218 Product Development jobs in Fremont

1 week ago Be among the first 25 applicants About Aerogen Pharma Aerogen Pharma is a US based clinical-stage specialty pharmaceutical company with a mission to develop inhaled drug/biologic and device combination that will transform the standard of care for acute and critically ill patients. Our goal is to create medically superior, proprietary and commercially differentiated combination products by combining proven therapeutic molecules with a unique, high-performance aerosol delivery system. About About Aerogen Pharma Aerogen Pharma is a US based clinical-stage specialty pharmaceutical company with a mission to develop inhaled drug/biologic and device combination that will transform the standard of care for acute and critically ill patients. Our goal is to create medically superior, proprietary and commercially differentiated combination products by combining proven therapeutic molecules with a unique, high-performance aerosol delivery system. We are embarking on an exciting and dynamic stage in our combination product development, moving into phase 3 clinical trial for one of the biggest breakthroughs in Neonatal care. We are a team of passionate industry experts who are leading, shaping, and driving a potentially transformative medical breakthrough for the treatment of neonatal respiratory distress syndrome (RDS) in the developed world. Additionally, in partnership with The Bill & Melinda Gates Foundation, we have an ambitious program in development to bring low-cost surfactant to the millions of premature babies with RDS born each year. Join us as we embark on this breakthrough and become inspired to deliver. What is the role? The Associate Director of Product Development is a critical role in Aerogen Pharma that will be responsible for key aspects of pharmaceutical development of AeroFact (biologic surfactant) or Synthsurf (Synthetic surfactant). The role will focus on phase appropriate product development of surfactant lyophilized formulations, manufacturing process optimization and scale up, and product characterization supporting pre-clinical and clinical studies. What are the key responsibilities? Leadership & Strategy : Oversee product development for biologics, proteins, and peptides, managing projects with CDMOs. Develop and execute strategies aligned with Aerogen Pharma's mission and regulatory standards. Product Development : Research, design and execute controlled experiments, with high attention to detail to development of stable and effective drug product, fit for commercialization. Conduct QbD experiments to identify CQAs that impact product performance and stability. Conduct registration enabling stability studies and product characterization studies per appropriate ICH guidances. Experience working on lipid based and / or protein based biologics is required. Experience with lyophilization process development and optimization is a plus. CDMO/CMO Collaboration: Serve as the primary liaison with external manufacturing / analytical partners. Ensure effective communication and coordination to meet project timelines and quality expectations. Regulatory Compliance : Prepare and review documentation for regulatory submissions (INDs, BLAs, NDAs). Ensure adherence to cGMP and regulatory requirements. Experience authoring late-stage regulatory dossiers, particularly BLAs is required. Cross-Functional Collaboration: Work closely with R&D, Manufacturing, Regulatory, and Quality Assurance teams to integrate product development within overall project goals. Troubleshooting & Problem Solving: Address and resolve formulation, process optimization, analytical issues during development and manufacturing. Implement corrective and preventive actions as needed. What education and experience are required? Ph.D. in Pharmaceutical sciences, Chemical engineering, Biochemical engineering or related field. 8-10 years in lipid formulations, liposomes or related drug delivery technologies. 2-5 years of manufacturing process development (lyophilization) is a plus. Extensive experience working with CDMOs is required. Late stage product development experience is required. Experience authoring CMC dossiers for FDA, EMA and other regulatory agencies is a must. Knowledge and experience in drug-device development, inhalation drug delivery is a plus. Knowledge of Good Manufacturing Practices, ICH, FDA, Health Canada and MHRA Regulations is required Excellent written and oral communication skills. What key skills will make you great at the role? Technical Expertise: Experience with lipid-based products (including proteins) and drug-device combination products is required. Experience With Manufacturing Process Development And Validation Is Preferred. Regulatory Knowledge: Deep understanding of regulatory requirements and submission processes for IND and BLA. Leadership Skills: Proven ability to lead and develop high-performing teams with excellent interpersonal and communication skills. Results oriented. Strong initiative, accountability and willingness to take ownership and drive projects tocompletion. Work independently with CDMOs without close supervision. Proven ability to operate effectively across a matrix organization to drive programs according to timelines; ability to articulate project objectives and priorities Dynamic thinker with a sense of urgency and a bias toward action Must be comfortable and confident challenging the status quo and pushing the teams to look at issues and opportunities from all angles Communication: Strong written and oral communications skills. Problem-Solving: Strong analytical skills with a proven track record of overcoming complex scientific challenges. Why Aerogen Pharma As a key member of Aerogen Group, the global market leader in high performance aerosol drug delivery, Aerogen Pharma is at a pivotal point in the company's life cycle. With plans to expand and centralize our US hubs over the next two years, we offer an environment where you can thrive professionally and learn from driven industry leaders in drug development and commercialization, inhaled devices, and neonatology. We foster an inclusive culture that empowers you to contribute to the transformation of Neonatal care, where potential is recognized, and professional development is encouraged. San Mateo, California Work experience General Project Management IT Consultant Languages English Seniority level Seniority level Director Employment type Employment type Full-time Job function Job function Product Management and Marketing Industries Technology, Information and Internet Referrals increase your chances of interviewing at TieTalent by 2x Get notified about new Associate Director Product Development jobs in San Mateo, CA . 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• Participate in the conceptualization, design, and development of aerospace components and systems.
• Conduct detailed engineering analysis, including structural, thermal, fluid dynamics, and stress analysis using FEA and CFD tools.
• Develop and refine 3D CAD models and engineering drawings in accordance with industry standards.
• Perform system-level integration and testing of aerospace hardware and software.
• Analyze test data, troubleshoot issues, and propose design modifications or corrective actions.
• Prepare comprehensive technical reports, design specifications, and presentations.
• Collaborate cross-functionally with manufacturing, quality assurance, and project management teams.
• Ensure designs meet performance, reliability, safety, and cost requirements.
• Support the fabrication and assembly of prototypes and flight hardware.
• Stay current with emerging aerospace technologies, materials, and manufacturing processes.
• Contribute to risk assessments and mitigation strategies for new product development.

• Bachelor's or Master's degree in Aerospace Engineering, Mechanical Engineering, or a related field.
• Minimum of 3-5 years of experience in aerospace product development, design, or analysis.
• Strong proficiency in CAD software (e.g., SolidWorks, CATIA, NX) and FEA/CFD analysis tools (e.g., Ansys, Abaqus).
• Solid understanding of aerospace materials, manufacturing processes, and testing methodologies.
• Knowledge of propulsion systems, spacecraft structures, or avionics is highly desirable.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong written and verbal communication skills, with the ability to convey complex technical information.
• Ability to work independently and as part of a collaborative, multidisciplinary team.
• Experience with flight hardware development and qualification processes preferred.
• Detail-oriented with a strong commitment to precision and accuracy.
• U.S. Citizenship or Permanent Resident (Green Card Holder) may be required for certain projects.

• Lead and support the development of new food and beverage products from initial concept through to successful commercialization, adhering to project timelines and budget.
• Conduct extensive research on consumer trends, market demands, ingredient functionalities, and competitive products to identify innovation opportunities.
• Formulate and test new product recipes, optimizing for taste, texture, shelf-life, nutritional profile, and cost-effectiveness.
• Source and evaluate new ingredients, ensuring compliance with regulatory standards (e.g., FDA, USDA) and company quality specifications.
• Collaborate closely with cross-functional teams including Marketing, Supply Chain, Operations, and Quality Assurance to ensure seamless product development and launch.
• Design and execute sensory evaluations and consumer testing to gather feedback and refine product formulations.
• Manage pilot plant trials and scale-up activities, troubleshooting issues and ensuring successful transition from lab to production.
• Prepare detailed product specifications, ingredient lists, nutritional facts, and processing instructions.
• Ensure all new products meet regulatory requirements for labeling and safety.
• Identify and implement process improvements in product development workflows.
• Maintain accurate and organized records of all formulations, experiments, and results.
• Stay current with advancements in food science, processing technologies, and clean label trends.
• Contribute to the intellectual property strategy through patentable innovations.
• Present project updates and findings to management and stakeholders.

• Bachelor's or Master's degree in Food Science, Food Technology, Chemical Engineering, or a closely related scientific field.
• Minimum of 3-5 years of progressive experience in product development within the Fast-Moving Consumer Goods (FMCG) food and beverage industry.
• Proven experience in formulation development, ingredient sourcing, and sensory evaluation.
• Strong understanding of food safety principles (HACCP, GMP) and regulatory requirements (FDA, USDA).
• Experience with pilot plant operations and scaling up recipes for commercial production.
• Excellent problem-solving skills, with a scientific and analytical approach to product development.
• Strong project management skills, with the ability to manage multiple projects simultaneously.
• Exceptional written and verbal communication skills, with the ability to collaborate effectively across departments.
• Ability to work both independently and as part of a collaborative team.
• Creative and innovative mindset with a passion for consumer products.
• Proficiency in recipe management software and Microsoft Office Suite.
• Comfortable with a hybrid work model, requiring regular presence in the San Jose, California, US R&D facility.

• Lead the full product development lifecycle for new and existing FMCG products, from ideation and concept generation to commercialization and post-launch analysis.
• Conduct thorough market research and consumer insights analysis to identify trends, unmet needs, and opportunities for innovation.
• Define product specifications, features, and benefits, ensuring alignment with consumer preferences and brand strategy.
• Collaborate cross-functionally with R&D, Marketing, Sales, Supply Chain, and Legal teams to ensure seamless product development and launch.
• Manage project timelines, budgets, and resources effectively to deliver products on schedule and within financial constraints.
• Oversee product testing, quality assurance, and regulatory compliance to ensure products meet all safety and performance standards.
• Develop and present business cases for new product concepts, including market potential, financial projections, and competitive analysis.
• Monitor product performance post-launch, gathering feedback and identifying opportunities for optimization or iteration.
• Stay abreast of competitor activities, industry best practices, and emerging technologies in the FMCG space.
• Mentor and guide junior team members within the product development department.
• Contribute to the long-term product roadmap and strategic planning for the FMCG portfolio.

• Bachelor's degree in Marketing, Business Administration, Engineering, or a related field; MBA is a plus.
• Minimum of 5-7 years of progressive experience in product development or product management within the FMCG industry.
• Demonstrated success in launching new products to market.
• Strong understanding of consumer insights, market research methodologies, and product lifecycle management.
• Excellent project management skills, with the ability to manage multiple complex projects simultaneously.
• Exceptional communication, presentation, and interpersonal skills, capable of influencing stakeholders at all levels.
• Analytical mindset with the ability to interpret data and make data-driven decisions.
• Proficiency in project management software and Microsoft Office Suite.
• Ability to thrive in a fast-paced, dynamic, and collaborative environment.
• Experience with sustainable or health-focused consumer products is highly desirable.

Molex is seeking an experienced New Product Development Manager to join our Copper Solutions team responsible for leading the development of high speed datacom and telecom solutions used in AI applications. The New Product Development Manager will work with customers (Hyperscalers/OEMs/ODMs), partners, and internal customers to ensure that we are developing new products that align with market technology needs. This leader will be taking those new products and partnering with customers to implement our technologies within their next generation platforms.

This role demands a blend of technical knowledge and business acumen, as well as a passion for innovation and a commitment to delivering high-quality, user-centric products that meet market demands. The New Product Development Manager will play a crucial role in shaping the future of AI hardware in the datacom industry, driving growth and maintaining a competitive edge in the market.

This person will work with all levels of the organization, including Senior Management and external customers, suppliers, and trade organizations.

Our Team

This person will work with all levels of the organization, including Senior Management and external customers, suppliers, and trade organizations. The information exchange is typically technical in nature and confidential. This position requires a high level of negotiation skills and business acumen.

What You Will Do

• Develops and implements strategic product and annual business plans targeting markets, industries and customers. Identifies product line trends and technologies. Leads long term product planning
• Increase pipeline growth, customer wins, and RPM release
• Work with MIE and cross functional teams to ensure CapEx and product costs are inline with market conditions
• Track capacity and drive capital investments supporting forecasted demand
• Drive the closure of any commercial negotiations with customers on new platform partnerships
• Identifies opportunities to establish and develop industry partner relationships
• Understand, support and contribute to current Molex Total Quality Management (TQM), Six Sigma, International Standards Organization (ISO) and Environmental, and/or Health and Safety (EH&S) Management Systems by following stated policies and procedures
• Perform other related duties as assigned by management
• Track and understand the competitive landscape and establish and drive our technology roadmap
• Develop relationships with our key customers and enable collaboration to align our customers technology roadmap to our own development plan
• Lead development projects making sure that it is completed on a timely basis and on budget
• Develop marketing collateral to promote new technologies and gain penetration in the market
• Drive product and technology release internally while working with marketing communications on launch strategies

Who You Are (Basic Qualifications)

• Bachelor degree in Business or Engineering
• 5+ Years of experience within the high speed Datacom Market OR 2+ Years of Sales Experience calling on Datacom accounts OR 2+ Years of Product Management Experience

What Will Put You Ahead

• Technical background (electrical or mechanical)
• Sales experience or product engineering
• SAP experience
• Experience in negotiating and working with contract manufacturers and electronics market OEM's

At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions. Any compensation range provided for a role is an estimate determined by available market data. The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location. If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy. For this role, we anticipate paying $130,000 - $180,000 per year. This role is eligible for variable pay, issued as a monetary bonus or in another form.

Hiring Philosophy

All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds. We are Military Ready and Second Chance employers. Learn more about our hiring philosophy here .

Who We Are

As a Koch company, Molex is a leading supplier of connectors and interconnect components, driving innovation in electronics and supporting industries from automotive to health care and consumer to data communications. The thousands of innovators who work for Molex have made us a global electronics leader. Our experienced people, groundbreaking products and leading-edge technologies help us deliver a wider array of solutions to more markets than ever before.

At Koch, employees are empowered to do what they do best to make life better. Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.

Our Benefits

Our goal is for each employee, and their families, to live fulfilling and healthy lives. We provide essential resources and support to build and maintain physical, financial, and emotional strength - focusing on overall wellbeing so you can focus on what matters most. Our benefits plan includes - medical, dental, vision, flexible spending and health savings accounts, life insurance, ADD, disability, retirement, paid vacation/time off, educational assistance, and may also include infertility assistance, paid parental leave and adoption assistance. Specific eligibility criteria is set by the applicable Summary Plan Description, policy or guideline and benefits may vary by geographic region. If you have questions on what benefits apply to you, please speak to your recruiter.

Additionally, everyone has individual work and personal needs. We seek to enable the best work environment that helps you and the business work together to produce superior results.

Equal Opportunities

Equal Opportunity Employer, including disability and protected veteran status. Except where prohibited by state law, some offers of employment are conditioned upon successfully passing a drug test. This employer uses E-Verify. Please click here for additional information. (For Illinois E-Verify information click here , aquí , or tu ).

#LI-AP3

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte whether it be in one of our labs, corporate offices, the field enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a results-driven environment that values innovation, collaboration, and compassion.

Location: This is an onsite position based in our South San Francisco location.

We are looking for a highly motivated individual to join the Veracyte R&D Team as a Principal Scientist for IVD product development. This exciting and challenging role is responsible for leading the development and validation of genomics-based molecular diagnostic assays under design control in the field of oncology. This position requires planning and managing technical studies aimed at establishing and validating genomics assay workflows, test kit components and controls, and performance of IVD assays, along with overseeing technical team members. To be a successful candidate, you will share our commitment to teamwork and collaboration and be excited by the challenges of applying your scientific expertise to develop genomic tests that improve patient diagnosis and treatment.

Responsibilities:

• Oversee development and validation of genomics-based molecular IVD assays using the design control process - inclusive of design, feasibility, optimization, guard-banding, verification, validation and design transfer.
• Mentoring (design, monitor, complete, troubleshoot) of laboratory project tasks performed by product development personnel.
• Lead product development efforts within a multi-disciplinary team that includes project management, clinical, bioinformatics, regulatory, quality and marketing groups.
• Participate in managing the Design History File for new products.
• May participate in other aspects of IVD development and testing to ensure that IVD products conform to product specifications.
• May participate in company audits as it relates to development and validation of IVD assays.

PhD in chemistry, biochemistry or molecular biology (or related studies) plus extensive relevant industry experience (10+ years, including 7 + years industry), or an B.S./M.S. in chemistry, biochemistry or molecular biology (or related studies) with additional relevant experience (15 + years, including 10+ years industry).

• Prior experience in developing genomics-based IVD assays or laboratory developed tests is required.
• Experience with various molecular platforms (e.g. next-generation sequencing, microarrays and/or qPCR), in the context of assay development and testing of clinical specimens, is required.
• Keen insight into experimental design, aimed at elucidating the biological factors that influence genomic results.
• Hands-on knowledge of the biochemistry underlying multi-component molecular biology methods at the sample preparation, assay and detection level.
• Familiarity with IVD regulations (FDA 21 CFR Parts 820 and ISO 13485:2016) or CLIA regulations.
• Demonstrated effective mentoring (design, monitor, complete, troubleshoot) of laboratory project tasks performed in the hands of others.
• Experience with gene expression is preferred but not required.
• Goal-oriented and timeline-driven to support company objectives. Demonstrated an ability to thrive in a fast-moving environment and acknowledge that product timeliness is essential to commercial success.
• Must be highly motivated team player and work well with others.
• Strong organizational, communication, and interpersonal skills.
• Excellent documentation skills including writing of technical documents.

#LI-Onsite

The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.

Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified Great Place to Work in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose.

Veracyte(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The companys growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The companys tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracytes exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.Veracyteis based inSouth San Francisco, California. For more information, please visit and follow the company on X (Formerly Twitter).

Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View ourCCPA Disclosure Notice.

If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to