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QC Analyst I
Legend Biotech 4.1
Quality control analyst job in Raritan, NJ
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QC Analyst I as part of the Quality team based in Raritan, NJ. Role Overview The QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. Key Responsibilities Be responsible for the completion of QC testing related to the manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment. Ensure testing is completed in compliance with all applicable procedures, standards and GMP regulations. Conduct analytical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories. Perform peer review/approval of laboratory data. Utilize electronic systems (LIMS) for execution and documentation of testing. Create, review and approve relevant QC documents, SOP's and WI's. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Work in a collaborative team setting with quality counterparts that include Quality Assurance, Manufacturing Operations, and Analytical/Process Development. Job duties performed require routine exposure to and handling of biological materials and hazardous chemicals. Requirements Bachelor's Degree in Science, Engineering or equivalent technical discipline is required. Minimum of 1 year relevant work experience, preferably within a biological and/or pharmaceutical industry is required. Experience in a Quality Control setting is preferred. Experience with processing samples in biosafety cabinets utilizing aseptic technique is strongly preferred. Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products is strongly preferred. Knowledge of Good Tissue Practices is required. Knowledge of CAR-T QC test methods and related equipment is preferred. Excellent written and oral communication skill are required. Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process. Candidates must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice. The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision. Comfortable with speaking and interacting with regulatory inspectors. This position may require occasional travel to partner sites in NJ or PA as business demands. This position may require up to 5% domestic or international travel as business demands. Ownership and Commitment Takes responsibility for one's results and deliverables; sets and achieves goals to support organizational priorities. Takes initiative; willing to take unpopular positions/actions when necessary; courageous and assertive. Works effectively in the face of ambiguity, shifting priorities, and rapid change; maintains a positive outlook in difficult situations; a change agent. Agility and Prioritization Identifies and focuses on activities of highest value and impact; makes informed decisions quickly. Results oriented; defines goals, metrics and actionable plans and manages work to deliver desired outcomes; has a sense of urgency. Considers resources, alternatives, constraints and desired outcomes to make effective decisions. Employs good project management principles to appropriately align time, resources, and budgets. Teamwork and Communication Appreciates diverse perspectives and is actively inclusive of others' input and ideas; treats others with respect. Articulates ideas clearly and succinctly in a variety of settings and styles; can get messages across that have the desired effect. Leverages personal credibility and interpersonal skills to help others make better decisions and positively impact outcomes; able to develop/maintain effective working relationships internally and externally Employs a global mindset in decision-making and errs on the side of over-communicating to create organizational transparency, trust and alignment. Continuous Improvement Takes initiative, actively shares knowledge, builds skills, promotes new ideas and embraces change. Generates new solutions to problems by challenging the status quo and conventional thinking. #Li-BG1 #Li-Onsite The anticipated base pay range is$61,454-$80,656 USD Benefits We are committed to creating a workplace where employees can thrive - both professionally and personally. To attract and retain top talent in a highly competitive industry, we offer a best-in-class benefits package that supports well-being, financial stability, and long-term career growth. Our offerings are designed to meet the diverse needs of our team members and their families, ensuring they feel valued and supported every step of the way. Highlights include medical, dental, and vision insurance as well as a 401(k)-retirement plan with company match that vest fully on day one. Equity and stock options are available to employees in eligible roles. We offer eight weeks of paid parental leave after just three months of employment, and a paid time off policy that includes vacation days, personal days, sick time, 11 company holidays, and 3 floating holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs - demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work. Please note: These benefits are offered exclusively to permanent employees. Contract employees are not eligible for benefits through Legend Biotech. EEO Statement It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. Legend may adjust base salary or other discretionary compensation at any time based on individual, team, performance, or market conditions. Legend Biotech maintains a drug-free workplace.
$61.5k-80.7k yearly Auto-Apply 1d ago

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Analyst II, Quality Control
Resilience 4.4
Quality control analyst job in East Norriton, PA
A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Position Summary As an Analyst II, Quality Control, supporting the Quality Control department at our East Norriton, PA facility, this role reports to the Technical Lead Manager and performs routine testing for manufacturing release and stability samples of gene (viral vector) and cell therapy products. The QC Analyst II partners closely with Manufacturing and QC Operations teams to ensure all required testing is completed in compliance with established standard operating procedures and testing methods, while meeting internal stakeholder needs. This role may require support for weekend testing as needed. Job Responsibilities * Perform routine sample analysis in support of manufacturing release and stability activities. * Sample testing of manufactured products using protein-based assays, molecular methods, and cellular assays. * Participate in method qualification/validation activities as necessary. * Analyze, document, and report experimental data in accordance with Resilience requirements. * Maintain, calibrate, and operate analytical equipment. * Qualify equipment related to testing. * Document work in accordance with cGMPs, established business processes and applicable SOPs. * Author SOPs, methods, protocols, training materials, and reports in alignment with applicable cGMPs, business standards, and intended use. * Own, author, and support QC change controls for the East Norriton site, as applicable. * Other activities as assigned Minimum Qualifications * Experience in mammalian cell culture. * Knowledge of general analytical methods. * Successful visual acuity test required for this role. Preferred Qualifications * BS in relevant discipline (immunology, cell biology, or related field). * 2 or more years relevant life science experience. * GMP Experience preferred. Sponsorship or support for work authorization, including visas, is not available for this position. Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $65,000.00 - $91,250.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.
$65k-91.3k yearly Auto-Apply 3d ago
Analyst II, Quality Control
National Resilience, Inc.
Quality control analyst job in East Norriton, PA
A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Position Summary As an Analyst II, Quality Control, supporting the Quality Control department at our East Norriton, PA facility, this role reports to the Technical Lead Manager and performs routine testing for manufacturing release and stability samples of gene (viral vector) and cell therapy products. The QC Analyst II partners closely with Manufacturing and QC Operations teams to ensure all required testing is completed in compliance with established standard operating procedures and testing methods, while meeting internal stakeholder needs. This role may require support for weekend testing as needed. Job Responsibilities Perform routine sample analysis in support of manufacturing release and stability activities. Sample testing of manufactured products using protein-based assays, molecular methods, and cellular assays. Participate in method qualification/validation activities as necessary. Analyze, document, and report experimental data in accordance with Resilience requirements. Maintain, calibrate, and operate analytical equipment. Qualify equipment related to testing. Document work in accordance with cGMPs, established business processes and applicable SOPs. Author SOPs, methods, protocols, training materials, and reports in alignment with applicable cGMPs, business standards, and intended use. Own, author, and support QC change controls for the East Norriton site, as applicable. Other activities as assigned Minimum Qualifications Experience in mammalian cell culture. Knowledge of general analytical methods. Successful visual acuity test required for this role. Preferred Qualifications BS in relevant discipline (immunology, cell biology, or related field). 2 or more years relevant life science experience. GMP Experience preferred. Sponsorship or support for work authorization, including visas, is not available for this position. Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $65,000.00 - $91,250.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.
$65k-91.3k yearly Auto-Apply 5d ago
Control Room Associate
Niagara Water 4.5
Quality control analyst job in Allentown, PA
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.
$30k-41k yearly est. Auto-Apply 60d+ ago
QC (Quality Check), Shipping & Packaging
Us207
Quality control analyst job in Allentown, PA
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.
$15 hourly Auto-Apply 60d+ ago
Quality Control Technician I - 2nd shift
Solesis
Quality control analyst job in Quakertown, PA
What we are looking for: The Quality Control Technician conducts inspection and testing activities at various manufacturing states including incoming, in process, and final release. 2nd Shift: Monday-Friday 3:00pm-11:00pm What you will do: Performs first article, in process, and final release testing for raw materials, as well as textile-based products. Utilizes a variety of testing equipment, including tensile testing machines, microscopes, and vision systems. Records and communicates test results manually and/or electronically. Inspects product for defects and contamination, according to Work Instructions (WI), Visual Inspection Criteria, SOP's, and internal specifications. Conducts extensive data collection to support the identification of trends to increase yields through process improvement. Enters visual inspections results as well as physical testing results into the applicable tracking databases. Packages and labels components in preparation for release. Generates certification documentation to accompany shipments. Enters information and uses ERP system to report quantities. Other duties as assigned Who you are: High School diploma or equivalent required. 0-1-year related experience preferred. Strong attention to detail. Intermediate computer skills. Proficiency in MS Word and MS Excel. Basic understanding of GMP and working within regulated industries. Demonstrated ability to communicate effectively with peers and management. Ability to multi-task change direction with shifting priorities. What we offer: Paid Breaks Generous Paid Time off and Holiday Pay Annual Bonuses Health Insurance: Medical with Rx plan / Dental / Vision 401k (retirement savings) with excellent company match Company Paid Short-Term and Long-Term Disability
$34k-48k yearly est. 47d ago
Chemistry Laboratory Technician
Us Cannalytics
Quality control analyst job in Bethlehem, PA
Are you looking for a job that's both challenging and fun? US Cannalytics is looking for a candidate that seeks a challenging Chemistry Laboratory Technician position in the exciting and ever-evolving medical cannabis industry. The successful candidate will be reliable, exhibit strong attention to detail and thrive in a fast-paced laboratory environment LABORATORY TECHNICIAN QUALIFICATIONS, must: Have a valid driver's license and high school diploma or equivalent. 21+ years old and subject to applicable employment requirements for the state of Pennsylvania for cannabis businesses including criminal background check. 2 years of relevant, professional (non-academic) laboratory experience or 1 year of laboratory experience plus a skills assessment. LABORATORY TECHNICIAN RESPONSIBILITIES: The laboratory technician is responsible and accountable for the testing, quality control, and tracking of cannabis material. The laboratory technician will ensure the safe, accurate, and timely testing of cannabis products. ESSENTIAL DUTIES: Proficiently utilize Microsoft Word and Excel, and other laboratory information management systems. Work in a timely manner, while striving to improve quality and maintain accuracy during all laboratory activities. Follow organizational policies and procedures for laboratory operations and comply with all state-specified rules and regulations for cannabis licenses, cannabis transport and cannabis testing, as applicable. Responsible for accurate measurements and documentation of all cannabis and cannabis materials, including sample weights/volumes, compliant cannabis tracking and destruction, and completion of supporting laboratory documentation. Adhere to Good Documentation Practices (GDP) for the completion of laboratory logs, forms, worksheets, or other documentation. Maintain laboratory reagent and supply inventory, including compliant documentation. Assists with the performance of sample intake and accessioning, and non-analytical test methods (foreign material, water activity, moisture content, etc.), as needed. Participate in and endeavor to complete training and be determined competent for assigned test methodologies including the following steps: a. Sample collection, intake and homogeneity. b. Sample preparation across all applicable matrices. c. Reagent preparation, including safe handling, storage and disposal. d. Sample loading and initial data analysis performed under the technical supervision of a Laboratory Chemist. e. Daily performance checks of applicable analytical equipment and method test parameters. f. Regular instrument cleaning and preventative maintenance for applicable analytical equipment. g. Basic troubleshooting of testing methodologies including all items listed within this sub-section. For test methods the employee has been trained and determined competent for: a. Independently prepare samples using aseptic techniques, including compliant documentation and necessary updates to laboratory workflow. b. Independently prepare reagents, solutions, and substrates for the equipment necessary for testing, including compliant documentation and necessary updates to laboratory workflow. c. Perform initial data analysis under the technical supervision of a Laboratory Chemist or Microbiologist. d. Assist in equipment and method validations or verifications, including compliant documentation and necessary updates to laboratory workflow. e. Successful completion of proficiency testing samples, completed as part of ongoing competency within the test method. Perform all other tasks and duties as assigned by Management, which may include cannabis sampling and transport. WORK ENVIRONMENT: The work environment characteristics described below 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. Work is performed in a production laboratory environment and requires use of personal protection equipment to limit exposure to chemicals or other hazards found within a laboratory environment. Work environment is fast-paced and will require frequent pivoting and multitasking, as well as the reprioritization of tasks based on demand/urgency. The work environment may expose employee to fumes or airborne particles, moving mechanical parts and vibration. The noise level in the work environment may be loud. Per state requirements for this industry, the facility is secured by user-specific access and is surveillance by cameras located throughout the laboratory except in restrooms. PHYSICAL DEMANDS: The physical demands described 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. Ability to concentrate and consistently produce accurate work. Frequent standing, walking, sitting, and use hands. Occasionally lift and/or move up to 40 pounds. Visual requirements to include close vision, color vision and ability to adjust focus. WORK HOURS: Wednesday - Saturday (training and competency determined on a Monday-Friday schedule) Job Type: Full-time, 10-hour shifts Benefits: Dental insurance Health insurance Paid time off Vision insurance Schedule: Tuesday-Saturday 10 hour shifts Overtime available Work Location: In person Job Type: Full-time Compensation: $20-$22 / hour Expected hours: 40 - 45 per week Education: High school or equivalent (required) BS in a natural science (preferred) Experience: Laboratory: 1 year (required) Analytical chemistry in a high-volume laboratory setting: 2 years (preferred) Laboratory sample extractions: 2 years (preferred) Agilent HPLC and/or GC: 2 years (preferred) Cannabis: 1 year (preferred)
$20-22 hourly 56d ago
Quality Control Technician
Polytek Development Corp
Quality control analyst job in Easton, PA
Polytek Development Corp. is a leading manufacturer of mold making and casting materials. Polytek is currently looking for a highly motivated, experienced, and extremely organized individual to join our rapidly expanding company. Essential Job Functions: Major tasks and other key responsibilities include: Perform QC tests on incoming raw materials as described in QC SOP. Perform QC tests on production samples as described in QC SOP. Mixing and curing test samples. Run Titrations, Viscosity measurements, Hardness measurements. Work with analytical equipment (including FTIR, TGA, rheometer, DSC). Hazardous chemical handling, storage, and disposal. Physical property testing (including viscosity, specific gravity, tensile/tear strength). Perform any testing and inspection required for customer returns. Perform any testing and inspection required for customer complaints and product non-conformance. Perform additional testing as required for off-specification raw materials and batches. Perform additional testing, ie. Soak tests, physical properties, product application, etc as directed. Interact with production personnel on pilot batches and production problems. Generate weekly QC Reports. Keep laboratory work area neat and uncluttered. Organize and maintain QC retain product samples and cured samples. Understand hazards of Polytek products through company provided training and reading SDSs and labels. Wear proper personal protective equipment (e.g., gloves and safety glasses) and follow all safety rules. Report safety concerns immediately to your supervisor. Perform other duties as assigned. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Must be able to work in a laboratory environment. Must be able to climb a ladder, frequently lift up to 8 lb, and occasionally lift up to 40 lb. Must be able to bend, squat, walk, stand, use hands to finger, handle or feel, reach with hands and arms, and repeatedly ascend/descend short flights of stairs/ladders for a full shift. Must be able to talk, hear and see with vision abilities including close/near, distance, color and peripheral vision, depth perception and ability to adjust focus. Must wear required Personal Protective Equipment (PPE) when entering laboratory or manufacturing areas. Education and Experience: Must be able to understand, speak, write, and read English. Bachelor's Degree in Chemistry or related field required. 1 - 3 years experience in quality control function in a chemical manufacturing environment is a plus. Skilled in quality processes and statistical techniques. Must have ability to work a flexible schedule, including occasional overtime. Must be proficient in Microsoft Office Suite. Must have the ability to work independently in a fast-paced environment. Strong verbal and written communication, organizational, and time management skills. 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.
$34k-48k yearly est. 5d ago
QC Laboratory Technician
Quva 4.5
Quality control analyst job in Bloomsbury, NJ
Our QC Laboratory Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing basic laboratory support functions related to the management of laboratory samples, materials, and testing supplies. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role working Monday through Friday from 8:00 AM to 4:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the QC Laboratory Technician Does Each Day: Verifies information on incoming lab samples and enters sample information into the laboratory database Place orders and stock laboratory supplies Light housekeeping, including operation of glassware washer Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPs Our Most Successful QC Laboratory Technicians: Are accurate and well organized, with strong attention to detail Express energy, show accountability, can multi-task and work in a fast-paced, quality-rich environment Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels Have good interpersonal skills and work effectively and efficiently in a team environment to accomplish goals Have strong verbal and written communications skills Minimum Requirements for this Role: A High School diploma or equivalent Able to successfully complete a drug and background check Proficient in Microsoft Office, Word and Excel Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: Bachelor's Degree in life science or related field 1 to 2 years' experience in data entry/clerical, or related responsibilities Benefits of Working at Quva: Set, full-time, consistent work schedule Comprehensive health and wellness benefits including medical, dental and vision 401k retirement program with company match 17 paid days off plus 8 paid holidays per year Occasional weekend and overtime opportunities with advance notice National, industry-leading high growth company with future career advancement opportunities Salary Range: $18.85-27.34/hour About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.” California Consumer Privacy Act (CCPA) Notice for Applicants and Employees
