Quality Technician - CAPS Process Control (2nd shift: Mon-Fri 2:30pm-11:00PM)
Quality control analyst job in Allentown, PA
Company: Central Admixture Pharmacy Functional Area: Quality Working Model: Onsite Days of Work: Wednesday, Tuesday, Thursday, Friday, Monday Shift: 5X8
Requisition ID: 7098
B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap and CAPS .
Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit
CAPS , part of the B. Braun Group of Companies in the U.S., is the nation's largest network of outsourcing admixture pharmacies, has been delivering high-quality, same-day, admixture services and solutions to hospitals and outpatient facilities for more than 28 years. Along with the nation's largest 503A sterile injectable outsourcing network, CAPS offers industry-leading batch compounding on a national scale through three 503B registered outsourcing facilities. With experience, capacity, and a passion for safety, CAPS is your 503B solution.
CAPS , part of the B. Braun Group of Companies in the U.S., is the nation's largest network of outsourcing admixture pharmacies, has been delivering high-quality, same-day, admixture services and solutions to hospitals and outpatient facilities for more than 28 years. Along with the nation's largest 503A sterile injectable outsourcing network, CAPS offers industry-leading batch compounding on a national scale through three 503B registered outsourcing facilities. With experience, capacity, and a passion for safety, CAPS is your 503B solution.
Position Summary:
Ensure and assist with site-specific quality compliance according to CAPS Standard Operating Procedures (SOPs) & specifications, quality review of documents, label control, assist with release activities and product inspections.
Essential Duties/Responsibilities:
Perform product inspection for defects, leaks and particulates.
Perform environmental monitoring of personnel (as needed) and complete documentation.
Assist in the media fill process validations to include inspection of filled units
Perform document review of compounding activities such as cleaning records, line clearance forms and inventory sheets:
Verify that raw materials meet specification
Verify and account for labeling
Review temperature and BMS alarms
Verify that product test results meet specification limits
Verify that all documentation is complete
Document non-compliance and work with supervisor/lead if further investigation is needed
Submit samples to the appropriate lab for particulate identification or microbial analysis.
Assist with equipment calibration program and maintenance record files.
Assist with raw material release and movement.
Under the direction of supervisor/lead, document and initiate quality events for deviation and complaint investigations.
Support internal & external audits.
Maintain quality records (equipment calibration and maintenance, training, deviation and complaint investigation, environmental monitoring, Certificate of Analysis, clean room certification etc.).
Participate in Quality Manager's staff meetings
Expertise: Knowledge & Skills
Knowledge of pharmacy operations and regulatory guidelines.
Ability to perform calculations.
Ability to work within established procedures and practices
Strong organizational skills and attention to detail
Ability to effectively troubleshoot issues.
Qualifications - Experience/Training/Education/Certification/Etc:
Required:
Minimum of High School Diploma/GED with work experience
Minimum of 2 years experience in a quality or manufacturing department of a pharmaceutical, Medical Device or Allied Health Science.
Schedule (2nd shift) Monday-Friday 2:30-11:00PM
Salary range is $20.39-$25.49/hr
Desired:
Experienced in aseptic operations.
Experience within a regulated environment
Associates Degree or higher level degree in Technician technical scientific discipline, Biology, Microbiology, Chemistry or Pharmacy.
Experience with Process Control, AQL, GMP and GDP
While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee frequently is required to use hands to handle or feel and reach with hands and arms. The employee is occasionally required to stand and walk. The employee must occasionally lift and/or move up to 45 pounds.
Responsibilities: Other Duties:
The preceding functions have been provided as examples of the types of work performed by employees assigned to this position. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed in this description are representative of the knowledge, skill, and/or ability required. Management reserves the right to add, modify, change or rescind the work assignments of different positions due to reasonable accommodation or other reasons.
Physical Demands:
The employee must occasionally lift and/or move up to 45 pounds.
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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Work Environment:
Indoors, cleanroom, working environment limited to a small area, wearing protective cleanroom attire, tolerating controlled temperatures and loud noise.
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually moderate.
The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate.
B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at .
Through its "Sharing Expertise " initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.
We are an equal opportunity employer. We evaluate applications without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here .
All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.
