Quality control analyst jobs in Reading, PA - 83 jobs

Piper Companies is seeking a Quality Control Analytical Scientist (qPCR) to join a growing biopharmaceutical organization pioneering gene therapies for rare genetic disorders. This onsite position in Exton, PA provides the opportunity to perform advanced molecular testing and DNA-based assays that directly support GMP manufacturing and product quality operations. Responsibilities of the Quality Control Analytical Scientist (qPCR): * Perform GMP-compliant qPCR testing to support bulk, drug substance, and final product analysis. * Conduct DNA extraction and assays including Vector Copy Number (VCN) and VSVG testing. * Support complementary methods such as cell culture, ELISA, and flow cytometry. * Review data for accuracy, integrity, and compliance with GMP and documentation standards. * Execute OOS investigations, CAPAs, and method troubleshooting as needed. * Maintain laboratory organization, calibration schedules, and audit readiness. Qualifications of the Quality Control Analytical Scientist (qPCR): * 3-5 years of QC experience in a GMP-regulated biopharma or biologics environment. * Strong proficiency in qPCR methodology, DNA extraction, and molecular analysis. * 2-3 years of mammalian cell culture experience preferred. * Familiarity with analytical platforms such as ELISA and flow cytometry. * Excellent attention to detail, communication, and documentation skills. * BS in Biochemistry, Biology, or related Life Science required. Compensation for the Quality Control Analytical Scientist (qPCR): * Pay Rate: $40/hour * Type: Contract-to-Hire (benefits included * Location: Onsite - Exton, PA * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays Application Period: This position opens for applications on 1/5/2026 and will remain open for a minimum of 30 days from the posting date. Keywords: Quality Control, QC Scientist, qPCR, Vector Copy Number, VCN, DNA Extraction, VSVG, GMP, Biologics, Gene Therapy, Molecular Testing, Analytical Methods, Cell Culture, ELISA, Flow Cytometry, CAPA, SOP, Data Integrity, Aseptic Technique, ALCOA, Good Documentation Practices, QC Assays, Biopharma, Exton PA #LI-JM1 #LI-ONSITE

Full-time Description Are you ready to catapult your lab career into supporting environmental sustainability? We are seeking an experienced Laboratory Analyst II to join our Inorganics team in Reading, PA. In this role, you'll perform analytical testing and sample processing that deliver the accurate, defensible data our clients depend on for environmental compliance and decision-making. You'll operate advanced instrumentation, interpret results, and ensure quality standards are met while expanding your technical expertise across diverse analytical methods. If you're ready to build technical expertise, expand your analytical skills, and grow your career in a collaborative, purpose-driven lab, we want to hear from you! **Please note - This position follows a Monday - Friday schedule of 6 AM to 2:30 PM, with rotating weekend and holiday coverage required.** Why You'll Love This Role Perform advanced sample preparation and analysis across specialized areas; Work with state-of-the-art instrumentation, technology, and Laboratory Information Management Systems (LIMS); Lead by example in quality, accuracy, and turnaround times that drive client trust and environmental compliance; Contribute to audits, SOP development, and process improvements that strengthen laboratory operations. What You'll Do Perform sample preparation, analysis, and quality control testing in accordance with Standard Operating Procedures (SOPs), approved methods, and regulatory standards; Accurately document all work and enter results into the Laboratory Information Management System (LIMS); Review and interpret data for accuracy, consistency, and reasonableness; escalate discrepancies or unusual findings; Perform analytical calculations and prepare reports as required; Maintain and troubleshoot laboratory instrumentation and equipment; perform routine calibrations and preventative maintenance; Support quality assurance and continuous improvement initiatives, including audits, corrective actions, and SOP revisions; Provide cross-training support and collaborate effectively with team members and management to meet deadlines and workload demands; Provide client-facing support, including phones and assist walk-in clients with sample intake as required depending on work location; Perform other duties as assigned. Requirements What Makes You a Great Fit Bachelor's Degree in Chemistry, Biology, Environmental Science; 2-3 years of professional hands-on laboratory experience, preferably within environmental testing; Experience with analytical techniques including ion chromatography (IC), flow injection analysis (FIA), segmented flow analysis (SFA), spectrophotometry (Spec), biochemical oxygen demand (BOD), and gravimetric (grav) methods strongly preferred; Demonstrated proficiency with laboratory instrumentation, standardized testing methods, and interpretation of analytical data across multiple techniques; Experience with LIMS and/or other laboratory management software strongly preferred; Proficiency in Microsoft Office (Word, Excel, Outlook) and Adobe Acrobat. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 10 paid holidays plus a generous time off plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position following a Monday through Friday schedule of 6 AM to 2:30 PM, with rotating weekend and holiday coverage; Flexibility to work outside of normal hours to support business needs and deadlines. Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future.

Job Description Join Berks Packing Co., Inc. as a Quality Control Technician on the 2nd Shift and immerse yourself in a dynamic environment where your skills directly impact food safety and quality. This role offers a unique opportunity to contribute to innovative practices in food manufacturing, ensuring excellence in every product we deliver to our customers. As part of a forward-thinking team, you will engage with the latest technologies and methodologies, enhancing your expertise in quality assurance. Your commitment to integrity and respect for industry standards will drive our commitment to customer satisfaction. Being part of this dedicated team means playing a key role in shaping the future of food safety and production. Take your career to the next level by applying your passion for quality and making a difference in a respected and traditional organization. Berks Packing Co., Inc.: What drives us Berks Packing is a 3rd generation family-owned and operated meat processor facility located in Reading, Pennsylvania. We have a long-standing tradition of providing excellent product quality and customer service. Berks has been a family favorite for over 92 years! Make a difference as a Quality Control Technician- 2nd Shift As a Quality Control Technician on the 2nd Shift at Berks Packing Co., Inc., you will be responsible for conducting thorough inspections of raw materials and finished products to ensure compliance with safety and quality standards. Your daily tasks will include monitoring production processes, identifying and documenting any deviations, and collaborating with production teams to implement corrective actions. You will perform routine quality assurance tests and maintain accurate records to support quality assurance protocols. Additionally, you'll be expected to contribute to continuous improvement initiatives by sharing insights and recommending enhancements to existing procedures. Attention to detail and adherence to safety regulations will be paramount in this role, as you work to uphold our commitment to excellence and customer satisfaction. Your proactive engagement with team members will foster an environment of respect and collaboration essential for maintaining high-quality standards. What we're looking for in a Quality Control Technician- 2nd Shift Successful Quality Control Technicians at Berks Packing Co., Inc. possess a unique combination of analytical and interpersonal skills critical for ensuring product quality in food manufacturing. Attention to detail is essential, allowing you to identify subtle inconsistencies in products and processes. Strong observational skills will enable you to accurately assess compliance with safety and quality standards. Excellent communication skills are necessary for effectively collaborating with cross-functional teams and articulating quality-related concerns or recommendations. Problem-solving abilities will empower you to investigate issues and implement corrective actions swiftly. A foundational understanding of food safety regulations and quality assurance practices will serve you well, as will a commitment to continuous learning in a fast-paced environment. Adaptability and a strong sense of integrity are crucial traits, as they ensure you uphold our core values while contributing to a culture of excellence focused on customer satisfaction. Join us! We believe in taking care of our team, both on and off the job. That's why we offer a mobile-friendly application process - because we know your time is valuable. If you're ready to take your management skills to the next level and join a team that values hard work and a good culture, complete our application today! A pre-employment physical and drug/alcohol screen is required. We conduct background checks as part of our pre-employment screening process and follow all EEOC and FCRA regulations regarding the use of criminal records in the hiring process.

