Quality Control Technician Jobs in Gloucester, NJ

LHH Recruitment Solutions has Quality Control Specialist opening for our client in the Conshohocken, PA area. This direct hire role allows you to collaborate with numerous departments to facilitate quality control and process improvement. This on-site position requires a bachelor's degree in Biological Science or similar, and 1+ years in a medical device manufacturing role. Ideal candidates will have experience in FDA, AATB and other applicable regulations and standards. Salary range: $25.00 - $28.00 per hour RESPONSIBILITIES: Inspect HCT/P products in accordance with standard operating procedures and regulatory requirements. Per organization, FDA and AATB. Define, sort, and document acceptable and unacceptable HCT/P products and/or medical devices. Prepare, create and document shipping documents and packages in accordance with standard operating procedures. Maintain a constant working knowledge of FDA 21 CFR 1271, FDA 21 CFR 820, AATB, other regulations and industry standards Communicate and escalate inspection or quality control issues to management/Quality Control as necessary. Initiate, review and document quality control records to include environmental monitoring, and HCT/P inspection. Support and collaborate on internal and external audits. File and maintain records in accordance with standard operating procedures and regulations and recordkeeping. Create, implement and present reports regarding any issues of products or processes, daily production quality, quality trends. Create and review case studies or regulatory standards and trends to stay abreast of issues in the field of quality control and quality assurance. REQUIREMENTS: Bachelor's degree in a relevant Biological Sciences or Similar and 1+ years manufacturing experience in medical device industry. Proven experience in FDA, AATB and other applicable regulations and standards. Proven ability to oversee multiple priorities and make sound business decisions. Knowledge of the practical application of engineering science and technology - applying principles, techniques, procedures, and equipment to design and production. QMS systems experience highly preferred.

Compensation: $33.75/hr to $39.50/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Healthcare benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, financial protection benefits, as well as HSA, FSA, and DCFSA account options. 401k retirement account access is offered starting on the 90th day with employer matching after one year of service. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Required Skills & Experience -Minimum one year of relevant GMP work experience in a lab setting -Bachelor degree in Biology or Chemistry -Working experience in a current Good Manufacturing Practices (cGMP) compliant QC laboratory or equivalent environment and solid understanding of cGMP and current Good Laboratory Practices (GLPs) -Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories such as qPCR, cell culture, Flow Cytometry, and/or ELISA -Ability to read/interpret technical documents such as SOPs, work instructions, test methods and protocols -Proficient with Microsoft Office applications Nice to Have Skills & Experience -1 year of experience working with mammalian cell culture -CAR-T, Cell and Gene Therapy, or Biochemistry laboratory experience -Basic knowledge of Compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC -Ability to complete equipment and software qualification protocols -Experience developing and setting long-term objectives -Experience working in Biosafety Level lab (BSL 2, BSL2+) or aseptic facility -Knowledge of EU/FDA guidance Job Description The QC CRS Analyst is responsible for conducting biochemical and testing of raw material, in-process, final product release and characterization samples, including CAR-T. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 5 -- 10 other Analysts within a functional Clinical Release and Stability Laboratory and report to the Senior QC Supervisor. Key Responsibilities: -Conduct analytical biological testing of clinical and commercial drug product/drug substance samples -Perform peer reviews and approvals of laboratory data -Use electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing including application of statistical concepts to laboratory data -Support of New Product Initiatives (NPI) including owning a project and perform project management functions with limited to no coaching from supervision/management -Perform Instrument Calibration and Preventative Maintenance -Update CRS-owned documents using the Document Management System (DMS) -Order/receive supplies and manage inventory -Support analytical method qualification, validation, and transfer into and out of the QC lab, owning change control actions, completing testing activities with mentorship from Sr. Analysts on transfer activities -Complete change control processes to integrate new methodologies and technologies into and out of the CRS Lab with limited oversight -Act as a peer subject matter expert in assessing talent by participating in panel interviews for job -Complete invalid assay and general laboratory investigation records -Complete corrective and preventative actions (CAPA) as assigned -Assist in the execution of internal audits

Contract to hire: $38/hr Essential Functions and Responsibilities Performs deviation investigations for all areas within Quality Control Perform out of specification investigations with an emphasis on QC analytical assays (flow cytometry, ELISA, and other cell-based assays) and microbiology assays Work cross-functionally to create relevant corrective/preventative actions (CAPA). Support maintenance of a database in support of QC metrics and KPI's. Revise quality documents in support of deviation mitigation and/or CAPAs. Support programs to improve on-time closure rates for all quality records Other responsibilities as determined. Required Education, Skills, and Knowledge Bachelor's degree in a relevant discipline (biological sciences or equivalent) 1-3 years of experience in the biopharmaceutical industry within a cGMP Quality Control role Basic knowledge of biological drug development with respect to Quality Control Extremely detail-oriented with strong analytical, written, and verbal communication skills Demonstrate sense of urgency; ability to recognize time sensitivity Flexible and adaptable style with an eagerness to take on challenges Preferred Education, Skills, and Knowledge Experience with cell and/or gene therapy products GMP regulated laboratory experience Knowledge of investigation writing The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation. Physical Demands and Activities Required: Must be able to Sit for an extended amount of time in front of the computer or biological safety cabinet Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadline Work Environment: This position will work in both an office and a manufacturing lab setting. When in the lab, must be able to work in Lab setting with various chemical/biochemical exposures, including latex and bleach. Able to work in cleanroom with biohazards, human blood components, and chemicals. Potential exposure to noise and equipment hazards and strong odors.

At RxSource, our passion drives us to be the bridge between pharma and patient. With offices in Canada, USA and Ireland we provide bespoke global clinical trial supply management services to pharma, biotech and CROs. Whether it's employing demand-led packaging, a local sourcing model or another flexible option, we guarantee on-time delivery without compromising quality. Our clients are our partners; success for them = success for us. We currently have an opening for a Quality Control Associate at our West Deptford, New Jersey facility. This role is a key position within our global Quality Assurance team and will be responsible for performing on-site quality activities. If you are a personable and proactive Quality professional with experience in clinical trial packaging and labelling, pharma manufacturing or pharma distribution, we would like to hear from you. What you will do: Release incoming goods Perform in-process and finished good quality inspections Initiate Quality Management System documentation (i.e. Deviation, CAPA, Change Control, etc.) Review batch records pre- and post-execution Perform periodic quality walkthrough inspections to verify compliance with SOPs Participate in process improvement initiatives Manage all controlled GMP documentation and document archives Assist with supplier and customer verification/qualification and approval Provide support for customer and regulatory inspections Review daily/weekly checks (e.g., temperature, sanitation, etc.) and facility maintenance reports Assist with facility qualification activities Your qualifications, skills and experience include: 2 or more years in a QA or QC role, clinical trial packaging or pharmaceutical manufacturing/distribution Working knowledge of Good Manufacturing Practices A degree or diploma from a recognized college or university Strong written and verbal communication skills Ability to prioritize Team player who works well with others A commitment to providing excellent internal and external customer service No matter your role at RxSource, successful team members are: Patient Champions, who put patients first and uphold strict ethical standards Achievers, who drive toward practical solutions Individuals Who Inspire Excellence in themselves and those around them High-quality and accountable executors, working towards goals and milestones with quality, precision, and speed

Supplemental Health Care is seeking a travel Cath Lab Technologist for a travel job in Philadelphia, Pennsylvania. & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: ASAP Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel Job Description: Supplemental Health Care has been named Best in Staffing based on real feedback from our working healthcare professionals, Supplemental Health Care is proud to be a partner to every person we work with. For our Cath Lab Technologists, that means experienced support from our dedicated recruiters to assist you in every step of finding your next job. We're currently hiring in Philadelphia, Pennsylvania to support hospitals in need of Cath Lab Techs. Cath Lab Technologist Contract Details: $2,280 - $2,536 per week 13-week contract with possibility to extend Hospital Setting Weekly pay Travel pay packages including housing and meals allowance are available Cardiology Technicians will be required to: Monitor patients' vital signs during tests Work with various types of cardiac equipment Assist in administration of catheterization Management of supplies and devices If you'd like more detail on this Cath Lab Tech assignment or are ready to get started with the placement process, please apply online now. Our team is standing by to respond as quickly as possible. Supplemental Health Care offers a wide variety of industry-leading benefits including: Full medical, dental, vision, life, and even pet insurance to provide you with the coverage you need whenever you need it. Round the clock support. No matter where you are or what time it is, Supplemental Health Care is standing by. Our Share the Care program is the most dynamic, profitable referral program in the industry. To learn more about Share the Care, check out shccares.com/referrals. SHC offers a 401k Retirement Savings Program to both full-time and part-time employees with a wide range of investment options. Discounted and free online access to CEU courses through Supplemental University. Through our online CEU options, you have access to the courses you need on your schedule. Requirements: ARRT American Heart Association BLS Minimum 1 year of Cath Lab experience Attention to detail and strong communication skills Supplemental Health Care will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable local, state, or federal law (including San Francisco Ordinance #131192, Los Angeles Municipal Code 189.00, the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act). For this type of employment, Kentucky state law requires a criminal record check as a condition of employment. For a copy of the Supplemental Health Care Privacy Policy, please visit Supplemental Health Care Job ID #1331199. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Cardiac Cath Lab Technologist About Supplemental Health Care At Supplemental Health Care, a simple belief in the power of caring guides a unique commitment to world-class service in healthcare staffing. For 40 years, we've supported talented professionals pursuing their life calling in hospitals, schools, home health, corrections, behavioral health, and other settings. At SHC, we inspire vital connections and enrich lives and inspire better outcomes. As recipients of the Best in Staffing Awards for both Client and Talent, Supplemental Health Care is proud to be among only 2% of staffing companies singled out for the distinction based on the real feedback of our employees and the clients we serve. SHC has also earned The Joint Commission's Gold Seal of Approval and is named among the Largest Health Care Staffing companies in the United States by Staffing Industry Analysts. We are also thrilled to recognize our very own SLP, Dr. Kelly Byrd as the American Staffing Association 2024 National Staffing Employee of the Year and Health Care Sector All-Star. We're honored to connect Dr. Byrd to employment, share her incredible story, and support her family literacy nonprofit. For everyone that we serve, SHC is the place where caring hearts thrive. Benefits Referral bonus Benefits start day 1 401k retirement plan Continuing Education Discount program Health savings account

