http://bauschandlomb.jobs2web.com/go/New-Jersey-Branding-Jobs/118191/ View New Jersey Branding Jobs at Bausch and Lomb en-us http://basf.jobs2web.com/images/bauschandlomb/logo.gif http://bauschandlomb.jobs2web.com/go/New-Jersey-Branding-Jobs/118191/ 720 Job Title:
Sr. Brand Manager, Global OTC Pharmaceutical Marketing

Req #:
5116BR

Job Description:
PURPOSE: Lead the development of robust category level strategies for key global OTC pharmaceutical brands and therapeutic areas within Ophthalmology. Collaborates closely with the Regional teams, R&D Project Management, Regulatory and Medical to ensure successful global launches, in-market performance and life cycle management of key global brands. Develops brand plans and supports Regional implementation. RELATIONSHIPS: Reports to the Global Head of OTC Marketing within the Pharmaceuticals Business Unit. Leads the Global brands team and the extended cross-functional team. Interacts extensively with all areas of the business - particularly Regional Marketing and Sales, R&D Project Management, Regulatory, Medical and Business Development. ESSENTIAL FUNCTIONS: BRAND AND THERAPEUTIC AREA STRATEGY: Leads Global brand team and extended cross-functional team to ensure successful global launches, in-market performance and life cycle management of key prescription pharmaceutical brands. Defines robust therapeutic area strategy to strengthen the in-market and pipeline portfolio in close collaboration with the R&D, Business Development and Regional Marketing and Sales. Develops Global brand plans to maximize key pipeline and in-market brands, including global launch plans, positioning, branding, life cycle management and forecasting. Supports Regional implementation of brand plans and sharing best practices to ensure excellent in-market execution. Partners with Marketing Intelligence to generate insights on customer needs, competitive dynamics and brand positioning / performance and incorporate these into strategies / plans. Ensures excellent matrix management and develops strong relationships with key internal and external stakeholders. Participates in cross-functional projects and select business development opportunities. BUDGET: Oversees the global brand budget and ensures that resources are appropriately allocated and high quality deliverables are produced. DEVELOPMENT OF PEOPLE: Supports Regional / local brand managers and helps to build capabilities within the Global brand and cross-functional teams; develops clear brand / team KPIs. Manage the application and communication of all B&L policies and procedures.

Qualifications
KEY SUCCESS FACTORS: EDUCATION, EXPERIENCE, KNOWLEDGE AND SKILLS: Bachelors Degree required. Masters degree preferred. 6 - 10 years relevant OTC Pharmaceutical marketing experience, demonstrating a steady career progression with increasing roles of responsibility. Prior experience launching a OTC Pharmaceutical product required. Prior experience in Global Marketing or in Marketing in more than one Region strongly preferred. Sales experience preferred. Strong analytical and quantitative analysis skills required. Strong influencing, cross-functional collaboration and customer service skills required. Ability to plan, organize, and deploy resources according to urgency/importance. Presentation/communications skills must be excellent. Strong Innovation and Adaptability: must be able to identify better ways of doing things and getting others excited about new approaches. OTHER: Works within B&L's established policies and procedures. Embraces B&L Values in spirit and actions. Up to 25% overnight travel.

Work Location NJ-Madison Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/MADISON-Sr_-Brand-Manager,-Global-OTC-Pharmaceutical-Marketing-Job-NJ-07940/514695/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/MADISON-Sr_-Brand-Manager,-Global-OTC-Pharmaceutical-Marketing-Job-NJ-07940/514695/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS Job Title:
Regulatory Affairs Associate Director - Brand

Req #:
5340BR

Job Description:
The Global Regulatory Associate Director handles all regulatory development aspects for prescription brand ("Brand") products. Participates on the product development team to provide regulatory guidance for Pharmaceutical Brand products. Manages relevant regulatory strategy components and interactions with Regulatory Authorities for Brand products. May perform due diligence efforts on new product opportunities. Specific

Job Duties:
? Responsible for developing a global product regulatory strategy for Brand pharmaceutical products ? Liaise with global regulatory counterparts to ensure regional requirements are incorporated into product strategy development ? Develop a product regulatory timeline aligned to Bausch & Lomb's product development, with key regulatory milestone, and activities for agency filing ? Coordinate with the Labeling Senior Manager for the development of product labels ? Ensure labeling content and product documentation is developed in accordance with regulatory requirements ? Participate as a member of the product development team(s) to build awareness of Regulatory Authority requirements and timing for submissions ? Coordinate with Global Submissions Manager to ensure timely and accurate submissions to Regulatory Authorities ? Act as a regulatory contact with Regulatory Authorities for assigned pharmaceutical Brand products ? Liaise with Bausch & Lomb country-specific pharmaceutical Regulatory Affairs personnel for international submissions and registrations ? Manage interactions with other Bausch & Lomb functions (e.g., Quality, Compliance) during Regulatory Authority inspections ? Provide regulatory guidance/input to internal product review boards ? Manage assigned personnel Technical Competencies: ? Knowledge of pharmaceutical brand industry regulatory affairs discipline throughout the product lifecycle, including Development, Promotion and Advertising, Labeling, CMC, Commercialization, and Operations ? Knowledge of domestic and international laws, regulations, and guidance that affect Brand products ? Knowledge of clinical development, including responsibilities for successful management of development milestones, and/or marketing authorization, meeting facilitation, labeling negotiations, and regulatory responses ? Ability to interpret Regulatory Authority policies and guidance and correctly apply them as appropriate in product development and labeling regulatory activities for Brand products ? Ability to influence and partner with cross-functional teams in a global pharmaceutical organization ? Ability to take innovative ideas from proof of concept to promote a successful product regulatory strategy and increase probability of regulatory approval ? Ability to critically review detailed scientific information and assess whether technical arguments are presented clearly and conclusions are adequately supported by data ? Ability to assess project risks, and where appropriate, recommend contingency plans and strategies to mitigate regulatory risks Professional Competencies: ? Demonstrated ability in analytical reasoning and critical thinking skills ? Strong capability to contribute and lead a team environment ? Strong business acumen and ability to see the business drivers outside of Regulatory Affairs ? Excellent communication skills; both oral and written ? Strong interpersonal skills with the ability to influence others in a positive and effective manner ? Demonstrated ability to contribute to a continuous learning and process improvement environment ? Capacity to react quickly and decisively in unexpected situations ? Detail-oriented with the ability to proofread and check documents for accuracy and inconsistencies ? Focused ability to influence operational excellence and performance metrics ? Risk adverse where needed with the ability to identify potential solutions to complex problems

Qualifications
? 8+ years relevant pharmaceutical industry and regulatory experience ? Pharmaceutical brand experience highly preferred ? Bachelors degree in science or health related field ? Advanced degree preferred (PhD, MD, MS, PharmD, or equivalent)

Work Location NJ - Madison Relocation Available Yes

Status Full-Time]]> http://bauschandlomb.jobs2web.com/job/MADISON-Regulatory-Affairs-Associate-Director-Brand-Job-NJ-07940/656248/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS http://bauschandlomb.jobs2web.com/job/MADISON-Regulatory-Affairs-Associate-Director-Brand-Job-NJ-07940/656248/?utm_source=J2WRSS&utm_medium=rss&utm_campaign=J2W_RSS