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<h3>Job Description</h3>
Job Description
Cresilon® is a Brooklyn-based biotechnology company that develops, manufactures, and markets hemostatic medical devices utilizing the company’s proprietary hydrogel technology. The company’s plant-based technology has revolutionized the current standard by stopping traumatic and surgical bleeds in seconds without the need for extended manual pressure. The company's current and future product lines target veterinary, human trauma, and human surgical applications. Cresilon's mission is to save lives. Learn more about the company at <a href="http://www.cresilon.com" target="_blank">www.cresilon.com</a>.
The Preclinical Principal Scientist will serve as a key scientific contributor, subject matter expert (SME) and Project Manager in the execution of Cresilon’s Preclinical Research Operations, including but not limited to in-vivo study design (Safety and Efficacy/Functionality evaluations), Preclinical Research Management, Vendor Management, and Preclinical Regulatory Strategy. This will include the development and execution of strategies for preclinical evidence necessary to competitively position a project’s product for domestic and international regulatory and clinical acceptance. This position as a hybrid role, with work off-site at CRO in NY/NJ area, work from home and on-site at Brooklyn NY.
Job Responsibilities:
The Preclinical Research Scientist will:
<ul>
<li>Lead, staff, and manage Cresilon’s Preclinical Research activities.</li>
<li>Provide preclinical scientific input and leadership on the evaluation of physical safety and efficacy for technologies and products at all stages of the product life cycle.</li>
<li>Plan, direct, coordinate and execute activities related to the design, initiation and follow-up of studies to support approval of Class I-III medical devices.</li>
<li>Develop, write, and/or review study protocols and reports. Act as technical mentor for the development of study experimental designs, protocols, and reports of junior associates.</li>
<li>Administrate and manage Cresilon preclinical regulatory strategy and communication.</li>
<li>Work with Contract Research Organizations (CROs) to execute both Biocompatibility / Safety and Efficacy/Functionality research, including negotiating, drafting, and managing research contracts and agreements with pre-clinical trial sites.</li>
<li>Ensure that company operates within the scope of regulatory compliance including Quality System Regulations (ISO 13485), health and safety, environmental protection regulations, and the core values of Cresilon. </li>
<li>Be a Subject Matter Expert (SME) for preclinical research department growth strategy. Actively interact with the internal and external scientific community to maintain state of the art knowledge.</li>
<li>Oversee the development of and modifications to preclinical models to address project needs.</li>
<li>Oversee the design and execution of preclinical functionality and safety in-vivo studies per project timelines.</li>
<li>Surveys the literature to identify and compare competitive product performance and safety risks.</li>
<li>Maintain current knowledge in existing regulations, requirements and standards, including but not limited to global regulatory requirements (ISO, FDA, etc) and compliance requirements (GLP, USDA, AAALAC, departmental SOP's, company policies, etc)</li>
<li>Work cross functionally with Regulatory and Quality to assess project risks, product safety and efficacy on NPD projects, including ensuring external facilities meet Cresilon standards for animal use and generating contracts and CRO audits, if necessary.</li>
<li>Manage budgetary requirements for all research projects to support efficacy and safety programs.</li>
<li>Lead the effort to publish surgical research in peer-reviewed journals.</li>
<li>Regularly interface with management to ensure research operations reflect overall corporate vision/strategy.</li>
<li>Work with VP of Technology and Director of R&amp;D to ensure long-term vision and goals met to reflect company’s charter.nd </li>
</ul>
Requirements
<ul>
<li>DVM, PhD or MD in a relevant discipline is preferred, A Bachelors in a technical or scientific field is required.</li>
<li>Minimum 6+ years’ experience in preclinical medical device research is required, preference given to veterinary surgical experience.</li>
<li>4+ years of people management experience preferred.</li>
<li>Extensive knowledge of surgery, anatomy, toxicology, and pathology is required.</li>
<li>Experience with planning, directing, and coordinating activities related to studies to support approval of Class I-III medical devices is highly preferred.</li>
<li>Experience in a medical device, pharmaceutical, or related setting with a proven record of success in supporting studies for R&amp;D projects is highly preferred.</li>
<li>Strong knowledge of ISO-10993 Standards, FDA Guidance and Regulations, and Animal Welfare Regulations.</li>
<li>Experience with surgical publication submission strategy is strongly preferred.</li>
<li>Strong communication skills (both written and verbal) is required with the ability to extract key facts from complex information and present concise summaries to management.</li>
<li>Demonstrated experience with large animal in vivo surgical research and CRO vendor management is required.</li>
<li>Previous experience in authoring and reviewing nonclinical regulatory documents as well as interactions with regulatory authorities is strongly preferred.</li>
<li>Excellent problem solving, conflict resolution, and analytical skills is required.</li>
<li>Ability to work eﬀectively both independently and collaboratively in a dynamic team-oriented environment is required.</li>
<li>Prior experience and ability to work well with external CROs and collaborators with professionalism and discretion is required.</li>
<li>Requires strong leadership and organizational skills including attention to detail and multi-tasking skills.</li>
<li>Able to understand and execute to project details but keep overall “big picture” view of projects, priorities, and strategies is required.</li>
<li>Medical Device product development experience, including knowledge of medical device regulations, regulatory/notified body requirements is preferred.</li>
<li>Good Laboratory Practices (GLP) experience preferred and working knowledge of Good Manufacturing Practices (GMP) </li>
<li>Experience in developing and commercializing regulated devices under Design Control (21 CFR 820) requirements, GLP/GMP, and ISO regulations is preferred.</li>
<li>Hands-on research experience with hemostatic devices and/or coagulation chemistry, strongly preferred. </li>
<li>Legal authorization to work in the United States.</li>
<li>This position is located in Brooklyn, NY and may require up to 30% travel (to monitor and execute out-sourced studies) </li>
</ul>
Cresilon is an equal-opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Cresilon makes hiring decisions based solely on qualifications, merit, and business needs at the time. 
Benefits
<ul>
<ul>
<li>Competitive annual base salary range of $130,000 - $210,000, depending upon job level and qualifications.</li>
<li>Paid Vacation, Sick, &amp; Holidays</li>
<li>Medical, Dental, and Vision Insurance, FSA: Dependent &amp; Healthcare, Commuter &amp; Parking Benefits, Long Term Disability Coverage</li>
<li>Company Paid Life and Short-Term Disability Coverage</li>
<li>Work/Life Employee Assistance Program </li>
<li>Monthly MetroCard Reimbursement</li>
<li>401(k) &amp; Roth Retirement Savings Plan with company match up to 5%</li>
</ul>
</ul>