Compensation details: 20.39-25.49 Hourly Wage
PIbc51bd97f5-
Quality Control Specialist
Quality control analyst job in West Reading, PA
At Customers Bank, we believe in working hard, working smart, working together to deliver memorable customer experiences and having fun. Our vision, mission, and values guide us along our path to achieve excellence. Passion, attitude, creativity, integrity, alignment, and execution are cornerstones of our behaviors. They define who we are as an organization and as individuals. Everyone is encouraged to have personal development plans. By doing so, our team members are on their way to achieve their highest potential and be successful in their personal and professional lives.
Must be legally eligible to work in the United States without sponsorship, now or in the future.
Who is Customers Bank?
Founded in 2009, Customers Bank is a super-community bank with over $22 billion in assets. We believe in dedicated personal service for the businesses, professionals, individuals, and families we work with.
We get you further, faster.
Focused on you: We provide every customer with a single point of contact. A dedicated team member who's committed to meeting your needs today and tomorrow.
On the leading edge: We're innovating with the latest tools and technology so we can react to market conditions quicker and help you get ahead.
Proven reliability: We always ground our innovation in our deep experience and strong financial foundation, so we're a partner you can trust.
What you'll do:
The Quality Control (QC) Specialist in Fraud Operations is responsible for ensuring that casework, investigations, alerts and transactions handled by the fraud team are accurate, complete and compliant.
Core Purpose:
* Detect and remediate errors, inconsistencies or missed steps in fraud handling.
* Ensure fraud operations staff follow internal procedures, regulatory requirements, and escalation paths.
* Act as the final checkpoint within the fraud operations team
* Case Review & Sampling: Conduct routine and targeted reviews of fraud alerts, disputes and investigations to confirm accuracy, completeness, and compliance with internal policies, established procedures, and applicable regulations.
* Accuracy & Compliance Verification: Ensure documentation, investigative decisions, and customer communications are correct, complete, and in adherence with regulatory requirements (e.g., Bank Secrecy Act, Reg E, NACHA) as well as bank policy.
* Error Tracking, Trending & Reporting: Identify errors and deficiencies, record trends, and develop and maintain processes for tracking and reporting quality metrics. Provide timely feedback to analysts and management.
* Root Cause Analysis & Remediation: Analyze recurring issues to identify systemic gaps or training needs and partner with management to implement corrective actions that strengthen fraud prevention effectiveness.
* Policy & Procedure Support: Assis in refining, document, and maintaining departmental procedures to ensure clarity, consistency and alignment with compliance and operational requirement.
* Training and Coaching: Develop and deliver results-based training or coaching to fraud operations staff when deficiencies are identified through quality reviews.
* Projects, Audits & Initiatives: Participate in departmental projects, audits, and initiatives as needed, ensuring that quality control insights are incorporated into broader fraud prevention strategies.
What do you need?
* 2-5 years of experience in fraud operations, financial crimes investigations or risk/compliance roles.
* Prior experience in quality assurance/control or audit strongly preferred
* Analytical Skills: Ability to review fraud cases, identify errors, spot trends, and conduct root cause analysis.
* Attention to Detail: Precision in reviewing documentation, decisions, and communications to ensure accuracy and compliance.
* Regulatory Knowledge: Working understanding of key banking regulations (e.g., Bank Secrecy Act, Reg E, NACHA) and internal fraud policies.
* Problem-Solving: Skills in diagnosing issues and recommending practical, risk-based solutions.
* Communication Skills: Clear verbal and written communication to provide feedback, draft reports and collaborate across teams.
* Coaching & Training Ability: Capacity to provide constructive feedback, develop training materials and deliver targeted coaching.
* Process Orientation: Ability to follow established procedures while recognizing opportunities for process improvements.
* Technical/System Skills: Familiarity with fraud monitoring systems, case management tools, and reporting software (Excel or Business Intelligence tools often helpful)
* Time Management & Prioritization: Skill in managing multiple reviews, projects and reporting deadlines efficiently.
Customers Bank is an equal opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
We also provide "reasonable accommodations", upon request, to qualified individuals with disabilities, in accordance with the Americans with Disabilities Act and applicable state and local laws.
Diversity Statement:
At Customers Bank, we believe in working smart, working together, and having fun while delivering innovative solutions and memorable experiences for our customers. We are committed to the continual advancement of a culture which reflects the value we place on diversity, equity, and inclusion. We honor the diverse experiences, perspectives, and identities of our team members, and we recognize that it is their passion, creativity, and integrity that drives our success. Step into your future with us! Let's take on tomorrow.
