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. 5d ago
Looking for a job?
Let Zippia find it for you.
Associate Scientist LCMS
Resolian
Chemist job in Malvern, PA
Responsibilities:
· Prepare reagents, standards, and control samples
· Analyze samples using various techniques specific to department
· Assist with method development
· Perform method validation or qualification
· Operate analytical equipment
· Lead troubleshooting activities
· Maintain analytical equipment
· Ensure lab area is clean and inspection ready at all times
· Remove lab waste
· Record tasks in accordance with Good Documentation Practices (GDP)
· Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11
· Follow applicable SOPs and procedural documents
· Review and evaluate data results
· Train lower level Scientists
· Other tasks as assigned
Education, Experience & Skills Required:
· BA/BS or higher with 5-6 years lab experience; all experiences will be evaluated
· Able to perform complex lab work
· Able to work in a regulated environment
· Able to work effectively and contribute within a team
· Able to work with computer systems
· Able to document clearly; knowledge of and experience in a regulatory environment
$55k-81k yearly est. 1d ago
Associate Scientist - Decisional Analytics
Insight Global
Chemist job in Spring House, PA
One of our large pharmaceutical clients in Spring House, PA is seeking an Associate Scientist to join their growing Decisional Analytics team within the Cell Therapy Development group under the R&D Cell & Gene Therapy organization. This group is responsible for generating rapid and robust, high throughput analytical platforms that support multiple cell therapy programs from early to late-stage clinical readiness for rapid progression of process development. This position will be focused on designing, optimizing, and executing assays to assess the attributes and quality of viral vectors and CAR-T cell therapy processes and products as a part of cell therapy manufacturing platforms. The primary function of the role is characterization of CAR-T cells, predominantly with flow cytometry. Other responsibilities include:
Developing and executing analytical assays with a particular focus on immune assays (Flow cytometry, Viral titer assays, potency and cell killing assays, ELISA, MSD platform, qPCR/dd PCR)
Actively participate with the program teams and lead efforts to design, optimize and execute bioanalytical methods to assess Cell therapy drug products during process development and product testing.
Support, develop and optimize CAR-T process development platforms with a focus on rapid decisional analytics.
Apply scientific expertise to evaluate alternative technologies, troubleshoot assays, and write technical documents involving CAR-T programs.
Support CAR-T process and development, perform cell cultures and decisional analytics assays associated with these activities as required.
Routinely support non-clinical study sample analytical testing and participate in routine lab operations, equipment maintenance, reagent qualifications, and/or other duties.
Analyze high volume data, present research findings and data to the group through both written and oral communication.
Qualifications:
Bachelor's or Master's Degree in a related field of study
Minimum of 1 year of Flow Cytometry experience
1+ years of ELISA and mammalian cell culture experience
Prior experience with CAR-T or Cell Therapy is preferred
Salary: $70,000 - $90,000 (can be flexible based off experience)
Hours: Monday-Friday, 8:00am-5:00pm
Hiring Method: Multiyear contract - After 1 year on contract, the individual will have the opportunity to apply for a permanent role or have their contract renewed for another year
PTO: 10 PTO days, 6 paid sick days & paid Holidays
Benefits: Medical, Dental, Vision and 401K plans available
Exact compensation may vary based on several factors, including skills, experience, and education.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.
$70k-90k yearly 4d ago
Development Chemist III
Quaker Chemical Corporation 4.6
Chemist 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
Associate Scientist Bakery and Cookies
Campbell Soup Co 4.3
Chemist job in Camden, NJ
Since 1869 we've connected people through food they love. We're proud to be stewards of amazing brands that people trust. Our portfolio includes the iconic Campbell's brand, as well as Michael Angelo's, Pace, Pacific Foods, Prego, Rao's Homemade, Swanson, and V8. In our Snacks division, we have brands like Cape Cod, Goldfish, Kettle Brand, Lance, Late July, Pepperidge Farm, Snack Factory, and Snyder's of Hanover. Here, you will make a difference every day. You will be supported to build a rewarding career with opportunities to grow, innovate and inspire. Make history with us. Why Campbell's… Benefits begin on day one and include medical, dental, short and long-term disability, AD&D, and life insurance (for individual, families, and domestic partners). Employees are eligible for our matching 401(k) plan and can enroll on the first day of employment with immediate vesting. Campbell's offers unlimited sick time along with paid time off and holiday pay. If in WHQ - free access to the fitness center. Access to on-site day care (operated by Bright Horizons) and company store. Giving back to the communities where our employees work and live is very important to Campbell's. Our "Campbell's Cares" program matches employee donations and/or volunteer activity up to $1,500 annually. Campbell's has a variety of Employee Resource Groups (ERGs) to support employees.
How you will make history here...
The Associate Scientist R&D will be responsible for supporting the Research & Development activities on the Fresh & Frozen Bakery and Cookies Product Development Teams.
In this role you will be supporting projects across the Bakery and Cookie Categories, primarily the Pepperidge Farm brand. The scope of the job encompasses supporting the entire Product Development process from idea conception through plant commercialization.
What will you do...
The Associate Scientist will be responsible for supporting benchtop, pilot plant, and ad-hoc project support. The individual may also work in a lab-based setting using applicable analytical testing equipment. They will be responsible for assisting with research, gathering and analyzing data and reporting findings on assignments/projects that are moderately complex. The Associate Scientist will perform a variety of duties requiring the application of technical knowledge using established processes/protocols. They will independently plan, prioritize, and execute work making basic technical decisions independently. Their day-to-day job responsibilities will require them to work in a team environment ensuring alignment with cross-functional partners, both internal (Marketing, Quality Assurance, Process Development, Packaging Development, Finance, Operations, and Procurement) and external (vendors/suppliers, Campbell's, co-manufacturers). They must be knowledgeable about experimental design (DOE), laboratory documentation, and general food science.
Primary Responsibilities
Support Product Development Scientists with sandboxing/product ideation, product feasibility testing, plant trials, start-ups, productivity and quality programs.
Assist with the assessment and validation of formulations from benchtop through commercialization with support and coaching from R&D manager. Project types include:
New product development
Cost savings opportunities
Quality improvement projects
Business continuity initiatives
Ensure all proper documentation is done accurately and on schedule, inclusive but not limited to:
Pre and post-trial documentation and communication to cross functional team
Electronic lab notebook maintenance of formula testing and results
Ability to interact and communicate effectively (written and verbal)
Conduct and maintain Quality Analytical Testing Data for Product Development team as needed.
Apply problem solving skills to identify, interpret and analyze the correct data and provide detailed directions to development projects.
Leveraging external suppliers to build knowledge to deliver results
Maintain benchtop workspace cleanliness and order
Easily adapts to changing priorities.
Who you will work with...
R&D management, scientists, product development and cross-functional team members.
What you will bring to the table... (Required Skills)
Bachelor's degree required from an accredited institution in science related field (Food Science, Engineering; or related field)
6 months to 2 years of related experience with a consumer-packaged goods background. Experience in a combination of any of the following: Snacks (such as crackers, chips, pretzels, and cookies) and Bakery (such as breads, buns/rolls, and cakes/frozen desserts).
Handle allergens including dairy, peanuts, tree nuts, soy, wheat, eggs and other food ingredient chemicals and allergens while wearing appropriate PPE.
Excellent analytical skills, strong attention to details, self-driven, ability to deal with ambiguity, good communication and interpersonal skills.
Ability to handle multiple assignments at any given time in a team environment.
Experience with Microsoft Office - including formula, data, graph application a plus
Must be able to lift up to 40 lbs
Anticipated travel up to 25%
Compensation and Benefits: The target base salary range for this full-time, salaried position is between
$57,800-$83,100
Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package.
The Company is committed to providing equal opportunity for employees and qualified applicants in all aspects of the employment relationship, including consideration for employment, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, protected veteran status, disability, age, religion, or any other classification protected by law.
$57.8k-83.1k yearly Auto-Apply 35d ago
Chemist (Manufacturing Associate)
Penn Life Sciences Inc.
Chemist job in Langhorne, PA
Penn Life Sciences is seeking a skilled Chemist (Manufacturing Associate) to join our team in Langhorne, PA. The Chemist (Manufacturing Associate) serves as a key manufacturing-facing technical resource, supporting investigations, documentation, and continued process verification to ensure consistent product quality and compliance with cGMP and regulatory requirements. The ideal candidate will bring hands-on experience in sterile manufacturing support, validation activities, and cross-functional collaboration within a regulated pharmaceutical environment.
This position's responsibilities will include, but not be limited to the following:
* Provide on-floor technical support to sterile manufacturing operations during routine production, validation, and qualification activities.
* Prepare, execute, and support the review of manufacturing-related validation documentation, including IQ, OQ, PQ, process validation, and continued process verification activities.
* Support deviation investigations, root cause analyses, and CAPA development related to manufacturing, validation, or qualification activities.
* Evaluate manufacturing changes and support change control activities related to processes, equipment, facilities, utilities, and procedures.
* Collaborate cross-functionally with Quality, Validation, Engineering, and Technical Services to ensure alignment across manufacturing activities.
* Support regulatory inspections, audits, and internal assessments related to manufacturing and validation activities.
We are looking for applicants with:
* Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or a closely related scientific discipline required; Master's degree preferred.
* 2-5 years of experience supporting pharmaceutical manufacturing, validation, or technical operations in a cGMP-regulated environment.
* Prior experience in sterile or aseptic manufacturing environments strongly preferred.
* Working knowledge of cGMP requirements (21 CFR Parts 210/211) and experience supporting validation and continued process verification activities.
* Strong technical writing, documentation review, and cross-functional communication skills.
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.
$46k-72k yearly est. 13d ago
Chemist
Onsite Personnel LLC 4.2
Chemist job in Philadelphia, PA
Job DescriptionSummary: QC Chemist:This position's purpose is to support the Quality Control lab for analysis of purified water, raw materials, finished and stability samples. Essential Duties and Responsibilities: QC Chemist
Sample of Raw materials and Purified water for Analysis
Arrange retain samples for raw materials and finished products
Performing daily analytical balance verification- as required
Performing calibration of pH meters and Fluoride Ion meters as required
Preparation and standardization of Volumetric solutions and test solutions as required
Arranging chemicals in the lab and checking for their expiration dates as required
Arranging quality control documents as needed as required
Performing wet analysis for raw materials and finished products, which includes Loss on drying, Viscosity, pH and water content etc.
Performing chart replacement for all chart records which monitor temperature and humidity as required.
Perform analysis using HPLC/UV-Visible spectrophotometer for raw materials, finished products and stability samples.
Qualifications: QC Chemist:
Ability to apply comprehensive knowledge of pharmaceutical cGMP's and quality system controls, procedures and records to ensure ongoing quality compliance.
Ability to perform all requirements independently with limited managerial oversight.
Excellent organizational abilities to meet accelerated timelines, manage multiple shifting priorities and maximize efficiencies in a dynamic customer-focused environment.
Superior attention to detail to ensure accuracy of work product.
Superior critical-thinking and problem-solving skills; ability to recognize and resolve discrepancies and issues.
Education/Experience: QC Chemist:
Minimum 2 years industrial experience in Quality Control laboratory functions.
Degree (BS or BA) in Biology, Chemistry, Biochemistry, or relevant related field.
Or sufficient technical depth or professional experience will be considered in lieu of technical degree.
Experience in quality systems, including validation, documentation, compliance department preferred.
HPLC analytical experience is a plus.
Onsite Personnel is an equal opportunity employer committed to hiring a diverse workforce in an inclusive culture environment. Onsite Personnel does not discriminate based on disability, veteran status or any other basis protected under federal, state, or local laws.
$46k-64k yearly est. 27d ago
Lab Chemist (2)
Monroe Energy LLC 4.2
Chemist job in Trainer, PA
Education, Experience, and Skill Requirements * Minimum 5 years relevant lab experience, Associate's degree with 2 yrs relevant Lab experience, or a Bachelor of Science degree in Chemistry * Prior CFR experience preferred - operating and/or maintaining
* General mechanical aptitude - ability to perform basic troubleshooting/repair of equipment
* Proficient with Microsoft Word, Outlook, and Excel, IT Skills - understanding data bases, Laboratory Information Management Systems (LIMS) and instrumentation networking.
* Demonstrated proficiency in all of Role Specific Competencies.
* This is a shift-work job that requires flexibility to work days, nights, weekends, and holidays.
Key Role Description
Assists with Lab technical activities related to all of the refinery processes and products including test methodology, equipment purchases, and equipment calibration and repair. Assists in managing daily operations to insure quality of results, efficient management of inventory to maintain continuity of operations, and the storage and handling of samples for regulatory compliance and inspection purposes.
Role Specific Competencies
At Monroe, we have identified nine specific competencies we expect all employees of our organization to possess. These competencies are incorporated as a part of our Selection, Performance Management/Review and Developmental processes. The competencies and activities for this role are detailed below:
Technical Knowledge - demonstrates the specific skills necessary for the assignments, understands the background and points of leverage to be effective in the role.
* Performs technical work in analytical or physical chemistry involving a variety of standardized chemical and physical tests.
* Monitors a specialized unit of a laboratory section or the operations of several units or performs complex and specialized chemical laboratory tests.
* Conducts analytical and physical tests on finished products.
* Requisition and maintainenance of chemistry supplies and equipment.
* Conducts analytical or physical testing of a variety of materials.
Knowledge of Work Areas and Responsibilities - demonstrates a clear understanding of role and responsibilities within specific area, flexible and agile in adapting to changes or exploring opportunities and challenges.
* Maintains schedule flexibility to meet the needs of the business: extended hours, evenings and/or weekends.
* Performs special projects as assigned by the Lab Leader.
* Attends operational meetings as needed.
Communications - Verbal and Written - includes written and verbal communications, delivers presentations and has good listening skills.
Problem Solving and Conflict Leadership - strives to understand contributing factors, works to resolve complex situations, and helps individuals to resolve conflicts.
Delivering Results - Sense of Urgency - defines appropriate goals, works toward achieving goals, articulates vision and steps for achievement, meets deadlines and provides timely status updates and follow-through.
Teamwork/Cooperation - accountable to team, works to meet established deliverables, appreciates view of team members and is respectful of others.
Initiative - takes action, seeks new opportunities, and strives to see projects to completion.
Work Reliability/Quality - strives to eliminate errors, accurate work is a priority, and seeks opportunities to improve product/services.
Integrity and Trust - honest, accountable, upholds ethics standards and maintains confidentiality.
$45k-64k yearly est. 57d ago
Chemist (Environmental)
Criterion Laboratories 4.1
Chemist job in Bensalem, PA
The Chemist is a key member of the laboratory team, and in close coordination with the Senior Chemist, is responsible for delivering consistent, accurate, and efficient environmental testing results. This role requires expert-level knowledge in analytical and organic chemistry, with a focus on metals, ions, VOCs, SOCs, and PFAS analyses. The Chemist operates a range of advanced instrumentation, including liquid chromatography, gas chromatography, ionic chromatography, atomic absorption spectrometry, and mass spectrometry, ensuring the highest standards of data integrity and laboratory quality.
Essential Duties and Responsibilities:
Analytical Testing:
Performs daily analyses by strictly adhering to established methods and Standard Operating Procedures (SOPs), including but not limited to metals, ions, volatile organic compounds (VOCs), semi-volatile organic compounds (SOCs), and per- and polyfluoroalkyl substances (PFAS).
Ensures all results meet regulatory and internal quality standards.
Instrumentation:
Operates, calibrates, and troubleshoots laboratory instruments such as liquid chromatography, gas chromatography, ionic chromatography, and mass spectrometry.
Performs preventive maintenance as recommended by manufacturers to maintain equipment reliability and data quality.
Quality Assurance:
Works closely with the QA Manager to ensure the integrity of all results produced.
Participates in method development, validation, and continuous improvement initiatives to enhance laboratory capabilities and compliance with state and federal regulations.
