Senior principal scientist jobs in Levittown, PA - 338 jobs
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Senior Scientist, Analytical Research & Development
Veranova
Senior principal scientist job in West Deptford, NJ
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 commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals 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.
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.
Role Overview:
The Sr. Scientist is responsible for the implementation, development, and validation of analytical test methods in support of process research, and cGMP production with emphasis on development of LC, GC, GC-MS and LC/MS, ELISA, SEC-MALS, CE-SDS, cIEF, etc) methods for small molecules, ADCs, Oligonucleotides and Peptides Major support functions include sample analysis by various analytical techniques including HPLC, GC, LC-MS/MS, GC-MS, ICP-MS, CE, SEC-MALS, CE-SDS, cIEF, NMR, KF, titrations, and instrumental and wet chemical techniques. Other duties may involve analytical method modification, development, and validation. The incumbent may function as the primary contact on one or more development projects. In- depth involvement with the project team concerning the chemistry of the project and analytical chemistry needs is expected
Core Responsibilities:
Develop and validate new analytical procedures. Independently, detects and solves complex problems of high technical difficulty.
Perform sample analysis using various analytical techniques (e.g., LC, GC, LC-MS, GC-MS, ICP-MS, ELISA, SEC-MALS, CE-SDS, cIEF, etc.), interpret results, and prepare high-quality documentation such as protocols, analytical reports, and summary reports.
Document all analyses per SOPs.
Prepare SOPs, test methods, and other GMP documentation.
Independently, detect and solve complex problems of high technical difficulty.
Apply knowledge and expertise from multiple disciplines (including QA, QC, Analytical and production) to achieve project goals.
Conduct investigations independently.
Troubleshoot analyses and instruments.
Support qualification of reference materials.
Develop new analytical procedures.
Validate analytical methods.
Prepare and review scientific reports.
Interface with internal and external clients.
Qualifications:
PhD in Analytical Chemistry or equivalent
Minimum of 8 years' experience in a GMP environment.
Minimum of 5 years' experience in method development and validation for small molecules Active Pharmaceutical Ingredients (APIs). Experience with Process Development of APIs.
Experience with LC, GC, GC-MS, LC-MS, IC, spectroscopy, and wet chemistry.
Experience mentoring staff members in an analytical department.
Formal project management training.
Experience with writing method validation protocols and reports desirable.
Experience with Microsoft Office and other complex computer software (UPLC, Empower 3) desirable.
Salary Range : $115,000 - $125,000 annual base salary
Our Commitment:
Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs.
Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.
Inclusive Culture: At Veranova, 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. Even if you don't meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.
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 .
$115k-125k yearly 3d ago
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Senior Scientist - Health Economic Resources
Tandym Group
Senior principal scientist job in Plainsboro, NJ
A recognized company in New Jersey is actively seeking a new SeniorScientist to join their growing Health Economics Resources initiatives. In this role, the SeniorScientist will be responsible for supporting the design, execution, and communication of observational studies using diverse RWD sources.
Responsibilities:
Support implementation of strategies to demonstrate the unmet need in disease with focus on outcomes meaningful to payers, clinical decision-makers, and regulators
Assist with research to generate evidence necessary to demonstrate product differentiation and value for commercial/market access needs support clinical development, regulatory and safety needs (real-world evidence and epidemiology studies)
Partner with CORE asset leads in development and execution of RWE studies delivered through hands-on analytics execution
Evaluate new and emerging data modalities (e.g., claims, EHR, social determinants of health, genomics, biomarkers, clinical notes) and conduct feasibility assessments to match study objectives with optimal RWD sources (claims, EHR, registries, patient-generated data)
Execute studies by managing table shells, analytic data file, analysis plan, programming, statistical methods, and quality control per regulatory and scientific standards
Conduct quality assurance and code validation, review programming code and data
Draft analysis reports and support the final publication/presentation of results
Perform other duties, as needed
Qualifications:
3+ years of experience in Real-World Evidence Generation and Epidemiology Analytics
Graduate (PhD or Masters) degree in Epidemiology, Biostatistics, Public Health, or related field
Working knowledge of the structure and caveats of Healthcare Claims Databases, Electronic Medical Records and/or Hospital Billing Data, Cancer Registry Data (SEER), Linked Dataset, etc.
Knowledge in Epidemiologic and Statistical concepts, such as confounding, bias, cumulative incidence, incidence rate, regression models, survival analyses.
Knowledge of Research Design and an ability to apply appropriate Statistical Methods common in outcomes research & epidemiology (survival analysis/modeling, regression analysis, IPTW, MAIC, causal inference, etc)
Hands-on proficiency in Statistical Programming (SAS, R, Python) on Real-World Oncology Claims / EHR Data & AI/ML frameworks
Solid problem solving and time management skills
Great interpersonal skills
Excellent communication skills (written and verbal)
Strong attention to detail
Highly organized
Able to multitask efficiently and effectively
Desired Skills:
Oncology experience
$94k-133k yearly est. 4d ago
Formulation Scientist
Net2Source (N2S
Senior principal scientist job in Skillman, NJ
Job Title: Formulation Scientist - Skin Health
Duration: 10-Month Contract
Work Hours: Monday - Friday, 8:30 AM - 5:00 PM
Locations: Skillman, NJ 08558 (4 days/week) / Summit, NJ 07901(1 day/week; may fluctuate based on business needs)
Experience Required:
2 to 4 years of formulation experience (mandatory)
Education:
Bachelor's Degree (BA/BS) required
Key Responsibilities:
Develop and optimize new product formulations and manufacturing processes.
Perform laboratory testing, evaluations, and multiple formulation iterations (batching).
Conduct stability studies to ensure technical accuracy and product performance.
Maintain accurate and detailed documentation throughout the product development lifecycle.
Collaborate effectively with cross-functional teams.
Manage timelines efficiently while maintaining attention to detail.
Apply strong analytical and problem-solving skills.
Communicate findings, progress, and challenges clearly and professionally.
Required Skills & Qualifications:
Strong formulation experience (required)
Background in Consumer Products, preferably Skin Health
Excellent time management and organizational skills
High attention to detail
Strong analytical and communication skills
Ability to work collaboratively in a team environment
$77k-113k yearly est. 1d ago
Scientist/Sr. Scientist - Repository
Coriell Institute for Medical Research 3.5
Senior principal scientist job in Camden, NJ
Coriell Institute for Medical Research is currently seeking an experienced Scientist (SeniorScientist depending on experience) to join the biobanking team.
The ideal candidate for this role is a PhD in genetics, cellular or molecular biology, biochemistry, or related field with postdoctoral experience and 2+ years of experience in project and resource management. We are interested in meeting candidates with proven ability to effectively collaborate with scientists and other department leads to oversee biobanking operations and biospecimen and associated data management pipelines. S/he will work to cultivate long-term relationships with project managers, internal and external stakeholders, and ensure effective and regular communications. This role also offers opportunities to publish and present to the wider scientific community. Potential candidates must be team players with excellent organizational, written and verbal communications skills.
Reporting to the Chief Biobanking Officer, the incumbent for this role will ensure that Coriell meets or surpasses biobanking standards for quality service and deliverables. Biobanking operational efforts include overseeing the growth of the biobanking collections via recruitment, submitter and biospecimen submission management; overseeing biospecimen processing, quality control and storage; overseeing biospecimen distribution; all under Coriell's quality management framework. Day to day responsibilities include but are not limited to:
Supporting delivering grant and contract requirements
Supporting internal and external reporting requirements
Supporting efficient, productive daily biobanking operations
Managing relationships with internal and external stakeholders
Supporting the Project Management team in ensuring deliverables are met in a timely manner
Serving as a technical expert providing scientific advice and leadership as needed
Developing and maintaining outreach efforts to submitters and end users of the biobank
Overseeing the submission of specimens to the biobank in accordance with the OHRP regulations, following guidelines established by Program Directors and Scientific Advisory Committees
Reviewing data (demographic, clinical, genomic) at the time of sample submissions to determine appropriateness and completeness
Contributing compelling, innovative ideas for continued strategic growth for the biobank
Representing and promoting Coriell and the biobanking collections at scientific meetings
Participating in Coriell strategic initiatives and task forces
Contributing to external funding opportunity applications
Adhering to internal standards, policies and procedures
Performing other duties as assigned.
Strong management skills, excellent communication, and the ability to work alongside senior management and contribute to the growth of the institution are vital for this role. If you are interested in applying for this opportunity, please email a cover letter and resume to *******************. Please include a detailed description of your relevant experience in your cover letter. Applicants are encouraged to highlight their background with non-profit, medical, healthcare, academic, and/or scientific research organization(s).
This role starts at $85,000/Year, but will be commensurate with relevant experience.
Coriell & Recruitment
Now in its 73rd year, Coriell Institute for Medical Research is an independent non-profit research center dedicated to the study of the human genome. Expert staff and pioneering programs in the fields of molecular and cellular biology, genetics, genomics and epigenomics, and biobanking drive our mission. To learn more, visit ****************
Any offer of employment extended by Coriell is contingent on an applicant's ability to be Authorized to Work in the United States of America. Upon date of hire, all employees are required to provide whichever valid Employment Authorization Documents they wish, as long as it is in compliance with Federal Regulations.
This /posting is to provide general guidance on the nature of work that will be performed in this position. It is not represented to be a full or exhaustive list of the duties, responsibilities, or qualifications needed for this role. Due to the nature of our work, the duties, responsibilities, and qualifications listed on this job description/posting are subject to change.
$85k yearly 1d ago
Scientist 2, Research & Development
Pyramid Consulting, Inc. 4.1
Senior principal scientist job in Skillman, NJ
Immediate need for a talented Scientist 2, Research & Development. This is a 10 months contract opportunity with long-term potential and is located in Skillman, NJ (Hybrid). Please review the job description below and contact me ASAP if you are interested.
Job ID: 26-00524
Pay Range: $35 - $43/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
Key Responsibilities:
Hours: 8:30am to 5:00pm (Monday through Friday).
86 Morris Avenue Summit, NJ 1 day per week.
May fluctuate based on needs.
A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations.
Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation.
Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline.