Join Berks Packing Co., Inc. as a Quality Control Technician on the 2nd Shift and immerse yourself in a dynamic environment where your skills directly impact food safety and quality. This role offers a unique opportunity to contribute to innovative practices in food manufacturing, ensuring excellence in every product we deliver to our customers. As part of a forward-thinking team, you will engage with the latest technologies and methodologies, enhancing your expertise in quality assurance. Your commitment to integrity and respect for industry standards will drive our commitment to customer satisfaction. Being part of this dedicated team means playing a key role in shaping the future of food safety and production. Take your career to the next level by applying your passion for quality and making a difference in a respected and traditional organization. Berks Packing Co., Inc.: What drives us Berks Packing is a 3rd generation family-owned and operated meat processor facility located in Reading, Pennsylvania. We have a long-standing tradition of providing excellent product quality and customer service. Berks has been a family favorite for over 92 years! Make a difference as a Quality Control Technician- 2nd Shift As a Quality Control Technician on the 2nd Shift at Berks Packing Co., Inc., you will be responsible for conducting thorough inspections of raw materials and finished products to ensure compliance with safety and quality standards. Your daily tasks will include monitoring production processes, identifying and documenting any deviations, and collaborating with production teams to implement corrective actions. You will perform routine quality assurance tests and maintain accurate records to support quality assurance protocols. Additionally, you'll be expected to contribute to continuous improvement initiatives by sharing insights and recommending enhancements to existing procedures. Attention to detail and adherence to safety regulations will be paramount in this role, as you work to uphold our commitment to excellence and customer satisfaction. Your proactive engagement with team members will foster an environment of respect and collaboration essential for maintaining high-quality standards. What we're looking for in a Quality Control Technician- 2nd Shift Successful Quality Control Technicians at Berks Packing Co., Inc. possess a unique combination of analytical and interpersonal skills critical for ensuring product quality in food manufacturing. Attention to detail is essential, allowing you to identify subtle inconsistencies in products and processes. Strong observational skills will enable you to accurately assess compliance with safety and quality standards. Excellent communication skills are necessary for effectively collaborating with cross-functional teams and articulating quality-related concerns or recommendations. Problem-solving abilities will empower you to investigate issues and implement corrective actions swiftly. A foundational understanding of food safety regulations and quality assurance practices will serve you well, as will a commitment to continuous learning in a fast-paced environment. Adaptability and a strong sense of integrity are crucial traits, as they ensure you uphold our core values while contributing to a culture of excellence focused on customer satisfaction. Join us! We believe in taking care of our team, both on and off the job. That's why we offer a mobile-friendly application process - because we know your time is valuable. If you're ready to take your management skills to the next level and join a team that values hard work and a good culture, complete our application today! A pre-employment physical and drug/alcohol screen is required. We conduct background checks as part of our pre-employment screening process and follow all EEOC and FCRA regulations regarding the use of criminal records in the hiring process.

TAIT partners with artists, brands, IP holders and place makers to bring culture-defining, never-before-seen experiences to life. With a legacy of innovation spanning over 45 years, TAIT has grown from pioneering in rock 'n' roll concert staging to setting the global standard for extraordinary live events and experiences through cutting-edge technology, precision engineering, and creative design. TAIT's 20 global offices have developed iconic productions and experiences in over 30 countries, all seven continents, and even outer space for renowned performers, theme parks, exhibits, and venues across the globe, including partnerships with Taylor Swift, Cirque Du Soleil, Royal Opera House, Nike, NASA, Bloomberg, Google, Beyoncé, and The Olympics Internship Overview The TAIT Internship program is a fully immersive, experiential program. Interns are placed in a department based on their major and interests, but it is up to them to set goals and define their experience at TAIT. We take pride in pushing the boundaries of what's possible, and we're committed to nurturing emerging talent. We're excited to offer a unique and rewarding internship experience that goes beyond the typical coffee runs and photocopying tasks. We're looking for motivated and passionate individuals to join us on this journey of growth, learning, and achievement! Are you ready to roll up your sleeves, challenge yourself, and make a real impact? If so, you're the kind of intern we're looking for. At TAIT, we understand that internships are a two-way street. While you'll be gaining valuable experience, you'll also be contributing to our team and projects in meaningful ways. We encourage you to set your goals, develop your skills, and help shape your own experience. Position Details Position: Control Fabrication Intern Job Specifications: Control Fabrication Interns will gain a key understanding of operations management in a custom fabrication environment. Control Fabrication Interns will experience multiple stages of the unique TAIT project lifecycle through support of operations functions such as Water Spiders, Carpentry, Customs, Staging, and Packaging. Location: West Lincoln Facility in Lititz, PA Duration: June 2026-August 2026 Compensation: $18/hr. Schedule: Interns are scheduled to work 40 hours per week on 1st shift dependent on projects and business needs Eligibility: This role is open to U.S. Residents only Intern Responsibilities + Participate in process alignment and analysis meetings + Assist with capacity planning/staffing requirements needed to achieve the production requirements and schedules + Assist with quarantines of non-conforming material + Develop an understanding of materials, parts, and elements pertaining to overall build + Take part in machining custom parts + Produce a quality product while focusing on TAIT brand quality and standards + Understanding the impacts of safety on an individual and facility level Qualifications To qualify for this internship, you must meet the following: + Currently pursuing a degree or equivalent in a related field: + Electrical Engineering + Electrical Fabrication + Electrical + Fabrication + Operations Management + Technical Theatre + Graduating in between December 2025 - May 2027 + GPA: 2.8 or Above + Familiarity with basic computer applications and software + Willingness to learn and develop skills in specific manufacturing tasks and processes + Please note that this internship is designed for individuals seeking an entry-level opportunity to gain practical experience in manufacturing and assembly processes. Potential Career Paths This position also provides a path for continued growth as a: Production Technician, Mechanical Fabricator I, or a Water Spider I based on skillset and additional training. Why Choose TAIT? + Gigs: You may be eligible for full time or part time conversion upon successful completion of your internship program* + Real-World Impact: Your work here won't just be busy work. You'll be an integral part of our team, contributing to projects that truly matter. Previous interns worked on actual projects that have been seen by millions of people! + Professional Growth: We're committed to helping you grow and learn. You'll gain hands-on experience in your chosen field and develop skills that will serve you well in your future career. + Mentorship: You won't be navigating this journey alone. Our team of experts will provide guidance, mentorship, and support to help you excel. + Innovation: We live on the cutting edge of innovation, and you'll be part of our team's creative solutions and groundbreaking ideas. + Networking: Build your professional network by connecting with industry leaders, fellow interns, and our experienced team. Are you ready to embark on a journey of growth, learning, and achievement? Join us and be a part of something special at TAIT. Your internship is not just a step in your career; it's a leap forward. Apply today! TAIT is an equal opportunity employer fully committed to diversity and inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran or any other protected characteristic as outlined by international, national, state, or local laws.

Job Description Multiple positions available: ELISA, PCR General Responsibilities: Perform testing in support of product manufacturing, employing manual and automated analytical equipment. Provide direct support of Quality Control analytical processes, test procedures, qualifications, validations, assay troubleshooting, equipment upkeep, logbook review, and inventory control. Essential Requirements: Must have direct subject matter expertise on the following techniques: ELISA, PCR Execution of sample and standard dilutions and volume calculations Microliter volume pipetting and plating Multi-Channel Repeater Micropipetting Setup and Operation of plate washer and plate reader Responsibilities: Execute Analytical Test Methods for in-process samples, bulk intermediate (drug substance), final drug product, and raw materials release, as well as stability testing. Primary testing responsibility will be conducting testing to support assays such as Residual p24, COL7/Lam332, BSA, and Trypsin assays. However, cross-training in cell culture and other analytical methods will be required (e.g. qPCR, flow cytometry platforms). Coordinate, schedule, and execute testing based on manufacturing schedules. Participate in the review process of SOPs and analytical test procedures as necessary to maintain compliance. Review Quality Control raw data for accuracy, completeness and compliance with effective SOPs to ensure the strength, identity, safety, purity and quality of the product. Troubleshoot and analyze nonconforming data. Perform timely response to Out of Specification (OOS) results, including notification to area management. Perform and document laboratory investigations to ensure that potential problems and root causes are identified, impact assessed and actions to prevent recurrence are considered and implemented. Execute associated CAPA. Ensure data integrity is maintained for all applications, programs, and executed work. Ability to document all work using Good Documentation Practices and ALCOA++ principles. Maintain laboratory housekeeping including organization, cleanliness, and logbooks. Perform internal audits and GEMBA walk-throughs of laboratory areas to maintain compliance. Author and/or execute protocols and generate technical reports. Author and manage change controls. Perform equipment standardizations and qualification, as necessary. Perform training of other employees. Communicate with the individual Operations Departments (Manufacturing, Quality Assurance, Facilities) to ensure that Company objectives are met on schedule. Computer Skills: To perform this job successfully, an individual should have knowledge of Microsoft Office software. Education: Minimum Bachelor of Science degree in a biochemistry, chemistry, or similar scientific discipline Essential Qualifications: 3-5 years Quality Control experience in GMP environment specifically in a similar role in the biologics industry 2-3 years' experience in mammalian cell culture in an academic or industrial laboratory Knowledge of basic laboratory skills (including aseptic technique, pipetting, biohazard control) Knowledge of Current Good Manufacturing Practice, Good Documentation Practices, and Industry standards required Familiarity with analytical equipment such as UV absorbance plate readers, Flow cytometers, microscopes, and pH meters is recommended. Excellent verbal and written skills with good interpersonal communication skills Must be open to occasional off shift and weekend work

QC Lab Technician - Lebanon, PA Hours are 7:00am - 3:00pm Monday thru Friday. The employee is expected to be proficient in the duties of the Quality Control Technician position as they appear below. It is also expected that the employee will have read and understand all Brentwood Industries policies and procedures for their intended position Employees may perform other related duties as required to meet the ongoing needs of the organization. Essential Responsibilities: Ensure the safe operation of all equipment during their shift. Know the location of all safety stops. Obtain probed regrind samples from appropriate departments and insure traceability. Know the proper technique of cleaning the lab mil and essential housekeeping duties. Produce a quality lab mil sample from regrind samples and provide these samples for inspection by a qualified quality control lab technician. Communicate all probing and sample preparation in a timely and concise manner. Test roll samples for proper gauge and determine pass/fail results based on pre-determined standards. Report excessively high or low gauge results to the lab lead and/or lab supervisor and also to calender operators. Prepare documentation for testing of roll stock samples. Complete testing of roll stock samples. Cut leaf strips from roll samples and press them into bars for testing. Prepare bars for testing including sanding flash. Conduct impact tests on roll samples and determine pass/fail results based on pre-determined standards. Perform specific gravity on specimens obtained from roll samples collected from the calender lines. Communicate results of all testing in a timely and concise manner. Set up and conduct the following ASTM tests with assistance: ASTM D790 Flexural testing ASTM D882 Tensile testing ASTM D792 Specific gravity testing ASTM D5420 Impact resistance testing ASTM D4226 Impact resistance testing ASTM D648 Heat Deflection Shrinkage/Stretch testing Essential Skills: EDUCATION and/or EXPERIENCE: High school diploma or equivalent preferred. LANGUAGE SKILLS: The ability to read, write (print legibly), speak and understand the English language at the high school level is required. The ability to communicate with other members of the Quality Control and Production departments and understand instructions, either verbal or written, is essential. MATHEMATICAL SKILLS: The ability to add, subtract, multiply, divide and calculate the average of numbers to the fourth decimal place is required. The ability to read digital micrometers and digital calipers as well as various other dial gauges and measuring devices is essential in order to perform the required duties listed above. REASONING ABILITY: The ability to ascertain the pass/fail status of a roll based on standards set forth in instructions whether verbal or written is imperative. The ability to grasp the concept that the end of a roll sample is the core of the next roll and determine the ramifications of that concept as they effect the status of the roll that follows is required. OTHER: By the completion of the 65 day trial period, the individual must possess or have developed most of the skills necessary to complete each duty satisfactorily. The employee must have developed a working knowledge of the Quality Control department and its function within the company. The employee must begin developing a working knowledge of all quality control software used in the lab. Brentwood offers professional growth potential, a pleasant work environment, and an excellent wage and benefits package including 401k w/employer match. Brentwood Industries, Inc., provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. At Brentwood, we have a passion for both our products and our people. Our goal as an employer is to help you excel as an individual and as part of a team by providing you with satisfying, motivating, and stimulating work experience. The varied nature of the environment at Brentwood allows you to work alongside industry professionals on a wide range of projects, contributing your knowledge and strengths to develop innovative, market-driven solutions. Please note: We are not working with external recruiters at this time and are not accepting unsolicited resumes.

At Niagara, we're looking for Team Members who want to be part of achieving our mission to provide our customers the highest quality most affordable bottled water. Consider applying here, if you want to: Work in an entrepreneurial and dynamic environment with a chance to make an impact. Develop lasting relationships with great people. Have the opportunity to build a satisfying career. We offer competitive compensation and benefits packages for our Team Members. Control Room AssociateThe team member in this position accurately maintains daily, weekly and monthly inventory levels in the WMS while maintaining proper inventory rotation and storage. Essential Functions Navigates through an advanced ERP System in order to successfully execute all daily aspects of the “Inbound & Outbound” inventory operations. Creates purchase orders (pallets, airgas etc.) Processes all recycle and destruction loads Ensures all finished goods, raw materials and sub-assembly components are maintained as per established guidelines and procedures. Processes all non-conforming material in Agile Coordinates with all involved parties to ensure accurate inbound receipts, intercompany transfers, and RMA's. Responsible for verifying true time inventory transaction records in the company's ERP system. Completes Oracle transaction activities from Receiving into Inventory, WIP, or Non-Conforming inventories. Responsible for the integrity and accuracy of all inventories by performing daily audits and maintaining a comprehensive Cycle Count program. Completes Oracle transaction activities associated with material movements. Responsible for the integrity, accuracy and control of all in house materials. Compiles records by SKU, quantities, Sub-Inventories, and validate EBS Oracle inventories against physical counts to investigate and adjust errors in computation or count and reports reasons for discrepancies. Maintains and compute inventory balance by running and preparing reports of inventory balances, shortages and discrepancies. Organizes warehouse for efficient storage and material distribution per supervisor instructions. Maintain accurate inventory levels through daily, monthly cycle counts and annual year-end physical inventories. Assists in maintaining accurate inventory reports by sub organizations, RMA's, HFI's, and WIP. Expired inventory disposition identification (SLOB). Maintains product rotation and storage disciplines (FIFO). Interacts and maintains positive relationships with all levels of leadership. Accomplishes special projects and other assignments/duties as required by management. Compliant to all safety rules and regulations, GMP's and all Niagara policies and procedures. Establishes and maintains high standards for quality, housekeeping and productivity. Regular and predictable attendance is an essential function of the job. Please note this job description is not designed to contain a comprehensive list of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without prior notice. Qualifications Minimum Qualifications: 2 Years - Experience in Field or similar manufacturing environment 2 Years - Experience in Position 0 Years - Experience managing people/projects *experience may include a combination of work experience and education Preferred Qualifications: 4 Years - Experience in Field or similar manufacturing environment 4 Years - Experience working in Position 2 Years - Experience managing people/projects *experience may include a combination of work experience and education Competencies This position embodies the values of Niagara's LIFE competency model, focusing on the following key drivers of success: Lead Like an Owner Makes safety the number one priority Keeps alert for safety issues and escalates immediately Effectively prioritizes tasks based on department goals Shows respect to others and confronts interpersonal issues directly Prioritizes resolution of customer issues effectively Responds promptly and honors commitments to internal and external customers InnovACT Makes recommendations to continuously improve policies, methods, procedures, and/or products Demonstrates adaptability by reacting appropriately to unexpected changes in situations or circumstances Increases performance through greater efficiency Find a Way Seeks to develop technical knowledge through learning from other experts Understands interdepartmental impact of individual decisions and actions Seeks solutions rather than placing blame Empowered to be Great Consistently looks for ways to improve one's self through growth and development opportunities Communicates clearly and promptly up, down, and across Communicates effectively to manage expectations Education Minimum Required: High School Diploma or GED Preferred: Associate's Degree Certification/License: Required: N/A Preferred: Forklift certification Foreign Language Required: Minimum Professional Proficiency Preferred: Full Professional Proficiency Benefits Our Total Rewards package is thoughtfully designed to support both you and your family: Regular full-time team members are offered a comprehensive benefits package, while part-time, intern, and seasonal team members are offered a limited benefits package. Paid Time Off for holidays, sick time, and vacation time Paid parental and caregiver leaves Medical, including virtual care options Dental Vision 401(k) with company match Health Savings Account with company match Flexible Spending Accounts Expanded mental wellbeing benefits including free counseling sessions for all team members and household family members Family Building Benefits including enhanced fertility benefits for IVF and fertility preservation plus adoption, surrogacy, and Doula reimbursements Income protection including Life and AD&D, short and long-term disability, critical illness and an accident plan Special discount programs including pet plans, pre-paid legal services, identity theft, car rental, airport parking, etc. Tuition reimbursement, college savings plan and scholarship opportunities And more! *********************************************** * *Los Angeles County applicants only** Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers, the California Fair Chance Act, and any other applicable local and state laws. Any employment agency, person or entity that submits a résumé into this career site or to a hiring manager does so with the understanding that the applicant's résumé will become the property of Niagara Bottling, LLC. Niagara Bottling, LLC will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity. Employment agencies that have fee agreements with Niagara Bottling, LLC and have been engaged on a search shall submit résumé to the designated Niagara Bottling, LLC recruiter or, upon authorization, submit résumé into this career site to be eligible for placement fees.

Job DescriptionDescription: The Quality Control (QC) Technician is responsible for inspecting, testing, and evaluating materials, components, and finished products to ensure compliance with company quality standards and customer specifications. The QC Technician supports production by identifying and documenting defects and working with other departments to resolve quality issues and improve processes. Responsibilities: Perform inspections of incoming materials, in-process assemblies, and completed buses to ensure compliance with engineering drawings, work instructions, and customer specifications. Document findings in inspection reports and maintain accurate records in accordance with company quality standards and ISO requirements. Conduct dimensional checks, functional tests, and visual inspections using gauges, tools, and other test equipment. Identify and isolate non-conforming materials or products; initiate non-conformance reports (NCRs) and support root cause analysis. Collaborate with production teams to resolve issues and ensure timely corrective actions. Support First Article Inspections (FAI), final inspections, and customer source inspections as required. Assist in audits and quality improvement initiatives to maintain and enhance the quality system. Adhere to all safety policies and procedures and promote a culture of continuous improvement. Requirements: Qualifications: High school diploma or GED required; technical certification or associate degree preferred. 2+ years of experience in manufacturing quality control or inspection role; experience in vehicle assembly, aerospace, or heavy equipment a plus. Ability to read and interpret blueprints, engineering drawings, and technical specifications. Familiarity with inspection tools such as calipers, micrometers, and height gauges. Strong attention to detail and ability to detect product irregularities. Basic computer skills for data entry and report generation. Knowledge of quality systems (e.g., ISO 9001) is a plus. Physical Requirements: Ability to stand for long periods and lift up to 30 lbs. Manual dexterity and good hand-eye coordination for inspections. Use of personal protective equipment (PPE) as required. Work Environment: Fast-paced, hands-on manufacturing environment with frequent standing, walking, Manufacturing/production floor environment. May be exposed to noise, dust, and fluctuating temperatures.