Safety and Compliance:
Maintains strict adherence to laboratory safety protocols and basic procedures.
Ensures compliance with all regulatory requirements, including those outlined by PADEP Chapter 252 and other relevant standards.
Collaboration and Mentorship:
Works directly with the Senior Chemist to expand knowledge and experience in various analyses and instrumentation. Mentors and guides less experienced laboratory analysts, fostering a collaborative and supportive team environment.
Expertise:
Possesses and applies expert knowledge in analytical and organic chemistry to support successful laboratory operations.
Stays current with industry advancements, new technologies, and best practices to continually improve laboratory performance.
Requirements
Required Knowledge and Experience:
Minimum of 2-5 years of relevant laboratory experience (as required by state regulations for supervisory roles).
Demonstrated experience with chromatography, inorganic analyses, and environmental testing methods.
Strong troubleshooting skills and ability to independently resolve complex laboratory issues.
Commitment to safety, quality, and continuous professional development.
Required Education, Certifications, and Licenses:
Bachelor's degree in Chemistry or a closely related field; advanced degree preferred. Completion of at least 24 credits in chemistry coursework. A masters or earned doctoral degree in a science discipline may be substituted for 1 year of experience.
Physical and Mental Requirements:
· This position may require standing, sitting, reaching, crawling, climbing, and squatting
· Ability to lift up to 20 lbs.
$45k-61k yearly est. 5d ago
Biology - Imaging R&D
Eli Lilly and Company 4.6
Chemist job in Philadelphia, PA
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Position Overview:Eli Lilly and Company (Lilly) Imaging Research and Development provides technical expertise for molecular and anatomical imaging to Lilly Research Laboratories. The Biologist will provide histopathology support by assisting in human tissue labeling to establish well-characterized tissue panels for compound screening and pathophysiological evaluation of target expression towards the discovery of new PET tracers for evaluation as development candidates.Responsibilities:• Design, develop, and execute human brain tissue characterization protocols (sample preparation and cryosectioning, staining, immunohistochemistry and autoradiography) for neuroscience research and imaging biomarker projects.• Assist in organization of tissue staining data from various research projects• Conduct and design radioligand binding assays such as autoradiography.• Implement digital pathology tools compatible with whole slide imaging scanner, autoradiography and confocal microscopy.Basic Qualifications:• Master of science degree, preferentially in Neuroscience with a minimum of 1 year experience in PET tracer discovery.Additional Skills/Preferences:Proficiency in immunohistochemistry, including immunofluorescence, automated histology equipment, spatial omics platform, gene silencing knowledge, and morphometry image analysis software (Visiopharm).• Provide strategic and technical expertise on the design and optimization of protein and transcript target detection.• Develop morphometric quantitative analysis methods using AI/ML software for target mapping in human samples• Experience in rodent and human tissue preparation and handling• Evaluation of small molecules and biologicals• Ensure good laboratory practice for data documentation as well as communicate research findings and recommendations to internal and external stakeholders through written reports, oral presentations and scientific communications.• In-depth knowledge of rodent and human neuroanatomy• Understanding of neuropathological hallmarks scoring• Use of real-time autoradiography is preferred• Ability to be pro-active, flexible, and capable of independent trouble shooting and problem solving. Work within a team-oriented lab environment and work within cross-functional project teams• Participate in scientific conferences and workshops to continue education/professional development• Good organizational and time-management skills• Excellent written and verbal communication skills
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$65,250 - $169,400
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
$65.3k-169.4k yearly Auto-Apply 19d ago
QC Scientist -I (Microbiologist)
Artech Information System 4.8
Chemist 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
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. 18d ago
Field Chemist
Heritage Environmental Services, LLC 4.4
Chemist job in Telford, PA
Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries.
Why Arcwood?
* Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves.
* Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges.
* Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant, Always.
* Collaborative Environment: Together we can achieve much more. Join a supportive and dynamic team where your ideas and efforts are recognized and rewarded.
Our Commitment: We are dedicated to fostering an inclusive and innovative workplace where every employee can thrive. As part of our team, you will have the freedom to contribute your expertise wherever needed, ensuring the success of our mission to protect the environment.
Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet.
Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future.
Field Chemist
As a Field Chemist you will be responsible for sorting and transporting hazardous and non-hazardous materials and waste, always ensuring compatibility and safety in all processes for each service provided to customers.
Essential Functions & Requirements:
* Prioritizes health and safety by adhering to policies, processes, and maintaining safe practices at all times
* Assists in the segregation of chemicals by hazard class and packs compatible materials in appropriate containers and prepares for transportation; completes necessary paperwork for each job
* Determines and loads supplies needed for job completion and travels to various industry, laboratory, and educational sites to perform lab pack services
* Assists in characterizing materials at field project sites
* Adheres to proper placarding and load segregation requirements when transporting hazardous materials
* Develops good customer relations by effectively communicating with site points of contact and others at customer location / site
* Appropriately directs Field Technicians / Drivers who are assisting with waste collection
* Maintains an introductory knowledge of high-hazard materials management / assessment and cylinder handling
* Maintains the ability to travel to support outside locations as needed
* Takes on additional duties as assigned to support the team and organization
Education:
* Bachelor's degree (required), with a focus in environmental science or science (preferred)
Experience:
* In lieu of degree 2+ years of related experience (required), previous experience in lab packing or environmental waste (preferred)
* Valid Driver's License and ability to obtain a Class B CDL with Hazmat endorsement within 6 months of hire date (required)
* Ability to pass a Motor Vehicle Record search to Company standards (required)
Competencies:
* Ability to work in a constant state of alertness and in a safe manner
* Ability to develop a working knowledge of all Federal, State, and local laws and regulations pertaining to the Environmental Services industry
* Excellent interpersonal skills to effectively communicate with internal and external customers
* Regular and predictable attendance to perform the functions and requirements of this role
Additional Requirements:
* Due to the potential exposure to atmospheres/waste/materials this position requires individuals to be clean shaven at all times in order to don a respirator for protection.
Benefits, Compensation, & Workforce Diversity:
Arcwood offers competitive pay and bonus incentives. Benefits include choice of medical, dental, and vision plans, flexible spending or health savings accounts, employee and dependent life insurance, short and long-term disability, 401(k) savings plan with 7% company match, and tuition reimbursement.
Equal Opportunity Employer - Veterans & Disabilities
A post-offer drug screen and background check will be required.
$46k-66k yearly est. 1d ago
Associate Scientist (Biologic Discovery)
Insight Global
Chemist job in Spring House, PA
Our large pharmaceutical client is seeking an Associate Scientist to join their growing Biophysics & Molecular Attributes Group in Spring House, PA. The Biophysics & Molecular Attributes Group within Biologics Discovery uses innovative biophysical, biochemical, and mass spectrometry based analytical tools to help select best therapeutic candidates for clinical development. You will be a critical member of the Higher Order Structure (HOS) team that characterizes developability attributes like thermal stability, chemical stability, solubility, and aggregation on a broad range of biologics platforms including monoclonal antibodies, multi-specific antibodies, antibody drug conjugates, antibody radio conjugates, and other therapeutic proteins. You will design and perform experiments using a variety of technologies like HPLC, DSF, DSC, cIEF, GXII, DLS, and more.
Key Responsibilities:
Execute automated methods for biophysical and structural characterization of antibody therapeutics. Integrate robotic liquid handling systems (e.g., Hamilton, Tecan) with analytical platforms to improve efficiency, consistency, and sample throughput.
Execute analytical analysis of biologics candidates using a wide variety of technologies such as size-exclusion HPLC, plate-based HIC/Heparin binding, DSF.
Evaluate results to deliver scientifically supported conclusions and recommendations that are documented in appropriate technical reports.
Maintain lab and equipment.
Collaborate with colleagues in the global organization to support discovery projects.
Assist in developing recommendations for improving standard procedures.
Required Skills & Experience
Master's or Bachelor's degree in a relevant scientific field
2 years of experience in protein characterization (biologics/large molecules)
Hands-on expertise in using and troubleshooting analytical techniques such as HPLC, DSF, DSC, cIEF, GXII, and DLS for protein and antibody analysis
Nice to Have Skills & Experience
Protein purification
Salary: $67,000 - $75,000 (can be flexible based off experience)
Hours: Monday-Friday, 8:00am-5:00pm
Hiring Method: Multiyear contract - After 1 year on contract, the individual will have the opportunity to apply for a permanent role or have their contract renewed for another year
PTO: 10 PTO days, 6 paid sick days & paid Holidays
Benefits: Medical, Dental, Vision and 401K plans available
Exact compensation may vary based on several factors, including skills, experience, and education.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.
$67k-75k yearly 1d ago
Development Chemist III
Quaker Chemical Corporation 4.6
Chemist 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 worlds 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 chemists 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 Masters 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, veterans 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
Associate Scientist Bakery and Cookies
Campbell Soup 4.3
Chemist job in Camden, NJ
Since 1869, we've connected people through food they love. We're proud to be stewards of amazing brands that people trust. Our portfolio includes the iconic Campbell's brand, as well as Cape Cod, Chunky, Goldfish, Kettle Brand, Lance, Late July, Pacific Foods, Pepperidge Farm, Prego, Pace, Rao's Homemade, Snack Factory, Snyder's of Hanover. Swanson, and V8.
Here, you will make a difference every day. You will be supported to build a rewarding career with opportunities to grow, innovate and inspire. Make history with us.
Why Campbell's…
Benefits begin on day one and include medical, dental, short and long-term disability, AD&D, and life insurance (for individual, families, and domestic partners).
Employees are eligible for our matching 401(k) plan and can enroll on the first day of employment with immediate vesting.
Campbell's offers unlimited sick time along with paid time off and holiday pay.
If in WHQ - free access to the fitness center. Access to on-site day care (operated by Bright Horizons) and company store.
Giving back to the communities where our employees work and live is very important to Campbell's. Our “Campbell's Cares” program matches employee donations and/or volunteer activity up to $1,500 annually.
Campbell's has a variety of Employee Resource Groups (ERGs) to support employees.
How you will make history here...
The Associate Scientist R&D will be responsible for supporting the Research & Development activities on the Fresh & Frozen Bakery and Cookies Product Development Teams.
In this role you will be supporting projects across the Bakery and Cookie Categories, primarily the Pepperidge Farm brand. The scope of the job encompasses supporting the entire Product Development process from idea conception through plant commercialization.
What will you do...
The Associate Scientist will be responsible for supporting benchtop, pilot plant, and ad-hoc project support. The individual may also work in a lab-based setting using applicable analytical testing equipment. They will be responsible for assisting with research, gathering and analyzing data and reporting findings on assignments/projects that are moderately complex. The Associate Scientist will perform a variety of duties requiring the application of technical knowledge using established processes/protocols. They will independently plan, prioritize, and execute work making basic technical decisions independently. Their day-to-day job responsibilities will require them to work in a team environment ensuring alignment with cross-functional partners, both internal (Marketing, Quality Assurance, Process Development, Packaging Development, Finance, Operations, and Procurement) and external (vendors/suppliers, Campbell's, co-manufacturers). They must be knowledgeable about experimental design (DOE), laboratory documentation, and general food science.
Primary Responsibilities
Support Product Development Scientists with sandboxing/product ideation, product feasibility testing, plant trials, start-ups, productivity and quality programs.
Assist with the assessment and validation of formulations from benchtop through commercialization with support and coaching from R&D manager. Project types include:
New product development
Cost savings opportunities
Quality improvement projects
Business continuity initiatives
Ensure all proper documentation is done accurately and on schedule, inclusive but not limited to:
Pre and post-trial documentation and communication to cross functional team
Electronic lab notebook maintenance of formula testing and results
Ability to interact and communicate effectively (written and verbal)
Conduct and maintain Quality Analytical Testing Data for Product Development team as needed.
Apply problem solving skills to identify, interpret and analyze the correct data and provide detailed directions to development projects.
Leveraging external suppliers to build knowledge to deliver results
Maintain benchtop workspace cleanliness and order
Easily adapts to changing priorities.
Who you will work with...
R&D management, scientists, product development and cross-functional team members.
What you will bring to the table... (Required Skills)
Bachelor's degree required from an accredited institution in science related field (Food Science, Engineering; or related field)
6 months to 2 years of related experience with a consumer-packaged goods background. Experience in a combination of any of the following: Snacks (such as crackers, chips, pretzels, and cookies) and Bakery (such as breads, buns/rolls, and cakes/frozen desserts).
Handle allergens including dairy, peanuts, tree nuts, soy, wheat, eggs and other food ingredient chemicals and allergens while wearing appropriate PPE.
Excellent analytical skills, strong attention to details, self-driven, ability to deal with ambiguity, good communication and interpersonal skills.
Ability to handle multiple assignments at any given time in a team environment.
Experience with Microsoft Office - including formula, data, graph application a plus
Must be able to lift up to 40 lbs
Anticipated travel up to 25%
Compensation and Benefits:
The target base salary range for this full-time, salaried position is between
$57,800-$83,100
Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package.
The Company is committed to providing equal opportunity for employees and qualified applicants in all aspects of the employment relationship, including consideration for employment, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, protected veteran status, disability, age, religion, or any other classification protected by law.
$57.8k-83.1k yearly Auto-Apply 36d ago
QC Chemist I
Penn Life Sciences Inc.
Chemist 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.
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. 19d ago
QC Scientist -I (Microbiologist)
Artech Information System 4.8
Chemist 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. 2h ago
Quality Control Analyst
Insight Global
Chemist job in Malvern, PA
The QC CRS Analyst is responsible for conducting biochemical and testing of raw material, in-process, final product release and characterization samples, including CAR-T. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 5 -- 10 other Analysts within a functional Clinical Release and Stability Laboratory and report to the Senior QC Supervisor. Key
Responsibilities:
-Conduct analytical biological testing of clinical and commercial drug product/drug substance samples
-Perform peer reviews and approvals of laboratory data -Use electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing including application of statistical concepts to laboratory data
-Support of New Product Initiatives (NPI) including owning a project and perform project management functions with limited to no coaching from supervision/management
-Perform Instrument Calibration and Preventative Maintenance
-Update CRS
-Owned documents using the Document Management System (DMS)
-Order/receive supplies and manage inventory -Support analytical method qualification, validation, and transfer into and out of the QC lab, owning change control actions, completing testing activities with mentorship from Sr. Analysts on transfer activities
-Complete change control processes to integrate new methodologies and technologies into and out of the CRS Lab with limited oversight
-Act as a peer subject matter expert in assessing talent by participating in panel interviews for job
-Complete invalid assay and general laboratory investigation records
-Complete corrective and preventative actions (CAPA) as assigned
-Assist in the execution of internal audits
REQUIRED SKILLS AND EXPERIENCE:
-Minimum one year of relevant GMP QC work experience in Pharmaceutical lab
-Bachelor degree in Biology or Chemistry
-Working experience in a current Good Manufacturing Practices (cGMP) compliant QC laboratory or equivalent environment and solid understanding of cGMP and current Good Laboratory Practices (GLPs)
-Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories specifically with Flow Cytometry
-Ability to read/interpret technical documents such as SOPs, work instructions, test methods and protocols
-Proficient with Microsoft Office applications (Outlook, One Note, Teams, Excel, Word, and PowerPoint)
NICE TO HAVE SKILLS AND EXPERIENCE:
-CAR-T, Cell and Gene Therapy, or Biochemistry laboratory experience
-Basic knowledge of Compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC
-Ability to complete equipment and software qualification protocols
-Experience developing and setting long-term objectives
-Experience working in Biosafety Level lab (BSL 2, BSL2+) or aseptic facility
-Knowledge of EU/FDA guidance
The average chemist in Ardmore, PA earns between $40,000 and $82,000 annually. This compares to the national average chemist range of $46,000 to $90,000.
Average chemist salary in Ardmore, PA
$57,000
What are the biggest employers of Chemists in Ardmore, PA?
The biggest employers of Chemists in Ardmore, PA are: