Quality Control Analyst Jobs in Norwood, MA

6 Month Contract Norwood, MA PR: $30-38/hour Shift: Tues-Sat, 1st shift All interviews to be held on Wednesday 11/27 with offers out slightly after. In this role, you will support cGMP microbiology methods for QC raw material, plasmid, drug substance, Stability and finished product testing for mRNA products produced at Moderna's manufacturing facility. This individual will contribute to non-testing projects and activities as needed example document certification, monthly biosafety cabinet cleaning etc. Job Responsibilities Execute compendial microbiological testing, and other methodologies as needed. Receive Environmental Monitoring Plates into MODA, Incubate, Microbial identification, Support testing for in-process samples, drug substance and drug product, including generation of testing data to support clinical studies. Assist in enumeration of test plates, review EM data, etc. Perform general laboratory support activities including reagent preparation, equipment maintenance, weekly and monthly cleaning of the BSCs, Document Certification, archival etc. Stock and perform inventory of lab supplies. Establish and maintain a safe laboratory working environment. Additional duties as may be assigned from time to time Education & Qualifications BS in a relevant scientific discipline with a minimum of 0 - 2 years (or MS in a relevant scientific discipline with 1 year) Quality Control experience in a cGMP organization Excellent troubleshooting and ability to communicate issues in a scientifically sound and understandable way. Familiarity with electronic databases (e.g. LIMS, SAP, LMS, or equivalent software) Strong written and oral communication skills as well as organizational skills Ability to prioritize, manage and complete multiple projects and tasks in a fast-paced environment efficiently and independently. Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations. A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

qPCR experience is required. Job Summary/Operations Involvement: Primary Duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations /validation/or development studies. Testing may include but not limited to samples from drug substances and drug product manufacturing, stability and various protocol studies using approved test methods or test methods derived from QC technical protocols. Specific Biochemistry Focus Areas: Product Testing: Area focuses on techniques such as SDS-PAGE Silver, QPCR, Potency, Kinetics assay, Enzyme Activity, pH, Osmo, A280 etc., in order to support in-process, release and stability testing. Role supports commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation. The introduction of new equipment and technology to improve sustainability and compliance is expected. Job Function and description 40-50% Testing execution, participate in training analysts, trouble shooting of methods 20-30%: QC operations support which entails data review, data trending, OE/5S/LEAN initiatives, maintenance of equipment and reagents, lab housekeeping, support for other QC groups. Compliance and quality systems (SOP revisions, input to quality systems records) 10-20% Involvement in various departmental and cross-functional teams and initiatives; inspection and regulatory support

Title: Quality Assurance Associate 2nd Shift Shift: 2nd Shift, 3 pm to 11pm Monday through Friday Status: 6-12 month contract Hourly rate: $55 an hour Please note, this is Quality Assurance role and not a QC role. Qualified candidates must have experience working in a QA role on the manufacturing floor. Additionally, this contract cannot be done on C2C or offer sponsorship of any kind. Quality Assurance Associate This individual in this office-based role will maintain on site quality presence at GMP facility in Lexington, MA by providing support for clinical phase manufacturing, batch record review and quality issue resolution. Will also support incoming raw material/excipient release, document management and training systems. Primary function is to assure the quality of manufactured products is in compliance with all applicable regulations, guidelines and internal procedures. Responsibilities: • Proactively promote GMP, GDP, and compliance concepts. • Support incoming raw material release. • Support Supply Chain and Manufacturing with dispensing of raw material for batch production. • Support QC, Analytical Research and Development (ARD) with CoA review, approval, and filing. • Perform quality oversight of clinical phase manufacturing executional compliance with GMP, including issuance of production batch records, line clearance, QA on the floor presence, raw material, component, and in-process material checks. • Support batch documentation review, deviations/investigations, change control and issue resolution for Intermediate and Drug Product (DP) Disposition. Qualifications: Minimum of BA/BS in a science related field • Minimum of 5 years of related work experience in pharmaceutical, biotech or medical industry • Knowledge of Good Manufacturing Practices (GMPs), Good Documentation Practices and application within pharmaceutical development.

