Quality control analyst jobs in Lansdale, PA - 168 jobs
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Global Process Chemist
Veolia | Water Tech 4.3
Quality control analyst job in Trevose, PA
Veolia Group is a global leader in environmental services, operating across all five continents with nearly 218,000 employees. Specializing in water, energy, and waste management. Veolia Group designs and
implements innovative solutions for decarbonization, depollution, and resource regeneration, supporting communities and industries in their ecological transformation. Within this framework, Veolia's Water Technology Business brings together a dedicated team of experienced professionals committed to tackling the world's most complex challenges related to water scarcity, quality, productivity, and energy. Together, we pursue a shared mission to create a more sustainable future.
Job Description
As a Global Process Chemist you will work closely with the Technology, Global Engineering and Regional Quality and EHS functions, being a key contact person for the development, roll out and sustainability of all initiatives relating to Veolia's CSM Chemical manufacturing operations with WTS business unit or related regional tolling operations.
In this critical role, you'll provide technical guidance, direction and training to plant staff and operators on process chemistry and safety, ensuring awareness and adhesion to process operation parameters and safety limits. You'll lead and provide onsite support for startup trials on new and/or improved processes, provide on-time coverage for troubleshooting, participate in root cause analysis and implement corrective and preventive actions.
Additionally, you will be responsible for supporting different new business opportunities, manufacturing process optimization, and cost-out initiatives in the business and ensure Safe Chemical Manufacturing. If you like the idea of doing meaningful work with a company that's doing big things to create a cleaner, more sustainable world for us all, here's more!
Key Responsibilities:
Support the Global Process Chemistry team to ensure all aspects of Process safety are addressed in projects and proper operating procedures are being applied at all reaction and blending plant operations.
Be the chemical expert to support the global reaction plants and tollers during start up and commissioning of new products and support for ongoing production challenges.
Maintain global communications to utilize resources in other regions and to ensure we meet the business needs of a global organization including Technology, Manufacturing, Sourcing, Product Quality, Business Units, and Supply Chain.
Represent Global Process Chemistry in team meetings and projects to ensure process chemistry and process safety requirements are covered from a regional point of view while ensuring consistency with global standards.
Support Cost-out initiatives by investigating the best operational strategy, in-house production vs tolling.
Support the regional tolling technology transfer leader by assembling and providing toll manufacture SOPs, conducting onsite EHS, Quality and Engineering audits, and following up on completion of corrective actions. Being a critical part of the qualification team through the entire qualification process, providing guidance and support of scale-up trials ensuring safe operation and delivering products meeting quality expectations.
Work closely together with the engineering team during the design and commissioning of new engineering projects at the Veolia CMS plants and provide technical process support
Assemble process safety information, including P&IDs, equipment design data, and process parameters needed for successful completion of Process Hazard Analyses (PHA/HAZOP)
Implement the company's internal standards for hazardous processes (e.g. flammable materials, combustible dust handling and neutralization reactions) etc.
Implement, maintain, and improve all aspects of the company's process safety program. Maintaining compliance with applicable OSHA, EPA, EU, and
country/state/local requirements including Process Safety Management, RMP, and Seveso.
Drive continuous system and process improvements based on Digitization and Lean Six Sigma methodology.
Qualifications
Core Requirements:
Master's degree in science, preferably Organic or Polymer Chemistry or equivalent University Degree. PhD is a plus!
Detailed understanding of chemical plant processes and process safety.
Expertise with chemical process instrumentation and WinCC
Experience in conducting employee Process Safety training
Support the process safety compliance culture associated with the Chemical Industry environment
Other Useful Skills and Experience:
5+ years of professional chemical industry experience
Familiar with WinCC or equivalent programs
Familiar with NFPA 30 standard, OSHA regulations, Process Safety Management, EPA and SEVESO experience
Knowledge of SAP is helpful
Familiar with Brilliant fulfillment / Lean Manufacturing / Six Sigma
Additional information
At Veolia, we realize diverse teams make smarter decisions, deliver better results, and build stronger communities. We're an organization that champions diversity and inclusion at every rung of the ladder and are proud to be an equal opportunity workplace. Because our people are our greatest assets, we also offer competitive compensation and benefits that include:
● Medical, Dental, & Vision Insurance Starting Day 1!
● Life Insurance
● Paid Time Off
● Paid Holidays
● Parental Leave
● 401(k) Plan - 3% default contribution plus matching!
● Flexible Spending & Health Saving Accounts
● AD&D Insurance
● Disability Insurance
● Tuition Reimbursement
Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law.
****Applicants are required to be eligible to lawfully work in the U.S. immediately; employer will not sponsor applicants for U.S. work authorization (e.g. H-1B visa) for this opportunity****
Veolia does not accept unsolicited resumes from external recruiting firms. All vendors must have a
current and fully executed MSA on file before submitting candidates. Any unsolicited resumes and
candidate profiles will be deemed the property of VWTS, and no fee will be due.
As an inclusive company, Veolia is committed to diversity and gives equal consideration to all applications, without discrimination.
$62k-93k yearly est. 1d ago
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Research And Development Chemist
Germer International-Pharmaceutical Recruiting
Quality control analyst job in Blue Bell, PA
Please note: For confidentiality purposes, this position is not located in Blue Bell. The role is based in the tri-state area.
This role will focus on the validation of analytical methods for products in development or for commercial products when needed. This position involves executing validation studies and optimizing or developing analytical methods when needed to support drug product applications. In addition to analytical method validation, this position will involve R&D T0 and Stability testing for 2-3 drug products in development
Key responsibilities.
Develops analytical methods that are accurate, precise, and specific for use in both the Quality Control department and the Research department. Methods primarily include HPLC and GC but also include ICP-MS, Karl Fisher, solid-state characterization, and others.
Documents the development of the method in the appropriate notebooks for future reference. Performs pre-validation work ahead of transfer to the Validation Department to demonstrate suitability for use.
Prepares test method procedures and supporting documentation for use in the Quality Control laboratory.
May be required to develop validation protocols and validate analytical methods used in the testing of raw materials, intermediate products, final products, and cleaning samples.
Assists in the maintenance and calibration of laboratory analytical instrumentation including, but not limited to HPLC and GC. Maintains accurate records regarding the maintenance and calibration activities.
May support manufacturing operations with testing of raw materials, intermediate products, final products, and cleaning samples. The incumbent is expected to operate in a neat and orderly manner and to provide accurate and timely test results.
Assists in the maintenance of the QC Laboratory. In addition to routine housekeeping and glassware cleaning, maintains and appropriate inventory of supplies and chemicals.
Documents sample preparation, equipment set-up and test results in Laboratory Notebooks or on the appropriate test record form. Documentation must be complete and verified by a second member of the quality group. In addition, laboratory log sheets, those related to equipment usage, calibration, and maintenance, reference standard inventory, QC chemical inventory, or those related to retention samples will be properly maintained.
EDUCATION/EXPERIENCE.
A Bachelor's Degree in Chemistry (Master's or PhD Degree is preferred)
A minimum of 7 years of experience in small molecule pharmaceutical laboratories, with a strong background/proficiency in LC, GC, Dissolution and chromatographic method validation and development.
