Quality control microbiologist jobs near me

Are you motivated to leverage your unique skills and experience with an industry leader trusted by the nations' strongest lending institutions? ServiceLink, the unrivaled best in the mortgage industry, seeks an action-oriented professional with a high degree of integrity and sound judgment to fill the position of Quality Control Analyst. The ideal candidate must share our unwavering focus on creating value for our customers and serve as a powerful force to promote unparalleled quality standards. If you thrive in a high-performance, Serve First culture, this may be the perfect position for you. It is an exciting time to join ServiceLink, where empowerment drives entrepreneurship. Applicants must be currently authorized to work in the United States on a full-time basis and must not require sponsorship for employment visa status now or in the future. 3+ years' experience in real estate appraisal quality control review at the AMC or mortgage company level. A DAY IN THE LIFE In this role, you will… · Perform quality control analysis of valuation reports in compliance with regulatory, industry and client requirements · Contact valuation providers to discuss revisions or obtain status as needed · Respond to and satisfy issues in a timely and consistent manner with accurate resolution · Meet daily, weekly, and monthly production goals set forth by management · Provide feedback to QC management that will improve processes and team productivity WHO YOU ARE You possess … · A confident understanding of the mortgage services industry with knowledge of appraisal industry guidelines and products · Prior appraisal or valuation review experience · The ability to multitask in a fast-paced environment, especially the ability to meet tight deadlines for our clients. · Exceptional customer service skills and mentality Responsibilities · Meet or exceed individual and departmental goals related to productivity and quality · Ensure valuation reports meet all regulatory and client standards · Maintain compliance with State and Industry regulations including Appraiser Independence Requirements · Identify any discrepancies or errors in valuation reports and provide detailed revision requests to the provider · Ensure appropriate escalation paths are followed · Ensure that all steps of the QC valuation process are completed accurately and within the required SLA (Service Level Agreement) timeframes · Contact valuation providers (appraisers, agents, etc.) as directed to discuss revisions or obtain status of the order · Attend departmental meetings as required · Participate in overtime, training, and onsite collaboration events as requested · Communicate daily with QC Managers on department operation protocols · Maintain a positive, professional business relationship with vendors and internal staff · Perform all other duties as assigned Qualifications · 3+ years' experience in real estate appraisal quality control review at the AMC or mortgage company level. · College degree preferred. · A penchant for excellence. You will use your strong attention to detail to maintain our quality standards. · The ability to multitask in a fast-paced environment, especially the ability to work in multiple systems at once. · The ability to quickly learn new skills, processes, and procedures. · USPAP certification; if not already certified, this role will require successful completion of the 15 or 7 hr. USPAP training course after hire, and successful maintenance of the certification during employment. · Knowledge of valuation processes, procedures, and technology. · Exceptional customer service, communication and writing skills. We can recommend jobs specifically for you! Click here to get started.

About Us: BlackSky is a real-time intelligence company. We own and operate the world's most advanced space-based intelligence platform and provide customers satellite imagery, automated analytics and high-frequency monitoring of strategic locations, economic assets and events from around the globe. BlackSky is trusted by the most demanding allied military and intelligence organizations and commercial companies to deliver foresight into critical matters that affect national security and the economy. BlackSky's data enables governments and businesses to see, understand and anticipate change as it happens, giving them the ultimate strategic advantage so they can act quickly. Our global team works with cutting-edge technology to make a difference around the world and prides itself on being people-first, customer-focused and fun. BlackSky is looking for a talented and creative Staff Image Annotation/Quality Control Analyst/Quality Engineer to support the development, operation, and capability evolution of Spectra AI, BlackSky's cutting edge AI/ML Platform. As part of the machine learning team, you are instrumental in shaping our computer vision products by managing the quality of data that trains AI/ML models. As an individual contributor, you will help manage and grow the entire labeling process that trains Spectra AI, overseeing remote data labeling teams and actively assess the quality of trained models, which create critical timely insights for our customers. While the locations listed in the job posting are ideal, we would love candidates near either our Herndon, VA or Seattle, WA offices. We may also consider remote candidates in certain states. Responsibilities: Own and architect vision, strategy, and technical roadmap for BlackSky's data labeling pipeline. Lead and manage external data labeling teams, providing oversight for labeling campaigns. Act as a key technical leader, partnering with stakeholders across the broader team (e.g., computer vision, mlops, platform) to meet customer-driven timelines and product requirements. Research for AI product development, identifying geographic areas where objects exist, developing object ontologies, building annotation instructions, and identifying imagery for annotation. Collaborate with machine learning and product teams to define metrics, assess, and report on the quality of machine learning models in development and production using statistical and quality assurance approaches. Create processes, tools, and scripts to manage and track data quality and labeling performance. Take part in the entire project lifecycle from requirements development to deployment. Mentor and guide other engineers on the team, leveraging your experience to teach others and foster a culture of technical excellence and innovation. Other job-related duties as assigned. Required Qualifications: Minimum of eight (8) years of hands-on experience as a data quality engineer, imagery analyst, GIS analyst, or quality assurance engineer in the space of satellites, computer vision, or machine learning. Bachelor's Degree or higher in one of the following fields: computer science, GIS, data science, mathematics, physics, statistics, or another scientific field, or equivalent experience (four years). Experience interpreting satellite imagery to identify objects, behaviors, or activities and working with GIS datasets. Hands on experience with annotation platforms such as LabelBox, SuperAnnotate, AWS Sagemaker, or CVAT and managing remote annotation workforces. Able to interdependently manage work projects defining, managing, and executing based on fixed objectives. Collaborates well with others and able to communicate ideas to those with other backgrounds. Experience with quality assurance practices, model testing & evaluation, and computing metrics & statistics from data. Attention to detail and ability to define, enforce, and follow rigorous process controls for managing data. Experience working with or managing Data Labeling teams such as CloudFactory, Hive, or iMerit. The program this role will support requires Us-born citizenship. Preferred Qualifications: Over ten (10) years of relevant professional experience. Experience with AI advancements in image annotation such as the Segment Anything Model (SAM), Embeddings, and other AI Assistance tools. Experience writing code and scripts, especially for processing large amounts of data. Proficiency with Python for automation and data manipulation tasks. Knowledge and experience working in an AWS Cloud environment. Demonstrated ability to lead and manage small teams. Life at BlackSky for full-time US benefits eligible employees includes: Medical, dental, vision, disability, group term life and AD&D, voluntary life and AD&D insurance BlackSky pays 100% of employee-only premiums for medical, dental and vision and contributes $100/month for out-of-pocket expenses! 15 days of PTO, 11 Company holidays, four Floating Holidays (pro-rated based on hire date), one day of paid volunteerism leave per year, parental leave and more 401(k) pre-tax and Roth deferral options with employer match Flexible Spending Accounts Employee Stock Purchase Program Employee Assistance and Travel Assistance Programs Employer matching donations Professional development Mac or PC? Your choice! Awesome swag The anticipated base salary range for candidates in Seattle, WA is $110,000-135,000 per year. The final compensation package offered to a successful candidate will be dependent on specific background and education. BlackSky is a multi-state employer, and this pay scale may not reflect salary ranges in other states or locations outside of Seattle, WA. BlackSky is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer All Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, sexual orientation, gender identity, disability, protected veteran status or any other characteristic protected by law. To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be 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. Department of State. #LI-Remote EEO/AAP/ Pay Transparency Statements: ***************************************************************** ************************************************************************************************

Responsible for all phases of laboratory preparations including preparing and organizing equipment, materials and supplies for the Biological Sciences laboratories. Prepares laboratory materials, supplies, and equipment in advance of need and supports the science laboratory courses as directed. Maintains living specimens, tracks inventory, follows all safety protocols and completes other duties as assigned. Minimum Qualifications EDUCATION AND EXPERIENCE High School Diploma, GED , or equivalent required. Four years of related experience, which should include (15) credit hours of college level course work in biological and/or microbiological science courses.

Why MSI? We thrive on solving challenges. As a leading MGA, MSI combines deep underwriting expertise with insurer and reinsurer risk capacity to create specialized insurance solutions that empower distribution partners to meet customers' unique needs. We have a passion for crafting solutions for the important risks facing individuals and businesses. We offer an expanding suite of products - from fully-digital embedded renters coverage to high-value homeowners insurance to sophisticated commercial coverages, such as cyber liability and habitational property - delivered through agents, brokers, wholesalers and other brand partners. Our partners and customers count on us to deliver exceptional service through a dedicated team that makes rapid resolutions a priority. We simplify the insurance experience through our advanced technology platform that supports every phase of the policy lifecycle. Bring on your challenges and let us show you how we build insurance better. Position Summary: The Internal Controls Associate works in the direction of the Internal Controls Director to design, develop and review internal control procedures for UCTS. Their duties include documenting key processes, procedures, executing high risk controls and collecting evidence that demonstrates the effectiveness of the control environment. Principal Responsibilities: Document MSI's standard operating procedures for processes and controls Perform risk assessments on as needed basis Assist in creating procedures to monitor the effectiveness of internal controls Analyze the results of control procedures and recommend changes when necessary to mitigate control deficiencies Maintain clear and concise written documentation of audit activities Directly participate in communications with internal / external audit entities Look for opportunities to improve operational and financial controls Bring issues and discrepancies to the attention of the appropriate leader and recommend solutions Interact directly with business leaders and stakeholders Ensure that MSI policies and procedures (including items such as quarterly controls) are properly completed at required intervals Execute and monitor high risk controls related to SOX (Sarbanes Oxley Act) Work with business segments to ensure proper controls are in place relative to production system access Coordinate with engineers to audit and validate user access to MSI end user production and financial systems. Validate that proper controls are in place for all code and product releases to production. Other responsibilities may be assigned related to various regulations such as NYDFS, PCI, Cyber, etc. as needed. Knowledge, Skills, and Abilities: A four-year degree with at least one-year prior applicable work experience required Working knowledge of the COSO and COBIT framework preferred Preferred knowledge in performing tests on IT General controls for SOX Experience in testing security controls is a plus Effective written and verbal communication skills Must possess excellent organizational skills Critical thinking skills Exhibits professional skepticism Ability to work independently, manage their own workload and prioritize tasks effectively Special Working Conditions: Fast-paced environment Must be able to interact effectively with various levels of management both inside and outside the organization Must be able to adapt and implement new control procedures as necessary Technical, Computer, And System-Specific Skills Required: Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) Experience with Microsoft Azure is a plus Experience with GRC tools is a plus Ability to learn any other appropriate program or software system used by the firm as necessary Education & Experience Bachelor's degree in Accounting, Finance, Computer Science or similar required 1-3 years' experience in auditing required Big four experience is a plus #LI-JW2 #LI-REMOTE Click here for some insight into our culture! The Baldwin Group will not accept unsolicited resumes from any source other than directly from a candidate who applies on our career site. Any unsolicited resumes sent to The Baldwin Group, including unsolicited resumes sent via any source from an Agency, will not be considered and are not subject to any fees for any placement resulting from the receipt of an unsolicited resume.

Do you have a passion for working in a laboratory? Do you thrive in a dynamic environment? We're looking for great teammates who have these qualities and want to make a difference by cultivating good manufacturing practices (GMPs) and company quality principles to deliver the product performance and quality for the consumers P&G serves. We have several types of Quality Control roles available at our Tabler Station Plant. As a QC Laboratory Analyst, you could work in an analytical or microbiological laboratory environment that stays in sync with Good Laboratory Practice (GLP) and current Good Manufacturing Practice (cGMP). The work will require collection, labeling, analysis, and results recording related to raw materials, intermediate products, finished goods, packaging materials and other samples. Tracking, trend analysis, and other Quality Control (QC) related responsibilities will be performed as directed by laboratory systems. In addition to laboratory testing, QC Analysts may be required to write control documents like Standard Operating Procedures (SOPs), deliver training, perform system health assessments, carry out "on the floor" coaching, , facilitate or participate in quality system failure investigations. Maintain cGMP principles and Good Documentation practices. Where do you fit in? Meaningful work on Day 1 We do various types of work including performing raw material, finished goods, intermediate, and development sample analysis according to standard analytical procedures. We perform routine instrument maintenance and calibration as needed during analytical work. We conduct limited instrument troubleshooting and problem diagnosis. We use discernment based on knowledge and experience as to the accuracy and reliability of analytical results. You will observe and identify problems with results and report to your supervisor. You will conduct analytical method development work with direct supervision and mentorship from Lab Leadership or other staff members. You may sample and label materials as needed according to written procedures or specific instructions, inspect appearance of raw materials during unloading as needed. Another responsibility will include coordinating the work with the Production Lead on night and weekend shifts to ensure appropriate prioritization of work. Key Analytical Work: Physical Measurements, Wet Chemistry, Chromatography including using GCs and HPLCs, Compendial Testing Key Microbiology Work: Traditional Plate Testing, Rapid Micro Screening Technology, MALDI-TOF, Autoclave Job Qualifications · Have a 2 year degree (or more) in a Science Field. · Commensurate experience of 5 years in a QC lab or GMP manufacturing operations will be considered. Starting Pay / Salary Range: $22.22/hr to $29.66/hr or ~$55,000/yr to $~73,000/yr (with built in overtime) with the potential opportunity to earn up to $42.08/hr or ~$103,000/yr (with built in overtime) as you grow in the organization. *Note: compensation for roles at P&G varies depending on a wide array of non-discriminatory factors including but not limited to the specific office location, role, degree/credentials, relevant skill set, and level of relevant experience. At P&G compensation decisions are dependent on the facts and circumstances of each case. Total rewards at P&G include salary + bonus (if applicable) + benefits. Your recruiter may be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the hiring process. We believe you will be an excellent fit here if, you: · Have computer literacy sufficient to use standard software (MS Office) as well as the ability to learn specific software and instrumentation. · Possess experience and knowledge of basic laboratory operations such as weighing, titrating, and preparing volumetric solutions. · Interpret analytical and microbiological method procedures and safety instructions using standard scientific terms and measures. · Perform routine calculations pertaining to analytical chemistry (e.g. dilution, concentration, test results). · Perform routine testing related to diluting, aliquot, and quantifying microbiological test results. · Have experience resolving operational or processes failures to understand root cause and able to develop an improvement plan · Have effective verbal and written communication skills with supervisor, other employees, and departments. · Are willing to wear appropriate safety equipment, such as safety shoes, hearing protection, and eye protection, wherever these things are necessary · Will work on a rotating shift schedule, including weekends. · Are able to work 24/7 rotating shifts and are available for overtime and call-in as needed. We want you to know: We are committed to providing equal opportunities in employment. We value diversity and do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Immigration Sponsorship is not available for this role. For more information regarding who is eligible for hire at P&G along with other work authorization FAQ's, please click HERE. Procter & Gamble participates in e-verify as required by law. Qualified individuals will not be disadvantaged based on being unemployed. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Job Schedule Full time Job Number R000134829 Job Segmentation Plant Technicians (Job Segmentation) Starting Pay / Salary Range $22.22 - $29.66 / hour