At R-V Industries, our work is much more than designing and building world-class industrial process equipment. Not only are we impacting everyday life in the world we serve, but we are providing a quality of life for our employees and their families. Every day, we come together to build stronger relationships with our vendors, our customers, and each other, so we can solve challenging problems, and continue to improve the safety, quality, and efficiency of all that we do. Caring matters at R-V. We care for each other, our safety, our quality, our learning, and our growth. We seek out diversity of thought, experience, and strengths in individuals, so we can continue to innovate as a team. We believe when we bring our true full selves to serve others, it elevates the quality of life for all. As with all s at R-V, this job is considered safety-sensitive. GENERAL JOB DESCRIPTION We are seeking an experienced Quality Inspector to join our team at our Honey Brook and Morgantown, PA locations. This position is responsible for providing day-to-day quality engineering support within our General Fabrication, ASME Section VIII, and NQA-1 markets. This position will play an integral role in the growth and improvement of the RVII organization through elevating first pass quality, increased project throughput, on-time delivery, and project expectations. DUTIES/RESPONSIBILITES Provide technical support to RVII manufacturing facilities Supports gathering and presenting key KPI measurements to the organization Participate in pre-job contract review. Develop and implement inspection and test plans for manufactured and purchased components Interface with vendors to ensure timely resolution of Quality non-conformances Conduct internal quality system process audits Coordinate and host outside inspection agencies and customer inspectors Prepare, revise, and implant Quality System procedures, policies, and work instructions Conceptualize and analyze designs to ensure technical outcomes are consistent with customer and company specifications Perform non-destructive and dimensional inspections in accordance with approved procedures, customer specifications, and governing codes. Maintain control and maintain an inventory of non-conforming products. Review contracts to determine deliverables and ensure compliance with specifications Plan, schedule, and coordinate NDE Inspection activities daily in conjunction with the manufacturing department. Maintain adherence with all M&TE requirements, testing requirements, and procedures SKILLS/QUALIFICATIONS NDE (Non-Destructive Evaluation) qualifications - minimum of Level II in VT/MT/PT/BLT/UT-T Must possess a valid American Welding Society - Certified Welding Inspector credential Must have advanced knowledge of ASME Y14.5 specification Must have fundamental knowledge of ASME Sections VIII and V Prior experience with ASME NQA-1 and 10CFR50 Appendix B preferred Ability to work independently and direct coworkers Bachelor's degree in engineering or quality related field with 2+ years of experience or 10+ years in Quality Control role Strong verbal and written communication skills Self-motivated with attention to detail and accurate reporting Proficient in MS Office suite products EDUCATIONAL/PHYSICAL REQUIREMENTS Two- or four-year college degree or relevant experience in inspection activities Everyday bending, crouching, stooping, standing, and overhead reaching Everyday exposure to moving machinery, dust, dirt, grease or other disagreeable elements Lifting up to 50-75 lbs. Must be able to pass and complete a physical assessment Must be able to perform the essential functions of the job with or without accommodation R-V Industries, Inc. is an equal opportunity employer. R-V Industries, Inc. is an equal opportunity employer. Monday-Thursday 6:00 am - 4:00 pm

Summary of Quality Control Technician - Precision Machining Inspector DAY SHIFT - MONDAY-THURSDAY 7:00am-4:30pm; Friday 7:00am-11am (estimated) We are seeking a detail / results oriented, Quality Control Technician for our plant in South Eastern Pennsylvania. We have been in business for more than 75 years and are considered a leader in our industry, making precision machined parts for a variety of OEM's. Family oriented culture with focus on Integrity, Accountability and Responsibility. What we do matters! The Quality Control Technician will monitor the quality of incoming and outgoing products or materials. Also, the position requires inspecting parts, analyzing measurements, and overseeing the capability of the production processes which must meet the dimensional specifications of the mechanical engineering drawing. Final and lot inspections are also critical aspects of this role which will be performed as required. Duties Include: Approve incoming materials by confirming specifications, conducting a visual and measurement test, and rejecting and returning unacceptable materials Approve in-process production by confirming required specifications, conducting visual and measurement tests, and communicating the required adjustments. Approve all finished products by confirming specifications and conducting required tests Return products for re-work if needed and complete documentation to confirm re-work Document and update inspection results by completing reports and logs Keep measurement equipment operating by following operating instructions, calling for repairs, and keeping gages calibrated. Roving manufacturing audits for part and systems compliance Approve first piece inspections using any combination of manual or advanced equipment and methods. Requirements include: Prefer a working knowledge of measuring equipment including CMM, Optical Comparator, Vision Systems, Non-Contact Measuring systems, Micrometers, Calipers, and all other handheld measuring tools. Effective communication skills. Detail oriented team player Strong blueprint reading skills. Familiarity with Geometric Dimensioning & Tolerancing. First Article inspections; Capability Studies. Developing and maintaining inspection reports. High School diploma or equivalent. 3+ year's experience in a fast paced precision machining environment Skills, Knowledge and Abilities Gage R & R studies. Inspection & Quality Planning. Ability to complete product layouts from blueprints. Material & Process Certifications and Test Report Verifications. Proficient in Microsoft Word & Excel and Quality software. Knowledgeable performing first piece, final inspection, in process and receiving inspection. Calibration of measuring instruments a plus. Operation of CMM and OGP vison system (or equivalent) a plus. SPC and Control / Run / Trend Analysis & Charting. Process / Equipment capability studies. Previous Aerospace Manufacturing Quality experience a plus. Background in ISO9001 and AS9100 a plus a plus. Lean Manufacturing experience & knowledge. Six Sigma Green Belt or equivalent knowledge a plus. FULL COMPREHENSIVE BENEFITS OFFERED SALARY TO COMMENSURATE WITH EXPERIENCE Must be a US citizen and be able to own a firearm due to ITAR and FFL requirements.

