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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.

Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our Rising Innovators for Scientific Excellence (RISE) Internship program is designed to ignite potential and accelerate learning the world of pharmaceutical innovation. We are seeking individuals for our 2026 Summer RISE Intern roles who have a mindset open to learning and growth, and a desire to make a difference. Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. Role Overview: Join the Analytical Research & Development (ARD) team within Veranova for a dynamic summer internship. Our program consists of a 10–12-week internship at our West Deptford, NJ location. The ARD Intern is responsible for the implementation of laboratory improvements, which may include reorganization of supplies to support a 5S or other organizational system and general laboratory improvements. Areas of improvement may include reference standards, metrology and/or general lab support. Job duties may change rapidly to support the daily operation of the laboratories, and the summer intern must be able to adjust to rapidly changing priorities. Core Responsibilities: • Assist in the execution of laboratory experiments, including analytical method development, validation, and GMP sample testing., • Operate and maintain analytical instruments such as HPLC, UV-Vis Spectrophotometer, and FTIR under supervision., • Follow established laboratory safety procedures and adhere to Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs)., • Assist in the maintenance and inventory management of reagents, chemicals, and consumables used in the lab., • Support the maintenance and continuous improvement of the 5S system in analytical laboratories, ensuring an organized and efficient work environment., • Assist in routine calibration and maintenance of laboratory instruments., • Collaborate with cross-functional teams, including Quality Control (QC), Chemical Development, and Quality Assurance (QA), to support analytical activities., • Maintain accurate and detailed records of laboratory work, ensuring compliance with documentation and regulatory requirements., • Provide general assistance to chemist (Cleaning of glassware, obtaining chemicals etc), • Communicates effectively in verbal and written form, • Provide weekly updates on project progress, • Volunteers to assist with tasks not directly related to a specific project., • Participates in self-development activities., • To carry out any other duties which are within the employee’s skills and abilities whenever reasonably instructed. Physical Demands & Work Environment • While performing the duties of this job it is required to stand, walk, and use hands to operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for job activity., • Must be able to lift and/or move up to 50 pounds., • Specific vision abilities include near, distance, peripheral, color perception, and the ability to adjust focus., • Regularly works with moving mechanical parts and may work with toxic or caustic chemicals., • The work may be performed in humid areas with low or high temperatures., • This work may need to work with respirator or operate with bunny suits., • Work may be required in areas where work potent and hazardous chemicals are utilized. Qualifications: • Working towards a BS in Chemistry, Chemical Engineering, Material Science, or related field, • Minimum Overall GPA of 2.7 required, • Demonstrated leadership skills with a true career aspiration to be a leader, • Must be adaptable, strive for excellence, and demonstrate a positive attitude in the face of adversity, • Strong interpersonal skills a must, coupled with a proven ability to build collaborative relationships to achieve results, • Proficiency with Microsoft Office required, • Strong problem solving and analytical skills essential, • Must be legally authorized to work in the US Preferred • Experience with 5S or other standardized workplace organization methods., • Prior experience working in a laboratory setting., • Understanding of laboratory safety procedures and best practices., • Knowledge of Current Good Manufacturing Practices (cGMP) and regulatory compliance in a pharmaceutical or analytical lab environment. Pay Range: $20 - $22 per hour Our Commitment: • Drive for Excellence: Our uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do., • Financial Wellness: We are committed to fair and transparent compensation practices. This includes competitive pay that reflects the scope and expectations of the role., • Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, and mentorship., • Inclusive Culture: An inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Additional Information: Applicants for this role must be authorized to work in the United States without further employer sponsorship. All your information will be kept confidential according to EEO guidelines. Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law. All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Job DescriptionDescription: 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., • 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. · This position may require standing, sitting, reaching, crawling, climbing, and squatting · Ability to lift up to 20 lbs.

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.

Job Description ARD Internship Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. At Veranova, we don’t just hire early talent - we invest in it. Our Rising Innovators for Scientific Excellence (RISE) Internship program is designed to ignite potential and accelerate learning the world of pharmaceutical innovation. We are seeking individuals for our 2026 Summer RISE Intern roles who have a mindset open to learning and growth, and a desire to make a difference. Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. Role Overview: The Summer Intern is responsible for the implementation of laboratory improvements, which may include reorganization of supplies to support a 5S or other organizational system and general laboratory improvements. Areas of improvement may include reference standards, metrology and/or general lab support. Job duties may change rapidly to support the daily operation of the laboratories, and the summer intern must be able to adjust to rapidly changing priorities. Work may be required in areas where work potent and hazardous chemicals are utilized. Visit Veranova.com to learn more. Our program consists of a 10–12-week internship at our West Deptford, NJ location. Core Responsibilities: • Assist in the execution of laboratory experiments, including analytical method development, validation, and GMP sample testing., • Operate and maintain analytical instruments such as HPLC, UV-Vis Spectrophotometer, and FTIR under supervision., • Follow established laboratory safety procedures and adhere to Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs)., • Assist in the maintenance and inventory management of reagents, chemicals, and consumables used in the lab., • Support the maintenance and continuous improvement of the 5S system in analytical laboratories, ensuring an organized and efficient work environment., • Assist in routine calibration and maintenance of laboratory instruments., • Collaborate with cross-functional teams, including Quality Control (QC), Chemical Development, and Quality Assurance (QA), to support analytical activities., • Maintain accurate and detailed records of laboratory work, ensuring compliance with documentation and regulatory requirements., • Provide general assistance to chemist (Cleaning of glassware, obtaining chemicals etc), • Communicates effectively in verbal and written form, • Provide weekly updates on project progress, • Volunteers to assist with tasks not directly related to a specific project., • Participates in self-development activities., • While performing the duties of this job it is required to stand, walk, and use hands to operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for job activity., • Must be able to lift and/or move up to 50 pounds., • Specific vision abilities include near, distance, peripheral, color perception, and the ability to adjust focus., • Regularly works with moving mechanical parts and may work with toxic or caustic chemicals., • The work may be performed in humid areas with low or high temperatures., • This work may need to work with respirator or operate with bunny suits. Qualifications: • Working towards a BS in Chemistry, Chemical Engineering, Material Science, or related field, • Minimum Overall GPA of 2.7 required, • Demonstrated leadership skills with a true career aspiration to be a leader, • Must be adaptable, strive for excellence, and demonstrate a positive attitude in the face of adversity, • Strong interpersonal skills a must, coupled with a proven ability to build collaborative relationships to achieve results, • Proficiency with Microsoft Office required, • Strong problem solving and analytical skills essential, • Must be legally authorized to work in the US Preferred • Experience with 5S or other standardized workplace organization methods., • Prior experience working in a laboratory setting., • Understanding of laboratory safety procedures and best practices., • Knowledge of Current Good Manufacturing Practices (cGMP) and regulatory compliance in a pharmaceutical or analytical lab environment. Pay Range: $20 - $22 per hour Our Commitment: • Drive for Excellence: Our uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do., • Financial Wellness: We are committed to fair and transparent compensation practices. This includes competitive pay that reflects the scope and expectations of the role., • Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, and mentorship. Applicants for this role must be authorized to work in the United States without further employer sponsorship. All your information will be kept confidential according to EEO guidelines. Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law. All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

Job Description Company Overview: 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., • 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)., • Competitive pay programs with excellent career growth trajectory, • Opportunities to see your efforts contribute toward the success of the business

Job Title: Quality Control Supervisor Location: G Street Facility, Philadelphia, PA Reports To: Quality Manager Position Summary The Quality Control Supervisor is responsible for leading the QC team and ensuring that all inspection and testing activities comply with ISO 9001 standards and company quality objectives. This role focuses on maintaining product quality, driving continuous improvement, and supporting internal and external audits. A key responsibility includes developing QC staff through training, implementing process improvements in the laboratory, and ensuring a strong safety culture. This role leads 6 technicians, a team lead, and an analytical chemist. Work Schedule • Full-time, on-site; Monday-Friday. supporting 1st Shift -- 7:30am to 4:30pm\n What you will do: \n • Supervise QC inspectors and technicians, including scheduling, coaching, and performance evaluations.\n, • Develop and deliver training programs on inspection techniques, measurement tools, ISO 9001 requirements, and laboratory safety protocols.\n, • Ensure all QC staff are trained in proper handling of equipment, chemical safety, and emergency procedures.\n, • Mentor team members to enhance technical skills and promote safe work practices.\n, • Oversee inspection and testing of raw materials, in-process components, and finished products.\n, • Review and approve inspection reports, test results, and non-conformance documentation.\n, • Identify opportunities to improve laboratory workflows, reduce testing time, and enhance accuracy.\n, • Implement new inspection methods, tools, and technologies to optimize QC processes.\n, • Collaborate with engineering and production teams to integrate quality improvements into manufacturing processes.\n, • Enforce compliance with all safety regulations and company policies in the QC lab.\n, • Conduct regular safety audits and risk assessments.\n, • Support internal audits and assist with external certification audits.\n, • Implement corrective and preventive actions (CAPAs) for identified issues.\n\n Minimum Qualifications \n • Bachelor's degree in Engineering, Chemistry, oQuality Management, or related field.\n, • 5+ years in a QC role within a manufacturing environment; at least 3 years in a supervisory capacity.\n, • Proficiency in inspection tools, measurement techniques, and quality software.\n, • Excellent leadership, communication, and problem-solving skills.\n\n Annual or Hourly Compensation Range The pay range for this position is $85,900.00 - $128,900.00. Many factors are taken into consideration when determining compensation, such as experience, education, training, geography, etc. We comply with all minimum wage and overtime laws. Benefits Ecolab strives to provide comprehensive and market-competitive benefits to meet the needs of our associates and their families. Click here to see our benefits. If you are viewing this posting on a site other than our Ecolab Career website, view our benefits at jobs.ecolab.com/working-here. Potential Customer Requirements Notice To meet customer requirements and comply with local or state regulations, applicants for certain customer-facing roles may need to: • Undergo additional background screens and/or drug/alcohol testing for customer credentialing., • Be fully vaccinated for COVID-19, including a booster if eligible, unless a religious or medical accommodation is requested by the applicant and approved by Ecolab. Americans with Disabilities Act (ADA) Ecolab will provide reasonable accommodation (such as a qualified sign language interpreter or other personal assistance) with our application process upon request as required to comply with applicable laws. If you have a disability and require accommodation assistance in this application process, please visit the Recruiting Support link in the footer of each page of our career website.

Looking for student currently enrolled in chemistry major, or chemistry-adjacent major with/or chemistry minor. Strong chemistry background and theory of various chemistry instruments and analytical chemistry techniques and procedures. Gain experience in analytical chemistry procedures and instrumen

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 ch

Are you looking for a fantastic career at Essential Utilities? We have an outstanding opportunity for a Chemist I based in the Bryn Mawr, PA area! Are you a future leader that wants to take your career to the next level? Let's talk!.

Are you looking for a fantastic career at Essential Utilities? We have an outstanding opportunity for a Chemist I based in the Bryn Mawr, PA area! Are you a future leader that wants to take your career to the next level? Let's talk!.

Bachelor's degree in Chemistry, Science, or a related field required;.

Degree (BS or BA) in Biology, Chemistry, Biochemistry, or relevant related field. Job Description Job Description Summary: 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 R

Job Description Job Description Description: 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. Required Education, Certifications, and Licenses: * B

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 lea