Auto-ApplyQC Scientist - I
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
QC Analytical Scientist, PCR
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 11/10/2025. Applications for this job will be accepted for at least 30 days from the posting date.
#LI-KP1 #LI-ONSITE
GMP QC Analyst I/ II
Quality control analyst job in Exton, PA
GMP QC Analyst I/ II
FLSA Status: Exempt
Salary Range: $65,000 - $70,000 / yr
We are seeking a highly motivated GMP QC Analyst I/ II to join our Cell & Gene Therapy (CGT) Quality Control team. The QC Analyst I/ II will be responsible for executing routine laboratory testing under cGMP conditions to support multiple client projects in various phases of development. This role is suitable for candidates seeking to gain hands-on experience in a dynamic, client-focused, cross-functional CGT laboratory.
The ideal candidate will have a strong foundation in biological sciences and laboratory techniques, along with a commitment to quality and regulatory compliance.
Responsibilities:
Perform analytical testing of all samples in accordance with GMP regulations and internal SOPs.
Execute a variety of biological assays including, but not limited to, ELISA, qPCR, dd PCR, and cell-based potency assays.
Perform aseptic cell culture work, including the maintenance, expansion and passaging of mammalian cell lines.
Support cell line banking activities, including preparation, cryopreservation and retrieval of cell stocks.
Support method qualification, transfer and validation activities for client-specific methods.
Prepare reagents, media, buffers, solutions, and test samples as per SOPs.
Calibrate and maintain laboratory instruments; report any malfunctions or deviations.
Perform laboratory cleaning and/or maintenance activities as assigned.
Participate in laboratory investigations, deviations, CAPAs, Effectiveness Checks, KLEs and change controls.
Assist in maintaining lab inventory and requesting of supplies/ forms.
Maintain accurate and complete documentation in compliance with data integrity standards and ALCOA+ and GMP data integrity standards.
Maintain a clean, safe, and compliant lab environment per company policies and regulatory guidelines.
Collaborate cross-functionally with QA, CGT R & D, and other departments.
May assist with biennial SOP review, peer-review, drafting of protocols and reports or other documentation at management's discretion.
What We're Looking For:
Degree in a related field (e.g., Biology, Cell Biology, Biotechnology, Biochemistry, Chemistry, life sciences)
QC Analyst I: Bachelor's degree with 1-3 years of experience or a Master's degree with 0-1 year of experience.
QC Analyst II: Bachelor's degree with 2-5 years of experience or a
Master's degree with 1-3 years of experience.
Working knowledge of aseptic technique, cell culture and basic molecular biology methods.
Ability to evaluate technical data and record data accurately and legibly
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
Insurance including Medical, Dental & Vision with significant employer contributions
Employer-funded Health Reimbursement Account
Healthcare & Dependent Care Flexible Spending Accounts
100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance
401k plan with generous employer match
Access to an Employee Assistance Program
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
#LI-SE7
Laboratory Analyst (Inorganics)
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.
Quality Control Inspector
Quality control analyst job in Macungie, PA
Quality Control Inspector Opportunity - Macungie, PA HTSS is seeking a highly meticulous Quality Control Inspector to join a respected electronics manufacturer in the Macungie area. This role is essential for ensuring the quality and reliability of electro-mechanical and printed circuit board PCB assemblies, offering a strong Temp-to-Hire path.
Compensation and Schedule
Location: Macungie, PA
Schedule: Monday-Friday, 7:30AM - 4PM
Pay Rate: $19/hour
Type: Temp-to-Hire
Core Responsibilities
As the QC Inspector, you will act as the final check on product quality:
Inspection: Inspect components and assemblies, verifying dimensions using precision measuring tools (e.g., calipers, micrometers).
Testing: Conduct functional tests on final assemblies according to established procedures, utilizing test equipment.
Documentation: Accurately document all inspection results, track defects, and maintain quality records.
Quality Assurance: Collaborate with production to resolve quality issues, suggest corrective actions, and ensure adherence to all quality system processes.
Support: Assist with inventory processes, ERP data scanning, and participate in rework/repair of defective assemblies, which may include light soldering.
Candidate Profile and Requirements
We are seeking a detail-focused professional prepared for a fast-paced environment:
Required Experience: Previous experience in a Quality Control or similar inspection role is mandatory.
Visual Acuity: Strong attention to detail and excellent visual acuity, including accurate color identification.
Technical Skills: Able to read and interpret blueprints, schematics, and technical drawings. Proficient with measuring instruments and Microsoft Office (Word, Excel).
Physical: Comfortable sitting or standing throughout the shift and lifting up to 30lbs.
Preferred: Prior experience in electronics manufacturing, familiarity with IPC-A-610 standards, and soldering experience are a definite plus.
Apply Today
If you are ready to apply your inspection expertise to a rewarding role, we want to hear from you.
Text "QC Inspector" to ************ to apply!
QC Inspector
Quality control analyst job in Sinking Spring, PA
Do you want to work for a construction company unlike any other? At JGM, we challenge the industry's status quo. Known as the team that delivers "When You Need It Yesterday", we've built a culture around safety, quality, and speed. At JGM, we're more than a company-we're 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 Tomorrow's 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:
* Medical, Vision & Dental
* PTO & Holidays
* 401(k) + Matching
* Life Insurance
* Short/Long 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 not all-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.
QC Inspector
Quality control analyst job in Reading, PA
About JGM Do you want to work for a construction company unlike any other? At JGM, we challenge the industry's status quo. Known as the team that delivers "When You Need It Yesterday", we've built a culture around safety, quality, and speed. At JGM, we're more than a company-we're 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 Tomorrow's 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:
Medical, Vision & Dental
PTO & Holidays
401(k) + Matching
Life Insurance
Short/Long 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 not all-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.
Quality Control Inspector - Welding
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
QC (Quality Check), Shipping & Packaging
Quality control analyst job in Allentown, PA
Job DescriptionNeeds 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.
Lab Analyst 1
Quality control analyst job in Allentown, PA
Job DescriptionCertified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries.
We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you.
We are currently looking for a Pathogen Lab Analyst to join our growing team!
$1000 HIRING BONUS!!!
Job Summary:
Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies.
Essential Responsibilities:
Accurately perform and read test results and notify Laboratory Management of deviations
Prepare and analyze samples for indicator organisms, pathogens, and chemistries
Apply aseptic/microbiological techniques in daily workload
Report inventory and expendable supplies/materials needed for testing requirements
Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control
Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc.
Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements
Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends
Perform all activities in a neat, safe, hygienic, and efficient manner
Share information in an open and timely manner
Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team
Responsible for the safety of oneself and others working within their area
Supervision:
This job does has no supervisory responsibilities.
Education & Experience:
Associate degree in Life Science or related field with two or more years of laboratory experience, preferred
Two or more years of experience in a commercial food-testing or analytical laboratory
Or equivalent combination of education and experience
Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures
Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures
Broad knowledge of concepts, practices, and procedures of a food testing laboratory
Ability to travel when necessary
Physical Demands/Work Environment:
Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components
Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens
Noise level varies from quiet to loud
Temperature varies from hot to cold
Interactive and fast-paced team oriented tasks
Overnight Travel is required at the discretion of management
Occasionally lift and/or move up to 25 pounds
Color vision and depth perception
Benefits:
Progressive 401k Retirement Savings Plan
Employer Paid Short- Term and Long-Term Disability, and Life Insurance
Group Medical
Tuition Reimbursement
Flexible Spending Accounts
Dental
Paid Holidays and Time Off
Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.
QC (Quality Check), Shipping & Packaging
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.
Auto-ApplyQuality Control Microbiologist
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.
Metal Anodizing/Plating/Chemical Treating Technician
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 ***************************
Quality Control Analytical Scientist (ELISA)
Quality control analyst job in Exton, PA
Piper Companies is seeking a Quality Control Analytical Scientist (ELISA) to join a rapidly growing biopharmaceutical organization advancing gene therapies for rare genetic disorders. This onsite position in Exton, PA offers hands-on involvement with ELISA and complementary analytical assays supporting GMP Quality Control operations.
Responsibilities of the Quality Control Analytical Scientist (ELISA):
* Perform GMP-compliant ELISA testing to support in-process, drug substance, and drug product analysis.
* Support additional analytical methods including cell culture, qPCR, and flow cytometry.
* Review and document results in compliance with GMP and data integrity standards.
* Conduct OOS investigations, CAPAs, and SOP revisions as required.
* Maintain laboratory organization, equipment calibration, and readiness for audits.
