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Chemistry Technician
Millersville University of Pennsylvania 4.1
Quality control analyst job in Millersville, PA
Requisition Number P01248 Position Type Staff Department Chemistry Working Title Chemistry Technician Classification State University Administrator 2 - Non-exempt - S9640 Information Nature of position Permanent, Full-time If Temporary, Start Date If Temporary, End Date If part-time, hours per week If part-time, percent time Days Worked Monday - Friday Hours/Shift worked 8:00 a.m. - 4:30 p.m. Union SCUPA- SUA & GFPC
Posting Detail Information
Job Summary/Basic Function
About the position:
The Chemistry Lab Technicians primary duties include overall responsibility for the safe and efficient operation of laboratories and ongoing function of instrumentation in the Chemistry Department. The Chemistry Technician is responsible for preparation of laboratories in introductory chemistry courses, chemistry laboratory safety, and maintenance of the water purification systems, instrumentation rooms, and department inventory of equipment and supplies. This position also provides regular maintenance for the department's NMR spectrometer and assists faculty with instrumentation operation, repair, and maintenance, including computer interfacing. The Chemistry Technician is responsible for overseeing the maintenance of a list of potentially hazardous chemicals that are used in the College's laboratories and collaborating with faculty and staff for safe usage, storage, and disposal of hazardous chemicals. The Chemistry Technician works closely with the university and college safety committees and the Director of Environmental Health & Safety to assist with chemical safety issues and training arising throughout the College and elsewhere on the campus. The Chemistry Technician also assists with function of the College Storeroom.
Join Our Team at Millersville University!
Position Salary: $54,983.00 annually
Plus a generous benefits package designed to support your well-being and future:
* Comprehensive Health Coverage - Medical, dental, and vision insurance
* Group Life Insurance
* Retirement Plans - Choose from two excellent options
* Tuition Waiver - Invest in your education or your family's
* Paid Time Off - Vacation, sick leave, and holidays to recharge
* Full Benefits Summary(PDF)
Why Millersville?
Nestled in beautiful Lancaster County, Pennsylvania, Millersville University is a proud member of Pennsylvania's State System of Higher Education. We're known for:
* Strong student-faculty connections
* 70+ undergraduate and 24 graduate programs
* A stunning campus and vibrant community
* Outstanding job placement for graduates
With over 66,000 alumni across the globe, our impact is far-reaching-and growing.
Our Mission & Values:
At Millersville, we live by our EPPIIC values of Exploration, Public Mission, Professionalism, Inclusion, Integrity, and Compassion.
We are deeply committed to Inclusive Excellence-creating a welcoming, supportive environment where everyone can thrive. We believe diversity is a strength, and we actively seek individuals who bring unique perspectives and experiences to our community.
Equal Opportunity for All:
Millersville University is an equal opportunity employer. We welcome applicants from all backgrounds and are committed to providing a workplace free from discrimination. Individuals from traditionally underrepresented groups are strongly encouraged to apply.
Duties and Responsibilities
Introductory Chemistry Preparation Room Duties:
* Set up and break down labs for introductory chemistry courses: set out equipment as needed and make sure reagents and supplies are available; verify proper operation of equipment; prepare unknown samples as needed.
* Order equipment and chemicals needed in the preparation room or on behalf of faculty, check status of outstanding purchases, and sign off as needed.
* Prepare stock reagent solutions for upcoming labs.
* Ensure introductory labs are clean, stocked (soap, distilled water, and paper towels), and ready for each session.
* Ensure that all materials are promptly put away, chemical and reagent bottles are properly cleaned and maintained, and that the labs and prep room are clean of clutter and dirty glassware.
* Ensure that lab equipment (pH meters, balances, stirrer/hot plates, centrifuges, etc.) are clean and maintained in working condition for all chemistry labs and stored properly between use.
* Train and supervise student assistants for the prep room and help guide student lab assistants in other teaching labs, as needed.
Chemistry Department Duties:
* Be responsible for the safe usage, collection, disposal, storage, and cleanup of hazardous chemicals.
* Supervise and perform the annual capital equipment inventory and maintain the departmental inventory databases.
* Maintain and operate the water purification systems to replenish stock.
