Senior Director, PQM Strategy Deployment & Excellence (Belgium/Italy)

Johnson & Johnson Innovative Medicine; Latina; In loco; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading global pharmaceutical company is seeking a Senior Director for PQM Strategy Deployment & Excellence in Italy. In this role, you will guide product quality excellence across innovative medicine initiatives, ensuring alignment with key partners and managing talented teams. The ideal candidate will have at least 15 years of experience in the Biotech or Pharmaceutical industry, strong leadership capabilities, and a proven track record in managing complex programs effectively. This full-time position offers a chance to make significant contributions to the organization.

Competenze

• 15+ years of experience in Biotech/Pharmaceutical Medical Device/Industry.
• 7+ years of people management & talent development experience.
• Ability to influence and negotiate with various stakeholders.

Mansioni

• Drive Product Quality Excellence leadership across global initiatives.
• Own and develop the PQM Strategy aligned with key business partners.
• Lead the initiative to foster data-driven approaches within the team.

Conoscenze

Leadership skills

Analytical thinking

Relationship management

Formazione

Bachelor's degree in Pharmaceuticals, Chemistry, Engineering, Sciences or similar

MBA, MS or PhD

Strumenti

Business Process Management (BPM)

Six Sigma

Descrizione del lavoro

Senior Director, PQM Strategy Deployment & Excellence (Belgium/Italy)

4 days ago Be among the first 25 applicants

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function

Quality

Job Sub Function

Business Process Quality

Job Category

People Leader

All Job Posting Locations

• Beerse, Antwerp, Belgium — Req #: R-047934
• USA (Raritan, Titusville) — Req #: R-046243
• Switzerland (Schaffhausen) — Req #: R-047927
• Italy (Latina) — Req #: R-047934

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all the postings, we recommend focusing on the specific country(s) that align with your preferred location(s).

We may also consider qualified internal candidates located in other Innovative Medicine manufacturing sites.

Position Summary

The Senior Director PQM Strategy Deployment & Excellence is part of the Product Quality Management organization and will drive Product Quality (PQ) Excellence leadership. He/she is responsible for the development, deployment and execution of the strategy and roadmap for Product Quality Management & alignment with the major business partners in Innovative Medicine (IM) Supply Chain, IM Quality and DPDS. The individual also provides functional management to PQM Stability CoE, Risk Management and PQM Support, Central Product Complaint Investigation and PQM Digital Excellence. The Senior Director PQM Strategy Deployment and Excellence is a member of the PQM Leadership Team.

Key Responsibilities

• Under the direction of the Vice President, Product Quality Management, provide Product Quality Excellence leadership to PQM and global initiatives across IM Quality and Supply Chain.
• Owns the development and deployment of the PQM Strategy, ensuring alignment of the Strategy and execution with IM Quality and other key PQM business partners such as Value Chain Management, Discovery Product Development and Supply (DPDS), Clinical Supply Chain and Small Molecule/BioTherapeutics development teams and within the IM Quality verticals.
• Owns the PQM elements for IM Quality.
• Owns PQM Stability Program Management CoE. Ensure compliance with all regulatory and IM and JnJ requirements while maximizing efficiency.
• Lead IM Stability Program Management (SPM) cross‑functional team to ensure IM SPM strategy is established and updated, SPM performance measures are in place and continuously improving through effective cross‑functional team collaboration.
• Owns quality system elements including but not limited to the Quality Management review process, internal audit, documentation management, training, etc. within PQM to ensure compliance and continuous improvements.
• Direct Product Risk Management activities within IM to ensure compliance with regulatory requirements. Ensure the successful application of Product Risk Management tools such as Criticality analysis, Product Risk Analysis (PRA)/Product Risk Management (PRM), FMEA, etc. within IM.
• Leads the initiative to develop and promote more data‑driven and innovative approaches within the PQM team. Supports PQM through better product analytics, dashboards and continuous improvement projects. Holds accountabilities for all activities performed within the PQM organization. Acts as a representative for PQM at IM Quality and other global digital forums and initiatives.
• Responsible for core PQM business processes such as PQM LRFP, Budget, Cascade, etc. Together with the team identifies, quantifies and drives improvement opportunities within PQM.
• Build organizational capability and ensure his/her group effectively executing JnJ’s performance management and talent development processes; having adequate resources and expertise to perform their duties related to product quality. Plan and manage the group’s budgets.
• Remains current in knowledge, skills and industry trends. Contributes to the strategy setting of the entire PQM organization. Train in new regulations, guidelines, procedures and processes. Make a positive contribution by making suggestions for improvement.
• Deliver portfolio of projects including product or therapeutic area projects flawlessly using proven project management tools.

Qualifications

• A Bachelor’s degree in Pharmaceuticals, Chemistry, Engineering, Sciences or similar.
• An advanced degree and/or Business (MBA, MS or PhD) is preferred.
• At least 15 years of senior level experience in Biotech/Pharmaceutical Medical Device/Industry and broad scientific expertise, having demonstrable experience in leading complex global programs and improvement initiatives, projects and groups of professionals are required. Multifunctional background preferred.
• A minimum of 7 years of people management & talent development experience is required.
• Must have strong leadership skills and operate as a leader with global mindset, understanding and appreciation of the global /enterprise context.
• Relationship management, excellent coaching and collaboration skills are required.
• Must be an analytical and strategic thinker with the ability to create integrated sector wide solutions to align with sector and enterprise requirements.
• Influence, shaping solutions, negotiation and consultative skills are required.
• Must be a thought leader experienced in shaping solutions, with strong communication and collaboration/partnership skills.

Required Skills

Preferred Skills

• Business Process Management (BPM)
• Business Requirements Analysis
• Compliance Management
• Consulting
• Developing Others
• Fact‑Based Decision Making
• Inclusive Leadership
• ISO 9001
• Leadership
• Leading Change
• Managerial Courage
• Process Governance
• Process Optimization
• Quality Control (QC)
• Quality Standards
• Quality Validation
• Six Sigma
• Standard Operating Procedure (SOP)
• Tactical Thinking

Seniority level

Not Applicable

Employment type

Full‑time

Job function

Management and Manufacturing

Industries

Pharmaceutical Manufacturing