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. The Validation Engineer I performs an array of well-defined validation activities in support of cGMP pharmaceutical/medical device contract manufacturing across multiple PCI facilities. In collaboration with validation management, the Engineer I assist with internal project teams and external validation firms on validation/qualification initiatives and ensures project schedules are met. Complies with requirements of the Safety Program, including PCI Health and Safety mandates and OSHA requirements. In carrying out duties, contributes and promotes a positive and equitable working environment emphasizing the PCI Values: Customer Focus, Innovation, Integrity, Collaboration, and Superior Performance. **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. • Author validation plans; assist with the development of specifications for user requirements, functional requirements, and design requirements, trace matrices, validation summary reports and test protocols for installation, operation, performance of equipment, functional requirements, risk assessments, and IQ/OQ/PQ. • Review commissioning, qualification and validation related system lifecycle documentation (user requirements, functional and design specifications, commissioning and qualification protocols). • Assist with direction on equipment/process change control development (equipment, utilities, facilities, and processes) used to develop and manufacture products in a cGMP environment. • Work closely with other validation department personnel as well as cross-functionally with Manufacturing, Engineering, Critical Utilities, Quality Assurance, and project management to achieve all project deliverables. • Assist management with mentoring and training of colleagues on policies and procedures including the requirements for validation. • Validation representative on validation projects leading by example on projects. • Develop and recommend science-based solutions with a focus on continuous improvement and compliance. • Perform risk assessment and mitigation steps to achieve attainment and maintenance of a validated state of compliance for all equipment, utilities, processes, materials, and facilities • Coordinate and execute validation protocol activities with consistent and effective communication with affected departments; working autonomously while keeping manager regularly updated. • Work in a highly independent fashion, with minimal to no direction in the execution of duties, while keeping team mates and manager informed and providing guidance to other engineers as needed. • Write protocols and technical study approaches. • Review document changes for validation and deviation impact. • Propose corrective actions to validation manager and appropriate departments to implement the required changes. **PROFESSIONAL SKILLS** • Knowledge of Industry guidelines (ISPE, PDA), US and international regulations (FDA, ICH, ISO, EMA) for validation of GMP facilities. • Possess strong knowledge of commissioning, qualification validation, practices, including applicable regulations. • Excellent technical writing, verbal communication and presentation skills.. • Proficiency in Microsoft Office including Word, Excel, Power Point, Project **QUALITIES** • Organized individual who is accustomed to working in a result oriented-focused, dynamic CMO environment. • Professional and collaborative team player must have strong interpersonal skills. • Honesty, integrity, respect and courtesy with all colleagues. • Ability to inspire others to strive for excellence. • Self-motivated and able to meet goals with minimal supervision. **PHYSICAL REQUIREMENTS & MENTAL DEMANDS** • Ability to lift 50 pounds • Must be able to stand for long periods of time each day • Travel and work at all PCI site locations/facilities • Ability to multitask with competing demands and at times shifting priorities. • Able to don ISO cleanroom gowning and PPE, as required by site procedures. **COMMUNICATIONS & CONTACTS** • Interacts with all department staff to resolve technical issues and initiate process improvements. • Must be able to work with multiple departments including Operations, Engineering, Facilities, Quality Control and Quality Assurance. **TRAVEL** Approximately 15% **EDUCATION** • Bachelor’s degree in Engineering or related scientific discipline required with a 1-3 years of Pharmaceutical industry experience or combination of work experience in Validation, QA, MFG, or Engineering. **EXPERIENCE** • Experience in pharmaceutical or biopharmaceutical environment in operations/engineering/manufacturing/quality environments. • Combination of equipment qualification, process validation, or cleaning validation is acceptable; QA pharmaceutical experience also preferred. • Validation experience with the following is highly preferred: Thermal characterization, Vacuum physics, Heat and mass transfer, Formulation, Aseptic Filling and Lyophilization. Steam Sterilization, • Experience in multiple regulatory inspections and knowledgeable in current industry standards and regulatory trends as they pertain to Validation of pharmaceutical or biopharmaceutical processes. \#LI- Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future (https://pci.com/) **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, Diversity, Equity, and Inclusion (DEI) 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._ Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don’t say no, we figure out how. PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled