General Manager (Atkinson)

Atkinson Resort & Country Club, located in Atkinson, NH , is pleased to announce an excellent career opportunity for a General Manager ! We are seeking a driven individual who is eager to contribute and grow a fast‑paced hospitality-focused property organization. As part of Troon , you’ll contribute to a global leader in golf and community management. Compensation : $165,000 - $185,000 annually, based on experienced. General Purpose The General Manager (GM) is responsible for the overall leadership, operational execution, and financial performance of Atkinson Resort & Country Club. This role provides direct oversight of golf operations, food and beverage, facilities, maintenance, and administrative functions while ensuring an exceptional experience for members, guests, and the public. The GM serves as the senior on-site leader and primary liaison between Troon, ownership/board leadership, members, and the surrounding community. The ideal candidate is a hands-on, visible leader who balances strong hospitality instincts with financial discipline, team development, and operational accountability. Directs and oversees all aspects of club or facility including its activities and relationships between guests, associates and community. Has the ultimate responsibility for maximum guest satisfaction and financial performance. Essential Duties Prepares and monitors annual budget, revenue goals and expenses as well as generating various (weekly, monthly, etc.) business volume forecasts. Monitors monthly and other financial reports/statements on a daily, weekly and monthly basis for the facility and takes effective corrective action when necessary. Establishes basic personnel policy, initiates and monitors policies relating to personnel actions and training along with professional development programs. Ensures all Human Resources procedures and policies are followed by management staff. Develops, maintains and administers a sound organizational plan and initiates improvements as necessary. Maintains membership with the PGA and CMAA and other professional associations. Attends workshops and meetings to keep abreast of current information and developments. Oversees the care and maintenance of all the facility’s physical assets and each individual facility. Coordinates marketing programs to promote the facility’s services to potential customers. Ensures the highest standards for food and beverage service on property. Implements policies and procedures for multiple departments, including compliance of all company standards relating to quality of products and services. Responsible for interviewing, hiring, training, planning, assigning, and directing work, evaluating performance, rewarding, and disciplining associates; addressing complaints and resolving problems. Directly manages department members that may include, but is not limited to: Head Professional(s), Golf Course Superintendent(s), Tournament Coordinator, Director, Instruction, etc. Assures that effective orientation and training are given to each new associate. Develops ongoing training programs. Regular and reliable attendance. Education/Experience Bachelor’s degree (BA); or five to ten years related experience and/or training; or equivalent combination of education and experience. (Multi-course facilities may require more experience.) Physical Demands Regularly stands, walks and sits. Occasionally may climb, balance, stoop, kneel, crawl, crouch, tastes or smells. Regularly uses hands to finger, feel or handle, reaches with arms and hands, talks or hears. Occasionally lifts up to 50 pounds. Environment/Noise Occasionally works in outdoor weather conditions. Noise level is moderate. Certificates/Licenses CMAA member, GCSSA, or PGA/LPGA membership preferred This job description is not intended to be all-inclusive and may be modified by Troon at any time to meet operational needs. This employer is an Equal Opportunity Employer and complies with all applicable federal employment laws, including providing required notices to applicants. Benefits & Other Compensation This position includes eligibility for the following benefits, subject to applicable plan terms: Healthcare Benefits – Medical, Dental, and Vision coverage Retirement Benefits – 401(k) with employer match Time Off – Paid time off (PTO) and leaves of absence, in accordance with applicable law and eligibility criteria Eligibility for benefits and the specific terms, conditions, and offerings are governed by the applicable plan documents and company policies, which may be amended at the Company’s discretion. About Troon: Founded in 1990 and headquartered in Scottsdale, AZ, Troon is the world’s largest professional club management company, that specializes in services in golf, hospitality, and residential communities. With more than 900 locations in 45 states and 27 countries, Troon is a leading employer in hospitality. Guided by values that emphasize being infectiously energetic, consciously kind, and humbly prosperous, Troon offers professionals the opportunity to grow and succeed within a globally respected organization. Learn more at www.troon.com. J-18808-Ljbffr

General Manager - Phoenix AZ Stock Yards Collective (Phoenix)

