture and Fermentation Development Purification Development Protein Analytical Chemistry Analytical Operations Pharmaceutical Development Drug Delivery Technology Development Potency Assay Development Cell and Gene Therapies This program provides a broad perspective and appreciation of the development of new processes, methods, and technologies at different production scales in the biotechnology industry. Candidates applying for the PTDU Intern Program should be passionate about science/engineering and thoroughly enjoy the challenges associated with complex problem-solving. Candidates must be highly self-motivated and able to work effectively as individuals and as part of multi-disciplinary teams in an atmosphere of casual intensity to develop medicines for unmet medical needs. Interns with a laboratory focus will work alongside scientists to design, execute, and analyze wet-lab or dry-lab-based experiments in support of the diverse development activities needed to produce therapeutics at scale for patients. Previous internship projects have included but are not limited to: Cell and molecular biology approaches to develop novel drug potency assays. Bioreactor, fermentation, and cell culture media studies. Drug analysis using tools like mass spectrometry, HPLC, NMR Protein structure and stability studies. Developing cell differentiation protocols in support of cell therapy programs. Updates to the PTDU Assay Information & Request (PAIR) System. Benchling templates and results schema update. Required Education You meet one of the following criteria: Must be pursuing a Bachelor's degree (enrolled student graduating in 2026 or 2027). Must have attained a Bachelor's degree no more than 2 years ago from the time of application (not currently enrolled in a grad program). Must be pursuing a Master's degree (enrolled student). Must have attained a Master's degree no more than 2 years ago from the time of application. Required Majors: Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Bioengineering, Pharmaceutical Engineering, Chemistry, Biology, Microbiology, Biophysics, or related disciplines. Preferred Knowledge, Skills, and Qualifications Detail-oriented, enthusiastic, and self-directed individual who is excited about tackling complex and creative scientific challenges in an industrial setting. Excellent communication, collaboration, and interpersonal skills. Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion. Ability to show a high degree of adaptive capacity. Relevant work experience in research labs or the biotechnology industry. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location for this position in California is $30.00 - $40.00 per hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off benefits. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Working in a team of media process technicians, media process technician I will manufacture dehydrated and liquid cell culture media. Formulation technician 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, turbidimeter 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 QUALIFICATION REQUIREMENTS: 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 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.

Reports to Operations Supervisor, Laboratory Supervisor or Laboratory Manager. Under limited supervision incumbent(s) will use their training in medical technology to perform clinical lab testing and/or other scientific examinations. Required to work independent of immediate supervision and assume the initiative for prompt and accurate performance of tests with appropriate documentation and proper notification of abnormal results. This is considered an entry level position and is the first of a two level job family. Clinical Laboratory Scientist I will perform all or part of the following duties: 1. Independently performs consistently moderate and somewhat complex clinical tests. Exhibits skills and proficiency in applying technical principles and techniques of medical technology. 2. Prepares and tests new reagents or controls and evaluates their usefulness based on standard criteria. 3. Performs test calibrations and runs Quality Control material at appropriate intervals. 4. Determines the acceptability of specimens for testing according to established criteria in testing procedures. 5. Determines calculated results utilizing testing data by means of manual or computerized procedures. 6. Accurately enters results of testing. Checks the computer review reports to monitor accurate reporting of laboratory results. 7. Evaluates the acceptability of routine analysis prior to releasing patient reports. Takes appropriate action in response to critical values or unusual or unexpected results, and documents action taken. 8. Responsible for performing preventative maintenance and/or calibration of laboratory equipment and properly documenting actions taken based on approved schedule. 9. Evaluates the results of instrument performance checks. Performs linearity, accuracy and precision checks as required. 10. Performs Q/C and calibrations with the appropriate frequency and evaluates results, to decide whether tests should be reported. Reports any shifts or trends to a Clinical Laboratory Scientist II or Supervisor. 11. Accurately performs and records proficiency testing. 12. Recognizes problems, and initiates troubleshooting steps to evaluate testing failures and other problems, if necessary. Notifies the supervisor, and contacts manufacturer for additional assistance or field service support, if required. 13. Monitors and maintains a consistent supply of reagents and consumables. 14. Promptly and courteously answers the phone and assists clients and other departments. 15. Maintains a safe and neat work area. 16. Maintains a cooperative working relationship with co-workers. 17. Provides on-going technical guidance to laboratory assistants, laboratory associates, and other Clinical Laboratory Scientists. Instructs and/or trains new employees in the proper performance of routine procedures. 18. Maintains professional growth and development through continuing education activities. 19. Follows established company and department policies and procedures. Follows the guidelines for safety, environmental, and infection control. 20. Demonstrates a high level of integrity and honesty in maintaining confidentiality. 21. May be required to perform Clinical Laboratory Scientist II level duties for a limited period of time, in order to establish competency prior to promotion as well as fill in for departmental absences. 22. Provides direct and constant supervision to unlicensed staff as necessary. Reports to Operations Supervisor, Laboratory Supervisor or Laboratory Manager. Under limited supervision incumbent(s) will use their training in medical technology to perform clinical lab testing and/or other scientific examinations. Required to work independent of immediate supervision and assume the initiative for prompt and accurate performance of tests with appropriate documentation and proper notification of abnormal results. This is considered an entry level position and is the first of a two level job family. Clinical Laboratory Scientist I will perform all or part of the following duties: 1. Independently performs consistently moderate and somewhat complex clinical tests. Exhibits skills and proficiency in applying technical principles and techniques of medical technology. 2. Prepares and tests new reagents or controls and evaluates their usefulness based on standard criteria. 3. Performs test calibrations and runs Quality Control material at appropriate intervals. 4. Determines the acceptability of specimens for testing according to established criteria in testing procedures. 5. Determines calculated results utilizing testing data by means of manual or computerized procedures. 6. Accurately enters results of testing. Checks the computer review reports to monitor accurate reporting of laboratory results. 7. Evaluates the acceptability of routine analysis prior to releasing patient reports. Takes appropriate action in response to critical values or unusual or unexpected results, and documents action taken. 8. Responsible for performing preventative maintenance and/or calibration of laboratory equipment and properly documenting actions taken based on approved schedule. 9. Evaluates the results of instrument performance checks. Performs linearity, accuracy and precision checks as required. 10. Performs Q/C and calibrations with the appropriate frequency and evaluates results, to decide whether tests should be reported. Reports any shifts or trends to a Clinical Laboratory Scientist II or Supervisor. 11. Accurately performs and records proficiency testing. 12. Recognizes problems, and initiates troubleshooting steps to evaluate testing failures and other problems, if necessary. Notifies the supervisor, and contacts manufacturer for additional assistance or field service support, if required. 13. Monitors and maintains a consistent supply of reagents and consumables. 14. Promptly and courteously answers the phone and assists clients and other departments. 15. Maintains a safe and neat work area. 16. Maintains a cooperative working relationship with co-workers. 17. Provides on-going technical guidance to laboratory assistants, laboratory associates, and other Clinical Laboratory Scientists. Instructs and/or trains new employees in the proper performance of routine procedures. 18. Maintains professional growth and development through continuing education activities. 19. Follows established company and department policies and procedures. Follows the guidelines for safety, environmental, and infection control. 20. Demonstrates a high level of integrity and honesty in maintaining confidentiality. 21. May be required to perform Clinical Laboratory Scientist II level duties for a limited period of time, in order to establish competency prior to promotion as well as fill in for departmental absences. 22. Provides direct and constant supervision to unlicensed staff as necessary. Clinical Laboratory Scientist I must have: 1. A Bachelor's of Science degree in medical technology or biological sciences from an accredited college or university. 2. A current California state Clinical Laboratory Scientist license to perform laboratory testing. 