Preclinical Principal Scientist, Research & Development

<h3>Job Description</h3>
Job DescriptionThe Role
We are looking for a Senior Climate Scientist with strong industry experience and a robust coding background to join our team. This role requires a blend of scientific expertise, technical proficiency, and communication skills, enabling you to not only contribute to our wildfire and climate models but also effectively pitch and discuss our models and systems with stakeholders.
Primary Responsibilities
<ul>
<li>Develop, refine, and validate climate and wildfire models to support underwriting and risk management.</li>
<li>Communicate complex scientific models and data-driven insights to both technical and non-technical audiences.</li>
<li>Collaborate closely with cross-functional teams, including engineering and underwriting.</li>
<li>Stay up-to-date with the latest climate science research, methodologies, and industry trends.</li>
<li>Design and implement Python-based analytical tools and models.</li>
<li>Analyze historical and predictive wildfire and climate data to improve model accuracy and effectiveness.</li>
<li>Assist in pitching our proprietary models and systems to potential clients, partners, and industry forums.</li>
</ul>
Requirements
Essential Experience of a Successful Candidate
<ul>
<li>PhD or Master's degree in Climate Science, Meteorology, Environmental Science, or a related field.</li>
<li>Proven industry experience in climate modeling, wildfire risk assessment, or similar domains.</li>
<li>Strong Python programming skills, including experience with data analysis libraries such as Pandas, NumPy, and geospatial tools.</li>
<li>Hands-on experience with climate and wildfire modeling techniques and tools.</li>
<li>Excellent communication skills, capable of simplifying complex models for diverse audiences.</li>
<li>Ability to work independently and within a collaborative team environment.</li>
</ul>
Useful Experience
<ul>
<li>Experience presenting at conferences or pitching scientific models to industry stakeholders.</li>
<li>Familiarity with machine learning techniques for climate data analysis.</li>
<li>Knowledge of geospatial data analysis and visualization frameworks.</li>
<li>Previous experience in the (re)insurance industry or working on natural catastrophe modeling.</li>
</ul>
Benefits
Why Join Kettle?
<ul>
<li>Be part of a mission-driven company tackling real-world challenges.</li>
<li>Work with a passionate and innovative team in a collaborative environment.</li>
<li>Opportunity to influence cutting-edge wildfire risk modeling in a dynamic industry.</li>
<li>Competitive salary and benefits package, including remote work flexibility.</li>
</ul>

Senior Climate Scientist

<h3>Job Description</h3>
Job DescriptionAbout CookUnity
Food has lost its soul to modern convenience. And with it, has lost the power to nourish, inspire, and connect us. So in 2018, CookUnity was founded as the first-of-its-kind platform that connects the world with the source of truly great food: chefs. Today, CookUnity delivers 35 million meals a year from the industry's best chefs to homes all over the country. Fresh. Ready-to-eat. And crafted with the passion that nourishes body and soul.
Unwilling to stop there, CookUnity is expanding beyond delivery to become an ever-innovating marketplace focused on our singular mission: empower Chefs to nourish the world.
If that mission has you hungry in more ways than one, you've found the right job posting.
The Role:
We are seeking an experienced Senior Machine Learning Scientist specializing in Recommendation and Search Systems to drive innovation and enhance our search and recommendation models. In this role, you will work on cutting-edge machine learning algorithms, develop scalable search and recommendation architectures, and collaborate with cross-functional teams to deliver personalized and relevant experiences to our users.
Responsibilities:
<ul>
<li>Architect, design, develop, and deploy the Machine Learning models that will serve real-time recommendations or search.</li>
<li>Research and implement state-of-the-art machine learning techniques such as deep learning, reinforcement learning, and collaborative filtering for recommendations and search ranking.</li>
<li>Be a leader in the Machine Learning community within CookUnity and work collaboratively across engineering and product teams.</li>
<li>Develop search ranking algorithms, query understanding, and relevance models to improve search experience.</li>
<li>Hands-on expertise with implementing end-to-end production ML systems at scale.</li>
<li>Collaborate with engineering, product, and data science teams to integrate models into production environments.</li>
<li>Act as an ambassador for AI within the organization, advocating for its adoption and showcasing its potential impact.</li>
</ul>
Requirements:
<ul>
<li>Bachelor's degree in Computer Science, Statistics, Mathematics, or a related field. A Master's degree is preferred.</li>
<li>5+ years of industry experience in building and deploying recommendation and search systems at scale.</li>
<li>Strong background in machine learning with experience and expertise in personalized machine learning algorithms, especially recommender and search systems.</li>
<li>Practical real-world experience with building scalable recommendations and search.</li>
<li>Knowledge of generative artificial intelligence applied to recommendation and search.</li>
<li>Demonstrated ability to design and implement effective machine learning systems.</li>
<li>Proficiency in programming languages such as Python, Kotlin or similar language.</li>
<li>Hands-on experience with machine learning frameworks such as TensorFlow, PyTorch, Scikit-learn, or similar.</li>
<li>Experience with cloud platforms (AWS, GCP, or Azure) and MLOps best practices.</li>
<li>Strong problem-solving skills and a clear understanding of algorithmic design.</li>
<li>Ability to communicate effectively with both technical and non-technical stakeholders.</li>
</ul>
Preferred requirements:
<ul>
<li>Experience in the food technology sector is a plus.</li>
<li>Experience working with Generative AI and its applications in personalization or search.</li>
<li>Contributions to research or publications in areas such as graph-based modeling, recommendation systems, customer retention (e.g., churn prediction), or lifetime value estimation.</li>
<li>Experience with Graph AI algorithms and network discovery techniques, including analyzing complex relationships and patterns within data networks.</li>
</ul>
Where You'll Be:
<ul>
<li>We offer you the flexibility to work where you work best!</li>
<li>This team operates within the Eastern Standard time zone for collaboration. </li>
</ul>
Benefits:
🩺Health Insurance coverage.
⛱ Unlimited PTO policy.
📈 We grow, you grow: Stock Options Plan granted on Day 1.
🌅 401k Plan.
🐣 Paid family leave.
🕯 Compassionate Leave: 3-5 days each time the need arises.
🥘 A generous amount of CookUnity credits to enjoy our amazing meals, added to your account, monthly.
🧘🏽️‍♀️ Wellness perks: access to a nutritional coach and fitness subsidies to build a healthy lifestyle.
👩🏾️‍🏫 Personalized Spanish coach.
&amp;#x1F31F; Awesome opportunity to join a company that is looking to change how we eat and how chefs work!
🗓️ 5- year Sabbatical: After 5 years with CookUnity, you get a 4-week paid sabbatical.
#LI-Hybrid
Learn More About CookUnity
We believe great leadership starts with alignment on vision, values, and ways of working. To give you deeper insight into who we are and what we're looking for, we invite you to explore: CookUnity's Leadership Principles – The values and behaviors that guide how we operate, collaborate, and scale.
We hope this provides valuable insight into our culture and product vision. If this excites you, we'd love to connect!
Compensation All final pay rates will be determined by candidates experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.Pay Range for this position$150,000—$200,000 USD
If you're interested in this role, please submit your application and if we think you might be a fit, we'll get in touch with you. Thank you for your time!
CookUnity is an Equal Opportunity Employer. We are dedicated to creating a community of inclusion and an environment free from discrimination or harassment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, citizenship status, protected veteran status, genetic information, or physical or mental disability.

Senior Machine Learning Scientist, Recommendation and Search Systems

<h3>Job Description</h3>
Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
Job Summary: We are seeking an experienced and highly skilled Senior Scientist to lead and advance the suspension cell culture operations within our US Protein Department. This role involves overseeing complex cell line cultivation processes, optimizing production workflows, and mentoring junior scientists to ensure the delivery of high-quality biologics. The ideal candidate will have extensive expertise in cell biology or biotechnology, demonstrated leadership abilities, and a strong track record in a laboratory or biomanufacturing environment.
Key Responsibilities:
<ul>
<li>Lead and manage suspension cell culture operations, ensuring adherence to protocols while driving improvements in process efficiency, yield, and quality.</li>
<li>Troubleshoot and resolve complex technical challenges in cell culture processes, working cross-functionally to minimize production disruptions.</li>
<li>Design, execute, and analyze experiments to optimize cell line performance and bioprocess parameters.</li>
<li>Maintain comprehensive documentation, including experimental data, batch records, and technical reports, ensuring compliance with regulatory and quality standards.</li>
<li>Provide mentorship, training, and guidance to associate scientists and technical staff, fostering professional development and technical excellence.</li>
<li>Collaborate with cross-functional teams to review and update SOPs, protocols, and production records, promoting continuous improvement and data integrity.</li>
<li>Lead special projects and initiatives as assigned by department leadership, contributing to strategic planning and innovation.</li>
</ul>
Qualifications:
<ul>
<li>Master's degree or Ph.D. in cell biology, biotechnology, or a related scientific discipline.</li>
<li>Minimum of 5 years of relevant experience in suspension cell culture or bioprocess development, preferably within a CRO, CDMO, or biopharmaceutical environment.</li>
<li>Proven leadership and project management skills with the ability to mentor and develop junior staff.</li>
<li>Strong problem-solving abilities with a hands-on approach to troubleshooting and optimizing cell culture processes.</li>
<li>Excellent verbal and written communication skills, capable of collaborating across teams and presenting complex data effectively.</li>
<li>Demonstrated knowledge of laboratory data documentation systems, quality standards, and regulatory compliance.</li>
<li>Highly organized, proactive, and capable of managing multiple priorities in a fast-paced environment.</li>
</ul>
#GS
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Cell Culture Senior Scientist

<h3>Job Description</h3>
Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
Job Summary:
We are seeking a skilled and detail-oriented Protein Purification Associate Scientist to join our US Protein Department. This role involves executing downstream processing activities including protein purification, characterization, and documentation. The ideal candidate will have a solid background in biochemistry, biotechnology, or a related field, along with hands-on experience in protein purification techniques in a laboratory or manufacturing setting. 
Key Responsibilities:
<ol>
<li>Perform protein purification using a variety of chromatography techniques such as affinity, ion exchange, size exclusion, and hydrophobic interaction. </li>
<li>Prepare buffers and reagents following SOPs and project-specific protocols. </li>
<li>Characterize protein products using SDS-PAGE, Western Blot, HPLC, UV spectroscopy, BCA assay, and other analytical methods. </li>
<li>Maintain accurate, complete, and timely documentation of experimental procedures and results. </li>
<li>Troubleshoot and optimize purification protocols as needed to improve yield and purity. </li>
<li>Collaborate closely with upstream, analytical, and quality teams to ensure project timelines and specifications are met. </li>
<li>Assist in the revision and creation of SOPs, batch records, and technical reports. </li>
<li>Support additional tasks and projects as assigned by the department supervisor. </li>
</ol>
Qualifications:
<ol>
<li>BS/MS in Molecular Biology, Cellular Biology, Biochemistry or related field with 1+ years of relevant experience in protein purification/characterization.</li>
<li>Familiarity with AKTA systems and chromatography software is a strong plus. </li>
<li>Strong organizational and documentation skills, with attention to detail and data integrity. </li>
<li>Ability to work independently and as part of a team in a fast-paced environment. </li>
<li>Excellent problem-solving and communication skills. </li>
<li>Experience in a CRO or CDMO setting is preferred. </li>
</ol>
#GS
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Protein Purification Associate Scientist

<h3>Job Description</h3>
Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.
Genscript is seeking an Associate Scientist, Molecular Biology for our Production team in Piscataway, NJ. 
The estimated salary range is $60,000 - $70,000, depending on experience. 
Job Responsibilities:
<ul>
<li>Perform molecular biology techniques, with a focus on molecular cloning, to support production workflows.</li>
<li>Design and execute experimental plans to optimize processes and meet project goals.</li>
<li>Troubleshoot technical issues in production protocols and propose effective solutions.</li>
<li>Participate in continuous improvement efforts to enhance workflow efficiency and product quality.</li>
<li>Analyze experimental data, document results, and maintain accurate records in accordance with company standards.</li>
<li>Collaborate with cross-functional teams to achieve production targets and timelines.</li>
<li>Stay updated on industry trends and advancements in molecular biology techniques.</li>
</ul>
Job Requirements:
<ul>
<li>Master's or PhD degree in Life Sciences (e.g., Molecular Biology, Biochemistry, Biotechnology, or related field) is preferred.</li>
<li>Bachelor's degree in Life Sciences with relevant work experience will also be considered.</li>
<li>Prior experience in molecular cloning techniques (e.g., plasmid construction, restriction digestion, ligation, PCR, transformation) is highly preferred.</li>
<li>Hands-on experience in a laboratory or production setting is a plus.</li>
<li>Fast learner with the ability to quickly adapt to new techniques and protocols.</li>
<li>Strong critical thinking and problem-solving skills to address complex technical challenges.</li>
<li>Results-driven mindset with a focus on delivering high-quality outcomes.</li>
<li>Excellent organizational skills and attention to detail.</li>
<li>Ability to work independently and collaboratively in a team-oriented environment.</li>
<li>Location Requirement: Must be able to work on-site in Piscataway, NJ.</li>
</ul>
#LI-EB1
#GS
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Associate Scientist, Molecular Biology

<h3>Job Description</h3>
Job DescriptionJob Title: Aseptic Technician - 2nd Shift Job Description
The role of an Aseptic Technician involves washing glassware and medical components using designated equipment, performing aseptic cleaning and packaging of products, and working in an ISO-6 cleanroom environment while wearing required PPE. This position requires loading and unloading manufacturing equipment, packaging processed products according to specifications, monitoring process systems and equipment for proper operation, and performing daily and weekly preventative maintenance tasks. Technicians will participate in safety committees and adhere to all safety rules and regulations, accurately complete required documentation for all tasks, and clean, sanitize, and disinfect workstations with meticulous attention to detail and high work accuracy.
Responsibilities
<ul>
<li>Wash glassware and medical components using designated equipment.</li>
<li>Work in an ISO-6 cleanroom environment while wearing required PPE.</li>
<li>Perform aseptic cleaning and packaging of products.</li>
<li>Load and unload manufacturing equipment.</li>
<li>Package processed products according to specifications.</li>
<li>Monitor process systems and equipment for proper operation.</li>
<li>Perform daily and weekly preventative maintenance tasks; assist maintenance team as needed.</li>
<li>Participate in safety committees and adhere to all safety rules and regulations.</li>
<li>Accurately complete required documentation for all tasks.</li>
<li>Clean, sanitize, and disinfect workstations before and after use.</li>
<li>Perform additional tasks as assigned by supervisor.</li>
<li>Will be assigned different processes depending on the client/project they are working with.</li>
</ul>
Essential Skills
<ul>
<li>Aseptic technique and sterilization.</li>
<li>Experience in cleanroom operations.</li>
<li>Attention to detail and high work accuracy.</li>
<li>Industry experience of 1-2 years or relevant laboratory/research experience.</li>
<li>Knowledge of sterile processing.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Previous GMP and SOP experience.</li>
<li>Good documentation practices.</li>
<li>Basic computer skills for using the internal database.</li>
<li>Understanding of GMP.</li>
</ul>
Work Environment
The work environment involves working in ISO level 6 and 7 cleanrooms, requiring gowning for extended periods of 6-10 hours with breaks in between. This setting is a contract steam and dry heat sterilization provider serving the pharmaceutical, compound pharmacy, medical device, and biotech industries. The role promises growth potential within the company.
Pay and Benefits
The pay range for this position is $23.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Fairfield,NJ.
Application Deadline
This position is anticipated to close on Jul 15, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Aseptic Technician- 2nd Shift