$18.9-27.3 hourly 54d ago
Laboratory Analyst II (Inorganics)
SPL 4.6
Quality control analyst job in Reading, PA
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.
$34k-47k yearly est. 19d ago
Quality Control Technician- 2nd Shift
Berks Packing Co
Quality control analyst job in Reading, PA
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.
$33k-47k yearly est. 60d+ ago
Quality Control Technician- 2nd Shift
Berks Packing Co., Inc.
Quality control analyst job in Reading, PA
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.
$33k-47k yearly est. 7d ago
Quality Control
Nucor Corporation 4.7
Quality control analyst job in Bethlehem, PA
Job Details Division: Nucor Rebar Fabrication Northeast Other Available Locations: N/A Welcome to Nucor, where our unique culture sets us apart. Joining Nucor means becoming part of North America's largest steel and steel products manufacturer, offering unmatched career opportunities and stability. We are known for our innovative sustainability practices and are the continent's largest recycler. Our vibrant culture, built on personal connections and teamwork, empowers every team member with the freedom to innovate and contribute to our collective success. Experience a workplace where safety, efficiency, and meaningful personal connections define every day, enriching both our teammates and the communities we serve. Nucor supports its teammates with top-tier benefits like Medical, Dental, Vision, and Disability Insurance, 401K and Roth accounts, Profit sharing, Pay-for-performance bonuses, Paid parental leave, Tuition reimbursement, Stock program, Scholarships and more. Basic Job Functions: * Must adhere to Nucor's safety programs and standards. * Demonstrate conduct consistent with Nucor's vision and values. * Perform and document all tests required (per the Quality Manual) during a production shift. * Participate in non-conformance root cause analysis. * Report and document any non-conformance to the Quality Manual requirements. * Report and document any non-conformance to tests performed. * Perform other tasks and duties as assigned Safety is the most important part of all jobs within Nucor; therefore, candidates must be able to demonstrate the ability to initiate, lead, and uphold safety policies, practices, procedures, and housekeeping standards at all times.Minimum Requirements: * Legally authorized to work in the United States without company sponsorship now or in the future. * High school diploma, GED or state/local equivalent Preferences: * Knowledge of CRSI quality standards * Proficiency in MS Office, including strong Excel and Word.Physical Demands: * Some heavy lifting may be necessary * Working conditions can be noisy, dusty, hot, cold Special Demands: * Must be able to work overtime when required * Some travel may be required * Must be able to work any shift * Must be familiar with and adhere to shop safety policies and procedures * Communication with various DOT customers * Communication with CRSI * Maintain and update CRIS QM as needed * Maintain DOT certifications with all states as needed * Understanding of ASTM coating and fabrication standards Nucor is an Equal Opportunity/Affirmative Action Employer - M/F/Disabled/Vets - and a drug - free workplace
$36k-43k yearly est. 60d+ ago
QC Inspector Trainee - Manufacturing
Onesource Staffing Solutions
Quality control analyst job in Phillipsburg, NJ
Job description: QC Inspector Trainee (Manufacturing) Phillipsburg, NJ Pay: $17-$20 per hour Schedule: Monday-Friday, 7:30 AM - 4:30 PM Type: Temp-to-Hire We're seeking a Quality Control Inspector Trainee to join our client's manufacturing team in Phillipsburg, NJ. A quality control (QC) inspector ensures products and processes meet established standards by inspecting materials, conducting tests, and documenting any defects. They use tools like micrometers and other instruments, analyze data, identify trends, and collaborate with production teams to implement corrective actions and improve overall quality. Their role is crucial for maintaining product consistency, ensuring safety, complying with regulations, and customer's specifications. Responsibilities: Conduct visual inspections and measurements on raw materials and finished goods to identify defects or deviations from standards. Documentation & Reporting: Record inspection results, document any non-conformities or defects, and assist in entering results into the computer system. Tool & Equipment Management: Operate and maintain testing equipment and instruments, ensuring their accuracy and reliability for consistent results. Skills and Qualifications Attention to Detail: A keen eye for identifying small flaws and discrepancies in products and processes. Analytical & Problem-Solving Skills: The ability to interpret data and validate test method procedures. Technical Knowledge: Understanding of measurement tools like calipers, gauges, and micrometers, preferred but training will be provided Organizational Skills: Necessary for managing tasks, prioritizing, and maintaining an orderly workspace. Physical Stamina: The job involves standing for long periods, lifting heavy objects (up to 60 lbs.) with team lift and moving materials. Basic Math Skills: Required for tasks such as counting, weighing, and measuring goods. Computer Literacy: Proficiency in using computers is preferred but training will be provided. Communication Skills: Ability to communicate effectively and professionally with other plant employees as well as vendors when needed. Why Join Temp-to-hire opportunity with a stable, growing manufacturing company. Full-time, consistent schedule. Weekly pay through OneSource Staffing. Supportive team environment with room to grow. How to Apply Apply today to join a growing and stable manufacturing team! Submit your resume to onesourcestaffing.com or Call OneSource Staffing - Easton Office at 610-750-9198 for immediate consideration. Benefits: Dental insurance Health insurance Vision insurance