3. Zero to three year's direct experience in a laboratory setting. 4. Demonstrated proficiency in computer skills such as word processing, statistical analysis, and laboratory information system. [All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. All duties and requirements are essential job functions.] Required California Laboratory Scientist generalist license. Position is for Tuesday-Saturday, 8am- 4:30pm, with weekend rotations. Skills & Requirements Clinical Laboratory Scientist I must have: 1. A Bachelor's of Science degree in medical technology or biological sciences from an accredited college or university. 2. A current California state Clinical Laboratory Scientist license to perform laboratory testing. 3. Zero to three year's direct experience in a laboratory setting. 4. Demonstrated proficiency in computer skills such as word processing, statistical analysis, and laboratory information system. [All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. All duties and requirements are essential job functions.] Required California Laboratory Scientist generalist license. Position is for Tuesday-Saturday, 8am- 4:30pm, with weekend rotations.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description As the Clinical Laboratory Technician you will be part of our Clinical Development and Medical Affairs team. The Clinical Development and Medical Affairs team oversees all clinical trials and clinical laboratory activities. THE ROLE: You will assist in building and establishing GRAIL's Clinical Lab, performing specimen testing and supporting the daily operations of the Clinical Lab. Specifically, you will: · Perform analytical testing activities including specimen testing, quality control, preparation and aliquoting of reagents. · Operate laboratory instruments and equipment. Troubleshoot and problem solve instrument issues as needed. · Monitor and perform equipment maintenance according to laboratory protocol. · Participate and comply with Quality and applicable regulatory requirements. · Maintain sufficient inventory of material, supplies and equipment in the laboratory for performance of duties. · Assist in building and establishing GRAIL's Clinical Laboratory. · Perform other miscellaneous laboratory duties as assigned and assist others as time allows. YOUR BACKGROUND: To be successful in this role, you will need to possess the following: · Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field. · Molecular diagnostics and Next-generation sequencing experience. · Ability to prioritize tasks with a high emphasis on quality. Strong organizational skills and meticulous attention to detail. · Ability to be able to work as part of a team within a highly collaborative environment. · Flexibility of work schedule to meet the needs of the Clinical Lab (may include weekends and Holidays) Additional Information Vishnu Kumar Associate Recruiter Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: *************** | Fax: ************

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.

The Clinical Laboratory Technician operates instruments under the supervision of a Clinical Laboratory Scientist. Follows established procedures for processing biological specimens for analysis. Performs clerical and phlebotomy functions as needed. Responsibilities Operates instruments under supervision of Clinical Laboratory Scientist: a. Operates instruments per SOP. b. Recognizes instrument malfunctions and notifies appropriate supervisory personnel when they occur. Performs routine quality control procedures and documents results according to SOP. Recognizes out of control results and immediately notifies supervisory personnel. Performs routine maintenance procedures and documents results according to SOP. Performs inventory of reagents and supplies as required by the department. Assists in putting away incoming supplies according to storage requirements. Performs specimen handling and processing (sorting, matching, prioritizing, centrifuging, and aliquoting) and/or microbiology specimen processing, plating and AFB processing. Performs specimen send-out protocol according to SOP. Prepares stains and reagents according to SOP. Performs phlebotomy functions, including adult, pediatric and neonates according to SOP as required. Performs and shares all the job responsibilities designated for the positions of Lab Assistant III, Lab Assistant II and Lab Assistant I as assigned. Acts under the direction of Laboratory Director in other necessary activities if consistent with training, education and professional ethics. Qualifications EDUCATION: Two years of college preferred EXPERIENCE: Experience in operating laboratory instruments and specimen processing. Knowledge of specimen send-outs and microbiology specimen processing (including AFB processing) Five years clinical laboratory experience (including phlebotomy) preferred CERTIFICATIONS/LICENSURE: Phlebotomy certification from a California Department of Health Services. OTHER SKILLS, ABILITIES & KNOWLEDGE: Ability to perform all phlebotomy functions, including adult, pediatric and neonates. Familiarity with medical terminology and basic typing skills.

