be responsible for the end-to-end data science pipeline – from data exploration to deploying models in a production environment. In a small team setting, you’ll grow versatile skills, collaborate closely with team members, enjoy flexibility, and have a direct impact on the business.
The role will involve exploring diverse datasets, developing innovative data products to tackle complex business goals, and crafting compelling narratives for different audiences. As a key player in our data science team, you’ll have the chance to deliver exciting projects, drive ongoing development of best practices, and help pioneer the team’s success. Your Day-to-Day: Collect, process, and organize data
from various sources in collaboration with Data Engineers. Conduct exploratory data analysis and use statistical and machine learning techniques to identify trends, patterns, and relationships in the data.
Develop, implement, and deploy predictive models and algorithms using a variety of machine learning techniques. Collaborate with cross-functional teams, including product managers, engineers, and marketing professionals, to translate data insights into actionable business insights. Stay up to date with the latest developments in data science and machine learning and apply these techniques to solve business problems. This role does not require travel. Requires sitting or standing at
will while performing work on a computer (or any other physical requirements).
What You Bring to The Team: Bachelor’s or master’s degree in a relevant field such as computer science, mathematics, statistics, or a related field or equivalent work experience. 3-4 years’ experience in Python, SQL/HQL, and Py Spark, with Databricks and MLFlow experience desired. Strong experience with machine learning concepts and techniques, and the ability to apply these techniques to real-world problems. Excellent communication and collaboration skills, and the ability to work effectively with people from different departments and levels of the organization, technical and non-technical.
What We Offer: · A great Team and culture – please see our Recruitment Video. · An exciting career as an integral part of a world-leading software company providing solutions for architecture, engineering, and construction. · Competitive Salary and benefits. · The opportunity to work within a global and diversely international team. · A supportive and collaborative environment. · Colleague Recognition Awards. #LI-Remote About Bentley Systems: Bentley Systems (Nasdaq: BSY) is the infrastructure engineering software company. We provide innovative software to advance the world’s infrastructure – sustaining both the global economy and environment.
Our industry-leading software solutions are used by professionals, and organizations of every size, for the design, construction, and operations of roads and bridges, rail and transit, water and wastewater, public works and utilities, buildings and campuses, mining, and industrial facilities. Our offerings, powered by the i Twin Platform for infrastructure digital twins, include Micro Station and Bentley Open applications for modeling and simulation, Seequent’s software for geoprofessionals, and Bentley Infrastructure Cloud encompassing Project Wise for project delivery, SYNCHRO for construction management, and Asset Wise for asset operations.
Bentley Systems’ 5,000 colleagues generate annual revenues of more than $1 billion in 194 countries. Equal Opportunity Employer: Bentley is an equal opportunity employer and considers all qualified applicants for employment without regard to race, color, interaction, interactionual orientation, gender identity, disability, protected veteran status, religion, national origin, age, or any other protected characteristic. This commitment extends to all aspects of employment, including, but not limited to, hiring, placement, promotion, compensation, and training.
EEO is the Law and EEO is the Law Supplement documents provide additional information about your rights as an applicant under the law. Bentley Policy on EEO, Affirmative Action and Pay Transparency Non-Discrimination Bentley participates in e-Verify / Bentley participate in e-Verify / Right to Work Notice Request an Accommodation: As an Equal Opportunity Employer, Bentley is committed to providing reasonable accommodations to applicants with disabilities. We encourage you to request a reasonable accommodation if you are not able to fully use or access our online application system.
You can make an accommodation request by calling 610-458-xyz X or sending us an email at xyz X@
thing of the past. We're the medical Companies of Johnson & Johnson, and you can count on us to keep working tirelessly to make that future a reality for patients everywhere, by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart.
We focus on areas of medicine where we can make the biggest difference: Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Arterial Hypertension. Visit us: At Janssen, we are dedicated to creating a future where disease is eradicated. As a Principal Scientist, you will own the development and implementation of sophisticated mathematical models and computational
tools to optimize bio therapeutics processes and cell culture media. You will supervise a team of modelers and data scientists, providing mentorship and expertise to drive innovative solutions.
Collaborating with multi-functional teams, including bioprocess engineers, analytical scientists, and statisticians, you will integrate modeling strategies into the overall bio therapeutics process development framework. Your expertise in mathematical modeling, statistical analysis, and data-driven approaches will improve process understanding and efficiency. Staying up-to-date with industry trends and new technologies, you will ensure the application of cutting-edge methods in bio therapeutics
process development. In this role, you will design experiments, analyze experimental data, and provide actionable insights.
You will effectively communicate your findings and recommendations to both technical and non-technical collaborators through presentations and reports. Additionally, you will drive innovation and continuous improvement in modeling methodologies to improve the robustness of bio therapeutics processes. Education: a Ph. D. in Simulation, Data Science and Analytics OR Chemical Engineering, Mechanical Engineering, Industrial Engineering, Mathematics, Statistics, or a similar field with a minimum of 6 years experience OR a Masters degree with a minimum of 12 years experience is required Experience and Skills: Required: Strong leadership skills demonstrated by successful management of a team of modelers and data scientists is required In-depth knowledge of bioprocessing, cell culture, protein purification, and related subject areas within the biomedical industry is required Proficiency in programming languages such as Python, R, or MATLAB, and experience with relevant software tools for modeling and simulation is required Excellent communication and teamwork skills, with the ability to work effectively in a multidisciplinary team is required Demonstrated expertise in applying data science and analytics principles in industrial applications, verifying performance and manufacturability, and driving form/fit/function is required Good written and oral communication skills are required Preferred: Familiarity with and hands-on experience with CMC process development is preferred Experience with regulatory filings is preferred Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers.
count on us to keep working tirelessly to make that future a reality for patients everywhere, by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart. We focus on areas of medicine where we can make the biggest difference: Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Arterial Hypertension.
Visit us: The Principal Scientist in the Large Molecule (LM) Drug Product Development and Delivery (DPD&D) team will work as a Scientific Integrator for late development biologic programs with a specific focus on the exciting area of cell therapy! Key Responsibilities: DPD&D scientific
integrator for late development asset(s) leading the development team to deliver on the overall program strategy. Build the program strategy in collaboration with the broader CMC Team (analytical, drug substance, regulatory, quality, supply chain, etc.
). Enables scientists to cultivate new scientific insights; and provide development opportunities working under indirect supervision with a high level of autonomy. Identifies and analyzes high-impact, complex and cross-departmental scientific/technical issues and gaps. Improves, changes or develops new business/work processes to share knowledge, build intellectual capital, build strategic technical capabilities and promote innovation
throughout the organization. Identifies novel scenarios and solicits acceptance of new insights, approaches, concepts through scientific leadership and acts as an internal expert with a direct impact on JRD/JSC scientific and/or business objectives.
May serve as the liaison between team members and senior leadership. Education: A minimum of a Bachelors degree with at least 10 years of relevant experience is required. Ph D or Pharm D is preferred Experience and Skills: Required: Significant expertise in Biomedical Dosage Forms, Drug Delivery systems and the overall drug development process through demonstrated experience and positive track record in multiple R&D or Commercial is required Parenteral drug product development and technology transfer experience is required Demonstrated matrix team leadership experience with a proven track record of directly leading sophisticated team(s) is required Ability to cultivate team efficiency and cohesiveness and to work collaboratively to implement, deliver and get results through the team is required Familiarity with Gx P compliance is required Familiarity with ICH regulatory guidelines is required Preferred: Experience in late-stage cell therapy development and fling is preferred IND/IMPD, BLA/MAA, and s BLA/Type II variation review/approval experience for biologics is preferred Education in shop, medical Sciences, Chemical Engineering or equivalent is preferred Demonstration of strong people leadership in past roles cultivating successful teams is preferred Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers.
to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at and follow n Research & Development, LLC is part of the Janssen medical Companies.
The candidate for this position will lead and perform activities related to equipment and system integrations for process development within the API-Protein group in Malvern, PA. The candidate's primary responsibilities will include leading and participating in system deployments, enabling instrument data flow, and optimizing digital pathways. This will include supporting monitoring
systems, bench instrument integration, laboratory/pilot-scale scale bioreactor and chromatography equipment and enabling overall data strategies to improve the efficiency of our business.
Key Responsibilities: Lead the design, deployment, and life cycle management of systems within the department and across departments, buildings, and sites as needed for various types of equipment, instruments, and data flows! Work closely with suppliers, IT partners, and business partners to ensure systems meet the intended function and business processes. Review status, data integrity, and accuracy of systems; report changes and updates to impacted teams, provide technical documents, and collaborate
closely with business partners creating data strategies to efficiently deliver our portfolio.
Work in a team environment as well as a contributing individually to meet project timeline and objectives. Required Qualifications: A Ph D in Biological/Data Sciences or equivalent field with at least 3 years of relevant post-doctoral experience in a medical environment; or a MS in Biological/Data Science or equivalent major with at least 8 years of relevant experience in a medical environment; or a BS in Biological/Data Sciences or equivalent major with at least 12 years of relevant experience in a medical environment. Knowledge and hands-on laboratory experience with upstream and downstream processes, instrumentation, PLCs, facility monitoring, or equivalent experience.
Coordinating with infrastructure IT, Business IT, and Lab IT colleagues for distributed system deployments, administration, and life cycle management. Sponsoring and coordinating on-site contract integrator colleagues supporting business needs/objectives. Experienced in maintaining written records in the form of (electronic) logbooks, protocols, scripts, and technical reports in both Gx P and non-Gx P environments. Highly organized and capable of managing/pursuing multiple projects independently with strong written and verbal communication skills.
Experienced in data reporting, team-based collaborations, and providing updates to management. Availability to work intermittently evenings and weekends. Preferred Qualifications: Automation networks, application licensing, and instrument data integration. Bioreactor systems including S88 process workflows and parameters, control strategies, associated parts, and data connection mechanisms. Chromatography purification systems including workflows and parameters and data connection mechanisms. Computerized SDLC. Integration of devices, PLCs, SCADAs, thick client deployments and connection to systems such as data historians.
Familiar with integration applications, data communication (i. e. - OPC), and digital sensor connections. Electronic chart recorders, alarm notification systems, and bench instrument integration. Electronic notebook workflow configuration and documentation. Experienced in running biochemical analytical methods. Overview knowledge of SQL databases. Overview knowledge of normal, emergency, and uninterrupted electric supply and panel drawings. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at and follow n Research & Development, LLC is part of the Janssen medical Companies.
This Senior Associate Scientist position in Biologics Drug Product Development & Delivery will be a lab-based role, responsible for experimental studies in pre-formulation, formulation, and analytical development of therapeutic proteins including monoclonal antibodies (m Abs), bispecifics, and fusion proteins. The candidate will work independently and with appropriate teams to support project needs
and meet project deliverables. This includes execution of studies to support formulation development and biophysical characterization across the portfolio.
Required Qualifications: B. S. in an appropriate scientific discipline with at least 6 years of related laboratory experience OR an M. S. with at least 3 years laboratory experience is required Demonstrated experience with therapeutic proteins and/or biologic products Demonstrated knowledge of GLP and GMP requirements Experience with characterization of biological molecules and development of analytical methodologies for characterization of drug product attributes. Expertise in biochemical, biophysical and/or analytical methodologies
such as HPLC, spectroscopy (e. g. UV, IR, Raman), light scattering (e.
g. SLS, DLS), particle analyzers (e. g. MFI, HIAC), and separation methods (e. g. CEX, c IEF, HIC) + Collect, analyze, document and interpret data as appropriate. Communicate data and data trends within the team and with functional leadership. Preferred Qualifications: • Ability to design and execute studies related to protein formulation and stability. Use scientific literature to understand protein behavior and/or support development challenges Author technical reports and make presentations of technical data Ability to identify protein liabilities and correlate protein behavior to data.
Capable of onboarding new techniques related to separations and/or particle characterization. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers.
past. We're the medical Companies of Johnson & Johnson, and you can count on us to keep working tirelessly to make that future a reality for patients everywhere, by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart.
We focus on areas of medicine where we can make the biggest difference: Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Arterial Hypertension. Visit us: Within the Laboratory Automation & Robotics team, you will leverage scientific and robotic systems expertise to drive the design, development, and implementation of laboratory automation workcell solutions for
various analytical workflow such as antigen binding, molecular, cell-based, flow cytometry, capillary electrophoresis, chromatography, and peptide mapping. You will collaborate with the Assay Automation team, Engineering, Assay Development, Data Science, IT, and end-users to drive our hands-free automation implementation.
You will play an integral role in improving sample throughput/capacity, while reducing hands-on time, time-to-result, repetitive strain, and assay variability. Key Responsibilities: Drive the design, development, and implementation of hands free end-to-end analytical workcell solutions (Driven by Biosero Orchestrator/Green Button Go®) Collaborate with Assay Automation,
Engineering, and Methods Development to influence and align on system components and workflow orchestration Collaborate with Laboratory Operations, Data Science, and IT to drive automated data flow within workcell solutions Optimize automated systems, expand capabilities, and support technical investigations Drive automated process/methods qualification, and operator training activities Collaborate with automation team members to support or maintain automated systems as needed Knowledge transfer and cross-training Ensure data integrity through accurate and timely data capture/entry into appropriate systems Author protocols, work instructions, SOPs, or presentations Education: A Ph.
D. M. S. or Bachelors of Science in Biology, Biological Sciences, Biochemistry, Computer Science, Engineering, or equivalent is required Experience and Skills: Required: A Ph. D. with 6 years experience, or a Masters/Bachelors of Science with 10 or more years of integrated automation experience is required Experience leading development and implementation of automated laboratory workflows and high-throughput methods within the biotechnology or medical industry; this includes systems configuration, liquid handling, and method programming is required Experience designing, programming, operating, and troubleshooting end-to-end integrated automation systems, such as Biosero, High Res® Biosolutions, or Thermo Scientific™ is required Experience with device and data systems integration is required Ability to identify/understand sophisticated customer needs and help craft automated solutions for laboratory workflows Experience leading evaluation and implementation of new and novel technologies is required Experience leading evaluation and implementation of new and novel technologies is required Experience with biological or biochemical assays; migration of bench techniques to hands-free automated systems is required Strong organizational and interpersonal skills (both written and oral), with the ability to closely collaborate with scientists, vendors, and external teams is required Experience working with multidisciplinary teams is required Preferred: Experience with various programming languages, such as Python, Visual Basic, C, C , etc.
is preferred Experience with analytical method development is preferred Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers.
and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, cardiovascular and metabolism, and pulmonary hypertension.
Please visit http: // for more information. The Senior Scientist, Gene Therapy within the Large Molecule Drug Product Development team will be a lab-based role, responsible for experimental studies in pre-formulation, formulation, characterization and analytical development of gene therapies
and other viral vector modalities for early, mid, and late-stage new molecular entity (NMEs). This includes development and optimization of the technical operations associated with gene therapy manufacturing, diluent compatibility/administration relevant studies, as well as execution of characterization plans and stability campaigns.
In addition, biophysical/analytical method development and data interpretation to analyze different biologics modalities is required. Key Responsibilities: Development and optimization of manufacturing process Design and execute studies relating to manufacturing process development, and overseeing the execution of development, small scale to GMP grade manufacturing
processes. Execution of characterization plans and stability studies with the goal of developing a better understanding of stabilization mechanisms.
Lead or participate in cross-functional teams at project-related meetings, lead or facilitate technical discussions, and successfully resolve problems with supplies, methods, project issues, and deviations. Perform technical analysis of the project data, including trending of data. Author technical reports and regulatory filling. Present data to peers and functional management. Collaborate with functional line management as well as scientists in related functional areas such as Research and Development, QC/QA, Clinical, Manufacturing, Toxicology, and Regulatory (CMC).
Perform duties consistent with good laboratory practices. Required: Ph. D. with 2-5 years' experience, Master's degree with 5-8 years of experience, or Bachelor's degree with more than 8 years' experience in an appropriate scientific discipline (Chemical or Biomedical Engineering, or related Engineering fields) is required. Experience with viral vector production/characterization. Ability to interpret and analyze data from biophysical assays and design appropriate experiments. Must have excellent strong written and verbal communication skills.
Preferred: Experience in gene therapy or viral modality manufacturing process. Experience implementing and maintaining high quality standards for all aspects of work conducted including adherence to regulatory GLP/GMP, departmental, and safety guidelines. Experience mentoring others in a matrix environment. Other: This role can be based in Malvern, PA or Spring House, PA and may require up to 10% of travel. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers.
and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care-and your career. CHOP's Commitment to Diversity, Equity, and Inclusion CHOP is committed to building an inclusive culture where employees feel a sense of belonging, connection, and community within their workplace.
We are a team dedicated to fostering an environment that allows for all to be their authentic selves. We are focused on attracting, cultivating, and retaining diverse talent who can help us deliver on our mission to be a world leader in the advancement of healthcare for children. We strongly encourage all candidates of diverse backgrounds and lived
experiences to apply. A Brief Overview To perform and report various laboratory tests prescribed by physicians. Has advanced experience and/or laboratory training that give this candidate the ability (advanced tech skill inventory) to perform this service in multiple or highly specialized sections of the laboratory as assigned.
Provides assistance to the Director and Supervisor for procedure development, product evaluation, quality monitors, review of technical/regulatory manuals and other technical duties. What you will do Accurately performs routine to highly complex diagnostic tests or procedures as assigned in multiple laboratory sections (advanced tech skill inventory) and reports
results through appropriate channels. Completes, evaluates and records all appropriate quality controls and quality assurance markers.
Activates troubleshooting procedures when necessary. Trains others to perform this responsibility when assigned. Assists others (as appropriate based on skill level) by demonstrating expertise of advance experience and or training (tech skill inventory) as necessary for laboratory operation and provides IMPACT feedback to the Supervisor. Maintains an awareness of laboratory science, products and procedures and makes recommendations for improvements to the Director or Supervisor. Assists with procedure development, product evaluations, quality monitors and regulatory compliance as assigned Performs preventative/safety maintenance on equipment and maintains a safe, clean and efficient work environment.
Takes initiative in problem solving equipment failures to the extent capable. Communicates unresolved issues to supervisor or designee. Complies with personal protective equipment (PPE) and other laboratory and hospital safety standards 100% of the time. Notifies supervisor of unsafe events. Responsibly controls and maintains inventory. Trains others to perform this responsibility when assigned. Provides professional, courteous and calm customer service to both internal and external customers.
Identifies appropriate resources and sources for re-directed inquiries. Acts as a reference source for laboratory procedures within their skill inventory as necessary. Takes charge of any unusual or problem situations and reports issue to Supervisor or Director. Regularly reviews operational procedure manuals, individual competency backssment, quality assurance monitors for completeness, accuracy and regulatory compliance. Assists the Supervisor with recommendations for content, accuracy and improvements. Actively identifies and pursues technical learning needs.
Actively participates in laboratory section continuing education/quality assurance meetings by providing instructional support and presentations. Successfully completes 12 units of approved continuing education activities during evaluation cycle. Education Qualifications Bachelor's Degree Required Bachelor's Degree Medical Technology, Medical Laboratory Science, or other science related fields Preferred Experience Qualifications At least three (3) years experience Required Skills and Abilities Exhibits the ability to work with computer programs and computer controlled equipment.
Exhibits the ability to handle and interpret data, multitask, and maintains confidential material. Exhibits good laboratory technique and safety practices. Exhibits good communication, technical and organizational skills. Experience and/or training in multiple laboratory sections and high complexity testing (advanced tech skill inventory). Exhibits the ability interpret scientific literature & regulatory compliance and apply to laboratory policy & procedure improvement or development. must demonstrate advanced technical skills inventory at a baseline level or higher.
Licenses and Certifications Medical Technologist (MT) - American Society for Clinical Pathology (ASCP) - upon hire - Preferred or Medical Laboratory Scientist (MLS) - American Society for Clinical Pathology (ASCP) - upon hire - Preferred To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must be fully vaccinated against COVID-19 and receive an annual influenza vaccine. Learn more. Employees may request exemptions for valid religious and medical reasons.
Start dates may be delayed until candidates are immunized or exemption requests are reviewed. EEO / VEVRAA Federal Contractor Tobacco Statement