$17-20 hourly 13d ago
Quality Control Technician - 3rd Shift
Blommer Chocolate Careers 4.5
Quality control analyst job in East Greenville, PA
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.
$41k-49k yearly est. 13d ago
Field Chemist
Heritage Environmental Services, LLC 4.4
Quality control analyst job in Telford, PA
Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries. Why Arcwood? * Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves. * Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges. * Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant, Always. * Collaborative Environment: Together we can achieve much more. Join a supportive and dynamic team where your ideas and efforts are recognized and rewarded. Our Commitment: We are dedicated to fostering an inclusive and innovative workplace where every employee can thrive. As part of our team, you will have the freedom to contribute your expertise wherever needed, ensuring the success of our mission to protect the environment. Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet. Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future. Field Chemist As a Field Chemist you will be responsible for sorting and transporting hazardous and non-hazardous materials and waste, always ensuring compatibility and safety in all processes for each service provided to customers. Essential Functions & Requirements: * Prioritizes health and safety by adhering to policies, processes, and maintaining safe practices at all times * Assists in the segregation of chemicals by hazard class and packs compatible materials in appropriate containers and prepares for transportation; completes necessary paperwork for each job * Determines and loads supplies needed for job completion and travels to various industry, laboratory, and educational sites to perform lab pack services * Assists in characterizing materials at field project sites * Adheres to proper placarding and load segregation requirements when transporting hazardous materials * Develops good customer relations by effectively communicating with site points of contact and others at customer location / site * Appropriately directs Field Technicians / Drivers who are assisting with waste collection * Maintains an introductory knowledge of high-hazard materials management / assessment and cylinder handling * Maintains the ability to travel to support outside locations as needed * Takes on additional duties as assigned to support the team and organization Education: * Bachelor's degree (required), with a focus in environmental science or science (preferred) Experience: * In lieu of degree 2+ years of related experience (required), previous experience in lab packing or environmental waste (preferred) * Valid Driver's License and ability to obtain a Class B CDL with Hazmat endorsement within 6 months of hire date (required) * Ability to pass a Motor Vehicle Record search to Company standards (required) Competencies: * Ability to work in a constant state of alertness and in a safe manner * Ability to develop a working knowledge of all Federal, State, and local laws and regulations pertaining to the Environmental Services industry * Excellent interpersonal skills to effectively communicate with internal and external customers * Regular and predictable attendance to perform the functions and requirements of this role Additional Requirements: * Due to the potential exposure to atmospheres/waste/materials this position requires individuals to be clean shaven at all times in order to don a respirator for protection. Benefits, Compensation, & Workforce Diversity: Arcwood offers competitive pay and bonus incentives. Benefits include choice of medical, dental, and vision plans, flexible spending or health savings accounts, employee and dependent life insurance, short and long-term disability, 401(k) savings plan with 7% company match, and tuition reimbursement. Equal Opportunity Employer - Veterans & Disabilities A post-offer drug screen and background check will be required.
$46k-66k yearly est. 22d ago
QC Receiving Specialist
Jax Diversified II Inc.
Quality control analyst job in Brookfield, NJ
Job DescriptionDescription: The Key Objective of the Quality Assurance Receiving Specialist is to contribute to the growth and profitability of Multi-Pak by effectively executing the functions of Quality Management while providing additional support to the other senior managers. Specifically, under the general direction of the Lead Quality Assurance Receiving Specialist, they are responsible for the following: inspection of all incoming bulk, components, primary and secondary labeling, and other packaging operating supplies per appropriate specification and/or procedure to ensure adherence to cGMPs and other regulatory requirements. He/she shall ensure that all incoming material meets the required specifications to be released for production. RESPONSIBILITIES: Essential Functions: • Ensure inspection activities are being performed not limited to verifying the quantities of all the pallets received in, performing the sampling for receiving inspection, signing off the receiving inspection report and logging into the Receiving inspection logbook. The inspection shall be performed for every incoming material - bulk, labeling material, and components. • Ensure receiving reports are created and documented correctly as per the SOPs and work instructions and are consistent with the product description detailed in the Inventory Checklist. • Assures material meets the appropriate specifications through appropriate inspection methods as described in the SOP and/or specification. • Responsible for managing the entire label issuance procedure including the inspection, label verification, issuance to the Label Room and verifying the returns from the production. • Responsible for intimating the Client services department and required personnel of the receiving inspection discrepancies. • Ensure the Transfer tags are created and documented correctly for the label transfers from Chapin warehouse to Clinton warehouse and vice versa. • Ensure samples are correctly stored and managed in the Chapin warehouse. • Manage the Quarantine area in both Chapin and Clinton warehouse. • Responsible for verifying the disposition of materials and signing the documentation for the same. • Responsible for maintaining accurate records and following good documentation practices for all materials inspected. • Maintain and manage all Component Specifications and Color Standards as required and provided by the client. Nonessential Functions/Demands: • Assists QA Department with documentation and QC Inspection when required. • A person in this position may occasionally be required to work in outdoor weather conditions. Requirements: • Associate's/Bachelor's Degree (preferred). • 1-2 years in related experience (especially in pharmaceutical industry). • Ability to demonstrate strong organizational skills. • Exercise judgment within defined procedures and practices. • Must be a strong team player with good problem solving, and good verbal and written communication skills. • Knowledge of GMP documentation and FDA required. • General knowledge of quarantine and warehouse operation. • Good knowledge of Microsoft Office programs. PHYSICAL/MENTAL DEMANDS: • Must be able to lift-up to 30 pounds frequently and 50 pounds on occasion. • Must be able to remain in the stationary position for up to 40% of the time. • Must be able to walk or stand up to 90% of the time. • The person in this position will need to occasionally move about inside the office to access office machinery, file cabinets, etc. • The person in this position will need to frequently move about inside the warehouse requiring them to position themselves through pallets and warehouse locations. • The person in this position is required to function in narrow aisles or passageways. • The person in this position will need to occasionally kneel, climb, crawl, climb and/or reach to perform inspections. • The person in this position is required to communicate to all other departments and must be able to exchange accurate information in these circumstances.
$35k-61k yearly est. 4d ago
Analyst II, Laboratory Operations
8427-Janssen Cilag Manufacturing Legal Entity
Quality control analyst job in Spring House, PA
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: R&D Operations Job Sub Function: Laboratory Operations Job Category: Professional All Job Posting Locations: Spring House, Pennsylvania, United States of America Job Description: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at *******************/innovative-medicine We are searching for the best talent for an Analyst II, Laboratory Operations to be located in Spring House, PA. Purpose: This position is part of the global Discovery, Product Development & Supply (DPDS) Operations Team responsible for operations within the Therapeutic Discovery (TD) and Preclinical Safety and Translational Sciences (PSTS) organizations. The Lab Operations team in DPDS Operations looks after the lab workspace to enable the scientists to focus on their science using a knowledge of project management, drug discovery instrumentation and automation, and process excellence to evaluate, develop and deliver drug discovery laboratory processes and infrastructure. The Analyst II functions by planning and performing operational activities and acquisitions linked to the lab workspace. They work effectively in multi-disciplinary teams and collaborates with internal and external partners - such as Safety, Business Operations, Facility Management, Finance - thus ensuring flawless execution of all projects and processes connected to the lab workspace. The function requires a hands-on mentality and the ability to work autonomously for longer term activities independently adapting to project developments and proposing next steps. You will be responsible for: Overseeing and managing the day-to-day activities involving provisioning, instrumentation, facility maintenance and upkeep to optimize laboratory operations. Managing laboratory projects end to end, from idea through onboarding and installation of new instruments. Coordinating laboratory moves for facility projects. Ensuring routine and unscheduled equipment maintenance is performed within acceptable timeframes, effectively collaborating with external partners/organizations. Collaborating with IT to manage and maintain computer and automation systems, including systems upgrades and issue resolution. Working closely with scientific staff and leaders to ensure a steady and ongoing relationship with intent for efficient operation, improved automation, and workflow process improvements. Collaborating effectively with