Company: Fusion Medical Staffing Job Details Fusion Medical Staffing is seeking a skilled Cath Lab Tech for a 13-week travel assignment in Pleasanton, California. As a member of our team, you'll have the opportunity to make a positive impact on the lives of patients while enjoying competitive pay, comprehensive benefits, and the support of a dedicated clinical team. Required Qualifications: One year's recent experience as a Cardiac Cath Lab Tech Current BLS (AHA/ARC) certification ARRT, RCES, or RCIS certification Current ACLS (AHA/ARC) certification Preferred Qualifications: Valid Radiologic Technologist license in compliance within state regulations PALS (AHA/ARC) or ENPC Certifications Other certifications and licenses may be required for this position Summary: The Cath Lab Technologist is responsible for assisting in diagnostic and interventional cardiovascular procedures in the cardiac catheterization lab. This role involves preparing patients and equipment, monitoring hemodynamic data, assisting physicians during procedures, and ensuring patient safety throughout the process. The technologist operates specialized imaging equipment, maintains sterile technique, and collaborates with the healthcare team to provide high-quality patient care. This position requires technical expertise in cardiovascular procedures, critical thinking skills, and the ability to work efficiently in high-pressure situations. Essential Work Functions: Prepare and position patients for cardiac catheterization, angioplasty, stent placement, electrophysiology studies, and other interventional procedures Assist physicians during procedures by passing catheters, wires, balloons, and stents, and operating fluoroscopy and hemodynamic monitoring equipment Operate and maintain imaging equipment, contrast injectors, and hemodynamic monitoring systems, ensuring proper functionality Scrub in and assist with sterile field setup, ensuring adherence to infection control and procedural protocols Perform sheath removal and hemostasis using manual compression or closure devices as directed Maintain accurate documentation, including patient records, imaging data, and equipment logs Assist with inventory management, stocking supplies, and ensuring proper storage of sterile instruments and medications Adhere to radiation safety protocols, ensuring proper use of lead aprons, shields, and dosimeters Ensure compliance with hospital policies, safety guidelines, and regulatory requirements Adhere to hospital safety protocols, infection control guidelines, and regulatory standards Perform other duties as assigned within the scope of practice Required Essential Skills: Critical thinking, service excellence, and good interpersonal communication skills The ability to read, write, and communicate in the English language Ability to read/comprehend written instructions, follow verbal instructions, and proficiency in PC skills Physical Abilities - Must be able to remain in a stationary position, move about, move equipment (50-100lbs), push, pull, and bend Interpersonal Skills - Must be able to work effectively with a variety of personnel (professional and ancillary) to present a positive attitude and professionalism Technical/Motor Skills - Must have the ability to grasp, perform fine manipulation, push/pull, and move about when assisting with procedures and/or using department equipment Mental Requirements - Must be able to cope with frequent contact with the general public and customers while meeting deadlines under pressure. Must be able to work under close supervision occasionally, as well as working without assistance from other personnel. Must be able to contend with irregular activity schedules occasionally and continuous concentration to detail Sensory - Must possess visual acuity and ability to effectively communicate Benefits Include: Highly competitive pay for travel professionals Comprehensive medical, dental, and vision insurance with first day coverage Paid Time Off (PTO) after 1560 hours Life and Short-term disability offered 401(k) matching Aggressive Refer-a-friend Bonus Program 24/7 recruiter support Reimbursement for licensure and CEUs Why Choose Fusion? At Fusion Medical Staffing, our goal is to improve the lives of everyone we touch, and we're always looking for people like you to join our mission. Your passion for helping others deserves a partner just as committed to supporting you - that's why we offer day one insurance, $0 copay for mental health services, scholarships and awards, exclusive discounts, and more. From your personal recruiter to our clinical and traveler experience teams, we're here to guide and celebrate you along your journey. You take care of others; we take care of you. Other Duties Disclaimer: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Other duties may be assigned. This job description is not a comprehensive list of all activities, duties, or responsibilities that are required of the employee for this job and is subject to change at any time with or without notice. Start your rewarding career as a Travel Cath Lab Tech with Fusion Medical Staffing and join our mission to improve lives. Apply now! *Fusion is an EOE/E-Verify Employer #pb15

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.

Fulfilling the promise of medicine The Permanente Medical Group, Inc. (TPMG - Kaiser Permanente Northern California) is one of the largest medical groups in the nation with over 10,000 physicians, 21 medical centers, numerous clinics throughout Northern and Central California, and an over 80-year tradition of providing quality medical care. We currently have the following opportunities: HEMATOLOGIST/ONCOLOGIST: Antioch (part-time), Dublin, Fresno, Modesto, Oakland, Roseville (part-time), Sacramento Downtown, South San Francsico, Vallejo HEMATOLOGIST/ONCOLOGIST - ONCOLOGY: Modesto, California Full-time annual salary range is $470,040 to $500,040 plus additional potential incentives up to $41,570*. Reduced schedules with pro-rated compensation may be available. *Some incentive opportunities are estimates based on potential premium pay. Per Diem Opportunities are also available throughout Northern & Central California. Per Diem pay range is $320 to $330 hourly. With TPMG you'll benefit from: Work-life balance focused practice, including flexible schedules and unmatched practice support. We can focus on providing excellent patient care without managing overhead and billing. No RVUs! We are committed to cultivating and preserving an inclusive environment for all physicians and employees. Multi-specialty collaboration with a mission-driven integrated health care delivery model. An outstanding electronic medical record system that allows flexibility in patient management. We have a very rich and comprehensive Physician Health & Wellness Program. We are Physician-led and develop our own leaders. Professional development opportunities in teaching, research, mentorship, physician leadership, and community service. EXTRAORDINARY BENEFITS: Competitive compensation and benefits package, including comprehensive vision, medical, and dental Interest Free Home Loan Program up to $250,000 (approval required) Relocation Assistance up to $10,000 (approval required) PSLF Eligible Employer Malpractice and Tail Insurance Life Insurance Optional Long-Term Care Insurance Paid holidays, sick leave, and education leave Shareholder track Three retirement plans, including a pension plan and 401(k) For more information about these opportunities, our wage ranges, or to apply, please visit our website at: ************************************************************** For immediate consideration, kindly reply with your CV. Or contact Bo Chau, Physician Recruiter at ************** / call ************** with any questions. We are an Equal Opportunity Employer and VEVRAA Federal Contractor Connect With Us: Facebook: @TPMGPhysicianCareers LinkedIn: /company/the-permanente-medical-group/ Twitter: @TPMGDocCareers Instagram: @TPMGPhysicianCareers

** **2026 Summer Intern - Product Technical Development - Laboratory (Wet-Lab or Dry-Lab)** **To Apply:** + As a **second** attachment (apart from your CV), please include a cover letter (not to exceed 1 page in length) that addresses the following questions: + What strengths are you most proud of that you will bring to your role as an intern at Genentech? + How does interning at Genentech fit in with your long term career goals? + Please describe a unique situation in either your academic, personal, or career areas ofyour life in which you took initiative that had a meaningful impact on either your school,community, or an organization. **Department Summary** Pharmaceutical Technical Development (PTDU) develops, delivers, and supports robust, cost-effective production methods and technologies for innovative therapeutics to meet the needs of Genentech's Research, Development, Commercial, and Product Operations groups. The group has long been recognized as a world leader in developing large-scale manufacturing processes, sophisticated analytical methods, and effective drug delivery systems. This internship position is located in **South San Francisco, on-site** **Program Highlights** + **Six Months (** **with a possible 6-month extension)** **, (40 hours per week) paid internship.** + **Program start dates are in May/June 2026.** + **A stipend, based on location, will be provided to help alleviate costs associated with the internship.** + Ownership of challenging and impactful business-critical projects. + Work with some of the most talented people in the biotechnology industry. + Final presentations of project work to senior leaders. + Lead or participate in intern committees to design and coordinate program events and initiatives. + Professional & personal development curriculum throughout the program, including networking opportunities, workshops, and panel discussions. + Participate in volunteer projects, social events, and team-building activities. **The Opportunity** As a Technical Development Intern, Laboratory focus, you may be assigned a project in one of the following areas within PTDUP: + Cell Culture and Fermentation Development + Purification Development + Protein Analytical Chemistry + Analytical Operations + Pharmaceutical Development + Drug Delivery Technology Development + Potency Assay Development + Cell and Gene Therapies This