Quality Control Analyst Jobs in Secaucus, NJ

EOY Contract with the possibility for conversion for the right associate. As an associate in quality, you will lead the review of various validation and qualification documents, ensuring compliance with quality standards. Your responsibilities include overseeing commissioning, validation, and qualification activities, managing change controls, investigations, and CAPAs, and participating in internal and external cGMP audits. You will also prepare and review SOPs, Annual Product Reports, and specifications for new packaging and manufacturing components. Requirements: · Bachelor of Science degree in Natural Sciences, and / or Engineering · 5+ years of GMP Quality Assurance, Manufacturing, Technical Services, or Validation experience in medical device, pharmaceutical or biopharmaceutical industry · 5+ years executing and / or reviewing Process Validation, Cleaning Validation, Computer Validation, Equipment / Utilities Qualification, Commissioning, and Method Validation documentation. · Demonstrated ability to interpret cGMP, 21CFR 210 and 211, other applicable regulations, standards and guidance.

JOB PURPOSE: The QC Technician duties are to ensure that product and deliveries entering the facilities according to buyer's specification, free of debris, hazards and contamination. Work with the Director and Assistant Director of FSQA/EHS to create and maintain a first-class safety environment and training program. ESSENTIAL POSITION RESPONSIBILITIES: · As the QC Technician you are required to inspect the transportation of the product for cleanliness, signs of rodents, leaks and excessive moisture. · QC Technician is responsible for taking samples of each product per lot. · The QC Technician also makes corresponding labels for samples and list related allergens. · Recording each pallet of cheese moisture listed by supplier and comparing it to moisture test conducted on-site assuring within proper range. · Inspecting pallets upon delivery assessing condition, making sure no damage is present and safe to use. · Sample and randomly test spices for foreign matter, such as hazards (metal, plastic, lead, glass and any other contaminants…) · Maintain and Rotate retention sample inventory, removing expired product organizing according date utilizing FIFO and GMPs. · Retrieve and submit environmental water samples to laboratory from each facility. · Test Gluten Free products for glutens. · Inspect and sign off on fire extinguisher monthly. · Work with each department of operations and disseminate finding. · Investigate all safety related incidents and accidents including OSHA and worker's compensation. · Coordinate with Human Resources on incident reporting to the insurance provider. · Perform safety inspections and observations at each facility of all areas including production and warehouse. · Develop reports and correspondence to be presented weekly, monthly, quarterly, and annually on safety and training related topics. · Develop training for existing and new hire employees focused on GMPs and Colonna Brothers policies and procedures. · Create, lead and maintain a safety practicing culture at each facility measuring effectiveness through inspection and tracking results. · Serve as a secondary point of contact for all company safety related issues and audits. · Create, maintain, and update materials for instruction to include power point presentations, books, binders, handouts, videos, and exams. · Perform remedial and recertification training for tenured who violate Colonna Brothers protocol and procedure. ADDITIONAL RESPONSIBILITIES: · Conduct multiple site training · Conduct safety committee meetings · Perform other duties as assigned · Adhere to all Colonna Brothers, OSHA and local safety and training procedures. · Maintain the integrity of the Colonna Brothers environmental, health, safety and security operating process. MINIMUM QUALIFICATIONS: Education · High school diploma or equivalent Job Experience · One (1) year of working in a safety sensitive environment or warehouse. · One (1) year of supervisory experience. Additional Skills · Demonstrate excellent attention to detail · Excellent presentation skills · Very effective communicator · Read and write in English · Must be very proficient with Microsoft applications including Word, PowerPoint, and Excel

Job Title: Process Chemist Department: Process R&D Job Type: Full Time Director of Process Chemistry We are seeking a highly motivated and skilled Process Chemist to join our Process R&D Department at Porton J-STAR. In this role, you will be responsible for the development, optimization, and scaling of chemical processes for pharmaceutical production. You will collaborate with cross-functional teams to ensure that our processes are efficient, cost-effective, and compliant with regulatory standards. This job description applies to activities and responsibilities associated with the process chemistry development group and support of GMP Operations. Responsibilities Follow existing synthetic routes, making processing improvements where necessary, while conducting multi-step organic synthesis Plan and organize routine operations to maximize production output. Design novel synthetic routes and carry out multi-step organic synthesis. Operate simple open access HPLC/UV, LC/MS, MS, NMR, GC/MS, and other analytical instruments required to monitor reaction processes. Consult with management, the Analytical Department, the Director of GMP Operations and others on issues concerning experiments prior to and during GMP production. Accurately make and check calculations, prepare raw materials, reagents and solutions in accordance with company SOP's. Faithfully record procedures and results in Batch Records or Solution Preparation Forms, notebooks, or other appropriate forms in an organized manner as dictated by departmental SOP and GMP regulations. Write reports on research as required. Promote compliance with cGMP regulations. Attend GMP training sessions. Support management and maintenance of the SOP and Document Control system. Work with clients to develop material release tests and specifications for materials supplied by J‑STAR. Help ensure that client project needs, requirements, and timelines are communicated to, and coordinated between, GMP Operations and Quality Control. Conduct process chemistry R&D for clients as an individual contributor, which includes, but is not limited to, research on synthetic routes to active pharmaceutical ingredients and chemical intermediates by route discovery, process optimization, safety evaluation, enabling technologies, high throughput screening and chemo/biocatalytic reaction discovery and optimization. This will include R&D under c-GLP and potentially under c-GMP conditions. Develop safe, timely and efficient chemical processes by using established, new and/or novel chemical methodologies and processes. Coordinate analytical chemistry methodology to process and/or catalysis discovery, development optimization and problem solving. Maintain an uncompromising focus on quality, documentation, confidentiality and scientific execution. Participate in idea generation for selective quotes/proposals to clients as well as successfully execute against accepted quotes. Initiate cross-department communication and develop coordinated R&D, processing schedules and deliverables Lead and contribute to scientific and technical discussions with co-workers and clients to plan, execute, resolve issues and problem solve. Communicate candidly, clearly and timely with clients, management and peers. Participate in weekly client updates as needed, prepare weekly reports, contribute to and lead campaign reports and participate in process chemistry technology transfer. Coordinate and author professional campaign reports, research summaries, and tech packages. Follow all company, site and laboratory Environmental, Health and Safety (EHS)-related protocols, processes, guidelines and SOPs. Actively participate in EHS discussions with peers and management for continuous improvement of EHS practices. Maintain a clean and well-organized hood, bench, glove-box and common work area that is free of clutter, excess chemicals/samples. Advocate for these principals and positively influence others in this regard. Qualifications Required MS, PhD degree in Organic Chemistry. Proven track record meeting aggressive targets as related to safe, timely and successful synthetic organic chemistry projects. Knowledge and experience base of working in a c-GMP environment is preferable, but not required Excellent written, verbal and presentation skills. Experience in small molecule drug development is preferable, but not required. Track record of scientific success as measured by publications and presentations. Ability to prioritize and manage numerous activities simultaneously. Ability to interact in an effective and appropriate manner with diverse population sets. Experience in working on and positively contributing to scientific teams. Ability to perform the physical requirements of the position.

