Trainee jobs at DSM Services USA Inc - 5 jobs

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position 2026 Summer Intern - Molecular Point of Care Systems Development We advance science so that we all have more time with the people we love. Department Summary At Roche, we believe the best solutions come by gaining different perspectives, asking and answering hard questions and challenging the status quo to develop small ideas and achieve big wins in innovation. Our success in creating a truly diverse and inclusive workplace will directly impact our ability to deliver on our purpose of “Doing Now What Patients Need Next.” Our Systems Development team focuses on product development on a state of the art molecular Point of Care platform. Primary responsibilities will include conducting and monitoring laboratory experiments on site to develop technical and theoretical understanding as part of product development. With guidance, you will analyze and brainstorm alternative approaches to solve problems and find solutions. You will also be responsible for coherence and compliance with Roche systems engineering principles and processes. This internship position is located in Pleasanton CA, on-site. The Opportunity After introduction to work processes, begins to organize, conduct and monitor laboratory experiments on site utilizing established and published procedures, and technical and theoretical understanding. Evaluates new equipment and techniques. With guidance, analyzes and brainstorms approaches to solve problems and find solutions. Assesses results for applicability, validity, and conformance to requirements and specifications. Summarizes experimental results, and reviews conclusions with supervisor and team members. Program Highlights Intensive 12-weeks, full-time (40 hours per week) paid internship. Program start dates are in May/June (Summer) A stipend, based on location, will be provided to help alleviate costs associated with the internship. Ownership of challenging and impactful business-critical projects. Work with some of the most talented people in the biotechnology industry. Who You Are Required Education: You meet one of the following criteria: - Must be pursuing a Bachelor's Degree (enrolled student) - Must have attained a Bachelor's Degree (not currently enrolled in a graduate program) Required Majors: Mechanical engineering, biomedical engineering or related field. Required Skills: Engineering background Experience working in a laboratory environment Equipment troubleshooting Engineering problem solving Data analysis Preferred Knowledge, Skills, and Qualifications Excellent communication, collaboration, and interpersonal skills. Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion. Previous work experience preferred Student organization and/or study abroad experiences Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location of California is $26.00-$33.00 hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off benefits. Who we are A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let's build a healthier future, together. Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Be Seen and Heard at EyePoint At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our: focus on science and innovation, we aim to offer a lifetime of clearer vision commitment to developing and commercializing innovative therapeutics to improve the lives of patients with serious retinal diseases Delivery of innovative therapeutics to protect vision, specializing in sustained-release treatments for serious retinal diseases. We See You. Your wellbeing Your professional worth Your future at EyePoint EyePoint offers robust total rewards in a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There's space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected. The Co-op will report directly to the Formulation Scientist. This position is located at our Watertown, MA site. The Co-op assignment will end on June 26, 2026. Responsibilities Primary responsibilities include, but are not limited to, the following: Individual Responsibilities Develop ocular formulations and manufacturing process for pre-clinical and clinical use. Interpret complicated data sets and provide sound recommendations Maintain knowledge with up-to-date scientific literature in the field of ocular drug delivery. Maintain a detailed and organized laboratory notebook Share findings in technical presentations and technical report Build expertise and knowledge around ocular formulation drug products. Ensure compliance with safety and regulations as well as experimental/laboratory best practices Qualifications Primary skills and knowledge required include, but are not limited to the following: Prior formulation development & characterization experience is a plus Level of Education Required: Currently enrolled in a university, pursuing a graduate degree in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or related discipline. Laboratory research experience (particularly formulations) is a plus (academic or industry) Excellent team player with strong interpersonal, written and verbal communication skills Personal Qualities: Bright, energetic, hard-working, and creative. Envision Your Future With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to improving the lives of patients with serious retinal diseases by developing and commercializing innovative therapeutics. The collective power of our values influences everything we do, and everything we do for you. Transformational Innovation We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. Unwavering Integrity We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us. Compassionate Excellence We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes. Inclusive Collaboration We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward. EyePoint is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. EyePoint is committed to fair and equitable compensation practices. The salary offer is commensurate with EyePoint's compensation philosophy and considers factors including but not limited to education, training, experience, market conditions, criticality of the role and internal equity. The target salary range for this position is listed below. #LI-Onsite Min USD $32.00/Hr. Max USD $42.00/Hr.