AnalytiChem is a global company founded in 2021 that assists analytical testing laboratories in the industrial, environmental, and materials markets to collect actionable data to optimize their business. Our mission is to enable our customers' science by providing a solutions-oriented and integrated range of products that help them collect their best data. We are experiencing rapid growth, both organically and through acquisition, with 8 companies worldwide and counting. Our brands include SCP Science, Chem Service, Bernd Kraft, OREAS, Chem-Lab, Northeast Laboratories and BioTRADING and we support customers in a wide range of industries from Industrial to environmental and animal health. If you are looking for a dynamic work environment in a fast-growing organization where you can make a difference, AnalytiChem might be the challenge you are seeking. What will you do We are looking for a reliable Quality Control Chemist to ensure that all external and internal requirements for production of chemical reference materials are met before our high-quality product reaches our customers, while managing a team of two (2) quality control analysts. You will be responsible for developing and performing various tests on candidate reference materials, including techniques such as Gas Chromatography (GC-FID & GC-MS), HPLC, FT-IR, pH-testing, UV absorption testing and alike. An excellent Quality Control Supervisor is highly experienced in various instrumental and wet chemical testing methods and passionate about top quality products. The goal is to assure the high quality of our operations and services aiming to the long-term success of our business. Your main skills Plan and perform quality control inspections on candidate reference materials Define standard methods and their acceptance criteria for analysis of CRM Perform HPLC, GC, UV, FT-IR and similar instrumental QC tests Perform titrations, pH-tests and other wet-chemistry tests Document results in lab notebooks and ERP systems Perform Proficiency Tests to demonstrate the lab competence Writing standards operating procedures and method documentations. Handle all non-conformities and corrective actions Communicate with external quality assurance officers and assessors during on-site inspections What we are looking for Proven experience as a quality control analyst or similar relevant role Thorough knowledge (min 3 years) of methodologies of quality testing techniques and methods Experience handling Reference Materials according to ISO 17025 and/or ISO 17034. Good knowledge of MS Office Good communication skills Great attention to detail and a results driven approach Reliable and Trustworthy BSc/BA in Chemistry or another relevant field

Duration: 03 Months (with a possibility of extension) Client: One of the largest Aerospace and Defense companies We are looking for an Inspector who perform routine visual and dimensional inspection operations on sub-assemblies, completed assemblies and work in-process. Duties: Perform highly repetitive visual/dimensional inspection operations on a select number of vendor supplied mechanical and electronic components. Perform visual, mechanical and electrical inspection operations and basic functional tests on a select number of vendor supplied mechanical and electronic components. Work from wiring diagrams, assembly drawings, specifications, and general instructions to perform in-process inspection duties. Follow detailed instructions and refer to inspection procedures to perform basic receiving inspection duties. Perform basic receiving inspection/in-process inspection duties with limited instructions and direction of supervisor or working leader. Visually inspect PCB assemblies for use in telemetry systems and other electronic equipment. Check and inspect electrical wiring connections and general component layouts for compliance with applicable drawing and specifications. Prepare and complete inspection forms/reports and records. Verify identification and proper mounting of components. Detect and report any operating difficulties or questionable conditions to your supervisor. Maintain work area and equipment in a clean and orderly condition. Follow prescribed safety regulations. Perform other related duties assigned by supervisor. Qualifications: High School Diploma or GED A minimum of 1 yrs. experience in Quality inspection of electronic components and in-process inspection of electronic printed circuit boards and assemblies. Ability to obtain required certifications: IPC-A-610 Acceptability of Electronic Assemblies Certification, IPC J-STD-001 Requirements for Soldered Electrical and Electronic Assemblies (Inspection module only). Certifications will be required no later than (2) weeks after being hired. Ability to read drawings and use standard measuring tools/instruments; Ability to use basic arithmetic including decimals and fractions. Basic computer skills required for data entry. Physical requirements of the job position requires the individual to have the ability to lift various items up to 50 lbs in weight. Ability to communicate and interface on various Quality related subjects daily.

Perform assay co-qualification, validation, and technical transfer of updated and new assays, as well as potential new products. Act as subject matter expert (SME) and train new laboratory personnel on assays. Perform all activities with respect to GMP/GDP compliance. Qualifications: Bachelor's degree in Biology, Biochemistry, Microbiology, Chemistry, or related scientific field or equivalent combination of education and experience. Minimum three (3) years of GMP experience in the pharmaceutical industry within a Quality Control Solid understanding and functional knowledge with hands-on experience with two (2) or more of the following: endotoxin, mycoplasma, bioburden, sterility. Experience in technical writing (e.g., technical reports, test methods, SOPs, protocols, deviations, CAPAs, change controls, etc.) Pay Scale: $115,000 - $125,000 ( Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer.

The Quality Technician in microbiology aseptic processes ensures products meet microbiological standards and are manufactured in a sterile environment. This role monitors quality assurance standards and encourages the team to consistently deliver excellent results. The Quality Technician is responsible for executing best practices, goals, and established standards for the team. Primary Responsibilities Perform tests to identify harmful microorganisms, maintain a sterile environment, and ensure regulatory compliance Document and analyze test results following good laboratory practices for microbiology and quality control laboratories Identify and address production issues, contributing to corrective action Inspect work daily, maintain cleanliness, organize supplies, and assemble sterile products using aseptic technique Handle biohazard spills, train new hires, and demonstrate the use of cleaning chemicals Uphold quality standards, follow GFSI, HACCP, and GMP guidelines, and participate in food safety inspections Support sanitation operations, monitor performance, and provide report Address customer complaints, conduct audits, and contribute to quality assurance improvements Promote continual improvement and collaborate on cross-functional projects Perform routine environmental monitoring within cleanrooms and production areas to detect microbial contamination Conduct microbiological assays on raw materials, in-process samples, and finished products using various techniques Accurately record and interpret test results, maintaining detailed documentation of activities, including deviations, investigations, and corrective actions Participate in investigations for out-of-specification (OOS) results, deviations, and complaints related to microbiology testing Ensure proper calibration and maintenance of laboratory equipment used for microbiological analysis and QC testing Prior Knowledge/Experience Bachelor's Degree in Microbiology, Biology, or related field 1-3 years of experience in quality; food processing experience preferred Strong understanding of aseptic techniques and microbiology principles Experience with various microbiological testing methods, including plate counting, membrane filtration, and rapid microbial detection Proficiency in data analysis, documentation, and recordkeeping Excellent attention to detail; ability to work independently and in team environments Familiarity with GMP regulations and quality systems Ability to utilize provided PPE - safety glasses, ear plugs/muffs, bump caps, dust masks, company uniform, safety shoes Ability to be respirator certified if required Physical ability to sit, stand, walk, climb, stoop for up to 8 hours; lift 55 lbs consistently; lift/hold objects overhead for extended periods Ability to climb and work on a 40-foot extension ladder for extended periods as needed; work at heights up to 50 feet Ability to maneuver and work in confined areas with variations in temperature, humidity, and air quality The following common allergens are processed in our facilities: wheat, eggs, dairy, and soy. Looking for a Career for Good? Puratos is a global purpose-driven company focused on bringing people together through food innovation for good. We offer a full range of innovative food ingredients and services for the bakery, patisserie, and chocolate sectors, serving artisans, retailers, industrial and food service companies in over 100 countries around the world. Our passion for innovation, pioneering spirit, and core values continue to propel our global ambitions. This coupled with our commitment to our communities is what makes working at Puratos so magical. We offer a competitive compensation and benefit package, designed to promote a Happier, Healthier You. This includes: Insurance coverage beginning the first of the month-no extra waiting period to get started Immediate 401(k) eligibility including a fully vested matching contribution Receive over 5 weeks total of paid time off within your first year of service Free life coaches, convenient onsite health exams, 24/7 access to Registered Nurses Puratos-paid insurance coverage to protect you and your family including Life and Disability insurance If you are a solution oriented and analytical thinker with a passion for leading and inspiring people, we invite you to experience the magic of being yourself and join us for “a career for good.”