* Supervise gas cylinder usage, return of empty cylinders, ordering of replacement cylinders, and arrangement of lease renewal.
* Maintain and oversee the instrumentation room and assist faculty with instruments use, as requested.
* Conduct routine preventive maintenance checks on laboratory equipment, e.g., pH meters, spectrometers, balances, and centrifuges. Make or arrange for repair of equipment, as appropriate.
* Maintain and update the chemical inventory for all prep room, teaching labs, and research rooms and advise on safe use and storage, especially for high hazardous waste materials.
* Perform routine weekly liquid nitrogen fills and biannual liquid helium fills for the NMR, monitor GC/MS helium pressure, and replace FT-IR desiccants.
* Act as technician/engineer for instrument maintenance, troubleshooting and repair for the NMR.
* Install and maintain all scientific software used for chemistry equipment and instruments, including sign-on credentials.
* Complete other projects and assume additional duties as assigned by the Chemistry Department chair.
* Responsible for keeping his/her education or training up to date with regard to maintaining current certifications and acquiring new ones, as needed.
* Use the equipment which the department possesses, including pH meters, spectrophotometers (UV-VIS, FT-NMR, FTIR, vacuum pumps, GCs, AA and HPLC), power supplies, electrical meters, balances, and various chemistry laboratory equipment.
College Duties:
* Oversee the College of Science and Technology waste disposal, generate the appropriate paperwork for this disposal, and work with the Director of Environmental Health & Safety to arrange for waste pick-up from our holding facility.
* Inspect the hazardous waste storage facility weekly and update logbook.
* Assist the College of Science and Technology Safety Committee in responding to and cleaning up chemical spills in Caputo, Roddy, and Brossman Halls.
* Serve as a member of the College of Science and Technology Safety Committee.
* Track Storeroom inventory and help coordinate plans for ordering to maintain appropriate stock based on historical usage data.
* All other duties as assigned.
Required Qualifications
* Bachelor's degree in Chemistry or B.S. in science with strong chemistry background and at least one year experience in a chemistry laboratory.
* Experience with function and operation of scientific instrumentation.
* Ability to multitask and prioritize daily tasks alongside broader responsibilities.
* Excellent oral, written, interpersonal communication skills.
* Proficiency in Microsoft Office including Word, Excel, PowerPoint, Outlook.
* Commitment to inclusive practices and working with diverse student populations.
* Valid driver's license.
* Successful interview.
* Successful completion of three background checks.
Preferred Qualifications
* Master's degree in chemistry or closely related field.
* Trained in OSHA and EPA best practices.
* Experience repairing and maintaining scientific instrumentation.
* Experience working in higher education or research setting.
Essential Functions
Please Note: These duties are to be performed with or without an accommodation. We are committed to providing reasonable accommodations in accordance with Americans with Disabilities Act (ADA).
* Ability to:
* work in person on campus.
* lift/pull/push up to 50 pounds.
* Moderate physical effort required.
* Exposure to physical and chemical risks requiring attention to safe behavior and material handling.
* Work is normally performed in a typical interior/office work environment.
* Dexterity of hands and fingers to operate a computer keyboard and mouse and work with scientific materials and instruments.
Posting Open Date 12/17/2025 Posting Close Date 01/05/2026 Special Instructions to Applicants
* This position is represented by a labor union and is subject to the terms and conditions of the SCUPA- SUA & GFPC Collective Bargaining Agreement.
* Ability to work in person on campus.
Quicklink for Posting/Requisition ********************************************
$55k yearly 9d ago
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QC Scientist - I
Integrated Resources 4.5
Quality control analyst job in Lititz, PA
Responsibilities:
• Experience with lab instrumentation/equipment such as pH, viscometer, FTIR, Near-IR, AA preferred.
• Hands on set-up and troubleshooting experience with HPLC and GC required.
• Experience with sample preparation required.
• Experience with a chromatographic data acquisition system required.
• Experience with Compendia USP and preferred experience with NF, EP and/or FCC required.
• Computer skills with utilization of Microsoft Office (Outlook, Word, and Excel) required.
• Problem solving skills required, preferred experience with laboratory investigations.