Join Blommer! We offer HEALTH & DENTAL BENEFITS DAY 1 OF HIRE! Blommer understands that our employees are our biggest assets. With this in mind we offer a generous benefits package, tuition reimbursement and 10 pounds of free chocolate for your birthday! Blommer has been providing delicious, high quality chocolate and cocoa products to customers since 1939. Built as a family business, we are continuing to grow and are looking for motivated and reliable associates to help in our mission of Bringing Chocolate to Life! Available Shifts: 3rd Shift : Sun-Thur 11p-7:30a JOB SUMMARY: The QC Technician is required to adhere to all aspects of quality assurance and quality control programs. This role requires quality standards are met by conducting appropriate testing methods and procedures. The QC Technician is required to perform these duties in a safe and responsible manner following all Blommer Chocolate safety policies. Responsibilities: Ensure requirements set forth in the Quality Assurance & Control Programs to support the safe manufacture of food are met; programs and may include but are not limited to: Environmental Monitoring, Sanitation Program, Shipping and Receiving, Allergen, Hold & Release, GMPs, Food Defense, Raw Material Sampling, Pre-ship Sampling. Operate and calibrate various laboratory equipment needed to validate product. Validate product through instrumentation testing & physical testing of raw materials, in process material and finished goods; tests include fat, particle size (Microtrac and micrometer), pH, moisture, allergen, free fatty acid, color (Hunter colorimeter), shell in nib. Monitor quality attributes for all manufactured products to ensure accurate product specification to customer requirements. Qualifications: Associate's degree in Food Science, Chemistry, or Microbiology OR one year laboratory experience preferable in food manufacturing environment. Proficient in current computer software - Microsoft Office Ability to utilize handheld data terminal such as scanner and tablet device. Blommer Chocolate Company 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. 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.

Needs to make sure that products being produced meet the expectations of the consumer. They examine jobs to make sure they meet quality expectations then assess the final product after production. Their role is to establish an acceptable variation range for jobs and identify when something fails to meet those requirements. Responsible for monitoring and ensuring that each stage of production is followed by all the necessary procedures and each product coming out of the production process. Document the results of their inspections and make recommendations on how to prevent common errors. Responsible for ensuring the quality control of all printing and sign products as well as packaging and shipment/delivery of all products. Responsible for checking in all vended products and ensuring they are ready for delivery or shipment. Duties and Responsibilities ● Must have attention to detail on quality and packaging for all outgoing shipments. ● Must be very organized while maintaining the ability to multitask. ● Coordinate with shipping companies like FedEx, UPS and others and ensure timely delivery. ● Work effectively with the center manager and sales team for quality delivery and escalations. ● The job requires repetitive lifting of sometimes heavy boxes. ● Must be a team player, dependable and have a good work ethic. ● Good written and verbal communication skills ● Excellent problem-solving and analytical skills ● Keen attention to detail ● Basic computer and math skills to calibrate and measure specifications ● Ability to use measuring devices like scales and tape measures ● In-depth understanding of company standards ● Understanding of target market and consumer needs ● Documentation and reporting skills ● Teamwork and collaboration ● Comfortable standing or walking for long periods of time Some cross training into bindery or other areas of the company will be required at times if another teammate is out. Experience Entry Level Job Full time Print Smith, Shipleap and Microsoft Office knowledge is a huge plus. Compensation: $15.00 per hour At AlphaGraphics, we offer careers for everyone! Whether you are just starting out, looking for that next great growth opportunity, or seeking a change, we have exciting roles to suit you. We pride ourselves on our training programs in management, sales, operations, print, signs, design, and marketing. Join us with or without experience, and we will succeed together as a team! We invite EVERYONE to apply! *AlphaGraphics centers (locations) are independently owned and operated. The posted positions are offered by individual franchisees who interview, hire, manage and pay the employees hired for positions in a specific local location (center) through their specific business.

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 our website ********************************** are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you Job Description Title: Quality control chemist- 2nd shift Duration: 12 Months Location: Myerstown, PA 17067 Description: The Raw Material testing team is responsible for Quality Control testing of APIs and excipients used in the manufacture of pharmaceutical and nutritional products. This is a fast-paced, energetic team that works together across two shifts to meet aggressive throughput times to support a lean manufacturing operation. Position Summary: In this position, the incumbent will be expected to draw upon previous analytical experience, as well as continuously learn Quality Control systems and effectively engage in relationships with peers in the laboratories, Manufacturing/Production, and personnel in other departments as needed. The incumbent will perform analysis on raw materials following prescribed procedures to provide the information base leading to material disposition, as well as assist in troubleshooting and problem solving as directed. Once the incumbent is assigned specific materials on which to perform the quality control tests, or provide development or troubleshooting, the incumbent will have considerable impact on results from his/her work. Material can be rejected and manufacturing procedures can be altered significantly either in schedule changes or in process itself. Position Duties & Responsibilities : Perform standard qualitative and quantitative analysis: • Utilize standard analytical chemistry techniques: wet analytical methods, HPLC, UV, GC, AA, polarimeter, FT-IR, NIR, RAMAN, etc.) to test raw materials in accordance with approved testing procedures, including those from company, the National Formulary (NF), the United States Pharmacopoeia (USP), the European Pharmacopoeia (EP), and the FDA. • Properly document and maintain records of all analysis information of assigned materials on data sheets and laboratory notebooks for permanent file. • Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with Supervisor and recommend additional testing if necessary. • Communicate to supervision in a timely manner all non-compliance situations, and assist in investigations. • Assist with troubleshooting analytical methodology and instrumentation malfunctions. • Perform special assignments as directed by supervisor, for example, revise existing analytical testing monographs to comply with compendia changes or other specific needs. • Accurate, complete and timely fulfillment of the job responsibilities will, in part, ensure GMP compliance as outlined in various Bayer and U.S. government rules and regulations. Documentation Review: • Review testing documentation performed by other analysts for compliance with BAYER, FDA, National Formulary (NF), United States Pharmacopoeia (USP), and European Pharmacopoeia (EP) procedures. Safety: • Adhere to the pertinent aspects of Corporate and plant safety programs and adhering to GMP's, ISO standards or other regulations. Qualifications Requirements/Preferences: • Bachelor's degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required. Chemistry degree is preferred. • At least 1-3 years of experience in a GMP laboratory environment. Master's degree in a related field with 1 year of experience may be considered. • Knowledge, practical application, and understanding of analytical chemistry is required to perform the functions of this position. • Basic experience with Personal Computer (PC). • Demonstrated capability for communicating ideas, concepts, and work results effectively to colleagues and supervision. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Must demonstrate initiative and a willingness to learn. • Good working knowledge of advanced laboratory instrumentation and personal computer skills are required. • Good working knowledge of advanced laboratory instrumentation and computers are required; This is defined as strong troubleshooting skills for assigned area such as HPLC, GC, AA, UV, TOC, NIR and/or dissolution and low error rates with microbiology or chemistry techniques for defined area • A working knowledge of organic chemistry, statistics, data processing and good manufacturing practices is required • Demonstrated ability to clearly communicate technical information in writing required. • Demonstrated ability to manage key projects and display area of expertise; i.e. clear/consistent notebook skills and function as an independent worker. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Demonstrated ability to take initiative and display a willingness to learn required. • A thorough understanding of National Formulary (NF); United States Pharmacopeia (USP); and European Pharmacopeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP's), quality control methods and procedures is required. • Competencies required: analytical problem solving, alertness, work within established policies and procedures, commitment to task, decisiveness, effective written and interpretive communication skills, and organization and planning skills. • Enter here Travel Requirements: None Thanks & Regards, Mayank Gupta, (M. Pharmacy) (Lead Pharma Technical Recruiter) Additional Information All your information will be kept confidential according to EEO guidelines.