fellow team/project members following procedures, priorities and timelines. Maintaining general laboratory safety standards. Qualifications / Requirements: Education: A minimum of a Bachelor's degree in a Scientific field, Engineering, Information Systems or Business is required. An advanced degree is preferred. Experience and Skills: Required: A minimum of 2 years of relevant experience is required. Strong interpersonal communication skills, effective organization, communication, and customer service skills are required. Excellent attention to details is required. Strategic and critical thinking, prioritization, and ability to execute on those strategies are required. Preferred: Proven project management success and change management experience is highly preferred. Solid working knowledge of laboratory or highly controlled facilities operations, information systems, instrumentation, automation, safety, and compliance are highly preferred. Prior laboratory experience on the bench or laboratory/operational management experience for science background candidates is preferred. Prior facility or laboratory renovation project management is a plus. Prior experience and understanding of laboratory automation is a plus. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via *******************/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource. #LI-Onsite Required Skills: Preferred Skills: Analytical Reasoning, Business Behavior, Coaching, Communication, Data Management and Informatics, Data Savvy, Ethical and Participant Safety Considerations, Inventory Management, Laboratory Operations, Laboratory Safety, Mental Agility, Molecular Diagnostics, Preclinical Research, Problem Solving, Research and Development, Toxicology, Use of Laboratory Equipment
$35k-54k yearly est. Auto-Apply 7d ago
Laboratory Analyst I - 2nd Shift (Inorganics)
SPL 4.6
Quality control analyst job in Reading, PA
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.
$34k-47k yearly est. 9d ago
Chemical Technician
Polytek Development Corp
Quality control analyst job in Easton, PA
Polytek Development Corp. is a leading manufacturer of mold making and casting materials. Polytek is currently looking for a highly motivated, experienced, and extremely organized individual to join our rapidly expanding company. Essential Job Functions: Major tasks and other key responsibilities include: Accurately follow directions on batch sheets. Accurately and thoroughly record required information on batch sheets. Dispense and weigh chemicals into mixing pots to make batches. Pack chemical products from mixing pots into 55-gal drums, 5-gal pails, 1-gal pails and smaller containers. Move pallets of drums/materials with forklift. Maintain/use raw materials inventory on a “first-in, first-out” basis. Print product labels with a computer and label product containers. Clean mixing pots. Keep the production area neat and uncluttered. Put chemicals back on the rack after use. Understand the hazards of chemicals through company-provided training and read MSDSs and labels. Wear proper personal protective equipment (e.g., gloves, safely glasses or goggles, respirators, aprons, coveralls) and follow safety procedures and rules. Report safety concerns immediately to your supervisor, the Plant Manager or Safety Committee Member. Strive for continuous improvement. Perform other duties as assigned. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Must be able to stand for prolonged periods of time and perform repetitive tasks. Must be able to lift and/or move items up to 50 pounds. Must be able to bend, squat, walk, stand, use hands to finger, handle or feel, reach with hands and arms, and repeatedly ascend/descend short flights of stairs/ladders for a full shift. Must be able to talk, hear and see with vision abilities including close/near, distance, color and peripheral vision, depth perception and ability to adjust focus. Must wear job-specific Personal Protective Equipment (PPE) for entirety of shift. Education and Experience: Must be able to understand, speak, write and read English. High school diploma or equivalent required. One year manufacturing experience preferred; on the job training to be provided. Basic computer experience. 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.
$36k-54k yearly est. 3d ago

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How much does a quality control analyst earn in Allentown, PA?

The average quality control analyst in Allentown, PA earns between $34,000 and $90,000 annually. This compares to the national average quality control analyst range of $40,000 to $86,000.

Average quality control analyst salary in Allentown, PA

$56,000

$34,00010%

$56,000Median

$90,00090%

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Quality Control Analyst Jobs
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Quality Control Analyst Allentown, PA Jobs

Quality control analyst jobs in Allentown, PA - 75 jobs

QC Analyst I

Analyst II, Quality Control

Analyst II, Quality Control

Control Room Associate

QC (Quality Check), Shipping & Packaging

Quality Control Technician I - 2nd shift

Chemistry Laboratory Technician

Quality Control Technician

QC Laboratory Technician

Laboratory Analyst II (Inorganics)

Quality Control Technician- 2nd Shift

Quality Control Technician- 2nd Shift

Quality Control

QC Inspector Trainee - Manufacturing

Quality Control Technician - 3rd Shift

Field Chemist

QC Receiving Specialist

Analyst II, Laboratory Operations

Laboratory Analyst I - 2nd Shift (Inorganics)

Chemical Technician

Learn more about quality control analyst jobs

How much does a quality control analyst earn in Allentown, PA?