We're growing and looking for a detail-driven, process-minded Business Analyst to join our Business Operations team. This role is critical to enhancing the quality and consistency of our work through rigorous review programs and operational controls. You'll be a key player in driving continuous improvement, ensuring compliance, and elevating our service delivery. The Gig: * Lead and manage quality assurance initiatives across Business Operations. * Design, test, and refine frameworks for quality review and control programs. * Conduct complex recurring quality audits and controls. * Gather and analyze functional and data requirements to support quality initiatives. * Facilitate discovery sessions and document findings with internal stakeholders. * Collaborate across departments to ensure alignment and timely execution. * Identify gaps and escalate deficiencies in quality programs and propose updates and strategies for mitigation. * Drive process standardization and improvement efforts through creative problem solving and efficiency tool implementation (ie. VBA, SQL, etc) * Own the end-to-end lifecycle of assigned work, from intake to resolution. * Support data analysis and research efforts across departments related to quality and control initiatives. * Maintain confidentiality and uphold company standards. * Other duties as assigned. What you need to make the cut: * Bachelor's degree in Business Systems, Finance, Accounting, or related field (preferred). * 2+ years of operations experience in benefits administration operations, HRIS, payroll, or insurance required. * Proven expertise in internal audit methodologies and operational control design. * Lean Six Sigma or similar methodology experience a plus. * Strong background in process review and risk identification. * Advanced proficiency in Microsoft Excel (pivot tables, lookups, nested functions, advanced functions). * Exceptional time management and organizational skills with the ability to manage conflicting priorities. * Strong critical thinking and problem-solving abilities. * Excellent communication and stakeholder engagement skills. * Project management experience is a plus. The pay range for this position is 45K to 71K per year (pay to be determined by the applicant's education, experience, knowledge, skills, abilities, balanced against internal equity and competitive market based geographic ranges). This role is eligible to participate in the annual bonus incentive plan.

Job Description At FEI Systems, we create innovative technology solutions to improve the delivery of health and human services because we know when cumbersome administrative processes stand in the way, those who need it most are often left without access to proper care and support. From comprehensive case management software to disaster recovery services and content management information systems used in delivering foreign aid, our solutions are improving the lives of millions of people. We're looking for a quality analyst who shares our commitment to leveraging technology to make a real impact in the world - a professional who knows, beyond all else, that the quality of our products and services is only as good as the company we keep. Job Summary: This individual works in a team environment and will be responsible for planning and conducting a wide range of quality control tasks, including analyzing requirements, test planning and strategy, developing and executing tests, evaluating results and reporting, and promoting organizational and product integrity. Responsibilities: Review documentation to understand testing requirements, test environments and objectives Use standardized testing methods, tools and procedures to ensure testing is efficient, effective and comprehensive Adhere to a unified team process Translate requirements into detailed test plans and test cases Execute manual/automated test plans Perform tests in terms of functionality, reliability, stress, and compatibility Document, troubleshoot, track and resolve requests and issues on a timely basis Ensure web applications are cross-browser/cross-platform compatible and respond accordingly to compatible devices and tablets Work with users to support User Acceptance Testing, Training, and more Advise Test Manager/Project Manager regarding overall quality of project and state of work Raise outstanding issues through established project management channels, as per project plan Required Skills: Self-motivating with excellent written and verbal communication skills Ability to work with and mentor other team members Strong analytical skills with attention to detail Positive attitude and driven Ability to read and understand workflow diagrams Passionate about product success Ability to handle overlapping assignments Ability to manage and oversee team member efforts Ability to understand and promote process improvements as needed supported by team 3-5 years of experience working as a QA Tester 2-3 years of experience in Testing Web based applications Preferred Technology Skills/Experience: Microsoft Test Manager Team Foundation Server SQL Experience and understanding of agile development life cycle Bachelor's degree in computer science or information technology related field (preferred) Location: Remote Status: Full time position with full company benefits NOTICE: EO/AA/VEVRAA/Disabled Employer - Federal Contractor. FEI Systems participates in E-Verify, a federal program that enables employers to verify the identity and employment eligibility of all persons hired to work in the United States by providing the Social Security Administration (SSA) and, if necessary, the Department of Homeland Security (DHS), with information from each new employee's Form I-9 to confirm work authorization. For more information on E-Verify, please contact DHS at **************. Applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, marital status, political affiliation, disability, or genetic information, except where it relates to a bona fide occupational qualification or requirement. FEI Systems creates an Affirmative Action Plan on an annual basis. Pursuant to federal law, the portions of FEI Systems' Affirmative Action Program that relate to Section 503 (Persons with Disabilities) and/or Section 4212 (Protected Veterans), are available for inspection upon request by applicants and employees during FEI Systems' normal business hours.

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic, and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek so they can do what they do best: improve the world around us. Information about Agilent is available at **************** Agilent Technologies, Inc. is looking to add a Quality Control Analyst to its high-performance quality team working at the state-of-the-art, contract API manufacturing facility that specializes in Nucleic Acid Chemistries located in Frederick, Colorado. The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in the capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life-changing, life-saving medicines. This position coordinates and conducts routine and non-routine testing to support process water monitoring, environmental monitoring, and compressed gas monitoring. Responsibilities also include testing to support cleaning verification for equipment release to support manufacturing activities. Understanding and experience with Standard Operating Procedures, current Good Manufacturing Practices (cGMPs), and other regulatory requirements are required. The QC Analyst will also work on complex problems to drive improvement. This position requires experience with in-process analysis utilizing analytical instrumentation for UV Analysis, HPLC, HPLC-MS, and density. The ability to support occasional weekend and evening work is required. Please note: This is a Night Shift, and the work hours are 8 pm to 5 am. Monday through Friday. Responsibilities/Duties: Exercise judgment within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results Outstanding communication skills, both written and oral, and the ability to communicate directly with peers and area managers Conducts analysis associated with clinical and non-clinical laboratory studies under current Good Manufacturing Practices (cGMP) regulations and guidance per Food and Drug Administration (FDA) and Organization for Economic Co-Operations and Development (OECD) Reviews data for compliance to specifications, reports results, and troubleshoots abnormalities Troubleshoots, investigates, and resolves laboratory testing failures and drives solutions to improve quality control laboratory programs through corrective and preventive actions Ensure equipment is performing well and coordinates preventative maintenance Maintain inventory and ordering of laboratory supplies Ensure good documentation practices are followed Qualifications A Bachelor's degree (B.S.) or equivalent in Chemistry or related life sciences field; or equivalent combination of education and experience 4+ years of relevant experience within the Industry Exposure and knowledge of FDA regulations and guidelines Knowledge of cGMP guidelines or international regulations (i.e., International Committee on Harmonization (ICH) Q7) Knowledge of analytical equipment and instrumentation utilized for the testing of in-process samples, raw materials, and microbiological samples Proficient with Microsoft Word, Excel, and Chemstation Familiarity with the following laboratory disciplines is highly desired: HPLC Density HPLC-MS IC Solution Preparation UV analysis FTIR Shift Differential for Night Shift. Night Shift is 8 pm to 5 am, Monday - Friday. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least October 15, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $39.65 - $61.96/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: NoShift: MorningDuration: No End DateJob Function: Quality/Regulatory

Job DescriptionWho we are REGENXBIO is an exceptional place to work. You'll have the opportunity to collaborate with some of the best and the brightest people, touch amazing science, and be a part of extraordinary plans. Our core values: Trust, Accountability, Perseverance, and Innovation drive everything we do. We aim to bring these values to life every day with all that we do, and we believe that what we do matters - to patients, to their families, and to their communities. As a member of our Bioanalytical Sciences team, you will be responsible for performing nonclinical and clinical sample testing (PK, Immunogenicity, PCR, etc.) following developed, qualified, and/or validated bioanalytical methods in support of REGENXBIO projects and programs. You will also be responsible for developing and validating bioanalytical methods for gene therapy products. You will also be responsible for performing QC review of documentation produced in the Bioanalytical laboratory, including assay runs, summary tables, reports, protocols and collaborate with various departments to ensure compliance with regulatory expectations.What you'll be doing Conduct assay operations and maintains accurate testing records. Review technical documents. Perform QC peer reviews and manages project-related activities. Troubleshoot analytical method issues and maintains lab inventories. Support Sample receipt/Accession, buffer preparation and lab maintenance Performs additional tasks or assist with special projects as assigned or needed. We set our employees up for success. To be successful in this role and help us achieve our goals, we are looking for someone with the following skills and qualifications: Bachelor's degree in a relevant scientific field with 2+ years of industry experience, or Master's with 1+ year. Hands-on experience with immunoassays (ELISA, MSD), cell-based assays, qPCR, and/or LC-MS. Analytical, problem-solving, and organizational skills with excellent attention to detail. Collaborative team player with strong written and verbal communication skills. Proficient in data analysis software (e.g., SoftMax) and Microsoft Office applications. By joining REGENXBIO, you will have the opportunity to be a part of a growing company and incredible team passionate about developing novel AAV gene therapy products to our patients. In addition, professional development is important to us. By joining our team, you'll have the opportunity to be exposed to challenging projects and development resources to help you grow personally and professionally. We are proud to offer a comprehensive rewards package which includes a market-competitive base salary, an annual performance-based bonus program, stock grants at all levels, and benefits such as health, dental, and vision insurance, retirement plan with 401(k) match, summer hours, and more! The estimated compensation range for this role is $66,000-$89,000 annually. The actual salary offered to the final candidate depends on a number of factors such as relevant work experience, skills, education, and years of experience.

Copper River Shared Services is seeking a skilled Document Control & Quality Analyst. The Document Control & Quality Analyst supports the development and maintenance of the organization's ISO 9001:2015 Quality Management System (QMS) through effective document control, audit support, and process improvement activities. This role bridges administrative document management and quality assurance functions, ensuring controlled documentation, data accuracy, and compliance with QMS requirements across the Copper River Family of Companies. Responsibilities (include but are not limited to): Manage controlled documents and records in accordance with ISO 9001:2015 and internal procedures. Review, process, and track change order submissions to minimize turnaround times. Maintain document control databases and ensure version accuracy and accessibility. Coordinate document publication, distribution, and archival processes. Assist in maintaining QMS documentation such as policies, procedures, and templates. Support internal audit preparation by gathering evidence and tracking corrective actions. Participate in quality meetings and contribute to data collection and metric tracking. Support standardization of QMS documentation across multiple business entities. Identify opportunities to streamline documentation workflows. Provide feedback on document control processes to enhance efficiency and compliance. Support training initiatives related to QMS document control and best practices. Essential Job Requirements: Education: Bachelor's degree in Quality, Business, or related field (or equivalent experience) Required Knowledge/Experience: 1-3 years of experience in document control, QMS support, or ISO 9001:2015 environments. Strong organizational and communication skills; proficiency with SharePoint and MS Office. Detail-oriented, proactive, and capable of managing multiple priorities About Copper River & The Native Village of Eyak: Owned by the Native Village of Eyak (NVE), a federally recognized Alaska Native Tribe, the Copper River Family of Companies are a collection of entities that deliver a complementary set of solutions and services to support the diverse missions and requirements of our clients. Proud participants of the Small Business Administration's (SBA) 8(a) Business Development Program since 2006, our companies consist of both current and graduation SBA 8(a) entities. It is our collective purpose to support the Tribe and diversify the NVE's ability to facilitate economic advancement. The income generated from our companies helps the Native Village of Eyak fund health and social services, economic development, natural resource/environmental education, jobs, job training, and other benefits to the NVE in a manner that is consistent with Alaskan Native cultural values and traditions. Copper River's Culture The Copper River Family of Companies has a positive, supportive, and thriving culture. At the foundation of our culture is a focus on collaboration. No matter your role or which operating company you work for, we are ONE TEAM working toward the same goals for our customers and for our collective owner- The Native Village of Eyak. How we treat each other is just as important as the work we deliver. Benefits Comprehensive medical, dental, and vision coverage Flexible Spending Account - healthcare and dependent care Health Savings Account - high deductible medical plan Retirement 401(k) with employer match Open leave policy and paid holidays Additional benefits including tuition reimbursement, transportation expense account, employee assistance program, and more! Note: These benefits are only applicable to full time, regular associates at Copper River. Disclaimer: The Copper River Family of Companies 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 Description Copper River Shared Services is seeking a skilled Document Control & Quality Analyst. The Document Control & Quality Analyst supports the development and maintenance of the organization's ISO 9001:2015 Quality Management System (QMS) through effective document control, audit support, and process improvement activities. This role bridges administrative document management and quality assurance functions, ensuring controlled documentation, data accuracy, and compliance with QMS requirements across the Copper River Family of Companies. Responsibilities (include but are not limited to): Manage controlled documents and records in accordance with ISO 9001:2015 and internal procedures. Review, process, and track change order submissions to minimize turnaround times. Maintain document control databases and ensure version accuracy and accessibility. Coordinate document publication, distribution, and archival processes. Assist in maintaining QMS documentation such as policies, procedures, and templates. Support internal audit preparation by gathering evidence and tracking corrective actions. Participate in quality meetings and contribute to data collection and metric tracking. Support standardization of QMS documentation across multiple business entities. Identify opportunities to streamline documentation workflows. Provide feedback on document control processes to enhance efficiency and compliance. Support training initiatives related to QMS document control and best practices. Essential Job Requirements: Education: Bachelor's degree in Quality, Business, or related field (or equivalent experience) Required Knowledge/Experience: 1-3 years of experience in document control, QMS support, or ISO 9001:2015 environments. Strong organizational and communication skills; proficiency with SharePoint and MS Office. Detail-oriented, proactive, and capable of managing multiple priorities About Copper River & The Native Village of Eyak: Owned by the Native Village of Eyak (NVE), a federally recognized Alaska Native Tribe, the Copper River Family of Companies are a collection of entities that deliver a complementary set of solutions and services to support the diverse missions and requirements of our clients. Proud participants of the Small Business Administration's (SBA) 8(a) Business Development Program since 2006, our companies consist of both current and graduation SBA 8(a) entities. It is our collective purpose to support the Tribe and diversify the NVE's ability to facilitate economic advancement. The income generated from our companies helps the Native Village of Eyak fund health and social services, economic development, natural resource/environmental education, jobs, job training, and other benefits to the NVE in a manner that is consistent with Alaskan Native cultural values and traditions. Copper River's Culture The Copper River Family of Companies has a positive, supportive, and thriving culture. At the foundation of our culture is a focus on collaboration. No matter your role or which operating company you work for, we are ONE TEAM working toward the same goals for our customers and for our collective owner- The Native Village of Eyak. How we treat each other is just as important as the work we deliver. Benefits Comprehensive medical, dental, and vision coverage Flexible Spending Account - healthcare and dependent care Health Savings Account - high deductible medical plan Retirement 401(k) with employer match Open leave policy and paid holidays Additional benefits including tuition reimbursement, transportation expense account, employee assistance program, and more! Note: These benefits are only applicable to full time, regular associates at Copper River. Disclaimer: The Copper River Family of Companies 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.

Selene Holdings is a multiple-lines business financial services firm with a mortgage servicing company, a loan diligence company, a title company, an insurance brokerage, and a real estate owned company. We have office locations in Dallas, TX, Jacksonville, FL, and Salt Lake City, UT. Founded in 2007 to address needs in the mortgage industry, Selene strives to provide amazing client and borrower experiences. A positive attitude coupled with proven creative thinking and actions are all attributes we seek in every one of our employees. If you want to make a difference, then Selene is the place for you! Position Summary: Quality Control Analyst focused on controlling a high quality product, enhancing loan review processes and developing specialist expertise for long term career growth. Essential Duties and Responsibilities include the following. Other duties may be assigned. Responsible for the Quality Control examination of loan reviews completed by Loan Review Analysts. Provide real time loan kick back feedback to Loan Review Analysts pertaining to errors and determining corrective actions. Ensure regulatory compliance for loans reviewed. Escalate error trends to management. Develop deep understanding of specific client guidelines. Handle escalated and countered client conditions with minimal guidance. Assists with loan review system testing and enhancement. Ongoing development of subject matter expertise - aim to become go to subject matter expert for various specialist loan review QC topics. Assist with problem solving, issue resolution and loan review guidance. Assist in providing guidance on daily matters, such as, questions regarding Underwriting Guidelines or Compliance questions relating to TRID, Reg X, TILA or others to LRAs. Maintains high level of confidentiality to protect privacy rights. Adheres to internal controls to reduce errors and customer complaints. Responsive to internal and external customers' needs in a timely, accurate and professional manner. 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. The qualified candidate must have: Maintains a current knowledge of underwriting guidelines, investor guidelines, regulatory compliance and TRID practices. Minimum 3-5 years mortgage underwriting and mortgage quality control within the origination or due diligence space. Strong understanding of condition clearing processes and their impact on loan grades. Basic understanding of the credit rating agency requirements. Knowledge of USPAP standards, supplemental valuation products and reconciliation. Ability to produce underwriting reports, analyze results, identify issues and take corrective actions. Experienced with reading, analyzing and understanding various loan servicer pay histories and servicing documentation. Developing leadership skills with the ability and experience to manage people. Effectiveness as a team player. Ability to easily prioritize job duties according to the needs of the company. Strong sense of professionalism and positivity. Excellent oral and written communication skills. Ability to develop rapport with all levels of associates and establish credibility. Excellent listening skills and the ability to use good judgment. Strong interpersonal/relationship building skills. Problem solving and decision making ability. Ability to produce quality work. Ability to think and solve problems strategically. Strong analytical and organizational skills. Excellent attention to detail. Ability to multi-task and consistently meet multiple deadlines. Education/Experience: Minimum 3-5 years' experience with emphasis on non-agency underwriting and QC desired. Experience in second level reviews; escalations and performance management required. Bachelor's degree preferred. Computer Skills: Working knowledge of and experience with Microsoft Office (Word, Excel, and Outlook). Previous experience with mortgage due diligence software, Andor, MSP, Black Knight/LPS and Fiserv preferred. Why Selene? Benefits Selene Finance LP is committed to the total wellbeing of its employees and therefore offers one of the best benefits packages available in the industry today, which includes: Paid Time Off (PTO) Medical, Dental &Vision Employee Assistance Program Flexible Spending Account Health Savings Account Paid Holidays Company paid Life Insurance Matching 401(k) Plan The job requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description is not an inclusive list of all duties and responsibilities of this position. Incumbents will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. Selene reserves the right to amend and change responsibilities to meet business and organizational needs. Privacy Policy - Selene (seleneadvantage.com)

Join us and celebrate the beauty of human experience. Create for happier, healthier lives, with love for nature. Together, with our customers, we deliver food innovations, craft inspired fragrances and develop beauty and wellbeing solutions. There's much to learn and many to learn from, with more than 16,000 employees around the world to explore ideas and ambitions with. In the USA, we develop, market and produce a wide array of solutions from our 25 most innovative sites, based across the country. Stretch your skills, create and get inspiration from passionate colleagues. Every day, your energy, your thirst for knowledge, and your creativity will shape our future, making a positive difference on billions of people. Every essence of you enriches our world. We are Givaudan. Human by nature. Basic Function (Purpose of Position): Under general supervision while following standard operating procedures and guidelines for internal safety, GPM and OSHA, evaluates a wide variety of flavoring products and incoming ingredients. Performs all sensorial, chemical, physical, and analytical testing for company products and processes as assigned. Makes calibration and minor equipment adjustments. Essential Functions: * Perform a wide variety of chemical, physical, and analytical tests as well as sensory evaluations for a wide variety of flavoring products and incoming ingredients as identified by current specifications. Enters test results into computer to determine if the product is to be approved or rejected. * Identifie lots that do not meet specification and completes initial investigation of non-conformance. Provides all collected information needed to trouble shoot the non-conformance to supervisor for review and direction. * Perform equipment calibrations and basic equipment maintenance per frequency noted in procedures. * Communicate rejections and information updates to key contacts in Quality, Operations, Purchasing and Customer Care on a daily basis. Types of communication include e-mail, notes entered into system, and verbal. Education/Experience/Skills/Job Knowledge: College degree in Biology, Chemistry or related field. 2-3 year's laboratory experience. Gas Chromatography knowledge. Familiar with variety software used and most production processes (varies by type of testing performed). Key Competencies for this position are: Communicates openly, thinks creatively, is open to change and learning, customer awareness, has a desire to achieve results, and is a team player. Organizational Relationships: Regular contact with operation managers, Quality Lab personnel, Operations, Planning, Purchasing, Customer Care and Flavor Chemists. Minimal, if any. Working Conditions: The normal conditions in which this job is performed are found indoors in a climate-controlled laboratory, but there may be occasional exposure to lower temperatures from refrigerated 2-10°C (35-50°F) storage areas. There is frequent stress due to time constraints of a project or equipment failure. Position requires frequent exposure to dust, fumes and gases and ongoing contact with raw materials and finished products. Must follow safety guidelines and procedures and perform all duties involving hazardous wastes in accordance with training received. Periodically, this position requires flexibility to work overtime during the week or weekend. Effect of Errors: All testing results are generated and entered into a database. This data is reviewed by the computer and acceptance or rejection direction is provided. Inaccurate testing results can lead to poor decisions by other quality personnel. There is a potential for loss of production batches. Failure to follow safety or hazardous waste training procedures may lead to injury to self or others. Must be able to report observations of unsafe acts to manager or safety manager. Physical Demands/Dexterity: The most frequent activities associated with this job are standing, twisting, walking, holding, filing, speaking, vision, hearing, data entry and writing by hand. Less frequent activities include carrying (up to 30 lbs.) for distances up to 20 feet, kneeling, lifting, sorting, pushing and pulling. Equipment Used: Gas Chromatograph, Scales, Glassware, Densitometer, Refractometer, Polarimeter, Omnis Autotitrator, Viscometer, Spectrophotometric Colorimeter, Peroxide meter, Turbidity meter, Karl Fischer titrator, Sieve testing equipment, Burette titration equipment, computer, and any new equipment that is setup in the lab. At Givaudan, you contribute to delightful taste and scent experiences that touch people's lives. You work within an inspiring teamwork culture - where you can thrive, collaborate and learn from other talented and passionate people across disciplines, regions and divisions. Every essence of you enriches our world. Diversity of perspectives fuels innovation and fosters deeper connections with our employees, customers, and partners. At Givaudan, we are dedicated to cultivating an inclusive environment where every individual's voice is valued and has the power to shape our world. Join us in making a difference together. Remote working: On-site At Givaudan, you contribute to delightful taste and scent experiences that touch people's lives. You work within an inspiring teamwork culture - where you can thrive, collaborate and learn from other talented and passionate people across disciplines, regions and divisions. Join us and Impact Your World Diversity drives innovation and creates closer connections with our employees, customers and partners. Givaudan embraces diversity and is committed to building an inclusive environment where everyone impacts our world.

Are you looking to catapult your career by driving high-impact transformation with household brands? Do you crave an entrepreneurial, fast paced, and engaging growth assignment working with incredible people from across the globe? At Dreyer's Grand Ice Cream, we are excited to start a new chapter of accelerated growth as part of Froneri - a global pure-play ice cream leader. Come help us transform DGIC into the #1 ice cream brand! With nearly 100 years of winning experience in the U.S, a robust portfolio of powerhouse brands that consumers know and love such as Häagen-Dazs, Drumstick, Dreyer's & Edy's, and the backing and coaching of European-based ice cream experts, we know we have the winning recipe. Headquartered in Walnut Creek, the Bay Area's hub for up-and-coming food trends, our teams across our offices and factories are raising the bar on all things ice cream. We are investing in significant capital expansions to grow our Operations and Supply chain and are transforming how we work at every level to become agile, accelerate growth and elevate our quality. With a renewed focus on frozen treats, our tight-knit team of ambitious innovators are fully immersed in the business and encouraged to flex and make decisions quickly. We are committed to pursuing every great idea and delivering the best ice cream experience for our consumers, when and where they want it. Unleash your potential at Dreyer's Grand Ice Cream and discover what a sweet career we have in store for you. Main Purpose of Job: To control product quality on the line to customer specification. To be achieved by monitor control points of the product and logged on relevant documentation. To action non-conformances and out of specifications resulting in full quality control and product safety. Role And Activity To lead the team to achieve required product quality. Ensure the required standards of product quality are achieved. To complete the paperwork at the required intervals. To complete the paperwork legibly and accurately. To report all non-conformances to the line manager, QA, shift manager. Ensure the person you have reported the non-conformances to complete and signs the relevant paperwork. Attend the taste panels. Work in an organized manner. Keep your workstations tidy and clean. Ensure food safety is not compromised. Operate good manufacturing standards and encourage the team to also operate GMP. Keep yourself aware of the production plan, be aware of changes to the plan and plan your daily routine to incorporate product changeovers. Play an integral part within the team to achieve the targets set for rework, downtime and wastage. Ensure that your working practices comply with company rules and procedures in order that you and any other person using the area of work can do so in safety. Collect all required samples in line with the QC sampling plan. Attend the weekly team brief. Represent the Froneri way of working through the behaviors and characteristics in our operating model and core values Measurable Outcomes Through a lead by example approach and consistently keeping your team informed of changes and the correct manner of operation. The customer complaints target is not maximized nor is the HOLD target. Paperwork audits show no non-conformances of your written work. To report all non-conformances and have the evidence of conversation by signature of the line manger on the relevant documentation. Target taste panel scores are achieved and WASP / WIBIT panels attended. Effective communication with your line manager and work colleagues to get it right first time. QA audit finds no non-conformance. The GMP target is not compromised, and your colleagues are aware of GMP and the audits. The yield target is achieved. Communicate with your line manager and work colleagues to prevent wastage, downtime and rework waste. Abide by Health and Safety requirements, notices and signs. Complete collection and logging of required samples. Attendance at the weekly team brief. Levels Of Responsibility Completion of LQC paperwork. Leading by example in all quality matters. Product quality within your area. Sample collection. Accept line only when signed off by the line manager and the machine operator. With aid of line management provide cover for absence of LQC. Behaviors and core values: must consistently showcase the desired behaviors that represent our core values. We take ownership Stay committed to responsibilities from start to finish Make sound decisions and get into the right level of detail Apply resources to initiatives that add growth, improve efficiencies, or reduce waste We do what is right Choose transparency over convenience, even if it means difficult conversations Set clear roles and responsibilities, enabling everyone to exercise appropriate initiative and judgment Speak up when you see something that does not align to our values and policies We seek to improve Strive to continuously improve and innovate to exceed expectations Value feedback from others and encourage open dialogue to understand how we can improve Learn from both successes and failures We are better together Ensure decisions are based on what's best for the whole business Practice inclusion by seeking diverse perspectives Treat everyone with fairness and respect Work Environment: In this position, the employee will regularly work with and around others; in a wet and/or humid environment; in areas of high noise level; and around mechanical, electrical, and pressurized equipment. The work is fast paced. Cold temperatures: parts of the facility, such as storage and production areas, may be kept at low temperatures. Requires use of cold-protective PPE. May involve standing, lifting, and walking in refrigerated zones for extended periods. Fast-paced: workers often operate under strict timelines to meet production quotas. High-speed manufacturing floor with frequent movement, line assignment changes, and tight production timelines. Standing for long hours: many roles require prolonged standing and repetitive tasks. Repetitive hand and arm movements required. Must be able to stand for hours with frequent bending, reaching, and lifting. Food safety regulations: employees must follow hygiene and safety guidelines, including wearing protective gear (gloves, hairnets, etc.). Team-oriented: workers collaborate to ensure smooth production and packaging. The position involves frequent exposure to nuts and other potential allergens. The pay scale for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. At Dreyer's Grand Ice Cream, it is not typical for an individual to be hired at or near the top of the range for their role, and compensation decisions are dependent on the facts and circumstances of each case. The pay for prospective employees in this role is $29 per hour, with opportunities for overtime, shift differential, cold premium pay and annual bonuses (variable depending on company performance). We offer a comprehensive group benefits package including medical, dental, vision, life, paid time off, paid holidays, paid parental leave, 401K plan with employer match and annual contribution available. Dreyer's Grand Ice Cream Inc. provides equal employment opportunities for all applicants, regardless of race, religion, gender, national origin, age, disability, marital status, veteran status, or any other protected characteristic.

Job Description Data Annotation Quality Control Analyst , Inc. Enabled Intelligence, Inc. provides extremely accurate, precise and secure data labeling and AI solutions to help our government and commercial customers effectively deploy reliable and unbiased artificial intelligence technologies. We leverage the unique talents of veterans, people with different abilities, and subject matter experts to unlock the value of data to improve the delivery of public services and mission critical national security programs. Every Enabled solution starts with a team of highly-trained, US based data analysts that have both subject-matter expertise as well as a deep understanding of the best techniques and tools for AI data annotation, model development, and testing and evaluation. At EI we respect and celebrate individuals from all walks of life. Our different backgrounds, cultures, experiences, and way of thinking make us stronger together and result in the most accurate and reliable AI solutions for our clients. We are extremely committed to a culture and environment where excellence can be achieved! If the idea of working in a collaborative, energetic and people focused environment where we are working together to build something meaningful excites you, Enabled Intelligence might just be the team you are looking for! Data Annotation Quality Control Analyst Data annotation is an essential component in training artificial intelligence/machine learning (AI/ML) algorithms. Accuracy of the data used to train AI models is one of the biggest factors in the effectiveness of the AI performance. As a member of the Enabled Intelligence Quality Control team, your role is to help ensure our clients receive the highest quality of data. You will review data such as geospatial imagery (EO, RGB, IR, SAR), Full Motion Video, and types of documents that have been annotated to identify and correct errors such as missed objects, miss-classifications and false positives. You will be responsible for recognizing patterns and sharing this analysis with project managers and the director of Quality Delivery. Joining our team means playing an integral role for the future of government AI/ML capabilities. Responsibilities Use advanced analytic tools to review data (EO, RGB, IR, SAR, FMV) that has been annotated to identify and correct errors such as missed objects, miss-classifications and false positives Diligently track and analyze patterns of errors and keep Project Managers and the Director of Quality Delivery up to date Process project data according to established procedures and guidelines Provide feedback and ideas on process improvements or concerns that may impact project performance Required Qualifications and Skills Strong computer skills including proficiency in Excel and PowerPoint Strong analytical skills, visual spacial recognition, pattern recognition and attention to detail Ability to follow directions and meet deadlines Ability to communicate reliably Ability to be a team player and work with individuals with different communication, learning and working styles Ability to work independently including managing your schedule, attending all required meetings and completing projects within a deadline Ability to work out of the Enabled Intelligence office located in Falls Church, VA Monday-Friday during normal business hours Must be a US Citizen Must be eligible to obtain a Top-Secret Security Clearance Desired Qualifications and Skills Previous imagery-based Data Annotation or feature extraction experience including EO, RGB, IR, SAR and/or FMV Previous Data Annotation Quality Control experience Ability to answer project questions and provide one on one performance feedback to Data Annotators Active US Security Clearance (Secret or above) Prior experience with business productivity tools like Microsoft Office, and/or Slack Highschool Degree Physical Requirements Prolonged periods of sitting at a desk and working on a computer Background Check & Security Clearance Applicants selected will be subject to background investigation. Applicants must be eligible to receive a US security clearance at the secret level or higher which requires US Citizenship. Job Posted by ApplicantPro

