job fairDiversityX | JobFairX
Job Seekers
For Employers
Sign In
JOB FAIRS NEAR ME
SEARCH JOBS
Calendar
JobAgentX
DiversityX | JobFairX
Job Seekers
For Employers
Sign In
JOB FAIRS NEAR ME
SEARCH JOBS
Calendar
JobAgentX
DIVERSITYX
DIVERSITYX
Job Seekers
JOB FAIRS NEAR ME
SEARCH JOBS
Calendar
INSTANTRESUME
Sign In
For Employers

Search Jobs

ServiceNow Lead
TechDigital Group
santa clara, ca
Compensation: 125.000 - 150.000
Top Skills' Details

• Ability to lead and own ServiceNow for global enterprise
• Dynamic Thought & People Leadership Skills... confident in ability to build awareness and generate "buy-in" with executives across other business units
• 15+ years of experience in Information Systems and Technology including an understanding of Service and Business Processes

Secondary Skills - Nice to Have

  • Design
  • Workflow
  • Cloud
  • Service desk
  • Service management

Job Description

  • Experience influencing stakeholders across the organization
  • Experience with large companies 7000+ emp
  • Experience working in a multicultural, international organization
  • Excellent written/verbal communication and presentation skills
  • Strong organizational, consultative, and conflict resolution skills
  • Good analytical skills, detail oriented, ability to effectively listen to and resolve customer issues
  • Good business acumen, ability to understand end to end business processes and work in a global environment
  • Solid teamwork and interpersonal skills to work well on cross-functional teams and at all levels of an organization
  • Relevance competency certification and education

Additional Skills & Qualifications

  • Drive the service and cloud platform vision across IT and the business
  • Manage and analyze business requirements / processes and define the right solutions
  • Evaluate system integration considerations to determine appropriate technology solutions.
  • Design, configure/code, tests and documents solutions based on user/business requirements.
  • Ensure SNOW platform is highly available, up to date and with high data quality
  • Continuously seeks ways to improve customer experience and users experience from SNOW platform
  • Explore ways to expand and integrate SNOW platform for new services
  • Integrate / maintain robust operation and project management processes
  • Follow up with stakeholders as needed
  • Employee Value Proposition (EVP)
  • Highly influential role aligned to a massive global instance of ServiceNow, a company fully invested in continuing the growth & utilization of the platform, and backing to create, design, build, implement, and lead the world's premier Service Management suite
#J-18808-Ljbffr
View On Company Site
Director of Supply Chain & Technical Sourcing - Propulsion
Slope
ms
Compensation: 125.000 - 150.000
A defense technology company is looking for a Director of Supply Chain to lead procurement and warehousing operations across multiple sites. This senior leadership role involves developing strategies to optimize supply chain performance and manage supplier relationships. Candidates should have over 10 years of experience in aerospace or regulated manufacturing and possess strong negotiation skills. A bachelor's degree in a relevant field is required, with an MBA preferred. The position is based in Mississippi and offers a competitive salary range.
#J-18808-Ljbffr
View On Company Site
Director Microbiology
Qpex Biopharma, Inc
san diego, ca
Compensation: 125.000 - 150.000

Overview

We are seeking an accomplished and strategic Director of Microbiology to lead our microbiology function within the Research and Discovery team. This role will play a critical part in driving the scientific and operational strategy for microbiological research supporting our Phase 1 clinical programs. The ideal candidate will have a Ph.D. in Microbiology or a related field, a proven track record in pharmaceutical industry settings, and experience managing high-performing teams in a fast-paced R&D environment.

Detailed Description

  • Lead microbiology research efforts that support early-phase clinical programs, including microbial characterization, mechanism-of-action studies, and assay development.
  • Drive the strategic direction of the microbiology function in alignment with overall R&D and corporate objectives.
  • Oversee daily operations of the microbiology lab, ensuring scientific rigor, compliance with GLP/GMP standards, and safety protocols.
  • Manage and mentor a team of scientists and research associates; foster a culture of innovation, collaboration, and continuous learning.
  • Partner with cross-functional teams (e.g., Regulatory, CMC, Clinical, QA) to ensure microbiological data supports preclinical and clinical milestones.
  • Serve as the microbiology subject matter expert in regulatory submissions and interactions with external partners, collaborators, and agencies.
  • Stay current with emerging trends and technologies in microbiology to inform strategic decision-making and maintain a competitive edge.

