Why Patients Need You

Our logistics and supply team makes sure that customers and patients have the medicines they need, when they need them. You’ll help bring medicines to the world even faster by embracing challenges, imagining what’s possible and taking action.

What You Will Achieve

Working with a dynamic team of Logistics and Supply Chain experts, you will play a critical role in ensuring the Quality and Compliance of Supply Chain cGMP operations.

You will help in the implementation of compliance programs, initiatives to support warehouse personnel and the development of behavioral & technical competencies for the organization within an environment of continuous improvement.  

It is your dedication and hard work that will make it possible for Pfizer’s customers and patients to receive the medicines they need, when they need them.

How You Will Achieve It

• Provide guidance, lead/co-lead projects, manage own time to meet objectives, and plan resource requirements for projects across the division.

• Contribute and lead global, cross-functional continuous improvement strategies to improve productivity and exceed customer satisfaction.

• Populate select monthly mandate dashboards and present progress in required forums.

• Enhance quality and compliance on a site and patient basis utilizing risk and mitigation plans.

• Analyze and compare information from multiple sources and identify cause and effect relationships supporting Corrective Action / Preventative Action investigations.

• Ensure compliance of our business processes and audit readiness by working closely with the business unit managers in Supply Chain.

Role Responsibilities:

• Work with and support QA on CAS Reports, Regulatory and Audit (Internal and External) commitments, CAPAs and other actions as needed

• Initiate quality investigations, events, change controls or planned temporary changes as needed.

• Track commitments and due dates to ensure on-time closure of quality records and commitments.  

• Lead responses to Supplier Corrective Action Report (SCARs) received by Supply Chain Warehouse

• Perform GMP document reviews for compliance

• Perform Batch Record review as required for drug transfers

• Author or approve GMP document revisions as needed.

• Identify deficiencies and work with the team on the necessary corrective actions

• Effectively participates in cross-functional team investigations for deviations and, when applicable, aids in authoring of remediation plans

• Assist in strengthening a Compliance culture and awareness by encouraging and communicating the compliance rules, escalation and remediation of compliance issues or improvements.

• Be a certified Trainer for the department.

Qualifications

Must-Have

• Applicant must have a High School Diploma (or Equivalent) and 8 years of relevant experience OR an associates degree with 6 years of experience OR a bachelors with at least 3 years of experience OR Masters with more than 1 year of experience.

• Demonstrated experience in Quality or cGMP warehousing

• Broad understanding of supply chain environment

• Demonstrated project management skills

• Excellent communication and interpersonal skills

• Strong knowledge of GMP standards and excellent MS Office skills

Nice-to-Have

• Experience with Method 1/Lean Six Sigma

• Experience supporting Quality investigations

• Experience presenting to Regulatory Auditors

PHYSICAL/MENTAL REQUIREMENTS

Ability to perform mathematical calculations.

Ability to read completed forms in English on site.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Off shift work may be required

Other Job Details:

• Last Date to Apply for Job: April 3rd, 2023

• Work Location Assignment: On Premise

Relocation assistance may be available based on business needs and/or eligibility.