Qualifications of the Quality Control Analytical Scientist (ELISA):
* 3-5 years of QC experience in a GMP-regulated biopharma or biologics environment.
* Proficient in ELISA execution, troubleshooting, and data analysis.
* 2-3 years of experience in mammalian cell culture preferred.
* Strong attention to detail and documentation accuracy.
* BS in Biochemistry, Chemistry, or related Life Science required.
Compensation for the Quality Control Analytical Scientist (ELISA):
* Pay Rate: $40/hour
* Type: Contract-to-Hire (benefits included)
* Location: Onsite - Exton, PA
* Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays
Application Period: This position opens for applications on 11/17/2025 and will remain open for a minimum of 30 days from the posting date.
Keywords: Quality Control, QC Scientist, ELISA, GMP, Biologics, Gene Therapy, Analytical Testing, Cell Culture, qPCR, Flow Cytometry, CAPA,
#LI-JM1 #LI-ONSITE
Laboratory Analyst (inorganics)
Quality control analyst job in Reading, PA
Full-time Description
LAUNCH YOUR PURPOSE DRIVEN CAREER IN ENVIRONMENTAL SCIENCE!
Are you ready to launch your career in environmental science and make a true impact? We're seeking a dedicated Laboratory Analyst 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 is a full-time position following a Monday - Friday schedule from 7 AM to 3:30 PM with some periodic overtime and weekends required.**
Why You'll Love This Role
Perform on the front line of science by generating analytical data to support compliance and decision-making;
Build hands-on expertise with advanced instrumentation, Laboratory Information Management Systems (LIMS), and modern analytical techniques;
Gain exposure to real-world applications of science in quality assurance, compliance, and client support;
Join a collaborative team where your work contributes directly to reliable results, operational excellence, and meaningful outcomes for clients and communities.
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 Chemistry, Environmental Science, or other related field;
Minimum of 1 year of hands-on experience in a professional or academic lab setting;
Experience with ion chromatography (IC), flow injection analysis (FIA), segmented flow analysis (SFA), spectrophotometry, biochemical oxygen demand (BOD), gravimetric analyses, mercury analysis, turbidity, or hardness testing strongly preferred;
Experience with ICP, ICP-MS, and EPA methods 200.7, 200.8, 6010, and 6020 strongly preferred.
Ability to manage and process high volumes of samples efficiently;
Proficiency with Microsoft Office tools (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 Monday through Friday from 7 AM to 3:30 PM; some periodic overtime including weekends is required;
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.
Lab Analyst 1
Quality control analyst job in Allentown, PA
Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries.
We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you.
We are currently looking for a Pathogen Lab Analyst to join our growing team!
$1000 HIRING BONUS!!!
Job Summary:
Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies.
Essential Responsibilities:
* Accurately perform and read test results and notify Laboratory Management of deviations
* Prepare and analyze samples for indicator organisms, pathogens, and chemistries
* Apply aseptic/microbiological techniques in daily workload
* Report inventory and expendable supplies/materials needed for testing requirements
* Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control
* Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc.
* Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements
* Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends
* Perform all activities in a neat, safe, hygienic, and efficient manner
* Share information in an open and timely manner
* Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team
* Responsible for the safety of oneself and others working within their area
Supervision:
* This job does has no supervisory responsibilities.
Education & Experience:
* Associate degree in Life Science or related field with two or more years of laboratory experience, preferred
* Two or more years of experience in a commercial food-testing or analytical laboratory
* Or equivalent combination of education and experience
* Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures
* Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures
* Broad knowledge of concepts, practices, and procedures of a food testing laboratory
* Ability to travel when necessary
Physical Demands/Work Environment:
* Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components
* Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens
* Noise level varies from quiet to loud
* Temperature varies from hot to cold
* Interactive and fast-paced team oriented tasks
* Overnight Travel is required at the discretion of management
* Occasionally lift and/or move up to 25 pounds
* Color vision and depth perception
Benefits:
* Progressive 401k Retirement Savings Plan
* Employer Paid Short- Term and Long-Term Disability, and Life Insurance
* Group Medical
* Tuition Reimbursement
* Flexible Spending Accounts
* Dental
* Paid Holidays and Time Off
Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.
Quality control chemist
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.
QC Inspector
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 wageand benefit package:
Medical, Vision & Dental
PTO & Holidays
401(k) + Matching
Life Insurance
Short/Long 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 not all-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.