This role will be based in our Cambridge, MA location until our new state of the art facility located in Burlington, MA is ready. Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing Quality Control professional looking to join and contribute to a commercial stage company with an established portfolio of unique advanced cell therapies and specialty biologics. Reporting directly to Quality Control Management at Vericel, this is a great opportunity to join a high growth company with a strong balance sheet supported by a talented team of professionals who are committed to improving the lives of the patients we serve. POSITION SUMMARY The Senior Quality Control (QC) Analyst is responsible for performing routine and non-routine assays of in-process samples, finished drug product (DP), and stability samples within the QC laboratory in accordance with SOPs for product release and validation. This role also participates in special projects, method development/transfers and cleaning study qualifications as needed. DUTIES AND RESPONSIBILITIES Perform microbiological, molecular and/or cell culture assays for in-process, final product and stability samples. Perform microbial limits, Bioburden testing, and identifying and trending microorganisms. Participate in method qualification/validation activities as necessary. Provide training and technical leadership to less experienced staff. Analyze, document, and trend QC data in accordance with Vericel requirements. Assist in the review of QC data and provide summaries to management as needed. Report out-of-specification or out-of-trend results in a timely manner to ensure appropriate actions are taken. Performance of QC general laboratory equipment calibration and maintenance, laboratory housekeeping and preparation of the laboratory for audits. Author and conduct periodic review to QC documents, including SOPs, protocols and forms. Assist QC Management, as needed, in the completion of OOS, deviations, change controls and CAPAs. Utilize a range of electronic systems such as LIMS and document/equipment management software. Collaborate with internal departments and teams to support QC testing, change controls, and CAPAs. Actively promote safety rules and awareness. Reports and takes initiative to correct safety & environmental hazards. Always demonstrate good safety practices including the appropriate use of protective equipment. Train on and maintain knowledge of current regulatory requirements and relevant internal procedures. Back up for QC instrument maintenance and calibration. Backup for QC sample receipt for internal testing, outside laboratory testing, login, processing, shipment, tracking, distribution of test results, and closure. Practice safe work habits and adheres to Vericel's safety procedures and guidelines. Work on special projects as needed and contribute towards continuous improvement. Other activities as assigned. QUALIFICATIONS, EDUCATION AND EXPERIENCE BS/MS degree in microbiology, molecular biology, biochemistry or a related discipline. BS, 5+ years' industry experience. MS, 3+ years' industry experience in cGMP lab environment. Ability to work independently with little supervision and/or function independently, exercise good judgement and work in a team-based environment. Demonstrate knowledge of cGMP/ICH/FDA/EU regulations, quality systems and regulatory requirements. Collaborative team player who fosters open communication and builds relationships with stakeholders. Exercise judgment and decision making when problem solving. Excellent written and verbal communication skills. Ability to manage competing priorities or projects. Ability to pay attention to detail as applied to data review and compliance. Strong organization, and communication skills with a positive attitude. Experience as a technical leader in a strong team environment and work independently to successfully balance short and long term project objectives. Preferred Qualifications: Experience with Deviation Management and Change Control. Experience with complex analytical methods or cell culture methods. Experience with assay/equipment validations/transfers. Excellent technical writing and investigational skills. WORKING CONDITIONS AND PHYSICAL DEMANDS Ability to lift 40 lbs. Required to work one day per weekend. Rotating holiday coverage May carry company issued cell phone for off-shift remote alarm coverage. Required to gown into classified manufacturing clean room areas. EEO Statement All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer. Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.

The Quality Control Technician is responsible for performing standardized qualitative and quantitative tests on work-in-process and finished products to ensure compliance with company and/or customer quality standards. Conduct organoleptic and analytical tests at various stages of compounding and packaging to ensure compliance with standards. May include the use of pH meters, HPLC, Malvern Mastersizer, and other instrumentation. Submit samples for microbiological testing, maintains test results, and calculates batch adjustments for certain products. Approve batches for packaging and conforming finished product for shipment and places non-conforming product on hold for further analysis. File and maintain retained samples. Calibrate, clean, and maintain laboratory equipment and instrumentation. Prepare reagents and solutions for use in testing. Observes conditions and practices in compounding, packaging, and finished goods storage areas, making recommendations for improvement. Skill Sets: Quality inspection, auditing and testing. Experience with implementation of corrective action programs (HACCP). Product or industry-specific experience. Strong computer skills. Knowledge of tools, concepts and methodologies. Knowledge of relevant regulatory requirements. Perform data collection, management and analysis. Regulation compliance assurance and reporting. Schedule: 9 AM - 5:30 PM (Mon-Fri) Pay Rate: $33.86/Hour

Immediate need for a talented Quality Assurance Associate II. This is a 12+months contract opportunity with long-term potential and is located in Waltham, MA, (Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID: 24-51470 Pay Range: $40 - $43/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Review and approve Master Manufacturing Records, Stability Protocols and Reports, Sampling plans, and associated manufacturing documents for the timely initiation of GMP manufacturing activities. Perform QA review of Executed Batch Records. Perform QA review of Quality Records, i.e. Deviations, CAPAs, OOS etc., as they occur. Perform QA review and approval on SOPs, forms, WI, and other document types. Provide SAP support for GMID and BOM approval. Provide Quality oversight and Quality guidance to resolve compliance issues for lots of drug substance, bulk drug product, drug product and clinical materials for use in clinical trials. Ensure all requirements, stipulated in the CMO Quality Agreements, are being met. Review and Approve Analytical related documents such as Test Methods, Test Method Transfer Plans and Assessments, if needed. Participate in Quality Risk Assessments Assist with internal and external audits. Support of data analysis and metrics for Quality Council, KPls, and other reportable forums may be requested. Assume additional responsibilities as assigned. Key Requirements and Technology Experience: Key skills; Deviation, Veeva, CAPA, Batch Records Bachelor's and/or 8+ years of relevant experience Minimum 5 years of experience in Quality Working knowledge and ability to apply Quality principles and cGMPs in conformance to standards, preferably gained from working in a manufacturing, QA or QC environment. Demonstrated ability to interact and communicate effectively, both written and verbal, with peers, management, auditors, and consultants. Must have excellent attention to detail, project and time management skills, and the ability to manage multiple priorities with aggressive timelines. Preferred experience with outsourced manufacturing and testing operations Working knowledge of MS Office products including Word, Excel, Outlook, PowerPoint, and Project. Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. 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. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

BioSens8 is creating novel quantitative and real-time biosensors fueled by our underlying platform technology. Our goal is to engineer continuous monitors which will give unprecedented and personalized insight into our body's health state. Our first application is in women's health to help women through infertility. Role Description This is a full-time on-site role for a postdoc level electrochemist. The electrochemist will be responsible for conducting research and development (R&D) related to biosensor engineering. Qualifications Current Postdoc in electrochemistry or related field NSF I-PERF (US citizens, nationals, or permanent residents eligible) Can distill and communicate results in an effective manner Self motivated and can work independently and in a team environment Passion for working in a fast paced startup environment

** Our client, a dynamic team that's solving the world's toughest challenges with groundbreaking science and technology, is looking to hire a Data Scientist. If you're passionate about innovation and want to be part of something bigger, we want to hear from you! If you are a chemist with strong data management experience, with a bachelor's degree in chemistry, we'd love to chat! As a Data Scientist II, you will be responsible for preparing analytical chemistry for loading into a database. Pay: 45-60/hr. Schedule: Monday-Friday, 8am-5pm Terms: 1 year contract with potential of extension Hyrid Opportunity What you will be doing: Extract and transform analytical chemistry data from public sources into spreadsheet templates that are loaded by others into a database. A thorough knowledge of analytical chemistry data and methods is needed to accurately extract and transform source data in preparation for database assimilation. Provide technical knowledge of analytical chemistry data and methods to support the data management team. Coordinate activities with data source subject matter experts to ensure integration, data integrity and data quality. What you bring to the company: BS in Chemistry. 5+ years of related work experience in management of analytical data. Good written and verbal communication skills. Team player, collaborative. Critical thinker, good problem solver. ** This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you**

The Sample Management group is looking for a highly motivated individual to be a key contributor within our team. As a member of the Sample Management group, the successful candidate will be primarily working within the Compound Hub, processing new client compounds and inventory requests through the Compound Hub Process Key Functions: Primary responsibility will be handling of all new compound orders, weighing solid samples within a weigh hood using an analytical balance in order to create solutions, which then move onto the Tecan Liquid Handler. Sample logistics including packaging and unpackaging samples from both internal and external locations. Responsible to ensure all service level agreements are achieved on a daily basis and to work with scientific staff directly to complete orders. Skills: A Bachelor's degree with experience working in a scientific lab, having an Client on compound inventory management and distribution utilizing automated systems. Should have a thorough knowledge of activities related to compound management, including inventory management, solution production, quality control and logistics management. Experience working with laboratory robotics Ability to diagnose and triage hardware and software issues quickly Good personal and communication skills. Ability to work well within a team Ability to multitask in a fast-paced environment Must understand customer focus, and be professional in the work place Must be self-motivated, well organized, reliable and able to prioritize workload Working knowledge of MS Office products Desired Traits & Experience: This is a service orientated position requiring attention to detail, ability to work as part of a team and interact routinely with the scientific staff. Knowledge of some or all of the following instruments/systems are required: Tecan evo, Biomicrolab Volume Checker, Biomicrolab Tube Sorter 0-12 months of experience Education A Bachelor's degree with experience working in a scientific lab

Provides analytical support to local and networked groups. Analytical support activities include analytical method development, test procedure writing, analytical method qualification, method transfer and sample analysis with established methods. Analyzes process development, tech transfer, and/or small-scale qualification lab samples, pilot plant samples, and CRO production samples. Possesses extensive knowledge of various laboratory instruments like Waters UPLCs, HPLC. Desirable knowledge with Waters BioAccord, GC-MS, ProteinSimple Maurice (iCE, cGE). Qualifications Required Bachelor's degree needed 3 - 5 years relevant experience About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

WHO WE ARE ODDITY is a consumer tech company that builds and scales digital-first brands to disrupt the offline-dominated beauty and wellness industries. The company serves over 40 million users with its AI-driven online platform, deploying data science to identify consumer needs, and developing solutions in the form of beauty and wellness products. ODDITY owns IL MAKIAGE and SpoiledChild. ODDITY LABS is our cutting-edge biotechnology R&D center, powering science-backed product innovation through the discovery and development of new molecules, probiotics, peptides, and other biological modalities. Unlike pharmaceuticals, ingredient innovation in the beauty and wellness industry has remained stagnant for decades. We are deploying patented, proprietary technologies and capabilities, including AI-based molecule discovery and advanced phenotypic databases, to understand the biological mechanisms that drive cellular behavior and develop uniquely efficacious products for beauty and wellness applications. Innovations from the ODDITY LABS will power game-changing products through ODDITY's current brands, as well as future brands. ODDITY operates with business headquarters in New York City, an R&D center in Tel Aviv, Israel, and a biotechnology lab in Boston. Our culture is fast-paced, innovative, agile, and offers every team member the opportunity to drive a big impact. THE OPPORTUNITY We're looking to hire a passionate Sr. R&D Chemist, Pre-formulation & Delivery to add to the ODDITY LABS Product Development Team. In this role, you will play a crucial role in the formulation and topical delivery of novel molecules through industry-leading personal care products. Your responsibilities will include analyzing physiochemical properties (solubility, stability, etc.) of our proprietary molecules and improving, optimizing, and maximizing active loading of poorly soluble API's by developing, adapting, and executing techniques/methodologies of optimizing solubility, stability and deliverability of the compounds in formulation. This role will also contribute in other ways to support our high-performing team as part of an industry-leading biotech R&D team. In this role, you will: Be responsible for analyzing, validating, improving and maximizing the effective formulation loading and delivery of poorly soluble compounds, including but not limited to solvent/excipient optimization, physical/chemical modifications, and delivery enhancements. Develop methods, assays and tests to quantify and validate the properties (solubility, stability, etc.) and their improvements. Evaluate existing methodologies and adapt them for optimal use while developing and establishing novel methods for improving the solubility, stability and delivery of new molecules. Manage external resources and projects with Contract Research Organizations regarding topics related to solubility, stability, compatibility, delivery, formulation, etc. Maintain responsibility for all materials, instruments, and data analysis across multiple projects. Refine and continuously evolve existing pipelines to enable data-driven decision-making, acceleration through the proof-of-concept to product stages, and product validation pipelines. This includes, but is not limited to, developing micro and nano-scale assays to support pre-formulation decisions and operations. Develop and/or standardize protocols to support synthesis and scale-up. Stay apprised of new pharmaceutical and chemistry trends and implement new technologies that further enhance the capabilities of ODDITY LABS. Develop and present new concepts in partnership with ODDITY LABS / ODDITY leaders. Support up to 3 team members across their developments, providing feedback, coaching, and mentorship. Foster a culture of innovation and be a leader within ODDITY LABS and across ODDITY teams. WHO YOU ARE You are a PhD in Chemistry, Chemical Engineering, or directly related technical field. You have a minimum 5-10 years of industry experience (pharma, biotech, etc.) in chemistry (analytical, medicinal, organic, etc.) or related fields, with at least 4 years focusing on topical/non-topical API characterization, analysis, pre-formulation, solubility enhancement, and/or other active ingredient delivery methods directly related to the job description You have extensive knowledge of both organic chemistry and current pharmaceutical methods and techniques for improving and modulating solubility and deliverability. You are familiar with industry standard analytical and screening methodologies in this area and comfortable both developing, performing, and executing all necessary experiments and techniques, including but not limited to: liposomal encapsulation, nanoemulsions, cyclodextrin complexation, salt formulation, ultrasonic homogenization, etc. You are a hard worker with a high level of accountability. You own tasks from ideation to completion. You work well in a fast-paced environment. You are a strong problem solver with a deep curiosity and desire to tackle challenging topical and non-topical delivery challenges in a fast-shifting environment, using both first principles and whatever other resources are at your disposal You are excited about building and growing a team, creating an environment that supports your team's personal / professional development and strong performance. You have excellent written and verbal communications with experience working with a diverse range of stakeholders. You are adaptable and a team player, willing to go the extra mile and jump in on ad hoc tasks to support the overall company growth. WHAT WE OFFER Competitive compensation and benefits package. This position will consider and sponsor candidates on a visa (OPT, STEM OPT, H1B, TN). This position is in-office in our Cambridge, Massachusetts office and laboratory. The salary for this position is negotiable and commensurate with experience. Note: We're currently hiring for many roles! Not the right fit, but interested in another position? Contact us ********************* This position is hiring for start in November/December 2024.