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym (mifepristone), the first approved treatment for hypercortisolism (Cushing's syndrome). Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation. What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease. Come spend your summer working with passionate colleagues and inspirational leaders, all while gaining world-class experience in one of the fast-growing biotechs in the Bay Area. The Patient Safety and Pharmacovigilance (PSPV) organization works collaboratively and strategically with colleagues across the product lifecycle to identify, evaluate, understand, and communicate the safety profile of Corcept products to protect patients worldwide. The PSPV intern will work under the supervision of the Head of Safety Systems and learn about core Patient Safety systems and reports, including safety data visualization, and the role of pharmacovigilance in a globally regulated industry. Responsibilities: Supports authoring or otherwise contributes to the preparation of data visualization reports Supports implementation of decisions from the PSPV systems, including signal management and data visualizations Contribute to health authority or other safety related query responses Ensures own work complies with established practices, policies and processes and any regulatory or other requirements Deliver a department presentation at the end of the program Participate as a member of the 2026 intern team group project that includes a company-wide presentation Preferred Skills, Qualifications and Technical Proficiencies: Knowledgeable in Microsoft Word, PowerPoint and Excel preferred Excellent verbal and written communication skills Ability to work in teams and independently Must be able to complete at least 10 consecutive weeks between June and August and it is a full-time internship (40 hours per week) Must be able to work at our Redwood City office for the duration of the internship, no relocation available Preferred Education and Experience: Currently enrolled as a sophomore, junior or senior an accredited university with a major in nursing, pharmacy or other medical/health/life sciences major GPA at least 3.0 The pay range that the Company reasonably expects to pay for this headquarters-based position is $26/hr - $32/hr; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience and education. Applicants must be currently authorized to work in the United States on a full-time basis. For information on how Corcept collects, uses, discloses, protects, and otherwise processes personal information and an explanation of the rights and choices available to you with respect to your personal information, please refer to our Privacy Notice link. Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs. Please visit our website at: ************************ Corcept is an Equal Opportunity Employer Corcept will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview. Though we use third-party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Corcept.

Be Seen and Heard at EyePoint At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our: focus on science and innovation, we aim to offer a lifetime of clearer vision commitment to developing and commercializing innovative therapeutics to improve the lives of patients with serious retinal diseases Delivery of innovative therapeutics to protect vision, specializing in sustained-release treatments for serious retinal diseases. We See You. Your wellbeing Your professional worth Your future at EyePoint EyePoint offers robust total rewards in a science-based entrepreneurial culture that empowers curiosity and innovation to help catapult your career. There's space for every voice and perspective to be heard in our on-site and remote environments where a variety of strengths and diverse backgrounds are connected. The Co-op will report directly to the Sr. Scientist. This position is located at our Watertown, MA site. The Co-op assignment will end on June 26, 2026. Responsibilities Primary responsibilities include, but are not limited to, the following: Individual Responsibilities Collaborate with cross-functional teams to support ongoing projects in Formulation Development R&D team. Assist in the preparation of samples for pre-formulation studies and solid-state characterization. Conduct experiments to evaluate the physicochemical properties of drug candidates, including solubility, stability, and polymorphism. Perform solid-state characterization techniques such as X-ray powder diffraction (XRPD), differential scanning calorimetry (DSC), and thermal gravimetric analysis (TGA). Document and analyze experimental data, contributing to reports and presentations. Single crystal growth. Collaborate with team members to troubleshoot experimental challenges and optimize methodologies Maintain laboratory equipment and ensure compliance with safety protocols. Qualifications Primary skills and knowledge required include, but are not limited to the following: A background in thermodynamics, polymorphism, crystallization, API, and formulation process development is preferred. Strong analytical and problem-solving skills. Familiarity with laboratory techniques and instrumentation is a plus. Excellent attention to detail and ability to work independently and in a team. Effective communication skills, both written and verbal. Level of Education Required: Currently pursuing a PhD or Masters Degree Preferred Field(s) of Study: Materials Science, Chemistry, Pharmaceutical Sciences Envision Your Future With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics. The collective power of our values influences everything we do, and everything we do for you. Transformational Innovation We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. Unwavering Integrity We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us. Compassionate Excellence We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes. Inclusive Collaboration We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward. EyePoint is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. EyePoint is committed to fair and equitable compensation practices. The salary offer is commensurate with EyePoint's compensation philosophy and considers factors including but not limited to education, training, experience, market conditions, criticality of the role and internal equity. The target salary range for this position is listed below. #LI-Onsite Min USD $32.00/Hr. Max USD $42.00/Yr.