Location: Yuba City, CA
from applicants. So whether you're looking for the buzz of a large city, the tranquility of nearby mountain bike trails or something in between, we encourage you to explore our organization. Job Summary: Plans and conducts segments of treatment programs designed to restore and improve physical, social and mental functions, while meeting department objectives.
Serves as co-leader in interdisciplinary approach to patient groups. Job Requirements: Education and Work Experience: Bachelor's Degree or equivalent (some certifications will require Bachelor's): Required Master's Degree: Preferred Licenses/Certifications: Physical Therapy licensure in state of practice: Required Cardiopulmonary
Resuscitation (CPR) or Basic Life Support (BLS OR HS-BLS OR RQIBLS) certification: Required Physical Therapist (PT): Required Essential Functions: Completes evaluations to ensure quality standards and addresses backssment areas that require attention.
Uses appropriate clinical techniques and tools and establishes individualized treatment plans for patients. Provides therapy interventions using appropriate treatment protocols and techniques. Establishes individualized care and discharge plans and ensures plans are communicated to appropriate parties. Completes comprehensive and accurate clinical documentation within established deadlines. Supervises assigned assistants. Performs other
job-related duties as assigned. Organizational Requirements: Adventist Health is committed to the safety and wellbeing of our associates and patients.
Therefore, we require that all associates receive all required vaccinations, including, but not limited to, measles, mumps, flu (based on the seasonal availability of the flu vaccine typically during October-March each year), COVID-19 vaccine (required in CA, HI and OR) etc. as a condition of employment, and annually thereafter. Medical and religious exemptions may apply. For more details: jobs-search. org/physical-therapist_yuba-city-c426297/physical-therapist-home-health-yuba-city-yuba-city_i1960087253
Aliso Viejo, California, and we have additional locations in the United States, Canada, United Kingdom, Germany, Japan, Australia and Brazil. How will you make an impact? The Lead Manufacturing Technician will be directly responsible for: Prepare components and build assemblies Ability to perform activities under a microscope Prepare bulk drug formulations Perform the following: Filing, capping, and crimping operations Packaging and labeling operations Sampling Visual inspections Real-time review of all executed documentation on the floor Oversee and assign daily production activities Ensure proper documentation (c GMP and GDP) Open/close work orders in Maximo and the enterprise resource
planning (ERP) system Oversee inventory on a daily basis in the ERP system Ability to address and resolve daily issues on the manufacturing floor Provide feedback and escalation to leadership Maintain production yield database Provide support for QMS including non-conformances (NCs), corrective and preventative actions (CAPAs), and change controls (CCs)) Additional tasks as required What will you do?
Maintain the operation schedule and allocate resources accordingly Oversee daily production activities Review all documentation and ensure completion following c GMP, QMS, and GDP guidelines. Use of Word, Excel and ERP to complete document reviews, training, and inventory Maintain
on the floor inventory for accuracy Revise documentation to ensure accuracy and compliance Communicate feedback to engineering on non-standard build requests, validation builds, clinical builds, etc.
How will you get here? High School Diploma Required 8+ years of related experience with high school diploma 6+ years of related experience with associate degree in science or engineering 4+ years of experience with bachelor's degree in science or engineering Demonstrates increased responsibility and leadership skills Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. These are just a few of the terms our employees use to describe their experiences as a part of the Glaukos family.
Those may seem like big aspirations, but here at Glaukos, we recognize the deep significance and profound meaning that comes from knowing that we can make a meaningful difference by helping improve eyesight of people worldwide. And because we're a rapidly growing company with a dynamic, fast-paced culture, individual employees are empowered with more diverse and enriching challenges that might not be possible at a larger company, and more fulfillment in knowing every person and every task is directly tied to making a difference in the life of others.
We offer competitive salary (based on experience), bonus eligibility, medical/dental/vision, life insurance, stock options, 401(k) Employer Match, Employee Stock Purchase Program, generous time off & paid holidays as well as time-off to volunteer in the community, plus the opportunity to work for a company that is pioneering a new glaucoma treatment class! Moreover, Glaukos Corporation has been Certified as a Great Place to Work the last three years! Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction including interactionual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
ABOUT US Founded in 1998, Glaukos Corporation is an ophthalmic medical technology and medical company focused on novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases. Our company was the first company to bring to market Micro-Invasive Glaucoma Surgery (MIGS), the micro-invasive procedure which revolutionized the treatment and management of glaucoma.
In 2012, we launched our first MIGS device-the i Stent®-in the United States, followed by our next-generation i Stent inject® device in September 2018 and i Stent inject® W in September 2020. In November 2019, Glaukos acquired Avedro, maker of the first and only FDA-approved cross-linking technology for progressive keratoconus. And we continue to seek to leverage our platform technologies to build a comprehensive and proprietary portfolio of micro-scale surgical and medical therapies for glaucoma, corneal health, and retinal diseases. Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol " GKOS" Our global headquarters is located in San Clemente, California with additional locations in Waltham and Burlington, Massachusetts.
Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employmentwithout regard to race, color, religion, interaction including interactionual orientation and genderidentity, national origin, disability, protected Veteran Status, or any othercharacteristic protected by applicable federal, state, or local law.
level, launched in February 2021. If you’re fascinated by the science behind highly effective skincare, age reversal and optimal health, we’d love for you to join us! We are looking for a passionate Associate Scientist to join our team. The ideal candidate is skilled in tissue culture, molecular and cellular biology, and drug screening techniques.
This person is expected to function well within a team setting, complete tasks on time, and communicate effectively with team leaders. The Associate Scientist will work within the research and development team on the validation and manufacturing of advanced human 3D skin models, testing new compounds, and studying their mechanism of action.
Experience in the field of Aging Biology, Cellular Senescence, Protein analysis, Immunohistochemistry, and Image analysis programs (such as Image J or Cell Profiler) is greatly appreciated.
ABOUT YOU • Ph D in Molecular Biology, Cellular Biology, Bioengineering, or a similar field, Masters degree with a minimum 7+ years experience of relevant industry experience. • A team player able to work in a collaborative/team-oriented environment. • Excellent communication and presentation skills. • Must be authorized to work in the United States. RESPONSIBILITIES • Work within our R&D team to execute cell-based assays and experiments, perform analyses, and report results. • Expertise in tissue
culture and molecular biology techniques including q RT-PCR and Protein Analysis • Demonstrate critical thinking and ingenuity by bringing new ideas to unveil scientific questions that align with our mission and product development.
• Foster and promote effective and efficient teamwork within the company. • Interpret results and troubleshoot technical problems. • Ensure that experiments are performed to a consistently high standard. • Accurate documentation in lab notebooks and internal databases with excellent organization and attention to detail. BENEFITS • Competitive, full-time salary + Bonuses • Full coverage Health and Dental Insurance and 401k • Career Development Planning To apply, please send an email to with the subject line “Associate Scientist”, and include a CV and cover letter in your application.
Science Jobs refer to employment opportunities within the various fields of science, such as biology, chemistry, physics, and environmental science. These positions often require a strong educational background in their respective disciplines and can range from academic research and teaching roles to industry-based positions in pharmaceuticals, technology, and more. Unique features of Science Jobs include a focus on innovation, evidence-based analysis, and the exploration of the natural world. They contribute significantly to technological advancements and the betterment of society through scientific discovery and application.
exciting products for customers and collaborating with cross-functional teams. The person will be responsible for taking products and processes from concept feasibility through to implementation into production for com mercialization. In this position, the person will work closely with the R&D team(s) in demonstrating reagent feasibility, assay development, generating product specifications, characterizing the product, developing manufacturing and QC processes, and transferring these stable processes to Manufacturing.
The ideal candidate will have extensive experience with analytical technologies associated with molecular biology with an emphasis on commercial product development from
concept to manufacturing. The person will characterize reagents to meet manufacturing requirements for critical reagent consumables. Candidate should have strong hands-on laboratory experience, including molecular biology techniques, sample preparation, analytical assay development and preferably sequencing instrument operation.
Primary Responsibilities: Hands-on testing and integration of assay and process workflows onto sequencing platforms. Plan, conduct, analyze, interpret, and report recommendations based on tested experimental results. Support product commercialization from design transfer to manufacturing. backss information to ensure data sufficiency and completeness of results.
Write batch records, experimental protocols, summaries, and reports.
Source and qualify external vendors, develop specifications, set up supply chain and manufacturing process. Work in ISO 9001 and 13485 regulated environments. Position Requirements: Masters or Ph. D. in Molecular Biology, Biochemistry, or related relevant industry experience in Biochemistry or Molecular Biology, with emphasis on product development and testing. Prior experience with q PCR assay development, RNA sequencing is strongly desired. Deep understanding of biochemistry, next-generation sequencing, development of analytical and functional assays, DOE, sequencing data analysis. Hand-on scientist with experience in QC assay development and validation.
Skilled at writing batch records, validation reports, with experience in quality management system, risk analysis and mitigation.
