Supply Chain Mgr

Posted 9 Days Ago
Be an Early Applicant
Juncos
Mid level
Biotech • Pharmaceutical
The Role
This role supervises Supply Chain operations, ensuring compliance with cGMP guidelines. Responsibilities include managing personnel involved in material management, coordinating daily activities, liaising with regulatory bodies, and enhancing business systems to optimize supply chain efficiency. The position requires collaboration with internal and external stakeholders to maintain performance targets.
Summary Generated by Built In

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PharmaLex is a highly successful and growing consulting company for the Healthcare industry around the world. PharmaLex offers professional development, plus a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in an atmosphere that values trust, respect, teamwork, creative talent, enthusiasm, and diligence.
Location - Juncos, PR 
Requirements:
Doctorate degree or Master's degree and 2 years of directly related experience or Bachelor's degree and 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.
Highly preferred: Industrial Engineering
• Experience managing Lines/Resource/Warehouse Capacity
• Advance knowledge in excel and Visualization/Digital tools (Smartsheet, Tableau)
• Experience with SAP a Rapid Response
• Expose to previous Supply Chain organizations
Job Description:
SUMMARY
Under minimal supervision provides Supply Chain work group supervision and technical expertise in support of successfully completing daily operations within scope of responsibility.
FUNCTIONS
- Ensures all work is completed with minimal disruption and in compliance with all cGMP guidelines.
- 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 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.
COMPETENCIES/SKILLS
Must have well developed skills from Supervisor I level in addition to the following:
- Facilitation and presentation skills.
- Strong analytical problem solving skills.
- Strong technical writing skills.
- Strong project management skills.
- Change management skills.
- Ability to influence staff and effect change outside of area of responsibility.
- Initiate and lead cross-functional teams to resolve complex issues.
- Good decision making skills.
- Technical expert for function.
- Possess an understanding and appreciation of the Amgen Values and Leadership Attributes.
- While performing the duties of this job, the environment for the staff member is of an office atmosphere.
- Computer terminals, telephones, and calculators are in use constantly.
- Assignments are received in task and objective oriented terms.
- Provides direction to subordinates using established policies and procedures.
- Work is reviewed upon completion for adequacy in meeting the task / objective.
- Administers policies and procedures that typically affect individual staff members within one or more functional work groups.
- Accomplishes tasks mainly through general supervision of nonexempt and experienced exempt employees.
- Monitors daily operations of a work group and actively assists, or provides direction to, subordinates as required.
- May perform ongoing operational tasks.
- Makes decisions regarding group operations.
- Erroneous decisions or recommendations or failure to achieve results might cause delays in program schedules and result in the allocation of more resources.
- Ensures tasks and projects are efficiently completed on schedule following established procedures and within budget.
- Majority of liaison is on internal basis with subordinates and supervisors at equivalent level or one level higher.
- Regularly conducts briefings to management.
- Liaison normally involves specific phases of a project or operation.
- External contacts are regular and generally involve coordinating operational issues.
PharmaLex is an Equal Opportunity Employer.

Top Skills

Excel
SAP
Smartsheet
Tableau
The Company
HQ: Burlington, MA
1,385 Employees
On-site Workplace
Year Founded: 1994

What We Do

PharmaLex is a leading provider of specialized services for the pharma, biotech and medtech industries.

We guide you from early strategic planning activities and non-clinical requirements through clinical development, regulatory submission processes and post-approval/maintenance post-launch activities. Our experts use technology enabled solutions to support you through the entire product lifecycle. We deliver exceptional results - going above and beyond the standard to deliver tailor-made solutions worldwide.

The PharmaLex Group now has over 3000 employees, with 68 offices in 32 countries and more than 1000 satisfied clients worldwide.

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