Proficient with Empower software.
Strong organizational skills.
Good communication skills
Good writing skills.
$53k-80k yearly est. 5d ago
Development Chemist III
Quaker Chemical Corporation 4.6
Quality control analyst job in Conshohocken, PA
At Quaker Houghton, we are experts in the development, production and application of chemical specialties, process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world's largest industrial companies and to this day our experience and expertise show in the actions and dedication of our Associates worldwide. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its associates and offers competitive compensation and benefit programs.
Summary:
Quaker Houghton is seeking a Development Chemist III to work in our Metalworking Fluid Development Laboratory in Conshohocken, PA. The laboratory supports multiple metalworking fluid product lines including soluble oils, semi-synthetics, and full synthetics. An individual in this role will be responsible for conducting product development, research projects, and product support for Quaker Houghton metalworking fluids. This will require working closely with commercial associates, other RD&E teams, customers, and external partners to design new products and execute tests both in the laboratory and in the field. We are seeking experienced candidates who are highly motivated, have strong collaboration skills, are creative problem solvers, and communicate effectively.
What will you do?
* Use knowledge of colloid chemistry, tribology, and testing techniques to formulate metalworking fluids that will meet customer needs and provide solutions to application problems.
* Work independently with minimal guidance from the laboratory manager.
* Act as a mentor to junior development chemists.
* Maintain a clear and orderly record all observations and data.
* Write detailed reports summarizing product development efforts, laboratory testing, and troubleshooting.
* Perform customer requested product analysis and testing to answer questions and address problems at commercial accounts.
* Provide legal and archival documentation for patent applications.
* Comply with safety regulations and lab procedures.
* Provide technical service and knowledge to customers and sales associates based upon the chemist's current level of expertise. Visit customers when required.
* Provide assistance to Manufacturing to improve the quality and efficiency of the manufacturing process. Assist Manufacturing and the Quality Assurance lab in solving quality and production problems.
* Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns.
* Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly.
Education, Experience, Skills & Competencies:
* This position requires a Bachelor Degree in Chemistry or equivalent with at least 7 years of experience, a Master's Degree in Chemistry or equivalent with at least 5 years of experience, or a Doctor of Philosophy in Chemistry or equivalent with at least 3 years of experience.
* Knowledge of colloid chemistry, surfactants, and tribology is required.
* Experience with the formulation of metalworking fluids and field support of machining and grinding operations is highly desired.
* Understanding of applied statistics and experimental design is not required, but highly desired.
* Must have the ability to operate in a fast-paced environment, to work on different projects at the same time, and to think analytically.
* Must have good prioritization and communication skills (oral and writing).
* Ability to write detailed reports and presentations which may be used to inform high-ranking members of the Technical Community.
What's in it for you:
* Competitive pay programs with excellent career growth trajectory
* Opportunities to see your efforts contribute toward the success of the business
* Work for a global leader in the industrial process fluids industry
Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce. Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veteran's status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities. Applicants with a disability who need assistance applying for a position may email ************************.
$66k-85k yearly est. 60d+ ago
Scientist/Quality control Scientist
Integrated Resources 4.5
Quality control analyst job in Ewing, NJ
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Title: Scientist I
Duration: 6 Months (Possibility of Extension)
Location: Ewing NJ 08628
Shift - Can be flexible, can start as early as 7:30 AM (end at 4 PM), up to 9 AM (end at 5:30 PM)
Job Description
The Analytical Scientist will be involved in the design, planning, organization and evaluation of drug product and combination drug/device product development.
They will perform analytical testing on formulation and manufacturing intermediate dosage forms as well as inhalation devices (aerosol performance testing) as part of a project team within Analytical Chemistry.
The position requires use and application of analytical chemistry principles, theories, and concepts. Work is directly supervised.
The Analytical Scientist will follow established procedures and methodologies and contributes to completion of routine scientific/technical tasks and has limited discretion to vary from established procedures.
Ability to work both closely with other team members from various disciplines as well as the ability to work independently when needed.
The Analytical Scientist will assist with the development of new procedures and methodologies (based on prior established techniques at this site) to develop solutions to solve scientific/technical problems of limited scope.
Qualifications
Mandatory and/or minimum requirements:
Prior experience with aerosol performance testing of inhalation dosage forms is required - (1 year or more of experience is required)
Prior experience with aerosol performance testing in a pharmaceutical environment (R&D preferred but QC setting acceptable)
Ability to work in a team-based / collaborative environment
Excellent documentation skills
Desirable attributes/qualifications:
Prior experience with Waters Alliance HPLCs and Empower
Prior experience creating technical documents including standard operating procedures and reports
Prior experience with MS Word, Excel, and PowerPoint for presenting data
Attention to detail in execution and documentation
Required levels experience and/or education: BS/MS in Chemistry or a related field, 3-7 yrs of experience (1-3 years could be considered depending upon relevance of experience to our needs)
Additional Information
Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus
Thank you for your time and consideration. I look forward to hearing from you!
Kind Regards
Ruchi Kumari
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
(DIRECT BOARD) # 732-844-8716 (F) 732-549-5549
LinkedIn: https://www.linkedin.com/in/ruchi-kumari
Gold Seal JCAHO Certified ™ for Health Care Staffing
“INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)
$47k-70k yearly est. 60d+ ago
QC Scientist -I (Microbiologist)
Artech Information System 4.8
Quality control analyst job in Fort Washington, PA
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
• The QC Scientist I will
provide testing and technical support in the QC laboratories.
• These functions include:
Collection, processing and testing of chemical components, bulk products, raw materials, packaging components, finished products, in-process materials, scale up, and cleaning validation samples
to conform to specifications and standard operating procedures (
SOPs)
.
•
Maintain inventory of testing supplies, t
emperature monitoring, water sample collection and testing, environmental monitoring and other duties as assigned. This position will have a general knowledge of SOPs, USP and other applicable pharmacopeia. Performs tasks with some guidance, but demonstrate the ability to comprehend and perform with experience.
• They will support the
review, data generation and/or writing of technical documents such as SOPs, laboratory investigations, test protocols and annual product reviews.
• This position complies with
cGMP,
safety training and regulations. Maintain an environment of respect and teamwork with all coworkers. All employees are required to cultivate an environment of quality & compliance in their actions.
• This includes attending all required training, adhering to the processes & procedures of their role and the company and displaying the highest level of integrity.
• Those who manage others are required to ensure their employees are trained appropriately, create & maintain an environment that promotes employee involvement and doing things right the first time.
Qualifications
•
A minimum of Bachelor's Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or related science is required.
•
Minimum 1 year of GMP/GLP microbiology lab experience in a pharmaceutical and/or OTC and/or regulated environment is required.
• Experience performing routine laboratory activities is required.
•
Basic knowledge/exposure of a LIMS system is preferred.
Strict compliance with good documentation practices and aseptic techniques is required.
• Ability to work independently, manage timeline and decision making is preferred.
• This candidate will be based in Fort Washington, PA and will be required to travel less than 10% domestically.
Additional Information
Sneha Shrivastava
Technical Recruiter (Clinical/Scientific)
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: ************ | Fax: ************
Connect with us on - LinkedIn | Facebook | Twitter
$61k-90k yearly est. 60d+ ago
Lead Quality Control Analyst
Honeywell 4.5
Quality control analyst job in Lansdale, PA
Honeywell in Lansdale, PA is seeking a Master‑Level Quality Assurance Specialist to champion excellence in aerospace and defense. As a subject matter expert in data capture, analysis, and quality systems optimization, you will ensure compliance with industry standards while driving continuous improvement through advanced analytics.
+ Data Capture & Analysis
+ Design and implement robust systems for capturing quality-related data across production and testing processes.
+ Apply statistical methods (SPC, Six Sigma, regression analysis) to identify trends, anomalies, and root causes.
+ Develop dashboards and automated reporting tools for real-time quality monitoring.
+ Quality Management System Expertise
+ Lead audits, inspections, and compliance reviews aligned with AS9100, ISO 9001, and defense industry standards.
+ Establish and maintain quality metrics (yield, defect rates, corrective actions).
+ Process Improvement
+ Recommend process changes that reduce variability and enhance reliability.
+ Utilize audit findings to correct and implement process and procedural improvements
+ Cross-Functional Collaboration
+ Interface cross-functionally , with suppliers, and customers to ensure quality expectations are met.
+ Present findings and recommendations to senior leadership using clear, data-backed insights.
**YOU MUST HAVE**
+ Education: Bachelor's Degree in Quality Assurance, Industrial Engineering, Data Analytics, or related field.
+ Technical Skills:
+ 5 years experience with ERP/MES systems and digital quality management tools
+ 5 years of demonstrated expertise in applying AS9100, ISO 9001, and IPC standards within quality management systems
+ 5 years of experience editing and indexing Command Media to ensure alignment with organizational and industry standards
+ Soft Skills
+ Proven analytical and problem‑solving expertise, with the ability to identify issues and implement effective solutions.
+ Excellent communication skills, adept at conveying complex information clearly to both technical teams and executive stakeholders.
+ Demonstrated leadership and mentoring experience, fostering collaboration, guiding team development, and driving performance.
+ This position requires access to technology, materials, software or hardware that is controlled by US export laws. In order to be eligible for this position, you must be a "US Person" under US export laws (or eligible for approval under a U.S. Government export license).
+ Ability to obtain and maintain a security clearance.
**WE VALUE**
+ Education: Master's Degree in Quality Assurance, Industrial Engineering, Data Analytics, or related field.
+ Technical Skills:
+ 8 years experience with ERP/MES systems and digital quality management tools
+ 8 years of demonstrated expertise in applying AS9100, ISO 9001, and IPC standards within quality management systems
+ 8 years of experience editing and indexing Command Media to ensure alignment with organizational and industry standards
+ Experience:
+ Minimum 7-10 years in aerospace/defense QA, with at least 3 years in a senior or lead role.
**U.S. PERSON REQUIREMENTS**
Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. citizen, U.S. permanent resident, or have asylum or refugee status in the U.S.
**ABOUT HONEYWELL**
Honeywell International Inc. (Nasdaq: HON) invents and commercializes technologies that address some of the world's most critical demands around energy, safety, security, air travel, productivity, and global urbanization. We are a leading software-industrial company dedicated to introducing state-of-the-art technology solutions to improve efficiency, productivity, sustainability, and safety in high-growth businesses in broad-based, attractive industrial end markets. Our products and solutions enable a safer, more comfortable, and more productive world, enhancing the quality of life of people around the globe.
**THE BUSINESS UNIT**
Honeywell Aerospace Technologies (AT) products and services are found on virtually every commercial, defense, and space aircraft in the world. We build aircraft engines, cockpit and cabin electronics, wireless connectivity systems, mechanical components, and more, and connect many of them via our high-speed Wi-Fi offerings. Our solutions create healthier air travel, more fuel-efficient and better-maintained aircraft, more direct and on-time flight arrivals, safer skies and airports, and more comfortable flights, along with several innovations and services that reflect exciting and emerging new transportation methods such as autonomous and supersonic flight. Revenues in 2023 for Honeywell Aerospace Technology were $14B and there are approximately 21,000 employees globally.
Honeywell helps organizations solve the world's most complex challenges in automation, the future of aviation and energy transition. As a trusted partner, we provide actionable solutions and innovation through our Aerospace Technologies, Building Automation, Energy and Sustainability Solutions, and Industrial Automation business segments - powered by our Honeywell Forge software - that help make the world smarter, safer and more sustainable.
Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.
$70k-90k yearly est. 10d ago
Senior Analyst, QC Chemistry, US Site (Hopewell, NJ)
Beone Medicines
Quality control analyst job in Pennington, NJ
**General Description:** Perform QC Chemistry laboratory activities with a primary focus on capillary electrophoresis techniques to support GMP manufacturing, testing, and release of material, intermediates and finished biological products (monoclonal antibodies) under FDA/EU regulations, applicable International Regulations, and BeOne Medicines' processes and procedures.
**Essential Functions of the Job:**
+ Perform routine and non-routine testing using capillary electrophoresis techniques (e.g., CE-SDS, CZE, ic IEF) in the QC Chemistry laboratory to ensure timely and compliant generation and reporting of in-process, release, and stability test results in support of manufacturing operations.
+ Review, interpret, and report analytical data in accordance with GMP regulations and internal procedures.
+ Lead troubleshooting efforts for analytical methods and instrumentation related to CE.
+ Conduct laboratory investigations, including OOS, Out of Trend, deviations, and invalid assays.
+ Implement corrective actions and preventive actions (CAPAs).
+ Participate in transfer and method validation activities, including protocol preparation, protocol execution, and report preparation.
+ Support routine operations, including but not limited to instrument qualification and maintenance, SOP generation and revision, test record keeping, etc.
+ Maintain equipment in a qualified and calibrated state, coordinating with metrology or vendors as needed.
+ Manage inventory of reagents and supplies for the laboratory.
+ Participate in internal and external GMP audits, as needed.
+ Train other junior level analysts and new hires on CE instrumentation, GMP practices, and data analysis.
+ Serving as subject matter expert in one or more areas of required testing.
+ Interacts with all levels of BeOne employees.
+ Undertake other duties as required.
**Education/Experience Required:**
+ Bachelor's or above in Chemistry, Biochemistry, or Biotechnology related scientific discipline.
+ Minimum of 4+ years of working experience in an FDA-regulated biotechnology, pharmaceutical company are required.
+ Familiar with Waters Empower Chromatography Data System.
+ Familiar with instrument and equipment validation. Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. Working knowledge with USP/EP and cGMP/EU GMP regulations.
+ Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level.
+ Credible and confident communicator (written and verbal) at all levels.
+ Strong analytical and problem-solving ability.
+ Hands-on approach, with a 'can do' attitude.
+ Ability to prioritize, demonstrating good time management skills.
+ Excellent attention to detail, with the ability to work accurately in a busy and demanding environment.
+ Self-motivated, with the ability to work proactively using own initiative.
+ Committed to learning and development.
**Computer Skills:**
+ Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint).
**Travel:**
+ Must be willing to travel approximately 10%.
+ Ability to work on a computer for extended periods of time.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
FLSA Status: Non-exempt/Hourly
Schedule: 8:00AM - 4:30PM, Monday - Friday. Occasional 2nd shift work required
Are you interested in growing your laboratory career at a fact-paced and expanding environmental testing laboratory? If so, we may have a great role for you; Criterion's Laboratory Analyst (PLM) role primarily performs precise and timely analysis of asbestos bulk samples using polarized light microscopy techniques. This role is responsible for adhering to quality assurance and quality control standards, following Criterion Laboratories' Laboratory Safety Procedures, ensuring a clean work environment, and fostering effective collaboration within a team environment.
Essential Duties and Responsibilities:
Uses polarized light microscopy to conduct detailed analysis of bulk samples for the identification and quantification of asbestos fibers.
Adheres to established analytical protocols and procedures to ensure reliable and reproducible results.
Maintains rigorous quality assurance practices to uphold data integrity and compliance with regulatory requirements.
Adheres to safety protocols to ensure a secure work environment for all personnel.
Maintains cleanliness and organization of the workspace to prevent contamination and ensure optimal working conditions.
Collaborates effectively with team members to achieve departmental objectives and contribute to a positive team culture.
Participates in training programs and stays abreast of advancements in polarized light microscopy techniques and asbestos analysis methodologies.
Requirements
Required Knowledge and Experience:
At least six (6) months experience performing analyses via polarized light microscopy
Familiarity with regulatory requirements and standards pertaining to asbestos analysis is preferred.
Strong attention to detail and the ability to maintain accuracy under tight deadlines.
Excellent organizational and communication skills, both verbal and written.
Demonstrated ability to work both independently and collaboratively within a team environment.
Commitment to maintaining high safety standards and promoting a culture of safety in the workplace.
Required Education, Certifications, and Licenses:
Bachelor's degree in a relevant scientific field (e.g., Geology, Biology, Chemistry, Environmental Science) and/or an equivalent amount of education and experience.
Physical and Mental Requirements:
Ability to perform microscopy work for extended periods, including sitting or standing.
Capability to lift and handle sample containers and equipment (up to 25 pounds).
$34k-49k yearly est. 35d ago
Development Chemist (at Gelest Inc.)
Mitsubishi Chemical Group 3.9
Quality control analyst job in Morrisville, PA
Gelest, Inc., part of the Mitsubishi Chemical Group, is hiring a Development Chemist to join our team in Morrisville, PA. This role offers the opportunity to contribute to our mission of delivering innovative specialty chemical solutions to customers worldwide.
The Development Chemist will play a key role in designing, developing, and optimizing chemical processes for specialty chemical products. This hands-on role involves synthetic organic chemistry, process development from lab to pilot scale, and data acquisition and analysis to ensure safe, reliable, and cost-effective manufacturing. The Development Chemist will collaborate closely with Product Development, Engineering, Production, and Quality teams to translate laboratory discoveries into scalable processes that meet business and regulatory requirements.
**PRINCIPAL ACCOUNTABILITIES:**
+ Design and perform laboratory experiments involving synthetic organic reactions, route evaluation, optimization, and troubleshooting.
+ Generate and analyze process data to identify improvement opportunities.
+ Scale laboratory processes to pilot and full production, ensuring robust transfer of technology and clear documentation.
+ Utilize analytical techniques (GC, NMR, FTIR, MS) to characterize materials, monitor reactions, and assess process performance.
+ Document experiments, observations, and recommended improvements in lab notebooks and technical reports.
+ Support process hazard assessments, safety reviews, and compliance with environmental, health, and safety regulations.
+ Maintain awareness of industry developments, new technologies, and specialty chemical manufacturing best practices.
+ Perform other duties as assigned.
**KNOWLEDGE/ EXPERIENCE/SKILLS:**
To perform the job successfully, an individual should demonstrate the following competencies:
+ Bachelor's degree in Chemistry, Chemical Engineering, or a related field. Master's degree preferred.
+ 1-3+ years of experience in specialty chemical synthesis, chemical process development, or scale-up preferred.
+ Hands-on experience with laboratory techniques and equipment preferred.
+ Background in synthetic organic chemistry, including multi-step synthesis and reaction mechanism understanding is preferred.
+ Experience with process development, including reaction kinetics, heat, and mass transfer, mixing, and scale-up considerations is preferred.
+ Hands-on experience with analytical instrumentation (GC, NMR, FTIR, MS) is preferred.
+ Excellent written and verbal communication, including technical reporting.
+ Commitment to maintaining a safe and compliant work environment.
+ Must be able to wear required PPE (safety shoes, glasses, gloves, hard hat; respirators as needed).
+ Must be able to climb ladders and stairs to collect samples and observe processes.
+ Must be able to lift up to 50 pounds and operate a forklift.
+ **Must be able to work 2nd shift:** Four (4) 10-hour shifts, Monday-Thursday, 12:30 PM - 11:00 PM
**Supplemental Company Information:**
Gelest, located in Morrisville, PA-conveniently accessible from Interstate 95, Route 1, and the PA/NJ Turnpikes-offers a rewarding career with competitive pay and a comprehensive benefits package, including:
+ Generous paid time off
+ Medical, Dental, Vision, and optional supplemental plans for employees and their families
+ 401(k) with a competitive company match
+ Company-paid Life Insurance, AD&D, Short-Term Disability, and Long-Term Disability
+ Eligibility for an annual performance bonus
+ Company-provided uniforms, work boots, and PPE
The salary range for this position is $27.00 (entry level) - $35.00 per hour. Factors such as scope and responsibilities of the position, candidate's work experience, education/training, job-related skills, internal peer equity, as well as market and business considerations may influence base pay offered. This salary will be subject to a geographic adjustment (according to a specific city and state), if an authorization is granted to work outside of the location listed in this posting.
$27-35 hourly 24d ago
QC Chemist I
Penn Life Sciences Inc.
Quality control analyst job in Langhorne, PA
Penn Life Sciences is seeking a detail-oriented QC Chemist I to join our team in Langhorne, PA. The QC Chemist I performs routine analytical testing in support of sterile drug product manufacturing, batch release, and stability programs within a cGMP-regulated environment. This role is responsible for generating accurate, compliant laboratory data while executing approved analytical methods and maintaining strict adherence to data integrity and documentation standards. The ideal candidate will have a strong foundation in analytical chemistry, a commitment to quality, and the ability to work effectively within a regulated Quality Control laboratory.
This position's responsibilities will include, but not be limited to the following:
* Perform routine analytical testing of raw materials, in-process samples, finished drug products, and stability samples using approved QC methods.
* Execute wet chemistry and instrumental analyses in compliance with validated methods, specifications, and cGMP requirements.
* Accurately document laboratory activities, results, and calculations in laboratory notebooks and electronic systems in accordance with ALCOA+ data integrity principles.
* Operate assigned analytical instruments and perform routine checks, calibrations, and basic troubleshooting in accordance with SOPs.
* Support stability programs, laboratory investigations (including deviations and OOS events), and analytical data review activities under supervision.
* Maintain laboratory organization, sample traceability, and inspection readiness while adhering to all applicable safety and regulatory requirements.
We are looking for applicants with:
* Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a closely related scientific discipline required.
* 0-3 years of analytical laboratory experience in a pharmaceutical, biotechnology, or regulated laboratory environment; academic laboratory experience will be considered.
* Working knowledge of analytical techniques such as HPLC/UPLC, UV-Vis spectroscopy, pH, Karl Fischer, TOC, dissolution, or particle size analysis.
* Understanding of good documentation practices and data integrity expectations within a QC laboratory.
* Strong organizational, analytical, and communication skills with a high attention to detail.
What we offer:
* 401(k) with company match
* Health, vision, and dental Insurance
* Childcare expense reimbursement
* Tuition reimbursement
* Annual bonus eligibility
* Annual merit increases
* Paid Time Off and Flexible Holidays
Penn Life Sciences is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, sexual orientation or any other protected status.
We encourage you to apply if you feel that you are a match! We look forward to hearing from you.
$49k-65k yearly est. 29d ago
QC Lab Technician
Rice's 4.3
Quality control analyst job in Moorestown, NJ
Since 1946, The Jet Pulverizer Company, Inc. has been committed to providing state-of-the-art processing equipment and services. The continuous technological advancement of our line of Micron-Master Jet Pulverizers and ongoing modernization and expansion of our Custom Grinding Division provide our customers with unsurpassed value and quality in both jet pulverizing equipment and custom grinding services. The Quality Technician plays a crucial role in ensuring the safety, quality, and compliance of products manufactured within our FDA-regulated micronization facility. This position involves monitoring production processes, conducting inspections, and collaborating with cross-functional teams to maintain high standards.
Requirements
Essential Duties of the QC Lac Tech:
PRIORITY - Product sample testing as required
Complete paperwork on a timely basis
Create sample composites and retains as indicated by customer need
Generate CoA's as required
Stock sample cups and lids
Monitor lab consumables and order as needed
Maintain clean lab
Monitor calibration status of instrumentation and calibrate as required
Perform routine inspections of raw materials, intermediate products, and finished goods.
Utilize precision measuring instruments and testing equipment to verify product specifications.
Identify any deviations from quality standards and report findings promptly.
Monitor micronization processes, including particle size reduction, blending, and packaging.
Collect samples at various stages of production for analysis.
Ensure adherence to standard operating procedures (SOPs) and regulatory guidelines.
Maintain accurate records of inspections, test results, and corrective actions.
Prepare quality reports and communicate findings to supervisors and management.
Collaborate with the Quality Assurance team to address non-conformities.
Assist during internal and external audits, including FDA inspections.
Ensure compliance with cGMP (current Good Manufacturing Practices) and other relevant regulations.
Support the implementation of quality management systems.
Provide guidance on quality-related matters to colleagues.
Foster a culture of quality awareness and accountability.
Must be willing to work overtime as needed, including some mandatory weekend shifts.
Experience/Skills
HS Diploma required. Associate degree preferred.
Computer proficiency - Microsoft Windows/Outlook, Microsoft Office
1 - 2 years lab experience
Experience working in an FDA-regulated environment (pharmaceuticals, medical devices, or related industries).
Proficiency in using measurement tools (calipers, micrometers, etc.) and analytical instruments.
Knowledge of cGMP, ISO standards, and quality control principles.
Strong attention to detail, problem-solving skills, and ability to work independently.
Excellent communication and teamwork abilities.
Salary Description $20 - $21 / hour
$20-21 hourly 11d ago
AVANTOR: Quality Control Lab Support
Elevated Resources
Quality control analyst job in Radnor, PA
Responsibilities:
LAB RELEASES
Maintain accuracy and transcribe large volumes of analytical data to support products on SAP system through data entry.
Review, obtain QC Supervisor approval and release non-GMP products in SAP.
Performs MMBE and MB1B SAP functions to also release or block non-regulated products in warehouse database. Also, update inventory out-of-balance screens and found inventory.
In support of maintaining the accuracy of analytical data and releasing products on-time, occasionally require Technical and/or IT support from Sr. QA Analysts to ensure proper alignment with Avantors methods and procedures; CofA error corrections and repush to the CofA website.
Creates 05 IL as needed
Work with Contract labs to coordinate test results and escalate priorities/rush jobs
SAMPLE SHIPMENTS
Assist with gathering documents to ship samples to outside labs
Sample shipment shipping documentation (i.e. MSO, Chain of Custody and MSDS) are generated and submitted.
Samples are packaged and delivered to Distribution for pick up and shipment.
Communicate with outside lab to ensure sample arrival, are on schedule for testing and for the lab to receive the CofA on time.
Capture, manage and make available to management sample shipments via Google Drive spreadsheet.
FINANCIAL
Inventories and orders office and lab supplies to ensure a smooth work process flow. Communicate with Receiving to ensure supply arrivals are delivered to the lab.
Upon receipt of office and lab supplies; packing slips, invoices are reviewed to ensure the QC Lab received all materials and all order transactions are invoiced correctly.
Responsible for generating purchase requisitions for purchase orders and maintaining office equipment preventative maintenance and notifying service techs for service.
Monthly P-Card reconciliation.
Capture, manage and make available to management PO requests, office and lab supply orders each via Google Drive spreadsheets.
OOS Investigations (20%) of the time:
The successful candidate with assist in OOS investigations and performing root cause analysis. The candidate will be responsible for events/CAPA's that are opened in response to the OOS investigations. Follow thru until completion.
Handle general administrative tasks, manages the meeting rooms booking as per needs
Works closely with Finance representatives to have all inventory records updated
Keep track of all docs needed by/for the accountancy company (invoices, contracts and other)
Archiving of company documents according local law
Maintains a record of entry and exit of documents and registers them
*Other duties as assigned
Job DescriptionDescription:
FLSA Status: Non-exempt/Hourly
Schedule: 8:00AM - 4:30PM, Monday - Friday. Occasional 2nd shift work required
Are you interested in growing your laboratory career at a fact-paced and expanding environmental testing laboratory? If so, we may have a great role for you; Criterion's Laboratory Analyst (PLM) role primarily performs precise and timely analysis of asbestos bulk samples using polarized light microscopy techniques. This role is responsible for adhering to quality assurance and quality control standards, following Criterion Laboratories' Laboratory Safety Procedures, ensuring a clean work environment, and fostering effective collaboration within a team environment.
Essential Duties and Responsibilities:
Uses polarized light microscopy to conduct detailed analysis of bulk samples for the identification and quantification of asbestos fibers.
Adheres to established analytical protocols and procedures to ensure reliable and reproducible results.
Maintains rigorous quality assurance practices to uphold data integrity and compliance with regulatory requirements.
Adheres to safety protocols to ensure a secure work environment for all personnel.
Maintains cleanliness and organization of the workspace to prevent contamination and ensure optimal working conditions.
Collaborates effectively with team members to achieve departmental objectives and contribute to a positive team culture.
Participates in training programs and stays abreast of advancements in polarized light microscopy techniques and asbestos analysis methodologies.
Requirements:
Required Knowledge and Experience:
At least six (6) months experience performing analyses via polarized light microscopy
Familiarity with regulatory requirements and standards pertaining to asbestos analysis is preferred.
Strong attention to detail and the ability to maintain accuracy under tight deadlines.
Excellent organizational and communication skills, both verbal and written.
Demonstrated ability to work both independently and collaboratively within a team environment.
Commitment to maintaining high safety standards and promoting a culture of safety in the workplace.
Required Education, Certifications, and Licenses:
Bachelor's degree in a relevant scientific field (e.g., Geology, Biology, Chemistry, Environmental Science) and/or an equivalent amount of education and experience.
Physical and Mental Requirements:
Ability to perform microscopy work for extended periods, including sitting or standing.
Capability to lift and handle sample containers and equipment (up to 25 pounds).
$35k-55k yearly est. 4d ago
Quality Control Inspector
Airborne Systems North America 3.4
Quality control analyst job in Pennsauken, NJ
SUMMARY: This position completes all or any combination of, inspection and/or testing tasks required to ensure that manufactured items conform to company and industry quality standards as well as to contract specifications when required. These duties require a high degree of accuracy and attention to detail.
SPECIFIC DUTIES/RESPONSIBILITIES:
* Inspects and measures materials, products, and work for conformance to specifications and standards throughout the manufacturing cycle.
* Accurately uses all standard measuring tools, including, but not limited to, rulers, calipers, and force gauges.
* Interprets blueprints, data, and other materials to determine specifications, inspection and testing procedures, and measuring instruments required.
* Records inspection data and quantities inspected on required inspection reports.
* Collects and files inspection and test records in accordance with established record maintenance procedures.
* Notifies supervisors and other personnel of production quality problems and assists in identifying and correcting these problems
* Discusses inspection results with those responsible for products and recommends necessary corrective actions.
* Completes all required record keeping, including time sheets, traceability forms, etc.
* Understand part numbers and revision levels
* Inspects customer repairs as needed.
* Assist with the training of new inspectors as needed
* Performs other related duties as required or assigned.
* Follows company rules and procedures.
QUALIFICATIONS:
* 1 to 2 years quality inspection experience in manufacturing.
* Functionally literate including able to read and write English documents.
* Able to perform basic computations (add, subtract, multiply, divide in all units of measure using whole numbers, fractions, and decimals).
* Capable of accurately using standard measuring tools.
* Capable reading and interpreting manufacturing drawings and work specification sheets.
* Detail oriented and able to maintain high accuracy standards.
* U.S. citizen, permanent resident alien or otherwise able to review all export-controlled technical information
EXPERIENCE: Six months to one year experience as a QC inspector in a manufacturing environment
EDUCATION: High school diploma or GED
WORK ENVIRONMENT: The work environment for this job is a manufacturing shop floor. The noise level is usually moderate due to sewing machines and traffic.
PHYSICAL DEMANDS: The position requires that the employee is regularly required to sit, talk, and hear. The employee is frequently required to use hands to fingers such as with a keyboard. The employee is occasionally required to stand; walk; reach with hands and arms. The employee must regularly lift and/or move up to 10 pounds. The employee must occasionally lift and/or move up to 25 pounds without assistance. Specific vision abilities include close, distance, and color vision and the ability to adjust focus.
SALARY RANGE: $18.45 - $20.64 / hour
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$18.5-20.6 hourly 60d+ ago
Analyst II, Laboratory Operations
8427-Janssen Cilag Manufacturing Legal Entity
Quality control analyst job in Spring House, PA
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at *******************
Job Function:
R&D Operations
Job Sub Function:
Laboratory Operations
Job Category:
Professional
All Job Posting Locations:
Spring House, Pennsylvania, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at *******************/innovative-medicine
We are searching for the best talent for an Analyst II, Laboratory Operations to be located in Spring House, PA.
Purpose: This position is part of the global Discovery, Product Development & Supply (DPDS) Operations Team responsible for operations within the Therapeutic Discovery (TD) and Preclinical Safety and Translational Sciences (PSTS) organizations. The Lab Operations team in DPDS Operations looks after the lab workspace to enable the scientists to focus on their science using a knowledge of project management, drug discovery instrumentation and automation, and process excellence to evaluate, develop and deliver drug discovery laboratory processes and infrastructure.
The Analyst II functions by planning and performing operational activities and acquisitions linked to the lab workspace. They work effectively in multi-disciplinary teams and collaborates with internal and external partners - such as Safety, Business Operations, Facility Management, Finance - thus ensuring flawless execution of all projects and processes connected to the lab workspace.
The function requires a hands-on mentality and the ability to work autonomously for longer term activities independently adapting to project developments and proposing next steps.
You will be responsible for:
Overseeing and managing the day-to-day activities involving provisioning, instrumentation, facility maintenance and upkeep to optimize laboratory operations.
Managing laboratory projects end to end, from idea through onboarding and installation of new instruments.
Coordinating laboratory moves for facility projects.
Ensuring routine and unscheduled equipment maintenance is performed within acceptable timeframes, effectively collaborating with external partners/organizations.
Collaborating with IT to manage and maintain computer and automation systems, including systems upgrades and issue resolution.
Working closely with scientific staff and leaders to ensure a steady and ongoing relationship with intent for efficient operation, improved automation, and workflow process improvements.
Collaborating effectively with fellow team/project members following procedures, priorities and timelines.
Maintaining general laboratory safety standards.
Qualifications / Requirements:
Education:
A minimum of a Bachelor's degree in a Scientific field, Engineering, Information Systems or Business is required. An advanced degree is preferred.
Experience and Skills:
Required:
A minimum of 2 years of relevant experience is required.
Strong interpersonal communication skills, effective organization, communication, and customer service skills are required.
Excellent attention to details is required.
Strategic and critical thinking, prioritization, and ability to execute on those strategies are required.
Preferred:
Proven project management success and change management experience is highly preferred.
Solid working knowledge of laboratory or highly controlled facilities operations, information systems, instrumentation, automation, safety, and compliance are highly preferred.
Prior laboratory experience on the bench or laboratory/operational management experience for science background candidates is preferred.
Prior facility or laboratory renovation project management is a plus.
Prior experience and understanding of laboratory automation is a plus.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via *******************/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
#LI-Onsite
Required Skills:
Preferred Skills:
Analytical Reasoning, Business Behavior, Coaching, Communication, Data Management and Informatics, Data Savvy, Ethical and Participant Safety Considerations, Inventory Management, Laboratory Operations, Laboratory Safety, Mental Agility, Molecular Diagnostics, Preclinical Research, Problem Solving, Research and Development, Toxicology, Use of Laboratory Equipment
$35k-54k yearly est. Auto-Apply 2d ago
Senior Quality Control Lab Technician
I.Rice & Company
Quality control analyst job in Philadelphia, PA
Job Description
An independent, family-owned business in Philadelphia, I. Rice & Co. has been making quality food products and flavors since 1884. With considerable growth and expansion, we are looking for qualified employees to help in a variety of positions. As a food manufacturing plant, I. Rice & Co. offers a diverse range of employment opportunities, from production coordination to warehouse stocking and inventory organization. With a passionate community, competitive pay, and generous bonus incentives, I. Rice offers ample opportunity for personal and professional growth.