<h3>Job Description</h3>
Job Description
Overview
Physician Affiliate Group of New York (PAGNY) is adding one Medical Physicist to the Radiation/Oncology group at NYC Health + Hospitals/Kings County. The Hospital is part of NYC Health + Hospitals. Kings County Hospital operates a world-renowned Level 1 Trauma Center, one of only three in Brooklyn, which serves 2.6 million residents of Brooklyn and Staten Island. 
The hospital maintains a strong academic affiliation with SUNY Downstate Health Sciences University To maintain its high healthcare delivery standards. 
The mission of NYC Health + Hospitals is to extend equally to all New Yorkers, regardless of the ability to pay comprehensive health services of the highest quality in an atmosphere of humane care, dignity, and respect. Their Values are built on a foundation of social and racial equity and has established the ICARE standards for all staff. 
NYC Health + Hospitals is the nation’s largest municipal health care delivery system in the United States. Dedicated to providing the highest quality health care services to all New Yorkers with compassion, dignity and respect, and regardless of immigration status or ability to pay. 
 
Responsibilities
<ul>
<li>
Collaborate with the chairman/physicians of the department on all aspects of running the service.
</li>
<li>
Perform annual physics program Audits in collaboration with chief therapist and chief of service
</li>
<li>
Calibrate and maintain patient management equipment in accordance with applicable regulations and protocols.
</li>
<li>
Perform all necessary acceptance testing and commissioning for all new patient management equipment.
</li>
<li>
Assure compliance with all radiation safety and protection regulations and requirements.
</li>
<li>
Actively participate in CQI/PI programs and activities/ACRO accreditation
</li>
<li>
Check patient charts to assure the prescribed delivery of radiation.
</li>
<li>
Teach resident physicians radiation therapy physics, and equipment operation and safety.
</li>
<li>
Provide technical input in design and construction of patient management rooms, and installation activities.
</li>
<li>
Assure the appropriate management of brachytherapy patients and radioactive sources.
</li>
<li>
Serve as consultant to hospital administration and other Departments.
</li>
</ul>
 
Qualifications
<ul>
<li>Masters degree or PhD in Medical Physicist </li>
<li>Certified in Medical Physicist – American Board of Radiology</li>
<li>Current NYS License as Medical Physicist - Therapeutic Radiology</li>
</ul>
Preferred Qualifications:
<ul>
<li>2 years or more experience preferred</li>
</ul>
Benefits include:
<ul>
<li>Competitive compensation package</li>
<li>10% 401K company contribution after one year of service</li>
<li>Choice of a three-tiered nearly FREE medical plan</li>
<li>Excellent dental insurance including orthodontics coverage</li>
<li>Generous paid time off program</li>
<li>Eligibility for loan forgiveness through the National Student Debt Forgiveness Center</li>
<li>Salary Amount: $245,000.00</li>
</ul>
Physician Affiliate Group of New York (PAGNY) is one of the largest multi-disciplinary groups in the country whose main purpose is to nurture and embolden the healthcare providers who take care of the most fragile and vulnerable patients in New York City. PAGNY is comprised of over 4,000 physicians and healthcare professionals who provide services to NYC Health + Hospitals (H+H), the largest public health system in the United States. Our practitioners are highly skilled professionals with outstanding credentials who deliver the highest level of quality healthcare to patients throughout New York City. 
Physician Affiliate Group of New York, P.C. (“PAGNY”) is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sex, sexual orientation, transgender status, gender dysphoria, national origin, age, religion, disability, military and veteran status, marital or parental status, citizenship status, genetic information or any other factor which cannot lawfully be used as a basis for an employment decision. We require applications to be completed online. 
If you wish to view PAGNY’s EEO policies, please click here. Please click here to view the Federal “EEO is the law” poster or visit <a href="https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm" target="_blank">https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm</a> for more information. 
The annual base salary listed complies with the New York City law on Salary Transparency in Job Advertisements. The annual base salary listed is for full-time employment and does not include bonuses/incentive compensation or benefits. Actual total compensation depends on many factors, including experience, specialties, historical productivity, and historical collections. Actual total compensation may differ.

Medical Physicist

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
The Associate Director, Statistics - Eye Care provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple disciplines to advance medicines to our patients.
This position will work a hybrid 3 day work schedule from one of the following AbbVie locations:
<ul>
<li>Irvine, CA</li>
<li>Lake County, IL&nbsp;</li>
<li>South San Francisco, CA</li>
<li>Florham Park, NJ</li>
</ul>
Responsibilities:
<ul>
<li>Provide statistical support for one or more clinical development projects through own efforts or those of a team. Lead/develop statistical strategy for project development and regulatory submission.</li>
<li>Provide statistical leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans.</li>
<li>Represent function/department on project team(s) to provide statistical input to compound/drug development and drive alignment with functional management. Partner with other functions (Clinical, Regulatory, Patient Safety, and GMA, etc.) to create development strategies for assigned projects.</li>
<li>Demonstrate extensive understanding of statistical concepts and methodology. Propose novel statistical methodological approaches to design of scientific studies. Provide sufficient detail to allow programming implementation. Ensure that all statistical analyses specified in scientific protocols and analysis plans are conducted appropriately.</li>
<li>Train and mentor staff on statistical methodology and operations. May supervise contract statisticians or junior statisticians. Gain expertise in innovative statistical methods. Assist functional leaders in recruiting qualified personnel and arranging training opportunities for professional development of staff.</li>
<li>Develop strategy for data presentation and inference. Ensure appropriate interpretation of statistical deliverables in collaboration with other functions. Collaborate in publication of scientific research. Ensure accuracy and internal consistency of reports and publications, including tables, listings, and figures.</li>
<li>Act as the liaison for statistical issues on AbbVie collaborative studies with CROs, academic institutions, government agencies, steering and/or data monitoring committees, joint ventures or licensing collaborators. Build external scientific connections which foster professional development and promote the reputation of the Statistics Department.</li>
<li>Ensure that all applicable regulatory requirements for work processes are met. Critically review regulatory submission documents. Participate in discussions with regulatory agencies as needed. Validate external statistical software to ensure compliance with SOPs and regulatory requirements.</li>
</ul>
Significant Work Activities:&nbsp;Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required
Qualifications 
<ul>
<li>MS (with 10+ years of experience) or PhD (with 6+ years of experience) in Statistics, Biostatistics, or a highly related field.</li>
<li>High degree of technical competence and excellent communication skills, both oral and written</li>
<li>Able to identify data or analytical issues, and assist with providing solutions by either applying own skills and knowledge or seeking help from others</li>
<li>Able to manage project timeline and quality of deliverables</li>
<li>Able to build strong relationship with peers and cross-functional partners to achieve higher performance. Highly motivated to drive innovation by raising the bar and challenging the status quo</li>
<li>Have strong leadership skills and experience in working/managing cross-cultural or oversea teams</li>
<li>Pharmaceutical or related industry knowledge required, including experience and understanding of drug development and life-cycle management in the regulated environment.</li>
<li>(SSG) Experience leading safety-related projects (eg, ISS, benefit-risk assessment, signal detection)</li>
<li>(GMA Stat) Competence in experimental and RWE study design, descriptive statistics, inferential statistics, statistical modeling, and statistical programming. Knowledge of methodologies for confounding control and bias minimization in observational studies preferred. &nbsp;</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;of this posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location, and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
​Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of any bonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's sole and&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

Associate Director, Statistics - Eye Care

<h3>Job Description</h3>
Job Description
Mount Sinai Services at NYC Health+Hospitals/Queens is seeking a Chief of Hematology/Medical Oncology for the Queens Cancer Center at the Queens Hospital Center. This Center of Excellence is the only state-of the-art comprehensive cancer center in the NYC Health+Hospitals System. This is an excellent opportunity to work in a mission-driven institution whose goal is to deliver exceptional care to the community.
The qualified candidate will join a collaborative team of medical oncologists/hematologists, radiation oncologists, and surgeons to deliver a wide array of oncologic and hematologic services. Offering a range of services, the Queens Cancer Center is strongly committed to caring for the whole patient and places a strong emphasis on providing patient-centered care. The Queens Cancer Center is a Commission on Cancer-designated Community Cancer Program employing a multidisciplinary approach to cancer research and treatment.
The ideal candidate will contribute to the leadership, direction and integration of the oncology/hematology service line at Queens Hospital Center/Queens Cancer Center and participate in the well-established and robust clinical research program. The research mission of the Queens Cancer Center is to advance the field of cancer/hematologic treatments and preventive measures and to facilitate the availability of these advancements to the community we serve.
Minimum Position Qualifications:
· Possess a medical degree (MD/DO) from an accredited university
· Has or has the ability to obtain a New York State Medical License
· Board Certified in Hematology and Medical Oncology
· Minimum of 5+ years of clinical/leadership experience
· Excellent communication, bedside manner, and organizational skills
· Strong work ethic and desire to participate in a team-oriented, collaborative mission-driven institution
All faculty have an academic appointment at The Icahn School of Medicine at Mount Sinai.
Responsibilities include:
<ul>
<li>Deliver direct clinical hematology/medical oncology care to patients at the Queens Cancer Center/Queens Hospital Center, including outpatient clinic and in-patient consultation.</li>
<li>Work collaboratively with leadership to optimize effective use of resources and operational performance of the Cancer Center.</li>
<li>Work collaboratively with leadership to create new patient services and define expectations and standards of patient care.</li>
<li>Actively participate in relevant committees and programs, including Cancer Committee and weekly Multidisciplinary Tumor Board Conference, contributing to the overall excellence in hematology/medical oncology services.</li>
<li>Demonstrate high standards of care through collaboration with physicians, surgeons, clinical professionals and staff.</li>
<li>Contribute to medical and surgical education programs, by participating in teaching residents and medical students.</li>
<li>Be committed to a professional and patient-centered care environment that places a high priority on clinical excellence.</li>
</ul>
The Mount Sinai Health System (MSHS) provides equal employment opportunity to all its employees and applicants for employment without unlawful discrimination on the basis of their actual or perceived race, creed, color, religion, national origin, sex, gender, gender expression, gender identity, age, disability, marital or parental status, sexual orientation, veteran, immigration, citizenship, or other protected status. EOE including Veterans and Disabled
Company DescriptionWho We Are: Over 42,000 employees strong, the mission of the Mount Sinai Health System is to provide compassionate patient care with seamless coordination and to advance medicine through unrivaled education, research, and outreach in the many diverse communities we serve. Formed in September 2013, The Mount Sinai Health System combines the excellence of the Icahn School of Medicine at Mount Sinai with seven premier hospital campuses, including Mount Sinai Beth Israel, Mount Sinai Beth Israel Brooklyn, The Mount Sinai Hospital, Mount Sinai Queens, Mount Sinai West (formerly Mount Sinai Roosevelt), Mount Sinai St. Luke’s, and New York Eye and Ear Infirmary of Mount Sinai. 
<h3>Company Description</h3>
Who We Are:\r\nOver 42,000 employees strong, the mission of the Mount Sinai Health System is to provide compassionate patient care with seamless coordination and to advance medicine through unrivaled education, research, and outreach in the many diverse communities we serve.\r\n\r\nFormed in September 2013, The Mount Sinai Health System combines the excellence of the Icahn School of Medicine at Mount Sinai with seven premier hospital campuses, including Mount Sinai Beth Israel, Mount Sinai Beth Israel Brooklyn, The Mount Sinai Hospital, Mount Sinai Queens, Mount Sinai West (formerly Mount Sinai Roosevelt), Mount Sinai St. Luke’s, and New York Eye and Ear Infirmary of Mount Sinai.

356 Science Jobs in New York, NY 10007, USA