Teva Pharmaceuticals
Associate Director, R&D Project Management - Innovative Medicines
Teva Pharmaceuticals, West Chester, Pennsylvania, United States, 19388
Associate Director, R&D Project Management - Innovative Medicines
Date: Nov 20, 2024
Location:
West Chester, United States, Pennsylvania, 19380
Company: Teva Pharmaceuticals
Job Id: 58436
Who we are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
The opportunity
We are seeking a seasoned Associate Director, R&D Project Management to lead the global development of our R&D Innovative Medicine products.
In this role, you will be responsible for delivering a product development strategy working in close partnership with a Senior Program Leader to establish, maintain and deliver the priority product plan for both early and late stage.
How you’ll spend your day
Manage Cross-Functional Teams: Drive the operational planning and delivery of development programs, ensuring timely and budget-conscious execution.
Innovate and Collaborate: Work closely with global project leaders and function leads to secure approvals, manage risks, and ensure resource allocation.
Manage Multiple Projects: Oversee a selection of projects, ensuring all documentation is accurate and up-to-date.
Lead quality risk management: Ensure significant risks to the programs have planned mitigations and are flagged in terms of likelihood and impact, to the relevant leadership.
Your experience and qualifications
Master’s degree in a life scientific field; Advanced scientific degree (M.D., D.O., Ph.D.) - preferred
Minimum of 7 years in the innovative pharmaceutical industry with a proven track record in project management
In-depth knowledge and understanding of innovative drug development, industry guidelines, and regulatory and submissions processes globally
Project Management Professional (PMP®) – preferred
Strong oral presentation skills and advanced experience leading cross-functional project teams – preferred
Proficiency in Planisware, Microsoft Project, SharePoint, PowerPoint, Word, Excel, and Outlook
Role location
This role is based in West Chester, PA – preferred or Parsippany, NJ with a requirement to be onsite three days a week. Willingness to travel domestically and internationally is essential.
Enjoy a more rewarding choice
We offer a competitive benefits package, including:
Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
Time Off: Paid Time Off including vacation, sick/safe time, caretaker time, 13 paid Holidays and 3 paid floating holidays.
Life and Disability Protection: Company paid Life and Disability insurance.
Additional benefits include, but not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:Internal Career Site (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
Important notice to Employment Agencies - Please Read Carefully
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
EOE including disability/veteran
Date: Nov 20, 2024
Location:
West Chester, United States, Pennsylvania, 19380
Company: Teva Pharmaceuticals
Job Id: 58436
Who we are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
The opportunity
We are seeking a seasoned Associate Director, R&D Project Management to lead the global development of our R&D Innovative Medicine products.
In this role, you will be responsible for delivering a product development strategy working in close partnership with a Senior Program Leader to establish, maintain and deliver the priority product plan for both early and late stage.
How you’ll spend your day
Manage Cross-Functional Teams: Drive the operational planning and delivery of development programs, ensuring timely and budget-conscious execution.
Innovate and Collaborate: Work closely with global project leaders and function leads to secure approvals, manage risks, and ensure resource allocation.
Manage Multiple Projects: Oversee a selection of projects, ensuring all documentation is accurate and up-to-date.
Lead quality risk management: Ensure significant risks to the programs have planned mitigations and are flagged in terms of likelihood and impact, to the relevant leadership.
Your experience and qualifications
Master’s degree in a life scientific field; Advanced scientific degree (M.D., D.O., Ph.D.) - preferred
Minimum of 7 years in the innovative pharmaceutical industry with a proven track record in project management
In-depth knowledge and understanding of innovative drug development, industry guidelines, and regulatory and submissions processes globally
Project Management Professional (PMP®) – preferred
Strong oral presentation skills and advanced experience leading cross-functional project teams – preferred
Proficiency in Planisware, Microsoft Project, SharePoint, PowerPoint, Word, Excel, and Outlook
Role location
This role is based in West Chester, PA – preferred or Parsippany, NJ with a requirement to be onsite three days a week. Willingness to travel domestically and internationally is essential.
Enjoy a more rewarding choice
We offer a competitive benefits package, including:
Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
Time Off: Paid Time Off including vacation, sick/safe time, caretaker time, 13 paid Holidays and 3 paid floating holidays.
Life and Disability Protection: Company paid Life and Disability insurance.
Additional benefits include, but not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.
Already Working @TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:Internal Career Site (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
Important notice to Employment Agencies - Please Read Carefully
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
EOE including disability/veteran