Skill Source is a leading placement service specializing in manufacturing operations both on the production floor and front office. We work hard finding the right complimentary fit for both client and qualified candidates. We facilitate this by asking not just the right questions technically but the right questions to fit you personally. We have a substantial client base to work with so there is a very good chance we can find you the next step in a more satisfying career. Submit your hard earned resume today and let us see what we can do for you! Job Description My growing client is looking for a skilled Metal Anodizing/Plating Technician. Full time position with a growing up and coming manufacturing company! Great pay and benefits! First shift position. Growth opportunities available. Qualifications At least 2yrs experience processing metal coatings (anodizing) onto metal parts (medical device or aerospace a plus) MUST have experience disposing hazardous materials in compliance with OSHA and/or HAZMAT guidelines Chemistry Degree - Associates or better strongly preferred. Additional Information These are permanent positions NOT contract! Excellent pay (Pay commensurate with experience) and benefits packages! Some of our clients pay FULL medical! Please feel free to review our other opportunities at ***************************

Full-time Description DEFINITION The Inspector is responsible for ensuring that all cast components meet customer specifications and internal quality standards. This role involves performing dimensional inspections, visual evaluations, and non-destructive testing (NDT) on investment castings throughout various stages of production. SUPERVISION RECEIVED This position reports directly to the Quality Assurance Manager SUPERVISION EXERCISED This position will not have any direct reports ESSENTIAL FUNCTIONS OF THE POSITION - NOTE: An employee assigned to this title shall perform a majority, but may not perform all, of the duties listed in this job description. Conversely, minor level duties performed on the job may not be listed. Work in a safe manner with a goal of zero harm. Create safety awareness by actively observing, auditing, and coaching safe work behaviors and conditions. Ensure compliance with safety and environmental rules and regulations. Demonstrates self-management skills, including time management, planning, scheduling, organizing, and prioritizing; ability to complete assigned duties in a timely manner and meet established deadlines Performs all necessary functions to adhere to ISO9001-2015 standards Examine castings for surface defects, cracks, porosity, and other imperfections according to established criteria. Use precision measuring instruments (e.g., calipers, micrometers, gauges, CMM) to confirm dimensional accuracy against engineering drawings and specifications. Record inspection results accurately in quality control logs and maintain traceability of parts. Conduct or assist with NDT methods such as dye penetrant, radiographic, or ultrasonic testing as required. Ensure proper execution of policies and procedures within areas of responsibility. Must have good attendance and be reliable. All other duties as assigned. Requirements KNOWLEDGE, SKILLS, AND ABILITIES · Ability to communicate information and ideas in speaking so others will understand. · Ability to establish and maintain effective working relationships with supervisors and senior managers, as well as employees. · Ability to operate a computer and secure information from established data processing, spreadsheet, word processing, database and graphics programs. · Ability to express ideas and communicate orally and in writing. Ability to read, write, speak, understand, or communicate in English sufficiently to perform the duties of this position. American Sign Language or Braille may also be considered as acceptable forms of communication. Understanding of applicable plant equipment and production process. Persons with mental or physical disabilities are eligible if they can perform the essential functions of the job after reasonable accommodation is made to their known limitations. If the accommodation cannot be made because it would cause the employer undue hardship, such persons may not be eligible. EDUCATION AND EXPERIENCE · High School Diploma or Equivalent preferred · Ability to read and interpret engineering drawings and specifications. · Certification in NDE (VT / PT / MT) is a plus. · Experience with CMM programming and operation is a plus. LANGUAGE SKILLS Ability to write routine reports and correspondence. Ability to speak effectively before the employees in the organization, communicate effectively with customers, suppliers and leadership throughout the organization. The ability to manage schedules, consider resources, and communicate these needs effectively throughout the organization. PHYSICAL DEMANDSReasonable accommodations may be made to enable individuals with known limitations or disabilities to perform the essential functions related to physical demands: While performing the duties of this job, the employee is frequently required to walk, sit, talk or hear, ascend and descend stairs, ramps, etc., use hands to finger, handle or feel objects, tools or controls, reach with hands and arms, climb or balance, stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to one hundred (50) pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. The employee must be able to be walking or standing for up to twelve (12) hours. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly exposed to moving mechanical parts, varying temperatures, high noise levels and dust. Salary Description $22-24 DOE

