Senior Manager, Project Management Office -Sun Pharmaceutical Industries, Inc (USA)

Senior Manager, Project Management Office -Sun Pharmaceutical Industries, Inc (USA)

Senior Manager, Project Management Office

Date:  Oct 31, 2023
Location:  Sun – Princeton – Corporate Office
Company:  Sun Pharmaceutical Industries, Inc (USA)
The Senior Manager is a lead position responsible for managing the day-to-day activities for new product launch projects with the objective to successfully commercialize and launch new products for SUN pharma. He/she develops end-to-end cross-functional project plans that detail critical path tasks, KPIs, milestones, scenario plans to mitigate impactful risks, timelines, and task owners. In addition, he/she must support and improve processes that impact key business areas like branded product label review & lifecycle management studies. This role will be the main point-of-contact between the brand, sales leadership, shared cross-functional project teams (local and global) and the PMO.
Area Of Responsibility
  • Coordinate and lead the Strategic Launch Planning Process with global alignment on all key requirements with sponsors & commercial leads.
  • Develop a robust, risk weighted scenario, launch plan with cross-functional teams while identifying critical gaps that the team needs to address. Understand and proactively recommend improvements in operational and go-to-market processes.
  • Ensure strategic alignment of the plan with commercial brand leads, along with a streamlined communication plan.
  • Ensures timely execution of critical tasks, milestones and deadlines. Follow-up with teams to continuously update the plan and prioritize activities as needed for the successful implementation of the project.
  • Lead regularly scheduled cross-functional meetings to ensure functional deliverables are understood and timelines are on track
  • Ensure that performance metrics are defined, tracked, and reported back to leadership teams
  • Assure all completed deliverables are stored in shared repository on time and dependency assessments are conducted regularly
  • Responsible for the preparation of project performance status & monthly status reports across all brands
  • Lead ad-hoc business projects & processes with global impact
  • Label Review Committee: Integrate & align all key global stakeholders across Brand, Regulatory, Medical & extended core teams on the thorough review of the label contents prior to submission. Continuously enhance the process and make impactful recommendations.
  • Lifecycle Management Studies: Integrate & align all key global stakeholders on the study progress and enhance the process continuously to address ongoing milestones, process gaps and next steps.
Education and Job Qualifications
  • BS/MS in Biology, Chemistry, Biochemistry, Biotechnology, or related scientific field is required
  • PMP desirable but not required
  • Proficiency with Enterprise Project Management tools
  • Strong Microsoft Project, PowerPoint and Excel skills
  • Strong passion for learning, building relationships & methodical in solving problems with teams
  • Ability to unite & lead cross-functional teams in a highly dynamic and changing environment (local and global)
  • Strong people skills & Ability to positively influence stakeholders to resolve impactful risks & conflicts
  • Excellent Emotional Intelligence, Communication & Listening skills
  • Situational, Social & Cultural Awareness
  • 8-10 years of Pharmaceutical industry experience with at least 5+ years of relevant Project Management experience in new product commercialization and/or clinical product development is required or equivalent
  • Strong exposure to Clinical trials, IND/ NDA filings – US and Global Regulatory Project Management is required
  • Understanding of branded product development & all aspects of the commercial launch processes
  • Understanding of program governance and business strategy development and execution
  • Strong understanding of manufacturing, supply chain process & regulatory strategies for successful commercial launch of the product.
  • Experience in project/program management of complex projects across diverse regions and cultures
  • Ability to build strong business relationships with all stakeholders & drive decision making
  • Solution centric approach to bring teams together to resolve priority risks & issues proactively with an eye on the big picture
  • Successful track record of delivering results through leading high performing teams
  • Process & Data driven to govern decisions
  • Ability to multi-task & handle complex issues in a balanced approach
  • Strong promoter of lessons learned and knowledge management
  • Ability to lead independently and inspire building teams locally and globally

The presently-anticipated base compensation pay range for this position is $109,000 to $133,000. Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan. Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.

The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. 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.

The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).

We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.

Notice to Agency and Search Firm Representatives:

Sun Pharmaceuticals (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Sun. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.

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Job Category: Phrama
Job Type: Full Time
Job Location: USA

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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