Commercial Associate Project Manager I (Onsite Required)

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2 Locations
In-Office
Pharmaceutical
The Role

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.


We are PCI. 


Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

   

Summary of Objective: 

The Commercial Associate Project Manager I assists with designated customer projects to ensure that objectives are accomplished within prescribed time frame and budget while adhering to applicable pharmaceutical regulations. 

PLEASE NOTE: This role will require you to be onsite and the work days are Friday-Saturday-Sunday-Monday from 8:00 AM--6:00 PM. You will train with the Commercial team onsite Monday-Friday until you are ready for your transition onto the Friday-Monday shift alignment.

 

Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.  

Essential responsibilities fall into four main areas– Scheduling, Component Management, Production Monitoring, and Shipments 

                                                   Scheduling 

  • Facilitate the creation of item number requests for new projects and updates to revisions to existing projects 

  • Create and route Lot Expiry (LE) forms for assigned projects per the packaging schedule. Ensure routing is successfully completed in time to meet Packet readiness timeline. 

  • Create scheduling request for each packaging order and deliver to the Scheduling team, schedule requests should be submitted as soon as reasonably possible to meet client demand 

  • Create Sales Order and Work Order in ERP system (JDE) upon receipt of customer PO.  

  • Own the packet routing process for assigned clients – providing the Quality team with the requisite amount of time to complete the process and deliver the packet to the Operations Team. 

  • Communicate required bulk delivery dates to customers to meet packaging demand 

  • Create and manage Original Promise Date (OPD) in JDE for any required adjustments that impact delivery dates 

  • Track packet issuance metrics for assigned customers 

 

                                         Component Management 

  • Monitor purchase order statuses to ensure on-time component delivery 

  • Maintain optimal component inventory levels to meet packaging orders – understanding component lead times and future forecast. Collaboration with Procurement is required.  

  • Order and ensure shipper labels and print mats/slugs are ready for maintenance and production requirements 

  • Responsible for the destruction of obsolete materials & expired materials as well as providing COFD to the customer (as required).  

  • Ensure obsolete materials are billed for and managed after a component revision or the end of a project once they are ship confirmed 

  • Collaborate with Central Parts or customer for the ordering of any TempTales 

 

                                            Production Monitoring 

  • Maintain communication with the Operations team during packaging runs to ensure all needs are met in a timely manner 

  • Facilitate the creation and routing of Change Orders that are required for packaging.  

  • Create sample requests as required by customers, ensure the appropriate instructions and documentation are contained for shipping. 

 

                                                    Shipments 

  • Partner with IQA to ensure timely release of components and bulk, ensuring all requirements are available ahead of component delivery 

  • Facilitate the documents required to transfer material between sites. 

  • Track releases of Finished Goods for timely shipment 

  • Prepare and distribute necessary shipping documents to the appropriate team members 

 

 

                                                         Miscellaneous 

  • Review and approve documentation including specifications and batch records, as required. 

  • Provide continuous support to Project Manager and team for day-to-day internal problem solving and trouble shooting.  

  • Training and onboarding for new employees within the same role, as requested 

  • This position may require overtime and/or weekend work.  

  • Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, rules.  

  • Attendance to work is an essential function of this position 

  • Performs other duties as assigned by Manager/Supervisor. 

 

 

Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 

Required: 

  • Associate degree in a related field and/or 1-3 years related experience and/or training (project coordinator, business analyst, etc.). 

  • College Level Mathematical Skills 

  • Intermediate Computer Skills: Ability to perform more complex computer tasks and has knowledge of various computer programs.  

  • Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs.  

  • Very High Reasoning: Ability to define problems, collect data, establish facts, and draw valid conclusions. Be able to interpret an extensive variety of technical instructions in math or diagram form and deal with several abstract/concrete variables.  

 

Preferred: 

  • Able to set and achieve challenging goals. 

  • Ability to adapt to a changing work environment.  

  • Ability to display excellent time management skills.  

  • Ability to identify and resolve problems in a timely manner.  

  #LI-JM1

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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The Company
HQ: Philadelphia, PA
2,259 Employees

What We Do

PCI is a leading provider of integrated pharmaceutical development services to the global healthcare market. With facilities in North America and Europe, PCI supports pharmaceutical and biotech companies with products destined for more than 100 countries around the world. PCI provides services for each stage of the product lifecycle – from early Phase I through commercial launch and long-term supply – and partners with customers to provide key insight and expertise in enabling successful commercialization and bringing lifesaving medications to patients. For more information, go to www.pci.com.

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