General Manager - Stock Yards PhoenixApplylocations: Phoenix AZtime type: Full timeposted on: Posted Todayjob requisition id: R279609ARE YOU A CURRENT US FOODS EMPLOYEE? PLEASE APPLY DIRECTLY THROUGH OUR INTERNAL WORKDAY CAREER SITEJoin Our Community of Food People!Support Stock Yards to ensure the Plant(s) grow profitably and contribute to the company objectives and success. RESPONSIBILITIES * Set up and execute operational plan for Plant(s) within the stated strategies and policies of the Company. Provide input to Stock Yards local teams and Region Vice President Stock Yards related to strategies and policies that impact managed plant(s).* Responsible for driving the plant(s) to achieve and surpass sales, profitability, cash flow, yield, specification metrics, business goals and objectives. Accountable for direction, management, and performance.* Responsible for creating relationships to drive sales to and through the broadline division teams. Partner with Area and Region leadership to drive and support COP growth in local markets. Partner with leadership to grow regional and national chain account opportunities.* Give extensive input to the operational excellence of the plant in terms of operations, productivity improvement, and equipment utilization. Continuously guide local team to execution of the above and ensure that execution is according to company guidelines.* Responsible for the measurement and effectiveness of all processes, internal and external. Provides timely, accurate and complete reports on the operational metrics of the plant.* Ensure that solid financial reports are produced and reviewed as appropriate.* Responsible to achieve AOP and related performance initiatives.* Motivate and lead a high performance management team; attract, recruit, and retain required members of the management team not currently in place, provide mentoring and coaching to all members of the team as a cornerstone to achieving higher personal effectiveness and continuing career development.* Provide day-to-day leadership and management to a manufacturing organization that mirrors the adopted mission and core values of the company.* Spearhead the development, communication and implementation of effective growth strategies and processes.* Represent the company with customers, employees, the community and business partners. SUPERVISION * Direct Line for applicable functional Leads: Warehouse, Production, Finance, Admin, Purchasing and Sales* Dotted Line for applicable functional leads; Finance, HR, FSQA RELATIONSHIPS * Internal: Broadline Division and Corporate Management at multiple levels.* External: Various governing agencies such as USDA, FDA, local authorities, auditing companies, vendors and customers QUALIFICATIONS Education/Training: High School Diploma or GED required. Bachelor’s degree preferred (or equivalent experience) Related Experience: Minimum of 8 years’ experience in a Leadership role in Sales, Manufacturing or Production, preferably in a meat processing environment Knowledge/Skills/Abilities: Knowledge of FSQA, Strong P & L experience, Sales, and strong leadership skills.This role will also receive an annual incentive plan bonus and long-term incentive.Benefits for this role may include health insurance, pre-tax spending accounts, retirement benefits, paid time off, short-term and long-term disability, employee stock purchase plan, and life insurance. To review available benefits, please click here: https://www.usfoods.com/careers/benefits.html.LI-EG1Compensation depends on relevant experience and/or education, specific skills, function, geographic location, and other factors as applicable by law (for example: state or local minimum wage thresholds). The expected base rate for this role is between$135,000 - $210,000 J-18808-Ljbffr

Associate Director / Director, Nonclinical Regulatory Affairs (Paramus)

Summary NS Pharma is a highly focused, research-driven biopharmaceutical company working in rare diseases. We’re exploring the potential of cutting-edge science as a subsidiary of Nippon Shinyaku Co., Ltd. In Japan Nonclinical Regulatory Affairs serves as the nonclinical regulatory lead with primary accountability for FDA and EMA interactions, leading and executing regulatory activities across global development stages, including IND-enabling, clinical development, and registration phases. This role is highly regulator-facing and requires the ability to engage directly, credibly, and scientifically with FDA and EMA reviewers on pre-clinical/nonclinical topics, including complex and high‑risk regulatory issues. The role coordinates the development of pre-clinical/nonclinical regulatory documentation and responses associated with Health Authority interactions and ensures alignment of scientific positions across submissions. The Associate Director/Director serves as a key interface between nonclinical functions, global regulatory teams, and external experts (including KOLs), ensuring scientifically sound, risk‑based, and regulatorily aligned nonclinical evidence generation strategies that support efficient global drug development. This is a hybrid role that requires two days in the Paramus, NJ office. Responsibilities Health Authority Interactions Act as the regulatory subject matter expert for FDA and EMA especially for pre-clinical/nonclinical matters, working in close alignment with global regulatory leadership. Lead and coordinate nonclinical regulatory interactions, including Pre‑IND, Type A/B/C, IND/CTA, and NDA/BLA meetings, covering meeting strategy, material review/preparation, internal alignment, and submission logistics. Define, articulate, and defend regulator-facing pre-clinical/nonclinical positions, including scientific rationales and risk‑based justifications. Provide content and review pre-clinical/nonclinical briefing documents and written responses to FDA and EMA, including clinical hold and major safety‑related questions, and ensure timely fulfillment of meeting follow‑up commitments. Pre-clinical/Nonclinical Regulatory Strategy Develop and execute global pre-clinical/nonclinical regulatory strategies across development stages in alignment with program objectives and applicable regulatory guidance. Provide scientifically sound, risk‑based interpretation and justification of nonclinical study findings to support regulatory decision‑making, aligned with ICH guidelines. KOL and External Expert Engagement Participate in and support KOL and external expert engagements related to nonclinical safety, toxicology, and translational risk. Integrate external scientific input into regulator‑facing pre-clinical/nonclinical strategies and regulatory documentation. Cross-functional Collaboration Collaborate closely with nonclinical safety, pharmacology, DMPK, clinical development, and CMC teams to ensure alignment of nonclinical regulatory positions across key submissions and regulatory communications. Serve as a key regulatory interface across U.S., EU, and Japan‑based R&D organizations, enabling global alignment while supporting regional regulatory requirements. Experience (Required) Strong background in nonclinical safety (toxicology) within pharmaceutical or biotechnology drug development. Significant experience with early-stage programs from preclinical to phase 1/2 development Hands‑on experience leading or co‑leading FDA interactions from a nonclinical regulatory perspective. Experience preparing regulator‑facing briefing documents and written responses. Experience supporting or leading KOL and external expert discussions related to nonclinical safety. Solid understanding of GLP toxicology studies and their regulatory application. Preferred Qualifications Working knowledge of pre-clinical/nonclinical pharmacology and/or DMPK. Experience in rare disease preferred but not required Experience with FDA clinical hold responses and/or complex EMA safety discussions. Familiarity with ICH M3(R2) and ICH S‑series guidelines. Experience in rare disease and/or oncology drug development. Experience working in global development teams (U.S.–Japan collaboration preferred). Experience working with a regulator (FDA/EMA) as a reviewer. Education Ph.D., Pharm.D., D.V.M., D.A.B.T., M.D., or equivalent degree in toxicology, pharmacology, pharmaceutical sciences, or a related field. Typically, 10 years of experience in nonclinical drug development within the pharmaceutical or biotechnology industry, including significant experience in pre-clinical/nonclinical regulatory affairs. Experience supporting at least one NDA/BLA and multiple IND/CTA submissions preferred. Experience working with a regulator (FDA/EMA) as a reviewer is desired but not necessary Compensation and Benefits Discretionary Bonus Programs and Long-term Incentive Plan Retirement Savings 401k with company match Medical, Dental & Vision Insurance, Life and AD&D Insurance, Short- and Long-Term Disability Insurance, Flexible Spending Account, Health Savings Account, and Employee Assistance Programs Generous Paid Time Off, Sick Time & Paid Holidays including a paid Year-End Shutdown. Career Development, Progression and Training Flexible Work Arrangement Programs J-18808-Ljbffr

Vice President of Procurement (San Antonio)

Overview Vice President, Procurement – Location: San Antonio, TX Are you ready to build and lead a world-class procurement organization while transforming the future of procurement for a rapidly growing international food manufacturer? This is a rare opportunity to shape enterprise strategy, drive innovation, and leave a lasting impact on a growing organization. This executive leadership role reports directly to the Chief Supply Chain Officer and is responsible for developing and executing the enterprise procurement strategy across 30 manufacturing facilities . You\'ll oversee strategic sourcing, commodity risk management, supplier partnerships, category management, indirect procurement, and digital transformation initiatives that directly impact profitability and long-term growth. Responsibilities Develop and execute the company\'s enterprise procurement strategy aligned with growth, margin expansion, supply continuity, and shareholder value. Lead procurement across ingredients, packaging, contract manufacturing, MRO, logistics, capital equipment, indirect spend, IT, facilities, and corporate services. Build best-in-class category management and strategic sourcing capabilities. Drive commodity risk management strategies across agricultural inputs including grains, edible oils, sweeteners, dairy, cocoa, and related commodities. Deliver measurable cost savings, working capital improvements, supplier innovation, and EBITDA growth. Lead procurement transformation through analytics, AI-enabled decision tools, automation, and digital technologies. Develop strategic supplier partnerships that improve innovation, resilience, quality, and customer value. Partner closely with Operations, Finance, Commercial, Quality, Engineering, and R&D to support enterprise objectives. Build, mentor, and develop a high-performing procurement organization while fostering a culture of accountability, collaboration, and continuous improvement. Qualifications 15 years of progressive procurement, strategic sourcing, or supply chain leadership experience. Executive leadership experience within commercial baking. Strong background managing commodity-based supply chains and agricultural inputs. Demonstrated success delivering cost savings, supplier performance improvements, working capital optimization, and procurement transformation. Experience leading procurement for complex, multi-site manufacturing organizations with $500M managed spend. Bachelor\'s degree required; MBA or advanced degree preferred. Why This Opportunity? This is a rare opportunity to influence enterprise strategy for a large, growing food manufacturer where procurement is viewed as a strategic business partner—not simply a purchasing function. The Vice President will have executive visibility, significant organizational impact, and the opportunity to shape the future procurement strategy of a international manufacturing organization. J-18808-Ljbffr

Scientific / Medical Director, Global Hematology Pipeline, Medical Affairs (Florham Park)

Overview 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description The Medical Affairs organization provides patients, healthcare providers and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie products safely and effectively, throughout the product lifecycle and the patient’s journey. This position can be based at our Mettawa, IL, Florham Park, NJ, or South San Francisco, CA locations and will follow a hybrid schedule of Tuesdays-Thursdays in office. Responsibilities Supports the creation and execution of disease and asset strategies. Supports pipeline medical evidence generation strategy and execution including company sponsored studies, research collaborations and investigator initiated studies. Leads creation of early scientific narratives, messaging, and communications activities including congress planning, medical education, publication strategies and plans. Provides in-house medical expertise for the disease area and assets, coordinating appropriate scientific activities with internal and external stakeholders as they relate to ongoing programs. May participate in due diligence or other business development activity as required by program needs, and contribute to translational strategy in partnership with discovery colleagues. Acts as a medical interface and actively solicits insights and opinion through the development and execution of medical expert engagement strategies, partnering with clinical development, commercial, access, area and affiliate colleagues to ensure that broad perspectives both internally and externally are incorporated into strategies and plans as appropriate. Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information. Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource. May assist in the development of medical education programs, advisories, and symposia. Assists with the scientific review, development, approval, execution, and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities. May interact with and coordinate appropriate scientific and medical activities with internal stakeholders (i.e., commercial, clinical operations, discovery, statistics, regulatory) as they relate to on-going medical affairs projects. Serves as the scientific team interface for key regulatory discussions. Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information. Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource. Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities. Qualifications Scientific Director Qualifications: Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred. 5-7 years of experience in the pharmaceutical industry or equivalent 7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred. Experience in multiple myeloma and cell therapies highly preferred. Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols. Proven leadership skills in a cross-functional global team environment. Must possess excellent oral and written English communication skills. Medical Director Qualifications: Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D). Relevant therapeutic specialty in an academic or hospital environment preferred. Completion of residency and/or fellowship is preferred. 0-2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3 years of experience is preferred. Experience in multiple myeloma and cell therapies highly preferred. Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols. Proven leadership skills in a cross-functional global team environment Ability to interact externally and internally to support global business strategy. Must possess excellent oral and written English communication skills. Additional Information 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. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html J-18808-Ljbffr