Pharmaceutical jobs in New York, New York - Page 2Crear alertas

TITLE: Senior Director, Pharmacy Services DEPARTMENT: Pharmacy Services REPORTS TO: Chief Operating Officer (COO) JOB SUMMARY The Senior Pharmacy Director is responsible for the overall operations, direction, leadership, and management of Saint Joseph's Medical Center and Saint Vincent's Medical Center Department of Pharmacy. The Senior Director of Pharmacy works collaboratively with institution leadership to implement and maintain pharmacy progress, best practices, and financial operations. The Senior Director of Pharmacy directs pharmacy personnel, ensures quality assurance, maintains distribution and technology systems, and provides fiscal oversight of Pharmacy cost center budgets and related forecasting of financial pharmacy initiatives. DUTIES AND RESPONSIBITITIES • Collaborating with healthcare executives to foster and build relationships aimed to align interdisciplinary services with initiatives such as quality metrics and financial performance., • Provides direction and coordinates day-to-day operations., • Advancing patient care services through the promotion of pharmacy best practices by the creation and adoption of emerging technologies and innovative services., • Oversees and adjusts all workflow systems processes, as needed, to meet operational requirements., • Monitors, analyzes and reports on established performance metrics on a regular basis., • Participates in staff meetings, planning meetings and other meetings as needed., • Actively participates as a member of the Pharmacy & Therapeutics Committee and other various committees that impact medication management., • Develops and implements management reporting systems for statistical and quality control documentation (metrics and dashboard oversight)., • Oversees the work of all pharmacists, pharmacy technicians and clerks including recruiting, hiring, disciplinary action, scheduling, team building, performance evaluation, etc., • Assures that all pharmacy staff are appropriately trained to perform necessary functions., • Ensures compliance with all licensure and governing body requirements including, but not limited to: Board of Pharmacy, Office of Pharmacy Affairs (340B Program), The Joint Commission (TJC)., • Maintains responsibility for assuring that the Department of Pharmacy is operating in accordance with the laws and regulations set forth by accrediting organizations and regulatory agencies., • Responsible for managing the operational budget of the Pharmacy departments., • Develops policies and procedures as they relate to medication management., • Maintains responsibility for assuring that the Department of Pharmacy is adequately serving the patients and clinical staff of the institution., • Maintains clinical pharmacy competencies commensurate to the Director of Pharmacy position ensuring the ability to train, education, and evaluate pharmacy staff for optimal oversight of the medical center's pharmacy program., • Develops and implements innovative systems and procedures designed to increase the efficiency, effectiveness and scope of pharmacy services., • Maintains responsibility for the financial management of the Department of Pharmacy hospital formulary., • Develops and implements training for staff to keep them abreast of advances in pharmacy technology and pharmacology., • Maintains control over the requisitioning and dispensing of all drugs and pharmaceutical supplies., • Attends conferences, seminars, and meetings as required. JOB REQUIREMENTS • NYS Registered Pharmacist, • Graduation from an accredited College of Pharmacy, • Eight (8) years of satisfactory, full-time experience as a Licensed Practicing Pharmacist, of which at least four (4) years shall have been in an administrative, managerial and supervisory capacity in a Hospital Pharmacy, • Ability to formulate, develop and implement pharmacy service programs and to direct and supervise pharmacy service personnel and staff activities, • Ability to work effectively with administrative staff, medical and nursing personnel, • Possession of a Master's degree in Hospital Administration; Business Administration; or Doctor of Pharmacy PHYSICAL AND MENTAL FACTORS Physical: Computer accessibility. Walking throughout Hospital areas and clinics, moving medications Mental: Must be able to effectively communicate with management and staff Salary Range: $205K-$215K Saint Joseph’s Medical Center is an equal opportunity employer.

About the Role: We are seeking a dynamic Senior Account Executive with a strong background in healthcare communications to join our team. This role is ideal for someone who thrives in a fast-paced agency environment and is passionate about delivering impactful promotional medical education and pharmaceutical advertising solutions. Key Responsibilities: • Serve as a primary point of contact for client accounts, ensuring exceptional service and strategic alignment with client objectives., • Manage day-to-day project execution across digital and print channels, including timelines, budgets, and deliverables., • Collaborate with internal teams-creative, medical, and digital-to develop and implement innovative campaigns that meet regulatory and brand standards., • Support the development of promotional medical education programs, including advisory boards, speaker training, and congress activities., • Contribute to strategic planning and provide insights that drive client success and account growth., • 3-5 years of experience in an agency setting focused on promotional medical education or digital/print pharmaceutical advertising., • Strong understanding of pharmaceutical marketing regulations and best practices., • Excellent project management skills with the ability to handle multiple priorities., • Exceptional communication and relationship-building skills. Desired Skills and Experience About the Role: We are seeking a dynamic Senior Account Executive with a strong background in healthcare communications to join our team. This role is ideal for someone who thrives in a fast-paced agency environment and is passionate about delivering impactful promotional medical education and pharmaceutical advertising solutions. Key Responsibilities: -Serve as a primary point of contact for client accounts, ensuring exceptional service and strategic alignment with client objectives. -Manage day-to-day project execution across digital and print channels, including timelines, budgets, and deliverables. -Collaborate with internal teams-creative, medical, and digital-to develop and implement innovative campaigns that meet regulatory and brand standards. -Support the development of promotional medical education programs, including advisory boards, speaker training, and congress activities. -Contribute to strategic planning and provide insights that drive client success and account growth. -Ensure compliance with industry guidelines and client-specific requirements. Qualifications: -3-5 years of experience in an agency setting focused on promotional medical education or digital/print pharmaceutical advertising. -Strong understanding of pharmaceutical marketing regulations and best practices. -Excellent project management skills with the ability to handle multiple priorities. -Exceptional communication and relationship-building skills. -Proficiency in digital platforms and familiarity with emerging trends in healthcare communications. Why Join Us? We combine scientific expertise with creative innovation to deliver meaningful solutions for our clients. You'll work with a collaborative team dedicated to advancing healthcare communications and making a real impact.

Title:- Medical Information Specialist II (Clinical) Location: Morristown , NJ 100% Remote Duration: Contract until Oct 2026 (Possible extension) Description: Medical Information Specialist will: • Manage and maintain scientifically accurate local and global response documents for Sanofi Consumer Healthcare (CHC) products • Support the team’s understanding and compliance with policies, procedures, and processes., • Leverage regional/local insights on content usage, to meet the need for new or updated content., • Look for efficiencies to optimize content creation and update., • Provide business stakeholders with actionable insights and recommendations based on knowledge of product/therapeutic area as well as customer interactions. Contribute to the identification and implementation of novel channels for dissemination of medical information. Scope of Responsibility Management Responsibilities: • Lead and manage direct reports within the US Medical Information team, providing mentorship, performance oversight, and strategic guidance to ensure high-quality medical content and inquiry handling., • manages and maintains scientifically accurate response documents for Sanofi Consumer Healthcare (CHC) products • localizes global scientific response documents (GSRDs) with local content as needed, • writes and reviews global medical information content., • ensures the quality and integrity of responses provided to health care professionals, patients, and consumers in the US and globally. • manages inquiries and responds to local and global escalations., • assists in review of medical compendia and contributes to NDA annual reports., • provides summaries of literature searches for NDA product annual reports for FDA submissions., • interacts with contact center team(s) and coordinates meetings, trainings and exchange as needed • performs regular contact center quality checks in US, • supports training of support function staff and outsourced partner(s) as needed., • executes processes and participates in cross functional projects by contributing with product knowledge and intra-departmental relations, along with editing, writing, database, and file management proficiency. • collaborates with Medical, Regulatory, R&D, and Quality colleagues across the company to ensure appropriate responses using a state of art tracking and repository systems. • performs literature research and critically evaluate scientific data., • performs ongoing literature reviews and extracts complex data from scientific literature and arranges the data in an organized format. • ensures consistent and accurate product information., • serves as a knowledge resource for all colleagues located around the world., • suggests improvements or updates to existing policies, procedures, work instructions, and work guides used in internal operations and with external vendors as needed. • Provides medically sound responses to complex inquiries forwarded from outsourced partner(s) and in-house sources and proposes solutions to identified issues. • Contributes to the identification and implementation of novel channels for dissemination of medical information, like chat bots, live chats, Apps etc. Education • Science degree, • Advanced degree (PharmD, PhD, MD, MS) in a health care related field desirable. Required knowledge and/or experience • Minimum of 3 years of related technical experience with at least 1 year management in a Medical Information or equivalent department within the Pharmaceutical /Consumer Health Industries • At least 1 year performing Medical Information related writing scientific response documents, responding to medical and non-medical related consumer healthcare product escalations. Knowledge of basic medical information requirements and compliance procedures and ability to understand consumers point of view. • Knowledge of Sanofi products, product labeling, and Federal Regulations pertaining to OTC and pharmaceutical products a plus. • Knowledge of Sales Force CRM and Veeva Vault Medical/RIM a plus MINAKSHI SANGWAN Recruiting Lead - US Recruitment O 732-339-3518 E W ___