Perform routine analytical tests on small molecule and polymer samples Analytical instrument maintenance and troubleshooting with guidance from senior scientists Contributes to multiple projects by providing analytical data and/or presenting results Collaboration with cross-functional teams (R&D, DE, Manufacturing, and Quality) Prepare and maintain technical documents including analytical test procedures, method development, and analytical findings Organizing lab supplies, chemicals, and test samples Fulfill all requirements of group, site, and company safety, ethics, and quality programs Qualification: BS or MS in Chemistry or related field Hands-on experience with analytical instruments such as LC, GC, IC, Titration, FT-IR, UV-vis, XRD, XRF, TGA, and DSC Good understanding of analytical chemistry and statistics Ability to quickly and effectively build relationships with cross-functional team members Excellent verbal and written communication skills Self-motivated, detail-oriented individual able to work in a fast-paced team environment

Salary Interval: Hourly The Middlesex Corporation is a nationally recognized and award-winning leader in the heavy civil construction industry. Since 1972, the family business founded by Robert W. Pereira has developed an extensive client and project list through its consistent efforts to safely build America's infrastructure. The Middlesex Corporation specializes in building and reconstructing highways, bridges, marine, rail, and transit facilities through its collaborative team approach and focus on core values. In addition, Middlesex Asphalt in Central Florida is one of the largest and most productive asphalt plants in the United States with Middlesex Paving earning an equally solid regional presence and reputation. Position Summary: We are seeking an experienced Quality Control Technician - Rail with proven leadership skills and a devoted work ethic who is looking for a successful career and the opportunity to grow with The Middlesex Corporation, a rapidly growing, successful, and well established heavy civil infrastructure company. As a Quality Control Technician - Rail, you will play a critical role in the overall leadership and successful and timely delivery of complex multimillion-dollar fast-track, complex heavy-civil, highway and bridge projects from pre-construction stage through project execution and completion. Responsibilities: Actively promote and carry out company Safety and Quality Policies and Procedures and ensure adherence to our The Middlesex Corporation's Core Values - “Safety First, In Everything We Do” and “Quality In All We Offer”. Actively participate in over-all day-today operational leadership and decision-making as the subject matter expert for all project quality management functions including self-performed work, materials or work performed by suppliers, vendors, subcontractors. Provide ongoing and regular quality control related technical input for construction planning, interpretation of design, development of efficient construction methods and quality controls processes for execution of the work. Manage and schedule all required quality testing, inspections and documentation including all third-party quality control related services. Manage the quality processes required per contract documents, specifications, drawings, engineering calcs for work activities such as crane/hoisting lifts, temporary works, falsework, shoring, formwork, safety systems, etc. Provide overall leadership to ensure work is constructed in compliance and work quality is accurately documented through clear and traceable record keeping and reporting. Develop and implement project specific Quality Control Plan that meets company policies, project requirements and is aligned with industry standards and best practices. Perform periodic audits to verify adherence to QA/QC Management Plan. Develop a comprehensive working knowledge of project contract documents, (drawings and specifications, and requirements by reference, etc. Maintain applicable industry reference standards and facilitate project access to relevant team members. Develop and implement a project Quality Control orientation program to ensure project team members are familiar with the requirements of the project QC Management Plan, and conduct to relevant project specific training, relative to Quality Control roles, responsibilities, processes, and procedures. Contribute to interpretation and dissemination and communication of project quality control requirements to relevant, staff including field crews and craft supervision. Assist in document management to ensure all project documents are updated and current to reflect any changes, revisions, etc. Assist in the procurement, buy-out, and management of subcontractors, suppliers/vendors to ensure subcontract /vendor agreements capture required quality related scope of work. Prepare and submit accurate Quality Control project status project reports. Manage project submittal process to ensure timely receipt, review and approval of submittals and shop drawings, as-builts, and other required documentation. Actively participate in RFI process to ensure timely receipt, review, response close out. Monitor project work for any non-compliance issues and ensure corrective measures are approved, executed and closed-out with documented acceptance. Manage project close-out including, timely management of punch list, commissioning, and transitional system operations turnover. Qualifications: Four-year engineering or construction management degree or equivalent combinations of technical training and relevant experience. Minimum of two (2) years of documented experience performing in a construction quality control management role on a heavy civil construction rail project. Comprehensive understanding of construction industry practices and standards as well as experience with supervision, estimating, scheduling, budget preparation and project status reporting. Experience utilizing project management software systems. Preferred Qualifications: Currently possess or the ability to attain; NETTCP Quality Assurance Technologist, and USACE Construction Quality Manager Certification. Heavy-Civil construction experience. We offer our full-time and eligible part time team members a comprehensive benefits package that's among the best in our industry. Benefits include medical, dental and vision plans covering eligible team members and dependents, employee assistance programs, life insurance, disability, top-tier 401k with matching, tuition reimbursement, industry leading referral program, and generous paid time off. Middlesex provides equal employment opportunities to all team members and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law. PI1709ad7b1760-26***********3