The Associate Scientist, Quality Control (QC) will execute QC operations in support of process development and validation. This role requires a candidate with technical lab experience and robust industry experience. The position demands previous expertise in technical skills such as Flow Cytometry, ELISA, and Cell Culture. Responsibilities * Execute QC operations in support of process development and validation, including in-process and lot release testing. * Implement innovative technologies, methods, and processes for process and product characterization. * Collaborate with other departments and external partners to support applicable projects. * Review all data in accordance with applicable procedures and cGMP requirements. * Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment. * Maintain laboratory and equipment. * Work and communicate effectively within the team to ensure timelines are met. * Perform peer review of testing data. * Complete all work in a timely manner. Essential Skills * Proficiency in ELISA, FACS, Flow Cytometry, and Cell Culture. * Experience in aseptic and bioanalytical techniques. * Hands-on experience with qPCR and quality control. * Minimum of 4 years technical lab experience and at least 2 years related industry experience. Additional Skills & Qualifications * B.S. in cell and molecular biology, immunology, biochemistry, or another Life Science field, with a master's degree preferred. * Ability to communicate effectively with peers, department management, and cross-functional peers. * Capability to set priorities of the group and manage timelines. * Ability to work with management. Work Environment The position requires hands-on work setting up and operating equipment in R&D and manufacturing environments. The employee will be required to wear all appropriate safety equipment, including eye protection, gloves, shoes, and lab coat. The role may require extended periods of standing. The work is split between 60% in the lab BSL 2 and desk, not in a cleanroom. Job Type & Location This is a Contract position based out of Frederick, Maryland. Job Type & Location This is a Contract position based out of Frederick, MD. Pay and Benefits The pay range for this position is $30.00 - $36.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Frederick,MD. Application Deadline This position is anticipated to close on Nov 25, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

1Resource Group is looking for some Lab Technician for a long term project in Manassas, VA for a growing semiconductor company. Responsible for analysis and reporting of various products, such as Crude Oil, Fuel Oils, Middle Distillates, Petroleum, and Petrochemicals, LPG and LNG gases, etc.. RESPONSIBILITIES - Responsible for conducting laboratory analysis. - Understand and keep current with all laboratory safety and reporting techniques. - Complete all laboratory reports as applicable. - Understand and keep current with all laboratory analysis methods. - Responsible for the maintenance and calibration of laboratory equipment. - The position requires a dependable and reliable individual; whose daily presence adds to the department's success. - Perform all other duties and responsibilities as assigned. REQUIREMENTS - Degree in Science or equivalent work experience in a laboratory setting. - Ability to understand ASTM standards and procedures. - Must be able to work with all chemical, petrochemical, and petroleum products. - Must be able to differentiate colors accurately by sight. - Must have reliable transportation to and from work. - Must have a flexible schedule as the position will include evenings, weekends and holidays, based on customer needs. Responsibilities Responsible for analysis and reporting of various products, such as Crude Oil, Fuel Oils, Middle Distillates, Petroleum, and Petrochemicals, LPG and LNG gases, etc. - Responsible for conducting laboratory analysis - Understand and keep current with all laboratory safety and reporting techniques - Complete all laboratory reports as applicable - Understand and keep current with all laboratory analysis methods - Responsible for the maintenance and calibration of laboratory equipment - The position requires a dependable and reliable individual; whose daily presence adds to the department's success - Perform all other duties and responsibilities as assigned Requirements REQUIREMENTS - Degree in Science or equivalent work experience in a laboratory setting. - Ability to understand ASTM standards and procedures. - Must be able to work with all chemical, petrochemical, and petroleum products. - Must be able to differentiate colors accurately by sight. - Must have reliable transportation to and from work. - Must have a flexible schedule as the position will include evenings, weekends and holidays, based on customer needs. Qualifications - Degree in Science or equivalent work experience in a laboratory setting - Ability to understand ASTM standards and procedures - Must be able to work with all chemical, petrochemical, and petroleum products - Must be able to differentiate colors accurately by sight

The MEP QC works closely with the project team, supporting and assisting the QC Manager, Project Manager and Project Superintendent in the management and administration of all facets of the project's mechanical, electrical, plumbing/piping, and fire protection operations. Job Duties: * Assess sub-contractors' capabilities to meet the quality requirements of the project as required. * Responsibility for the performance of all MEP inspection and testing activities. * On Design-Build projects, assist with design reviews and contract document/code conformance. * Complete responsibility for the entire MEP & FP submittal process. * Assure that the contract obligations' for testing and record keeping are adhered to. * Control calibrated measuring and test equipment used on the project. * Keep calibration records and ensure that all testing equipment has current calibration records. Ensure proper turnover of complete quality control package(s). Responsible for ensuring that turnover documentation is maintained, organized and turned over on schedule. * Maintain project quality records for the construction phase of the project and quality audit plans, performance and management thereof. * Perform evaluations of sub-contractors' facilities to determine their capabilities in meeting the quality requirements. * Conduct periodic Quality Program training for site supervisory personnel. * All other duties as normally required by our QC Department, and as required by day-to-day business. * Work with in precise limits and standards of accuracy * Work within the BLHI company policy, BLHI Safety Manual and OSHA Safety rules. Perform other duties as assigned by the supervisor as needed. Requirements: * Five (5) years of formal training and experience on industrial, commercial, or federal projects. * Must have a comprehensive understanding of mechanical, electrical, plumbing and controls systems as it pertains to installation, coordination, operation, and start-up and commissioning. * Ability to effectively interact with project team members, clients, subcontractors, and craft employees. * Must be capable of obtaining or possess inspection licenses and/or certifications as required

Job DescriptionBenefits: 401(k) 401(k) matching Dental insurance Health insurance The full-time Pharmaceutical Quality Control Associate is responsible for completing the necessary quality checks that include but are not limited to ensuring the accuracy of repackaged medications, obtaining necessary approvals in order to move repackaged products to the next phase of processing and other duties as assigned by their supervisor. Each associate will be fully trained on how to review the necessary records as well as how they will review each type of pharmaceutical and/or OTC which could include: Oral solids Liquid cups Vials Oral Syringes Powders Overwrapping Kitting The associate will be trained and will be held responsible for maintaining the equipment, where assigned, on a shift basis which can include cleaning and general equipment troubleshooting. The technician will identify any quality control issues with their supervisor. Mandatory Qualifications: High School Diploma or equivalent North Carolina Pharmacy Technician Certification Ability to physically perform light lifting Ability to follow written and oral instruction Good organizational skills Visual acuity Basic Math Skills Strong attention to detail Working knowledge of computer hardware & PC Windows Ability to read, write and speak English Preferred: Associates Degree or higher Previous pharmaceutical repackaging experience Previous hospital or healthcare experience Job Type: Full-time Pay: $13.50 $15.50 per hour