Operations Consulting - Connected Supply Chain QMS - Director

Profile

Specialty/Competency: Operations

Industry/Sector: Pharma and Life Sciences

Time Type: Full time

Travel Requirements: Up to 60%

A career in Connected Supply Chain, within Operations Consulting, will provide you with the opportunity to help our clients optimise all elements of their operations to move beyond the role of a cost effective business enabler and become a source of competitive advantages. We focus on product innovation and development, supply chain, procurement and sourcing, manufacturing operations, service operations and capital asset programmes to drive both growth and profitability.

You'll be a part of a team that helps organisations in transforming their supply chains into a strategic asset. You’ll work with our clients to develop a supply chain strategy, optimise their supply chain footprint and logistics, manage transportation and distribution, and develop an integrated business planning solutions.

To really stand out and make us fit for the future in a constantly changing world, each and every one of us at PwC needs to be a purpose-led and values-driven leader at every level. To help us achieve this we have the PwC Professional; our global leadership development framework. It gives us a single set of expectations across our lines, geographies and career paths, and provides transparency on the skills we need as individuals to be successful and progress in our careers, now and in the future.

As a Director, you'll work as part of a team of problem solvers, helping to solve complex business issues from strategy to execution. PwC Professional skills and responsibilities for this management level include but are not limited to:

Support team to disrupt, improve and evolve ways of working when necessary.

Arrange and sponsor appropriate assignments and experiences to help people realise their potential and support their long-term aspirations.

Identify gaps in the market and spot opportunities to create value propositions.

Look for opportunities to scale efficiencies and new ways of working across multiple projects and environments.

Create an environment where people and technology thrive together to accomplish more than they could apart.

I promote and encourage others to value difference when working in diverse teams.

Drive and take ownership for developing connections that help deliver what is best for our people and stakeholders.

Influence and facilitate the creation of long-term relationships which add value to the firm.

Uphold the firm's code of ethics and business conduct.

Job Requirements and Preferences :

Basic Qualifications :

Minimum Degree Required :

Bachelor Degree

Minimum Years of Experience :

7 year(s)

Preferred Qualifications :

Preferred Knowledge/Skills :

Demonstrates proven expertise of, and is recognized as a leader within industry and regulatory agencies involving, Quality Management Systems, preferably within or with the FDA, emphasizing the following areas:

Driving strategy and implementation efforts on Quality Management Systems-related client engagements, including these focus areas- new business development; client engagement delivery, (i.e. remediating warning letters, consent decrees, an development and execution of effective, efficient and sustainable quality management systems; regulatory agency interactions; and, intellectual property development); and,

Participating and delivering thought -leadership conferences and roundtables, organizing think-tank-like discussions around controversial topics in an effort to generate the dialogue needed between industry and the regulators that can lead to potential solutions.

Demonstrates proven expertise and success with identifying pharmaceutical, biotech, medical device and diagnostic businesses with potential quality issues and business development targets, including providing the following areas:

Insights into the trends and expectations of regulatory agencies;

Guidance on developing effective assessment and remediation frameworks and/or practices;

Experiential guidance, subject matter specialty, and optimized standard industry practices with Quality Management Systems relating to practices involving Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), Good Pharmacovigilance Practices (GPP), and/or Good Laboratory Practices (GLP).

Demonstrates proven expert-level abilities and success in roles leading large or multiple teams through the design and implementation of people, process and technology changes, including:

Building solid and collaborative relationships with team members- fostering a productive teamwork environment; leading teams to generate a vision; leveraging diverse views; and helping to develop and grow team members throughout the course of every engagement;

Exhibiting capability in thought leadership, emphasizing new business development and project extensions, including client lead maturation, proposal development, and close;

Managing and delivering significant business results that reflect strategic and creative thinking, individual initiative and optimized engagement management- developing a business vision and leading complex projects while functioning at the highest levels of client organizations;

Identifying and addressing client needs ( i.e. building, maintaining, and utilizing networks of client relationships; managing resource requirements, project workflow and budgets);

Communicating complex material effectively in written and oral formats to various audiences; and,

Conducting and directing quantitative and qualitative analyses of large and complex data.

Demonstrates proven intimate abilities and success as a team leader, including leading teams to generate a vision, to establish direction and motivate members, as well as create an atmosphere of trust, leverage diverse views, coach staff, to encourage improvement and innovation.

Demonstrates proven thought leader-level abilities and success with directing efforts across pharmaceutical, biotech, and / or medical device companies, emphasizing the following areas:

Identifying and addressing client needs with major regulatory agencies (e.g. FDA, EMA, PMDA, etc.);

Developing and sustaining extensive client relationships using networking, negotiation and persuasion skills to identify and sell potential new service opportunities;

Preparing and presenting complex written and verbal materials including RFPs; and,

Defining resource requirements, project workflow, budgets, billing, collection.

At PwC, our work model includes three ways of working: virtual, in-person, and flex (a hybrid of in-person and virtual). Visit the following link to learn more: https://pwc.to/ways-we-work.

PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy.

All qualified applicants will receive consideration for employment at PwC without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. PwC is proud to be an affirmative action and equal opportunity employer.

For positions based in San Francisco, consideration of qualified candidates with arrest and conviction records will be in a manner consistent with the San Francisco Fair Chance Ordinance.

For positions in Albany (NY), California, Colorado, Nevada, New York City, Washington State, or Westchester County (NY), please visit the following link for pay range information: https://pwc.to/payrange-v1-advisorydirector

Company info

PwC US
Website : http://www.pwc.com