Qualifications

  • Ph.D. in Microbiology, Molecular Biology, or a closely related scientific discipline.
  • Minimum of 8 years of industry experience in microbiology within a pharmaceutical, biotech, or related setting, including leadership roles.
  • Proven experience supporting Phase 1 or early-stage clinical programs.
  • Demonstrated success in directing research and discovery activities.
  • Strong leadership and people management skills; experience building and developing high-functioning scientific teams.
  • Excellent analytical, problem-solving, and strategic thinking capabilities.
  • Effective communicator with the ability to present complex scientific information clearly to both technical and non-technical stakeholders.

Preferred Experience

  • Experience developing antibiotic combination therapies, especially beta-lactam/β-lactamase inhibitor programs or synergy-based approaches.
  • Deep understanding of resistance mechanisms in Gram-negative pathogens (P. aeruginosa, Acinetobacter, Enterobacterales) and approaches to overcoming them.
  • Direct experience working with non-tuberculous mycobacteria (NTM), including M. abscessus or M. avium complex models.
  • Proven success advancing antibacterial agents through preclinical and IND-enabling stages.
  • Experience with translational microbiology and PK/PD modeling to support dose selection.
  • Familiarity with regulatory expectations for microbiology data packages in IND/NDA submissions.
  • Background in molecular or genomic characterization of resistance and target validation.
  • Demonstrated experience managing CRO collaborations and multi-site external research partnerships.
  • Knowledge of BSL-2 and BSL-3 containment standards and microbiological safety practices.
  • Publication record or conference presentations in antimicrobial research or drug resistance mechanisms.

Additional Information

The base salary range for this full-time position is $210,000 - $250,000. Individual pay is determined by several factors, which include but are not limited to: job-related skills, experience, and relevant education or training. The range does not include the comprehensive benefits, bonus, long-term incentive, applicable allowances, or any additional compensation that may be associated with this role.

EEO

Shionogi Inc. is an equal opportunity employer supporting individuals with disabilities and veterans. All qualified applicants will receive equal consideration for employment opportunities based on valid job requirements without regard to race, color, religion, sex (including pregnancy), marital status, national origin, age, ancestry, citizenship, disability, genetic information, status as a disabled veteran, a recently separated veteran, Active Duty Wartime or Campaign Badge Veterans, and Armed Forces Service Medal Veterans, or any other characteristic protected by applicable law. It is the policy of Shionogi Inc. to undertake affirmative action for protected veterans and individuals with disabilities in compliance with all federal, state, and local requirements to recruit a diverse pool of protected veteran and individuals with disabilities applicants and to ensure that our employment practices are, in fact, non-discriminatory.

If you are qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request accommodations by calling or by sending an email to

#J-18808-Ljbffr
View On Company Site
JobAgentX
Land More Interviews with AI-Matched Jobs & a Tailored Resume
Try JobAgentX ↗
Director of Clinical Services – STRTP (In-Person)
Ruby's Place
castro valley, ca
Compensation: 125.000 - 150.000
A nonprofit organization is seeking a Head of Service (Clinical) in Castro Valley, CA. This in-person position requires a commitment to trauma-informed care, experience in mental health services, and a valid license in Psychology. The incumbent will conduct assessments, provide psychotherapy, and facilitate family reunification sessions. Excellent organizational and interpersonal skills are required. The role offers a salary of $115,000 per year with benefits including medical coverage and a matched retirement plan.
#J-18808-Ljbffr
View On Company Site
Visionary School Principal & Instructional Leader
Tolleson Union High School District # 214
avondale, az
Compensation: 125.000 - 150.000
A prominent school district in Arizona is seeking an experienced Principal to lead their high school. The Principal will be responsible for managing staff, overseeing curriculum and educational programs, ensuring compliance with academic standards, and fostering a positive school climate. Candidates must have a Master's degree in Education, significant teaching and leadership experience, and a valid Arizona principal certificate. This is a full-time position offering a supportive environment for educational growth.
#J-18808-Ljbffr
View On Company Site
Director of Data Management & AI Platform (Databricks)
Molina Healthcare
az
Compensation: 125.000 - 150.000
A healthcare organization is seeking a Director of Data Management to lead the enterprise data management strategy and modernization across healthcare domains. This senior leadership role involves managing core payer data, leading the Databricks lakehouse strategy, ensuring compliance with regulations, and developing cross-functional teams. Ideal candidates will have over 10 years of experience in healthcare data management and strong knowledge of data engineering practices. Compensation ranges from $117,731 to $229,576 annually, depending on location and experience.
#J-18808-Ljbffr
View On Company Site
Platform Engineering Director – Data & Analytics
Corning Inc.
charlotte, nc
Compensation: 125.000 - 150.000
A leading technology company is seeking a Director of Data & Analytics Platform Engineering to lead the development of enterprise-scale platforms. This role is critical for enabling data-driven decision-making across the organization. The ideal candidate will have extensive experience in platform engineering, a passion for innovation, and strong leadership skills. Responsibilities include defining roadmaps, leading teams, ensuring compliance with governance standards, and optimizing platform performance. This position supports immigration sponsorship and offers a competitive compensation package.
#J-18808-Ljbffr
View On Company Site
Head of Customer Success – DACH Region
NTT DATA Business Solutions
workfromhome, ok
Compensation: 125.000 - 150.000
Ein führendes internationales Technologieunternehmen sucht einen Head of Customer Success Management für die DACH-Region. Sie übernehmen die strategische, kaufmännische und operative Verantwortung und stellen nachhaltiges Umsatzwachstum sowie hohe Kundenzufriedenheit sicher. Ein fundiertes Verständnis für SAP-Operations kombiniert mit fließenden Deutsch- und Englischkenntnissen ist erforderlich. Die Stelle bietet flexible Arbeitszeiten und ein unterstützendes Teamumfeld.
#J-18808-Ljbffr
View On Company Site
Senior Product Manager — AI & Knowledge Discovery Platform
Scribd, Inc.
workfromhome, ca
Compensation: 125.000 - 150.000
A tech company specializing in document solutions is seeking a Senior Product Manager to lead the product strategy and vision. The successful candidate will have over 5 years of product management experience and a passion for improving user quality while achieving business goals. You will work collaboratively with design, engineering, and other departments to shape a seamless user experience. This role supports flexible working arrangements with occasional in-person attendance required.
#J-18808-Ljbffr
View On Company Site
JobAgentX
Land More Interviews with AI-Matched Jobs & a Tailored Resume
Try JobAgentX ↗
Remote Senior Product Manager, International Checkout & Growth
Stord Inc.
workfromhome, ga
Compensation: 125.000 - 150.000
A leading consumer experience company in Atlanta is seeking a Senior Product Manager to shape modern warehouse operations. The role involves collaborating with fulfillment teams and stakeholders to enhance operational metrics. Ideal candidates should have e-commerce SaaS experience, an analytical mindset, and a strong ownership mentality. Responsibilities include engaging with users, defining the product roadmap, and driving product adoption. This position offers the chance to significantly impact customer experience and business growth.
#J-18808-Ljbffr
View On Company Site
Program Director, Arts Internship
Enterprise for Youth
san francisco, ca
Compensation: 125.000 - 150.000

Founded in 1969, Enterprise for Youth empowers San Francisco youth ages 14 to 25 through a continuum of workforce development programs. We offer job-readiness training, paid internships, and access to employment opportunities—preparing youth with the skills and experience needed to thrive in the workplace and pursue their dreams. Our work centers equity, opportunity, and economic mobility for young people from under-resourced communities.

POSITION OVERVIEW

This is a mission-critical leadership role ideal for someone who thrives at the intersection of youth development, arts and culture, partnership building, and program strategy. The Program Director will cultivate relationships with San Francisco’s most respected arts institutions, inspire and support young people who are passionate about the arts, and contribute to a gold‑standard internship model that blends professional development with arts‑specific career exploration.

Enterprise for Youth is proud to be the California designee for the Arts Internship program—an exciting, multi‑year, multi‑million‑dollar investment to launch and grow a paid summer arts internship program for high school students in San Francisco. The Program Director, Arts Internship Programs will lead this high‑profile initiative from inception, scaling from 20 interns in Year 1 with planned growth of 20‑25% over 3 years.

The Program Director will be responsible for overseeing the entire lifecycle of an internship program, spanning from recruitment and onboarding of interns and partners, designing and implementing programming focused on workforce readiness, coordinating payroll processes, and supporting with data and evaluation.

KEY RESPONSIBILITIES

  • Lead the vision, design, and execution of the Arts Internship program in San Francisco.
  • Integrate the arts internship requirements into pre-existing programming with an explicit focus on arts‑specific offerings.
  • Manage and grow the annual program budget (over $1MM total), ensuring responsible use of funds, tracking outcomes, and aligning spending with goals.
  • Update, facilitate, and oversee a holistic curriculum blending general career readiness (resume writing, professional communication, networking, college essay writing) with arts‑specific career skills (arts management, arts administration, curation, production).
  • Responsible for hiring, training, and managing seasonal and permanent staff, facilitators, and interns, while supporting the Program Team’s leadership with payroll, HR onboarding, and data collection (pre‑ and post‑program and session surveys).
  • Oversee the development and execution of communications and social media strategies for programming, in close collaboration with Communications staff.

Partnership Development

  • Maintain, build, and nurture relationships with prestigious San Francisco arts and cultural organizations—such as SF MOMA, African American Shakespeare Company, 826 Valencia, A.C.T., SF Ballet, and more—to secure meaningful internship placements.
  • Act as a liaison and thought partner to internship host sites, ensuring alignment of youth experience with educational goals and partner needs.
  • Represent Enterprise for Youth and the Arts Internship at events, conferences, and convenings.

Youth Recruitment & Engagement

  • Develop and implement inclusive outreach and recruitment strategies to identify and enroll high school students—particularly those from communities underrepresented in the arts.
  • Create systems of support to help interns navigate their first workplace experience and explore pathways into college and careers in the arts.
  • Work closely with families, schools, and community‑based organizations to ensure strong wraparound support.
  • Serve as the primary contact for arts internships participating in regular reporting, convenings, and knowledge‑sharing.
  • Share outcomes, best practices, and innovations from San Francisco with other grantees across the country.
  • Ensure program fidelity with the core expectations and values while adapting to the unique context of San Francisco.

Administrative/General

  • Participate in agency‑wide meetings and events, special projects, and other tasks as assigned.
  • Support organization‑wide fundraising initiatives including development of grant proposals.

QUALIFICATIONS

Required

  • 5–8 years of progressive leadership experience in youth development, arts education, workforce development, or nonprofit program management.
  • A strong commitment to racial equity, youth empowerment, and expanding access to the arts.
  • Demonstrated success in managing complex projects, teams, and partnerships.
  • Experience working with high school students from diverse and under‑resourced backgrounds.
  • Excellent interpersonal, written, and verbal communication skills.
  • of professionalism and comfort representing Enterprise externally with funders, civic leaders, and partners.

Preferred

  • Knowledge of San Francisco’s arts and cultural landscape.
  • Background or training in arts education, creative youth development, youth workforce development, and/ or nonprofit arts management.
  • Experience with program evaluation and reporting for funders.
  • Proficiency in Salesforce or other CRM systems.

WORK CULTURE & BENEFITS

Enterprise for Youth offers a collaborative and inclusive work environment where creativity, initiative, and flexibility are valued. Benefits include:

  • Generous PTO (vacation, sick, personal, and holiday leave)
  • Health, dental, and vision insurance
  • 401(k) with employer match
  • Hybrid work model with an office in downtown San Francisco

HOW TO APPLY

Please submit your resume and a cover letter that outlines your interest in the role and your relevant experience to at . Applications must be submitted by October 17, 2025 .

Enterprise for Youth is an equal opportunity employer and welcomes applicants of all backgrounds. We strongly encourage people of color, LGBTQ+ individuals, and those with lived experience in under-resourced communities to apply. We comply with the San Francisco Fair Chance Ordinance and Chapter 12T of the San Francisco Administrative Code.

