Quality control analyst jobs in San Buenaventura, CA - 36 jobs

Quality Control Analyst III in Camarillo, CA Build your future at Curia, where our work has the power to save lives. The Quality Control Analyst III is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives. We proudly offer * Generous benefit options (eligible first day of employment) * Paid training, vacation and holidays (vacation accrual begins on first day of employment) * Career advancement opportunities * Education reimbursement * 401K program with matching contributions * Learning platform * And more! Responsibilities * Perform complex testing and data evaluation, such as HPLC, ELISA, etc. * Troubleshoot equipment issues promptly and communicate resolutions to management * Participate in or assist with test method validations * Evaluate data for trends * Support and/or investigate OOS events by performing thorough root cause analyses, assessing potential product impact, and implementing appropriate CAPAs * Interact with outside departments including attending meetings, providing updates, etc. * Coordinate testing performed at outside testing labs, raw materials, etc. * Maintain a detailed and accurate recording of activities and results * Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries * Perform risk assessment as needed * Write/revise test methods, standard operating procedures, etc. * Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures * Support equipment upkeep * Prepare and order supplies, as necessary * Enter data into relevant data management systems and perform tracking and trending of data. Compile data and provide/present data summaries to management * Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry * Collaborate with cross-functional departments to coordinate testing, scheduling needs, and prioritization * Lead departmental projects and participate in cross-functional teams, including continuous improvement initiatives and new customer project teams * Lead the stability program, including management of test points, reporting of data, and investigations of out of specification or aberrant stability results Required * Bachelor's Degree in Chemistry or related field and 5+ years related work experience; OR * Master's Degree in Chemistry or related field and 3+ years related work experience; OR * PhD in Chemistry or related field and 1+ years related work experience * Experience working in cGMP or GLP pharmaceutical industry environment * Willing to work flexible hours (nights and weekends), as-needed (overtime eligible) Knowledge, skills and abilities * Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public * Ability to meet deadlines and work under pressure with limited supervision * Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently * Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations * Ability to write reports, business correspondence, and procedures * Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations * Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis * Ability to define problems, collect data, establish facts, and draw valid conclusions * Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and handle several abstract and concrete variables * Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems * Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus Other Qualifications * Must pass a background check * Must pass a drug screen * May be required to pass Occupational Health Screening Pay Range: $85,000-$106,500/year Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer. #LI-AC1

Science & Research Camarillo, California, US + Added - 04/12/2025 Apply for Job Pay Rate Low: 37 | Pay Rate High: 39 _Our client, a global CDMO, offering products and services across the drug development spectrum is looking for a skilled Sr. QC Analyst to join their team in Camarillo, CA!_ **Job Title:** QC Analyst III **Location:** Camarillo, CA **Job type:** 6 month contract - hire **Pay rate:** $37 - $39/ hr. **Job Summary:** We are seeking a highly skilled and detail-oriented Senior QC Analyst to perform complex analytical testing in support of pharmaceutical product development and manufacturing. The ideal candidate will have advanced experience in chromatography techniques (e.g., HPLC, UPLC, GC), method validation, data analysis, and regulatory compliance. This position plays a critical role in ensuring product quality, supporting investigations, and driving continuous improvement across the QC function. **Key Responsibilities:** + Perform complex analytical testing including Liquid Chromatography (HPLC/UPLC), Gas Chromatography (GC), and other instrumental and wet chemistry techniques. + Troubleshoot analytical instruments and resolve method or equipment-related issues. + Participate in and assist with test method validations, verifications, and transfers. + Evaluate and analyze test data to identify trends, outliers, or potential issues. + Support OOS (Out of Specification) and OOT (Out of Trend) investigations, including CAPA (Corrective and Preventive Action) documentation. + Coordinate testing activities with external laboratories, including raw material and specialized testing. + Execute, author, and review SOPs, test methods, protocols, reports, investigations, change controls, and data summaries. + Utilize risk assessment and root cause analysis tools (e.g., 5 Whys, Fishbone) to support investigations and process improvements. + Manage aspects of the stability program, including scheduling, testing, and reporting, and investigate aberrant stability results. **Qualifications:** + Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field. + 3-6+ years of relevant experience in a regulated laboratory environment (pharmaceutical, biotech, or similar). + Strong technical expertise in HPLC, UPLC, GC, and other analytical techniques. + Working knowledge of cGMP regulations, ICH guidelines, and regulatory expectations. + Experience with method validation and stability programs preferred. + Ability to manage multiple tasks and work independently in a fast-paced environment. + Experience with electronic data systems (e.g., Empower, LIMS, TrackWise, MasterControl). _Note: This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_ \#INDBH \#LI-DNP We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Quality Control Supervisor $29.00 - $45.00/ Hr. ***Will start 100% On-Site in Oxnard, CA. Must relocate to Henderson, NV in January 2027*** As the largest machine tool builder in the western world, we need world-class talent in all of our departments. And we're not just looking for people for the production floor. Haas is a very vertically integrated company, with a wide range of high-tech career opportunities available. Oh, and yes, we are the same Haas that owns the Stewart-Haas Racing NASCAR teams, and the Haas F1 Team from the Netflix series: Drive to Survive. Quality Control Supervisor supervises and coordinates activities of workers engaged in production-inspection of machined parts and finished assemblies, applying knowledge of inspection procedures, inspection equipment set-up and operating techniques. Essential Duties and Responsibilities include the following. Other duties may be assigned. Address supplier quality issues through on-site assessment and internal corrective action. Establishes working relationship with all internal customers. Maintain a flexible staff workload to fill any void in area of responsibility. Coordinates supportive activities anticipating need and scheduling coverage. Reports on area performance and communicates effectively to management and team members of area as required. Draft performance evaluations of staff in a timely manner. Conducts staff meetings for continuous improvement activities. Meets daily production requirements. Motivates staff and conducts training activities - sets the example. • Employees are expected to follow instructions, procedures and to escalate any issue impacting workflow, quality, etc. • Employees must exhibit honesty and integrity as well as demonstrate adherence to rules, procedures and policies. Supervisory Responsibilities Supervisory Responsibilities Supervised Employees Directly supervises employees. The supervisory responsibilities include the following: supervises in accordance with the organization's policies and applicable laws. Supervisors must also train employees, plan, assign, and direct work, address complaints and resolve problems. 11 to 25 Qualifications Qualifications To perform this job successfully the candidate must be able to perform each essential duty adequately. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Minimum Qualifications 3+ years related supervisor experience. Desired Qualifications Education Bachelor's Degree BA/BS/BFA/BSA from a four-year college or university is required, plus additional related experience, training and/or equivalent combination of education and experience. Preferred Major Mechanical Engineering Manufacturing Engineering Industrial Engineering Minimum Years of Experience 10+ years Language Skills Must have the ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, and/or governmental regulations in English. Must be able to write analytical and/or technical reports, business correspondence, procedure manuals, and create instructional reference material. Able to speak effectively before groups, customers, employees of the organization and/or the general public. Mathematical Skills Must be able to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume. Must have the ability to apply concepts of arithmetic, algebra, and geometry. Reasoning Ability Must have the ability to define problems, collect data, establish facts, and draw valid conclusions. Must be able to interpret an extensive variety of technical instructions such as mathematical and/or diagram form and deal with several abstract and concrete variables. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Physical Activity Duration Sitting Occasionally Standing Frequently Walking Occasionally Bending (neck) Frequently Bending (waist) Rarely Squatting Frequently Twisting (neck) Frequently Twisting (waist) Frequently Climbing Frequently Kneeling Frequently Crawling Frequently Reaching (above shoulder level) Frequently Reaching (below shoulder level) Frequently Hand Use Duration Repetitive use of hand Frequently Simple grasping Frequently Power grasping Frequently Fine manipulation Frequently Pushing & Pulling Frequently Vision Close vision Yes Distance vision Yes Color vision Yes Peripheral vision Yes Depth perception Yes Adjust focus Yes Lifting Requirements Duration 0-10 lbs. Frequently 11-25 lbs. Frequently 26-50 lbs. Frequently 51-60 lbs. Occasionally 61+ lbs. Occasionally Equipment Use Duration This position requires computer use, including monitor, keyboard, mouse, trackball, touchpad, etc. Frequently Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Noise Level The noise level in the work environment is usually: Loud Work Environment Duration This position operates in a general office or engineering lab environment Frequently Employee will work around machining or on the production floor Occasionally Employee is exposed to moving mechanical parts and vibration Frequently Employee is exposed to hazardous chemicals, fumes or airborne particles Occasionally Employee is exposed to outside weather conditions, extreme cold or extreme heat Frequently Employee is exposed to risk of electrical shock Never

Employment Type: Contract Duration: 2 years + Note: Onsite Essential 3 Key Consulting is hiring a Sr Associate Quality Control for a consulting engagement with our direct client, a leading global bio-pharmaceutical company. Job Summary: Candidate will be working on site Targeting candidates with 4-6 years of industry/ non academia experience Quality Control Raw Materials is searching is for an analytical scientist to support testing for Raw Materials of routine samples for use within our network manufacturing operations. This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing. The ideal candidate enjoys tackling challenges and excels at time management with attention to detail. Day-To-Day Responsibilities: Performing analytical testing for HPLC, UPLC, Gas Chromatography, GC-MS and/or IC-PMS Interacting cross-functionally with a wide variety of people and teams Troubleshoot, solve problems and communicate with stakeholders. Participate in initiatives and projects that may be departmental or organizational in scope. Evaluate lab practices for compliance and operational excellence on a continuous basis. Qualifications 4-6 years of experience in HPLC, GC, GC-MS and/or ICP/MS. Bachelors Degree in any science field. Demonstrated experience in investigations and QC processes. Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision. Strong communication skills (both written and oral), facilitation and presentation skills. Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories, preferably with GMP experience. Compendial experience. Understanding of biopharmaceuticals process and related unit operations Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy. Independent, self-motivated, organized, able to multi-task in time-sensitive environments. Top Must have Skill Sets: HPLC, GC, GC-MS or ICPMS experience, pertaining to routine use and troubleshooting GMP laboratory experience Teamwork and motivation to problem solve and improve self, operations, and processes Red Flags: Jumpy job history Interview Process: Interviews will be conducted via Webex. First interview with hiring manager, second interview with team We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this position, please feel free to look at other positions on our website *********************** You are welcome to also share this posting with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Job Description Key Responsibilities * Perform testing of raw materials, intermediates, final products, and stability by following analytical methods. * Maintain, calibrate, and operate equipment and instruments supporting cell bioassays, Flow Cytometry, ELISA, and PCR assays. * Track and test products according to stability protocols. * Work with internal and external resources to maintain the lab in an optimal state. * Monitor and trend data, complete routine record review of test data and related documents for in-process testing, drug substance, and drug product release. Generate Certificates of Analysis (CoAs) for product release. * Assist in the preparation of dossiers and data packages for interactions between Kite (Gilead) and regulatory agencies; participate in Pre-Approval Inspections. * Develop, revise, and review SOPs, qualification/validation protocols, and reports. * Conduct investigations regarding out-of-specification (OOS) results and manage deviations related to analytical procedures. Provide updates at daily and weekly meetings. * Monitor GMP systems to ensure compliance with documented policies. * Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies as appropriate. * Gather metric information for continuous improvement of areas of responsibility. * Perform other duties as required. Basic Qualifications * BS degree in a scientifically oriented field and at least 2 years related work experience. OR * MS degree in a scientifically oriented field and at least 0 years related work experience. Preferred Qualifications * At least 2 years of industry experience in a biotech and/or pharmaceutical quality-related role. * Strong knowledge of GMP, SOPs, and quality control processes. * Experience identifying, writing, evaluating, and closing OOS investigations. * Proficient in MS Word, Excel, PowerPoint, and other applications. * Strong written and verbal communication skills. * Ability to communicate and work independently with scientific/technical personnel. * Well-versed in analytical techniques such as Flow Cytometry, ELISA, PCR, and cell bioassays for biopharmaceutical testing. * Working knowledge of quality systems and regulatory requirements (21 CFR Part 11/210/211). * Flexibility to work alternate schedules, including weekends, as business needs require. The salary range for this position is: $80,325.00 - $103,950.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: ****************************************************************** * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit ******************* Sign up to follow @KitePharma on Twitter at *************************** For jobs in the United States: Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance. For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Kite Pharma Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Job DescriptionKey Responsibilities Perform testing of raw materials, intermediates, final products, and stability by following analytical methods. Maintain, calibrate, and operate equipment and instruments supporting cell bioassays, Flow Cytometry, ELISA, and PCR assays. Track and test products according to stability protocols. Work with internal and external resources to maintain the lab in an optimal state. Monitor and trend data, complete routine record review of test data and related documents for in-process testing, drug substance, and drug product release. Generate Certificates of Analysis (CoAs) for product release. Assist in the preparation of dossiers and data packages for interactions between Kite (Gilead) and regulatory agencies; participate in Pre-Approval Inspections. Develop, revise, and review SOPs, qualification/validation protocols, and reports. Conduct investigations regarding out-of-specification (OOS) results and manage deviations related to analytical procedures. Provide updates at daily and weekly meetings. Monitor GMP systems to ensure compliance with documented policies. Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies as appropriate. Gather metric information for continuous improvement of areas of responsibility. Perform other duties as required. Basic Qualifications BS degree in a scientifically oriented field and at least 2 years related work experience. OR MS degree in a scientifically oriented field and at least 0 years related work experience. Preferred Qualifications At least 2 years of industry experience in a biotech and/or pharmaceutical quality-related role. Strong knowledge of GMP, SOPs, and quality control processes. Experience identifying, writing, evaluating, and closing OOS investigations. Proficient in MS Word, Excel, PowerPoint, and other applications. Strong written and verbal communication skills. Ability to communicate and work independently with scientific/technical personnel. Well-versed in analytical techniques such as Flow Cytometry, ELISA, PCR, and cell bioassays for biopharmaceutical testing. Working knowledge of quality systems and regulatory requirements (21 CFR Part 11/210/211). Flexibility to work alternate schedules, including weekends, as business needs require. The salary range for this position is: $80,325.00 - $103,950.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: ****************************************************************** * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit ******************* Sign up to follow @KitePharma on Twitter at *************************** For jobs in the United States: Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance. For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Kite Pharma Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.

· Top 3 Must Have Skill Sets: Previous experience with Microbiology testing, aseptic technique and working in a GMP lab. · Candidate must be willing to work a Sunday-Thursday day shift. · The candidate must be extremely flexible with their schedule as this lab tests samples that are time sensitive and an unexpected need to perform weekend and after hours work may arise. · Day to Day Responsibilities: Candidate will perform routine Microbiology assays as well as lab support activities · Job Details: Under general supervision, the candidate will perform Microbiology assays which may include: Bioburden, Bioburden Verification, Water Membrane Filtration, Biological Indicators and Growth Promotion of media, among other tests. · Additional duties include cleaning of the labs, equipment maintenance and assisting with work order execution, restocking, and ordering supplies. Candidate will also be responsible for data entry into LIMS. Candidate must be willing to work Sun-Thur day shift. Qualifications Microbiologist/ Associate Quality control Additional Information All your information will be kept confidential according to EEO guidelines.

Summary The Quality Systems Associate supports multiple quality functions including investigations, documentation control, labeling, and training. This role performs RMA inspections, deviations and product complaint investigations, manages document control activities, and supports labeling and packaging specification processes. The Associate ensures compliance with internal procedures, regulatory requirements, and quality standards while collaborating with cross-functional teams to maintain the integrity of the Quality Management System (QMS). Essential Duties Investigation ·Perform investigation of deviations and product complaints (PC). ·Follow up with internal teams and suppliers for open actions and gather data through interviews. ·Complete status reports, draft RCIs, and participate in MRB meetings and status updates. ·Answer and document PC-related phone calls. ·Perform RMA inspections for all returned materials/products and document findings. Labeling and Packaging Support ·Support label specification creation and revisions for new product introductions and updates. ·Review supplier artwork, packaging assessments, and initiate DCRs for PI revisions and label updates. ·Upload PMGs to the website to ensure current information for patients. ·Verify SPL postings or deletions for compliance. Documentation Management ·Perform daily document control activities including physical file put-away, check-in/out, and record retention records. ·Locate archived documents and assist with digital formatting. Support document storage solutions and transfer boxes to permanent storage areas. This position may be assigned additional responsibilities at the discretion of management to support evolving departmental needs and organizational objectives Knowledge, Skills, Experience Needed Education ·Bachelor's degree in Life Sciences, Engineering, or related field. (preferred) Experience ·2+ years in quality, documentation, or operations within a regulated industry Skills / Competencies: Technical Skills ·Basic understanding of GMP/GDP and QMS workflows. ·Proficiency in document control systems, LMS administration, and Microsoft Office Suite. ·Ability to interpret and update labeling specifications and artwork. · Familiarity with QMS systems, LMS platforms, and basic GMP/GDP principles. Soft Skills ·Attention to Detail - Ensures accuracy in documentation and labeling. ·Communication - Clear and professional interaction with internal teams and suppliers. ·Organization - Manages multiple tasks and deadlines efficiently. ·Problem-Solving - Identifies issues and escalates appropriately. ·Collaboration - Works effectively across departments. Miscellaneous Requirements: ·Maintain a strong attendance record ·Adhere to company's drug-free workplace policies Physical Requirements: Office-based with occasional work in controlled environments. ·May be required to work longer than the typical 8-hour workday. ·Sedentary position that may require pro-longed periods of desk work. ·Requires light physical duties in keeping work areas clean and organized. Regularly required to walk the production and warehouse areas. May require lifting boxes or equipment weighing up to 50 pounds. About GSMS Founded in 1986 by a veteran of the US Air Force, GSMS has grown to be the leading provider of generic pharmaceuticals to the federal government. Based in Camarillo, CA, the GSMS team is relentlessly focused on providing critical medicines to our veterans, active-duty military members, and their families while delivering significant cost-savings to the government. Our expertise covers all aspects of the federal healthcare market, including contracting, compliance, data analytics, packaging, labeling, distribution, sales, and customer relations. With over 200 team members and 90 manufacturer partners, GSMS is well positioned to grow our market leadership position and bring innovative solutions to our customers and investors. The hiring range for this position in Camarillo, CA (Remote) is $24.04 - 27.88 per hour. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills and experience among other factors. A bonus may be provided as part of the compensation package, in addition to a full range of other health and welfare benefits.

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. **Job Description** **Key Responsibilities** + Perform testing of raw materials, intermediates, final products, and stability by following analytical methods. + Maintain, calibrate, and operate equipment and instruments supporting cell bioassays, Flow Cytometry, ELISA, and PCR assays. + Track and test products according to stability protocols. + Work with internal and external resources to maintain the lab in an optimal state. + Monitor and trend data, complete routine record review of test data and related documents for in-process testing, drug substance, and drug product release. Generate Certificates of Analysis (CoAs) for product release. + Assist in the preparation of dossiers and data packages for interactions between Kite (Gilead) and regulatory agencies; participate in Pre-Approval Inspections. + Develop, revise, and review SOPs, qualification/validation protocols, and reports. + Conduct investigations regarding out-of-specification (OOS) results and manage deviations related to analytical procedures. Provide updates at daily and weekly meetings. + Monitor GMP systems to ensure compliance with documented policies. + Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies as appropriate. + Gather metric information for continuous improvement of areas of responsibility. + Perform other duties as required. **Basic Qualifications** + BS degree in a scientifically oriented field and at least 2 years related work experience. **OR** + MS degree in a scientifically oriented field and at least 0 years related work experience. **Preferred Qualifications** + At least 2 years of industry experience in a biotech and/or pharmaceutical quality-related role. + Strong knowledge of GMP, SOPs, and quality control processes. + Experience identifying, writing, evaluating, and closing OOS investigations. + Proficient in MS Word, Excel, PowerPoint, and other applications. + Strong written and verbal communication skills. + Ability to communicate and work independently with scientific/technical personnel. + Well-versed in analytical techniques such as Flow Cytometry, ELISA, PCR, and cell bioassays for biopharmaceutical testing. + Working knowledge of quality systems and regulatory requirements (21 CFR Part 11/210/211). + Flexibility to work alternate schedules, including weekends, as business needs require. The salary range for this position is: $80,325.00 - $103,950.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: ****************************************************************** * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit ****************** . Sign up to follow @KitePharma on Twitter at ************************** . **For jobs in the United States:** Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance. For more information about equal employment opportunity protections, please view the 'Know Your Rights' (********************************************** poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT (********************************************************* YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. **For Current Kite Pharma Employees and Contractors:** Please apply via the Internal Career Opportunities portal in Workday. **Change The World With Us** Everyone at Kite is grounded by one common goal - curing cancer. Every day, we aim to establish a direct line between that purpose and our day-to-day work. We are creating Kite together, with the recognition that the best teams are built by the best people. We maintain an attitude of curiosity, and creativity with each challenge as we develop a new market for cancer therapies. We appreciate and respect one another, and most importantly, we don't take success for granted. While we've come a long way to make what others viewed as impossible, possible, we know one thing is certain. Today is just the beginning.

Under general supervision, this position performs routine laboratory testing and related activities in support of Quality Control operations. The role requires adherence to current Good Manufacturing Practices (cGMP), safety guidelines, and regulatory requirements while supporting analytical testing, documentation, and laboratory operations. **Key Responsibilities** + Perform routine laboratory procedures and analytical testing in a regulated QC environment + Document, calculate, compile, interpret, and enter laboratory data accurately and in a timely manner + Operate, maintain, and troubleshoot laboratory instruments and specialized equipment as required. + Maintain laboratory reagents and maintain an inspection ready area + Maintain complete and compliant laboratory documentation, including logbooks, worksheets, and electronic records + Follow all applicable safety guidelines, cGMPs, and CFR requirements + Maintain training records and comply with written procedures and laboratory systems + Support controlled document updates and change implementation activities + Identify and escalate compliance, safety, or data integrity issues as appropriate + May recommend and implement improvements related to routine job functions **Ideal Candidate Profile** The ideal candidate is a motivated, reliable individual who is eager to grow in a regulated Quality Control laboratory environment. This role is well-suited for: + Recent graduates or early-career professionals with a Bachelor's degree in Biology, Chemistry, Biochemistry, or a related scientific field + Candidates with hands-on QC GMP laboratory experience, even if a degree is not held + Individuals who are highly trainable and enthusiastic about learning analytical testing techniques + Team-oriented professionals with strong time management, reliability, and organizational skills + Candidates comfortable working with basic computer systems and laboratory documentation + Familiarity with GMP principles is preferred but not required **Preferred Qualifications:** + Ability to follow regulatory requirements, written procedures, and safety guidelines + Ability to review and evaluate data and documentation in accordance with company and regulatory standards + Strong organizational skills with the ability to manage multiple priorities and meet deadlines + Excellent attention to detail + Strong written and verbal communication skills + Flexibility and adaptability in a fast-paced, regulated environment + Understanding of when and how to appropriately escalate issues + Ability to identify, recommend, and implement improvements related to routine job functions + Commitment to continuous learning and compliance with cGMP and safety requirements. **Top must have skills:** + cGMP Compliance & Documentation + Laboratory Execution & Analytical Skills + Reliability, Organization & Time Management **About US Tech Solutions:** US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit *********************** . "US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran"

Join our dynamic team as a Quality Control Technician, where you will play a crucial role in ensuring the highest standards of product quality in a cleanroom environment. You will be responsible for inspecting incoming and final products, contributing significantly to our quality assurance processes. Responsibilities + Manage the equipment calibration and maintenance program, maintaining inventory and status of measuring devices. + Provide support for all testing related to manufacturing, including first article inspections, in-process release inspections, final QC release of finished goods, and document reviews. + Ensure all inspections and procedures are properly completed and documented. + Support environmental monitoring of cleanrooms and address microbial failures with effective solutions. + Review quality assessment results to determine acceptance or rejection of manufactured products during the inspection process. + Participate in the investigation of source materials for products and components. + Complete customer surveys and questionnaires. Essential Skills + Bachelor's degree in a technical or scientific field, or High School Diploma with 1-3 years of experience in quality assurance. + Understanding of global pharmaceutical product regulations with experience in ISO 9001 and/or 21 CFR Parts 210, 211, and/or Part 820. + Experience in quality systems including corrective actions, change control, quality audits, and validation of manufacturing processes or product development in a pharmaceutical or medical device environment. + Solid organizational and planning skills. + Ability to communicate effectively, both verbally and in writing, and demonstrate good interpersonal skills interdepartmentally and with external vendors and contractors. + Ability to work effectively and efficiently in a team environment. + Passion for innovation and drive for solutions. + Personal accountability for results and integrity. + Eagerness to learn and continuously improve. + Uncompromising dedication to quality. + Good general mathematical and computer skills. Additional Skills & Qualifications + Experience with labeling, quality control, quality assurance, blueprint reading, GMP, documentation, quality inspection, deviation management, attention to detail, and document control. + Proficiency in the use of calipers and quality inspection techniques. + Ability to work effectively in a high-paced cleanroom environment. Work Environment This role requires working within a cleanroom environment where precision and attention to detail are paramount. Candidates should be comfortable working in a fast-paced setting, utilizing small measuring devices and computer skills to ensure the highest level of product quality. Job Type & Location This is a Permanent position based out of Camarillo, CA. Pay and Benefits The pay range for this position is $49920.00 - $49920.00/yr. Medical, Dental, Vision, FSA, Life and AD&D, 401(k) Workplace Type This is a fully onsite position in Camarillo,CA. Application Deadline This position is anticipated to close on Jan 19, 2026. 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Job Description Job Title: Quality Control Inspector II F Reports To: Quality & Process Planning Manager Job Purpose The Quality Control Inspector II is responsible for ensuring that all products meet established quality standards and customer specifications. This role performs inspections, checks, and tests during the manufacturing process, records observations, and recommends improvements. The position requires proficiency with ERP systems to produce quality reports for internal and external use, while supporting company-wide quality initiatives and continuous improvement efforts. Duties & Responsibilities Ensure compliance with all quality check procedures throughout the production process. Perform required physical testing in accordance with Work Instructions. Develop inspection plans aligned with company and customer-specific requirements. Conduct required visual checks and verify masking accuracy against blueprints and purchase orders. Act as subject matter expert for multi-process orders. Approve internal masking with resource owners to prevent process failures. Record inspection data, document pass/fail status, and report rejections with photo evidence as needed. Tag and hold parts for review when disposition is required. Complete logbooks for Copper Sulfate and 24-hour humidity tests. Review Shop Travelers for accuracy, completion, and compliance. Verify packaging instructions are followed before shipment and ensure traceability. Inspect expedited, regular, and rework orders for proper processing. Perform random sampling inspections on large quantity orders. Gather required measurement tools and take photos, sharing findings with customers and production teams. Promote accuracy in job scanning and identify opportunities to improve shop floor efficiency. Utilize ERP software to document corrective actions and prevent recurring quality issues. Educate production staff on quality control issues and support improvement efforts. Assist Quality Engineering and Specialists with troubleshooting and corrective actions. Maintain communication via email and phone as required. Ensure inspection benches are organized and clean; maintain 5S standards and audits. Perform other duties as assigned by management. Qualifications 3-5 years of quality control inspection or related experience. High School Diploma or equivalent required. Basic blueprint reading and interpretation. Proficiency with Microsoft Office Suite and ERP systems. Strong verbal, written, and customer service skills. Experience using measuring tools (meters, gauges, calipers, etc.). Ability to work full-time, including overtime and weekends as needed. Key Competencies Strong verbal and written communication skills. Attention to detail and accuracy. Basic math and analytical skills. Documentation and reporting skills. Hand-eye coordination. Ability to stay organized and maintain good housekeeping practices.

Responsibilities of the QC Technician II include implementing and recording various testing methodology within the laboratory. Monitor plant cleaning activities by conducting regular swabbing of production equipment. This position is responsible for the quality, safety, and compliance of the laboratory operations as well as the timely release of test results. Hourly Pay: $32.00 - $34.00 Essential Duties and Responsibilities include the following. Other duties may be assigned. * Direct and implement various analytical tests on incoming samples of raw materials (RM), product components (Intermediates), and Finished Products to assure the Quality of the component. These include but are not limited to: * Logging samples into the Sample Data Base. * Performing analytical tests using the following testing equipment and recording results: * Fourier Transform - Infrared Spectrometer (FTIR). * Handheld & Benchtop Densitometers (SG-Specific Gravity) * Refractometers (RI-Refractive Index) * Small Scale Flash Point Tester (Flashpoint) * Total Acidity - manual titrations * pH meter * Hot plate (boiling point testing) * Turbidity (TURB) * Absorbance (ABS) * Moisture * Support OH R&D Analytical testing and tasting panels. * Analytical Testing for Regulatory (i.e., FP/BP, ABV). * Conduct small scale taste test to compare incoming sample to a prior batch or lot. * Compare test results with specification ranges to determine batch to batch consistency of the product. Trouble shoot batches that do not meet specifications. * Perform daily calibration checks of lab equipment (RI, SG, pH, FTIR, TURB, and ABS). * Monitor plant cleaning activities by conducting Allergen testing, and other environmental microbial and pathogen swabbing. * Review production schedule to find or order retain samples for batch comparison. * Clean lab / glassware. * Organization and cataloguing of retain library. * Filing sample folders and paperwork. * Create transmittals and associated sample request forms and labels for outside testing, gather / prepare these for shipment. * Release products in a usable status by entering data in ERP system and create paperwork for shipping department (CoA, SDS, and Required customer documents). * Build continuous improvement by developing and implementing new procedures based on trends, new issues, and analyses. * Report food safety issues to the Corporate Food Safety Manager or Director of Quality. Supervisory Responsibilities This position does not have any supervisory responsibilities. Competencies To perform the job successfully, an individual should demonstrate the following competencies: Optimizes Work Process- Knowing the most effective and efficient processes to get things done, with a focus on continuous improvement. Collaborates- Building partnerships and working collaboratively with others to meet shared objectives. Self-Development- Actively seeking new ways to grow and be challenged using both formal and informal development channels. Communicates Effectively- Developing and delivering multi-mode communications that convey a clear understanding of the unique needs of different audiences. Analytical - synthesizes complex or diverse information; collects and researches data; uses intuition and experience to complement data; designs workflows and procedures. Teamwork - balances team and individual responsibilities; exhibits objectivity and openness to others' views; gives and welcomes feedback; contributes to building a positive team spirit; puts success of team above own interests; able to build morale and group commitments to goals and objectives; supports everyone's efforts to succeed. Safety and security - observes safety and security procedures; determines appropriate action beyond guidelines; reports potentially unsafe conditions; uses equipment and materials properly. Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and/or Experience Bachelor's degree (B.S.) from four-year college or university in chemical or food science; preferred. Two years of related experience and/or training; or equivalent combination of education and experience. Language Skills Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to write speeches and articles for publication that conform to prescribed style and format. Ability to effectively present information to top management, public groups, and/or boards of directors. Mathematical Skills Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. Reasoning Ability Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, musical notes, etc.,) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables. Computer Skills To perform this job successfully, an individual should have knowledge of Database software, Internet Software; Inventory software; Manufacturing software; Spreadsheet software and Word Processing software. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to stand; walk; sit; talk or hear and taste or smell. The employee is occasionally required to use hands to finger, handle, or feel and reach with hands and arms. The employee must frequently lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly exposed to fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; extreme cold and extreme heat. The noise level in the work environment is usually loud. At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a wide variety of candidates, and we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. At Glanbia our culture will celebrate individuality, knowing that together we are more. Nearest Major Market: Los Angeles

Are you a hands-on problem solver with a passion for science and technology? Join our team as an R&D Technician and play a crucial role in our research and development projects. If you have a keen eye for detail, strong technical skills, and a drive to innovate, we want to hear from you. Take the next step in your career and help us create groundbreaking solutions that make a difference. Who is Meissner? The goal at Meissner is to be more than simply good; it is to be extraordinary. Extraordinary performance comes from extraordinary people. Meissner as a group is passionate about helping our clients manufacture lifesaving and life enhancing drugs, therapies, and vaccines. We develop, manufacture, supply and service advanced microfiltration products and single-use systems worldwide. We know that when you are passionate about what you do, it s more than just a job. Meissner is focused on the development of the whole individual, and we have programs and tools in place to help us stay at our best mentally and physically. In alignment with our commitment to support the growth and development of the whole individual, Meissner has inaugurated a Learning and Development department to solely focus on cultivating our team. When you grow, we grow. How you will make an impact: Research and Development technicians are at the forefront of innovation and scalability for Meissner Filtration Products. The Research and Development Technician supports development, testing, quality, and production of new products and technology. They will work directly with the R&D Scientific and Engineering team in the manufacturing of new products and bring these technologies up to production. Run equipment following procedures to test different parameters to evaluate the effects of changing process conditions. Assemble / Disassemble mechanical equipment containing chemical solutions and clean equipment in preparation for next runs. Prepare chemical formulations using ingredients and solvents. This is an on-site role based out of our headquarters in Camarillo, CA. The skills and experience you ll need: High School Diploma or GED. Must have a strong mechanical acumen and ability to perform basic math, understanding addition, subtraction, measurement, ratios, and percentages. Familiar with MS Office software including Outlook, Word, Excel on the PC. Must be able to record and enter data into a spreadsheet. Must have strong English Language written and verbal communication skills. Don t meet every single requirement? Apply anyway. What we can offer you: Full Medical, Dental and Vision coverage with HSA Employer Contributions for eligible plans Additional Perks- HQ Onsite Full Gym, Ultramodern Coffee Bars, Free EV Charging Stations, Employee Discounts 401k, Profit Sharing, 401k Advisory Services Company Sponsored Life Insurance Employee Assistance Program Paid Time Off, Paid Holidays, Anniversary Holiday Ready to make an impact? Let s talk. This position may require you to access information that is subject to U.S. export regulations. You may only access such information if you are a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. government. Meissner is proud to be an Equal Opportunity Employer. US BASE PAY SCALE $20.16 - $25.84/hr The base pay scale for this role is what Meissner reasonably expects to pay for the position although actual pay may vary from this scale depending on an applicant's experience.

**Kelly Science & Clinical** is seeking a **Chemist I** for a **temp-to-hire (contract-to-perm)** position with one of our industry partners in **Valencia, CA** . If you're passionate about hands-on laboratory work and eager to grow your scientific career, let The Experts at Hiring Experts help you take the next step. **Summary:** The Chemist I performs routine and specialized laboratory tasks to support product manufacturing, quality control, and process operations. This role is ideal for a detail-oriented individual who works well independently, thrives in a dynamic laboratory environment, and values safety, organization, and accuracy. Strong communication and teamwork skills are essential. **Responsibilities:** + Transfer, pipette, and weigh materials for laboratory processes + Mix and pour epoxy materials + Log radionuclide use and activities in Microsoft D365 + Perform daily cleaning and maintenance of production labs and facilities + Conduct gamma camera scanning + Communicate effectively with other groups within the company to ensure timely product manufacture + Follow all safety, health, and environmental regulations + Complete daily duties and orders unsupervised **Qualifications:** + Minimum education: Bachelor's or Associate's degree in a related field OR equivalent experience + Minimum experience: 6 months of related laboratory experience, college coursework, or internal experience + Experience handling standard laboratory equipment (pipettors, balances, mixers, ovens) is a plus + Experience with containment apparatus (hoods, gloveboxes) is a plus + Excellent manual dexterity and steady hand + Proficiency in Microsoft Excel, Word, Outlook, and Access + Safety-oriented, neat, and organized + Sound judgment and decision-making ability + Ability to lift up to 30 lbs **Additional Details:** + **Shift:** Onsite + **Pay Rate:** $25.00-$26.00/hour + **Employment Type:** Temp-to-Hire (Contract-to-Perm) + **Location:** Valencia, CA As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Entech Instruments Inc., a California-based company specializing in scientific instrumentation and sample extraction and introduction technologies for GC-MS platforms, is seeking a candidate with experience in the analysis of volatile and semi-volatile compounds in drinking, ground, and wastewater using one or more of the following EPA methods: 8260, 8270, 8275, 524, 525, 624, 625, and 608. The ideal candidate has extensive experience developing GC-MS applications with a detailed history of using sample preparation and introduction techniques such as SPME, SBSE, SPE, dynamic headspace, and purge & trap. In addition, the ideal candidate should have a mastery of sample preparation methods for targeted testing of organics in water for water safety applications. Experience with other applications such as; food safety, flavors & aromas, pharmaceuticals, metabolomics, and materials analysis is highly desirable. Entech's recently introduced Sorbent Pen technology and VASE (Vacuum Assisted Sorbent Extraction), is set to revolutionize the GC-MS research and testing industry by enabling solvent-free exhaustive extractions of volatile and semi-volatile compounds in a rapidly growing number of sample matrices. The chosen candidate will have the opportunity to shape their career, actively participating in ongoing research and development, creating new applications, publishing journal articles and app notes, and presenting findings at conferences and to government agencies. Responsibilities: • Develop and validate new analytical methods for the quantification of VOCs & SVOCs in drinking, surface, and groundwater. • Establish and nurture relationships with customers to ensure consistent application and method execution. • Maintain communications with EPA and FDA to expedite the adoption of new methods. • Establish and train a laboratory team to support the primary mission. • Author journal articles and application notes. • Assist with continued product R&D. • Troubleshoot analytical instrumentation as needed. • Work with sales and marketing to develop and publish data online, case studies, technical information, and videos that highlight the technology's method efficiencies and advantages. • Prepare presentations for customer visits, conferences, and trade shows. Requirements: • Must be enthusiastic about new product development and willing to participate in rigorous experimentation with short production timelines. • Extensive GC/MS experience is required. • Experience with some or all of the following; SPE, LLE, Soxlet, Quechers, SPME, SBSE, Purge/Trap, Dynamic Headspace and other sample preparation experience. • Experience with EPA methods, including EPA 8260, 8270, 8081, 8082, 8011, 624, 625, 608, 524, and 525. • Experience with Agilent, Thermo, or Shimadzu GC-MS systems and associated software. • Excellent communication skills in English, both oral and written for technical documentation, reporting of experimental results, and oral presentations. • Must be able to present technical concepts and simulated or experimental results. • Some travel required. Education: M.S. or PhD preferred Educational profile should include: Gas Chromatography, Liquid Chromatography, Mass Spectrometry, Mass Spectrometer Instrumentation, Chemistry, Chemical Engineering, Applied Chemistry, Applied Physics Salary Range DOE 401k Full Medical, Vision, and Dental Job Type: Full-time

Quality Control Analyst II in Camarillo, CA Build your future at Curia, where our work has the power to save lives. The Quality Control Analyst II is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives. We proudly offer * Generous benefit options (eligible first day of employment) * Paid training, vacation and holidays (vacation accrual begins on first day of employment) * Career advancement opportunities * Education reimbursement * 401K program with matching contributions * Learning platform * And more! Responsibilities * Perform complex testing and data evaluation, such as HPLC, ELISA, etc. * Troubleshoot equipment issues promptly and communicate resolutions to management * Participate in or assist with test method validations * Evaluate data for trends * Support and/or investigate OOS events by performing thorough root cause analyses, assessing potential product impact, and implementing appropriate CAPAs * Interact with outside departments including attending meetings, providing updates, etc. * Coordinate testing performed at outside testing labs, raw materials, etc. * Maintain a detailed and accurate recording of activities and results * Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries * Perform risk assessment as needed * Write/revise test methods, standard operating procedures, etc. * Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures * Support equipment upkeep * Prepare and order supplies, as necessary * Enter data into relevant data management systems and perform tracking and trending of data. Compile data and provide/present data summaries to management * Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry * Collaborate with cross-functional departments to coordinate testing, scheduling needs, and prioritization * Lead departmental projects and participate in cross-functional teams, including continuous improvement initiatives and new customer project teams * Lead the stability program, including management of test points, reporting of data, and investigations of out of specification or aberrant stability results Required * Bachelor's Degree in Chemistry or related field and 3+ years related work experience; OR * Master's Degree in Chemistry or related field and 1+ years related work experience; OR * Experience working in cGMP or GLP pharmaceutical industry environment * Willing to work flexible hours (nights and weekends), as-needed (overtime eligible) Knowledge, skills and abilities * Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public * Ability to meet deadlines and work under pressure with limited supervision * Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently * Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations * Ability to write reports, business correspondence, and procedures * Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations * Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis * Ability to define problems, collect data, establish facts, and draw valid conclusions * Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and handle several abstract and concrete variables * Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems * Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus Other Qualifications * Must pass a background check * Must pass a drug screen * May be required to pass Occupational Health Screening Pay Range: $72,000-$89,800/year Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer. #LI-AC1

Employment Type: Contract Business Unit: Clinical Process and Chemical Analysis Duration: 18+ months (with likely extensions) Notes: Onsite 3 Key Consulting is hiring a Senior Associate Quality Control for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: This Associate, in the Bioassay group, within client's quality control organization will work in a dynamic team environment to support testing, and projects within the group. The successful candidate will be responsible for Bioassay lab activities including analytical testing and analysis, tracking and trending of data, lab cleaning, and equipment maintenance. Why is the Position Open? Backfill, and additional workload. Top Must-Have Skill Sets: Pipetting Aseptic technique Cell culture Degree: Biology Degree (Bachelors), will consider new grad Day to Day Responsibilities: Sample potency testing using qualified cell or antigen/receptor based methodology Testing Execute routine and non-routine testing procedures and assays Perform data analysis of testing results and communicate results to appropriate sources Comply with safety guidelines Learn and comply with GLP, and cGMPs, which includes, but are not limited to, the maintenance of training records, laboratory notebooks, written procedures, equipment monitoring systems and laboratory logbooks. Material/Data Management Responsible for documenting, computing, compiling, interpreting, and entering data Responsible for the inventory management of all media, and reagents Ensure the timely disposal of tested samples. Red Flags: HPLC Gels Interview process: Phone screening followed by in-person interview. We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

Top skill sets: Biology, biochemistry, or any related field (back ground) Degree: BS. Or MS. In the science field Day to day responsibilities / first 30 days: Reading SOPs, shadowing senior analysts in the lab Basic Qualifications • Bachelor's degree OR • Associate's degree & 4 years of directly related experience OR • High school diploma / GED & 6 years of directly related experience Preferred Qualifications • Bachelor's degree and 4 years directly related experience. • Attention and dedication to quality. • Must be a team player. • Ability to organize work, handle multiple priorities and meet deadlines • Strong written and oral communication skills • Must be flexible and adaptable to changing priorities and requirements • Demonstrates understanding of when and how to appropriately escalate. Knowledge with Tecan and automated cell counter. Job Details: This is a new position-person will be working with a team-group is about 10 and everyone gets individual tasks to do. They do work together based off deadlines. Under general supervision, this position will perform routine procedures and testing in support of the General Testing and Raw Materials group. Specific responsibilities include: • Performing routine laboratory procedures • Routine testing includes but is not limited to, gene expression methods, cell proliferations methods, receptor/antigen binding methods, maintain culture cells. • Will also be responsible for documenting, computing, compiling, interpreting, reviewing, and entering data. • Providing and communicating results, maintaining/operating specialized equipment, and initiating and/or implementing changes in controlled documents. Responsible for general lab duties, such as chemical inventory, lab cleaning and instrument cleaning. • Must learn and comply with safety guidelines, cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory notebooks, written procedures, equipment monitoring systems and laboratory log books. Qualifications Top skill sets: Biology, biochemistry, or any related field (back ground) Degree: BS. Or MS. In the science field Day to day responsibilities / first 30 days: Reading SOPs, shadowing senior analysts in the lab Basic Qualifications • Bachelor's degree OR • Associate's degree & 4 years of directly related experience OR • High school diploma / GED & 6 years of directly related experience Preferred Qualifications • Bachelor's degree and 4 years directly related experience. • Attention and dedication to quality. • Must be a team player. • Ability to organize work, handle multiple priorities and meet deadlines • Strong written and oral communication skills • Must be flexible and adaptable to changing priorities and requirements • Demonstrates understanding of when and how to appropriately escalate. Knowledge with Tecan and automated cell counter.