Quality Technician- Pennsauken NJ (near Philadelphia) Job Summary: The primary responsibility of this role is to perform analytical and microbiological testing using established methodologies to ensure that all products meet food safety, quality specifications, and aseptic requirements. This includes testing finished goods, in-process items, and conducting equipment swabbing. The role utilizes approved laboratory techniques and performs complex calculations to ensure timely and accurate results. Key Responsibilities: (Other duties may be assigned as necessary) Monitor and verify food safety preventive controls and critical factors (e.g., thermal process, sterilization) to ensure compliance. Perform package checks on production lines, ensuring that quality standards are met, and report any issues to QA management. Support testing of new or revised product formulas and packaging materials to ensure their safety and compliance. Conduct Pre-Operational Inspections, cleaning verification swabs, and allergen swabs as part of quality assurance processes. Educate and support team members on food safety responsibilities and best practices for good manufacturing procedures. Analyze data to identify trends and patterns, leading continuous improvement efforts and projects to enhance product and process quality. Place non-conforming products on hold, troubleshoot issues, and collaborate with leadership to investigate, determine root cause, and identify non-conforming product range. Education/Experience: High school diploma or general education degree (GED) required. Associate's or Bachelor's degree preferred. Experience in manufacturing quality assurance in a highly regulated environment such as food or pharmaceutical manufacturing, preferred not required.

Packaging and Labeling Design Specialist & Inventory Manager Are you ready to grow your career in a fast-paced environment with cross-functional collaboration great opportunities for advancement? Come join a dynamic team with 5 production facilities located in New Jersey, Massachusetts and California. Our client is looking for a detail-oriented Packaging and Labeling Design Specialist & Inventory Manager to develop and implement innovative and compliant packaging and labeling solutions - while also overseeing the management of packaging/labeling inventory. In this role you will regularly collaborate with the Quality Assurance (QA) team to ensure that packaging designs meet customer requirements, company specifications, and regulatory and quality standards. Other responsibilities include managing packaging materials, ensuring product inventory accuracy, and supporting QA efforts in product testing and batch quality control. Key Responsibilities: Packaging and Labeling Design Design & Development Regulatory Compliance Material Selection Labeling Accuracy Prototyping and Testing Syndigo Content Management Inventory Management Inventory Control Stock Rotation Batch Management Supply Chain Collaboration Collaboration with QA Team Quality Assurance Coordination Documentation and Records Product Testing Support Continuous Improvement Required Qualifications: Bachelor's degree in Graphic Design, Packaging Engineering, Supply Chain Management, or related field. 2+ years of experience in packaging design, labeling, or inventory management. Previous experience working with Quality Assurance teams in a manufacturing or production environment is preferred. Knowledge of relevant regulatory requirements for packaging and labeling (FDA, MSC, BAP, ISO, etc.). Strong proficiency in design software (e.g., Adobe Illustrator, Photoshop, CAD software). Familiarity with inventory management systems (e.g., Navision, or other ERP software). Attention to detail and ability to identify compliance issues or potential defects. Strong communication skills for effective cross-functional collaboration with design, QA, production, and logistics teams. Preferred Qualifications: Experience in sustainable packaging solutions and eco-friendly materials. Knowledge of supply chain best practices and inventory optimization techniques. Don't let this opportunity pass you by - this challenging and rewarding opportunity could be yours if you apply today! The above requirements and qualifications are meant to describe the general nature of the position and do not represent all duties to be performed by the selected candidate. Please note that only candidates who are under consideration for the position will be contacted. The Company is an equal opportunity employer. All employment is decided on basis of qualifications, merit, and business needs without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or veteran or disability status.

