Business Unit Intern
PCI Pharma Services
Summary
Execute documentation preparation for 24/7 production environment. Manage lot & expiration form creation, administrative planning tasks, and outbound finished goods shipments. Identify potential process improvements to improve efficiency.
Job description
Essential Duties and Responsibilities
- Support cGMP documentation creation and transactions as it pertains to lot/expiration form creation, outbound finished good shipments, and inventory reporting
- 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
Required:
- Working toward Bachelor's Degree in related field
- College Level Math Skills
- Advanced Computer Skills: Ability to perform the most complex computer tasks and operate various computer programs
- Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs
- High Reasoning: Ability to solve practical problems and deal with a variety of concrete variables in situations where there is only limited standardization. Ability to interpret a variety of instructions that may be provided in various forms
Preferred:
- Ability to effectively present information to various people as the job requires
- Ability to work independently and/or part of a team
- Ability to display original thinking and creativity
- Ability to hold oneself in a professional manner
Requirements
- Working toward Bachelor's Degree in related field
- College Level Math Skills
- Advanced Computer Skills
- Full Professional Proficiency in English
- High Reasoning ability
Benefits
- Paid Time Off
- Health Insurance
- Dental Insurance
- Vision Insurance
- Flexible Spending Account
- 401(k)
- Performance Bonus
Company overview
PCI Pharma Services is a global contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical supply chain solutions to pharmaceutical and biopharmaceutical companies worldwide. Founded in 1991 and headquartered in Philadelphia, Pennsylvania, the company has established itself as a trusted partner in the healthcare industry, offering integrated services that span the entire drug development lifecycle. PCI specializes in drug development support, clinical trial supply management, contract drug manufacturing, sterile and non-sterile drug product packaging, and global pharmaceutical logistics. With a global footprint encompassing 30 GMP-compliant facilities across multiple continents, the company serves as a strategic partner that follows the molecule from early development through commercial launch. PCI's expertise enables clients to accelerate time-to-market while ensuring regulatory compliance and quality standards. The company's comprehensive service portfolio includes analytical services, formulation development, commercial manufacturing, packaging, supply chain management, and distribution, making it a one-stop solution for pharmaceutical companies seeking to outsource their development and manufacturing needs.