• Ability to work individually as well as in a team.
• Self-motivated.
Job Description
Experience: A minimum of 1 years of analytical laboratory experience within the pharmaceutical or consumer healthcare industry.
Qualifications
Education: Bachelor Degree in Chemistry, related science or the equivalent.
Additional Information
Contact me at 732-549-5307
$55k-83k yearly est. 60d+ ago
Quality Control Analytical Scientist (ELISA)
ZP Group 4.0
Quality control analyst job in Exton, PA
Piper Companies is seeking a Quality Control Analytical Scientist (ELISA) to join a clinical stage company developing gene and cell therapies for rare diseases in Exton, PA. RESPONSIBILITIES: * Perform ELISA testing to support product manufacturing using manual and automated analytical equipment.
* Execute and maintain Quality Control analytical processes, including test procedures and validations.
* Troubleshoot assays and ensure proper equipment maintenance and calibration.
* Review logbooks and documentation for accuracy and compliance.
* Manage inventory and support qualification activities for QC operations.
QUALIFICATIONS:
* BS in biochemistry, chemistry, or similar field
* 3-5 years of Quality Control experience in a GMP-regulated environment, with a focus on ELISA methodology within the biologics industry.
* Strong understanding of Current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and applicable industry standards.
* Working knowledge of analytical instruments such as UV absorbance plate readers, flow cytometers, microscopes, and pH meters is preferred.
COMPENSATION/ BENEFITS:
* Pay Rate: $40/hr.
* Contract to hire
* Medical, Dental, Vision, 401K, PTO, Sick Leave if required by law, and Holidays
* Requires onsite availability Tuesday - Saturday
This job opens for applications on 11/13/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: Quality Control, Analytical Scientist, Gene therapy, Cell therapy, ELISA, Assay troubleshooting, plate reader, plate washer, micro pipetting, volume calculations, biochemistry, chemistry, Microsoft office, Exton pa, clinical stage, cell culture , flow cytometry
#LI-LR1 #LI-ONSITE
$40 hourly 47d ago
Controls Integration Intern
Tait Towers 4.3
Quality control analyst job in Lititz, PA
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: Controls Integration Intern
Job Specifications: Controls Integration Interns are tasked with making multiple elements work together as one cohesive system. Controls Integration Interns have essential responsibilities in project coordination especially focused on project sites around the world and exists on the uniquely TAIT line between technology and art.
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
+ Fulfill shop testing and setup responsibilities
+ Develop knowledge of one or more integration-related technical fields (including motion control, hydraulics, functional safety, industrial automation, rigging)
+ Communicates frequently with rest of project team about tasks and risks
+ Comprise part of field engineering and installation team, ultimately implementing technology on site for the customer
+ Setting up, configuring, testing, and programming entertainment automation systems
+ Building and putting the finishing touches on staging structures, automated machinery, and high-performance aerial rigging
+ Variety of markets: theme parks, theaters, concerts, cruise ships
+ Technical project leadership
Qualifications
To qualify for this internship, you must meet the following:
+ Currently pursuing a degree or equivalent in a related field:
+ Controls Engineering
+ Computer Science and Engineering
+ Technical Theatre
+ Physics
+ Other relative degrees
+ 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: Associate Control Integrator, TAIT Crew Associate
Why Choose TAIT?
+ Housing: We offer a housing stipend our onsite interns in PA, NY, FL, CO, NV, and CA. This benefit applies to interns who live more than 50 miles from the worksite and would need to relocate to the area to complete their internship.
+ 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.
$18 hourly 21d ago
Quality Control Specialist [Temp to Perm]
Castle Creek Biosciences LLC
Quality control analyst job in Exton, PA
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
$37k-66k yearly est. 21d ago
Quality Control Technician
Ster Seating
Quality control analyst job in Exton, PA
Full-time Description
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.
$33k-47k yearly est. 60d+ ago
Quality Control Inspector - Welding
R-V Industries Inc. 3.9
Quality control analyst job in Honey Brook, PA
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
$37k-54k yearly est. 9d 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. 17d ago
Laboratory Analyst (Inorganics)
Suburban Testing Labs 3.2
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 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 are looking to deepen your technical skills, support team development, and contribute to meaningful scientific outcomes, 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 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: 9 paid holidays plus a generous PTO 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. 50d ago
QC-QA Lab Technician
Brentwood Industries, Inc. 4.3
Quality control analyst job in Reading, PA
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.