DIRECT HIRE MUST HAVES: Bachelor's degree in a relevant discipline (biological sciences or equivalent) Minimum (5) years of experience in the biopharmaceutical industry within a cGMP Quality Control role Overview Senior Quality Control Specialist, QC Operations Strategy will be responsible for planning and managing projects with minimal oversight, utilizing principles and methodologies from Lean, Six Sigma, and Project Management to drive continuous improvement for all QC functional areas, and the creation and maintenance of QC workforce models to ensure patient demand is met. T This role is responsible for identifying and driving continuous improvement in collaboration with QC functional areas, and the creation and maintenance of the QC workforce models to ensure patient demand is met. This position is also responsible for maintaining knowledge of lean labs principles and various operational excellence strategies within the department by providing lean focused leadership, training, coaching, and mentorship to QC personnel. The Senior Quality Control Specialist, QC Operations Strategy must have experience with lean labs, different operational excellence concepts, tier governance, workforce modeling and planning, and be a highly collaborative team player who works well in dynamic environments. Essential Functions and Responsibilities Drive deployment, hypercare, change management, and maintenance of ongoing lean labs implementation in Quality Control. Build and maintain QC workforce models. Utilize SME knowledge of lean methodologies to collaborate with QC leadership to define strategy, plan, and oversee the execution of key initiatives that deliver significant business value. Collaborate with other continuous improvement professionals to cascade needs and projects throughout the business and achieve solutions that drive positive business results. Collaborate closely with the Senior Manager, Quality Control, Operations Strategy as well as other QC functions to strategically plan future projects such as new product introduction, laboratory capacity planning, facility transfers and expansions, and other pipeline projects. Develop and upkeep planning tools to allow for site growth within the quality control organization such as headcount capacity models for increased manufacturing capabilities and onboarding of new quality control assays, tests, and processes that contribute to the release of lots and materials. Facilitate the deployment, hypercare, change management, and maintenance of new and ongoing lean labs implementation in Quality Control. Collect and analyze data from QC workforce models to allow for opportunity identification, solution development, and sustainability. Monitor and routinely evaluate KPIs, metrics, heat maps, and A3s to measure performance of quality functional areas. Act as subject matter expert to QC's lean capabilities by facilitating training and coaching of problem solving using the lean tool kit. Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations. Must adhere to Iovance Biotherapeutics' core values, policies, procedures, and business ethics. Perform miscellaneous duties as assigned. Required Education, Skills, and Knowledge Bachelor's degree in a relevant discipline (biological sciences or equivalent) Minimum (5) years of experience in the biopharmaceutical industry within a cGMP Quality Control role Experience with different operational excellence concepts including (but not limited to) lean labs, lean practioner, tier governance, coaching kata, gemba walks, job instruction, Kaizen, A3 problem solving, change management, leader standard work. Fundamental knowledge of Quality Control operational and laboratory practices including, but not limited to, microbiology, analytical testing, sample management, quality records, and training. Advanced proficiency in MS Office (Word, Excel, PowerPoint, Visio) Successfully interface with multi-disciplined teams in a global setting Extremely detail-oriented with strong written, and verbal communication skills Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity Advanced strategic planning and implementation Demonstrate sense of urgency; ability to recognize time sensitivity Flexible and adaptable style with an eagerness to take on challenges Problem solver who not only identifies issues but leads efforts to resolve them

Avo Photonics is a dynamic contract engineering services company that designs, develops, and manufactures custom opto-electronic products for a large customer base. We seek a diligent, dedicated, and meticulous person who will help further our success and reputation in the industry. The successful candidate will have at least three years of manufacturing experience. Responsibilities: Support Process Engineering team by assembling prototypes and provide critical feedback on process viability for manufacturing Perform directed design of experiments; record structured data against controlled experiments and generate reports on procedure and results Perform documented performance checks, calibrations, and preventative maintenance on equipment including laser welders, seam sealers, die bonders, wire bonders, and more Collect measurements to ensure workstations are meeting ESD and cleanroom standards Review work instructions and provide training on developed processes to Manufacturing team Troubleshoot equipment and optical workstations to quickly resolve authorized production-impacting issues Requirements: A.S. (B.S. preferred) in the Sciences or Engineering 3 years of manufacturing experience 2 years experience in an engineer facing role Excellent communication skills and willingness to learn Avo Photonics offers competitive salaries and a comprehensive benefits package. Avo Photonics is not accepting unsolicited assistance from search firms for this employment opportunity. All resumes submitted by search firms to any employee of Avo Photonics by any method without a valid written contract in place with Avo Photonics will be deemed the sole property of Avo Photonics. No fee will be paid in the event the candidate is hired by Avo Photonics as a result of the referral or through any other means.

Core Group Resources is America's leading recruitment company. Founded by a service academy graduate who has offshore experience, Core Group Resources' expertise is unmatched in the marine offshore market, finance, IT, renewables, & non-profit for executive search, staffing, and expertise identification.*Marine QA/QC Coordinator Job Summary* We are seeking a qualified Marine Quality Assurance/Quality Control (QA/QC) Coordinator to support its expanding Vessel Construction Management (VCM) projects. This role focuses on ensuring shipyard QA/QC materials and processes meet contract specifications, industry standards, and published drawings. *Marine QA/QC Coordinator Responsibilities* * Oversee shipyard QA/QC materials and processes to ensure compliance with specifications and standards. * Conduct internal audits and monitor shipyard QA programs for quality oversight. * Identify deficiencies in workmanship, materials, and construction quality, coordinating corrective actions. * Promote a safety-first culture, ensuring compliance with industry and internal safety standards. * Maintain accurate documentation of inspections, KPIs, non-conformance issues, and corrective actions. * Support process improvements and administrative functions within the VCM team. * Coordinate the installation and integration of Owner Furnished Equipment (OFE) with shipyard personnel, subcontractors, and vendors. * Conduct periodic inspections to verify compliance with construction specifications. * Assist with meeting coordination, documentation, and assume administrative responsibilities in the absence of the Communications Supervisor. * Support additional vessel construction management programs as needed. *Marine QA/QC Coordinator Position Requirements* * High school diploma or GED. * Associate's or Bachelor's degree in quality management, marine engineering, naval architecture, or a related field. * Experience in shipbuilding and/or ship repair projects preferred. * Experience with marine quality inspections, auditing, and testing preferred. * Ability to read and interpret blueprints/drawings and ensure compliance with project specifications. * ISO 9001 Auditor Certification preferred. * Must be capable of working in a shipyard environment (climbing ladders/gangways, confined spaces, exposure to varying weather conditions). #LI-Onsite

American Medical Staffing is seeking a travel Cath Lab Technologist for a travel job in Browns Mills, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: ASAP Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel You have a lot of choices when you consider your next professional role and we know it can be hard to wade through all the calls, emails and messages from medical staffing agencies who see you as just a number. Consider a different approach with a travel nurse staffing agency that provides high-end, customized career support for your future. American Medical Staffing (AMS) puts you first, and we are currently seeking a RADTECH - Cath Lab for a Hospital contract position in Browns Mills, New Jersey Have questions about compensation, population, unit/caseload details, experience requirements or scheduling? No problem! Text the job title and location to our recruitment team today at and we will answer all of your questions on the spot. Adventure Awaits! With AMS, you will enjoy benefits like: COMPENSATION that is competitive, negotiable, and paid weekly BONUSES when you refer others $500 for you and $500 for them BENEFITS on Day 1, including medical, dental, vision, and supplemental benefits RETIREMENT PLANS after 90 days of employment REIMBURSEMENT for travel and other incidentals PAID TIME OFF that is flexible to your needs EXPERT SUPPORT for compliance, credentialing/licensure, and CEU MENTORING specific to the travel nurse experience Along with the support of AMS in the lead-up to your assignment (e.g., credentialing, negotiating pay, etc.), we also have a team of coaches you can connect with for advice, training and development, or just to network. Like you, these advisors are AMS clinicians who have a passion for high-quality care, knowledge-sharing, and the agency experience in a hospital. We want you to feel as empowered as possible. Which is why, for over 20 years, we have helped professionals like you grow and chart a new course in their careers. Here are just a few things your peers say about us: I like that my recruiter works with me to get the best assignments and I love that my recruiter checks up on me.-Angela S, Hospital RN at American Medical Staffing Everyone at AMS has always been attentive and authentic with me.-Jeanne W, Hospital RN at American Medical Staffing Without fail, my recruiter calls and checks on me to see how I am doing and if I need anything. This has created a close, trusting bond.-Michael H, Hospital RN at American Medical Staffing Read More Testimonials by visiting have a lot of options when it comes to who you partner with, and we understand that. So, as you head out and discover what is next, consider the WHOLE experience you want to have. American Medical Staffing is not just along for the ride or there for one assignment. We want to help you create genuine moments in your career that are authentic, empowering, and extraordinary. American Medical Staffing (AMS) is an Equal Employment Opportunity Employer and does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, membership in an employee organization, retaliation, parental status, military service, or other non-merit factor American Medical Staffing Job ID #55201. Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: RADTECH:Cath Lab,07:00:00-15:00:00 About American Medical Staffing American Medical Staffing is a staffing agency headquartered in Baltimore, MD. Our goal is to CREATE an extraordinary experience for our health care professionals. Our roots are nurse owned and operated so we know what clinicians want - lots of options, a smooth and informed placement process, competitive and accurate pay, great customer service and responsiveness to requests, and advocacy when there is an issue. When AMS was founded in 2001, we started our company with a mission to be a better agency than our competitors. We have always put a heavy emphasis into what is best for our employees, not necessarily just our clients or our company. You are not an expense as you may be to a hospital; you are an asset. We take employee advocacy seriously; you are not just a number to us. The end result is that you don`t work for us; we work for you. Since starting in Baltimore, MD, we continue to grow throughout the country. Check out our industry leading reviews on Google and Indeed to see how much our clinicians enjoy working with us! · Benefits: AMS offers an array of benefits for any employee working 30 hours or more! Those eligible employees who choose to participate will pay the premiums with deductions from their pre-tax earnings. We offer a complete benefits package including Health Insurance, 401K with up to 2% match, Life, Vision, and Dental. From health and wellness support, financial or legal needs, or help with life's everyday challenges, our Employee Assistance Program provides you with resources, services and discounts to help you manage your unique concerns and save time, energy and money. We also offer additional Employee Perks that you can enjoy as an AMS employee: Scrubin - Uniform Discounts Working Advantage - unlimited access to thousands of exclusive discounts and special offers nationwide for theme parks, shows, tours, attractions, sports, concerts, hotels, rental cars, retail gift cards, movie tickets and much more Hotel Engine - Save up to 60% when booking hotel rooms, with access to more than 700,000 deeply discounted hotels worldwide. Discounted Pet Insurance Wellness Program, including fitness, nutrition and financial wellness Betterhelp - 1 month of free therapy, followed by a discounted rate for our Healthcare Professionals and their family members. Win Win Referral Bonus - $500 for you, and $500 for them! Benefits 401k retirement plan Life insurance Medical benefits Dental benefits Vision benefits