#J-18808-Ljbffr
View On Company Site
Director, Biopharma Business Development — Remote
Sentynl Therapeutics, Inc.
workfromhome, ca
Compensation: 125.000 - 150.000
A leading biopharmaceutical company is seeking a Director of Business Development based in San Diego, CA, or offering remote arrangements. This role requires 10+ years of experience in the biopharmaceutical industry, with at least 5 years in business development, along with strong negotiation skills and financial acumen. The Director will lead licensing and acquisition strategies, working closely with cross-functional teams to deliver transformative therapies to patients with rare diseases. Competitive salary offering between $180K to $230K.
#J-18808-Ljbffr
View On Company Site
Director of Port Ops Finance & Analytics — Hybrid Leader
Carnival Corporation & plc
miami, fl
Compensation: 125.000 - 150.000
A leading cruise line is seeking a Director of Port Ops Planning, Finance & Analytics based in Doral, Florida. This role requires strong financial expertise and leadership skills to manage port operations costs and reporting. The successful candidate will oversee a team, improve forecasting accuracy, and implement efficient systems for financial transparency. A hybrid work model is available, and the position includes benefits like health coverage, employee stock options, and travel privileges.
#J-18808-Ljbffr
View On Company Site
Senior Demand Planning Director - CPG, Equity Eligible
Getconfido
new york, ny
Compensation: 125.000 - 150.000
An innovative CPG tech company based in New York is seeking a seasoned demand planning professional to join their team. This role requires over 5 years of hands-on demand planning experience, where you'll collaborate with cross-functional teams including product and sales to optimize workflows and maximize platform value. This position is based at the NYC Headquarters with a competitive salary between $150,000 and $200,000, along with equity and benefits.
#J-18808-Ljbffr
View On Company Site
Associate Director, CDMO Alliances & Strategy
Otsuka Pharmaceutical Co., Ltd
princeton, nj
Compensation: 125.000 - 150.000
A global pharmaceutical company is seeking an Associate Director for CDMO Alliance Management in Princeton, NJ. This role involves managing relationships with Contract Development and Manufacturing Organizations, leading contract negotiations, and ensuring the alignment of partner activities with company goals. Candidates should have 8-12 years of experience in alliance management within the pharma/biotech industry and strong skills in risk management and communication. Competitive salary offered.
#J-18808-Ljbffr
View On Company Site
JobAgentX
Land More Interviews with AI-Matched Jobs & a Tailored Resume
Try JobAgentX ↗
Director of Pricing Automation & Strategy
Beacon Roofing Supply, Inc
greenwich, ct
Compensation: 125.000 - 150.000
A leading building products distributor is seeking a Director of Pricing Optimization in Connecticut to modernize B2B pricing through automation, analytics, and streamlined processes. The ideal candidate will have over 10 years of experience in pricing and revenue management and strong leadership skills. This position offers a competitive salary range of $180,000 - $290,000 annually, alongside benefits such as medical insurance and 401(k) matching.
#J-18808-Ljbffr
View On Company Site
Senior Director Supply Chain - USL
Upsher-Smith Laboratories
maple grove, mn
Compensation: 125.000 - 150.000
Senior Director Supply Chain - USL page is loaded## Senior Director Supply Chain - USLlocations: Maple Grove, MNtime type: Full timeposted on: Posted 20 Days Agojob requisition id: 9476**Job Summary**The Senior Director Supply Chain provides strategic leadership for material and supplier sourcing activities. The Senior Director is responsible for the procurement of materials, products and/or services in support of the sales plan and general business operations for Upsher-Smith.This position will lead strategy, operations, and governance for all outsourced drug substance and product manufacturing — ensuring supply reliability, regulatory compliance, cost optimization, and procurement excellence across the value chain. The ideal candidate is a seasoned manufacturing and supply chain leader who brings deep experience in external partnerships, technology transfers, and end-to-end procure-to-pay (P2P) management within a regulated pharmaceutical environment.**Essential Functions***Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.** Identifies and develops strategic direction for the Supply Chain function while overseeing end-to-end outsourced production for Upsher-Smith’s commercial and clinical products, ensuring uninterrupted global supply.* Lead technology transfers from Upsher-Smith’s internal manufacturing sites to external partners with efficiency, precision, and compliance.* Responsible for S&OP process include demand planning and supply planning to ensure USL achieves optimal inventory levels. Collaborates with commercial organization to achieve targeted service levels.* Utilizes S&OP to direct review of short-term (monthly) and long-term (quarterly & annual) forecast to minimize backorders, Failure to Supply, excess inventory and maintain high level of customer service.* Build and manage high-performing strategic relationships with key CMOs and CDMOs across global markets.* Partner closely with QA and Regulatory Affairs to ensure all external manufacturing and procurement partners operate in full compliance with FDA, EMA, PMDA, and other global health authority standards.* Oversee the external manufacturing and procurement budgets, ensuring fiscal accountability, cost optimization, and long-term value creation.* Develop and track key performance indicators (KPIs) across the external manufacturing and procurement ecosystems to ensure measurable results.* Establish and lead governance frameworks for partner oversight, including executive business reviews, performance scorecards, and contract negotiations.* Analyzes and plans, anticipating obstacles and resource constraints, and develops contingency strategies to meet organizational priorities.* Develops and manages Department budgets within annual approved plan.* Evaluates staff performance, provides coaching, guidance, direction, and facilitates short and long-term development.* Champion the development and optimization of the end-to-end procure-to-pay (P2P) process — from supplier selection, sourcing strategy, and contract execution to purchase order, payment, and supplier performance tracking.* Establishes departmental policies and procedures and manages team to those standards.* Makes strategic decisions in an environment of constantly changing priorities. Uses processes, tools and metrics to monitor, manage and improve performance, output and efficiencies to prevent critical deviations or delays from the business objectives.* Manages outside resources by planning and monitoring pricing trends, availability of supplies and supplier performance supporting quality and delivery expectations. Leads the team for resolution of invoice discrepancies and quality issues (SCARs) to ensure continued supply of quality materials.* Responsible for establishing and maintaining supplier relationships. Establishes supplier performance metrics through the development of strategic and tactical supplier management plans.* Negotiates supplier contracts to attain price, service advantages and supply continuation.* Recognizes legal consequences of supplier transactions and purchase orders.* Represents Procurement in the participation and contribution to Supplier Risk Management, Alliance Management, S&OP, and process change control.*The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time which reflects management’s assignment of essential functions.***Minimum Education, Experience, Skills*** Bachelor’s degree in Chemistry, Engineering, Pharmacy, Biology, Supply Chain, or a related discipline required. Advanced degree (MS, MBA, or PhD) strongly preferred.* 12+ years in supply chain/operations with 7+ years in pharma/biotech; 5+ years leading teams.* Proven leadership of end-to-end supply chains including CMOs/CDMOs, serialization, cold-chain, and distribution to U.S. channels.* Deep knowledge of GMP/GDP, DSCSA, FDA/ICH, and audit readiness.* Proficiency with ERP (e.g., SAP), planning tools, and serialization/EPCIS systems.* Strong financial acumen (COGS, PPV, inventory capitalization), contract negotiation, and vendor management.* Experience with generics, rare disease/specialty products, or temperature-sensitive therapies.* Global distribution/launch experience (EU/Canada/APAC) and trade compliance exposure.* Experience standing up S&OP in a high growth organization.Compensation Range:$192,000.00 - $308,000.00Upsher-Smith Laboratories, LLC is committed to providing equal employment opportunity to all applicants and employees according to all applicable equal opportunity and affirmative action laws, directives and regulations of federal, state and local governing bodies and agencies. In keeping with this commitment, Upsher-Smith Laboratories, LLC will recruit, hire, train and promote persons in all job titles, without regard to race, color, creed, religion, sex (including factors related to pregnancy or child birth), national origin, age, marital status, familial status, disability, sexual orientation, gender identity status with regard to public assistance, employment status, local human rights commission activity, status as a protected veteran, genetic information, atypical hereditary cellular or blood trait, or any other protected category.
#J-18808-Ljbffr
View On Company Site
Development Asset Lead, Senior Director
Biogen, Inc.
cambridge, ma
Compensation: 125.000 - 150.000
## **About This Role**The Senior Director, Development Asset Lead (DAL) is responsible for leading one or more preclinical or clinical-stage assets within Biogen’s development portfolio. This role provides strategic, cross-functional leadership to maximize asset value and ensure effective execution of the integrated asset plan (IAP). The DAL partners across research, development, and commercial functions to align scientific strategy, operational execution, and business considerations such as time, risk, and value. As leader of the asset team, the DAL drives development strategy, oversees progress toward key milestones, and represents the program within governance forums. This role reports to the **Head of Development Asset Leadership** and is responsible for guiding the most complex or late-stage assets, including programs approaching regulatory filing or major stage-gate decisions.## **What You’ll Do*** Lead development and continuous refinement of the integrated asset plan to maximize value and efficient execution* Define asset strategy, goals, timelines, and risk mitigation plans in partnership with program management* Drive cross-functional alignment and accountability for delivery of integrated development plans* Represent the asset at portfolio governance forums and senior leadership discussions* Integrate scientific, regulatory, and commercial considerations into development strategy and decision-making* Partner with Research, Development Units, and functional leaders to support portfolio planning and asset prioritization* Ensure effective program execution through collaboration with program management and functional teams* Foster a high-performing, collaborative team culture across the asset team* Contribute to departmental communities of practice to share insights and identify program synergies## **Who You Are**You are a strategic and collaborative leader with deep drug development expertise and the ability to guide complex, cross-functional teams. You bring strong scientific insight and business acumen to navigate development decisions and drive programs toward successful outcomes.## **Required Skills*** Bachelor’s degree required; advanced degree strongly preferred (MS, MD, PhD, PharmD, or MBA)* 13+ years of experience in pharmaceutical or biotechnology drug development* Proven leadership of cross-functional teams delivering complex development programs* Deep understanding of clinical development strategy and integrated asset planning* Strong knowledge of Minimum and Target Product Profile (MPP/TPP) concepts* Experience with IND-enabling activities, clinical pharmacology, and safety considerations* Working knowledge of global regulatory requirements for drug development and registration* Ability to translate emerging scientific and clinical data into development strategy* Strong executive communication and stakeholder management skills* Demonstrated ability to lead within a matrixed organizational environment## **Preferred Skills*** Prior experience leading cross-functional development programs or portfolio assets* Experience preparing programs for major development milestones or regulatory filings* Therapeutic area expertise within neuroscience or related disciplinesJob Level: Management**Additional Information**The base compensation range for this role is: $274,000.00-$377,000.00Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families *physical, financial, emotional,* and *social well-being*; including, but not limited to:* Medical, Dental, Vision, & Life insurances* Fitness & Wellness programs including a fitness reimbursement* Short- and Long-Term Disability insurance* A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)* Up to 12 company paid holidays + 3 paid days off for Personal Significance* 80 hours of sick time per calendar year* Paid Maternity and Parental Leave benefit* 401(k) program participation with company matched contributions* Employee stock purchase plan* Tuition reimbursement of up to $10,000 per calendar year* Employee Resource Groups participationWe are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. to learn more about our DE&I efforts.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission.## **Caring Deeply. Achieving Excellence. Changing Lives.****Scam Advisory:** Please be cautious of scam recruitment offers claiming to be from Biogen. All legitimate correspondence from a Biogen employee will come from a "@biogen.com" email account. Learn more about scams and fraudulent job postings .
#J-18808-Ljbffr
View On Company Site
Director-Manufacturing
Elanco Tiergesundheit AG
fort dodge, ia
Compensation: 125.000 - 150.000
Director-Manufacturing page is loaded## Director-Manufacturinglocations: Fort Dodge, IAtime type: Full timeposted on: Posted Todayjob requisition id: R **At Elanco (NYSE: ELAN) – it all starts with animals!****As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.** **At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.****At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.****Making animals’ lives better makes life better – join our team today!**## Your Role: Director – OperationsAs **Director – Operations**, you will lead biologics manufacturing operations at Elanco’s **Fort Dodge, Iowa** site—one of the company’s key production facilities supporting its global animal health portfolio. In this role, you will provide strategic and operational leadership for biologics production, overseeing large manufacturing teams while driving safety, quality, and operational excellence in a highly regulated environment.You will partner across manufacturing, quality, engineering, and process development to ensure reliable product supply, continuous improvement of manufacturing processes, and successful commercialization of new products.## Your Responsibilities• Lead biologics manufacturing operations to ensure the safe, compliant, and efficient production of high-quality biological products. • Develop and lead a large production organization, coaching frontline leaders and building high-performing teams. • Drive operational excellence initiatives, including LEAN and continuous improvement programs to improve efficiency, reliability, and cost performance. • Partner with Process Development and technical teams to support new product introduction, technology transfer, and validation activities. • Manage operational planning including departmental budgets, capital investments, and strategic initiatives to support site and business objectives.## What You Need to Succeed (minimum qualifications)• **Education:** Bachelor’s Degree in a scientific, engineering, or related discipline • **Experience:** Minimum of 5 years of experience in biologics manufacturing, production operations, or regulated pharmaceutical/biotechnology manufacturing • **Top Skills:** Operational leadership of manufacturing teams and expertise in regulated biologics or pharmaceutical production environments## What Will Give You a Competitive Edge (preferred qualifications)• Experience in animal health, biologics, vaccine, pharmaceutical, or biotechnology manufacturing • Demonstrated experience leading large teams in regulated environments (cGMP, USDA, FDA, or similar) • Experience implementing LEAN manufacturing, operational excellence, or continuous improvement initiatives • Strong experience with biologics production processes, fermentation, purification, or vaccine manufacturing • Experience managing significant operational budgets and capital investment projects## Additional Information• **Travel:** Up to 10% annually • **Location:** Fort Dodge, IA – Onsite## Physical Requirements### Occasionally (1–33%)Sitting, reclining, reaching (extended hands/arms), reaching across midline, handling, feeling, crouching/squatting, crawling, balancing, stooping, kneeling, jumping, stairs, ramp, ladder, lifting/lowering, carrying, pushing/pulling.### Frequently (34–66%)Standing, walking, fingering (pinch/pick).### Constantly (67–100%)Change of position.**Light Work (Level 2):** Exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently.Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected statusElanco Animal Health Incorporated (NYSE: ELAN) is a global leader in animal health dedicated to innovating and delivering products and services to prevent and treat disease in farm animals and pets, creating value for farmers, pet owners, veterinarians, stakeholders, and society as a whole. With nearly 70 years of animal health heritage, we are committed to helping our customers improve the health of animals in their care, while also making a meaningful impact on our local and global communities. At Elanco, we are driven by our vision of Food and Companionship Enriching life and our Elanco Healthy Purpose(TM) CSR framework – all to advance the health of animals, people and the planet. Learn more at .
#J-18808-Ljbffr
View On Company Site
Associate Director, CDMO Alliance Management
Otsuka Pharmaceutical Co., Ltd
princeton, nj
Compensation: 125.000 - 150.000
## **Position Summary:**The Associate Director, CDMO Alliance Management, GEM will serve as Otsuka’s representative and business partner toward our network of Contract Development and Manufacturing Organizations (CDMOs). This leader is responsible for the end-to-end lifecycle of partner management—from initial selection and complex contract negotiations to long-term strategic relationship building. The Associate Director ensures that the external manufacturing network is high-performing, risk-resilient, and fully aligned with Otsuka’s strategic business objectives.## ## **Key Responsibilities:****Contract and Partner Management**:* Serve as the central point of contact and business partner for CDMOs, ensuring alignment between partner actions and company goals.* Lead the identification and selection process for new CDMO partners and participate in all contract negotiations, including centrally managing the repository of all active agreements.* Contribute to the Governance and Business Review meetings with CDMO executive leadership to ensure long-term collaboration.**Performance Monitoring and Improvement:*** Define, set, and monitor key performance indicators (KPIs) to hold CDMOs accountable for delivery and quality.* Support comprehensive risk assessments focused on stable supply chains and quality assurance at partner sites.* Facilitate discussions and drive the implementation of improvement measures based on KPI performance data and identified risks.* Conduct business-side assessments during GMP audits led by the Quality Team to ensure commercial and operational viability.**Internal and External Coordination:*** Support the internal decision-making process regarding new CDMO selections and major capital investments.* Act as the lead for cross-departmental coordination when major incidents occur, ensuring rapid resolution while daily operations remain with functional teams.* Collaborate with internal departments to identify supply risks stemming from regulatory shifts, demand volatility, or manufacturing deviations, and lead the execution of countermeasures at the CDMO level.**Qualifications and Preferred Experience:*** Education: Bachelor’s degree in Science, Engineering, Business, or a related field (MBA or advanced degree preferred).* Professional Experience: 8–12+ years of experience in alliance management, strategic sourcing, or external manufacturing within the pharmaceutical or biotech industry.* Strategic Soft Skills: Proven ability to influence and collaborate with cross-functional stakeholders in a complex, matrixed organization.* Operational Excellence: Strong background in risk management, business continuity planning, and performance analytics (KPIs).* Communication: Exceptional negotiation and communication skills, with the ability to navigate sensitive partner relationships and internal executive reporting.* Proven ability to work with international colleagues.* Knowledge of CDMO landscape and manufacturing processes across one or multiple modalities (e.g., small molecule, biologics, sterile fill-finish, etc.).* Thorough knowledge of GMPs (CFR title 21, parts 210-211 and Part 600), along with EU, MHRA and other global health authority regulations.* Strong, proven supplier relationship management skills. Negotiation and contract management skills a plus**Competencies** **Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change. **Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business. **Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders. **Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka. **Respectful Collaboration -** Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals. **Empowered Development -** Play an active role in professional development as a business imperative.Minimum $169,222.00 - Maximum $253,000.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate’s job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.**Application Deadline**: This will be posted for a minimum of 5 business days.**Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.Come discover more about Otsuka and our benefit offerings; .**Disclaimer:**This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request.**Statement Regarding Job Recruiting Fraud Scams**At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.To ensure that you are communicating about a legitimate job opportunity at
#J-18808-Ljbffr
View On Company Site
Auto Service Store Manager — Lead, Earn Bonuses Up to $100K
Atlantic Coast Enterprises
delray beach, fl
Compensation: 125.000 - 150.000
An established industry player is seeking a dynamic Store Manager for a busy automotive service location. This full-time role involves leading a team to deliver exceptional customer service and drive sales. You will be responsible for managing daily operations, hiring and training staff, and fostering a collaborative environment. With a competitive salary and numerous benefits, this is an exciting opportunity to build a rewarding career in the automotive industry. If you are a motivated leader with a passion for customer service, this position could be your next great adventure!
#J-18808-Ljbffr
View On Company Site
Back Next

JobFairX

  • MilitaryX
  • DiversityX
  • HealthcareX

For Job Seekers

  • Calendar
  • JobAgentX
  • FAQ
  • Search Jobs

Employers

  • JobFairX
  • Contact us

Social

  • Facebook
  • Linkedin
©2026, DiversityX. All Rights Reserved.|Terms of Use|Privacy Policy

Land more interviews at your job fair

Let JobAgentX match you with employers and tailor your resume for each job you interview for.

See Matched Jobs