senior scientist

Tremco Commercial Sealants & Waterproofing

<div>
 
 
 Tremco Construction Products Group
 
 (CPG), part of RPM International Inc., unites industry-leading building envelope solutions manufacturers, service providers and trusted brands&mdash;including Tremco, Nudura, Dryvit, Willseal, Weatherproofing Technologies, Inc. and Weatherproofing Technologies Canada&mdash;to deliver comprehensive, integrated building systems. With operations spanning North America, Europe, Asia-Pacific, India and Latin America, Tremco CPG has a global presence supported by regional businesses and distributors who understand local market needs for commercial, industrial and residential construction and restoration projects.
 
 
 
 
 
 
 GENERAL PURPOSE OF THE JOB: Tremco is
 
 seeking an applicant with a demonstrated knowledge of coating formulating across multiple chemistries, with a focus on reactive, one component systems and butyl technologies, and would be responsible for all efforts regarding new developmental projects and operational and supply chain support regarding them. The incumbent in the role will advance projects effectively once given guidance from senior leadership and communicate project updates to assist in tactical decision making regarding the area of their expertise. They will demonstrate competency regarding adaptability, resourcefulness, collaboration, and accountability to drive projects to completion when working individually or within a group dynamic.
 
 
 
 
 
 
 ESSENTIAL DUTIES AND RESPONSIBILITIES:
 
 
 <ul>
 <li>
 Lead and supervise research projects that deliver business results
 </li>
 <li>
 Lead multiple project activities through a defined product development process
 </li>
 <li>
 Oversee the design of experiments to evaluate and optimize the performance attributes of these technologies
 </li>
 <li>
 Understand process capability, design selection criteria, and/or structure-property relationships for developed products
 </li>
 <li>
 Assure and validate proper documentation of responsible technical and experimental activities
 </li>
 <li>
 Present work and subject matter cross-functionally to facilitate discussion of project management
 </li>
 <li>
 Explores conceptual ideas to prove or disprove concepts
 </li>
 <li>
 Ability to travel up to 25%
 </li>
 </ul>
 
 
 
 
 
 EDUCATION REQUIREMENT:
 
 Bachelor's degree in chemistry or chemical engineering or higher.
 
 
 
 
 
 
 EXPERIENCE REQUIREMENT:
 
 
 <ul>
 <li>
 4+ Years' experience reactive chemistry with deep knowledge in polymer synthesis.
 </li>
 <li>
 Polymer knowledge in polyurethane, acrylics, STPU and STPE, and other hybrid systems
 </li>
 <li>
 Knowledge of solvent-based coatings and sealants (commercial deck coatings and roof systems)
 </li>
 </ul>
 
 
 
 
 
 PHYSICAL DEMANDS:
 
 Incumbent must be able to stand, walk, sit, use hands, reach, climb, balance, kneel, talk, hear, taste, smell, and lift up to 50 lbs.
 
 
 
 
 
 
 BENEFITS AND COMPENSATION:
 
 
 
 The salary range for applicants in this position generally ranges between $90K and $100K and is negotiable depending on experience plus incentive compensation. This range is an estimate, based on potential employee qualifications, operations, needs, and other considerations permitted by law.
 
 
 
 
 
 The Company offers a variety of benefits to its employees, including but not limited to health insurance, paid holidays, paid time off, 401(k) Savings and Trust &amp; Plan with company match, Company Pension Plan, Performance Based Bonus/Commission, and continuing education.
 
 
 
 
 
 
 
 All qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.
 
 
 
</div>

Senior Scientist

Q-CTRL

About the team Q-CTRL's Quantum Sensing Research team performs basic and applied research in quantum sensing and quantum-enabled navigation. It is a highly dynamic team comprising approximately 30 specialists in theoretical and experimental atomic physics, cold-atom interferometry, navigation modelling, and modern Bayesian estimation and signal processing techniques. The Quantum Sensing Research and Quantum Sensing Engineering teams work closely together, translating novel quantum sensing research into a useful capability and product. We are focussed on pushing the boundary of what is possible in quantum sensing and ensuring our R&D has real-world impact. About the role We are seeking a new Senior Scientist to help improve the calibration, noise measurement, signal extraction, and validation procedures of Q-CTRL's quantum inertial sensors for the use in GPS-denied or contested environments. You will work closely with experts in quantum sensing to deliver novel navigation capabilities that solve pressing challenges in maritime and aeronautical positioning and navigation. A key focus of the role will be developing and implementing methods for the extraction of useful real world outputs and performance metrics of our sensors while in the field, as well as the calibration and noise characterisation of these sensors. You will be operating in the crossover of ultra precise next generation quantum sensors and classical inertial navigation systems, pushing these to their limit to extract signals of value from real world systems. The test and validation procedures, performance metrics and signal processing algorithms you develop will inform the continued improvement of our quantum sensors and their deployment for a given navigation end-user or application. What you'll be doing: <ul> <li>Perform essential research and development into novel quantum control solutions and sensor fusion algorithms to enhance the performance of real world quantum sensors (including atom interferometers and magnetometers).</li> <li>Analyse sensor performance in realistic environments, and measure, characterise and calibrate noise metrics for performance enhancement.</li> <li>Work closely with our quantum control engineers, experimental physicists, and sensor hardware specialists to deploy your developed test and validation procedures on real quantum sensor hardware.</li> <li>Collaborate with your colleagues in the Quantum Sensing (Inertial) Team, the Quantum Sensing Division, and the company more broadly.</li> <li>Share your insights into sensor test, characterization, calibration and validation with the broader Quantum Sensing Division, company, external stakeholders and customers through verbal presentations and written outlets (e.g., academic publications, technical reports, blog posts).</li> <li>Other duties within the Employee's skills and experience, or with reasonable training.</li> </ul> Ideally you'll have: <ul> <li>A PhD in Physics, Engineering or a closely related discipline.</li> <li>Experience in the theory, calibration, optimisation, testing and validation of inertial sensors and inertial navigation systems.</li> <li>Experience with atom interferometry, Cold and/or ultracold atomic systems, Quantum sensing in warm atomic vapours, Pulse-level optimisation and quantum control techniques.</li> <li>Experience developing error budget, noise characterisation and sensor metrology.</li> <li>Demonstrated ability to account for real world effects of sensor misalignment using coordinate systems transformations, scale factor and transfer function inversion and co-location limitations.</li> <li>Finally, you will have a strong desire to work with a world leading team and a company that is fundamentally building the future of the quantum technology industry.</li> </ul> It would be fantastic if you have these skills but not essential: <ul> <li>Expertise with Python and Rust programming language for scientific computing.</li> <li>Experience designing, operating and testing inertial navigation system hardware and working closely with both theoretical and experimental teams.</li> <li>Demonstrated experience in improving sensor performance through careful calibration and noise/error measurements.</li> </ul> About Q-CTRL Q-CTRL is the global leader in AI powered quantum control infrastructure software. We build the tools that make quantum technology useful, solving the hardest challenges in quantum computing and quantum sensing to deliver real world impact. Founded in 2017, we operate globally with offices in Sydney, Los Angeles, San Francisco, Berlin, and Oxford. Our teams bring together technical and multi disciplinary expertise across the product lifecycle, and we're hiring talent to help scale every part of the business. We work quickly to turn cutting edge science into deployable technology. In 2024 we raised US$113 million in Series B funding, the largest aggregate investment for a quantum software company. Six months later we delivered the first commercial quantum advantage with Ironstone Opal, our field validated quantum navigation solution for defense and industry. At Q-CTRL, we prioritize outcomes over hours. We offer flexibility, equity potential, and competitive benefits that reflect our high performance culture. If you're ready to help shape the future of quantum, we'd love to hear from you! To recruitment agencies, we do not accept unsolicited branded profiles and are not responsible for any fees related to unsolicited resumes.

Senior Scientist, Inertial

<div><div>What you&rsquo;ll need to succeed as Senior Scientist, Data Science at XPO</div><div>
Minimum qualifications:</div><ul><li>
Bachelor&rsquo;s degree or equivalent related work or military experience</li><li>
2 years of hands-on experience in delivering solutions in at least two of the following: data science, data analysis, geospatial, finance, econometrics, cloud computing, big data and database management</li><li>
Experience with statistical modeling, data analytics and visualization using R and Python (Numpy, Pandas, Scipy, Plotly and Matplotlib)</li><li>
Significant experience applying one or more analytical methods: regression (preferably mixed models), data classification and reduction (cluster, factor, principle components, decision trees), Bayesian inference or other advanced machine learning techniques</li><li>
Deep understanding of statistical modeling, machine learning, deep learning or data mining concepts, and a track record of solving problems with these methods</li><li>
Technical database knowledge (Oracle, NoSQL, data modeling) and experience optimizing SQL queries on large data</li><li>
Ability to write SQL fluently, recognize and correct inefficient or error-prone SQL, and perform test-driven validation of SQL queries and their results</li><li>
Proficiency in Microsoft Office and Windows applications</li><li>
Availability to work periodic 24/7 on-call support as required by the team&rsquo;s rotation schedule</li></ul><div>
Preferred qualifications:</div><ul><li>
Master's degree in Computer Science, MIS, Engineering, Business or a related field</li><li>
Data science specialization from Coursera, Udacity, Data Camp, etc.</li><li>
5 years of experience in data science, or data analysis with a focus on advanced analytics, statistical modeling, machine learning, and AI</li><li>
5 years of hands-on experience in delivering solutions in at least two of the following: data science, data analysis, geospatial, finance, econometrics, cloud computing, big data and database management</li><li>
Ability to quickly learn and achieve proficiency in new software applications</li></ul><div></div><div> 
About the Senior Scientist, Data Science job</div><div>
Pay, benefits and more:</div><ul><li>
Competitive compensation package</li><li>
Full health insurance benefits available on day one</li><li>
Life and disability insurance</li><li>
Earn up to 15 days of PTO over your first year
</li><li>9 paid company holidays</li><li>
401(k) option with company match</li><li>
Education assistance</li><li>
Opportunity to participate in a company incentive plan</li></ul><div></div><div> 
What you&rsquo;ll do on a typical day:</div><ul><li>
Conceive and develop end-to-end solutions focused on data science and engineering, using machine learning and deep learning algorithms, statistical concepts, data modeling, software development, cloud computing and visualizations</li><li>
Resolve technical issues in existing processes and current development work; solicit assistance from other roles and groups, and drive resolution to ensure the integrity of platform quality and project timelines</li><li>
Understand and improve shared standard patterns, templates and artifacts for data science platform architecture, data science development approaches, data models, new technology adoption and rollout</li><li>
Collaborate with IT and business teams to identify and document use cases, performance and capability requirements, and criteria for successful solution delivery</li><li>
Mentor other team members on technical skills, methodologies, problem solving approaches and standard patterns used at XPO</li><li>
Generalize and share technical approaches among other developers, and simplify and communicate completed work to broader audiences across the company</li><li>
Help support data consumers to ensure they have reliable access to trusted data</li></ul> 
About XPO
XPO is a top ten global provider of transportation services, with a highly integrated network of people, technology and physical assets. At XPO, we look for employees who like a challenge and can communicate effectively in all situations. We want to leverage your skills and years of experience to drive positive results while ensuring a bright future for yourself and XPO. If you&rsquo;re looking for a growth opportunity, join us at XPO. 
We are proud to be an Equal Opportunity employer. Qualified applicants will receive consideration for employment without regard to race, sex, disability, veteran or other protected status. 
All applicants who receive a conditional offer of employment may be required to take and pass a pre-employment drug test. 
The above statements are not an exhaustive list of all required responsibilities, duties and skills for this job classification.</div>

Senior Scientist, Data Science - Hybrid

Castle Biosciences, Inc.

<div>Castle Biosciences Earns &quot;Top Workplaces USA Award&quot; for Phoenix, Pittsburgh, and Friendswood!
You won't find a work culture and benefits package like ours every day. Come join our team and a group of colleagues who love working at Castle!
Learn more at www.CastleBiosciences.com
Castle Biosciences Inc. is growing, and we are looking to hire a full-time R&amp;D, Senior Scientist working from our Friendswood, TX office location, with a start date of February 1, 2026.
Why Castle Biosciences?
Exceptional Benefits Package:<ul><li>
Excellent Annual Salary + 20% Bonus Potential</li><li>
20 Accrued PTO Days Annually + 10 Paid Holidays</li><li>
401K with 100% Company Match up to 6%</li><li>
3 Health Care Plan Options + Company HSA Contribution</li><li>
Company Stock Grant Upon Hire</li></ul>
A DAY IN THE LIFE OF A Senior Scientist
The Senior Scientist will work with R&amp;D colleagues to develop evidence to support launched products in dermatology, while also collaborating across Castle Biosciences to produce key scientific materials such as publications, abstracts, slide decks, and other literature for internal training and external education. This role will spend the most time on data analysis, data presentation, collaboration with Marketing, Sales, and Medical Affairs, as well as publication planning, writing, and editing.
REQUIREMENTS<ul><li>
PhD level training in life sciences</li><li>
Experience related to Atopic Dermatitis preferred</li><li>
The ability to successfully communicate and teach in a complex and competitive environment.</li><li>
Strong interpersonal, organizational, and communication skills, written and oral.</li><li>
Demonstrated team player.</li></ul>
SCHEDULE<ul><li>
Monday &ndash; Friday, in-office 5 days a week from 9:00 am to 5:30 pm, exempt position, working from the Friendswood, TX office.</li><li>
Off-hour work will be required to facilitate communication and meet deadlines.</li></ul>
READY TO JOIN OUR BIOTECH TEAM?
We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon!
Castle Biosciences Awards and Research Developments!
WORK AUTHORIZATION
All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas.
ABOUT CASTLE BIOSCIENCES INC.
At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes.
Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.
Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.
If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail ReasonableAccommodationsRequest@castlebiosciences.com.
This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
** No third-party recruiters, please</div>

R&D, Senior Scientist (FWD)

Merck

<div>Job Description
Our Company&rsquo;s Research Laboratories located in South San Francisco is currently seeking an in vivo Senior Scientist to join our Lab Animal Resources group. The Senior Scientist, under the guidance of Laboratory Animal Veterinarians, will provide comprehensive study support and world class animal care to impact drug development and discovery and improve human health. Comprehensive study support encompasses conducting all aspects of a study including meeting with investigators, ordering animals, compound formulation and administration, sampling, tissue collection, body scores or weights, coordinating the use of imaging modalities, sampling processing, shipping and receiving compounds or samples, as well as some routine veterinary and animal colony management tasks. The ideal candidate should be team oriented, value workplace collaboration and can work with minimal to no supervision.
NOTE: This role will require some weekend and holiday study support and clinical care.
Key Responsibilities:<ul><li>
Contribute to execution of in vivo studies in rodents including animal ordering, compound administration, dosing (all routes with emphasis on intravenous), surgical procedures, clinical observations, sampling, and tissue collection</li><li>
Manage study timelines and maintain accurate, timely, and well-organized records of animal treatments, study data, procedures, inventories, research protocols, and reports</li><li>
Carry out research and medical treatment regimens for research animals under the guidance of the Veterinarian including weekends and holidays</li><li>
Work independently and be proactive in seeking opportunities, while also contributing positively to team dynamics</li><li>
Support activities and in the areas of inspection readiness, safety initiatives, cost containment, efficiency, productivity, energy conservation, waste minimization, operational excellence, and lean practices</li><li>
Learn new procedures to support additional in vivo studies and vivarium operations as needed</li></ul>
Qualifications:
Education:<ul><li>
Bachelor&rsquo;s (with 7 years) or Master&rsquo;s (with 4 years) in Biology, Animal Science, or related in vivo field and relevant experience
</li></ul>Required Experience and Skills:<ul><li>
Demonstrated in vivo research experience including handling, dosing and sample collection</li><li>
Expertise with anesthesia and surgical procedures (e.g., osmotic pump implantation, orthotopic oncology models, telemetry)</li></ul>
Preferred Experience and Skills:<ul><li>
ALAT, AAALAS certification</li><li>
Expertise with PK studies, cardiovascular, renal, and/or metabolic models</li><li>
Expertise with rodent echocardiography</li></ul>
#EligibleforERP
Required Skills:
Animal Care, Animal Handling, Animal Science, Animal Welfare, Blood Specimen Collection, Dosing, In Vivo Studies, Laboratory Animal Sciences, Surgical Procedures
Preferred Skills: 
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another&rsquo;s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as &ldquo;remote&rdquo;.
The salary range for this role is
$128,800.00 - $202,700.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee&rsquo;s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles&rsquo; Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully 
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
Domestic/International
VISA Sponsorship:
Yes
Travel Requirements:
No Travel Required
Flexible Work Arrangements:
Not Applicable
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
N/A
Job Posting End Date:
11/20/2025<ul><li>A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. 
</li></ul> 
Requisition ID:R371215</div>

Senior Scientist, In Vivo Research

Mars

<div>
 
 Job Description:
 
 
 
 The position is responsible for the development and deployment of new product recipes for canine and feline dry, wet and care &amp; treat products within NA. The position is accountable to for maintenance and continuous improvement as well as partnering in innovation for all NA production sites. This position will work strategically and co-functionally to provide formulation and technical support for existing products, lead the formulation activities associated with new product development and raw material development while maintaining quality design and delivering desired product performance to both the consumer and pet. The position will also work to explore and implement efficiency, cost savings and business continuity initiatives. The position will work closely with cross-functional partners with other R&amp;D functions, Supply, Finance and Commercial to enable the successful delivery of the business OGSM. The role operates in a pet friendly, open office environment supporting pet nutrition.
 
 
 
 What are we looking for?
 
 
 
 
 Minimum Requirements
 
 
 
 <ul>
 <li>
 Bachelor's degree in Biological/Agricultural Engineering, Food Science Technology, Animal Science/Nutrition or equivalent
 </li>
 <li>
 3+ years&rsquo; experience in recipe formulation in a research and development and/or a technical role in the field of raw materials or finished product CPG
 </li>
 <li>
 Experience in Formulation Optimization software
 </li>
 <li>
 Travel up to 10%
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 Advanced degree in Biological/Agricultural Engineering, Food Science Technology, Animal Science/Nutrition or equivalent
 
 
 </li>
 </ul>
 
 What will be your key responsibilities?
 
 
 
 <ul>
 <li>
 Engage in Innovation, Renovation, and Business Continuity projects by developing recipes that meet product &amp; performance targets and attributes
 </li>
 <li>
 Finalize and execute recipes and raw materials in the factory consistent with business processes and company standards
 </li>
 <li>
 Run quarterly recipe optimization cycles and report on quality and cost
 </li>
 <li>
 Provide input for finished product testing plans to drive the efficient use of available budget
 </li>
 <li>
 Responsible for engaging in efficiency activities as part of productivity and cost reduction efforts to meet NA business targets
 </li>
 <li>
 Understand supplier capabilities to deliver against our specification targets and drive continuous
 
 
 </li>
 </ul>
 improvement programs at the site level
 
 
 <ul>
 <li>
 Deliver agreed Value Leadership projects and initiatives.
 </li>
 <li>
 Partner to solution crisis events that impact raw materials and recipes at our NA sites
 </li>
 <li>
 Demonstrate a quality culture in actions, words and spirit
 
 
 </li>
 </ul>
 Decisions:
 
 
 <ul>
 <li>
 Apply nutrition updates and maintain product integrity as reflected in the recipe software
 </li>
 <li>
 Drive timely response to Sentinel findings and to changes in the nutrient matrix stemming from variability
 
 
 </li>
 </ul>
 in Raw Material nutrient values that affect product cost and compliance
 
 
 <ul>
 <li>
 Provide input on test plans and acceptance criteria for new raw material vendors
 
 
 </li>
 </ul>
 Recommendations
 
 
 <ul>
 <li>
 Product renovation, cost and quality improvement programs
 </li>
 <li>
 Formulation representation for Concessions and Risk Assessments
 
 
 </li>
 </ul>
 
 What can you expect from Mars?
 
 
 
 <ul>
 <li>
 Work with diverse and talented Associates, all guided by the Five Principles.
 </li>
 <li>
 Join a purpose driven company, where we&rsquo;re striving to build the world we want tomorrow, today.
 </li>
 <li>
 Best-in-class learning and development support from day one, including access to our in-house Mars University.
 </li>
 <li>
 An industry competitive salary and benefits package, including company bonus.
 
 
 </li>
 </ul>
</div>

Senior Scientist, Formulation

<div>Job Description
We are seeking a strategic and technical team player with expertise in cell culture commercialization. The primary objective of the Biologics Drug Substance Commercialization (BDSC), Cell Culture Sciences department is to provide the technical leadership and laboratory capabilities in support of late-stage pipeline commercialization and post-market commercial manufacturing support. BDSC supports stage 1 &amp; 2 process validation deliverables (2011 FDA process validation guidance) including various pipeline commercialization activities, process characterization, control strategy development, technology transfer to internal and external manufacturing sites, manufacturing investigations, process validation, second generation process development and authoring of regulatory submissions.
Under the general scientific and administrative direction of the Director in Biologics Cell Culture Sciences group and working in conjunction with internal and external partners, this individual will support late stage and commercial large molecule biologics program activities. The individual will be responsible to support development activities, commercialization activities of late-stage pipeline and/ or post-market commercial manufacturing biologics. For commercial programs, activities include site-to-site process transfers, manufacturing investigations and trend evaluations, process enhancements, next generation process development and characterization, process validation, and regulatory submission authoring
In this role, the successful candidate will be responsible to<ul><li>
Coordinate project planning, resourcing, progress reporting, troubleshooting and people management.</li><li>
Responsible for process development, process characterization and regulatory filing activities to ensure a smooth and clear path to successful PPQs and BLAs for the company's pipeline.</li><li>
Ensures project results meet requirements regarding technical quality, reliability, schedule, and cost.</li><li>
Solves technical and non-technical problems throughout the life of the project, tries to resolve problems during the design and planning phases whenever possible.</li><li>
Provides timely and accurate information and status updates to project sponsors and management.</li><li>
Champion compliance and safety; promote a culture of diversity, inclusion, and equity.</li></ul>
Minimum Education Requirement and Experience:<ul><li>
Bachelor&rsquo;s degree in Chemical Engineering, Bioengineering, Biological Engineering, or a related field with six (6) years of relevant industry experience</li></ul>
OR<ul><li>
Master&rsquo;s degree in Chemical Engineering, Bioengineering, Biological Engineering, or a related field with four (4) years of of relevant industry experience</li></ul>
OR<ul><li>
Ph.D. in Chemical Engineering, Bioengineering, Biological Engineering, or a related field with a no minimum relevant knowledge</li></ul>
Required Experience and Skills:<ul><li>
Strong fundamental knowledge in mammalian cell culture processing of biologics (large molecule products), recent advances, and challenges in the field</li><li>
Expertise in planning, execution, analysis, and documentation of all stages of cell culture process commercialization.</li><li>
Experience with late-stage commercial process development (CPD), technology transfer (TT), scale-down model qualification (SDMQ) and process characterization (PC).</li><li>
Experience authoring technical documentation in support of the following: process characterization (PC), process performance qualification (PPQ), risk assessment (RA), control strategy, process comparability reports, and/or regulatory submissions (BLA/MAA/JNDA etc.).</li><li>
Adaptability and agility to prioritize and deliver complex objectives, often on tight timelines, in a rapidly changing environment.</li><li>
Experience and aptitude to work and collaborate in internal and external cross-functional, matrixed teams.</li><li>
Action-oriented, mindset for creativity; ability to take initiative, innovate, iterate, and problem-solve.</li><li>
Excellent interpersonal and communication skills</li></ul>
Preferred Experience and Skills:<ul><li>
Experience in CMC development teams.</li><li>
Experience with cell culture process development for biologics.</li><li>
Experience with high throughput microbioreactor systems, and advanced in situ analytics for process monitoring and control</li><li>
Experience with state-of-the-art cell culture processes including intensified inoculum/fed-batch and perfusion process development.</li><li>
Background in data science approaches related to cell culture and predictive modeling e.g., (metabolic flux (MFA) analysis, omics, machine learning; experience integrating PAT efforts)</li><li>
Experience with on-the-floor Good Manufacturing Practice (GMP) manufacturing support, familiarity with manufacturing batch record reviews and/or operations.</li><li>
Experience with mathematical modeling, theoretical scaling calculations, drug substance comparability, scale down establishment, computational fluid dynamics (CFD) modeling, Quality by Design (QbD) and Lean Six Sigma principles.</li><li>
Experience supporting/writing regulatory filings (IND, MAA, BLA) and inspections with multiple agencies (FDA, EMA, JNDA, TGA).</li><li>
Demonstrated commitment and experience to coach and mentor staff to maximize talent development and utilization.</li></ul>
Required Skills:
Biological Engineering, Bioreactors, Cell Cultures, cGMP Regulations, Chemical Engineering, Chromatographic Techniques, Computational Fluid Dynamics (CFD), Design of Experiments (DOE), Flux Analysis, GMP Compliance, Mammalian Cell Culture, Process Design, Process Optimization, Process Scale Up, Process Verification, Production Process Development, Small Molecule Synthesis, Technical Writing Documentation, Technology Transfer
Preferred Skills: 
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another&rsquo;s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as &ldquo;remote&rdquo;.
The salary range for this role is
$114,700.00 - $180,500.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee&rsquo;s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles&rsquo; Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully 
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
Domestic
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Not Applicable
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
11/26/2025<ul><li>A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. 
</li></ul> 
Requisition ID:R374276</div>

Senior Scientist, Engineering

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