QUALITY CONTROL SENIOR LAB TECHNICIAN
This permanent, full-time position supports the Quality Assurance department. The Senior Lab Technician plays a critical role in maintaining and enhancing our commitment to food safety and quality. This hands-on position combines technical expertise with leadership, performing daily functions in the lab, while also supporting the Director of Quality Assurance with administering department operations, validating program CCPs, and participating in audits. Knowledge of laboratory principles is required. Product testing includes brix, pH, water activity, titrations, viscosities and organoleptic evaluations. Environment is a clean and modern lab working with terrific people.
Essential Job and Duties
- Perform analytical tests on raw materials and finished products
- Maintain extensive record keeping
- Assist with auditing and maintaining SQF, GMP, & HACCP programs at the plant
- Calibrate laboratory equipment
- Participate in company audits
- Work with production to make adjustments to batches in order to adhere to product specifications
- Run batch freezer to make finished product for further study and sensory evaluation
- Measure and verify raw materials needed for batching
- Respond to customer questions or concerns in a professional and appropriate manner
- Inspection of inbound receipts
- Maintain the finished goods retention library
- Sample finished product for microbial analysis
- Maintain raw material specification documentation and product specification documentation
- Maintain finished product specification documentation
This position is supported by a team of technicians performing similar tasks. Our products, equipment, and methods are continually evolving. The duties associated with this position will change and evolve as needed. This individual is required to be willing and able to take on new responsibilities as needed.
Education and Experience
- Bachelor's Degree in Food Science, R&D, or related course of study preferred
- 5 years of related quality assurance or lab experience
- Experience with FDA, USDA, GFSI, SQF, FSMA, GMP, GLP, HACCP preferred
Skills and Expectations
- Ability to prioritize and organize ones work load
- Ability to work in a team environment as well as individually in an environment with changing priorities
- Comfortable working on an active busy production floor among batching and packaging equipment.
- Ability to manage time effectively
- Maintain proper lab conditions and equipment maintenance
- Maintain proper record keeping and perform data entry
- Be capable of working in various work settings of the facility including laboratory, office and plant areas
- Perform basic math skills
- Proficient computer skills, including above average knowledge of MS Excel
- Understand and perform scaling/measuring in standard and metric formats
- Food industry experience preferred.
- Lifting and carrying up to 50 pounds
- Being able to withstand extended periods of time on one's feet
- Working and walking in a wet environment
Benefits
Benefits and Compensation
- Weekly pay with direct deposit
- Health insurance
- Various supplemental insurance policies available after 90-day introductory period
- Life insurance available after completion of 90-day introductory period
- 401-K retirement plan available after one year of employment
- Option to participate in uniform program
- Annual bonus incentives
I.Rice is an equal opportunity employer and derives our staff skills through a diverse and talented workforce. This person will work closely with all departments and persons in our facility and must conduct themselves professionally at all times.
$44k-63k yearly est. 18d ago
Chemistry Laboratory Technician
Us Cannalytics
Quality control analyst job in Bethlehem, PA
Are you looking for a job that's both challenging and fun? US Cannalytics is looking for a candidate that seeks a challenging Chemistry Laboratory Technician position in the exciting and ever-evolving medical cannabis industry. The successful candidate will be reliable, exhibit strong attention to detail and thrive in a fast-paced laboratory environment
LABORATORY TECHNICIAN QUALIFICATIONS, must:
Have a valid driver's license and high school diploma or equivalent.
21+ years old and subject to applicable employment requirements for the state of Pennsylvania for cannabis businesses including criminal background check.
2 years of relevant, professional (non-academic) laboratory experience or 1 year of laboratory experience plus a skills assessment.
LABORATORY TECHNICIAN RESPONSIBILITIES:
The laboratory technician is responsible and accountable for the testing, quality control, and tracking of cannabis material. The laboratory technician will ensure the safe, accurate, and timely testing of cannabis products.
ESSENTIAL DUTIES:
Proficiently utilize Microsoft Word and Excel, and other laboratory information management systems.
Work in a timely manner, while striving to improve quality and maintain accuracy during all laboratory activities.
Follow organizational policies and procedures for laboratory operations and comply with all state-specified rules and regulations for cannabis licenses, cannabis transport and cannabis testing, as applicable.
Responsible for accurate measurements and documentation of all cannabis and cannabis materials, including sample weights/volumes, compliant cannabis tracking and destruction, and completion of supporting laboratory documentation.
Adhere to Good Documentation Practices (GDP) for the completion of laboratory logs, forms, worksheets, or other documentation.
Maintain laboratory reagent and supply inventory, including compliant documentation.
Assists with the performance of sample intake and accessioning, and non-analytical test methods (foreign material, water activity, moisture content, etc.), as needed.
Participate in and endeavor to complete training and be determined competent for assigned test methodologies including the following steps: a. Sample collection, intake and homogeneity. b. Sample preparation across all applicable matrices. c. Reagent preparation, including safe handling, storage and disposal. d. Sample loading and initial data analysis performed under the technical supervision of a Laboratory Chemist. e. Daily performance checks of applicable analytical equipment and method test parameters. f. Regular instrument cleaning and preventative maintenance for applicable analytical equipment. g. Basic troubleshooting of testing methodologies including all items listed within this sub-section.
For test methods the employee has been trained and determined competent for: a. Independently prepare samples using aseptic techniques, including compliant documentation and necessary updates to laboratory workflow. b. Independently prepare reagents, solutions, and substrates for the equipment necessary for testing, including compliant documentation and necessary updates to laboratory workflow. c. Perform initial data analysis under the technical supervision of a Laboratory Chemist or Microbiologist. d. Assist in equipment and method validations or verifications, including compliant documentation and necessary updates to laboratory workflow. e. Successful completion of proficiency testing samples, completed as part of ongoing competency within the test method.
Perform all other tasks and duties as assigned by Management, which may include cannabis sampling and transport.
WORK ENVIRONMENT:
The work environment characteristics described below are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Work is performed in a production laboratory environment and requires use of personal protection equipment to limit exposure to chemicals or other hazards found within a laboratory environment.
Work environment is fast-paced and will require frequent pivoting and multitasking, as well as the reprioritization of tasks based on demand/urgency.
The work environment may expose employee to fumes or airborne particles, moving mechanical parts and vibration.
The noise level in the work environment may be loud.
Per state requirements for this industry, the facility is secured by user-specific access and is surveillance by cameras located throughout the laboratory except in restrooms.
PHYSICAL DEMANDS:
The physical demands described are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Ability to concentrate and consistently produce accurate work.
Frequent standing, walking, sitting, and use hands.
Occasionally lift and/or move up to 40 pounds.
Visual requirements to include close vision, color vision and ability to adjust focus.