As a Distinguished Engineer at Capital One, you will be a part of a community of technical experts working to define the future of banking in the cloud. You will work alongside our talented team of developers, machine learning experts, product managers and people leaders. Our Distinguished Engineers are leading experts in their domains, helping devise practical and reusable solutions to complex problems. You will drive innovation at multiple levels, helping optimize business outcomes while driving towards strong technology solutions. At Capital One, we believe diversity of thought strengthens our ability to influence, collaborate and provide the most innovative solutions across organizational boundaries. You will promote a culture of engineering excellence, and strike the right balance between lending expertise and providing an inclusive environment where the ideas of others can be heard and championed. You will lead the way in creating next-generation talent for Capital One Tech, mentoring internal talent and actively recruiting to keep building our community. Distinguished Engineers are expected to lead through technical contribution. You will operate as a trusted advisor for our key technologies, platforms and capability domains, creating clear and concise communications, code samples, blog posts and other material to share knowledge both inside and outside the organization. You will specialize in a particular subject area, but your input and impact will be sought and expected throughout the organization. Team Description: In this role, you will be supporting the Bank Tech organization. You will lead development and implementation that will enable business initiatives, working with other leaders and teams across the enterprise to enable these solutions. As a candidate for this role, you're able to seamlessly switch from diving deep into technology with engineers to driving high-level, strategic discussions. You are a naturally curious technologist and stay on top of emerging trends, including prototyping of nascent technologies. You are not afraid to question any existing processes and solutions, yet you display a keen sense of business value proposition and focus on the right priorities. If you are ready to provide thought leadership and build engineering excellence across Capital One's engineering teams, come join us in our mission to change banking for good. Key responsibilities: Articulate and evangelize a bold technical vision for your domain Decompose complex problems into practical and operational solutions Ensure the quality of technical design and implementation Serve as an authoritative expert on non-functional system characteristics, such as performance, scalability and operability Continue learning and injecting advanced technical knowledge into our community Handle several projects simultaneously, balancing your time to maximize impact Act as a role model and mentor within the tech community, helping to coach and strengthen the technical expertise and know-how of our engineering and product community Explore new cloud technologies and identify applications to leverage their potential Develop patterns for cloud to enable emerging business initiatives Collaborate with tech leaders to drive tech strategy Evangelize cloud strategy, solutions and best practices across the enterprise Basic Qualifications Bachelor's Degree At least 10 years of experience with software programming At least 7 years of experience with solution architecture or software engineering At least 5 years of experience with cloud computing (AWS, Microsoft Azure, Google Cloud) Preferred Qualifications: Master's Degree in Computer Science or a related field 10+ years of professional experience in the full lifecycle of system development, from conception through architecture, implementation, testing, deployment and production support 7+ years of experience using Python or Java, or Go, and SQL 5+ years on AWS Serverless Technologies 3+ years of experience with Kafka, Airflow, Spark, AWS Glue/Kinesis 3+ years of experience with streaming and event driven technologies Capital One will consider sponsoring a new qualified applicant for employment authorization for this position. The minimum and maximum full-time annual salaries for this role are listed below, by location. Please note that this salary information is solely for candidates hired to perform work within one of these locations, and refers to the amount Capital One is willing to pay at the time of this posting. Salaries for part-time roles will be prorated based upon the agreed upon number of hours to be regularly worked. McLean, VA: $263,900 - $301,200 for Distinguished Engineer New York, NY: $287,800 - $328,500 for Distinguished Engineer Philadelphia, PA: $239,900 - $273,800 for Distinguished Engineer Wilmington, DE: $239,900 - $273,800 for Distinguished Engineer Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate's offer letter. This role is also eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). Incentives could be discretionary or non discretionary depending on the plan. Capital One offers a comprehensive, competitive, and inclusive set of health, financial and other benefits that support your total well-being. Learn more at the Capital One Careers website. Eligibility varies based on full or part-time status, exempt or non-exempt status, and management level. This role is expected to accept applications for a minimum of 5 business days.No agencies please. Capital One is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to sex (including pregnancy, childbirth or related medical conditions), race, color, age, national origin, religion, disability, genetic information, marital status, sexual orientation, gender identity, gender reassignment, citizenship, immigration status, protected veteran status, or any other basis prohibited under applicable federal, state or local law. Capital One promotes a drug-free workplace. Capital One will consider for employment qualified applicants with a criminal history in a manner consistent with the requirements of applicable laws regarding criminal background inquiries, including, to the extent applicable, Article 23-A of the New York Correction Law; San Francisco, California Police Code Article 49, Sections 4901-4920; New York City's Fair Chance Act; Philadelphia's Fair Criminal Records Screening Act; and other applicable federal, state, and local laws and regulations regarding criminal background inquiries. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation, please contact Capital One Recruiting at ************** or via email at RecruitingAccommodation@capitalone.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations. For technical support or questions about Capital One's recruiting process, please send an email to ********************** Capital One does not provide, endorse nor guarantee and is not liable for third-party products, services, educational tools or other information available through this site. Capital One Financial is made up of several different entities. Please note that any position posted in Canada is for Capital One Canada, any position posted in the United Kingdom is for Capital One Europe and any position posted in the Philippines is for Capital One Philippines Service Corp. (COPSSC).

Compensation: $27-$33/hr Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Shift: 3/12h shifts - 6PM-6AM; rotates week over week! OT Available 10 PTO days, 6 sick days per 12 months, renewed upon extension. *Please note - sick days and PTO days cannot be used interchangeably, and do not carry over upon extension. Requirements: A minimum of a bachelors degree in chemistry, or a Scientific related field Minimum 1 year of working in current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify gaps in processes or systems Experience with HPLC, pH testing, Osmo testing, conductivity, or protein concentration Strong pipetting techniques Knowledge and awareness of compendial (USP, EP, JP, etc.) requirements and standards for QC testing Ability to read and interpret documents such as SOPs, work instructions, test methods and protocols Day-to-Day: The QC Analyst In-Process Laboratory position supports the Quality Control In-Process and conducts biochemical, microbiological, and general chemical testing of in-process or final product samples submitted to the QC laboratories. The position requires analytical testing to be completed in compliance with all applicable procedures, standards and GMP regulations. This position requires high attention to detail, organizational leadership, interpersonal skills, a quality mindset, critical thinking, and technical writing skills. This position will be the shift leader and primarily work independently. Key Responsibilities: -Perform analytical testing in compliance with applicable GMP regulations while maintaining a safe work environment in compliance with all applicable environmental, health, and safety regulations. -Conduct biochemical, microbiological, and/or general chemical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories. -Perform peer review of laboratory data -Utilize electronic systems i.e. LIMS, MES, LES, Empower, Trackwise, etc. for execution and documentation of testing -Maintain Laboratory Housekeeping including: sample management, reagent prep, instrument standardization/calibration -Complete Document Revisions