$36k-44k yearly est. Auto-Apply 60d+ ago
Quality Control Microbiologist
Us Tech Solutions 4.4
Quality control analyst job in Myerstown, PA
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
Title: Quality Control Microbiologist
Duration: 12 Months
Location: Myerstown, PA 17067
Job Description:
Microbiology Team working in a fast paced environment, supporting manufacturing and packaging of OTC Drug and Nutritional products, across multiple shifts, by performing all aspects of Microbiological testing.
POSITION SUMMARY
This position is in the Quality Assurance department and the incumbent will be expected to continuously learn Quality Assurance systems, manufacturing, and effectively engage in relationships with peers in the laboratories, Manufacturing/Production and personnel in other departments as needed. Once the incumbent is assigned specific products on which to perform the quality assurance 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. Perform analysis on raw materials, intermediates, purified water systems, environmental monitoring and finished products, following prescribed procedures to provide the information base leading to raw material/intermediates/product disposition. Assist in troubleshooting and problem solving as directed, within the Microbiology area; focus is on Microbiological testing.
Position Duties & Responsibilities
Perform standard qualitative and quantitative analysis on: purchased raw materials, in-process products, pure drug substances and finished pharmaceutical preparations employing standard procedures, in accordance with approved testing procedures of BAYER, the National Formulary (NF) and the United States Pharmacopoeia (USP).
Utilize standard "bench" microbiological aseptic technique
Maintain records of all analysis information of assigned products on data sheets for permanent file and proper entry of information on laboratory forms.
Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with Supervisor and recommend additional testing if necessary.
Adhere to the pertinent aspects of Corporate and plant safety programs and adhering to GMP's, ISO standards or other regulations.
Assist in investigating non-compliance investigations.
Assist with troubleshooting analytical methodology and instrumentation malfunctions.
Perform special assignments as directed by supervisor.
Assist in validation of manufacturing and production lines and equipment pertinent to microbiology (e.g. equipment and room cleaning validation).
Prepare microbiological testing media/diluents.
Perform testing of water samples from Purified (Reverse Osmosis) Water, USP systems.
Perform microbiological environmental monitoring in production areas and in the Microbiology Laboratory.
Qualifications
Requirements/Preferences
Education Requirement(s):
Bachelor's degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required.
Skill & Competency Requirements:
At least 1 year of lab experience is required:
Assigned within the Microbiology area and/or previous experience in microbiology processes is preferred.
Knowledge, practical application, and understanding of microbiology are necessary to perform the functions of this position.
Good documentation practices
Ability to work collaboratively in a team-based environment is required.
Good working knowledge of personal computer skills are required;
Working knowledge of aseptic techniques, environment monitoring methods, Gram staining and microbiological test methods is required.
Competencies required: analytical problem solving, work within established policies and procedures, effective written and interpretive communication skills, and organization and planning skills.
Preferences:
A working knowledge of statistics, data processing and good manufacturing practices is desirable.
A thorough understanding of National Formulary (NF); United States Pharmacopoeia (USP); and European Pharmacopoeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP's), quality control methods and procedures preferred.
Thanks & Regards,
Mayank Gupta
(
Lead
Pharma Technical Recruiter)
Additional Information
All your information will be kept confidential according to EEO guidelines.
$39k-53k yearly est. 2h ago
Metal Anodizing/Plating/Chemical Treating Technician
Skillsource 3.3
Quality control analyst job in Valley, PA
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 ***************************
$33k-39k yearly est. 60d+ ago
QC Inspector
JGM
Quality control analyst job in Coatesville, PA
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.
$27k-43k yearly est. 11d ago
Quality Control Inspector - B3
Sunset Grown
Quality control analyst job in Jonestown, PA
Our Jonestown Distribution Center, a 218,000 sq. ft. refrigerated facility operating 24/7, is currently seeking a Quality Control Inspector to join our team. The essential function of this position is to assist the Quality Control team with daily activities and ensure that all product meets customer specifications and to proactively prevent rejections.
Rotational Full Time Shift: 3 Day & 4 Day Week: 6:00 PM - 5:30 AM
Primary Function:
The Quality Control Inspector will assist Quality Control Inspection Supervisor with all daily activities and to ensure that all
product meets customer specifications. This position collaborates with the Quality Control Inspection Supervisor, and
other warehouse personnel to proactively prevent rejections.
Values: To perform the job successfully, the incumbent's behavior must be consistent with the PRIDE values expected of
all Mastronardi Produce employee's: be Passionate; have Respect; be Innovative; be Driven and strive for Excellence.
Primary Responsibilities:
* Ensure that all product meets or exceeds customer specifications.
* Ensure allocation is followed, validate correct product is pulled and shipped to customer.
* Assist Quality Control Inspection Supervisor to ensure that all product inspections are being performed, labeling
specification are adhered to, and non-conformance product is pulled and corrected.
* Flex Between the shipping dock, receiving dock and production to assist Quality Control Inspection Supervisor
with Quality issues and/or inspections.
* Report any exceptions to the customer specifications to Quality Control Inspection Supervisor.
* Send out Quality Issues Emails for Non-Compliant Product.
* Oversee floor operations when the Quality Control Inspection Supervisor is unavailable.
* Remember recent rejections and rejection trends.
* Ensure Product packaging is in presentable condition for our customers.
* Ensure Presentation is of highest standards.
* Performs any other Quality Control related tasks or special projects as assigned.
* Provide training when required.
Education/Background Requirements:
* 1 Year College degree or 6 Months year of experience in a related field required.
* Previous experience in produce industry preferred.
Specific Knowledge, Skills and Abilities Required
* Must pass Drug Test, Background Check and pre-employment Skills Testing.
* Must sign a confidentiality agreement upon hire.
* Must be a self-starter and willing to work flexible hours.
* Proficiency in use of English language with the ability to communicate effectively and professionally.
* Proficient in computer-use skills (MS Office: Word, Excel and PowerPoint).
* Strong organizational, analytical and problem-solving skills. Need to be creative, adaptable and able to accurately
work with a sense of urgency.
* Spanish as a second language would be an asset.
* Inspection/audit experiences, working in software applications are considered assets.
* Proficient in basic computer skills, JDA or NAV experience preferred.
* Ability to use and read measuring devices such as scales, calipers, ruler.
* Excellent communication and interpersonal skills.
Working Conditions:
* Environment includes an expansive refrigerated warehouse, where the temperatures range is 45-55 degrees
(except office areas). The background noise approaches 70 dcbs.
* Must be capable of lifting up to 35 lbs.
Please note: Mastronardi Produce has accommodation processes and policies in place and provides accommodation for
employees with disabilities. If you require a specific accommodation because of a disability or documented medical need,
please contact the Human Resource office so that arrangements can be made for the appropriate accommodation to be
put into place.
$27k-43k yearly est. 29d ago
Quality Control Inspector
Medtec LLC DBA Civco Radiotherapy
Quality control analyst job in Avondale, PA
The Quality Control Inspector I is responsible for inspecting, testing, and auditing raw materials and finished products, as well as releasing finished products.
Attention to detail is an expectation.
Demonstration of commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures.
Inspect and release raw materials, components, sub-assemblies, and finished devices according to procedure.
Drives continuous improvement activities with cross-functional team members.
Generate non-conformances and escalate to the Material Review Board in a timely manner.
Interacts with production areas, manufacturing and design engineering, marketing, quality, and management.
Job Duties:
Promotes a work environment of continuous improvement that supports CQ Medical's Quality Policy, Quality System, and the appropriate regulations.
Assists with communicating business-related issues or opportunities for improvement to management.
Accountable for compliance with applicable US and International regulations and directives including, but not limited to, Food & Drug Administration (FDA), Canadian and European Union regulations.
Works in a team environment to achieve metrics.
Interprets engineering drawings, schematic diagrams, sampling tables, or formulas and confers with management or engineering staff to determine quality and reliability standards.
Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance, mechanical, or chemical characteristics.
Records test data, applying statistical quality control procedures using GMP documentation practices.
Recommends modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability.
Quarantines all incoming material until testing is accepted.
Quarantines all non-conforming material during any step of the manufacturing process until the Material Review Board dispositions the material.
Purging of records as required.
Maintains a neat and organized work area.
Remains current on all required training.
Conducts calibrations and works with 3
rd
party calibration providers to ensure inspection equipment meets specifications.
Conducts transactions in the Quality Management System and/or ERP system to detail the disposition of incoming and in-process materials.
Working Conditions:
50 lbs. of lifting required for this role
Hearing protection, safety glasses, safety shoes, and gloves are required for this role
Required exposure to biohazard
Job Qualifications:
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
Ability to write routine reports and correspondence.
Ability to speak effectively before groups of auditors or employees of our organization.
Ability to interact effectively with individuals and teams.
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, percent, and interpret bar graphs.
Decision-making ability.
Ability to use testing equipment.
Must be able to manage multiple tasks and perform with accuracy and a high attention to detail.
Ability to identify priorities and function independently required.
Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Identify various discrepancies (product, process, documentation, etc.)
Analytical and problem-solving skills.
Computer proficiency, including data entry. MS Office Suite (Word, PowerPoint, and Excel) experience required.
Education and/or Experience
High school diploma or general education degree (GED).
Medical device or manufacturing experience a plus.
Preferred demonstration of leadership.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
$27k-43k yearly est. 8d ago
Quality Control Inspector
CQ Medical Careers
Quality control analyst job in Avondale, PA
The Quality Control Inspector I is responsible for inspecting, testing, and auditing raw materials and finished products, as well as releasing finished products.
Attention to detail is an expectation.
Demonstration of commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures.
Inspect and release raw materials, components, sub-assemblies, and finished devices according to procedure.
Drives continuous improvement activities with cross-functional team members.
Generate non-conformances and escalate to the Material Review Board in a timely manner.
Interacts with production areas, manufacturing and design engineering, marketing, quality, and management.
Job Duties:
Promotes a work environment of continuous improvement that supports CQ Medical's Quality Policy, Quality System, and the appropriate regulations.
Assists with communicating business-related issues or opportunities for improvement to management.
Accountable for compliance with applicable US and International regulations and directives including, but not limited to, Food & Drug Administration (FDA), Canadian and European Union regulations.
Works in a team environment to achieve metrics.
Interprets engineering drawings, schematic diagrams, sampling tables, or formulas and confers with management or engineering staff to determine quality and reliability standards.
Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance, mechanical, or chemical characteristics.
Records test data, applying statistical quality control procedures using GMP documentation practices.
Recommends modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability.
Quarantines all incoming material until testing is accepted.
Quarantines all non-conforming material during any step of the manufacturing process until the Material Review Board dispositions the material.
Purging of records as required.
Maintains a neat and organized work area.
Remains current on all required training.
Conducts calibrations and works with 3
rd
party calibration providers to ensure inspection equipment meets specifications.
Conducts transactions in the Quality Management System and/or ERP system to detail the disposition of incoming and in-process materials.
Working Conditions:
50 lbs. of lifting required for this role
Hearing protection, safety glasses, safety shoes, and gloves are required for this role
Required exposure to biohazard
Job Qualifications:
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
Ability to write routine reports and correspondence.
Ability to speak effectively before groups of auditors or employees of our organization.
Ability to interact effectively with individuals and teams.
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, percent, and interpret bar graphs.
Decision-making ability.
Ability to use testing equipment.
Must be able to manage multiple tasks and perform with accuracy and a high attention to detail.
Ability to identify priorities and function independently required.
Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Identify various discrepancies (product, process, documentation, etc.)
Analytical and problem-solving skills.
Computer proficiency, including data entry. MS Office Suite (Word, PowerPoint, and Excel) experience required.
Education and/or Experience
High school diploma or general education degree (GED).
Medical device or manufacturing experience a plus.
Preferred demonstration of leadership.
$27k-43k yearly est. 7d ago
Quality Control Inspector - B3
Sunset 4.0
Quality control analyst job in Jonestown, PA
Our Jonestown Distribution Center, a 218,000 sq. ft. refrigerated facility operating 24/7, is currently seeking a Quality Control Inspector to join our team. The essential function of this position is to assist the Quality Control team with daily activities and ensure that all product meets customer specifications and to proactively prevent rejections.
Rotational Full Time Shift: 3 Day & 4 Day Week: 6:00 PM - 5:30 AM
Primary Function:
The Quality Control Inspector will assist Quality Control Inspection Supervisor with all daily activities and to ensure that all
product meets customer specifications. This position collaborates with the Quality Control Inspection Supervisor, and
other warehouse personnel to proactively prevent rejections.
Values: To perform the job successfully, the incumbent's behavior must be consistent with the PRIDE values expected of
all Mastronardi Produce employee's: be Passionate; have Respect; be Innovative; be Driven and strive for Excellence.
Primary Responsibilities:
• Ensure that all product meets or exceeds customer specifications.
• Ensure allocation is followed, validate correct product is pulled and shipped to customer.
• Assist Quality Control Inspection Supervisor to ensure that all product inspections are being performed, labeling
specification are adhered to, and non-conformance product is pulled and corrected.
• Flex Between the shipping dock, receiving dock and production to assist Quality Control Inspection Supervisor
with Quality issues and/or inspections.
• Report any exceptions to the customer specifications to Quality Control Inspection Supervisor.
• Send out Quality Issues Emails for Non-Compliant Product.
• Oversee floor operations when the Quality Control Inspection Supervisor is unavailable.
• Remember recent rejections and rejection trends.
• Ensure Product packaging is in presentable condition for our customers.
• Ensure Presentation is of highest standards.
• Performs any other Quality Control related tasks or special projects as assigned.
• Provide training when required.
Education/Background Requirements:
• 1 Year College degree or 6 Months year of experience in a related field required.
• Previous experience in produce industry preferred.
Specific Knowledge, Skills and Abilities Required
• Must pass Drug Test, Background Check and pre-employment Skills Testing.
• Must sign a confidentiality agreement upon hire.
• Must be a self-starter and willing to work flexible hours.
• Proficiency in use of English language with the ability to communicate effectively and professionally.
• Proficient in computer-use skills (MS Office: Word, Excel and PowerPoint).
• Strong organizational, analytical and problem-solving skills. Need to be creative, adaptable and able to accurately
work with a sense of urgency.
• Spanish as a second language would be an asset.
• Inspection/audit experiences, working in software applications are considered assets.
• Proficient in basic computer skills, JDA or NAV experience preferred.
• Ability to use and read measuring devices such as scales, calipers, ruler.
• Excellent communication and interpersonal skills.
Working Conditions:
• Environment includes an expansive refrigerated warehouse, where the temperatures range is 45-55 degrees
(except office areas). The background noise approaches 70 dcbs.
• Must be capable of lifting up to 35 lbs.
Please note: Mastronardi Produce has accommodation processes and policies in place and provides accommodation for
employees with disabilities. If you require a specific accommodation because of a disability or documented medical need,
please contact the Human Resource office so that arrangements can be made for the appropriate accommodation to be
put into place.
$26k-33k yearly est. 27d ago
QC Analytical Scientist, PCR
ZP Group 4.0
Quality control analyst job in Exton, PA
Piper Companies is seeking a QC Analytical Scientist, PCR to join a clinical stage biotechnology company near Exton, PA. This is an onsite role in Exton, PA and is a contract to hire opportunity. Responsibilities: * 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:
* 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:
* Pay Rate: $40/hour
* Benefits Available: Medical, Dental, Vision, 401K, Sick Leave as required by law
This job opens for applications on 12/15/2025. Applications for this job will be accepted for at least 30 days from the posting date.
#LI-KP1 #LI-ONSITE
$40 hourly 15d ago
Quality Control Technician
Ster Seating LLC
Quality control analyst job in Exton, PA
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.
$33k-47k yearly est. 23d ago
Quality control chemist
Us Tech Solutions 4.4
Quality control analyst job in Myerstown, PA
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.
How much does a quality control analyst earn in East Lampeter, PA?
The average quality control analyst in East Lampeter, 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 East Lampeter, PA