
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.
Global Pharmaceutical Equipment Engineer, is a subject matter expert in high-speed automation with emphasis on device assembly and packaging. This position will be responsible for developing standards and best practices in the equipment and automation space for all PCI sites. This position will work with engineers and engineering leaders to ensure we uphold the highest standards consistently across PCI sites manufacturing drug-device combination products. Working closely with clients and internal stakeholders, this position will evaluate emerging technologies in the drug delivery device space, identify product opportunities, work with equipment vendors to implement new technologies to our equipment set, skill set requirements by site and define a roadmap for success.
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:
- Lead engineering standards and best practices for assembly & packaging equipment specification, build management, and commissioning in all PCI sites.
- Strategic focus for equipment specific technology development appropriate to the PCI CDMO working environment.
- Work with Business Development and new clients to define equipment and process requirements Provide subject matter expertise and hands-on work during equipment design, FAT, SAT and validation to augment facility-based NPI resources.
- Maintain Quarterly Business reviews for responsible OEMs and drive KPIs to best in class.
- Develop a skill set gap analysis for engineers and technicians in the equipment and troubleshoot high speed automation assembly and packaging equipment.
- Develop an ongoing technical training academy to enhance equipment knowledge for our sites, support troubleshooting and reduce mean to time to recovery on equipment issues.
- Knowledge of and adherence to all PCI, cGMP and cGCP policies, procedures, rules and regulations as applicable to assigned tasks.
- This position may require overtime and/or weekend work.
- Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, rules.
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:
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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.

PCI is your world leading CDMO, providing integrated end-to-end drug development, manufacturing, and packaging solutions to increase product speed to market and opportunities for commercial success. PCI brings the proven experience that comes with more than 90 successful product launches each year and over five decades in the delivery of CDMO services. With 30 sites across Australia, Canada, North America, the UK, and Europe and over 6000+ dedicated employees, together, delivering life changing therapies. Leading technology and continued investment enable us to deliver development to commercialization solutions throughout the product lifecycle, collaborating with our clients to improve the lives of patients globally.