You've got problem-solving instincts, a passion for patient care, and the technical training to deliver quality results. You're also looking for great benefits, the support of an all-star team, and an opportunity to grow your career. Join our front line of #HealthcareHeroes! Our mission is to advance the health and wellbeing of our communities as a leader in clinical laboratory solutions. Quality is in our DNA -- is it in yours? This opportunity is part-time on second shift 3:30pm-12am. With a rotating Saturday and holiday schedule. Location: 10 Risho Ave East Providence, Rhode Island 02914 In this role, you will: Perform a vital part of the patient care process through moderate and high complexity testing Analyze, review, and report testing results Recognize when corrective action is needed and implement effective solutions Work in a fast-paced laboratory environment with biological and chemical hazards Champion safety, compliance, and quality control All you need is: ASCP certification or equivalent Associate or Bachelor of Science degree in Medical Technology; or Bachelor of Science in Chemical, Biological, or Physical Science with 1 year of Medical Technology training Clinical rotation in the MLS or MLT program completed Strong reading, writing, and analytical skills Ability to operate general laboratory equipment, including but not limited to: telephones, computers, automated analyzers, centrifuges, microscopes, manual and automated pipettes, and audible alarms. New MLS/MLT graduates encouraged to apply Bonus points if you've got: 2+ years of laboratory training or experience performing high complexity testing within area of specialty We'll give you: Appreciation for your work A feeling of satisfaction that you've helped people Opportunity to grow in your profession Free lab services for you and your dependents Work-life balance, including Paid Time Off and Paid Holidays Competitive benefits including medical, dental, and vision insurance Help saving for retirement, with a 401(k) plus a company match A sense of belonging - we're a community! We also want you to know: This role will have routine access to Protected Health Information (PHI). Employees will be trained on reasonable safeguards and are expected to maintain strict confidentiality, as well as abide by all applicable privacy and security standards. Employees are expected only to access PHI when it is required to fulfill job duties. Scheduled Weekly Hours: 20 Work Shift: Job Category: Laboratory Operations Company: East Side Clinical Laboratory, Inc. Sonic Healthcare USA is an equal opportunity employer that celebrates diversity and is committed to an inclusive workplace for all employees. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, age, national origin, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

How You Will Make an Impact: The Quality Control Inspector will inspect and ensure units are manufactured to sales agreement, as well as Morgan's engineering drawings, standards, and specifications. The Nuts and Bolts: Inspect and ensure all units are manufactured to sales agreement. Inspect and ensure all units are manufactured to Morgan's engineering drawings, standards, and specifications. Direct others within the work area to complete rework items. Conduct in-process quality audits and review standards and specification requirements with production supervisor when errors or defects are detected. Perform final inspection function per Morgan and Customer specification and standards. Work with manufacturing to ensure on-time delivery and budgetary goals are met. Direct and coordinate the quality process, provide continuous quality improvements, and ensure the integrity of Morgan's product quality, manufacturing, certification and release activities. Train the workforce on quality standards and specifications. Adhere to the company safety regulations and assist in the training and awareness of safety guidelines to new employees in the department. Maintain a clean, orderly and safe work environment. Perform other duties as required by management. Required Credentials: Previous experience in a quality control/quality assurance position. Prefer 3 years of experience in a manufacturing or a quality assurance environment. Clear and effective communication Skills. Ability to concentrate for extended periods of time and follow established safety and procedures. Computer experience using Microsoft Office. Preferred but not required: High school diploma or equivalent. You Must Be Able to: This job operates in a manufacturing plant environment. While performing the duties of this job, the team member is regularly required to talk or hear. The team member frequently is required to stand (sometimes for extended periods); walk; use hands to finger, handle or feel; and reach with hands and arms, and lift up to 35 pounds. The team member may, at times, sit, bend, stoop, squat, reach overhead, or crawl (may be in confined spaces). The QC Technician is expected to perform repetitive tasks with the team member's hands, and have the ability to climb ladders and/or work in high places. How We Make an Impact: Celebrating our 70th year as the largest truck body builder in North America, Morgan Truck Body LLC is proud to produce, deliver, and service quality products. With a foundation built on innovative design and quality construction, Morgan has experienced tremendous growth. In addition to dry freight truck bodies, Morgan specializes in satisfying unique and custom truck body needs, including electric vehicles, mobile service units, and refrigerated products, serving farmers, ranchers, contractors, landscapers, equipment and material haulers, and more! Our shared values are the foundation upon which Morgan does business: people integrity results passion Some of Our Total Rewards We offer big company perks with small company culture: Comprehensive benefits package including Medical, Dental, Vision, and Life 401(k) Savings Plan with Company Match Tuition Reimbursement Paid holidays and increasing vacation time with years of service Generous Footwear and Eyewear Reimbursement Programs Paid Job and Leadership Development training Morgan Truck Body LLC is a business unit of the J.B. Poindexter & Co., Inc. family and provides equal employment opportunities to all team members 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. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Whether you are just beginning your career or taking the “next step,” please visit our careers page *************************** #LI-TK1 #VIQ PandoLogic. Category:Quality Control, Keywords:Quality Control / Quality Assurance Technician, Location:Putnam, CT-06260

**Profile insights** Find out how your skills align with the job description **Skills** Do you have experience in **Laboratory experience** **Education** Do you have a **High school diploma or GED** * 401(k) 5% Match * 401(k) matching * Dental insurance * Health insurance * On-the-job training * Opportunities for advancement * Pet insurance

As a Medical Laboratory Technician (MLT) in the Microbiology Dept. at IDEXX, you will be a key contributor at one of the largest veterinary diagnostic companies in the world. You will perform laboratory testing that helps veterinarians diagnose and treat pets. You will join a fast-paced work environment that encourages teamwork, quality, and offers opportunities for personal growth. This is a full-time role with competitive benefits. Want to see what it is like to work in our lab? Check out these videos from our lab employees talking about working at IDEXX: ****************************** Development Opportunities in Labs for Mallory Cormier, Senior Labs Lead Why Taylor Gardner, Medical Laboratory Technician, Chose IDEXX IDEXX reference laboratories is a global network united by a shared commitment to enhancing pet care where the true strength in our name is the people behind it. Our reference laboratories make it possible for our customers to discover more with our unrelenting commitment to innovation, personalized support, guidance, and expertise, while providing the most complete and advanced menu of diagnostic tests along with technology and tools. In This Role: You will be using automated analyzers, microscopes and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries and diseases in support of veterinarian animal treatment. You will be performing diagnostic tests on blood, urine, fecal or pet biopsy samples that we receive in our lab by the thousands, every day. You will be responsible for setting up and running lab tests and reading and releasing results according to SOPs (Standard Operating Procedures). You can expect to specialize in the following area: Microbiology Processing clinical samples for the identification of bacteria and fungi using automated and manual methods. What You'll Need to Succeed: Ideally, you will have experience setting up, running, and reading lab tests, and operating laboratory equipment (microscopes, pipetting and / or clinical diagnostic analyzers). You have experience with diagnostic microbiology testing. You must have experience in culture reading You have a positive attitude and love to bring that energy into the lab every day to support your colleagues You are looking forward to working in a team You concentrate on the details and can work reliably and precisely You have a great sense of team spirit and responsibility You possess a High School diploma or equivalent combination of education and experience is required. A 2-, 3- or 4-year degree in a Science-related field is preferred. It is not required to work in our lab, but if you were a Veterinary Technician (RVT, LVT, CVT) or Medical Laboratory Technician (MLT or MT), this experience and education would be a plus. Able to meet the physical requirements that go with working in a lab - standing and sitting for extended periods of time, phone & computer use, extended reach, lifting up to 50lb, and specific vision ability - close, color, depth perception, and ability to adjust focus. This is a laboratory, so there is potential exposure to biohazards, agents known to cause zoonotic diseases, and hazardous chemicals. What You Can Expect From Us: Competitive Hourly Pay Opportunity for annual cash bonus and merit pay increase consideration Health / Dental / Vision Benefits Day - One 5% matching 401k On the job training and career advancement opportunities Additional benefits including but not limited to financial support, pet insurance, mental health resources, volunteer paid days off, employee stock program, foundation donation matching, and much more! Opportunity to do meaningful work where you positively impact the lives of people and pets all over the world This is a benefitted position (not contingent or temporary) Schedule: The schedule for this position is: Monday-Friday, every other Saturday (when working a Saturday, then you will have a day off during the week) The hours of this position are: 9:30am-6:00pm Hourly pay is targeting: $32 -34 / hr but based on experience level Hours have the ability to be flexible for a highly experienced candidate The shifts and hours may vary slightly depending on business needs. Reliable and dependable attendance is an essential function of the position. Why IDEXX? We're proud of the work we do, because our work matters. An innovation leader in every industry we serve, we follow our Purpose and Guiding Principles to help pet owners worldwide keep their companion animals healthy and happy, to ensure safe drinking water for billions, and to help farmers protect livestock and poultry from disease. We have customers in over 175 countries and a global workforce of over 10,000 talented people. So, what does that mean for you? We enrich the livelihoods of our employees with a positive and respectful work culture that embraces challenges and encourages learning and discovery. At IDEXX, you will be supported by competitive compensation, incentives, and benefits while enjoying purposeful work that drives improvement. Let's pursue what matters together. IDEXX values a diverse workforce and workplace and strongly encourages women, people of color, LGBTQ+ individuals, people with disabilities, members of ethnic minorities, foreign-born residents, and veterans to apply. IDEXX is an equal opportunity employer. Applicants will not be discriminated against because of race, color, creed, sex, sexual orientation, gender identity or expression, age, religion, national origin, citizenship status, disability, ancestry, marital status, veteran status, medical condition, or any protected category prohibited by local, state, or federal laws. This Medical Laboratory Technician (MLT) position will be based out of our North Grafton, MA location. Does this sound like the opportunity for you? Apply today! #LI-JF1 #IND-LAB

Quality Control Analyst - Contract - Cambridge, MA Proclinical is seeking a Quality Control Analyst for a contract role in Cambridge, MA. Primary Responsibilities: The successful candidate will be responsible for ensuring the completeness, consistency, and accuracy of regulatory filings, laboratory data, and reports. This role offers flexibility for remote work, with some on-site presence expected. Occasional travel to CMO/CTL sites may also be required. Skills & Requirements: Degree in chemistry, biology, biochemistry, or a related scientific field. Experience in a GMP Quality Control function within the pharmaceutical/biotech industry. Knowledge of method transfer and analytical method implementation. Strong technical writing skills, particularly for investigations. Proficient in data analysis and interpretation with excellent attention to detail. Solid problem-solving skills and experience in conducting investigations and implementing CAPA. Strong organizational skills with the ability to manage multiple tasks autonomously. Excellent communication and teamwork abilities. Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred. The Quality Control Analyst's responsibilities will be: Verify the integrity and traceability of regulatory dossier sections. Review regulatory dossier sections against associated reference methods and reports for accuracy. Review analytical data for accuracy and completeness. Ensure data integrity in laboratory notebooks, worksheets, logbooks, and electronic data. Review complex notebooks involving analytical method validation, verification, and transfer testing. Ensure electronic data generation follows applicable procedures. Discuss necessary corrections to analytical data or reports with clients. Adhere to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). Consult with management regarding assignment priorities and communicate any deviations/discrepancies. Provide feedback and suggest improvements to the review process. Perform additional duties as assigned by management. If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at a.maldonado@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.

6 Month Contract Norwood, MA PR: $30-35/hour Shift: 3rd shift, 10pm - 8am, Mon - Fri Seeking a contract role in Quality Control Sample Management Associate II based at their Norwood, MA site. The individual in this role will perform cGMP QC sample management activities for QC Chemistry, Microbiology, Bioassay, and various Development labs. Job Responsibilities Sample coordination including cross functional collaboration with internal and external labs Receipt, processing, distribution and shipment of the following sample types: In-Process, DS, Formulation and DP Equipment cleaning Stability Raw Materials Coordinating domestic and international sample shipments Communication with external Contract Test Labs (CTLs) Interact with Development teams in a GMP compliant manner Inspect product and raw material retention samples LIMS (LabVantage) sample logging and result entry AQL visual inspection of drug product Stability program support Controlled temperature unit management, maintenance and troubleshooting Clean room gowning Managing/stocking of QC lab supplies Write/revise SOPs, protocols and reports Complete and maintain cGMP documentation for work performed Participate in authoring quality systems records such as deviations, change controls, CAPAs. Support non-conformance investigations Establish and maintain a safe laboratory working environment This position will support first shift QC Sample Management operations at Moderna, Wednesday through Saturday Additional duties as may be assigned from time to time Education & Qualifications Education: Bachelor's degree in a relevant scientific discipline Experience: At least two years in a cGMP laboratory setting Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations. General laboratory operations (Pipette and analytical balance use.) Strong technical writing skill Proficiency with Microsoft Office Programs Quick learner with electronic databases (e.g. LIMS, SAP, LMS) Strong written and oral communication skills as well as organizational skills General knowledge of industry standards and guidelines for quality control laboratory operation Demonstrated ability to work effectively under established guidelines and instructions Ability to collaborate effectively in a dynamic, cross-functional matrix environment. Be able to follow the relevant Standard Operation Procedures as written. Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment. A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.