Key Requirements and Technology Experience:
Key skills; Consumer Products - Skin Health
BA Degree 2 to 4 years' experience
Our client is a leading Pharmaceutical Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.
$35-43 hourly 1d ago
Polymer Scientist
Insight Global
Senior principal scientist job in Raritan, NJ
*This will be a 12-month contract with potential extensions
*5 days on site in Raritan
Required Skills & Experience
•BS degree in polymer science, chemistry, material science, or related science is required
•A minimum one (1) year related working experience is required if BS or MS degree
•Previous experience in polymer characterization including thermal analysis (DSC, DMA, TGA), rheology, and x-ray diffraction testing (XRD) is required (at least 2/3 skills)
•Must be able to work independently and effectively collaborate and communicate with other team members
Nice to Have Skills & Experience
-Experience in a GLP/GMP environment
-Experience with medical devices
-Experience with test method development
Job Description
A large life sciences/medical device client of ours is looking for a Polymer Science to join their team for a 12+ month contract. They will focus on polymer characterization, including rheology, thermal analysis (DSC, DMA, TGA), and x-ray diffraction (XRD), in support of new product development and life-cycle management. The associate will work closely with an appointed scientist to execute test methods, analyze and report results, and develop new procedures as needed. Key responsibilities include and maintaining instruments, preparing samples, ensuring timely testing and data reporting, maintaining accurate documentation and calibration records, and adhering to GMP/GLP practices. Additional tasks may involve microscopy, wet chemistry, and training other personnel.
$77k-112k yearly est. 3d ago
Formulation Scientist
Ztek Consulting 4.3
Senior principal scientist job in Raritan, NJ
Role: Formulation Scientist, on-site in Raritan, NJ- Full-time
Experience Required: 8 - 20 + Years
Must Have Technical/Functional Skills
• Product formulation and launch experience.
• Biomaterials and material development.
• Medical device and combination product design and development; PMA familiarity.
• Problem-solving using Analytical tools.
• Design of Experiments (DOE) and applied statistics.
• Protocol development, reporting, and documentation.
• In-vitro/ex-vivo characterization of prototypes.
• Biochemical test method development and validation.
• Strong communication and collaboration across teams.
• Ability to work in ambiguous environments and deliver outcomes.
• Experience with self-directed teams and multitasking.
• Effective prioritization and decision-making.
• Travel up to 20% may be required (domestic and international)
$65k-94k yearly est. 2d ago
Product Development Scientist Formulation
Source One Technical Solutions 4.3
Senior principal scientist job in Skillman, NJ
Source One is a consulting services company and we're currently looking for the following individual to work as a consultant with our direct client, a global pharmaceutical manufacturing client in Summit, NJ .
No Third-Party, No Corp to Corp, No Sponsorship Now or Future
Title: Product Development Scientist - Formulation
Location: Skillman NJ
Hybrid Work Locations; Skillman, NJ 4 days/week then in Summit, NJ 1 day per week. Hours: 8:30am to 5:00pm (Monday through Friday). May fluctuate based on needs.
Contract Duration: 10 months, with likely extension
Pay Rate: $43.28 per hour (w2)
*PLEASE NOTE: Apply only if you have FORMULATION Experience this is required
Job Description:
Consumer Products - Skin Health
A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations.
Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation. Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline.
FORMULATION Experience is required
BA Degree 2 to 4 years' experience
$43.3 hourly 1d ago
Associate Principal Scientist, Data Science - Princeton, NJ
Dsm-Firmenich
Senior principal scientist job in Princeton, NJ
Associate PrincipalScientist, Data Science
We are seeking a highly skilled data scientist specialized in Formulation Performance Modeling and Formulation Creation across a portfolio of Innovation projects, as well as ensuring the team is deploying the latest, state-of-the-art technologies and skills to develop, manage and govern various products in food, perfumery and beauty. The candidate would join dsm-firmenich's Data Science team within Science and Research and with focus on Data Science model development and on the translational task between Data Science and Business Units key users and stakeholders.
This role offers the opportunity to drive interdisciplinary science projects that integrate the latest advances in cheminformatics, data science, AI and while working in close collaboration with leading domain perfumery and flavour experts.
Your Key Responsibilities:
Use data science and AI to drive a fast-paced ingredient discovery pipeline that generates maximum value for dsm-firmenich's, perfumery and beauty, taste, texture and health segments.
Develop and implement ML and AI models for predicting and optimizing performance of formulations in diverse applications.
Contribute to formula creation and product development tools with Data Science models and data pipelines.
Translate scientific research findings into practical applications that can drive business growth. Identify opportunities for commercialization of research outcomes and collaborate with business units to realize these opportunities.
Contribute to the development and adoption of Data Science best practices and by our global community of data scientists, scientists and experts in perfumery and beaty, taste, texture and health segments.
Stay up to date on the latest advancements in cheminformatics, formulation design, computational biology, molecular AI and modeling approaches.
Apply modern software development and machine learning tools and practices in your daily work, including a high level of proficiency in Python, git, and team co-development workflows. Familiarity with good use of coding agents preferred.
Team-up with other data scientists and chemistry and physics science experts around the globe to drive project success.
We Bring:
Highly motivated, professional and committed multicultural and interdisciplinary team.
Opportunity to put your scientific skills into practice with innovations in health, nutrition and beauty.
Grow and develop your skills through our in-house training courses.
Being a part of company shaping a strong legacy heritage through industrial innovations and cutting-edge technology.
A commitment to science-based innovations with 2000 scientists and 700 mm annual S&R investments.
You Bring:
Ph.D., master's degree or similar experience in Physics, Chemistry, Engineering, Structural Biology, Computer Science, AI, or a related field.
3-7 years of additional academic or industry work experience in the chemical industry, bio- and cheminformatics or formulation space.
Record of accomplishments demonstrating high drive and keen entrepreneurial innovation.
Strong skills in computational chemistry, cheminformatics, statistics, structural biology, including hands-on development experience of modern AI tools.
Deep understanding of Data Science methods, formulation performance applications, generative AI technologies in chemistry and physics, science informed ML methods.
Proficiency Python, good code management, git, and working with CI/CD pipelines.
Excellent problem-solving skills and proven ability to work both independently and collaboratively.
Effective communication and collaboration skills with the ability to convey complex concepts to non-experts.
Entrepreneur mindset and ability to provide insights based on data analysis to inform business decisions.
The salary or hourly wage scale provided reflects the pay range dsm-firmenich expects to pay the successful candidate for the position. Individual pay offered will be based on the applicant's job-related skills, experience, relevant education, or training, and primary work location. This position is also eligible for bonuses and benefits, which are not included in the pay scale provided. Salary $128,000-$183,000.
About dsm-firmenich
At dsm-firmenich, we don't just meet expectations - we go beyond them.
From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.
And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future.
Because real progress only happens when we go beyond, together.
The application process
Interested in this position? Please apply online by uploading your resume in English by October 10, 2025.
Inclusion, belonging and equal opportunity statement
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.
We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve.
We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.
And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work.
Agency statement
We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role
$128k-183k yearly 60d+ ago
Scientist II
Artech Information System 4.8
Senior principal scientist job in Fort Washington, PA
LanceSoft is a nationally certified Minority Business Enterprise (MBE) that has established itself as a pioneer in providing highly scalable, cost-effective workforce solutions to a diverse set of customers across various industries in the United States. Headquartered in Virginia, LanceSoft currently operates out of several locations in the US and Canada.
Title: Scientist II
Location: Fort Washington, PA
Duration: 12 Months
Job Description:
II. Position Summary:
Provides testing, technical and troubleshooting support in the QC laboratories. These functions include:
Collection, processing, method development and testing of chemical components, bulk products, raw materials, packaging components, finished products, marketed product stability, in-process materials, scale up, validation and cleaning validations to conform with specifications and standard operating procedures (SOPs).
Thorough knowledge of SOPs, USP and other applicable pharmacopeia.
Possess foresight to recognize task needs and performs the trained task without the request of management.
Reviews and/or writes the following documents: APR, SOPs, QSRs, Instrument qualification, protocol/report writing, trending and review/analysis of data.
Performs statistical analysis in support of APRs, Stability, and Product Release.
Complies with cGMPs, safety training and regulations.
Performs more advance technical projects under the supervision of management.
Maintains an environment of respect and teamwork with all coworkers.
The Company's management reserves the right to add, delete or otherwise alter assigned duties at any time. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
III. Responsibilities
:
(Define key accountabilities and/or activities.) Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies' policies, procedures and guidelines, this position:
Ensure quality and compliance in all my actions by:
o Attend GMP training on the schedule designated for my role and as appropriate for my role
o Adhere to strict compliance with procedures applicable to my role.
o Exercise the highest level of integrity in the tasks that I perform
o In a timely and prompt manner, identify report and seek correction for deviations noted in my workplace.
o Embrace a behavior of employee involvement and commitment to doing the job right the first time
Systems Knowledge
• Be a Power User in the applicable systems and roles assigned.
• Trained to the role in which you are assigned as required for your job function in the applicable systems
• Utilize tools within MS office and other systems to improve business effectiveness
• Exposure to & working knowledge of electronic batch records and/or other automated processes/systems (labs)
• Working knowledge of SAP or ERP system; including other relevant systems per role
• Working knowledge of an automated system.
Product Knowledge
• Understanding of product family, product size and put-up, and product characteristics (color, viscosity) associated active and excipient. Critical parameter associated with all processing steps.
Training
• Can act as SME and be a curriculum owner.
• Partner with training department to create training materials including curricula.
• Can act as qualified trainer in specific areas.
• Participate in all trainings.
• Ensure all trainings are completed on-time.
Investigations
• Assists in gathering information and documentation as required.
• Participates in investigations as required.
Compliance - Safety, GMP, Facilities
• Provide support during regulatory inspections /audits as directed. Support may be in the form of scribes, runner, and document gathering.
• Attend GMP training on the schedule designated for the role and as appropriate for the role.
• May provide statistical analysis in support of the APR and Stability processes.
• Adhering to strict compliance with procedures according to the roles and responsibilities.
• Exercises the highest level of integrity in the tasks performed
• In a timely and prompt manner, identify report and seek correction for deviations noted in the workplace.
• Embrace a behavior of employee involvement and commitment to doing the job right the first time.
• Strong working GMP knowledge. Communicates and identifies GMP gaps.
• Can participate in all types of audits & Inspections.
• Leads areas in ensuring all operations (processes) are completed in a compliant and safe manner.
• Assists in coordination efforts in case of emergency- spill, fire etc.
• Takes necessary action to eliminate and immediately address safety hazards. Communicate any observed unsafe behaviors immediately.
• Understands the safety concerns and promotes a safety conscience culture for their job function.
• Wears the appropriate PPE when working in manufacturing and other hazardous working environments and advocates standards of safety.
• Contributes and attends all EHS programs as assigned.
• Promptly communicates deficiencies to management.
• Maintains facility and work area in good working condition.
• Works with team to ensure all aspects of business remain compliant.
Documentation Management
• Edits documentation (i.e. Standard Operating Procedures, work instructions) as necessary.
• Perform/assist in the completion and documentation of the process steps as per the documentation directives.
• Complete visual verification of the process and document these steps in the appropriate system.
• Document all activities per the GMP requirements.
Process Excellence, Lean, Continuous Improvement, ME2
• Completes PE/ Lean awareness training.
• Proactively identifies opportunities for continuous improvement and proposes actions to address these opportunities.
• Participates and leads continuous improvement implementations and kaizen events. Understands and applies PE tools in daily work activities.
Leadership
• Job expert that less experienced personnel can go to for assistance.
• Provides leadership in absence of supervisors (for short periods).
• Assist management through change and transformation activities.
• Facilitates departmental meetings and may assist in the coordination of other scheduled meetings. In absence of management, attends meetings on his/her behalf.
• Continuously demonstrates all GLP values; specifically: integrity and credo based actions, self awareness and adaptability, results and performance driven, organization and talent development, and collaboration and teaming. Demonstrated behaviors include: fairness, honesty, consistent and ethical behaviors, empathy and collaboration.
• Contributes and supports an environment that fosters diversity and inclusion.
• Exhibits and lives core values and behaviors.
• Contributes to a climate of open communication, engagement and ownership within team.
• Builds working relationships
• Provides feedback to site management
• Supports strategic and tactical plans in alignment with site's mission and plans.
IV. Requirements
:
Education: Bachelor's Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or related science is required
Experience:
Minimum 2 years of GMP/GLP quality control lab experience in a pharmaceutical and/or OTC and/or regulated environment is required.
Physical Demands: Capable of performing routine laboratory activities. Light to moderate lifting
Knowledge, Skills and Abilities: Basic knowledge/exposure of a LIMS system is preferred
Additional Information
Regards,
Anuj Mehta
************
$70k-102k yearly est. 3d ago
Machine Learning Scientist
Align Technology 4.9
Senior principal scientist job in Morrisville, PA
This position is ideal for an early-career machine learning scientist to join the AI & Machine Learning team as a Machine Learning Scientist, supporting photo-based diagnostics and remote treatment monitoring. Partnering with other machine learning specialists and product marketing, you'll provide technical solutions to complex problems in computer vision and 3D data analysis to support Align's product portfolio. This role is key to building out Align's core technology capabilities.
* Use data science and machine learning to solve complex, multidisciplinary challenges in applied research and turn technology know-how into execution in a dynamic business environment
* Develop algorithms and models in collaboration with business partners, product managers, and software engineers to solve key business initiatives
* Design and implement machine learning techniques to improve treatment planning, customer engagement, and device manufacturing based on historical data
* Collaborate effectively with other data science teams globally to ensure technology re-use and transfer of new capabilities to drive innovation
* Quickly learn and assimilate new business processes, ideas and concepts to formulate conclusions and deliver results.
* Identify features and data needed for machine learning solutions.
* Help to deliver a vision for our product evolution using machine learning
* Stay current on the emerging directions in AI-technologies and support the development of the AI/ML roadmap
* Stay current on specific AI-technologies and apply them in an appropriate manner to applicable projects
$64k-95k yearly est. Auto-Apply 26d ago
Scientist
Mindlance 4.6
Senior principal scientist job in Spring House, PA
Mindlance is a national recruiting company which partners with many of the leading employers in the Life Sciences, IT, and Financial Services sectors, feel free to check us out at ************************* Job Description The successful candidate will be responsible for performing multiple biochemical assays to screen compounds and profile lead candidates for pharmaceutical targets. Job requirements include ability to work with purified proteins, compound plate creation and tracking and perform biochemical assays. The successful candidate will work as part of an interactive research team; will report results of studies back to team members and in a timely, thorough, and coherent manner. Such a position requires an energetic, highly organized and motivated person.
Requirements include compound plate creation using dispensers such as ECHO, compound ordering and tracking, execution of biochemical assays using automated liquid handlers and spectroscopic readers and generation of electronic notebooks that document all performed work. Good communication skills as well as an aptitude to perform research activities in a collaborative and result-driven setting are a must.
Qualifications
The successful candidate will possess an M.S. with 1-3 years of experience or a B.S. /B.A. with 2-4 years of experience or the equivalent training/experience.
Additional Information
All your information will be kept confidential according to EEO guidelines.
$65k-93k yearly est. 3d ago
Scientist
Lancesoft 4.5
Senior principal scientist job in Raritan, NJ
Leads formulation design efforts from concept through to prototyping phases, Design Reviews and Validation. Collaborate with external suppliers and internal partners to develop products. Drive product characterization to ensure rigorous technical understanding and relationships to pre-clinical clinical outcomes.
Lead raw material suppliers through raw material iterations, correlating to product design window Drive execution of Learning Plans.
Participate in multi-functional discussions and design reviews, including product creation at multiple scales (modeling, lab, pilot and manufacturing).
Participate in clinical procedures and activities, translating learning into viable prototypes Generic Managerial Skills.
Strong communication skills.
Candidates must be highly proficient in reading, writing, and speaking English language.
Ability to multitask, including ability to understand customer requirements, retrieve relevant information, and provide responses satisfactorily and with immediacy is required.
Employee must be able to effectively prioritize and manage multiple activities and responsibilities.
Ability to understand and follow complex written procedures is required.
Ability to function in a team environment and deliver on team objectives is required.
Ability to make decisions and solve problems while exhibiting situational judgement.
$90k-121k yearly est. 14d ago
Formulation Scientist
Net2Source (N2S
Senior principal scientist job in Skillman, NJ
Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap - Right Talent - Right Time - Right Place - Right Price and acting as a Career Coach to our consultants.
Company: One of Our Clients
Job Description:
Job Title: Formulation Scientist
Location: Skillman, NJ 08558
Duration: 09+ Months (Extendable)
Pay Rate: $40.00 - 43.28 hourly. on W2 without benefits.
Description:
A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations. Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation. Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline.
FORMULATION Experience is required
Consumer Products - Skin Health
BA Degree 2 to 4 years' experience
Awards and Accolades:
America's Most Honored Businesses (Top 10%)
Awarded by USPAAC for the Fastest Growing Business in the US
12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020)
Fastest 50 by NJ Biz (2020, 2019, 2020)
INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list)
Top 100 by Dallas Business Journal (2020 and 2019)
Proven Supplier of the Year by Workforce Logiq (2020 and 2019)
2019 Spirit of Alliance Award by Agile1
2018 Best of the Best Platinum Award by Agile1
2018 TechServe Alliance Excellence Awards Winner
2017 Best of the Best Gold Award by Agile1(Act1 Group)
$40-43.3 hourly 5d ago
Associate Scientist (Biologic Discovery)
Insight Global
Senior principal scientist 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 2d ago
Postdoctoral Researcher
Coriell Institute for Medical Research 3.5
Senior principal scientist job in Camden, NJ
The Chen Lab at the Coriell Institute for Medical Research is seeking a highly motivated Postdoctoral Researcher (Fellow) to join an interdisciplinary research program focused on AI-assisted drug development targeting NRF2 for the treatment of esophageal cancer.
Position Requirements
PhD or equivalent degree in a biomedical research field
Strong research experience in cell and molecular biology, preferably in the cancer research area. Animal model experience is preferred but not required
Demonstrated ability to give scientific presentations and publish scientific papers
Demonstrated ability to work independently and collaboratively in a multidisciplinary research environment
Research Focus
The successful candidate will work on cutting-edge projects integrating experimental cancer biology with artificial intelligence-driven drug discovery, with a specific focus on NRF2 signaling pathways in esophageal cancer. The position offers opportunities to contribute to translational research with strong clinical relevance.
Salary and Benefits
Salary and benefits will follow NIH Postdoc guidelines, commensurate with experience
This role will be eligible to participate in Coriell's Health & Welfare benefits, receive an employer-paid Long-term disability plan and Basic Life Insurance Policy, and will be enrolled in a 401(a) plan that receives a 7% monthly employer contribution (Base Salary). The role receives an annual allotment of 20 days of PTO, 7 paid sick days, and up to 10+ paid holidays.
About the Chen Lab
The Chen Lab focuses on understanding molecular mechanisms driving esophageal cancer progression and therapeutic resistance, with an emphasis on translating basic discoveries into novel treatment strategies. The lab integrates cellular, molecular, animal, and computational approaches, fostering a collaborative and innovative research environment. Learn more here.
Coriell & Recruitment
Founded in 1953, Coriell is an independent non-profit biomedical research center that
conducts groundbreaking research to identify the genetic and epigenomic causes of
disease and accelerates scientific discovery by generating world-class biomaterials
through establishing and curating key biobanks that now contain some of the world's
most extensive collection of cell lines, DNA, and other biomaterials for use by the
international research community. To learn more, visit ****************
Any offer of employment extended by Coriell is contingent on an applicant's ability to be Authorized to Work in the United States of America. Upon date of hire, all employees are required to provide whichever valid Employment Authorization Documents they wish, as long as it is in compliance with Federal Regulations.
This /posting is to provide general guidance on the nature of work that will be performed in this position. It is not represented to be a full or exhaustive list of the duties, responsibilities, or qualifications needed for this role. Due to the nature of our work, the duties, responsibilities, and qualifications listed on this job description/posting are subject to change.
$45k-66k yearly est. 2d ago
Associate Principal Scientist, Data Science - Princeton, NJ
Dsm-Firmenich
Senior principal scientist job in Princeton, NJ
**Associate PrincipalScientist, Data Science** We are seeking a highly skilled data scientist specialized in Formulation Performance Modeling and Formulation Creation across a portfolio of Innovation projects, as well as ensuring the team is deploying the latest, state-of-the-art technologies and skills to develop, manage and govern various products in food, perfumery and beauty. The candidate would join dsm-firmenich's Data Science team within Science and Research and with focus on Data Science model development and on the translational task between Data Science and Business Units key users and stakeholders.
This role offers the opportunity to drive interdisciplinary science projects that integrate the latest advances in cheminformatics, data science, AI and while working in close collaboration with leading domain perfumery and flavour experts.
**Your Key Responsibilities:**
+ Use data science and AI to drive a fast-paced ingredient discovery pipeline that generates maximum value for dsm-firmenich's, perfumery and beauty, taste, texture and health segments.
+ Develop and implement ML and AI models for predicting and optimizing performance of formulations in diverse applications.
+ Contribute to formula creation and product development tools with Data Science models and data pipelines.
+ Translate scientific research findings into practical applications that can drive business growth. Identify opportunities for commercialization of research outcomes and collaborate with business units to realize these opportunities.
+ Contribute to the development and adoption of Data Science best practices and by our global community of data scientists, scientists and experts in perfumery and beaty, taste, texture and health segments.
+ Stay up to date on the latest advancements in cheminformatics, formulation design, computational biology, molecular AI and modeling approaches.
+ Apply modern software development and machine learning tools and practices in your daily work, including a high level of proficiency in Python, git, and team co-development workflows. Familiarity with good use of coding agents preferred.
+ Team-up with other data scientists and chemistry and physics science experts around the globe to drive project success.
**We Bring:**
+ Highly motivated, professional and committed multicultural and interdisciplinary team.
+ Opportunity to put your scientific skills into practice with innovations in health, nutrition and beauty.
+ Grow and develop your skills through our in-house training courses.
+ Being a part of company shaping a strong legacy heritage through industrial innovations and cutting-edge technology.
+ A commitment to science-based innovations with 2000 scientists and 700 mm annual S&R investments.
**You Bring:**
+ Ph.D., master's degree or similar experience in Physics, Chemistry, Engineering, Structural Biology, Computer Science, AI, or a related field.
+ 3-7 years of additional academic or industry work experience in the chemical industry, bio- and cheminformatics or formulation space.
+ Record of accomplishments demonstrating high drive and keen entrepreneurial innovation.
+ Strong skills in computational chemistry, cheminformatics, statistics, structural biology, including hands-on development experience of modern AI tools.
+ Deep understanding of Data Science methods, formulation performance applications, generative AI technologies in chemistry and physics, science informed ML methods.
+ Proficiency Python, good code management, git, and working with CI/CD pipelines.
+ Excellent problem-solving skills and proven ability to work both independently and collaboratively.
+ Effective communication and collaboration skills with the ability to convey complex concepts to non-experts.
+ Entrepreneur mindset and ability to provide insights based on data analysis to inform business decisions.
The salary or hourly wage scale provided reflects the pay range dsm-firmenich expects to pay the successful candidate for the position. Individual pay offered will be based on the applicant's job-related skills, experience, relevant education, or training, and primary work location. This position is also eligible for bonuses and benefits, which are not included in the pay scale provided. Salary $128,000-$183,000.
**About dsm-firmenich**
At dsm-firmenich, we don't just meet expectations - we go beyond them.
Join our global team powered by science, creativity, and a shared purpose: to bring progress to life.
From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.
And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future.
Because real progress only happens when we **go beyond, together** .
**The application process**
Interested in this position? Please apply online by uploading your resume in English by October 10, 2025.
**Inclusion, belonging and equal opportunity statement**
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.
We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve.
We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.
And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work.
**Agency statement**
We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role
$128k-183k yearly 60d+ ago
Scientist-IV
Artech Information System 4.8
Senior principal scientist job in Raritan, NJ
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 Technical Operations Contractor is responsible for technical aspects of the Lifecycle Management structure and strategy for parenteral drug products including SIMPONI pre-filled syringes, STELARA pre-filled syringes, and Risperdal Consta Injection.
The candidate will provide this technical support at U.S. based contract manufacturing sites such as Baxter Bloomington, IN and Alkermes, Wilmington, OH.
The candidate will support technology transfers, implementation of continuous process verification programs, investigations, change control initiatives, and continuous process improvement programs.
FUNCTIONAL KNOWLEDGE, SKILLS, AND ABILITIES:
• Strong expertise with regard to pharmaceutical products & manufacturing processes with a focus on parenteral products
• Good knowledge regulatory requirements and GMP's understands the technical aspect of the lifecycle strategy of products
• applies the science based risk approach and regulatory/GMP intelligence
• ability to create, maintain, and upgrade product technical knowledge and author documentation regarding these activities
• ability to monitor technical process and product performance across internal and external manufacturing sites and employ statistical methods to assess
• ability to participate in risk assessments with a quality and compliance perspective
PERSONAL & INTERPERSONAL SKILLS / LEADERSHIP SKILLS:
• Ability to participate on cross functional / cross-region project teams
• Ability to manage complexity and change
• Ability to interact at different levels of the organization (including Sr. Management)
• Ability to work under pressure and resolve conflicts
• Ability to work independently under general direction, having a good sense of prioritization of assigned
tasks and manage time accordingly
• Ability to participate in a result oriented project team
PERSONAL ATTITUDE & MINDSET:
• Can-do mentality, agility & flexibility able to work with stretched goals and deadlines
• Works with others towards the project team's goals
• Understands culture differences
• Communicates, motivates, negotiates and is an assertive person having impact
• Shows a high sense of responsibility regarding professional activities
Qualifications
DEGREE REQUIREMENT:
Minimum requirements: BS/BA with 3 to 5 years' experience in pharmaceutical development or pharmaceutical manufacturing or
related post graduate academic experience/education.
Additional Information
This is a time sensitive and critical position a quick response would be of great help.
Contact Information:
Sneha Shrivastava
Technical Recrutier
**************
$85k-124k yearly est. 3d ago
Associate Scientist - Cell Therapy API Development
Insight Global
Senior principal scientist job in Spring House, PA
Our large pharmaceutical client in Spring House, PA is seeking an Associate Scientist to join their growing Cell Therapy API Development organization and support blood sample management and testing activities. This individual will be completing apheresis formulation, cryopreservation of samples, managing and tracking sample inventory, maintaining and ensuring accuracy across databases as well as owning sample delivery and coordination across internal teams. Training is provided for this role and this team provides a lot of opportunity for growth! Other responsibilities include:
Completing formulation of apheresis material and working with multiple species' blood samples to support the pipeline portfolio and explore novel and innovative approaches to safety assessment in drug development.
Sample coordination which includes:
Managing request forms to determine material needed (new formulations or reserved material)
Forecasting, coordinating, and submitting samples of fresh apheresis material to other internal teams for requested testing
Keeping records of orders, COA, etc.
Executing cryopreservation for samples and storing material
Maintaining internal databases and ensuring correct sample information is updated and accurate which includes authoring eLNs of formulation and updating Sharepoint with inventory and DA analysis
Tracking and coordinating inventory which includes:
Getting quotations for new leukapheresis material from collection agencies based on forecasts
Placing orders through procurement group to ensure funds are used from appropriate projects for collections
Tracking and following up with vendors
Qualifications:
Bachelor's or Master's Degree in a related field of study
2+ years of relevant lab-based experience including cell cryopreservation
Previous experience with mammalian cell culture and aseptic techniques
Familiar with formulation of apheresis material
Salary: $75,000-$90,000 (flexible based on 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 annually & 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.
$75k-90k yearly 4d ago
Scientist-I
Artech Information System 4.8
Senior principal scientist job in Spring House, 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
List major responsibilities and duties of the position. List most complex or difficult parts of job first. Describe scope of responsibilities.
• Assist with activities as assigned by the the Clinical Scientist or Study Responsible Physician which support the monitoring and reporting of clinical trials .
• Member of the clinical Work Group (WG) for each study assigned.
• Assist with study-specific data review activities in support of database locks.
• Support monthly medical monitoring data review activities.
• Assist with tracking of safety events, review of new SAEs, and Narrative as appropriate.
• Assist/Coordinate activities in support of external data requests
• Other activities as determined by study team and phase of trial (ie start-up, execution or close out).
PRINCIPAL RELATIONSHIPS:
• Describe the primary working relationships (internal & external) and primary interfaces.
• Clinical Team: SRP/SRSs, Clinical Scientist, MRP, GI-Derm/Immunology VP
• Contacts Inside the Company: Integrated Data Services, Global Medical Safety, Global Clinical Operations, programming & biostatistics
• Contacts Outside the Company: vendor and CRO/ARO contacts as appropriate
• Internal J&J Use Only Revision Date: April 27, 2016
• Supervision: This position reports to Clinical Scientist/SRP
Qualifications
EDUCATION AND EXPERIENCE REQUIREMENTS:
• Describe the minimum knowledge, skill and ability requirements for the position. Include any degrees or certifications which are required and/or desirable.
• Bachelor's degree (or equivalent) required and 1-2 years relevant work experience preferred.
• Bachelor's degree in a scientific displine or nursing preferred. Candidates with additional degrees such as Masters (or equivalent) will also be considered but not required.
• Good organization skills, good written and verbal communication skills
• Excellent independent time management skills
• Proven ability to plan and track deliverables and timelines
• Individual must work well in a dynamic environment and be able to prioritize and respond to changing needs of the business.
• Proficient Microsoft Office applications and use of Internet, EXCEL, POWERPOINT, WORD
Additional Information
For more information, Please contact
Sneha Shrivastava
************
How much does a senior principal scientist earn in Levittown, PA?
The average senior principal scientist in Levittown, PA earns between $74,000 and $146,000 annually. This compares to the national average senior principal scientist range of $83,000 to $169,000.
Average senior principal scientist salary in Levittown, PA
$104,000
What are the biggest employers of Senior Principal Scientists in Levittown, PA?
The biggest employers of Senior Principal Scientists in Levittown, PA are: