Quality control analyst jobs in Oxnard, CA - 98 jobs

Quality Control Microbiologist II - Camarillo, CA The Quality Control Microbiologist II performs quality activities in support of product production and releases. The QC Microbiologist performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. 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. 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! Essential job duties * Lead and/or support quality event investigations for out-of-specification (OOS), out-of-trend (OOT) or nonconformance events * Perform environmental monitoring of clean rooms (under ISO and EU specifications) * Perform and review QC testing (Endotoxin, Bioburden, TOC, Conductivity, Growth Promotion Assay, etc.) for manufacturing, raw materials, in-process materials, intermediates and final product * Demonstrate technical proficiency in test procedures and ensure QC activities are carried out using applicable regulatory requirements (FDA, USP, ICH etc.) * Participate in audits, client investigations, and project-related activities * Lead and/or support activities associated with Change Control, CAPAs, client audit response, work orders, etc. * Receive and process samples to meet production/client timelines * Read, trend and report environmental, personnel, in-process, raw material, finish product and water bioburden testing results * Prepare and send out samples for microbiological identification * Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met * Work closely and collaborate in a team environment with QC Analytical and Quality Assurance, Manufacturing, Technical Services, Materials Receiving, and Research and Development * Ensure the successful implementation and execution of new QC methods/procedures and equipment * Perform trending of QC data and present information to Management * Perform general laboratory housekeeping * Author, review, and approve microbiology test results and analytical methods as needed * Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met * Support Manufacturing with client-specific testing requirements * Inspection of media fills Education, experience, certification and licensure * Bachelor's Degree in Microbiology or related field * Minimum 3-5 years' industry experience in a GMP sterile finish or pharmaceutical cleanroom environment * Willing to work flexible hours (nights and weekends), as-needed Knowledge, skills and abilities * Proficient in the validation/qualification of lab microbiological techniques preferred * Knowledgeable in FDA cGMPs (21 CFR 211); ISO 9001, 13485 and 17025 a plus * Knowledgeable in USP , , , and * Strong organizational skills and the ability to prioritize/multitask * Proficient in Microsoft Office Suite (excel) * Attention to details and following GMP methods and instructions * Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently * Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, and customers * Ability to write reports, business correspondence, and procedures * Ability to define problems, collect data, establish facts, and draw valid conclusions Physical requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is occasionally required to stand; walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, 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 has the potential of being exposed to fumes or airborne particles and toxic or caustic chemicals (wearing proper Personal Protective Equipment will be required in these situations). The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; outside weather conditions; and may be expected to work with electronic equipment (always being aware of one's environment and taking proper precautions is required). The noise level in the work environment is usually moderate. Employee may be responsible for moving and/or generating hazardous waste for treatment, storage and disposal. Affected employee will need to be familiar with the applicable training requirements included in the customized Resources, Conservation and Recovery Act. Employee will understand waste labeling, secondary containment, chemical compatibility, storage time limits, container size and quantity limits, container integrity when waste is left unattended and improper disposal of hazardous materials. Other Qualifications * Must pass a background check * Must pass a drug screen * May be required to pass Occupational Health Screening Pay Range: $70,304-$88,000/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.

Resillion is a strategic partner for quality assurance. We offer worldwide services on the field of quality technology, testing, conformity, interoperability and assurance, from initiation to launch - for the software system, cybersecurity, the device, digital products and media content. With a passion for quality, Resillion provides end-to-end solutions to support customers in their strategic digital initiatives and offers a holistic approach for both software and hardware. Via our office in Europe, the United Kingdom, the USA, India and China, we bring together more than 500 experts who are committed to success. We combine the best human and artificial intelligence (AI) on advanced solutions for quality technology in the liver. Resillion offers deep sector knowledge and works together with the world's leading companies in telecom, media, energy & utilities, health care, finance and consumer electronics. ***************** Job Description Set up playback devices, QC bays and monitors/scopes according to established specifications. Verify correct format, aspect ratio, audio configuration, and file metadata based on client specifications and previous title history. Take accurate line count and video/ audio measurements using industry standard waveform scopes and audio meters. Perform thorough mastering level quality control inspection noting any and all audio/ video impairments and anomalies. Ensure reports are consistent and accurate across all previous versions of a given title, which may require tracking new anomalies back to original sources and other aspect ratios/ formats. Troubleshoot any technical issues with the playback of assigned jobs. Provide additional information regarding a particular job or specific anomaly as needed. May be required to perform other duties as needed (including, but not limited to: file transmission and data management, training other operators, client review sessions, etc.) Qualifications Solid understanding of a wide variety of film, video and audio impairments and their underlying causes. Extensive experience with all SD and HD formats and timecode 2K, UHD and 4K and HDR-10 and Dolby Vision experience a huge plus. Extensive experience with any and all file-based workflows (including, but not limited to Tiff, DPX, J2K, ProRes, IMF packages). Solid Clipster proficiency including building. cp files and understanding of timeline output settings/ bin clip properties Experience with ColorFront Transkoder for QC or Production a plus Ability to read and understand MaxFaLL and MaxCLL HDR reports. Superior attention to detail and accuracy. Ability to think in a logical and organized manner and work efficiently under tight deadlines with minimal supervision. Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications: 3 to 5 years of experience as a Mastering Quality Control operator, working in a professional Post Production facility or studio. Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information Location: Burbank, CA Employment Type: Part-Time- On as needed basis Schedule: Swing Shift Salary: $28.00-30.00 Per Hour

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.

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.

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.

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"

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 We are looking for a Quality Control Microbiologist I at our Santa Monica facility. Shift Tuesday to Saturday days Responsibilities (include but are not limited to): * Perform and review environmental monitoring of cleanrooms including surface, viable air, non-viable air, and personnel monitoring. * Perform microbiological testing of raw material, in process, final product, protocol/validation-related, and critical utility samples. * Collect water samples to ensure all sample collected per schedule. * Performs bioburden testing of water and product. * Prepares growth promotion and other applicable nutrient substrate media qualification. * Data entry and data trend as needed. * Assist in investigations regarding out of specifications (OOS) results, address and manage deviations related to micro procedures. * Routine maintenance of lab equipment and lab spaces. * Conducts procedure updates in QC lab and GMP reviews of logbooks. * Coordinates waste management, LEAN and 5S efforts as required. * Perform other duties as assigned. Knowledge: * Basic Knowledge of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs). * Basic Knowledge of general Microbiology techniques such as Gram staining, aseptic technique, and plate streaking technique. * Knowledge of USP and other regulatory requirements. * Proficiency in Microsoft Office applications. * Ability to work effectively in a team environment. * Strong verbal, written, and interpersonal communication skills are required. Basic Qualifications: * Bachelor's OR * Associate and 2+ years of relevant experience OR * High School Diploma/GED and 3+ years of relevant experience Preferred Qualifications: * Prior Quality Control Microbiology laboratory experience preferred. * Experience in aseptic techniques and clean room operations. * Ability to gown for entry into Aseptic core and supporting areas, and lift approximately 25 lbs. * Knowledge of GMP, SOPs, LIMS, and quality control processes for clinical manufacturing. * Proficient in MS Word, Excel, Power Point and other applications. * Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment. * Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities. * Ability to be flexible with schedule and work overtime as needed. The salary range for this position is: $69,445.00 - $89,870.00. 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 Description We are looking for a Quality Control Microbiologist I at our Santa Monica facility. Shift Tuesday to Saturday days Responsibilities (include but are not limited to): Perform and review environmental monitoring of cleanrooms including surface, viable air, non-viable air, and personnel monitoring. Perform microbiological testing of raw material, in process, final product, protocol/validation-related, and critical utility samples. Collect water samples to ensure all sample collected per schedule. Performs bioburden testing of water and product. Prepares growth promotion and other applicable nutrient substrate media qualification. Data entry and data trend as needed. Assist in investigations regarding out of specifications (OOS) results, address and manage deviations related to micro procedures. Routine maintenance of lab equipment and lab spaces. Conducts procedure updates in QC lab and GMP reviews of logbooks. Coordinates waste management, LEAN and 5S efforts as required. Perform other duties as assigned. Knowledge: Basic Knowledge of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs). Basic Knowledge of general Microbiology techniques such as Gram staining, aseptic technique, and plate streaking technique. Knowledge of USP and other regulatory requirements. Proficiency in Microsoft Office applications. Ability to work effectively in a team environment. Strong verbal, written, and interpersonal communication skills are required. Basic Qualifications: Bachelor's OR Associate and 2+ years of relevant experience OR High School Diploma/GED and 3+ years of relevant experience Preferred Qualifications: Prior Quality Control Microbiology laboratory experience preferred. Experience in aseptic techniques and clean room operations. Ability to gown for entry into Aseptic core and supporting areas, and lift approximately 25 lbs. Knowledge of GMP, SOPs, LIMS, and quality control processes for clinical manufacturing. Proficient in MS Word, Excel, Power Point and other applications. Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment. Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities. Ability to be flexible with schedule and work overtime as needed. The salary range for this position is: $69,445.00 - $89,870.00. 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.

Come Join Us! From apartments in New York to hospitals and stadiums in Dallas, libraries at prestigious universities to creating modern retail experiences, our teams contribute architectural glass and building products to projects that shape the way people live, work, heal, learn, and play. At OBE, the work of our employees truly matters. With over 6,500 employees, we operate more than 80 manufacturing and distribution facilities in five countries. You can see some of our favorite projects here. Start your journey with OBE and help us build the future. About the Position We are currently searching for an experienced and analytical Quality Control Staff to join our production department. As the Quality Control, you will uphold the safety regulations of our company and oversee the production process to guarantee that all our products meet quality expectations. The chosen candidate will perform regular product evaluations, record inspection results, and recommend improvements to the production process. To excel in this role, applicants should demonstrate great attention to detail with technical and math abilities. What You'll Get To Do Perform quality assessments on all incoming material from vendors, outgoing products for shipping and customer complaints. Reject all products and material that fail to meet quality expectations. Read drawings, plans and specifications to understand the requirements of the products and services. Perform Inspection and testing acceptance criteria Measure product dimensions examine functionality and compare the final product to the specifications. Recommend improvements to the production process to ensure quality control. Document inspection outcomes by completing detailed reports and performance records. Teach the production team about quality control concerns to improve product excellence Oversee the production process Resolve quality related issues in a timely manner. Control and maintenance of all quality documentation, such as: creation, review, approval, modification, elimination and distribution. Review, disposition and oversee rework of nonconforming product. Recommend Corrective/ Preventive actions to eliminate the causes of actual or potential non Qualification Requirements A minimum of 1-year experience in a similar role High School diploma or equivalent qualification Certification in quality control is preferred Good math and technical skills Understanding of quality control standards and testing techniques. Basic computer skills (excel & word) Dependable, organized with ability to prioritize effectively Good communication skills Ability to problem solve, multi-task, attention to detail and work independently Measuring equipment (Caliper, tape measure, etc.) Position Pay Range $24-$27 USD What OBE Offers You Benefits that benefit you - industry competitive benefits at the lowest cost to the employee Work-life balance - PTO and holidays, including floating holidays you can choose Compensation that rewards your hard work - A pay-for-performance culture with potential for annual raises and bonuses Training - We will equip you with the knowledge and skills you need to succeed OBE Privacy Policy OBE will not discharge or discriminate against employees or applicants for discussing, disclosing, or inquiring about their own or others' pay.

The Quality Control is responsible for overseeing and managing all aspects of quality control processes within the organization. This role involves leading a team of quality control inspectors, implementing quality standards, and ensuring compliance with industry regulations. The ideal candidate will have strong leadership skills, attention to detail, and a deep understanding of quality control practices, particularly in GMPs (Good Manufacturing Practices) and HACCP (Hazard Analysis and Critical Control Points). What We Offer: Comprehensive Medical, Dental, and Vision Insurance Enjoy discounts on organic meals daily Opportunities for career growth Key Responsibilities: team of quality control inspectors. Assign tasks and responsibilities to team members and ensure the timely completion of quality control activities. Conduct regular performance evaluations and provide feedback to team members. Develop, implement, and maintain quality control procedures and standards in compliance with GMPs and HACCP. Oversee the inspection and testing of products to ensure they meet quality specifications. Analyze quality data and identify trends or areas for improvement. Ensure compliance with industry regulations and company policies. Maintain accurate records of quality control activities, inspections, and test results. Prepare and present reports on quality performance and improvement initiatives. Identify opportunities for process improvements and lead quality improvement projects. Collaborate with cross-functional teams to address quality issues and implement corrective actions. Stay updated with industry trends and advancements in quality control techniques, particularly GMPs and HACCP. Develop and deliver training programs for quality control staff. Ensure all team members are knowledgeable about quality standards and procedures, with a strong focus on GMPs and HACCP. Requirements Qualifications: Minimum of 5 years of experience in quality control or quality assurance, with at least 2 years in a supervisory or lead role. Experience in the [specific industry] is preferred. Knowledge: In-depth knowledge of Good Manufacturing Practices (GMPs) and Hazard Analysis and Critical Control Points (HACCP) standards. Skills: Strong leadership and team management skills. Excellent analytical and problem-solving abilities. Proficiency in quality control software and tools. Strong communication and interpersonal skills. Physical Requirements: Ability to lift up to 35 pounds. Ability to stand for extended periods and perform repetitive tasks. Comfortable working in a manufacturing or production environment. Benefits: Competitive salary and performance-based bonuses. Health, dental, and vision insurance. Professional development opportunities.

The Quality Control Inspector is responsible for managing quality against the three stages of production (before, in process and final repairs) of vehicles in accordance with factory and county specifications as well as ensuring vehicles are repaired per estimate and according to county standards. Pay Range: $24.00 - $26.00/hour RESPONSIBILITIES Review approved estimates/supplements against repaired vehicle Notify management of any additional repairs needed Maintain all safety and health personal protective equipment, including respirators, in the manner recommended by the equipment manufacturer Ensure full use of all required safety and health personal protective equipment across all locations for the contract Comply with all laws and regulations pertaining to paint, thinners and other hazardous materials. Reports any deviations to management Cooperate and assist other personnel in the repair and prepping of vehicles Understand, keep abreast of and complies with federal, state and local regulations that affect body shop operations, such as hazardous waste disposal, OSHA Right-to-Know, etc. Operate all tools and equipment in a safe manner Other duties as assigned QUALIFICATIONS High School Diploma or equivalent required One-year certificate from college or technical school; or 3-6 months related experience and/or training (or equivalent combination of education and experience) Must have 1 year of work related experience Must have a valid Driver's License Must have the following Certifications: Damage Analysis and Estimating Certification for Collision Repair I-CAR Effective oral and written communication skills with all levels of the organization Strong organizational skills with the ability to manage time and multiple priorities to completion Problem solving skills with an analytical thought process Ability to adapt to a rapidly changing environment Must be able to lift, lower, carry, push or move objects up to 50 lbs. Various tasks may require intermittent standing or prolonged sitting, and the ability to walk, reach, kneel, crouch and handle work related supplies and tools. Additional details related to physical requirements may be outlined in the Company's Performance Work Statement or Contract with the client. BENEFITS Constellis offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects its commitment to creating a diverse and supportive workplace. Medical, Vision & Dental Insurance Paid Time-Off Program & Company Paid Holidays 401(k) Retirement Plan Insurance: Basic Life & Supplemental Life Health & Dependent Care Flexible Spending Accounts Short-Term & Long-Term Disability Personal Development & Learning Opportunities On-the-job Training, Skills Development & Certifications Employee Referral Program Corporate Sponsored Events & Community Outreach WORKING CONDITIONS Work is typically based in a busy service center/maintenance garage environment and subject to frequent interruptions. Frequent work outside and in inclement weather conditions is required, including heat, cold and humidity. May be exposed to fumes or airborne particles, toxic or caustic chemicals and vibration. Must be willing to wear Personal Protective Equipment as required by established Company Safety Standards. Normal work hours are Monday-Friday 6:00 am to 2:30 pm, however some extended or weekend hours may also be required.

The Quality Control Inspector is responsible for managing quality against the three stages of production (before, in process and final repairs) of vehicles in accordance with factory and county specifications as well as ensuring vehicles are repaired per estimate and according to county standards. Pay Range: $24.00 - $26.00/hour RESPONSIBILITIES Review approved estimates/supplements against repaired vehicle Notify management of any additional repairs needed Maintain all safety and health personal protective equipment, including respirators, in the manner recommended by the equipment manufacturer Ensure full use of all required safety and health personal protective equipment across all locations for the contract Comply with all laws and regulations pertaining to paint, thinners and other hazardous materials. Reports any deviations to management Cooperate and assist other personnel in the repair and prepping of vehicles Understand, keep abreast of and complies with federal, state and local regulations that affect body shop operations, such as hazardous waste disposal, OSHA Right-to-Know, etc. Operate all tools and equipment in a safe manner Other duties as assigned QUALIFICATIONS High School Diploma or equivalent required One-year certificate from college or technical school; or 3-6 months related experience and/or training (or equivalent combination of education and experience) Must have 1 year of work related experience Must have a valid Driver's License Must have the following Certifications: Damage Analysis and Estimating Certification for Collision Repair I-CAR Effective oral and written communication skills with all levels of the organization Strong organizational skills with the ability to manage time and multiple priorities to completion Problem solving skills with an analytical thought process Ability to adapt to a rapidly changing environment Must be able to lift, lower, carry, push or move objects up to 50 lbs. Various tasks may require intermittent standing or prolonged sitting, and the ability to walk, reach, kneel, crouch and handle work related supplies and tools. Additional details related to physical requirements may be outlined in the Company's Performance Work Statement or Contract with the client. BENEFITS Constellis offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects its commitment to creating a diverse and supportive workplace. Medical, Vision & Dental Insurance Paid Time-Off Program & Company Paid Holidays 401(k) Retirement Plan Insurance: Basic Life & Supplemental Life Health & Dependent Care Flexible Spending Accounts Short-Term & Long-Term Disability Personal Development & Learning Opportunities On-the-job Training, Skills Development & Certifications Employee Referral Program Corporate Sponsored Events & Community Outreach WORKING CONDITIONS Work is typically based in a busy service center/maintenance garage environment and subject to frequent interruptions. Frequent work outside and in inclement weather conditions is required, including heat, cold and humidity. May be exposed to fumes or airborne particles, toxic or caustic chemicals and vibration. Must be willing to wear Personal Protective Equipment as required by established Company Safety Standards. Normal work hours are Monday-Friday 6:00 am to 2:30 pm, however some extended or weekend hours may also be required.

Job Description Full Time + Benefits (Medical, Dental, Vision, 401k with Company Match, PTO) Job Type: On-site Hourly Range: $19.50 - $23.00, DOE Fralock is an engineered solutions provider of specialty components and subassemblies using advanced materials for high reliability, severe environment, and technically challenging applications. We develop and manufacture custom integrated solutions. Established in 1967, we are a critical solutions provider to Fortune 500 corporations, government, and targeted OEMs in a variety of industries including Semiconductor Equipment Manufacturing, Medical and Life Science, Aerospace and Defense, Industrial, Electronics, and Energy. Fralock is headquartered in Valencia, CA with manufacturing locations located throughout Northern and Southern California. VISION To be recognized by our customers as a leading solutions provider of proprietary engineered advanced materials for high reliability, severe environment, and technically challenging applications. MISSION To create value, profitably grow, and share our success with all stakeholders. CULTURE Respect - We treat others the way they want to be treated. Integrity - We practice a high standard of ethics in our business dealings with customers, suppliers, and employees. Responsiveness - We have a sense of urgency in responding to internal and external requests and work proactively to solve problems. Excellence/Competence - We empower our people to continuously improve and execute high quality work. Teamwork - We work together to achieve Fralock business objectives by communicating at a high level, by listening and having clarity in our expectations of one another. Individual Accountability and Personal Responsibility - We do what we have committed to do when we committed to doing it. Continuous Improvement across all segments of the company This position requires access to information controlled under the International Traffic in Arms Regulations (ITAR) or the Export Administration Regulations (EAR), the successful candidate must be a "U.S. person" as defined in the ITAR and EAR (which generally means (i) be a citizen or national of the United States; or (ii) be a lawful permanent resident of the United States; or (iii) have been admitted to the United States as a refugee, or have been granted asylum, as specified under applicable law. Main Functions Perform inspections, checks and tests for quality control for the manufacture of products. Interpret complex drawings, standards, procedures, and test data. Document results of inspections. Maintain calibration system. Typical Duties Follow procedures, work, and inspection instructions in the job orders Perform inspections using CMM, Keyence, calipers, micrometers, or templates Work with Production/Receiving Inspection/Purchasing when parts are found out of tolerance Document results of inspections using First Article Report AS9102, customer-specific inspection documents, Fralock Dimensional Reports, copies of CMM report or written results in the job order Compare actual measurements to drawing tolerances using calibrated tools and inspection systems. Perform visual inspections using IPC-A-600, IPC-A-610, and J-STD-001 criteria to assess workmanship, soldering, and cosmetic requirements. Identify, tag, and document nonconforming items; coordinate with Quality and Engineering for resolution. Issue certificate of conformance Maintain CMMs and inspection tools in good condition, including inspection stamp Perform calibration of calipers, micrometers and templates, and coordinates outside calibration Update and maintain Master Calibration List Inspect materials and components upon receipt to confirm documentation, certifications, and traceability meet requirements. Conduct in-process checks to verify critical features and detect defects early in production. Perform final inspections to confirm product readiness for shipment, including dimensional, visual, and functional checks. Capture and upload inspection photos, ballooned drawings, and other evidence into QMS/ERP. Participate in containment and root cause investigation activities when quality issues arise. Maintain an organized, clean work area that supports ESD and FOD prevention. Required Skills PC literate (Excel, Word, e-mail) Knowledge in blueprint reading and geometrical tolerances; use of hand-held inspection tools and templates Minimum 2 years of quality inspection experience in a controlled manufacturing environment (aerospace, medical, or equivalent). Good communication skills both oral and written; English language proficiency for technical documentation and communication Proficiency in reading and interpreting engineering drawings and GD&T. Familiarity with basic measurement tools and inspection equipment. Competence in using MS Excel, Word, and ERP/QMS data entry. Strong attention to detail and ability to follow documented procedures. Preferred Skills Familiar with CMM inspection and Statistical Process Control (SPC) Familiarity with ISO 9001/ AS 9100 and/ or ISO 13485 Standard Experience in Aerospace, Medical or Automotive industry Knowledge of IPC-A-600, IPC-A-610, and J-STD-001 standards. Experience with flex/rigid-flex PCBs, SMT assemblies, or precision machined components. Proficiency with vision systems, CMMs, and SPC tools. AS9102 FAIR completion experience. Knowledge in calibration Education Requirements High School Diploma Experience Requirements 2 years minimum in a quality related field Physical Requirements Ability to multi-task Sitting/Walking/Standing Lifting in accordance with employee safety handbook Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of a position. Fralock provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QC Microbiologist to work for a Greater Los Angeles area cosmetics contract manufacturing company. Pay Rate: $20-24/hour depending on experience. 2nd shift: 1:00pm - 9:30pm plus OT and weekends as needed Summary:Responsible for all aspects of microbiological issues, including but not limited to the following: writing and validating microbiological procedures, testing samples and interpretation of results. Responsible for obtaining samples and coordination the timing and testing of each sample as described in the SOP. Responsibilities: Perform microbiological testing of bulk samples, finished goods, raw materials and other samples as outlined in SOP's. Perform preservative efficiency/challenge testing. Review, interpret and perform test protocols as directed. Develop and coordinate document control related to microbiological testing. Maintains and coordinates equipment calibration to support QC compliance in key aspects. Maintain various logbooks with departmental data. Support the department by typing memos, reports and spreadsheets with distribution and filing as required. Email, fax or make telephone calls as needed. Understand, exercise, and monitor all GMP and safety requirements and procedures in the work environment. Support other areas of QC with clerical support as needed. Will require use of gloves, safety glasses Performs other duties as assigned. Experience: Bachelor's Degree in Microbiology or related field. At a minimum, completed two years of course work and laboratory experience in Microbiology. Knowledge of microbiological methodologies and practices. Excellent English written and verbal communication skills. Advanced statistical and mathematical skills. Please send resumes to *********************** and visit our website at ******************* for additional job opportunities!!!

Quality Control Microbiologist II - Camarillo, CA The Quality Control Microbiologist II performs quality activities in support of product production and releases. The QC Microbiologist performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. 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. 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! Essential job duties • Lead and/or support quality event investigations for out-of-specification (OOS), out-of-trend (OOT) or nonconformance events • Perform environmental monitoring of clean rooms (under ISO and EU specifications) • Perform and review QC testing (Endotoxin, Bioburden, TOC, Conductivity, Growth Promotion Assay, etc.) for manufacturing, raw materials, in-process materials, intermediates and final product • Demonstrate technical proficiency in test procedures and ensure QC activities are carried out using applicable regulatory requirements (FDA, USP, ICH etc.) • Participate in audits, client investigations, and project-related activities • Lead and/or support activities associated with Change Control, CAPAs, client audit response, work orders, etc. • Receive and process samples to meet production/client timelines • Read, trend and report environmental, personnel, in-process, raw material, finish product and water bioburden testing results • Prepare and send out samples for microbiological identification • Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met • Work closely and collaborate in a team environment with QC Analytical and Quality Assurance, Manufacturing, Technical Services, Materials Receiving, and Research and Development • Ensure the successful implementation and execution of new QC methods/procedures and equipment • Perform trending of QC data and present information to Management • Perform general laboratory housekeeping • Author, review, and approve microbiology test results and analytical methods as needed • Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met • Support Manufacturing with client-specific testing requirements • Inspection of media fills Education, experience, certification and licensure • Bachelor's Degree in Microbiology or related field • Minimum 3-5 years' industry experience in a GMP sterile finish or pharmaceutical cleanroom environment Knowledge, skills and abilities • Proficient in the validation/qualification of lab microbiological techniques preferred • Knowledgeable in FDA cGMPs (21 CFR 211); ISO 9001, 13485 and 17025 a plus • Knowledgeable in USP , , , and • Strong organizational skills and the ability to prioritize/multitask • Proficient in Microsoft Office Suite (excel) • Attention to details and following GMP methods and instructions • Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently • Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, and customers • Ability to write reports, business correspondence, and procedures • Ability to define problems, collect data, establish facts, and draw valid conclusions Physical requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is occasionally required to stand; walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, 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 has the potential of being exposed to fumes or airborne particles and toxic or caustic chemicals (wearing proper Personal Protective Equipment will be required in these situations). The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; outside weather conditions; and may be expected to work with electronic equipment (always being aware of one's environment and taking proper precautions is required). The noise level in the work environment is usually moderate. Employee may be responsible for moving and/or generating hazardous waste for treatment, storage and disposal. Affected employee will need to be familiar with the applicable training requirements included in the customized Resources, Conservation and Recovery Act. Employee will understand waste labeling, secondary containment, chemical compatibility, storage time limits, container size and quantity limits, container integrity when waste is left unattended and improper disposal of hazardous materials. Other Qualifications • Must pass a background check • Must pass a drug screen • May be required to pass Occupational Health Screening Pay Range: $70,304-$88,000/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.

· 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.

Resillion is a strategic partner for quality assurance. We offer worldwide services on the field of quality technology, testing, conformity, interoperability and assurance, from initiation to launch - for the software system, cybersecurity, the device, digital products and media content. With a passion for quality, Resillion provides end-to-end solutions to support customers in their strategic digital initiatives and offers a holistic approach for both software and hardware. Via our office in Europe, the United Kingdom, the USA, India and China, we bring together more than 500 experts who are committed to success. We combine the best human and artificial intelligence (AI) on advanced solutions for quality technology in the liver. Resillion offers deep sector knowledge and works together with the world's leading companies in telecom, media, energy & utilities, health care, finance and consumer electronics. ***************** Job Description Performing A/V linear passes, checking and confirming accuracy, sync, and quality of audio, video, and subtitles Performing logic and navigation QC, and confirming functionality and presence of all assets against client specs Checking video assets for quality issues, including any dropouts, corruption, blocking, etc. Performing compatibility testing, checking for basic functionality on a matrix of devices based on product specs Writing up any issues observed in a clear, accurate, technically proficient manner Qualifications Experience utilizing various devices for both physical media and streaming playback (set top boxes, gaming systems, streaming media players, etc.) Experience with FileMaker Proficiency in Excel Deep understanding of DVD & Blu-Ray production processes, Surround Sound, Dolby ATMOS, HD, UHD, and regional products (domestic and international), etc. Excellent verbal and written communication skills A love of television and movies and a genuine curiosity about the technology involved in creating them Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Location: Burbank, California Employment Type: Part-Time, On-Site Schedule: Flexible hours Salary: $20.00-22.00 Per Hour

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job Description 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 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.

Resillion is a strategic partner for quality assurance. We offer worldwide services on the field of quality technology, testing, conformity, interoperability and assurance, from initiation to launch - for the software system, cybersecurity, the device, digital products and media content. With a passion for quality, Resillion provides end-to-end solutions to support customers in their strategic digital initiatives and offers a holistic approach for both software and hardware. Via our office in Europe, the United Kingdom, the USA, India and China, we bring together more than 500 experts who are committed to success. We combine the best human and artificial intelligence (AI) on advanced solutions for quality technology in the liver. Resillion offers deep sector knowledge and works together with the world's leading companies in telecom, media, energy & utilities, health care, finance and consumer electronics. ***************** Job Description Title responsibilities include, but are not limited to, the following: Performing A/V linear passes, checking and confirming accuracy, sync, and quality of audio, video, and subtitles Performing logic and navigation QC, and confirming functionality and presence of all assets against client specs Checking video assets for quality issues, including any dropouts, corruption, blocking, etc. Performing compatibility testing, checking for basic functionality on a matrix of devices based on product specs Writing up any issues observed in a clear, accurate, technically proficient manner Qualifications The ideal candidate would possess: Experience utilizing various devices for both physical media and streaming playback (set top boxes, gaming systems, streaming media players, etc.) Experience with FileMaker Proficiency in Excel Deep understanding of DVD & Blu-Ray production processes, Surround Sound, Dolby ATMOS, HD, UHD, and regional products (domestic and international), etc. Excellent verbal and written communication skills A love of television and movies and a genuine curiosity about the technology involved in creating them Additional Information Location: Burbank, California Employment Type: Part-Time Schedule: Day Shift Salary: $20.00-22.00 Per Hour