618013 Senior Quality Control Specialist, QC Operations Strategy Direct Hire Philadelphia, PA Senior Quality Control Specialist, QC Operations Strategy will be responsible for planning and managing projects with minimal oversight, utilizing principles and methodologies from Lean, Six Sigma, and Project Management to drive continuous improvement for all QC functional areas, and the creation and maintenance of QC workforce models to ensure patient demand is met. T This role is responsible for identifying and driving continuous improvement in collaboration with QC functional areas, and the creation and maintenance of the QC workforce models to ensure patient demand is met. This position is also responsible for maintaining knowledge of lean labs principles and various operational excellence strategies within the department by providing lean focused leadership, training, coaching, and mentorship to QC personnel. The Senior Quality Control Specialist, QC Operations Strategy must have experience with lean labs, different operational excellence concepts, tier governance, workforce modeling and planning, and be a highly collaborative team player who works well in dynamic environments. Essential Functions and Responsibilities Drive deployment, hypercare, change management, and maintenance of ongoing lean labs implementation in Quality Control. Build and maintain QC workforce models. Utilize SME knowledge of lean methodologies to collaborate with QC leadership to define strategy, plan, and oversee the execution of key initiatives that deliver significant business value. Collaborate with other continuous improvement professionals to cascade needs and projects throughout the business and achieve solutions that drive positive business results. Collaborate closely with the Senior Manager, Quality Control, Operations Strategy as well as other QC functions to strategically plan future projects such as new product introduction, laboratory capacity planning, facility transfers and expansions, and other pipeline projects. Develop and upkeep planning tools to allow for site growth within the quality control organization such as headcount capacity models for increased manufacturing capabilities and onboarding of new quality control assays, tests, and processes that contribute to the release of lots and materials. Facilitate the deployment, hypercare, change management, and maintenance of new and ongoing lean labs implementation in Quality Control. Collect and analyze data from QC workforce models to allow for opportunity identification, solution development, and sustainability. Monitor and routinely evaluate KPIs, metrics, heat maps, and A3s to measure performance of quality functional areas. Act as subject matter expert to QC's lean capabilities by facilitating training and coaching of problem solving using the lean tool kit. Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations. Must adhere to company's core values, policies, procedures, and business ethics. Perform miscellaneous duties as assigned. Required Education, Skills, and Knowledge Bachelor's degree in a relevant discipline (biological sciences or equivalent) Minimum (5) years of experience in the biopharmaceutical industry within a cGMP Quality Control role Experience with different operational excellence concepts including (but not limited to) lean labs, lean practioner, tier governance, coaching kata, gemba walks, job instruction, Kaizen, A3 problem solving, change management, leader standard work. Fundamental knowledge of Quality Control operational and laboratory practices including, but not limited to, microbiology, analytical testing, sample management, quality records, and training. Advanced proficiency in MS Office (Word, Excel, Powerpoint, Visio) Successfully interface with multi-disciplined teams in a global setting Extremely detail-oriented with strong written, and verbal communication skills Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity Advanced strategic planning and implementation Demonstrate sense of urgency; ability to recognize time sensitivity Flexible and adaptable style with an eagerness to take on challenges Problem solver who not only identifies issues but leads efforts to resolve them The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation. Physical Demands and Activities Required · Must be able to remain in a stationary position standing or sitting for prolonged periods of time. · Must be able to move about inside an office and exert up to 10 pounds of force occasionally or a negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects. · Must have visual acuity to perform activities such as: preparing and analyzing data and figures, viewing a computer screen, and extensive reading. · This position requires repetitive motion, substantial movements (motions) of the wrist, hands, and/or fingers. · Must be able to communicate with others to exchange information. Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines Work Environment This job works in a professional office environment and a manufacturing lab setting. Potential exposure to latex, bleach, loud noise, lab equipment hazards, strong odors, and chemical/biochemical is possible. Requires operating standard office equipment and keyboards. The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time. We are committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, our employees and applicants will be considered without regard to an individual's race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law ***Pay rate is commensurate with experience. Target pay rate range is $95-110K***

Assist with the development of sterility assurance principles at the site in the areas of aseptic processing, and contamination control. Support the site compliance to the global microbial control standards/procedures on environmental monitoring, critical utilities, contamination control strategy, clean-room management, microbiological methods and validations, sterilization and aseptic processing controls, disinfectant efficacy studies and microbial risk assessments. Assist with the design of the contamination control strategy. Develop microbial contamination/Cross contamination risk assessments Qualifications: Bachelor's degree in a relevant discipline (biological sciences or equivalent) Minimum four to Five (4-5) years of experience in the pharmaceutical industry within a Quality Control Sterility Assurance role or Microbiology role\ Experience running or validating microbiology rapid safety methods (endotoxin, mycoplasma, and sterility). SME on 2-3 of the Rapid Safety assays (Sterility via BacT, Endotoxin via EndoSafe, Mycoplasma via BioFire and/or qPCR) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer.