2,584 Pharmaceutical Research jobs in the United States

About the job Pharmaceutical Data Scientist

Pharmaceutical Data Scientist needs basic industry-relevant scientific knowledge; should have at least a B.Sc in a scientific discipline related to the pharmaceutical industry (Biology, Chemistry, Pharmacology, Biochemistry, etc)

Pharmaceutical Data Scientist requires:

• Basic industry-relevant scientific knowledge; should have at least a B.Sc in a scientific discipline related to the pharmaceutical industry (Biology, Chemistry, Pharmacology, Biochemistry, etc)
• Ability to multitask efficiently, prioritize quickly, and manage time effectively
• Database and computer skills; talent for analyzing and visualizing complex data
• Advanced proficiency with Microsoft Excel

Pharmaceutical Data Scientist duties:

• Record and maintain relevant information detailing new scientific innovations into internal caseload management information systems
• Assist team members with basic legal requests (e.g. non-disclosure agreements, material transfer agreements, fee-for-service agreements)
• Utilize internal databases to provide clear reports and information, updated on a regular basis, to monitor activity, support innovation sourcing partnerships, progress against objectives and drive decisions on new scientific areas and strategies

**Pharmaceutical Development Scientist I**
**Position Summary:**
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
Catalent's Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacturing. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.
Catalent Pharma Solutions in Kansas City, MO is hiring a Pharmaceutical Development Scientist I. The Pharmaceutical Development Scientist I will serve as technical representative for formulation design and development of oral solid dosage forms. This individual will design and execute experiments and processes necessary for developing formulations of pharmaceuticals oral solid. The Scientist I will also lead clinical trial manufacturing endeavors and ensures that all work is carried out in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs).
**This is a full-time salaried position on-site: Monday - Friday, 7:30am-4:30pm.**
**Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.**
**The Role:**
+ Develop and execute laboratory work plans/schedules independently, using customer milestones and Division/site performance standards and metrics
+ Authors technical documents, such as protocols, batch records, test methods, technical reports, and operating procedures. Review technical documents for accuracy, thoroughness and regulatory compliance
+ Trains, coaches or mentors team members on technical development or business issues. May have limited responsibility to direct work of technical staff, including work assignments. Supervised customer interaction on team meetings
+ Utilize knowledge of high-shear granulation, fluid-bed technology, roller compaction, compression, encapsulation
+ Executes efficiency improvement project with moderate guidance. Identify and recommend business opportunities on a project specific basis
+ Has advanced knowledge of the principles, theories and concepts applicable to a limited range of work in pharmaceutics and knowledge of principles and concepts in other disciplines
+ Applies technical and functional knowledge to assist in experiment/project design that will enable department to meet goals
+ All other duties as assigned
**The Candidate:**
+ Candidate must have either a Bachelor's degree in related scientific field with six years of related work experience, OR a Master's of Science with four years related work experience, OR a Doctorate (PhD) in scientific field would be acceptable without any experience
+ Hands on experience in oral solid dosage form development and manufacturing preferred. Must show knowledge of techniques in design of experiments and statistics, and cGMP and Good Documentation Practices in accordance with applicable regulatory guidance and Site SOPs
+ Must have the ability to: learn and retain technical information, proactively address work issues at both an individual level and a team level, communicate proficiently with internal and external stakeholders
+ Must have experience developing and executing minimally complex procedures or methods with high quality and becoming familiar with drug development milestones and their context. Recognizes and elevates changes in project scope or execution for review by project manager and department director and able to prioritize and suggest alternatives or contingencies to achieve the correct technical solutions with most efficient resource utilization
+ Must be able to: propose deviations from established procedures and methods based upon sound judgment, assess training needs and formulate development plans for subordinates, recognize unmet customer needs.
+ Must be proficient with performing and interpreting physical testing; bulk/tap density, sieve analysis, flow analysis, solid fraction results and provide options based upon the data
+ Must have a work strategy focused on personal and team efficiency. Well organized with ability to multitask. Ability to work effectively under pressure to meet deadlines. May publish or present externally every 2-3 years
+ **Physical requirements:** stand, walk, sit, use hands to manipulate, and reach with hands and arms for up to 8 hours per day. Frequent sitting, standing, walking, reading of written documents and use of computer monitor screen. Able to work with respirator (P100, PAPR, etc.). Occasional lifting and/or moving up to 50 pounds.
**Why you should join Catalent:**
+ Defined career path and annual performance review and feedback process
+ Diverse, inclusive culture
+ Positive working environment focusing on continually improving processes to remain innovative
+ Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
+ 152 Hours + 8 paid holidays
+ Several Employee Resource Groups focusing on D&I
+ Dynamic, fast-paced work environment
+ Community engagement and green initiatives
+ Generous 401K match
+ Company match on donations to organizations
+ Medical, dental and vision benefits effective day one of employment
+ Tuition Reimbursement - Let us help you finish your degree or start a new degree!
+ WellHub program to promote overall physical wellness
+ Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories
**Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ( to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .

At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world's most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.
Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we're working at the pace of change on diagnostic tools that address the world's biggest health challenges, driven by knowing that behind every test there is a patient waiting.
Learn about the Danaher Business System ( which makes everything possible.
The Senior Clinical Research Scientist reporting to the Director, Clinical Research, develops and independently writes clinical documentation including clinical protocols, clinical study reports and clinical justifications in support of research and new product development, registration and commercialization of products.
This position is part of Clinical Affairs and will be an Onsite Role in Sunnyvale, CA. The senior clinical research scientist will work on advanced, complex projects requiring state of the art knowledge in oncology and/or infectious disease molecular diagnostics. This is an exciting opportunity to collaborate with other Cepheid scientists, external partners, Government Affairs, Medical and Scientific Affairs on developing the product evidence strategy plan (PESP).
In this role, you will have the opportunity to:
+ Manage strategies for obtaining clinical evidence using the product evidence strategy plan process (PESP)
+ Develop strategies for clinical trials and ensure that activities are conducted in compliance with current applicable regulations, laws and guidance including but not limited to US and EU and global regulation as well as with Cepheid's policies and procedures.
+ Establish scientific methods for design and implementation of clinical protocols and have oversight for clinical strategy, protocol development and clinical study reports for US and OUS registration studies
+ Prepares scientific content of clinical study reports and review clinical and analytical sections for regulatory submissions to ensure data meets all necessary regulatory standards.
+ Review pertinent literature, prepare white papers/manuscripts, and provide education to Cepheid staff as needed.
The essential requirements of the job include:
+ Bachelor's degree in Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology with 5+ years of related work experience OR Master's degree in Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology with 3+ years of related work experience OR Doctoral degree in Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology with related work experience.
+ Experience with in vitro diagnostic (IVD) products, preferably in molecular diagnostics or immunodiagnostics, in oncology and/ or infectious disease
+ Proficiency in Microsoft Office Suite
It would be a plus if you also possess previous experience in:
+ A Masters or PhD in Clinical Sciences, Health/Life Sciences, Molecular Biology, Biochemistry and/or Human Physiology
+ Strong scientific background with deep understanding of oncology/infectious disease and the molecular diagnostic area
+ Preferred experience in IVDD/IVDR or MDD/MDR regulations
Physical Demands:
+ Ability to travel up to 10% overnight, domestic and international
Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.
The salary range for this role is $111,100 - 152,800. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
The EEO posters are available here ( .
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation.
Operating Company: Cepheid

Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients. It’s our work, our passion, and our legacy. We invite you to join us.  

Hybrid

Employee Value Proposition:  

At Taiho Oncology, we are dedicated to transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging your expertise to drive innovative clinical research and contribute to groundbreaking therapies. We offer a collaborative and inclusive work environment where your ideas and contributions are valued. Join us to advance your career, work with passionate and skilled professionals, and make a meaningful impact on the fight against cancer. At Taiho Oncology, you will find purpose, growth, and the opportunity to be at the forefront of cancer research.

Position Summary:  

The Senior Manager, Clinical Research Scientist has responsibility assisting in design, execution and reporting of current and future clinical oncology trials ranging from phase 1 - 3. Additionally, this role position supports the responsible medical monitor in the execution of key tasks involved in the design, conduct, monitoring and review of study data, analysis and reporting of clinical trials.

Performance Objectives:

• Collaborates with other key team members (Medical monitor, Project Manager, Clinical Operations, Data Management, Biostatistics, PV, PK, Biomarkers and Medical Writing etc.), to deliver high quality clinical trial results.
• Use scientific expertise to support the creation of relevant high-quality clinical documents such as study protocols and clinical study reports (CSRs), investigator brochures, DSUR, NDA/MAA registration documents and publications.
• Reviews and summarizes ongoing clinical data (from EDC and listings) to monitor the quality of the study, ensure clean data flow into the study database and compliance with the protocol.
• Keeps the latest knowledge in clinical development through publications and scientific conferences and leverages the knowledge for designing and summarizing clinical studies.
• Keeps Sr. Medical Director current on status of clinical trials and provides ongoing risk assessments for the study conduct and operational risks.
• Performs other duties as required.

Education/Certification Requirements:  

• Masters level degree in pharmaceutical or related medical science is preferred.  Bachelor’s level candidates with substantive prior pharmaceutical experience will also be considered.  

Knowledge, Skills, and Abilities:

• 3-5 years of experience in clinical drug development in pharmaceutical industry.
• At least 2 years in drug development industry in oncology and with previous exposure to clinical development, such as reviewing of the quality of ongoing and final clinical study data, protocols and CSRs, investigator brochures, DSUR, NDA/MAA registration documents and publications.
• Ability to critically review and interpret Clinical data.

The pay range for this position at commencement of employment is expected to be between $165K - $195K annually. This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including annual bonus/incentive comp plans, potential long term incentive plan, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if a candidate/employee receives an offer of employment.  

If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. 

#Loca tion-Princeton,NJ #Location-Pleasanton,CA #LI-Hybrid

**Job Description**
Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Orthopedic Surgery-Res Adm
**Work Type:** Full Time (Total FTE between 0.9 and 1.0)
**Shift:** Shift 1
**Work Schedule:** 8 Hr (8:00:00 AM - 4:00:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page ( Range:** $27.47 - $38.81 per hour
Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush's anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
**Summary:**
This position is designs, initiates and performs complex scientific research experiments and prepares final reports and papers based on experimental results. Plans and directs experiments for research which includes the planning and execution of procedures for the collection, maintenance, culture and banking of research specimens. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
**Required Job Qualifications:**
- Master's Degree in basic sciences or relevant field.
- 3 years of research experience.
- Strong software skills and experience with word processing, spread sheets and data base management.
- Excellent communication and analytical skills.
- Good technical writing skills.
- Ability to prioritize and manage own work.
- Clear interest in collaborative, multidisciplinary teamwork.
- Highly-motivated, enthusiastic and detail-oriented.
- Ability to work independently.
**Preferred Job Qualifications:**
- Doctoral Degree.
**Responsibilities:**
- Responsible for the methods, management and organization of laboratory. Plans, directs and conducts research experiments and activities.
- Identifies research projects, experiments and potential research directions related to research activities; collects, evaluates, interprets and provides documentation of research data to accomplish research objectives. Maintains careful records of all work performed.
- Provides direction and training to other laboratory personnel, residents and students.
- Provides assistance with data collection and preparation of manuscripts, research papers, and/or grant proposals for presentation and/or publication.
- Maintains a safe laboratory environment and ensures compliance with governmental and University policies, procedures, rules and regulations.
- Operates and maintains laboratory and specialized scientific equipment in the lab space. Ensures that laboratory supplies are maintained on a consistent basis.
- Collaborates with statistician, research coordinators and staff from other departments.
- May be responsible for animal handling and for working with animal tissues.
- Other duties as assigned.
Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
**Position** Research Scientist
**Location** US:IL:Chicago
**Req ID** 20126

**Summary:**
Meta Platforms, Inc. (Meta), formerly known as Facebook Inc., builds technologies that help people connect, find communities, and grow businesses. When Facebook launched in 2004, it changed the way people connect. Apps and services like Messenger, Instagram, and WhatsApp further empowered billions around the world. Now, Meta is moving beyond 2D screens toward immersive experiences like augmented and virtual reality to help build the next evolution in social technology. To apply, click "Apply to Job" online on this web page.
**Required Skills:**
Research Scientist Responsibilities:
1. Perform research and develop solutions to computer software and computer hardware problems.
2. Research, design, and develop new optimization algorithms and techniques to improve the efficiency and performance of Meta's platforms.
3. Design and implement large-scale distributed software systems to serve large numbers of complex requests simultaneously and without failure.
4. Utilize technical research background, train new ranking models, and run experiments.
5. Create tools for migrating large bodies of user data across systems for new products, scalability efforts, and development of new core infrastructure.
6. Use machine learning, statistics, or other data techniques to build algorithms.
7. Suggest, collect, and synthesize system requirements from stakeholders and create effective feature roadmaps.
8. Analyze and resolve computer challenges from a system engineering standpoint.
9. Work on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
10. Demonstrate good judgment in selecting methods and techniques for obtaining solutions.
**Minimum Qualifications:**
Minimum Qualifications:
11. Requires Master's Degree (or foreign equivalent degree) in Computer Science, Engineering, Information Systems, Analytics, Statistics, Mathematics, Physics, Applied Sciences, or a related field and 5 years of experience in Job offered or related occupation
12. Requires 5 years of experience in the following:
13. 1. Algorithms, data structures, or systems software
14. 2. Solving analytical problems using quantitative approaches
15. 3. Gathering, manipulating, or analyzing complex, high-volume, high-dimensionality data from varying sources
16. 4. Communicating complex research in a clear, precise, and actionable manner
17. 5. Research in topics closely related to machine learning, NLP, recommendation systems, pattern recognition, signal processing, data mining, artificial intelligence, information retrieval, or computer vision
18. 6. Developing highly scalable classifiers and tools leveraging machine learning, statistics, regression, rules-based models, or mathematical models and
19. 7. Java, C++, Perl, PHP, or Python
**Public Compensation:**
$263,803/year to $290,180/year + bonus + equity + benefits
**Industry:** Internet
**Equal Opportunity:**
Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.
Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at

**Be visionary**
Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research?
We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins.
**Job Description**
We are seeking applicants for a Cheminformatics Research Scientist position that will be part of a Teledyne FLIR team responsible for in-depth research, discovery and problem-solving related to detection of Chemical, Biological, Radiation/Nuclear, and Explosive (CBRNE) threats for US Government and Commercial markets. Our products are based on "outside-the-lab" platforms, and include hand-held, wearable, emplaced, and UxV mounted sensors and detectors. Teledyne FLIR's sensors and detectors generate feature-rich data sets that lead to accurate detection and identification of threats. The research scientist is expected to understand the principles of our core technologies and conduct development and testing of cheminformatics and machine learning algorithms to improve accuracy and reliability of sensor and detector outputs.
**Primary Duties & Responsibilities:**
+ Use Data Science methods, including, but not limited to, Artificial Intelligence/Machine Learning approaches to perform sample classification, molecule identification, data processing (e.g. filtering, baselining), feature recognition, feature extraction, alarm threshold determination, pattern matching, statistical trending, scoring of detection quality, and integration of other information into decision making.
+ Collaborate with other technologists within Teledyne on application of AI/ML to system level data fusion, e.g. combining CBRNE sensor outputs with other information in AR/VR or other situational awareness modalities
+ Plan, design, and conduct data acquisition on sensor prototypes to drive algorithm development
+ Report results to manager and project team for 1 or more projects on a weekly basis
+ Compile reports and participate in customer reviews in West Lafayette and in the field.
**Job Qualifications:**
+ Background must include:
+ PhD degree in a cheminformatics-related field, such as chemistry, biology, biochemistry, engineering, or computer science, or an MS degree with 3+ years of experience
+ Experience in data science, modeling, algorithm development, and/or AI/ML methods
+ Experience using (and analyzing data outputs from) analytical spectrometers, mass spectrometers, and chemiresistive sensors strongly preferred
+ Wet chemistry lab experience
+ Microsoft Office (Excel, PowerPoint, etc.) skills required
+ Excellent analytical and problem-solving skills
+ Ability to effectively communicate and interact with team members and customers
+ Experience with machine learning models such as random forest, multilayer perceptron, convolutional neural networks
+ Experience with transformer networks and encoders/decoders is strongly preferred
+ Deep Python or R programming expertise, or equivalent experience with a related programming language such as C, C++, C#, etc.
+ Experience using visual statistical analysis software
+ Proven experience required
+ Perform basic test design - define the question being asked and develop single-variable experiments to answer
+ Act independently to drive experimentation & testing
+ Drive toward solutions to project goals
+ Compile data in a way it can be shared across the organization on a weekly basis
+ Able to troubleshoot and resolve science and project issues
+ Work professionally as part of a cohesive team, and communicate with team members to ensure project goals and timelines are met
Applicants must be either a U.S. citizen, U.S. national, legal permanent resident, asylee, refugee or must be eligible to apply for and obtain the appropriate export control license from the U.S. Departments of State or Commerce.
#FLIR
Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions.
Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws. ?
You may not realize it, but Teledyne enables many of the products and services you use every day **.**
Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

**Description:** The Advanced Programs and Exploitation (APEX) team with Lockheed Martin in Boulder is looking for a Research Scientist to support ongoing programs and internal research and development efforts. The APEX team is focused on mission processing applications of remote sensing payloads and fusion of various data types. This position will work alongside research scientists, FPGA engineers, and software engineers on the APEX team to accomplish to develop, test, and deliver prototype and fully capable systems.
This position will be expected to:
- participate in the development, integration, and enhancement of remote sensing processing and tracking algorithms and software.
- evaluate, refine, and develop tracking & processing algorithms.
- help our team evolve ground-based mission processing applications of remote sensing payloads onto flight hardware for onboard mission processing operations.
- develop a thorough understanding of R&D mission processing code written in C++.
- add features to a complex legacy code base.
- develop models and detailed simulations to predict and assess system performance.
- possibly work on AI/ML algorithm applications.
**Basic Qualifications:**
- Degree in a STEM (Science, Technology, Engineering, or Math) field from an accredited institution.
- Proficiency in MatLab and another programming language
- Ability to obtain a TS/SCI Clearance required for this role.
**Desired Skills:**
- Proficient in C++ & Python
- Experience with hardware acceleration technologies (e.g., GPUs, FPGAs)
- Understanding of AI/ML algorithms and architectures (e.g., CNNs, RNNs, transformers).
- Experience in remote sensing
- Experience with software version control such as GIT
- Applied mathematics or algorithm development experience
- Strong experience in software design and development.
- Active security clearance
**Security Clearance Statement:** This position requires a government security clearance, you must be a US Citizen for consideration.
**Clearance Level:** TS/SCI
**Other Important Information You Should Know**
**Expression of Interest:** By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings.
**Ability to Work Remotely:** Part-time Remote Telework: The employee selected for this position will work part of their work schedule remotely and part of their work schedule at a designated Lockheed Martin facility. The specific weekly schedule will be discussed during the hiring process.
**Work Schedules:** Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits.
**Schedule for this Position:** 4x10 hour day, 3 days off per week
**Pay Rate:** The annual base salary range for this position in California and New York (excluding most major metropolitan areas), Colorado, Hawaii, Illinois, Maryland, Minnesota, New Jersey, Vermont, Washington or Washington DC is $73,400 - $129,260. For states not referenced above, the salary range for this position will reflect the candidate's final work location. Please note that the salary information is a general guideline only. Lockheed Martin considers factors such as (but not limited to) scope and responsibilities of the position, candidate's work experience, education/ training, key skills as well as market and business considerations when extending an offer. **Benefits offered:** Medical, Dental, Vision, Life Insurance, Short-Term Disability, Long-Term Disability, 401(k) match, Flexible Spending Accounts, EAP, Education Assistance, Parental Leave, Paid time off, and Holidays. (Washington state applicants only) Non-represented full-time employees: accrue at least 10 hours per month of Paid Time Off (PTO) to be used for incidental absences and other reasons; receive at least 90 hours for holidays. Represented full time employees accrue 6.67 hours of Vacation per month; accrue up to 52 hours of sick leave annually; receive at least 96 hours for holidays. PTO, Vacation, sick leave, and holiday hours are prorated based on start date during the calendar year. This position is incentive plan eligible.
**Lockheed Martin is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics.**
**The application window will close in 90 days; applicants are encouraged to apply within 5 - 30 days of the requisition posting date in order to receive optimal consideration.**
At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work.
With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility.
If this sounds like a culture you connect with, you're invited to apply for this role. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs , and apply for roles that align with your qualifications.
**Experience Level:** Experienced Professional
**Business Unit:** SPACE
**Relocation Available:** Possible
**Career Area:** Software Engineering
**Type:** Full-Time
**Shift:** First

**Summary:**
Meta Platforms, Inc. (Meta), formerly known as Facebook Inc., builds technologies that help people connect, find communities, and grow businesses. When Facebook launched in 2004, it changed the way people connect. Apps and services like Messenger, Instagram, and WhatsApp further empowered billions around the world. Now, Meta is moving beyond 2D screens toward immersive experiences like augmented and virtual reality to help build the next evolution in social technology. To apply, click "Apply to Job" online on this web page.
**Required Skills:**
Research Scientist Responsibilities:
1. Perform research and develop solutions to computer software and computer hardware problems.
2. Research, design, and develop new optimization algorithms and techniques to improve the efficiency and performance of Meta's platforms.
3. Design and implement large-scale distributed software systems to serve large numbers of complex requests simultaneously and without failure.
4. Utilize technical research background, train new ranking models, and run experiments.
5. Create tools for migrating large bodies of user data across systems for new products, scalability efforts, and development of new core infrastructure.
6. Use machine learning, statistics, or other data techniques to build algorithms.
7. Suggest, collect, and synthesize system requirements from stakeholders and create effective feature roadmaps.
8. Analyze and resolve computer challenges from a system engineering standpoint.
9. Work on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
10. Demonstrate good judgment in selecting methods and techniques for obtaining solutions.
11. Develop ML techniques on feature/data/architecture track to improve performance of ads ranking models.
12. Monitor the ML system health (prediction, model staleness, calibration) and fix potential issues.
13. Coordinate and align on the plan for ML model iteration as a model owner and maintain centralized online modeling experiments.
**Minimum Qualifications:**
Minimum Qualifications:
14. Requires a Master's degree in Computer Science, Engineering, Information Systems, Analytics, Statistics, Mathematics, Physics, Applied Sciences, or a related field
15. Requires completion of a university-level course, research project, internship, or thesis in the following:
16. 1. Algorithms, data structures, or systems software
17. 2. Solving analytical problems using quantitative approaches
18. 3. Gathering, manipulating, or analyzing complex, high-volume, high-dimensionality data from varying sources
19. 4. Communicating complex research in a clear, precise, and actionable manner
20. 5. Research in topics closely related to machine learning, NLP, recommendation systems, pattern recognition, signal processing, data mining, artificial intelligence, information retrieval, or computer vision
21. 6. Performing research that enables learning the semantics of data (images, video, text, audio, or other modalities) and advances the technology of intelligent machines
22. 7. Devising better data-driven models of human behavior
23. 8. Adapting standard machine learning methods to best enterprise modern parallel environments: distributed clusters, multicore SMP, or GPU
24. 9. Developing highly scalable classifiers and tools leveraging machine learning, statistics, regression, rules-based models, or mathematical models
25. 10. Java, C++, Perl, PHP, or Python
**Public Compensation:**
$218,402/year to $240,240/year + bonus + equity + benefits
**Industry:** Internet
**Equal Opportunity:**
Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.
Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at