PRIMARY FUNCTION • Associate Director/Director plays a key role as clinical technical lead on global Phase I-III and other clinical pharmacology centric projects, • Serves as a team member supporting multiple facets of Clinical Pharmacology, including study design, PK and PK/PD analyses, and overall drug development support. This position is also the scientific and medical/clinical liaison between internal teams and external groups such as clinical operations, vendors (CROs, central laboratories, etc.), investigators, medical monitors, regulatory authorities, medical affairs, commercial, Key Opinion Leaders, Advisory Boards, • The candidate will have an excellent knowledge of Clinical Pharmacology principles, such as PK, PK/PD, drug metabolism, drug-drug interactions, PBPK, PopPK modeling and E-R analysis. Provides peer-reviewed interpretation of clinical pharmacology data and incorporates appropriate analyses into reports required for regulatory submissions MAJOR RESPONSIBILITIES AND DUTIES • Accountable and responsible for the Clinical Pharmacology support for the HUTCHMED global portfolio, • Provide scientific insights that drive global clinical development decisions and support global regulatory submissions, • Responsible for ensuring appropriate Clinical Pharmacology representation on drug/ dosage form development and clinical teams and provision of PK/PD expertise and leadership to a project, • The incumbent will complete assigned work in a resourceful, self-sufficient manner and will be able to create alternative approaches to achieve desired results if needed, • Responsible for ensuring planning and direction of Clinical Pharmacology components of clinical programs (including clinical development plan/life cycle plan) and studies (including synopsis and protocol preparation; clinical phase oversight, reporting), • Responsible for ensuring leadership of multifunctional study team to design, deliver and report the assigned clinical pharmacology studies and ensuring overall scientific accountability for the designated studies, • Responsible (with members of Clinicians and Statisticians) for ensuring appropriate dose-finding strategies during clinical drug development that will ensure optimal doses in first in human studies and dosage regimens in patients, • Responsible for summarizing and interpreting results of pharmacokinetic, pharmacodynamic analyses with respect to their impact on development and clinical use of drugs, • During the pre-clinical stages of drug development, works with Drug Discovery team to ensure that sufficient preclinical PK/PD knowledge exists to support progression into first in man studies, • Accountable for ensuring that there are valid methods for measuring drug and metabolite concentrations (or any biochemical biomarkers) in human studies, • Coordinates with medical writers (and other team members) in the data review, analysis and reporting of the Clinical Pharmacology study, • Responsible, in conjunction with medical writer, for overall content and accuracy of study report before forwarding for final sign-off. Assist with internal and external dissemination of results to Development Team, Investigators etc., • Provides recommendations for clinical doses and dosing algorithms (including drug interaction advice, food effects, special group dosing etc.) to the Clinical and Development teams and in regulatory documentation such as labeling, • Stays abreast of literature, government guidelines, internal guidance on clinical trial conduct including Good Clinical Practice and internal SOPs, regulations for specific projects to which assigned, in order to be a team resource of clinical pharmacology and therapeutics knowledge in terms of both medical background and clinical trial design, • Participates in multidisciplinary teams in assessing potential in-licensing opportunities, as requested by line management, • Acts as technical lead for specific development projects, Phase I/III and Clinical Pharmacology centric studies, • Manage and initiate external collaborations with leaders in clinical pharmacology and Key Opinion Leaders MINIMUM REQUIREMENTS • PhD in clinical pharmacology, quantitative pharmacology, pharmacokinetics, or related field / MD/ PharmD preferred, • Biologics including monoclonal antibody, bispecific antibody, and antibody-drug conjugate experience is preferred, • Experiences in Oncology/Autoimmune disease field is preferred, • Proven expertise in pharmaceutical/biotech industry (8-15 years) with adequate knowledge in ICH guidelines, Good Clinical Practice applicable to Clinical Pharmacology, • Direct experience with clinical pharmacology summary documents required for Regulatory submissions, • Comprehensive understanding of worldwide clinical regulatory requirements with working knowledge of drug development process with a proven record in drug development from IND through regulatory submission and commercialization, • Experience in clinical development and new drug registration, • Mastery of statistics applied to clinical research, • Ability to work with pharmacometrician for PopPK modeling, E-R analysis, PBPK, and PK-PD modeling, and interpret the data to support the clinical development, • Good ability to interpret complex clinical data and experimental results, • Ability to develop network internally and externally to communicate in situations requiring special tact and diplomacy, • Self-motivated and self-disciplined individual with superb problem-solving and leadership skills, • Excellent English (writing and speaking) and excellent mastery of English medical terminology PREFERRED SKILLS AND EXPERIENCE: • Knowledge of FDA, EMA and ICH guidelines and regulations, • Record of successful publications in the area of clinical pharmacology/pharmacometrics, • Comprehensive understanding of worldwide clinical regulatory requirements with working knowledge of drug development process with a proven record in drug development from IND through regulatory submission and commercialization. Prior direct interaction with regulatory agencies and advisory boards is required, • Candidate must demonstrate thorough understanding of principles of clinical pharmacology including clinical study design, analysis, and interpretation, and application of these approaches to drug development, guidelines in the design of clinical trials and development plans KEY COMPETENCIES: • Ability to organize and work simultaneously on multiple projects, • Ability to work in a matrix, project-oriented environment, • Excellent written and oral communication skills, interpersonal/influencing skills, and ability to work in a continually changing environment, • Supports the success of a group being led by providing clarity, support and tools needed to excel as things change, • Maintains a functional, perspective and acts on the belief that solutions and plans are stronger when appropriate collaboration occurs across and beyond the organization, • Actively builds relationships and networks with others across and beyond HUTCHMED working constructively across organizational boundaries despite differences in interests, perspectives and need

100% ONSITE Florham Park NJ Pay: $36-$41/hr MUST BE LOCAL IN NEW JERSEY REQUIRED: BS/MS in science Background or MS in Regualtory Affairs and 1+ year of expereince within the pharmaceutical industry as a Regulatory Affairs professional. Publishing related software tools e.g. Documentum, eCTDXPress/ISIPublisher, ISI Toolbox/DocuBridge/Insight platform, Adobe Acrobat. Regulatory Affairs Submissions Job Description: The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams, this individual establishes and maintains submission content planners and associated timelines, facilitates tactical submission team meetings, prepares content planners for publishing, interfaces with publishing vendor, and fulfills Submission Management functions on Project Teams in support of Development, Marketing, and post-marketing regulatory authority applications. This individual is recognized as a very knowledgeable in their discipline expert and in regulatory affairs submission management. Responsibilities : • Manages low to medium impact (with respect to internal visibility, risk, complexity and criticality) submission projects to ensure the timely delivery of high quality dossiers that meet technical specifications defined by regulatory authorities and can be easily navigated and reviewed by a regulatory agency., • Acts as RA Submissions support to project teams providing guidance and communication of established submission processes and standards. Provides input to project publishing timelines and deliverables., • Participates in submission team meetings. Expedites, manages, and coordinates multiple concurrent interrelated activities for submission projects in the delivery of low to moderately complex published submissions within the required timelines. Anticipates obstacles and proposes solutions within the team., • Coordinates submission publishing with offsite publishers/provides notification to ensure all required resources are available to meet submission timelines. Prepares content planner for publishing and works with vendor to resolve publishing issues. May perform in-house publishing tasks, • Facilitates the creation or procurement of submission content deliverables such as cover letters and forms, • Performs detailed quality reviews of published output to ensure compliance with Regulatory Standards and Health Authority guidances including verification of content, bookmarks, hypertext links and tables of content in low to moderately complex submissions. Facilitates team reviews., • Contributes to the development of optimal business processes and standards within the department to ensure high levels of customer support and to achieve high quality submissions., • Contributes to the implementation of internal process and standards documents relating to publishing and publishing deliverables., • Suggests and contributes to process improvements, including changes to software and business processes. May participate on internal project teams to update business software., • Demonstrates ability to influence without direct authority. Builds and maintains positive relationships internally and externally., • Position accountability/scope: oSupervision required. Receives project assignments from manager but has responsibility for managing own projects with oversight. Reviews project progress with manager on a regular basis with direction provided by manager. May assist with onboarding staff.

Day to Day: We are looking for a Chargebacks & Rebates Analyst to join one of our large generic pharmaceutical organizations in the Florham Park, NJ, area. We do not need an individual who is a Gross-To-Net Subject Matter Expert, but an individual with chargebacks & rebates experience (preferably someone with iContracts experience). This role will focus on managing and enhancing gross-to-net analytics, reporting, and forecasting. The consultant will work cross-functionally with Finance, Sales, and Commercial teams to ensure deductions and accruals are accurate, well-documented, and timely. Gross-to-Net Accruals & Analysis, including supporting the monthly close process by reviewing, validating, and booking GTN accruals (e.g., chargebacks, rebates, admin fees, returns, and Medicaid). *This position is hybrid, 3 days onsite per week in Florham Park, NJ. Must Haves: -Pharmaceutical experience -5-7 years of Financial Analysis, Chargebacks/Rebates experience -Experience with iContracts, Model N or a similar software (preferred, flexible) -Advanced experience with Excel and comfortable presenting information/data through PowerPoint slides

Pharmaceutical Sales Representative. We're looking for sales professionals who want to work on our Pharmaceutical Sales Rep team and who are determined to make life better for patients. Responsibilities – Pharmaceutical Sales Representative.

The Director, Pharma Commercial Strategy defines and drives IQVIA Digital's segment-level strategy for pharmaceutical clients. Develop and own the segment strategy for IQVIA Digital offerings across large pharma and other prioritized segments, including Key Accounts and EBP (pre-commercial, small, a

Job Title: Independent Medical Education Manager-Contract Location: 50% onsite-Madison, NJ 07940 Hours: Mon-Fri 8am-5pm Responsibilities: • Help ensure compliance and quality of supported medical education programs within the assigned therapeutic area via tracking of outcomes and educational effectiveness: o Assist with analysis of program outcomes for adherence to learning objectives and proposed outcomes levels o Assist in review of program outcomes reports for adherence to outcomes templates o Observe, monitor, and evaluate supported IME live activities and enduring materials • In collaboration with Medical Education TA Leads, develop and maintain Hematology medical education resources including, but not limited to: o CME Digital Activity Guides o Quarterly educational outcomes infographics, highlighting key insights/metrics, unfilled educational gaps, and activity spotlights o Slide library • Maintain calendar of live IME events for Hematology programs, • Assist Medical Education TA leads in development of Request for Education (RFEs), • Work collaboratively, effectively, and efficiently with all internal and external customers, partners, and stakeholders, • Evaluate opportunities for innovation, idea generation, continuous improvement, and process enhancements to continually evolve the Medical Education department and enhance its value to the organization, • Medical Education Provider Interfacing Activities: o Communicate with external Medical Education Providers on all grant-related information, to ensure receipt of project status reports, launch dates, outcomes reports within pre-established timelines and guidelines, resource tools and publications o Manage Provider Capability on-site/teleconference presentations Qualifications: • Advanced science degree in the medical field, PharmD, PhD, NP or equivalent with a minimum of 1-2 years of experience working in the pharmaceutical, medical education and/or clinical environment. Medical Education experience and proficiency in a grant management system preferred., • Strong computer skills including SharePoint Online and MS Office 365 [Word, Excel (Pivot tables), PowerPoint, Outlook], • Strong project management skills and ability to multitask and ensure time management, • Strong analytical and problem-solving skills, • Demonstrated ability to work effectively and collaboratively within a matrixed organization, • Strong written and verbal communication skills; strong attention to detail, • Demonstrated track record of being a team player, • Creativity and innovation displayed in past accomplishments"

Job Description Company: Pharmaceutical Company Contract Position: 1 year with potential extension Location: Nutley, NJ Job Posting: EZIJP00004277 Description: This position is responsible for performing proactive/high quality administrative support to multiple members within the Global Regulatory Operation Services (GRSO) department. He/she may be assigned to support other departments or projects/events within Medicine Development Center. Major Duties and Responsibilities: • Personal assistant to GRSO’s Head, including calendar/meeting management., • Support day to day administrative activities for the GRSO department, such as being the point of contact for general inquiries about the department, knowledge of all administrative systems/software (i.e. Concur, travel agency, ReadSoft), procurement of office/meeting supplies, arranging/coordinating IT support as needed., • Document management: creation of template (in Word, Excel, PowerPoint) and management of documents such as monthly reports, Unit objectives, department’s budget. Maintain and update GRSO’s internal website as needed and no less than once a month., • Manage GRSO’s monthly FTE reporting for all US/Canada colleagues., • Coordinate both domestic and international travel arrangements for GRSO colleagues, as well as supporting or arranging (as needed) executive level visitors from the home office and other regions. Research travel options and other travel arrangements (i.e. car service, train, flights, hotel) via the company’s travel system/agency. Assist with passport/visa requirements for international travel., • Expense Report Submission: Process travel and entertainment expense reimbursements using ADP Concur for GRSO’s Head and GRSO’s members as needed. Track expenses, compile and submit P-card expense reports on a monthly basis., • Invoice Processing: Manage, process and coordinate approval of invoices via ReadSoft on a monthly basis. Contact vendors to resolve any discrepancies or problems. Answer all vendor inquiries. Advise supervisor of any invoice errors or non-compliance issues. Scan copies of invoices, correspondence, and checks for filing., • Meeting support (remote and in-person): assist with remote meeting setup and administrative support during meetings (i.e. logistics, audio-visual services, meeting minutes). Coordinate and assist with overall aspects of pre, during and post on/off-site meetings (i.e. logistics, agenda, meeting supplies, food services) as needed., • Assist HR Business Partner with candidate interview schedules, new hire on-boarding and other HR activities as required. Any other team-initiated program and ad-hoc duties as required. Qualifications: • Associate degree is required. BA/BS degree preferred., • 4+ years related administrative experience supporting multiple individuals., • Must have strong organizational skills and excellent judgment and reasoning abilities., • Individual must be customer and employee focused, able to multi-task, work under minimal supervision, and demonstrate resiliency and high productivity in a fast-paced environment., • Must have an ability to handle sensitive and confidential information and documents appropriately. Maintain appropriate archive for all relevant and legal documents., • Must have excellent verbal and written communication skills, exceptional interpersonal skills and ability to work cooperatively and collaboratively with others., • Must have proficient computer skills with Outlook, and Microsoft Office programs (Word, Excel, PowerPoint).

About Kerry Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role We are seeking a highly skilled and innovative RD&A Scientist to join our Beverage team. This role is responsible for developing and optimizing beverage formulations across various formats including sparkling, still, juice, and functional beverages. The ideal candidate will bring deep technical expertise, strong sensory capabilities, and a collaborative mindset to drive product innovation and meet customer expectations. Key responsibilities • Develop and prepare beverage formulations, syrups, and concentrates at lab and pilot plant scale., • Test and refine formulations to meet specific taste profiles and regulatory standards., • Customize beverage ingredients independently or within cross-functional teams., • Calculate calories and understand the role of sweeteners and nutrients in formulations., • Facilitate sample shipments for internal and external stakeholders., • Support beverage and taste development under GMP and safety standards., • Manage multiple tasks and deadlines with speed and accuracy., • Master formulation techniques for RTD (Ready-to-Drink) and RTM (Ready-to-Make) formats., • Apply exceptional sensory skills to define and discriminate flavor profiles under tight timelines., • Demonstrate a deep understanding of beverage processing techniques and nutritional value calculations., • Communicate formulation concepts effectively in commercial settings with customers., • Apply mathematical skills to work with dilutions, percentages, and ppm calculations., • Exhibit self-motivation and resourcefulness in solving complex formulation challenges. Qualifications and skills • Bachelor’s Degree in Food Science, Biology, Chemistry, or a related Applied Science., • Minimum of 5 years of experience in beverage development and formulation., • Strong scientific and analytical aptitude., • Proficiency in Microsoft Office; experience with SAP is a plus., • Excellent problem-solving skills and ability to work independently and collaboratively. The typical hiring range for this role is $75,602 to $123,432 annually and is based on several factors including but not limited to education, work experience, certifications, location, etc. In addition to your pay, Kerry offers benefits such as a comprehensive benefits package, incentive and recognition programs, equity stock purchase and retirement contribution (all benefits and incentives are subject to eligibility requirements). Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at: Know Your Rights: Workplace Discrimination is Illegal (dol.gov). Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a “starter kit,” investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.

Director of Purchasing(Food Manufacturing) • Strong knowledge of SAP or any other ERP system., • 5+ years of purchasing experience in food manufacturing or related industry., • Strong negotiation and vendor management skills. The Purchasing Manager is responsible for sourcing, negotiating, and procuring raw materials, packaging, and supplies required for food production. This role ensures timely delivery of high-quality ingredients while maintaining cost efficiency and compliance with food safety standards. Are you looking to make a career change to a stable company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance and paid PTO.Does this position match your future career goals? Then this opportunity could be the right fit for you. • Great Opportunity, • Top Benefits, • Growth Opportunities, • Competitive Salary Responsibilities: • Analyze market data and consumer trends to inform purchasing decisions., • Collaborate with buyers and merchandisers to expand product categories., • Forecast product demand to maintain sustainable inventory levels., • Develop product positioning, packaging, and pricing strategies to grow market share., • Provide regular reports on market conditions, cost fluctuations, and supply chain performance., • Create strategic roadmaps for new product development and category expansion., • Oversee sourcing and negotiation processes with suppliers., • Develop and manage sourcing strategies aligned with business objectives., • Lead major supplier negotiations and manage contract development., • Ensure compliance with cost, quality, and legal standards., • Monitor inventory levels and coordinate with production teams to forecast material needs. Qualifications: • Bachelor’s Degree in Supply Chain, Marketing, or Engineering., • 5+ years of purchasing experience in food manufacturing or a related industry., • Strong knowledge of SAP or other ERP systems., • Solid understanding of category management, marketing, and sales principles., • Experience with supplier relationships, JIT, Lean manufacturing, and inventory management., • Proficient in data analysis and forecasting methods., • Skilled in communicating go-to-market strategies across cross-functional teams., • Experience in supplier qualification and auditing., • Strong organizational, leadership, and multitasking abilities. Jasleen Kaur Ajulia Executive Search is a search firm specializing in Manufacturing, Finance, IT, Legal and Pharmaceutical positions. This is a confidential search for one of our preferred clients. It is a direct hire position that includes competitive compensation and full comprehensive benefit package. #ZR

Head of Analytical Development: NYC Position Overview We are seeking a Director or Senior Director of Analytical Development to lead and expand the analytical development function. This individual will play a pivotal role in supporting late-stage programs, ensuring robust analytical strategies for drug substance and drug product, and driving method development, validation, and transfer activities. This is a hands-on leadership role for someone who thrives in a dynamic environment, enjoys rolling up their sleeves, and is committed to building best-in-class analytical capabilities. The ideal candidate will be comfortable commuting to the New York site four days per week and collaborating cross-functionally with CMC, Quality, and external partners. Key Responsibilities • Lead the Analytical Development team responsible for method development, qualification, validation, and transfer for drug substance and drug product., • Develop and implement analytical strategies to support late-stage development, scale-up, and commercialization., • Oversee characterization studies, stability programs, and specification setting in alignment with regulatory requirements., • Partner closely with Process Development, Quality, and Regulatory teams to ensure seamless integration of analytical deliverables., • Manage relationships with CDMOs and external testing labs, ensuring timelines and quality standards are met., • Provide technical leadership and mentorship to a growing team, fostering a culture of scientific excellence and accountability., • Contribute to regulatory submissions (IND, NDA) and represent Analytical Development in health authority interactions as needed. Qualifications • Ph.D. or M.S. in Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline., • 10+ years of experience in analytical development within the biotech or pharmaceutical industry, with a strong focus on small molecule late-stage development and commercialization., • Proven track record of leadership in method development, validation, and transfer for complex modalities (biologics experience strongly preferred)., • Deep understanding of ICH guidelines, regulatory expectations, and CMC requirements for global filings., • Excellent communication and collaboration skills; ability to work effectively in a fast-paced, matrixed environment., • Willingness and ability to be onsite in New York 4 days per week. Why Join? • Opportunity to shape analytical strategy for a late-stage pipeline with high-impact programs., • Work in a well-funded biotech with strong pharma partnerships and a clear path to commercialization., • Collaborative, science-driven culture where your contributions make a tangible difference.

7 Month Contract*** Title: Commercial Rebates and Returns Manager ** Day to day: Insight Global is seeking a highly skilled Rebate and Returns Manager to manage commercial rebates, administrative fees, billbacks and other after sales expenses; ensure prompt payment to Wholesalers, Retailers, Distributors and Group Purchasing Organizations. This candidate will be preparing executive summary level reporting to the customer, field force and Contracts and Pricing management. This role requires close interaction with Credit and Collections, handling payment reconciliations as well as variance analysis against customer claims. Backfilling contract management as needed and working closely with A/R, A/P and GTN Team. Building and maintaining all customer incentive programs in revenue management system. Communicating technical aspect of the processing any assisting in resolution of system imperfections and setting preventive measures of reoccurrence. Educational Qualifications • 5-year experience in commercial finance, familiar with pharmaceutical regulations and GMP., • 2-3 years’ experience in rebates, chargebacks, contracts; Model-N or similar Revenue Management System, SAP, • Familiarity in commercial product returns/recall operations, • Inmar experience a plus Knowledge and Skills (Functional / Technical) • Working knowledge of Microsoft Office with ability to use advanced Excel spreadsheet functions, formulas and pivots., • Excellent written and oral communication skills., • Ability to communicate with all levels of personnel including senior management and external customers., • High-level analytical skills to collect information, research data and develop rational solutions., • Excellent interpersonal, written, and oral communication skills, • Collaborative attitude as well as strong analytical and investigative skills, • Ability to multi-task, work under pressure and meet deadlines, • Capability to follow verbal and/or written instructions, • Customer oriented: must recognize the importance of customer relationships

Station Trainer Jamaica, NY Are you looking to make a career change to an exciting company? This exciting opportunity as a Station Trainer offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance, paid PTO etc. Does this position match your future career goals? Then this Station Trainer could be the right fit for you. Responsibilities: • Deliver comprehensive training through multiple modalities, including instructor-led and virtual instructor-led sessions, e-learning, self-directed learning, on-the-job training (OJT), and supporting training materials, • Facilitate and oversee Cargo Classroom instruction and OJT, including final assessments and required sign-offs, • Ensure all training and equipment operations comply with Swissport Corporate and NOAM Training Policies, Safe Systems of Work (SSOW), and Standard Operating Procedures (SOPs), • Actively promote and reinforce best practices across station operations, • Conduct internal quality assurance activities, including operational audits, to support compliance and continuous improvement, • Continuously evaluate training effectiveness to ensure staff competency, confidence, and role-specific proficiency, • Maintain training and operational compliance standards across the station, • Collaborate regularly with subject matter experts (SMEs) to ensure training content remains accurate, relevant, and aligned with operational needs, • Serve as a role model by consistently demonstrating best-practice behaviors and procedures, • Provide objective feedback, coaching, and performance guidance to improve individual and team effectiveness, • Accurately document and report all training activities using approved systems to ensure reliable tracking and data integrity, • Support nearby stations with training and operational needs as required, • Forecast and plan initial and recurrent training requirements in coordination with Regional Training Managers, local HR, and Operations teams, • Deliver and facilitate initial and recurrent training programs in accordance with global and local standards, • Administer required examinations, evaluations, and training documentation to maintain regulatory and corporate compliance, • Support new hire onboarding and training tracking to ensure a smooth transition into operational roles, • Assist with on-the-job coaching programs for assigned functions and serve as tier-one support for locally certified coaches, • Maintain operational currency and familiarity with station procedures and equipment Qualifications: • Minimum of one (1) year of industry experience in airline cargo operations, • High School Diploma or equivalent experience demonstrating problem-solving ability, stakeholder collaboration, and effective prioritization, • Ability to travel up to 10%, including travel within the United States and Canada, • Ability to pass required security clearances and possess a valid driver’s license, • Strong verbal and written communication skills, with the ability to influence without direct authority, • Working knowledge of computer systems, with proficiency in Microsoft Office Suite strongly preferred, • Customer service–oriented mindset with a commitment to operational excellence, • Flexibility to work various shifts, including off-peak hours, to support training requirements, • Demonstrated understanding of adult learning principles, instructional design, and training evaluation methodologies preferred, • Ability to thrive in a fast-paced, dynamic, and evolving operational environment, • Proven ability to develop and deliver engaging presentations, slide decks, and training materials Salary: $27-$32/ hour Benefits: • Medical Insurance, • Dental Insurance, • Vision Insurance, • 401K, • Paid Time Off, • Direct Hire Ask for: Deb #Talroo #iHire #ih Ajulia Executive Search is a New Jersey based Executive Search Firm specializing in retained searches in multiple sectors, including Manufacturing, Finance, IT, Legal, and Pharmaceutical. We have a nationwide client base and offer services in temporary and direct hire placements.

The ideal candidate will bring strong leadership, organizational expertise, and deep industry knowledge across the pharmaceutical, biotech, or medical device sectors, along with a proven track record of success in previous roles. Previous experience that provides the knowledge, skills, and abilities

Account Planning, Adaptability, Customer Feedback Management, Hospital Sales, Interpersonal Relationships, Lead Generation, Market Analysis, Pharmaceutical Sales Training, Sales Calls, Sales Metrics, Sales Pipeline Management, Sales Presentations, Sales Process Management, Sales Territory Management

Managing a digital brand focused on websites (management of website tactics required, pharma agency background required). Experience in pharmaceutical marketing is required. Experience in managing pharma brand launch in rare disease is preferred.

Client Activation Manager - Pharma & Health. Previous experience in the Healthcare and Pharmaceutical industries is preferred but not required.

The Administrative Assistant / Receptionist provides front-office support and administrative coordination to ensure smooth daily operations within a fast-paced biotech/pharmaceutical environment. Administrative Assistant / Receptionist. This role serves as the first point of contact for employees, g

• Drive with Purpose – important medical deliveries to people in need, • Follow delivery routes and time schedules for accepted routes/jobs., • Deliver a variety of pharmaceuticals and equipment., • Use own vehicle to complete accepted delivery jobs., • Load and unload totes/bags., • Totes/bags are generally under 20lbs, • Handle delivery paperwork as instructed., • Use own smartphone to enter delivery information., • 21 or older., • Valid driver’s license for at least 3 years, • No more than 3 combine at-fault accidents and/or moving violations in the past 3 years, • Own your own vehicle. This route requires a 2011 or newer SUV or larger vehicle., • Carry current vehicle insurance and can meet $100/300k Bodily Injury coverage minimum requirement., • Can pass a criminal background check, motor vehicle record check and drug screen., • Location may require you to obtain LLC if you do not already have one. #Tier2

If you have a spotless driving record, a dependable vehicle and the drive to come through for people in need, please fill out our driver form to become one of our delivery contractors. • Drive with Purpose – important medical deliveries to people in need, • Drive packages, not people – never worry about who’s getting in your car, • Follow delivery routes and time schedules for accepted routes/jobs., • Deliver a variety of pharmaceuticals and equipment., • Use own vehicle to complete accepted delivery jobs., • Load and unload totes/bags., • Totes/bags are generally under 20lbs, • Handle delivery paperwork as instructed., • Use own smartphone to enter delivery information., • 21 or older., • Valid driver’s license for at least 3 years, • No more than 3 combine at-fault accidents and/or moving violations in the past 3 years, • Own your own vehicle. This route requires a 2011 or newer Sedan, SUV or Minivan., • Carry current vehicle insurance and can meet $100/300k Bodily Injury coverage minimum requirement., • Can pass a criminal background check, motor vehicle record check and drug screen., • Location may require you to obtain LLC if you do not already have one. #Tier2

A company is looking for a Senior Vice President, Corporate Brand & Impact.Key Responsibilities Serve as a senior strategic counselor to a global pharmaceutical client across corporate brand and health equity workstreams Lead development and execution of large-scale corporate brand and reputation

Key Responsibilities Evolve and expand data and analytics offerings in pharmaceutical marketing, enhancing capabilities in segmentation and predictive modeling Design measurement frameworks linking marketing initiatives to business outcomes and develop actionable insights from key marketing data

Key Responsibilities Lead the design and execution of RWE analyses for pharmaceutical clients, translating complex drug development questions into actionable research plans Derive complex real-world endpoints and provide technical oversight on real-world data methodologies Set methodological sta

Key Responsibilities Lead product communications for pharmaceutical and biotech clients, including managing clinical data and regulatory milestones Develop and execute product communication strategies that align with corporate brand narratives and integrate patient advocacy Mentor junior team me

A company is looking for a Pharmacist Clinical Refill Center.Key Responsibilities Dispense medications and interpret IV admixture orders, preparing primary IV solutions Manufacture nonstandard pharmaceutical preparations and maintain appropriate records Supervise support personnel and ensure the

A company is looking for a Fixed-Term Coordinating Center Associate to provide customer service support for pharmaceutical programs.Key Responsibilities Handle inbound and outbound contacts related to specific programs and provide consistent customer service support Document all communications an

Key Responsibilities Serve as the primary client contact for a high-profile pharmaceutical client, providing strategic counsel and building trust Lead the development and execution of integrated corporate brand communications strategies and major campaigns Manage a multi-disciplinary account tea

Spring & Bond is a digital media agency and consultancy specializing in helping pharmaceutical and medical device manufacturers create robust, omnichannel media strategies for both healthcare professionals (HCPs) and consumer audiences. The Manager, Beyond Insights (BI) oversees a team of analysts a

A company is looking for a Pharmaceutical Promotional Copywriter (Remote).Key Responsibilities Write creative marketing copy across various digital mediums according to project specifications Research clients and competitors to support creative strategy and execution Collaborate with design and

A company is looking for a Marketing Automation Specialist to join a global pharmaceutical client in a fully remote role.

Key Responsibilities Lead Generation & Pipeline Development: Identify current users and generate new leads targeting top pharmaceutical accounts Relationship Building: Engage with senior executives to develop meaningful relationships that contribute to sales growth Sales Process Management: Mana

Regulatory and Medical Affairs - Medical Education Manager. Regulatory and Medical Affairs - Medical Education Manager. Advanced science degree in the medical field, PharmD, PhD, NP or equivalent with a minimum of 1-2 years of experience working in the pharmaceutical, medical education and / or clin

A company is looking for a Junior Copywriter/Proofreader to create impactful pharmaceutical promotional materials.Key Responsibilities: Develop and source new content while ensuring alignment with audience and channel strategy Maintain organized annotations throughout the creative process and com

Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries.Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world.Our vision is to be our customers' mos

A data analytics firm seeks a Project Lead/Manager to leverage AI and data science in solving business challenges for pharmaceutical clients.

Job Description Introduction Axtria is a leading global provider of cloud software and data analytics to the Life Sciences industry. We help Life Sciences companies transform the product commercialization journey to drive sales growth and improve healthcare outcomes for patients. We are acutely aware that our work impacts millions of patients and lead passionately to improve their lives. Since our founding in 2010, innovation has been our winning differentiation, and we continue to leapfrog competition with platforms that deploy Artificial Intelligence and Machine Learning. Our cloud-based platforms - Axtria DataMax™, Axtria InsightsIQ™, Axtria SalesIQ™, and Axtria MarketingIQ™ - enable clients to efficiently manage data, leverage data science to deliver insights for sales and marketing planning, and manage end-to-end commercial operations. We work with over 100 Life Sciences companies, many with multiple engagements globally across 75+ countries. We continue to win industry recognition for growth and are featured in some of the most aspirational lists – INC 5000, Deloitte FAST 500TM, NJBiz FAST 50, SmartCEO Future 50, Red Herring 100, and several other growth and technology awards. Axtria is looking for exceptional talent to join our rapidly growing global team. People are our biggest perk! Axtria is recognized for its organizational culture in both US and India, including certification by the Great Place to Work® Institute. Our transparent and collaborative culture offers a chance to work with some of the brightest minds in the industry. Axtria Institute, our in-house university, offers the best training in the industry and an opportunity to learn in a structured environment. A customized career progression plan ensures every Axtrian is setup for success and able to do meaningful work in a fun environment. We want our legacy to be the leaders we produce for the industry. Will you be next? Role Overview Seeking an experienced R&D SME to support a global pharmaceutical client. The role bridges business and technical teams translating R&D needs into client data and analytics solutions that ensure clarity, compliance, and business value. Key Responsibilities • Domain Leadership: Serve as the R&D/Clinical expert for data onboarding and governance. Guide stakeholders across discovery, pre-clinical, and clinical functions, aligning data efforts to business goals., • Elicit business needs and translate into functional requirements, data mappings, and test scenarios. Partner with technical teams to ensure data is structured and integrated to support analytics and insights., • Apply deep knowledge of pharma data governance, access management, and compliance standards (GxP, FAIR). Contribute to metadata standards, data catalogs, and controlled access models., • Stakeholder Engagement: Communicate complex R&D and data concepts clearly to senior business and IT leaders. Lead workshops and reviews to drive decisions and ensure alignment.Required Experience, • 7–10+ years total experience; majority in pharma R&D with primary focus on Discovery and Clinical areas., • Strong grasp of R&D workflows, clinical operations, and related regulatory processes., • Knowledge of pharma data sources (internal/external: discovery, clinical, real-world, omics)., • Proven skill in translating business priorities into functional designs and test scenarios., • Experience with data governance, quality, metadata, and access controls., • Excellent client-facing, communication, and presentation skills., • We are hiring for Berkeley Heights, NJ., • U.S. Citizens and those authorized to work in the U.S. are encouraged to apply. The salary range reflected is based on a primary work location of Berkeley Heights, New Jersey. The actual salary may vary for applicants in a different geographic location. #LI-NS1 Powered by JazzHR B8B8yfO0KW

Utilize product management tools (Jira, Confluence, Aha!, Productboard) to manage roadmaps, documentation, and communication. We are seeking a strategic, customer-centric, and execution-focused Product Manager to lead the evolution of our patient support program (PSP) solutions for pharmaceutical an

Experience partnering directly with executives and senior leaders. Executive partnership skills to act as the CPOs right hand and keep communication flowing smoothly. Founded by a practicing physician and a senior pharmaceutical executive, Impiricus was created to cut through the noise and put physi

As a Copywriter at Avalere Health, you will develop content for pharmaceutical brand communications for healthcare professionals and patients. Collaborate with art directors, writers, and editors as well as other team members to develop creative concepts.

A leading pharmaceutical company in Elizabeth, NJ is seeking an Account Rep Bio-Pharmaceutical to join their sales team. The ideal candidate should have sales experience, a strong service orientation, and the ability to thrive in a performance-driven environment.

Pharmacy Name: Meta Specialty Pharmacy.Location: 1230 Metcalf Ave, Bronx, NY - 10472.Meta Specialty Pharmacy in Bronx is seeking a dedicated and highly skilled Pharmacist to join our team.We are looking for a professional who can dispense medications accurately, provide excellent pharmaceutical care

A pharmacist appropriately enters and updates clinical intervention in the electronic health record system for all rejected orders. The Pharmacist is responsible for the provision of pharmaceutical care to all patient age groups including geriatric, adult, adolescent, pediatric, and neonatal patient

Ready for a change from bedside Nursing? Our home infusion nurses care for our specialty infusion patients 1:1 in the patient's home. Amerita, an affiliate of BrightSpring Health Services, is a specialty infusion company focused on providing complex pharmaceutical products and clinical services to p

Regional Director, IV Infusion Sales. At Amerita, we're not just delivering Infusion services-we're building relationships that improve patient outcomes and drive business success. We are the leading provider of Infusion services focused on providing complex pharmaceutical products and clinical serv

Data Science Consulting, Strategy & Transformation Consulting.Guidehouse Life Sciences is an engine of innovation, helping pharmaceutical, biotech, medical device, and diagnostic companies develop custom solutions that tackle today's challenges, while anticipating tomorrow's opportunities.You will h

Advanced degree in Pharmacy, Regulatory Affairs, Life Sciences, or related field preferred. We are seeking a highly experienced Pharmaceutical Regulatory & Compliance Consultant with deep expertise in U. The ideal candidate will have extensive experience in pharmaceutical manufacturing and wholesale