WORK HOURS:
Wednesday - Saturday (training and competency determined on a Monday-Friday schedule)
Job Type: Full-time, 10-hour shifts
Benefits:
Dental insurance
Health insurance
Paid time off
Vision insurance
Schedule:
Tuesday-Saturday
10 hour shifts
Overtime available
Work Location: In person
Job Type: Full-time
Compensation: $20-$22 / hour
Expected hours: 40 - 45 per week
Education:
High school or equivalent (required)
BS in a natural science (preferred)
Experience:
Laboratory: 1 year (required)
Analytical chemistry in a high-volume laboratory setting: 2 years (preferred)
Laboratory sample extractions: 2 years (preferred)
Agilent HPLC and/or GC: 2 years (preferred)
Cannabis: 1 year (preferred)
$20-22 hourly 51d ago
QC (Quality Check), Shipping & Packaging
Us207
Quality control analyst job in Allentown, PA
Needs to make sure that products being produced meet the expectations of the consumer. They examine jobs to make sure they meet quality expectations then assess the final product after production. Their role is to establish an acceptable variation range for jobs and identify when
something fails to meet those requirements.
Responsible for monitoring and ensuring that each stage of production is followed by all the
necessary procedures and each product coming out of the production process.
Document the results of their inspections and make recommendations on how to prevent
common errors.
Responsible for ensuring the quality control of all printing and sign products as well as
packaging and shipment/delivery of all products.
Responsible for checking in all vended products and ensuring they are ready for delivery or
shipment.
Duties and Responsibilities
● Must have attention to detail on quality and packaging for all outgoing shipments.
● Must be very organized while maintaining the ability to multitask.
● Coordinate with shipping companies like FedEx, UPS and others and ensure timely
delivery.
● Work effectively with the center manager and sales team for quality delivery and
escalations.
● The job requires repetitive lifting of sometimes heavy boxes.
● Must be a team player, dependable and have a good work ethic.
● Good written and verbal communication skills
● Excellent problem-solving and analytical skills
● Keen attention to detail
● Basic computer and math skills to calibrate and measure specifications
● Ability to use measuring devices like scales and tape measures
● In-depth understanding of company standards
● Understanding of target market and consumer needs
● Documentation and reporting skills
● Teamwork and collaboration
● Comfortable standing or walking for long periods of time
Some cross training into bindery or other areas of the company will be required at times if
another teammate is out.
Experience
Entry Level Job
Full time
Print Smith, Shipleap and Microsoft Office knowledge is a huge plus. Compensation: $15.00 per hour
At AlphaGraphics, we offer careers for everyone! Whether you are just starting out, looking for that next great growth opportunity, or seeking a change, we have exciting roles to suit you.
We pride ourselves on our training programs in management, sales, operations, print, signs, design, and marketing. Join us with or without experience, and we will succeed together as a team!
We invite EVERYONE to apply!
*AlphaGraphics centers (locations) are independently owned and operated. The posted positions are offered by individual franchisees who interview, hire, manage and pay the employees hired for positions in a specific local location (center) through their specific business.
$15 hourly Auto-Apply 60d+ ago
Quality Control
Nucor Corporation 4.7
Quality control analyst job in Bethlehem, PA
Job Details Division: Nucor Rebar Fabrication Northeast Other Available Locations: N/A Welcome to Nucor, where our unique culture sets us apart. Joining Nucor means becoming part of North America's largest steel and steel products manufacturer, offering unmatched career opportunities and stability. We are known for our innovative sustainability practices and are the continent's largest recycler. Our vibrant culture, built on personal connections and teamwork, empowers every team member with the freedom to innovate and contribute to our collective success. Experience a workplace where safety, efficiency, and meaningful personal connections define every day, enriching both our teammates and the communities we serve.
Nucor supports its teammates with top-tier benefits like Medical, Dental, Vision, and Disability Insurance, 401K and Roth accounts, Profit sharing, Pay-for-performance bonuses, Paid parental leave, Tuition reimbursement, Stock program, Scholarships and more.
Basic Job Functions:
* Must adhere to Nucor's safety programs and standards.
* Demonstrate conduct consistent with Nucor's vision and values.
* Perform and document all tests required (per the Quality Manual) during a production shift.
* Participate in non-conformance root cause analysis.
* Report and document any non-conformance to the Quality Manual requirements.
* Report and document any non-conformance to tests performed.
* Perform other tasks and duties as assigned
Safety is the most important part of all jobs within Nucor; therefore, candidates must be able to demonstrate the ability to initiate, lead, and uphold safety policies, practices, procedures, and housekeeping standards at all times.Minimum Requirements:
* Legally authorized to work in the United States without company sponsorship now or in the future.
* High school diploma, GED or state/local equivalent Preferences:
* Knowledge of CRSI quality standards
* Proficiency in MS Office, including strong Excel and Word.Physical Demands:
* Some heavy lifting may be necessary
* Working conditions can be noisy, dusty, hot, cold Special Demands:
* Must be able to work overtime when required
* Some travel may be required
* Must be able to work any shift
* Must be familiar with and adhere to shop safety policies and procedures
* Communication with various DOT customers
* Communication with CRSI
* Maintain and update CRIS QM as needed
* Maintain DOT certifications with all states as needed
* Understanding of ASTM coating and fabrication standards
Nucor is an Equal Opportunity/Affirmative Action Employer - M/F/Disabled/Vets - and a drug - free workplace
$36k-43k yearly est. 60d+ ago
QC Scientist -I (Microbiologist)
Artech Information System 4.8
Quality control analyst job in Fort Washington, PA
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
• The QC Scientist I will
provide testing and technical support in the QC laboratories.
• These functions include:
Collection, processing and testing of chemical components, bulk products, raw materials, packaging components, finished products, in-process materials, scale up, and cleaning validation samples
to conform to specifications and standard operating procedures (
SOPs)
.
•
Maintain inventory of testing supplies, t
emperature monitoring, water sample collection and testing, environmental monitoring and other duties as assigned. This position will have a general knowledge of SOPs, USP and other applicable pharmacopeia. Performs tasks with some guidance, but demonstrate the ability to comprehend and perform with experience.
• They will support the
review, data generation and/or writing of technical documents such as SOPs, laboratory investigations, test protocols and annual product reviews.
• This position complies with
cGMP,
safety training and regulations. Maintain an environment of respect and teamwork with all coworkers. All employees are required to cultivate an environment of quality & compliance in their actions.
• This includes attending all required training, adhering to the processes & procedures of their role and the company and displaying the highest level of integrity.
• Those who manage others are required to ensure their employees are trained appropriately, create & maintain an environment that promotes employee involvement and doing things right the first time.
Qualifications
•
A minimum of Bachelor's Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or related science is required.
•
Minimum 1 year of GMP/GLP microbiology lab experience in a pharmaceutical and/or OTC and/or regulated environment is required.
• Experience performing routine laboratory activities is required.
•
Basic knowledge/exposure of a LIMS system is preferred.
Strict compliance with good documentation practices and aseptic techniques is required.
• Ability to work independently, manage timeline and decision making is preferred.
• This candidate will be based in Fort Washington, PA and will be required to travel less than 10% domestically.
Additional Information
Sneha Shrivastava
Technical Recruiter (Clinical/Scientific)
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: ************ | Fax: ************
Connect with us on - LinkedIn | Facebook | Twitter
How much does a quality control analyst earn in Lansdale, PA?
The average quality control analyst in Lansdale, 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 Lansdale, PA
$56,000
What are the biggest employers of Quality Control Analysts in Lansdale, PA?
The biggest employers of Quality Control Analysts in Lansdale, PA are: