Graduate, Engineering (NPI)

Posted 4 Days Ago
Be an Early Applicant
2 Locations
In-Office
Entry level
Pharmaceutical
The Role
Supports engineering leads with new product introduction projects from business development handover through equipment qualification and operational handover. Responsibilities include URS development, design reviews, FAT and SAT support, commissioning, IQ/OQ/PQ activities, project tracking, vendor coordination, GMP documentation, change control, SOP updates, equipment readiness, and continuous improvement. The graduate will develop expertise in regulated pharmaceutical packaging and device assembly equipment while building project management and cross-functional collaboration skills.
Summary Generated by Built In

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.

   

Key Responsibilities

Project Support

  • Support Engineering Leads in the delivery of projects from Business Development handover through to PQ and final transition to operations.
  • Assist in the development of User Requirement Specifications (URS) and contribute to design review activities.
  • Provide support during equipment build and acceptance phases, including Pre-FAT, FAT, and SAT activities.
  • Assist with commissioning and qualification activities (IQ, OQ, PQ), including execution support and data collection.
  • Help track project timelines, milestones, and action logs to support on-time delivery.
  • Support the handover of equipment to Operational Engineering, ensuring readiness and completeness.

Cross-Functional Coordination

  • Liaise with Engineering, Quality, Validation, Supply Chain, Procurement and Operations teams to support project execution.
  • Assist in coordinating activities between internal stakeholders and external equipment vendors.
  • Support inventory checks and pallet build for components supplied to vendors for machine build and FAT stage gates.
  • Help ensure facility and room readiness in collaboration with site teams ahead of equipment installation and qualification. Procurement, layouts, requisition control development.
  • Participate in cross-functional meetings and follow up on assigned actions.

Documentation & Compliance

  • Support the preparation, review, and maintenance of project and validation documentation in line with GMP requirements.
  • Assist with change control processes, ensuring accurate documentation and timely progression.
  • Contribute to the development and update of Standard Operating Procedures (SOPs)
  • Help compile and manage spares lists, including identification of critical spare parts.
  • Help design and manage equipment change part storage units.
  • Ensure documentation is completed in a timely and compliant manner to support audits and inspections.
  • Develop an understanding of cGMP requirements & regulatory compliance standards.
  • Ensure safe work practices are followed at all times and report any near misses to the Environmental Health & Safety (EHS) Department.

Continuous Improvement

  • Contribute to continuous improvement initiatives across engineering and NPI processes.
  • Support identification of process inefficiencies and assist in implementing practical improvements.
  • Help standardise documentation and project tracking tools where applicable.
  • Participate in Lean or operational excellence initiatives where applicable.

Learning & Development

  • Develop an understanding of the full equipment lifecycle within a Contract Development and Manufacturing Organisation environment, from URS through to PQ.
  • Gain hands-on exposure to regulated engineering practices, including GMP, validation, and equipment qualification.
  • Build knowledge of pharmaceutical packaging and device assembly equipment (e.g., labellers, cartoners, casepackers, PFS assembly).
  • Learn from experienced Engineering Leads and cross-functional teams through active participation in project activities.
  • Take ownership of personal development, supported by mentoring and structured learning opportunities.
  • Complete structured training on assembly equipment, packaging equipment, vision systems, and serialisation.
  • Develop core project management skills including planning, communication and risk awareness.
  • Undertake additional tasks or ad hoc projects as required to meet business needs within the scope of the role.
  • Travel on company business as required (vendor, supplier or customer-based).

Knowledge & Experience

Essential:

  • Educated to degree Level 8, or equivalent, in a relevant Engineering discipline (e.g. Electrical, Electronic, Mechanical, Mechatronic, Automation, or similar)
  • Strong interest in electrical and mechanical equipment within a regulated manufacturing environment.
  • Excellent written and verbal communication skills.
  • Proficient utilisation of Microsoft Office applications (Excel, Word, PowerPoint).
  • Strong organisational and time management skills.
  • Analytical mindset with attention to detail.
  • Ability to work collaboratively in a cross-functional team environment.
  • Self-motivated with a proactive approach to learning.

Desirable:

  • Internship, placement or work experience within pharmaceutical, biopharmaceutical, food or regulated manufacturing environment.
  • Basic understanding of cGMP principles.
  • Exposure to project management methodologies and electrical and mechanical equipment.
  • Experience using project tracking tools (e.g. MS Project, Smartsheet).

Skills & Aptitudes:

  • Strong interpersonal skills.
  • Eagerness to learn and develop professionally.
  • Ability to manage multiple tasks in a structured manner.
  • Problem-solving capability with a logical approach.
  • Customer-focused mindset.
  • High level of integrity and professionalism aligned to PCI Values and Behaviours.

Scope and Authority:

  • Supports Strategic projects under supervision of Engineering Leads.
  • No direct budget or people management responsibility.
  • Responsible for adhering to company SOPs, Health & Safety and regulatory guidelines.
  • Accountable for supporting the Engineering and NPI teams in the planning, coordination, delivery, and install of project equipment throughout the engineering lifecycle.

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.

Skills Required

  • Degree Level 8 or equivalent in a relevant engineering discipline, such as electrical, electronic, mechanical, mechatronic, or automation engineering
  • Strong interest in electrical and mechanical equipment within a regulated manufacturing environment
  • Excellent written and verbal communication skills
  • Proficiency with Microsoft Office applications, including Excel, Word, and PowerPoint
  • Strong organizational and time management skills
  • Analytical mindset and attention to detail
  • Ability to work collaboratively in a cross-functional team environment
  • Self-motivated with a proactive approach to learning
  • Internship, placement, or work experience in pharmaceutical, biopharmaceutical, food, or regulated manufacturing
  • Basic understanding of cGMP principles
  • Exposure to project management methodologies and electrical and mechanical equipment
  • Experience using project tracking tools such as MS Project or Smartsheet

PCI Pharma Services Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about PCI Pharma Services and has not been reviewed or approved by PCI Pharma Services.

  • Retirement Support Feedback suggests the company provides a 401(k) with an employer match in the mid‑single‑digit range, with immediate vesting noted in certain cases. This is viewed as a solid component of the overall package.
  • Leave & Time Off Breadth PTO and paid holidays are commonly available, and some roles indicate vacation is accessible from early tenure. Availability of time off is frequently described as a positive element of the package.
  • Affordable Benefits Health insurance is sometimes described as reasonably priced depending on plan tier. Feedback suggests core medical, dental, and vision coverage is part of a standard offering.

PCI Pharma Services Insights

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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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