program provides a broad perspective and appreciation of the development of new processes, methods, and technologies at different production scales in the biotechnology industry. Candidates applying for the PTDU Intern Program should be passionate about science/engineering and thoroughly enjoy the challenges associated with complex problem-solving. Candidates must be highly self-motivated and able to work effectively as individuals and as part of multi-disciplinary teams in an atmosphere of casual intensity to develop medicines for unmet medical needs. Interns with a laboratory focus will work alongside scientists to design, execute, and analyze wet-lab or dry-lab-based experiments in support of the diverse development activities needed to produce therapeutics at scale for patients. Previous internship projects have included but are not limited to: + Cell and molecular biology approaches to develop novel drug potency assays. + Bioreactor, fermentation, and cell culture media studies. + Drug analysis using tools like mass spectrometry, HPLC, NMR + Protein structure and stability studies. + Developing cell differentiation protocols in support of cell therapy programs. + Updates to the PTDU Assay Information & Request (PAIR) System. + Benchling templates and results schema update. **Required Education** You meet one of the following criteria: + Must be pursuing a Bachelor's degree (enrolled student graduating in 2026 or 2027). + Must have attained a Bachelor's degree no more than 2 years ago from the time of application (not currently enrolled in a grad program). + Must be pursuing a Master's degree (enrolled student). + Must have attained a Master's degree no more than 2 years ago from the time of application. **Required Majors:** Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Bioengineering, Pharmaceutical Engineering, Chemistry, Biology, Microbiology, Biophysics, or related disciplines. **Preferred Knowledge, Skills, and Qualifications** + Detail-oriented, enthusiastic, and self-directed individual who is excited about tackling complex and creative scientific challenges in an industrial setting. + Excellent communication, collaboration, and interpersonal skills. + Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion. + Ability to show a high degree of adaptive capacity. + Relevant work experience in research labs or the biotechnology industry. **Relocation benefits are not available for this job posting.** The expected salary range for this position based on the primary location for this position in California is $30.00 - $40.00 per hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off benefits. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants (***************************************************************************************************** .

Mon-Fri 6a - 230pm Senior 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 31, 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.

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.

The Clinical Laboratory Technician operates instruments under the supervision of a Clinical Laboratory Scientist. Follows established procedures for processing biological specimens for analysis. Performs clerical and phlebotomy functions as needed. Responsibilities Operates instruments under supervision of Clinical Laboratory Scientist: a. Operates instruments per SOP. b. Recognizes instrument malfunctions and notifies appropriate supervisory personnel when they occur. Performs routine quality control procedures and documents results according to SOP. Recognizes out of control results and immediately notifies supervisory personnel. Performs routine maintenance procedures and documents results according to SOP. Performs inventory of reagents and supplies as required by the department. Assists in putting away incoming supplies according to storage requirements. Performs specimen handling and processing (sorting, matching, prioritizing, centrifuging, and aliquoting) and/or microbiology specimen processing, plating and AFB processing. Performs specimen send-out protocol according to SOP. Prepares stains and reagents according to SOP. Performs phlebotomy functions, including adult, pediatric and neonates according to SOP as required. Performs and shares all the job responsibilities designated for the positions of Lab Assistant III, Lab Assistant II and Lab Assistant I as assigned. Acts under the direction of Laboratory Director in other necessary activities if consistent with training, education and professional ethics. Qualifications EDUCATION: Two years of college preferred EXPERIENCE: Experience in operating laboratory instruments and specimen processing. Knowledge of specimen send-outs and microbiology specimen processing (including AFB processing) Five years clinical laboratory experience (including phlebotomy) CERTIFICATIONS/LICENSURE: Phlebotomy certification from a California Department of Health Services. OTHER SKILLS, ABILITIES & KNOWLEDGE: Ability to perform all phlebotomy functions, including adult, pediatric and neonates. Familiarity with medical terminology and basic typing skills.