Posted:
10/14/2024, 6:48:51 PM
Location(s):
Groton, Connecticut, United States ⋅ Connecticut, United States
Experience Level(s):
Junior ⋅ Mid Level
Field(s):
Operations & Logistics
ROLE SUMMARY
Internal Packaging Operations is part of Clinical Supply Operations (CSO) in the Global Clinical Supply (GCS) organization. Our purpose is to provide packaging solutions based upon a commitment to reliability, trust, confidence and ease of customer interaction to deliver quality packaged clinical supplies to the patient.
The Packaging Coordinator (PC) interfaces globally with Supply Chain Leads (SCL), Operational Strategy Leads (OSL), Clinical Research Pharmacists (CRP), and all other groups within and outside Global Clinical Supply necessary to bring a packaging request to completion. The PC acts as a Project Manager to ensure that these activities are performed at Pfizer internal packaging facilities within agreed to timelines and meeting the initial request parameters.
How You Will Achieve It
Provide Clinical Packaging support to internal and external partner lines while maintaining an organizational culture that values flexibility, continuous improvement and an agility to meet business needs
Support the development of practical and efficient clinical supply packaging designs for jobs designated for internal packaging activities
Coordinate and communicate multiple study packaging and/or labelling requirements to partner lines and internal packaging operations colleagues
Utilize project management skills to support project planning and scheduling and help assess risks to complete the packaging operation
Following standard operating procedures, prepare and approve packaging and labelling documentation and generate internal study paperwork to support packaging operations
Work with partner lines to drive the progress of the packaging operation to ensure timelines are met
Occasional interaction with suppliers and vendors as needed to support development and progression of packaging activities
Be compliant with Good Manufacturing Practices
Be inspection ready and support GMP audits.
Support assigned facility, equipment, process management tasks (such as validation tasks, periodic reviews and SOP authoring) and contribute to continuous improvement initiatives.
This position will primarily interface with the following:
Internal Packaging Operations Team
GCS Clinical Supply Operations workstreams
Global Clinical Supply stakeholders
Quality Assurance, Analytical Research and Development
BASIC QUALIFICATIONS
Bachelor’s Degree in relevant course of study and 0-2 years of experience
Relevant project management experience
Demonstrated communication skills
Proficiency in Microsoft office
PREFERRED QUALIFICATIONS
Experience working in a GMP regulated work environment
Knowledge of clinical trial study design
Clinical supply, pharmaceutical or related experience
Experience with enterprise-wide applications or systems (e.g. AXIS, CSDS, GDMS)
PHYSICAL/MENTAL REQUIREMENTS
Excellent planning, prioritization and organizational skills
Strong oral and written customer focused communication skills
Proven interpersonal, facilitation, and negotiation skills
High attention to details
Ability to manage time and dynamic changes effectively
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
On site presence is required to support physical operations.
Occasional travel to vendor sites may be required.
Work Location Assignment: Hybrid
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Website: https://www.pfizer.com/
Headquarter Location: New York, New York, United States
Employee Count: 10001+
Year Founded: 1849
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Biotechnology ⋅ Health Care ⋅ Medical ⋅ Pharmaceutical ⋅ Precision Medicine