div class="job-description-container">Role: Commercial SME(Commercial Analytics Consultant (Pharmaceutical Domain)
Location: New Jersey– Hybrid role
. https://www.interview.micro1.ai/intro/dc1838d2-367f-4c54-b907-96e9463ff98e/?skill=c2bf2d05-09c0-46ed-8b90-f6096af1e1d9&ping=ok
.Union, New Jersey5 days ago
Our passionate, global workforce augments local expertise and diverse mix of skills with data, science, and technology to deliver bespoke engagement solutions that help clients reimagine how they engage with their patients, payers, people, and providers to improve treatment outcomes. Learn more: https://www.greatplacetowork.com/certified-company/7003732 .
p>As one of the world's top three credit ratings agencies, Fitch Ratings plays a critical role in global capital markets by providing supplementary credit analysis, ratings, research, and commentary to financial market participants. For over 100 years, Fitch Ratings has been creating value for global markets through its rigorous analysis and deep expertise, which have resulted in a variety of market leading tools, methodologies, indices, research, and analytical products.
li>Critically reviewing and interpreting local, state, and federal environmental regulations, permitting, compiling, and drafting regulatory applicability determinations, and communicating findings, to co-workers, clients, and regulatory agencies. Our experts are leaders in their fields, developing and delivering innovative solutions in diverse markets including Buildings, Transport, Planning & Urban Design, Water, Environment & Health, Energy, and Management Consulting.
p>Univar Solutions is a leading, global distributor of chemicals and ingredients essential to the safety, health, and wellbeing of our daily lives from life-saving medicines and vitamins to hand sanitizers and industrial materials used for cleaning, construction, and more. All searches must be initiated by Univar Solutions Talent Acquisition team and candidates must be submitted via Applicant Tracking System (ATS) by approved vendors who have been expressly requested to make a submission for a specific job opening.
MINIMUM WORK EXPERIENCE: Typically 10 or more years of increasing responsibility and complexity in terms of any applicable professional experience including 5 years of combined marketing and/or sales experience, or the equivalent required; 3 or more years of management experience. This includes sales and market share analysis, identifying underperforming categories, developing plans and programs to drive sales and market share in Generic Pharmaceutical products.
Accountable for developing plans that will result in increased sales, market share and/or profitability through product category analysis, strategy development, supplier profitability and contribution, category maintenance and new product launches. Responsible for the management of the pharmaceutical category inclusive of Brands, Generics, and Specialty drugs and develop the product category strategy in meeting the goals of the organization and its customers across segments.
p>Essential Duties & Key Responsibilities: - Participate in discussions with SourceBlue and Turner Business Unit (BU) Business Development (BD) teams and project leadership about client prospects to secure SourceBlue (SB) business opportunities.
- Manage vendor submittals, factory testing, delivery of products, start-up of equipment, equipment training for owners' staff, warrantees, and record documents for purchased equipment.
em> Proven ability to manage and coordinate multiple projects in a fast-paced, highly professional environment Excellent verbal and written communication, and interpersonal skills Strong customer service orientation Excellent organizational and time management skills Knowledge and understanding of financial indicators, ability to analyze PNL Ability to translate strategies into operational and tactical goals and track performance Ability to prioritize and execute tasks in a high-pressure environment and make sound decisions in emergency situations Ability to motivate teams and lead through influence Leadership and coaching skills Compensation The expected salary range for this position is $120,000 - $150,000 annually. Education and Experience Bachelor''s degree in Science, Business Management, Operations or related discipline 10+ years of relevant experience in the pharmaceutical industry (Testing, Inspection, Certification) 3-5 years of supervisory experience Travel Frequent travel required (34%-66%) Knowledge/ Skills/ Abilities Language Skills English Advanced Reasoning Skills/Abilities Advanced Mathematical Skills Intermediate Computer Skills Microsoft Office (Work, Excel, PowerPoint, Outlook) Intermediate Language Skills French Basic Preferred Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.
p>Keywords: Associate Creative Director, ACD, Pharmaceutical Advertising, Healthcare Advertising, Pharma Marketing, DTC Advertising, HCP Marketing, Regulated Advertising, Integrated Campaigns, Creative Leadership, Concept Development, Figma, Sketch, Adobe Creative Suite, Photoshop, Illustrator, InDesign, AI in Creative, Generative AI, Campaign Development, Brand Strategy, MLR Review, Legal Review, Fair Balance, Patient-Centric Design, Contract Creative Director, Healthcare Agency, Digital Marketing, Visual Storytelling, Pharmaceutical Campaigns. The Associate Creative Director - Pharmaceutical Advertising will play a hands-on leadership role, shaping and delivering integrated creative campaigns for both DTC and HCP audiences while guiding teams through concept development, execution, and regulated review processes.
The position focuses on Veeva CRM, Vault PromoMats, Medical Information/MedInquiry, MedComms, Network, and other related platforms, while partnering closely with business stakeholders to translate requirements into effective system solutions, drive process improvements, and support day-to-day operations. - 3-5+ years of hands-on experience supporting, administering, configuring or optimizing Veeva Vault and/or Veeva CRM/Vault CRM within a pharmaceutical, biotechnology, life sciences, healthcare, or another regulated environment.
Leadership skills to motivate the team to achieve broad operational targets with impacts on own job discipline, multiple job disciplines, and department. Negotiate with senior management, customers, and external parties of divergent interests to reach an agreement of strategic importance while being guided by the business segment and the organization's functional strategy.
p>This job is a part of the Facilities Management functional area which focuses on all aspects of the operations of a set of assets, providing support to the Facility Managers regarding all repairs and investment plans. About the Role:
As a CBRE Facilities Director, you will serve as the primary client leader for the delivery of facilities management services to a Life Sciences/ Pharmaceutical client.
p>Responsibilities: The Sun Internship Program will allow students the opportunity to gain valuable experience that will integrate the knowledge and theory learned in the classroom with practical application and skill development in a professional setting. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.
Bridgewater, NJ30+ days ago
With strong project management capabilities, problem‑solving skills, and hands‑on content design and communication experience, you will deliver impactful materials with speed and accuracy-helping brand teams scale their content and omnichannel execution. Execute scalable content creation across various digital platforms (social media, display ads, banners, website, digital brochures, and emails, including Veeva RTE) to support omnichannel orchestration and personalization.
Florham Park, New Jersey30+ days ago
li style="margin-bottom:0in;font-size:10pt">Serve as the primary technical liaison to development laboratories and CMOs for key projects, and collaborate with Shionogi Japan colleagues on technology transfer activities while overseeing drug development and manufacturing processes. Overview: The Senior Manager, Pharmaceutical Sciences applies broad pharmaceutical sciences and CMC expertise to develop and maintain commercial products that are safe, effective, compliant, and robust across the product lifecycle.
This role partners across process and formulation development, CMC and Regulatory, Quality, and manufacturing/commercialization stakeholders to inform control strategy and support regulatory filings, ensuring development programs are supported by scientifically sound, compliant analytical strategies. The PAS Director provides strategic and operational leadership for a team that develops, qualifies, and applies analytical methods to characterize, release, and support stability for clinical drug substance and drug product.
Jersey City, NJ24 days ago
Together we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Syneos Health (Nasdaq:SYNH) is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
This role bridges drug development, manufacturing, and quality control to deliver high-quality eCTD submissions.
Key Responsibilities:.
Compliance & Risk Management:
- Identify/escalate CMC regulatory risks and propose mitigation strategies.
Florham Park, NJ30+ days ago
This role will provide technical leadership for an oral suspension product and a sterile injectable product, including formulation/process development, technology transfer, external manufacturing (CDMO/CMO) oversight, investigations, and post-approval lifecycle management. Serve as the primary technical liaison to development laboratories and CMOs for key projects, and collaborate with Shionogi Japan colleagues on technology transfer activities while overseeing drug development and manufacturing processes.
Powered by the Omni marketing orchestration system, OM connects best-in-class capabilities that enable our full-service media agencies OMD, PHD, and Hearts & Science to deliver more relevant and actionable consumer experiences, more productive and proactive client experiences, and more collaborative and rewarding talent experiences for the more than 24,000 people serving the world's leading brands in OM agencies around the globe. SSCG Media Group (SSCGMedia.com) is one of the largest full-service,100% pharma-focused strategic media planning and buying groups in the world and is a proud member of Omnicom Media.
West Caldwell, NJ30+ days ago
Able to wear safety glasses, hearing protection, full face/half mask respirator, latex gloves, Tyvek suit and other safety equipment as needed. Communicate with IPC Operator and Supervisor on all issues concerning quality, components, and machine performance.
p>Education Minimum Requirements:
p>Education Minimum Requirements: Minimum 3 years relevant industry experience for applicants with a Bachelor of Science degree, or 0 years of relevant industry experience for applicants with a Master of Science degree in Chemistry, Pharmaceutical Sciences, or related fields.
In your role as Scientist, you will be part of a team of Analytical Chemists working on cross-functional scientific teams to enable novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization and statistical data analysis.
Somerset, New Jersey30+ days ago
Who You Are: We are seeking a detail-oriented Pharmaceutical Operator to support manufacturing operations and ensure the consistent production of high-quality pharmaceutical products in a regulated environment. We are committed to innovation, quality, and excellence in the pharmaceutical industry, continuously seeking talented professionals to join our dynamic team.
The mission of College of Pharmacy and Health Sciences is to create a values-based student-centered learning experience that prepares graduates who are committed to improving the health of individuals and populations through leadership roles in pharmacy practice health care research and related health care fields. Job Summary Fairleigh Dickinson University College of Pharmacy and Health Sciences invites applications for a 12-month tenure-track faculty position at the rank of Assistant or Associate Professor in the Department of Pharmaceutical Sciences.
Fairfield, NJ30+ days ago
Responsible for coordinating, arranging and preparation of customer meetings on-site for the purpose of project team execution that can include campaign reviews, ad-hoc process related meetings, etc. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer, and more interconnected world.
p>Responsibilities: The Sun Internship Program will allow students the opportunity to gain valuable experience that will integrate the knowledge and theory learned in the classroom with practical application and skill development in a professional setting. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.
p>This role is part of Alcon's Research & Development function, a team that innovates boldly and delivers new products and services to help revolutionize the eye care industry, advance optimal patient outcomes and help people see brilliantly. The Pharmaceutical Medical Science Liaison - Dry Eye Medical (Science/Tech/Engineering Path) is primarily responsible for presenting scientific and clinical information on Alcon products and gathering insights to influence company strategies.