Supply Chain Manager

Mentor Technical Group • Juncos, PR • 5h ago

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.

Responsibilities:

Ensures all work is completed with minimal disruption and in compliance with all cGMP guidelines and Amgen procedures.

Direct and coordinate daily activities of personnel responsible for material receipt, storage and transport.

Ensures materials are received, stored and transported according to established performance standards and all applicable procedures and regulations.

Interacts with internal and external regulatory agencies to ensure compliance with cGMP, DOT, OSHA requirements.

Collaborate with other sites to maintain optimal flexibility for the storage of all materials and product.

Identify and oversee implementation of new and improved business and compliance systems and tools.

Partner with key internal customer groups and/or external suppliers to ensure successful operations and performance targets are achieved.

Responsible for business continuity programs for assigned areas.

Participate on global functional teams to coordinate and improve the transportation and Logistics of material movement and storage across the Amgen Supply Chain.

Direct and coordinate daily activities of personnel responsible for developing and managing Product demand and forecasts.

Organize and communicate on a regular basis the total demand and supply requirements to senior management.

Coordinate the Master Production Schedule for Finished Goods and effectively communicate any impact created by, and to the supply plan.

Manage the process of gathering, evaluating and feedback of global demand requirements.

Provide and coordinate the development of business case scenarios that demonstrate the impact of current or proposed operations plans.

Manage the preparation and communication of the Company wide Inventory Distribution Plan to achieve corporate goals of customer satisfaction and risk management.

Develop and coordinate the long-range production requirements based on Marketing forecasts, product approval and release timelines, clinical requirements, SKU put-up information and business planning timelines estimates.

Education:

Ph.D OR MS + 2 years of directly related experience OR BS + 4 years of directly related experience OR Associate's degree and 10 years of directly related experience OR High school diploma / GED and 12 years of directly related experience.

Preferred Qualifications:

Educational background in Life Science and/or Engineering

Written and Verbal communication in English and Spanish

In-depth experience in Root Cause Analysis (Fishbone, Six Boxes, Fishbone, 5 Why's)

Supply Chain experience (receiving, suppliers, warehouse, shipping)

Strong Technical Writing Skills

Skilled in performance of GMP operations

Compliance/Regulatory knowledge and interaction experience

Experience leading cross-functional teams for RCA and problem solving

Ability to communicate and collaborate with technical and management staff within manufacturing, process development, supply chain, and quality.

Strong presentation skills.

Project management skills.

Specific responsibilities include but are not limited to:

Complete Root Cause Analysis

Apply Process Expertise - capable of understanding process and controls require to assess for potential causal factors

Assess process performance by observation of floor operations and review of performance data.

Support trouble shooting to identify Causal Factors and potential corrections

Evaluate operational procedures

Evaluate training requirements for technical aspects of the process

Identify training opportunities

Use and perform Risk Assessments as required to identify and understand risks and failure modes

Define CAPAs

Evaluate process improvement opportunities

Negotiate Actions with Partners

Deliver timely robust plan to address Root Cause

Perform Impact to Process /Equipment /System Assessment

Team with Product Development to understand potential impact to product quality attributes

Assess Equipment/Systems information for potential impact to product quality attributes

Assess for Data Integrity

Assess for Process Validation Impact

Author Investigation Report

Use Technical Writing techniques proficiently

Perform Data Verification

Ensure timely report approval

Support Peer Review

Follow current standard procedures/templates

Serve as SME to define deviation designation when called upon

Facilitate Process and Equipment Risk Assessments and make recommendations to mitigate risks

Participate in regulatory inspections

Participate in the assessment or implementation of special projects or initiatives.

Make strategic planning to support product supply and business performance metrics.

Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.

Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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