Supervisor QC Reference Laboratory - New York - CLICK AND APPLY! Permanent and full-time position. Bachelor s or higher degree in clinical laboratory technology, or Bachelor's or higher degree from a program with a major in biology, chemistry, or the physical sciences, and an advanced certificate in clinical laboratory technology, or Education and training sufficient to qualify for licensure as a Clinical Laboratory Technologist prior to 2009 as specified in NYS-ED Regulation 79-13.4. Bachelor s degree with at least four years of pertinent clinical laboratory experience subsequent to qualifying of which at least two years have been spent working in a clinical laboratory having a director at the doctoral level. Master s degree with at least two years of pertinent clinical laboratory experience subsequent to qualifying of which at least two years have been spent working in a clinical laboratory having a director at the doctoral level. Current active NY State License as a Clinical Lab Technologist. Proposed annual salary is $123,600.00 /yearly. This position is responsible for ensuring the daily function of the Laboratory. This includes scheduling and supervising the staff, supply management, review of daily records, and overall day-to-day functions of the QC/Reference Laboratory. APPLY NOW! OR reach out to Megan directly at (accepts texts) / . OR schedule a quick call with Megan using this link: megankarecruiting

Laboratory Technologist - Hematology/Chemistry - NightsHere at NewYork-Presbyterian Hospital, Laboratory Technologists are redefining the limits of science and medicine. We study some of the most complex and rarely seen medical conditions - with unmatched energy and expertise. Join our team as a Laboratory Technologist and make tomorrow better for countless human beings.Within the NewYork-Presbyterian Clinical Laboraotries, you'll find a patient-focused, engaging, supportive and team-oriented environment. Join a highly skilled technical team of Laboratory Technologists in our robust and fully automated Chemistry/Hematology sections and take on this important role, responsible for performing all patient tests, reading slides, performing quality control procedures as well as standard preventative maintenance. Here you'll have an opportunity to work with nationally accredited colleagues and contribute to lifesaving results.This is a full-time position, working nights, Monday - Friday from 12am - 8am, with rotating weekends and holidays. Preferred Criteria ASCP certification Excellent written and verbal communication skills Experience with performing standard Coagulation testing including PT,APTT, DDIMER, Fibrinogen, Heparin assay and automated CBCs with experience in doing differentials Required Criteria A Bachelor's degree in Medical Technology (or equivalent experience) New York State Clinical Laboratory Technologist licensure from the New York Education department Strong commitment to providing an outstanding patient experience Competitive sign-on bonus up to $10K: Extra Night Shift Sign-on Bonus New graduates eligible Experiential bonus commensurate with experience Join a healthcare system where employee engagement is at an all-time high. Here we foster a culture of respect, diversity, and inclusion. Enjoy comprehensive and competitive benefits that support you and your family in every aspect of life. Start your life-changing journey today. Join a healthcare system where employee engagement is at an all-time high. Here we foster a culture of respect, diversity, and inclusion. Enjoy comprehensive and competitive benefits that support you and your family in every aspect of life. Start your life-changing journey today. Please note that all roles require on-site presence (variable by role). Therefore, all employees should live within a commutable distance to NYP. NYP will not reimburse for travel expenses. __________________ 2024 “Great Place To Work Certified” 2024 “America's Best Large Employers” - Forbes 2024 “Best Places to Work in IT” - Computerworld 2023 “Best Employers for Women” - Forbes 2023 “Workplace Well-being Platinum Winner” - Aetna 2023 “America's Best-In-State Employers” - Forbes “Silver HCM Excellence Award for Learning & Development” - Brandon Hall Group NewYork-Presbyterian Hospital is an equal opportunity employer. Salary Range: $53.15-$66.65/Hourly It all begins with you. Our amazing compensation packages start with competitive base pay and include recognition for your experience, education, and licensure. Then we add our amazing benefits, countless opportunities for personal and professional growth and a dynamic environment that embraces every person. Join our team and discover where amazing works.

We are a leading global contract development and manufacturing organization dedicated to the advancement of cell and gene therapy products. We believe in the transformative potential of cell and gene therapies and we are shaping the future of medicine. We open doors in the regenerative medicine industry for those looking to transform medicine while continuously improving an innovative, growing company. The Supervisor, QC Microbiology will organize, and direct staff to meet and exceed cGMP requirements, and establish KPI's, while adhering to quality control-microbiological and technical standards. The QC Environmental Monitoring Supervisor will also provide oversight of day-to-day activities including adjustment of workflow, test performance, and quality compliance. Essential Functions and Responsibilities Below is the summary of the role responsibilities. This is not an exhaustive list of all responsibilities, duties, skills, efforts, requirements or working conditions associated with the role. While this is intended to be an accurate reflection of the current job, management reserves the right to revise the job or to require that other or different tasks be performed as assigned with or without notice. Ensures compliance with regulatory agency requirements by enforcing a quality culture throughout the department. Schedules and monitors daily operation of department based on projected client demands. Conducts routine walkthroughs of the facility to ensure compliance with regulatory and quality practices. Approval of investigations and documentation of non-confirming events and environmental excursions. Recommends process improvements to achieve greater efficiency within the department and between sites. Participates in department and cross functional meetings. Maintains audit readiness within the department by ensuring proper training of staff, reviewing documentation, and ensuring laboratory cleanliness. Interacts with internal and external customers to ensure proper sampling, reporting, and resolution of questions and concerns. Other duties as assigned. Qualifications Bachelor's degree in a Microbiology or relevant field Minimum of 7+ years of experience with environmental monitoring or within the biopharmaceutical industry or equivalent. Minimum of 2 years of experience in a supervisory or lead role. Strong knowledge of FDA and EU regulatory standards. cGMP experience required. Strong knowledge of microbiological test methods and philosophies. Strong knowledge of quality systems and ability to interpret Quality standards of implementation and review. Proficient with computer software with MS Office and LIMS (MODA experience preferred). Competencies/Candidate Profile Collaboration, accountability, adaptability, can-do, leadership, technical capacity, problem solving, customer-centric, communication, project management, and presentation skills Supervisory Responsibility Determines staffing levels; recruits, interviews, selects, hires, and employs appropriate number of employees. Provides oversight and direction to the employees in accordance with the organization's policies and procedures. Coaches, mentors, and develops staff, including overseeing new employee onboarding and providing career development planning and opportunities. Empowers employees to take responsibility for their jobs and goals. Delegates responsibility and holds staff accountable by providing regular feedback. Fosters teamwork and cohesiveness among department members; expeditiously initiates conflict resolution when issues arise. Creates a workplace culture that is consistent with the mission, vision, guiding principles, and values of the organization. Leads employees using a performance management and development processes to include goal setting, feedback, and performance development planning. Appropriately communicates organization information through department meetings, one-on-one meetings, appropriate email, and regular interpersonal communication. Quality Requirements Build Quality into all aspects of your work by maintaining compliance to all quality requirements. Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function). Attend all required Quality & Compliance training at the specified interval. Direct Reports QC Microbiology Analysts

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Expert who would like to lend your expertise to train AI models? About the opportunity: Outlier is looking for talented Chemistry Experts to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by… Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to Chemistry Evaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise: A bachelor's or higher degree in Chemistry or a related subject Experience working as a Chemistry professional Ability to write clearly about concepts related to Chemistry in fluent English Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project. PLEASE NOTE: We collect, retain and use personal data for our professional business purposes, including notifying you of opportunities that may be of interest and sharing with our affiliates. We limit the personal data we collect to that which we believe is appropriate and necessary to manage applicants' needs, provide our services, and comply with applicable laws. Any information we collect in connection with your application will be treated in accordance with the Outlier Privacy Policy and our internal policies and programs designed to protect personal data. This is a 1099 contract opportunity on the Outlier. ai platform. Because this is a freelance opportunity, we do not offer internships, sponsorship, or employment. You must be authorized to work in your country of residence. If you are an international student, you may be able to sign up for Outlier if you are on a visa. You should contact your tax and/or immigration advisor with specific questions regarding your circumstances.

Driven by a commitment to research, quality, and service, PDI provides innovative products, educational resources, training, and support to prevent infection transmission and promote health and wellness. Encompassing three areas, our Healthcare, Sani Professional and Contract manufacturing divisions, we develop, manufacture, and distribute leading edge products for North America and the world. We have several locations across the US and are looking for new Associates to join our team! POSITION PURPOSE This role is part of the R&D Microbiology team and involves leading the application and interpretation of standards and regulations related to PDI's microbiological and sterility assurance control programs. Key responsibilities include analyzing data, developing tactical plans, implementing procedures, and leading remediation projects. Additionally, you'll conduct scientific research to support PDI's growth strategies, ensuring that our products meet stringent microbiological and sterility standards. The position is a key component of scientific advancement in skin antiseptics and medical device sterilization. Primarily, the role supports new market launches with input across all facets of project progression including scientific insights, prototype assessment and registration testing to meet regulatory requirements. This position requires strong cross-functional collaboration and communication. In addition, developing equity building studies that enhance PDI's current portfolio to provide a competitive edge in a challenging marketplace. ESSENTIAL FUNCTIONS AND BASIC DUTIES RESEARCH & DEVELOPMENT: Act as a sterilization and microbiology subject matter expert (SME), by supporting new product development, changes to existing commercial products. Guide product development teams with scheduling, budget estimates, deliverables, as needed to ensure project and product launch success, and compliance with applicable regulations, industry standards. Develop innovative microbiology solutions to support product development and meet regulatory requirements. Provide technical solutions to product development and engineering teams using various fields of science and sterilization theory and practice. Lead cycle development, validation, requalification activities, as well as product-specific sterilization qualifications and adoptions. LABORATORY SUPPORT: Analyze samples, ensure compliance, and prepare, sterilize, and evaluate products with precision. Optimize laboratory space to ensure an efficient flow of work. Develop and refine methods, utilizing various techniques and instrumentation for accurate results Create new SOPs where gaps exist. Maintain SOP version revisions for continuous improvement initiatives. Maintain detailed records and partner with teams to ensure compliance and efficiency. CROSS-FUNCTIONAL SUPPORT: Lead formulators to determine the correct method and dosage for sterile products Work with packaging and operations to ensure appropriate sterility assurance level Identify technical and project risks. Drive quick problem-solving, manage risks, and align teams on project goals. Prepare technical reports and technical presentations for internal meetings. Provide input to regulatory strategies as it relates to sterilization validation and verification PERFORMANCE MEASUREMENTS Ability to work in partnership with the product development and regulatory functions. Communicate scientific findings clearly and make meaningful contributions to projects. Support work stream timelines and be able to balance priorities according to stakeholder needs. Able to communicate and cooperate with other team members and cross function teams effectively. Demonstrate ability to add value to the organization through scientific excellence. Take ownership for assigned projects and self-lead initiatives. QUALIFICATIONS EDUCATION/CERTIFICATION University Degree in a Biological Science required Masters/Ph.D. an advantage REQUIRED KNOWLEDGE Previous experience in a regulated R&D environment supporting Sterile Products. Strong Microbiology understanding. Working knowledge of FDA regulations EXPERIENCE REQUIRED 5+ years' experience in sterilization or microbiology for regulated products Responsible for ensuring compliance with standards governing Ethylene Oxide, Dry Heat, X-Ray and Gamma sterilization Experience in working in GxP laboratory facilities. SKILLS/ABILITIES Excellent communication skills (verbal / written). Ability to explain science to management. Prudent risk taker. Identifies opportunities and takes risks to achieve objectives. Simplify complex ideas, collaborate effectively, deliver results, and innovate in sterility assurance. Able to work on multiple projects of varying complexity. Computer literate (Outlook / Word / Excel). SALARY RANGE $65,000 - $90,000 annually BENEFITS PDI is pleased to offer comprehensive and affordable benefits for our associates, which includes: Medical, behavioral & prescription drug coverage Health Savings Account (HSA) Dental Vision 401(k) savings plan with company match and profit sharing Basic and supplemental Life and AD&D insurance Flexible Spending Accounts (FSAs) Short & long-term disability Employee Assistance Program (EAP) Health Advocacy Program PDI also offers many voluntary benefits such as: Legal services, critical illness, hospital indemnity, accident coverage, ID theft and fraud protection, pet insurance and employee discounts. At PDI, we are also committed to helping our associates maintain a healthy and sustainable work/life balance and are proud to provide associates with paid time off programs including: sick & safe leave, vacation, company & floating holidays, paid parental leave, and depending on the position we also offer summer hours and flex place/flex time options.

Our client is seeking Full-Time Clinical Lab Techs for their Microbiology Lab! Full time Monday - Friday Shifts: 4:30 PM - 1:00 AM OR 9AM - 5:30 PM Perform routine and emergency tests on blood and other body fluids using a variety of automated and manual instrumentation promptly. Maintain equipment and records according to department procedures and regulatory agencies guidelines in the areas of QA and QC. Use independent judgment to solve technical and procedural problems. In some instances, the ability to stand or sit for extended periods of time is necessary. Pay Range based on experience: $88,757 - $109,063.43 $5,000 Sign on Bonus Requirements Must have an active New York license At least 2 years of work experience preferred Bachelor's Degree in physical science, medical technology preferred. Benefits 1199 Members Medical & Dental 403B matching up to 8% of salary Room for Growth Great leadership and support, utilizing the latest advances in computer technology.

An exciting new opportunity for an experienced financial services professional within the Data Reporting and Controls team. As a Firmwide Regulatory Reporting & Analysis (FRRA) - Data Controllers & Reporting (DCR) - Associate within the Data Controllers & Reporting Team, you will be focused on working with the teams involved in production processing and reporting activities including strategic initiatives for US Regulatory Reports i.e. FR Y-9C, Call Report & CCAR. The Firmwide Regulatory Reporting & Analysis (FRRA) team resides within Corporate Finance. The group is responsible for the execution and delivery against the Firm's regulatory reporting requirements to its U.S. regulators and has end-to-end responsibility for U.S. regulatory reporting and capital stress testing, including the design, implementation, and oversight of the execution, analysis, and control and governance frameworks. Its mandate includes determining the appropriate investment in people, processes and technology to improve the accuracy, completeness and consistency of the Firm's U.S. regulatory reporting and capital stress testing submissions, as well as the implementation of new requirements and guidelines as they are published. We are the Data Controllers & Reporting (DCR) team within FRRA. DCR is a diverse, global organization of 100+ talented employees united by shared goals & priorities. We are responsible for completeness and accuracy of data in the firm's target state financial reporting platform. Our mission across the 25+ firmwide & local jurisdictions we support globally, is to drive completeness and accuracy of data through activities spanning from data sourcing, data validations, adjustment processing & reconciliations. Job Responsibilities: Be responsible for BAU activities spanning from data sourcing, data validation and completeness, adjustments processing and performing reconciliations Executing overall operating model, procedures for functional areas in the reporting space Managing client relations, communications and presentations Supporting business users of the FRI application with User queries, Issue Resolutions Identify and execute process improvements to the existing operating model, tools and procedures Interacting with Controllers, Report owners and RFT (Risk & Finance Technology) partners Act as an interface with Control partners, ensuring compliance with risk and controls policies Escalating issues as needed to the appropriate team(s) and management Partnering with projects team through the full project life cycles Leading programs/initiatives for reporting automation and operating model optimization Required Qualifications, Skills, and Capabilities: Bachelor's degree in Accounting, Finance, or a related discipline 3+ years of financial services or related experience Strong oral and written communication with the ability to effectively partner with managers and stakeholders at all levels Strong working knowledge of MS office applications (MS Excel, MS Word, MS PowerPoint), specifically with reconciliations, summarizing and formatting data Experience using data management & visualization tools in a reporting setting: AWS Databricks, Alteryx, SQL, Tableau, Visio, Preferred Qualifications, Skills, and Capabilities: Familiarity with US Regulatory reporting (E.g. Y9C, Call, CCAR etc.), controllership functions, banking & brokerage products, and US GAAP accounting principles Control mindset and exposure to establishing or enhancing existing controls Strong verbal and written communication skill with the ability to present information at varying levels of detail depending on the audience Strong process and project management skills Enthusiastic, self-motivated, effective under pressure and strong work ethic and keen attention to detail and accuracy Aptitude and desire to learn quickly, be flexible, and think strategically Client & business focused; able to work collaboratively and build strong partnerships with clients and colleagues at all levels

Quality Control Associate - Brilliant Earth, Secaucus, NJ Our Jewelry team is dedicated to delivering excellence from the time a customer places an order to the moment a customer opens their package. The team coordinates and executes day-to-day operations of jewelry production, while maintaining strong relationships with our partners. Join our team of committed problem solvers who are passionate about ensuring that every Brilliant Earth purchase meets the highest standards of quality and craftsmanship. To learn more about what it means to be a member of our Operations team, click here to check out our recent blog post! Responsibilities: Execute quality assurance best practices to ensure products meet Brilliant Earth's high-quality standards. Perform finishing and cleaning for fine jewelry products, including rhodium plating, ultra sonic and steaming. Adhere to guidelines to ensure gemstones and metals are handled properly. Perform data entry in our ERP/MES systems, ensuring accurate product tracking in the system. Meet daily processing timelines and quotas. Communicate and work cross-functionally with other teams, providing updates on status, issues and concerns. Maintain the workspace in a clean, organized and efficient manner. Adhere to product security and safety protocol and procedures. Qualifications: Experience physically working with Jewelry and knowledge of Jewelry production / manufacturing processes. Computer skills and ability utilize MES/ERP systems Highly organized with a focus on execution and exceptional attention to detail Exceptional time management skills and accountability Ability to adapt quickly in a fast-paced environment Team player with demonstrated communication skills and ability to work collaboratively. Interest in socially and environmentally responsible organizations and products Ability to safely access the workspace, which requires walking up 1 flight of stairs B1 level English Proficiency (Common European Framework of Reference for Languages) What We Offer: At Brilliant Earth, we're passionate about the employee experience. That's why we offer an excellent training program and endless opportunities for career growth! In addition, we offer competitive compensation and a robust benefits package, including: Career Growth. We want to see you sparkle! Through regular 1-1's with your manager, a variety of training opportunities, and an annual 360 review process for all employees, our leaders are dedicated to creating clear pathways for growth. Ask the hiring team for more information on how Brilliant Earth creates a culture of collaboration and growth during your interview conversations! Diverse, mission-minded team. We were founded to cultivate a more transparent, sustainable, compassionate, & inclusive jewelry industry. Learn more about our impact and team diversity Here! Lifestyle Spending Account. At Brilliant Earth, we're committed to your well-being. Enjoy company reimbursements for eligible wellness expenses, such as gym memberships, massage, counseling, and more! Continued Education. Company-sponsored learning in leadership, professional skills, diversity & inclusion, and access to tuition reimbursement for role-specific trainings. Employee Discounts. As an employee at Brilliant Earth, you'll receive a generous discount on our jewelry. Mental Wellness Perks. We offer access to mental health resources, such as self-care apps and seminars. Our Employee Assistance program offers 24/7 access to counseling! Giving Back and Volunteer Opportunities. In addition to our giving back programs, our teams support local initiatives and spend time together by volunteering. Medical, Dental, and Vision. We offer multiple plans to choose from, including a $0 monthly premium option for employee health insurance and employer HSA contributions. Insurance kicks in on the first day of your 2nd month! 401k match. We know that saving for the future is important. That's why we offer a generous 401k match. Paid Time Off. We know it's important to recharge and relax - you'll accrue 3 weeks of PTO in your first year. Parental Leave. We aim to support our growing families. Employees can utilize our paid parental leave to bond and care for their new additions. Disability and Life insurance. 100% employer-paid. Pre-Tax Commuter Benefits. How to Apply & What to Expect: Everyone at Brilliant Earth has a voice - we want to hear yours! If you are interested in growing with Brilliant Earth, send us a resume and cover letter letting us know why you are interested in joining our mission and our team. Please include a sentence about your favorite shape of diamond. You'll receive an email when we've received your application, and can expect an update within a week of applying. The interview process for this role includes a phone call with the recruiting team and an on-site interview with our VP, Product Operations. #IND333 More About Us At Brilliant Earth, our mission is to cultivate a more transparent, sustainable, compassionate, & inclusive jewelry industry. We believe in creating jewelry you can feel good about wearing, without ever compromising between quality and conscience. We are hard-working team players that welcome challenges and rise to any occasion. Our community of collaboration, respect and encouragement is fostered by frequent team events, cross-departmental meetings and celebrating our wins, big and small. As one of the fastest growing e-commerce jewelers in the world, we're searching for bright and passionate people who are excited to make an impact from day one and grow with the company to take on greater responsibility over time. Brilliant Earth recognizes the value of diversity and inclusion on our team, as we work together to reinvent fine jewelry in a thoughtful and modern way. At Brilliant Earth, we celebrate each other - our successes, the lessons along the way, and the unique perspectives each individual brings to our team. It is our intent to maintain a work environment and hiring process which is free of harassment or discrimination because of sex, race, religion, color, national origin, physical or mental disability, genetic information, marital status, age, sexual orientation, gender identity, military service, veteran status, or any other status protected by Federal, State or local laws. We are committed to complying with all Federal, State and local laws providing Equal Employment Opportunities, and all other employment laws and regulations. If you need assistance or reasonable accommodation completing an application or at any stage of the interview process, please reach out to us at accommodations@brilliantearth.com.

Job Description: Contract 10Months Worker will need steel toe shoes and safety glasses 2nd shift This is a 2nd shift position: 2:00PM - 10:30PM with overtime availability Long assignment with goal to convert right candidate to FTE The Senior Finishing Technician performs visual quality inspections and modifies rolls of indicators according to customer specifications. How you will do it Independently set up and operate equipment in accordance with current good manufacturing practices and standard operating procedures Responsible to finish operations on the appropriate jobs in the order needed to meet production schedules Follow the Finishing work instructions and other instructions as trained Maintains rewind tables calibrated Basic understanding in the use of conventional measuring tools and techniques to assure compliance with specification Inspect the product for defects and any non-conforming material Repair and splice Time Temperature Indicator rolls Ensure the products are properly stored (freezer, chilled enclosure, room temperature - per produce specification) Number Time Temperature Indicators Performs periodic preventive and maintenance activities. Manages and operates ink jet equipment. Tracks modifications performed to the Finished Label Inventory Maintains and adheres to all company safety policies and procedures. Maintains work area organization and documentation to satisfy ISO and GMP standards. Maintains good communication and working relationships with all departments and effectively functions within a team environment. Exhibits professional etiquette that exemplifies the values of the organization. Attendance at the worksite is required on a regular and on-going basis. What we look for High School Diploma or GED At least 2 years of experience Key Skills & Competencies: Ability to read and interpret documents such as work instructions, safety rules, operating and maintenance work instructions, procedure manuals and MSDS sheets. Must have sufficient English reading, writing and speaking skills to review work instructions and communicate effectively throughout the organization. Must be able to perform basic arithmetic using units of measure, whole numbers, common fractions and decimals. Must understand and be able to convert measurement units to/from Imperial to Metric. Ability to maintain quality and safety control standards. Knowledge of light equipment operation in the performance of job responsibilities. Ability to prepare routine administrative paperwork. Ability to read, sort, check, count, and verify numbers. Ability to lift and manipulate heavy objects. Ability to detect problems and report information to appropriate personnel. Ability to read, analyze and interpret complex written and verbal information. Must have the ability to effectively communicate orally and in written form both internally and externally. Must be familiar with and be able to communicate via e-mail. Must be familiar with and be able to use computer software including word processing & spreadsheets (Microsoft products preferred), and ERP System.

Essential Functions Ensure that all samples received by the laboratory are logged in according to the appropriate procedure including labeling, logging, and acknowledging. Ensure instrumentation is running, troubleshoot issues, and make or coordinate repairs as Perform analysis as requested on the required turnaround Clean and maintain equipment and Maintain inventory of standards and supplies; order replacements as Ensure all analysis is performed within the specifications of the appropriate Provide SOP updates and details for corrective actions as Report non-conformances to the QAM and Laboratory Utilize laboratory information management system (LIMS) functions, including generating work lists, obtaining, and updating project status, and ensuring reported data is properly qualified. Performs other job-related duties and projects as Supervisor Responsibilities No Supervisor responsibilities Required Qualifications Bachelor's degree or higher in Chemistry, Chemical Engineering, Applied Physics, Other Physical Sciences as approved. Minimum 5 years' experience in general chemistry laboratory or 4 years' experience in an appropriate laboratory, Instrumental troubleshooting & maintenance. Master's Degree in an Engineering or applied science discipline can substitute for 2 years' experience. Familiarity with various sample Detailed knowledge of EPA Methodology - Specifically the following list: EPA Method 29, 306, SW-846 0060 & 0061 EPA Method 5, 17, 201A, 202, 200.8, 6020, 245.1, 1631 Functional operational knowledge of CVAAS, ICP/OES, ICP/MS Knowledge, Skills & Abilities Intermediate skill level in Microsoft Office programs, including Work, Excel, and Strong written and verbal communication skills, both with internal customers and external Ability to accurately read, write, and interpret laboratory Professional behavior and Ability to be organized and attention to Ability to prioritize and multi-task, follow up on pending issues, meet deadlines and work General familiarity with laboratory safety, previous laboratory experience Work Environment While performing the duties of this job, the employee regularly works in a laboratory setting. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Sitting and/or standing for extended periods and the use of hands to finger is common. Hearing and vision within normal ranges is helpful for normal conversations, to receive ordinary information and to prepare or inspect documents. Duties frequently involve repetitive motions and eye/hand/foot coordination. While performing the duties of this job, good manual dexterity for the use of laboratory equipment is needed. The employee is occasionally required to walk, lift, carry, push, pull, climb, stoop, kneel, crouch, reach, handle, grasp, and feel. Occasional heavy lifting is expected. Exertion of up to 30 lbs. of force may occasionally be required. Use of applicable Personal Protective Equipment is mandatory. Travel Not applicable Other Duties Please note this job description is intended to describe the general nature and level of work performed by employees assigned to this position. It is not designed to contain or be interpreted as a comprehensive list of all duties, responsibilities, and qualifications. Additional job-related duties may be assigned. Alliance reserves the right to amend and change responsibilities to meet business and organizational needs as necessary with or without notice. EEO Commitment: We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, national origin, ethnicity, sex, pregnancy, sexual orientation, gender identity/expression, including transgender identity, religion, disability, age, genetics, active military or veteran status and any other characteristics protected under applicable federal or state law.

Medical Laboratory Technician to work in Microbiology/Core Laboratory under the direct supervision of supervisor/technologist. Will be responsible for performing a variety of complex and routine test within the Laboratory complying with all safety and regulatory requirement. Required to work weekends and scheduled holidays based on the department needs. Participate in interdepartmental collaboration within the institution, to provide the highest quality patient care

QC CHEMIST QUALIFICATIONS Have a valid driver's license. Be at least 21 years old. Must be able to meet the eligibility requirements for employment within a cannabis business set by the State of New Jersey. Have 2 years of relevant professional, post academic laboratory experience. Must have at a minimum, a bachelor's degree in a natural science, to include, but not be limited to, biology, chemistry, or environmental sciences. QC CHEMIST RESPONSIBILITIES The HPLC or GCMS QC Chemist positions require a bachelor's degree in a hard science and a minimum of two years of professional (non-academic) laboratory experience, and are responsible and accountable for the testing, instrumentation and testing methodology, quality control and tracking of cannabis material-ensuring the safe accurate and timely testing of NJ cannabis products. The ideal candidate possesses core skills in analytical chemistry, data analysis and instrument maintenance and troubleshooting for gas chromatography or high-performance liquid chromatography instrumentation. Premium skills such as Quality Assurance, ISO / IEC 17025, and method development and validation within a cannabis testing laboratory are highly valued. A valid driver's license is also required for this role. ESSENTIAL DUTIES Follow policies and procedures for the daily operations and fully comply with state medical marijuana regulations Use of aseptic technique to handle, prepare, and analyze samples Expertise in sample preparation and testing methods using analytical instrumentation (HPLC, LC-MS/MS, ICP-MS, GCMS) Responsible for inventory of supplies and cannabis tracking and destruction Responsible for accurate weighing and recording all product weights Works in a timely manner and strives to improve quality and maintain accuracy Perform area and instrument cleaning, maintenance and calibration including compliant documentation of associated logs Develop, performs, or assists in method validations Analyzes data from testing performed and submits to laboratory director or lab director designee Performs all other tasks and duties as assigned, which may include cannabis sampling, transport, and sample preparation Job Type: Full-time Pay: $26.00 - $28.00 per hour Benefits: Dental insurance Flexible schedule Health insurance Paid time off Vision insurance Schedule: 10 hour shift 8 hour shift Day shift Monday to Friday Overtime Weekends as needed Experience: analytical, non-academic: 1 year (Required) Work Location: In person

Goodwill NYNJ Ecommerce Quality Control - Full Time Position To receive merchandise and sort & separate items based on quality standards for listing. • Receive incoming totes from stores & record seal information as directed. • Research items online for matching descriptions and value by using different market places. • Accept and reject items based on quality standards. • Use provided manifesting software to print SKUs and safely apply them to a variety of items. • Comply with production expectation. • May need to lift up to 50lbs. • Additional duties as required. • Minimum high school diploma. • Ability to read and write English. • Basic computer & internet research skills. • Ability to deal with change and work in a dynamic environment. • Able to work under minimal supervision and process the expected number totes per day. • Able to work as part of a team involved in the quality control of items for Goodwill's E-Commerce (Online) department. Duties will be performed in an industrial warehouse environment. This job requires you to stand/move for long periods of time. Covid-19 Update - In alignment with New York City's decision to lift the private employer vaccination requirements, effective November 1, 2022, Retail Employees in NYC are now exempt from submitting vaccination proof and/or no longer required of submitting proof of weekly PCR/Antigen(Rapid) testing if they have requested medical/ religious accommodation. Retail stores in NJ and Upstate continue to be exempt as per New Jersey and New York State Guidelines.