Salary: Do you want to work for a construction company unlike any other? At JGM, we challenge the industrys status quo. Known as the team that delivers When You Need It Yesterday, weve built a culture around safety, quality, and speed. At JGM, were more than a company-were a family. Working side by side, we support one another, building trust by knowing we can count on each other. Driven by our core values, mission, and purpose, we stay focused on our vision for the future. The result? A team environment that fuels exceptional employee satisfaction, which in turn drives extraordinary client experience and continued company growth. The only question is: Are you ready to join our growing family and be part of something truly special? Be an integral part of the JGM family by living our core values: We Plan. We Adapt. We Succeed. Uncompromising Safety & Quality. Family is Our Foundation. Create Value Through Better Solutions. Whatever it Takes. Commitment to Self-improvement. Our Purpose (FOREVER): Develop Elite Leaders Today, So We Can Build Tomorrows Future Our Vision (ONE DAY): Driven to be the Safest, Fastest, and Most Effective Industrial Construction & Fabrication Partner in North America Our Mission (TODAY): Solve Our Clients Toughest Challenges with Safety and Quality Top of Mind Position Overview JGM is seeking a talented QC Inspector to join our growing team! The perfect candidate is a professional who thrives on tackling challenges in an exciting, fast-paced environment. This position will inspect raw materials, in-process work and finished products for conformance to shop drawings, specifications, and codes by performing the below duties. Responsibilities Conduct complete layout inspections, measuring dimensions (length, height, angles, radii, etc.) using precision instruments (micrometers, calipers, gauges, etc.) to ensure compliance with drawings, specifications, and codes. Verify quality at all stages: incoming materials, in-process work, and final products. Visually inspect parts, welds, bolts, coatings, and assemblies; compare pieces to detect variations; enforce standards and legal requirements. Interpret and apply shop drawings, specifications, ASTM codes, AISC standards, DOT requirements, and welding/bolting/painting codes. Maintain accurate inspection records, defect lists, and calibration of measuring equipment; coordinate with departments to resolve quality issues. Support operator training on measurement, visual acceptability, and processes; assist with internal and external audits. Manage NDE (Non-Destructive Examination) training, testing, certification, and documentation; maintain CWI certification. Review and approve quality-related purchase orders, reports, and testing requirements. Assist in developing procedures, quality summaries, and corrective actions; enforce non-conformance protocols. Serve as liaison with outside inspectors; investigate shop/field errors and support resolutions. Perform other QA-related tasks as required by supervision. Qualifications Strong knowledge of welding symbols and diagrams, and inspection tools. Highly proficient in reading blueprints and other printed instructional material. Basic Math & Geometry/Trigonometry. Familiar with variety of weld processes: Flux Core Arc Welding (FCAW), Sub Arc Welding (SAW), Gas Metal Arc Welding (GMAW), and/or Gas Tungsten Arc Welding (GTAW) Ability to perform and document inspection activities during fabrication and welding of structural piece members. Microsoft Office. CWI preferred. Self-motivated, collaborative team member. Safety focused. Operates equipment and champions safety initiatives. Education High School Degree or GED Equivalent preferred Minimum of seven years related experience and/or training in steel fabrication; or an equivalent combination of higher education and experience in the steel fabrication industry or closely related fields. Physical Requirements The demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires prolonged walking, standing, sitting, bending, squatting, stooping, climbing, regular lifting and carrying to move up to 50 lbs., talking, hearing, reaching, feeling, grasping, and push/pulling. Must be able to work in various weather conditions/temperatures. Regular mental and visual attention much or all the time with manual coordination. General office environment conditions. Flexibility required to travel. JGM offers a competitive wage and benefit package: Participate in the companys yearly performance bonus program Medical, Vision & Dental PTO & Holidays 401(k) + Matching Life Insurance Short/Long-Term Disability Employee Assistance Program Generous Referral Program Training and Further Education This job description is subject to change based on the needs of the business and is notall-inclusive. JGM is an Equal Opportunity Employer. Employment decisions are made 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.

Piper Companies is seeking a Quality Control Analytical Scientist (Flow Cytometry) to support GMP analytical testing for a late-stage biopharmaceutical organization advancing gene therapies for rare genetic disorders. This onsite role in Exton, PA offers hands-on experience with flow cytometry and related cell-based assays supporting clinical manufacturing. Responsibilities of the Quality Control Analytical Scientist (Flow Cytometry): * Perform GMP-compliant flow cytometry assays to support in-process, drug substance, and drug product testing. * Execute methods such as percent transduction efficiency and CD90 analysis. * Support additional testing platforms including cell culture, ELISA, and qPCR. * Review results for accuracy, data integrity, and compliance with GMP documentation standards. * Conduct investigations, CAPAs, and method troubleshooting as needed. * Maintain laboratory organization, equipment calibration, and readiness for audits. Qualifications of the Quality Control Analytical Scientist (Flow Cytometry): * 3-5 years of QC experience in a GMP-regulated biopharma or biologics environment. * Strong experience with flow cytometry, gating strategies, and data analysis. * 2-3 years of mammalian cell culture experience preferred. * Familiar with analytical assays such as ELISA and qPCR. * BS in Biochemistry, Biology, or related Life Science required. Compensation for the Quality Control Analytical Scientist (Flow Cytometry): * Pay Rate: $40/hour * Type: Contract-to-Hire (benefits included) * Location: Onsite - Exton, PA * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays Application Period: This position opens for applications on 1/5/2026 and will remain open for a minimum of 30 days from the posting date. Keywords: Quality Control, QC Scientist, Flow Cytometry, FACS, GMP, Analytical Testing, Biologics, Gene Therapy, Cell Culture, ELISA, qPCR, Transduction Efficiency, CD90, Gating Strategy, Data Integrity, CAPA, SOP, Aseptic Technique, QC Assays, Biopharma, Exton PA #LI-JM1 #LI-ONSITE

Full-time Description At SPL, we turn science into impact. We're searching for a driven Laboratory Analyst I to join our Inorganics team in Reading, PA. In this role, you'll receive hands-on training from industry experts, work with advanced analytical instrumentation, and perform testing and data analysis that support client, regulatory, and internal quality requirements. The data you produce will help ensure accuracy, compliance, and confidence in results that matter. If you're ready to build technical expertise, expand your analytical skills, and grow your career in a collaborative, purpose-driven lab, we want to hear from you! Please note: This position works our second shift schedule Monday - Friday from 2:00 PM - 10:00 PM. What You'll Do Perform sample preparation, analytical testing, and data entry in accordance with approved methods, SOPs, and quality standards; Operate and maintain laboratory instruments, performing routine calibration, troubleshooting, and preventative maintenance; Accurately document and review results within the Laboratory Information Management System (LIMS) or designated systems; Support the laboratory's quality system by following Good Laboratory Practices (GLP), assisting with audits, corrective actions, and continuous improvement initiatives; Adhere to safety and compliance protocols to maintain a safe and efficient laboratory environment; Assist with general laboratory housekeeping, inventory management, and cross-training as needed; Perform other duties as assigned. Requirements What Makes You a Great Fit Associate's or Bachelor's Degree in Science or related area. Equivalent experience may be considered in lieu of degree; Previous hands-on experience in a professional or academic lab setting; Experience with ion chromatography (IC), titrations, gravimetric analyses, pH, and/or alkalinity strongly preferred; Ability to manage and process high volumes of samples efficiently; Proficiency with Microsoft Office tools (Word, Excel, Outlook) and Adobe Acrobat; Strong analytical, organizational, and problem-solving skills, with a high level of attention to detail. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 10 paid holidays plus a generous time off plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position following a standard Monday through Friday schedule; Flexibility to work outside of normal hours to support business needs and deadlines; Must be able to work 2nd shift schedule Monday - Friday from 2:30 PM - 10 PM and be able to support a monthly Sunday rotation and holiday rotation. Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future.