<h3>Job Description</h3>
Required: experience leading manufacturing process involving CNC Machining and Welding.
The Director of Manufacturing Engineering plays an integral part in plant operations, special projects, OPEX, and is responsible for developing and maintaining motivated team and for supporting budgetary and production targets. The position has direct reports but must be able to work in partnership with Engineering, Quality, Supply Chain and Production in support of the departmental objectives.
<ul>
<li>The Manufacturing Engineering team is responsible for developing the standard processes used to manufacture, including selection and definition of all tooling, equipment, fixtures, and anything else related to the process. The team is responsible to ensure all production processes are defined using the standard work formats and templates as well as to create any training documents required to ensure production operators can perform the work in accordance with the documented standard.</li>
<li>Support the Operations team in the achievement of KPI’s related to shipping volume targets, on-time delivery, past due backlog, customer lead time, efficiency, utilization, and overtime premium expense.</li>
<li>Support and drive continuous improvements in manufacturing metrics including quality, yields, cycle time, productivity, and cost. Promote process improvement, and LEAN manufacturing methodologies and 5S processes.</li>
<li>Recommend changes in work practices to improve production standards and product quality.</li>
<li>Oversee the Operational Excellence (cost reduction) plans for the site. Coordinate and manage the projects at a tactical level and develop the project tracking tools to report out to senior management.</li>
<li>Coordinate, review, and present data for the purchase of capital equipment, tooling improvements to audiences at various levels of the company.</li>
<li>Author annual performance reviews and develop continuing education and advancement paths for entire department.</li>
</ul>

Director of Manufacturing Engineering

<h3>Job Description</h3>
Position Overview 
The Senior Medical Director will serve as the clinical lead for ophthalmology programs, with a focus on Ophthalmology indications. This role will oversee the design, execution, and analysis of clinical trials and play a key role in shaping development strategy. 
Key Responsibilities 
<ul>
<li>
Lead cross-functional study execution teams across clinical operations, clinical science, biometrics, regulatory affairs, CMC, pharm/tox, drug safety, commercial, and alliance management
</li>
<li>
Serve as medical monitor for clinical studies, ensuring patient safety and data integrity
</li>
<li>
Author and review clinical development plans, study protocols, amendments, informed consent forms, investigator brochures, INDs, annual reports, clinical study reports, and regulatory submissions
</li>
<li>
Organize and lead scientific advisory board meetings, engaging with external experts to inform program strategy
</li>
<li>
Identify and assess new clinical opportunities in collaboration with research and portfolio teams
</li>
<li>
Anticipate program risks and develop mitigation strategies
</li>
<li>
Represent the company at external meetings, conferences, and with regulatory authorities 
</li>
</ul>
Qualifications 
Education
<ul>
<li>
MD with residency training in Ophthalmology
</li>
</ul>
Experience
<ul>
<li>
8+ years of clinical ophthalmology research in the biopharmaceutical industry
</li>
<li>
Proven experience leading Phase I=III clinical trials
</li>
<li>
Gene therapy experience strongly preferred
</li>
<li>
Experience contributing to NDA/BLA/MAA submissions
</li>
<li>
Skilled in writing clinical research protocols, serving as a medical monitor, and interpreting clinical data
</li>
</ul>
Skills
<ul>
<li>
In-depth knowledge of ICH-GCP and FDA regulatory guidelines; international regulatory familiarity is a plus
</li>
<li>
Strong communication skills, both written and verbal, including public speaking
</li>
</ul>

Sr Director, Clinical Development (Ophthalmology)

<h3>Job Description</h3>
Job Title:- Senior Sourcing Manager
Duration: 6 Months
Location:- Foster City, CA
 
 JOB DESCRIPTION:
. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis, and cancer. Company operates in more than 35 countries worldwide, with headquarters in Foster City, California.
 
 KEY RESPONSIBILITIES:
The Senior Manager, Strategic Sourcing &amp; Supplier Management, will lead strategic sourcing activities and projects as assigned across multiple categories. This may include leading supplier selection projects, contract negotiation, project management, managing supplier or contract manufacturer relationships, providing strategic sourcing support for other members of the strategic sourcing team or new product development as well as purchasing and inventory management of components. You will have responsibility for indirectly leading and influencing others, bidding, selecting and managing multiple activities and projects. This position is based at the site in Foster City, CA, and is eligible for the GFlex program allowing remote work up to 2 days per week.
 
 ESSENTIAL FUNCTIONS:
• Lead or provide support to members of the strategic sourcing and supplier management team for projects and activities such as contract negotiations, supplier selection, planning and preparation for CMO and supplier business reviews.
• Lead/support strategic sourcing projects as required in developing and maintaining processes in areas such as contract management process, end to end supplier RFP process, establishing a process for managing supplier performance data or others as assigned.
• Lead/support preparation, reviewing, challenging, and tracking of RFPs/RFQs/RFIs for new business with external suppliers and in consultation with functional stakeholders (Manufacturing Operations, Technical Development. Quality Assurance, Analytical Operations etc.).
• Negotiate Confidentiality Agreements, Master Services Agreements and Work Orders.
• Responsible for procurement, purchase order placement and inventory management of components as required.
• Support annual business review meetings (BRMs) with assigned suppliers as needed.
• Lead and participate in Operational Excellence projects.
• Coordinate/lead meetings internally and with suppliers, publishes meeting minutes.
• Participates in solving issues of high complexity.
• Communicates issues to line manager and project teams in a timely manner.
• Support product team needs for the selection of suppliers to provide required supplies from development through commercialization.
• Collaborate and establish regular meetings with key stakeholders and partners to ensure outsourced needs are met.
• Organize and participate in teleconferences and face-to-face meetings with global suppliers; work closely with teams to establish agenda and keep track of key decisions.
 
QUALIFICATIONS
• 8+ years of experience in a pharmaceutical/biotech organization or relevant manufacturing environment and a BA or BS degree; an MA/MBA degree may be considered as 2 years of relevant experience and Ph.D. may be consider as 4 years’ experience.
• Prior experience leading manufacturing service providers and/or direct material suppliers.
• Strong computer skills and experience with an ERP system (SAP).
• Understanding of activities related to the CMC development of biopharmaceuticals.
• Knowledge of GMPs and associated regulations (21CFR parts 11, 210, 211, 820)
• Ability to lead cross functional teams
• Strong people management skills
• Experience negotiating contractual agreements
• Experience with combination Products preferred
• Strong verbal and written communication skills
• Ability to manage multiple programs/projects; sound organizational and time management skills
• Ability to develop concise presentations to convey complex issues to senior management
• Ability to work under uncertainty and to resolve conflict in a constructive manner
• Ability to solve highly complex problems through ingenuity and collaboration with subject matter experts and other key stakeholders
• Ability to work in a fast-paced environment
• Project management experience and/or certification are a plus
• This position may require up to 20% domestic and/or international travel
 
 CORE VALUES
• Integrity (Doing What’s Right)
• Inclusion (Encouraging Diversity)
• Teamwork (Working Together)
• Excellence (Being Your Best)
• Accountability (Taking Personal Responsibility)

Senior Sourcing Manager

<h3>Job Description</h3>
Arhaus was founded in 1986 on a simple idea: Furniture and décor should be sustainably sourced, lovingly made, and built to last. Today, we partner with artisans around the world who share our vision, creating beautiful, heirloom-quality pieces that can be used—and loved—for generations.
 
Arhaus is seeking a Senior Art Director to join their Creative team. The ideal candidate will be able to translate strategic insights into brand defining creative storytelling, have a high attention to detail, be able to drive creative innovation, and manage the creative design process. As a Senior Art Director, you'll be responsible for the concepting, execution and on-time delivery of high-quality creative materials across marketing channels with a focus on building the Arhaus brand, engaging customers, and driving business results.
 
Essential Duties &amp; Responsibilities: 
 
<ul>
<li>Lead and manage the creative design process from concept to completion, ensuring that all deliverables support Arhaus brand pillars, engaging customers, and driving business results</li>
<li>Partner with copywriters and marketing partners to brainstorm, design and develop creative work for various campaigns, including print ads, digital banners, social media content, and other marketing materials.</li>
<li>Design materials that enhance the Arhaus brand and the overall customer experience </li>
<li>Drive innovation with editorial storytelling approach that elevates customer engagement</li>
<li>Provide expertise that pushes the team to do the most effective and elevated work possible</li>
<li>Demonstrate exceptional creative concepting ability across multiple marketing channels, as evidenced by a diverse portfolio of work </li>
<li>Translate strategic insights into effective and highly creative ideas</li>
<li>Oversee and mentor designers, providing guidance and feedback to ensure their professional growth and the quality of their work.</li>
<li>Partner with Marketing leads to grow the business and explore new business opportunities</li>
<li>Manage multiple projects and deliverables simultaneously</li>
<li>Maintain accountability for overall quality of creative work</li>
<li>Conduct and participate in design reviews with a range of stakeholders across the organization</li>
</ul>
 
Requirements: 
<ul>
<li>Bachelor or Master’s degree in Advertising, Communications, Design, or other related field (or other relevant equivalent)</li>
<li>7+ years of experience in Art Direction </li>
<li>Fluent in Adobe Suite</li>
<li>Strong conceptual and visual storytelling skills, with an exceptional portfolio showcasing a range of campaign work..</li>
<li>Strong understanding of design principles, typography, color theory, and layout design.</li>
<li>Ability to balance big-picture creative thinking with hands-on design execution.</li>
<li>Strong project management skills and ability to function as project leader influencing others as well as individual contributor. Able to work well in cross-functional teams.</li>
<li>Strong leadership skills and the ability to mentor and guide junior team members.</li>
<li>Team Player – Must be able to manage and work with various members of creative, ecommerce and social teams</li>
<li>Must be organized and able to prioritize, multi-task and work independently </li>
<li>Fluent in English, with excellent communication, presentation, and social skills</li>
<li>Strong communication, presentation, and interpersonal skills including the ability to communicate design concepts appropriately to different audiences and varying levels of the organization</li>
<li>Excellent presentation, teambuilding and communication skills, as well as a strong customer service mentality, to build and maintain relationships</li>
</ul>
 
Arhaus is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Arhaus is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Arhaus are based on business needs, job requirements, and individual qualifications, without regard to race, color, sex, sexual orientation, gender identity, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Arhaus will not tolerate discrimination or harassment based on any of these characteristics. Arhaus encourages applicants of all ages.

Senior Art Director

<h3>Job Description</h3>
Job Title: Lab Technician /Agriculture Technician 
 Location: Kunia, HI 96759
 Duration: 3-6 Month Contract 
 Pay Range: $20 – $25/hr

Position Summary:
We are seeking entry-level Lab Technicians with an agriculture-related background (Agriculture, Botany, Crop Science, Horticulture, Entomology, etc.) to support lab-scale research and product development for Client. This is an excellent opportunity to gain hands-on experience in a lab environment working with cutting-edge agricultural research and technologies.

Key Responsibilities:
<ul>
<li>Assist in preparing, evaluating, and documenting lab-scale agricultural samples used in crop research, product testing, and development programs.</li>
<li>Support agronomic studies by conducting plant evaluations, seed treatments, pest/pathogen trials, or soil/media analyses as needed.</li>
<li>Operate, troubleshoot, and maintain lab and agricultural testing equipment for accurate results and process reliability.</li>
<li>Keep detailed lab notebooks, digital records, and reports in accordance with study requirements and protocols.</li>
<li>Conduct internet and literature reviews related to plant science, pest resistance, seed technology, or soil health to support R&amp;D projects.</li>
<li>Work closely with research scientists and other lab technicians to execute tasks that support both agricultural field trials and lab-based experiments.</li>
<li>Ensure compliance with EHS (Environmental, Health, and Safety) guidelines, SOPs, and company safety protocols in all lab and field activities.</li>
<li>Ability to manage multiple assignments, interface with research teams, agronomists, and technical supervisors, and deliver results in a timely manner.</li>
</ul>

Ideal Background:
<ul>
<li>Recent graduates or professionals with degrees or hands-on experience in:</li>
<li>Agriculture</li>
<li>Crop Science</li>
<li>Botany</li>
<li>Horticulture</li>
<li>Entomology</li>
<li>Plant Physiology</li>
<li>Agronomy or related fields</li>
<li>Interest in agricultural innovation, crop protection, or plant health research.</li>
<li>Comfortable working in both lab and field environments when required.</li>
<li>Detail-oriented, organized, and eager to contribute to real-world agricultural solutions.</li>
</ul>
 
This role is ideal for candidates who are passionate about sustainable agriculture, plant research, and contributing to global food security through science and innovation.
 
Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian's platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals. Dexian's brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit <a href="https://dexian.com/" target="_blank">https://dexian.com/</a> to learn more. Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.

Agriculture Technician

<h3>Job Description</h3>
Medical Director - Endocrinology (Obesity) Location: United States (Remote)
A growing biotech with an expanding late-phase pipeline is seeking an experienced Medical Director to lead clinical development efforts in endocrinology, with a focus on obesity. This is a high-impact role where your medical expertise will directly influence trial design, patient safety, and regulatory strategy-driving therapies that could transform lives.
Why This Role Stands Out
<ul>
<li>
Lead late-stage clinical trials with direct influence on strategy and execution
</li>
<li>
Work across disciplines to bring innovative treatments to market
</li>
<li>
Engage with key opinion leaders and regulatory authorities at the forefront of endocrinology
</li>
</ul>
What You'll Do
<ul>
<li>
Contribute to and execute the Clinical Development Plan for obesity programs
</li>
<li>
Serve as Medical Monitor, ensuring patient safety and data integrity in late-phase trials
</li>
<li>
Lead trial design and provide guidance to study teams, sites, and investigators
</li>
<li>
Collaborate on critical clinical documents including protocols, investigator brochures, and regulatory submissions
</li>
<li>
Interpret and communicate clinical data to drive decision-making
</li>
<li>
Partner with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, and Medical Affairs
</li>
<li>
Maintain strong external relationships with KOLs, clinical consultants, and investigative sites
</li>
</ul>
What You Bring
<ul>
<li>
MD (Board Certification or PhD in Endocrinology or related field preferred)
</li>
<li>
5+ years of industry experience (or equivalent academic/clinical background); candidates with less experience may be considered for an Associate Medical Director role
</li>
<li>
3+ years in clinical trial design and execution
</li>
<li>
Proven ability to manage safety monitoring, data analysis, and cross-functional collaboration
</li>
<li>
Excellent written and verbal communication skills
</li>
<li>
Strong leadership and problem-solving capabilities
</li>
<li>
Ability to work in a fast-paced, high-accountability environment
</li>
</ul>

Medical Director - Endocrinology (Obesity)

<h3>Job Description</h3>
The Maintenance Coordinator leads the mechanic department to ensure the timely and effective repair, maintenance, and optimization of all cutting and sewing equipment. This role is responsible for minimizing downtime, maintaining equipment reliability, and ensuring that parts and supplies are adequately stocked to support uninterrupted production. The Maintenance Coordinator manages the department through training, communication, and organization, while driving performance toward the facility’s key performance indicators (KPIs). The position provides hands-on technical support and supervision to uphold operational excellence, quality standards, and safety across the facility.
<ul>
<li>Bachelor’s degree or equivalent experience required.</li>
<li>Minimum of 10 years working in a manufacturing environment, with at least 5 years in a management position.</li>
<li>Preferably proficient and knowledgeable in cutting and sewing machines, including but not limited to:</li>
<li>Cutting Equipment: Lectra, Gerber, Yi systems</li>
<li>Sewing Equipment: Single &amp; multi-needle lockstitch, chain stitch, bar-tack, buttonhole, felling machines, irons</li>
<li>Ongoing training in industrial equipment maintenance and technologies required.</li>
<li>Must read, write, and speak English fluently.</li>
<li>Bilingual in Creole and/or Spanish preferred.</li>
</ul>

Maintenance Coordinator

<h3>Job Description</h3>
Onward Search Education is a specialized education staffing and talent solutions company that helps educators, therapists, and school health professionals find top jobs with the nation's top schools. We're currently seeking a Physical Therapist to join a school team in Lake County, IL.
This role offers the opportunity to make a meaningful impact on student mobility, independence, and physical development within a supportive educational setting.
 
Position Details:
<ul>
<li>Position: Physical Therapist</li>
<li>Location: Lake County, IL</li>
<li>Duration: 2025/2026 school year</li>
<li>Schedule: Monday–Friday, school hours</li>
<li>Student Population: PreK– middle school</li>
</ul>
 
Responsibilities:
<ul>
<li>Deliver direct physical therapy services in accordance with students’ IEP goals.</li>
<li>Conduct evaluations and monitor motor function and physical development.</li>
<li>Collaborate with educators and related service providers to promote accessibility and inclusion.</li>
<li>Maintain accurate documentation and ensure compliance with special education requirements.</li>
<li>Participate in IEP meetings and contribute professional insight on accommodations and interventions.</li>
</ul>
 
Qualifications:
<ul>
<li>Master’s or Doctoral degree in Physical Therapy.</li>
<li>Active Illinois Physical Therapy license.</li>
<li>Prior school-based experience preferred.</li>
<li>Strong communication, documentation, and interdisciplinary collaboration skills.</li>
</ul>
 
What We Offer:
<ul>
<li>Competitive pay and benefits package.</li>
<li>Access to a wide network of schools and districts for diverse placement options.</li>
<li>Streamlined hiring process to get you started quickly.</li>
<li>Ongoing communication and advocacy throughout your placement.</li>
<li>Personalized support from dedicated recruiting professionals.</li>
<li>Opportunities for professional growth and development.</li>
</ul>
 
Why Apply: If you’re passionate about creating positive change and supporting students’ success, this is the opportunity for you! Work alongside a dedicated team of educators and support staff, helping students reach their full potential.
 
Ready to join us? Apply today – we can’t wait to hear from you!

Physical Therapist [79738]

<h3>Job Description</h3>
OIA Global Since its founding in 1988, OIA Global has grown into a $1 billion world-class logistics and packaging company that employs over 1,300 professionals in 28 countries. Our knowledge, solution design experience, and installed infrastructure give our customers the confidence and capability to extend their supply chains from emerging production areas to key commercial markets.
 
Summary: Senior Export Coordinator
As a Senior Export Coordinator, you will review and process export transactions, including all related activities, for one or more major accounts. You will provide excellent and timely customer service. Day to day duties will include preparation of freight quotes, tracking of freight and processing invoices. The Export Agent maintains a strong attention to detail, while ensuring compliance with all government export and transportation regulations.
 
Duties and Responsibilities:
<ul>
<li>Promote a positive relationship with the client by ensuring excellent and timely customer service at all times.</li>
<li>Receive, review, and process high-volume and/or complex export transactions for client(s), including booking, documentation, and billing.</li>
<li>Process data through the Company’s system and submit shipment information to various government agencies as required.</li>
<li>Check the shipments in the warehouse as needed to ensure that the shipping documents correspond to the actual shipments.</li>
<li>Process bills of lading for outgoing shipments.</li>
<li>Track and review shipping status to ensure timely departure/delivery of freight; enter milestone data.</li>
<li>Ensure shipments of hazardous materials are checked and processed in accordance with all applicable regulations under the International Air Transport Association and, Code of Federal Regulations.</li>
<li>Create quotations for individual shipments, including estimating prices for the shipper, and selecting transportation companies to use.</li>
<li>Departmental Training and Development.</li>
<li>Departmental Leadership and Support.</li>
</ul>
Required Skills and Abilities:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
<ul>
<li>Proficiency in Microsoft Office, particularly Excel, Word and Outlook.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Ability to pay close attention to detail.</li>
</ul>
Education and Experience:
<ul>
<li>Minimum 5 years relevant work experience handling full-cycle export transactions in the freight forwarding industry.</li>
<li>Familiarity with CargoWise’s Enterprise system a plus.</li>
</ul>
Physical Requirements:
<ul>
<li>Prolonged periods of sitting at a desk and working on a computer</li>
<li>The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</li>
</ul>

Senior Ocean Export Coordinator

<h3>Job Description</h3>
Location: Upstate NY (Relocation from Canada welcome!)
 
Please note: We are only considering W2 candidates at this time. Applications from third-party vendors or C2C arrangements will not be considered.
 
ADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Headquartered near San Francisco, California, and with operations in the Eastern and Western US, Canada and Singapore, our company is involved in almost every facet of global pharmaceutical and biotechnology facility design and process engineering and quality system projects.
 
ADVENT's services include process engineering, automation engineering, project engineering, facility/system design, start up and commissioning, validation and compliance consulting for distinguished and successful biotechnology and pharmaceutical manufacturing companies.
The successful candidate will work with a group of engineers involved in the design, automation, commissioning and start-up of various processes, systems and facilities. A combination of strong technical aptitude, automation engineering skills and technical writing are the desired skill set.
 
This is an outstanding opportunity to join our growing team!
 
&amp;#x1F4BC; Full-Time | Onsite
About the Role:
We’re looking for a detail-driven HEPA Certification Coordinator to manage and maintain HEPA filter compliance across our pharmaceutical cleanroom facilities. You’ll work with internal teams and external vendors to ensure air quality standards are met and documented.
 
What You’ll Do:
<ul>
<li>Oversee HEPA filter certification and scheduling</li>
<li>Ensure compliance with GxP and industry standards</li>
<li>Coordinate with vendors and internal teams</li>
<li>Maintain accurate documentation and reports</li>
<li>Support investigations and continuous improvement</li>
</ul>
 
What You Bring:
<ul>
<li>3+ years in pharma manufacturing with cleanroom experience</li>
<li>Knowledge of HEPA standards, GxP</li>
<li>Strong communication and organizational skills</li>
<li>Bachelor’s in engineering, Science, or related field</li>
</ul>
 
Perks &amp; Benefits:
<ul>
<li>Competitive salary</li>
<li>Full health, dental, vision, and retirement benefits</li>
<li>Tuition reimbursement, PTO, and more</li>
</ul>
 
&amp;#x1F4E9; Ready to make an impact? Apply now and help us maintain the highest standards in cleanroom air quality.

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