QC Analyst 2 Job Title: Quality Control Laboratory Analyst 2 - Radiopharmaceuticals About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company beginning operations in Springfield, NJ. The state-of-the-art facility will provide contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. The company expects rapid growth in the next few years. Evergreen is a small team, where all team members support each other in a variety of activities. Job Description: We are seeking a highly motivated and detail-oriented Quality Control Laboratory Analyst 2 to join our team. This individual will play a key role in ensuring the highest standards of quality and compliance in our radiopharmaceutical release processes. The ideal candidate will have a background in pharmaceutical or life sciences, and hands-on experience with analytical techniques such as GC (Gas Chromatography), TLC (Thin Layer Chromatography), and HPLC (High-Performance Liquid Chromatography). Key Responsibilities: Perform quality control testing and analysis release testing of radiopharmaceutical products to ensure compliance with internal and external specifications and regulatory standards. Independently operate and maintain laboratory equipment, ensuring calibration and proper functionality. Maintain a clean, safe, and organized lab environment, adhering to all safety and pharmaceutical regulations, including radiation safety protocols. Perform daily lab tasks, including solution preparation, drug product analysis, and documentation of all testing. Utilize laboratory techniques including GC, TLC, and HPLC to perform a variety of testing procedures. Maintain thorough and accurate documentation of testing activities, results, and reports in accordance with SOPs (Standard Operating Procedures). Train and mentor new team members, offering support and guidance to ensure smooth onboarding and integration into laboratory operations. Maintain strict attention to detail while working with hazardous materials and ensure proper handling of radioactive substances as per safety guidelines. Qualifications: 2-5 years of experience in the pharmaceutical, life sciences, or radiopharmaceutical industry Bachelor's degree in a scientific field (e.g., Chemistry, Biochemistry, Pharmaceutical Sciences), or equivalent relevant work experience. Proficiency and hands-on experience with laboratory techniques such as GC, TLC, and HPLC. Ability to work independently and as part of a team, managing multiple tasks and priorities. Strong problem-solving skills and attention to detail, with an understanding of GMP, GLP, and other regulatory requirements. Previous experience in training or mentoring new staff members is a plus. Working Environment: Laboratory setting with exposure to radiation and other chemical hazards. Required to wear personal protective equipment (PPE) such as lab coats, gloves, and safety goggles. Fast-paced laboratory setting with occasional lifting and movement of materials. Commitment to maintaining a clean, organized, and safe working environment.

Laboratory Technologist - Hematology/Chemistry - NightsHere at NewYork-Presbyterian Hospital, Laboratory Technologists are redefining the limits of science and medicine. We study some of the most complex and rarely seen medical conditions - with unmatched energy and expertise. Join our team as a Laboratory Technologist and make tomorrow better for countless human beings.Within the NewYork-Presbyterian Clinical Laboraotries, youll find a patient-focused, engaging, supportive and team-oriented environment.Join a highly skilled technical team of Laboratory Technologists in our robust and fully automated Chemistry/Hematology sections and take on this important role, responsible for performing all patient tests, readingslides, performing quality control procedures as well as standard preventative maintenance. Here you'll have an opportunity to work with nationally accredited colleagues and contribute to lifesaving results.This is a full-time position, working nights, Monday - Friday from 12am 8am, with rotating weekends and holidays. Preferred Criteria ASCP certification Excellent written and verbal communication skills Experience with performing standard Coagulation testing including PT,APTT, DDIMER, Fibrinogen, Heparin assay and automated CBCs with experience in doing differentials Required Criteria A Bachelors degree in Medical Technology (or equivalent experience) New York State Clinical Laboratory Technologist licensure from the New York Education department Strong commitment to providing an outstanding patient experience Competitive sign-on bonus up to $10K: Extra Night Shift Sign-on Bonus New graduates eligible Experiential bonus commensurate with experience Join a healthcare system where employee engagement is at an all-time high. Here we foster a culture of respect, diversity, and inclusion. Enjoy comprehensive and competitive benefits that support you and your family in every aspect of life. Start your life-changing journey today. Join a healthcare system where employee engagement is at an all-time high. Here we foster a culture of respect, diversity, and inclusion. Enjoy comprehensive and competitive benefits that support you and your family in every aspect of life. Start your life-changing journey today. Please note that all roles require on-site presence (variable by role). Therefore, all employees should live within a commutable distance to NYP. NYP will not reimburse for travel expenses. __________________ 2024 Great Place To Work Certified 2024 Americas Best Large Employers Forbes 2024 Best Places to Work in IT Computerworld 2023 Best Employers for Women Forbes 2023 Workplace Well-being Platinum Winner Aetna 2023 Americas Best-In-State Employers Forbes Silver HCM Excellence Award for Learning & Development Brandon Hall Group NewYork-Presbyterian Hospital is an equal opportunity employer. Salary Range: $53.15-$66.65/Hourly It all begins with you. Our amazing compensation packages start with competitive base pay and include recognition for your experience, education, and licensure. Then we add our amazing benefits, countless opportunities for personal and professional growth and a dynamic environment that embraces every person. Join our team and discover where amazing works. RequiredPreferredJob Industries Other

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Expert who would like to lend your expertise to train AI models? About the opportunity: Outlier is looking for talented Chemistry Experts to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by… Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to ChemistryEvaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise: A bachelor's or higher degree in Chemistry or a related subject Experience working as a Chemistry professional Ability to write clearly about concepts related to Chemistry in fluent English Payment:Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.