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 Senior Manufacturing Specialist is responsible for assisting the manufacturing team in a variety of complex tasks in accordance with the FDA and other regulatory agencies expectations while following all safety and quality guidelines of PCI. Incumbent collaborates with the manufacturing department in the execution of production across multiple shifts against department operational goals. This position will be the SME within the operations processes and is expected to be extremely versed in validation, regulatory and quality requirements as it pertains to cGMP. As the process operations subject matter expert, the incumbent is expected to take a lead role in process improvement initiatives.
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.
Ensure efficient operation of process floor activities by developing/improving processes, materials, GMP and safety controls
Collaborate with the Quality, Operations, Material Management, Engineering, MTS, Validation, Facilities, Finance, and R&D teams to optimize processes, applying Lean principles
Drive efforts to address regulatory compliance issues related to production.
Work closely with Operations Management to provide guidance to staff in alignment with cGMP requirements, department goals and corporate quality standards
Proactively identify, assess, and mitigate operational and organizational risks; escalate key risks and issues to manufacturing senior management and cross-functional support teams
Ensure manufacturing SOPs and batch records reflect practice, and are aligned to cGMPs/ISO and corporate standards
Author and perform investigations, deviations, CAPAs, and other GMP documentation and ensuring timely completion
Ensure work done by enabling/support groups is completed to standards. Participates in inspections conducted by external regulators, as required
Identify continuous improvement opportunities to improve processes and practices and makes changes in conjunction with supervisors and operators
Partner with cross-functional groups to evaluate and drive resolution of operational issues and proactively drive continuous improvement projects to completion
Successfully participate in media fill / aseptic proficiency test and maintains qualification if applicable.
Works within defined processes steps and methods, and will assist in developing procedures for new assignments or tasks
As the SME, assist in manufacturing operations to provide training and guidance as necessary
As the SME, you will train potential operations trainers and operators
Acts as Liaison and SME for new projects, creates processes and appropriate SOPs
Other duties as assigned
Special Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions.
Ability to lift 25 pounds
Ability to stand, sit or remain in the same position for long periods of time
May be required to travel between sites
Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Interacts with cross functional support teams such as Quality, Operations, Materials Management, Engineering, MTS, R&D, Validation, etc.
TRAVEL
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.
10+ years' experience with GMP, ISO and/or an FDA regulated environment is required.
6+ years of experience in a cGMPs/ISO environment in an operations role. Strong understanding of cGMPs
Strong technical writer and SME in writing all Quality system documents (CAPAs, Deviations, Change Controls, etc.)
SME in troubleshooting, investigation, root cause and risk analysis in a cGMP environment for complex issues within the production environment
Strong understanding of validation principles and practices to ensure compliance within operations
Bachelor's Degree in a Science or Engineering related field preferred
Intermediate/advanced PC skills, MS Office and Microsoft project applications is required
Ability to prioritize and manage multiple resources in a production environment with flexibility to meet organizational needs
Proven leadership, initiative, project management, and problem-solving skills
Skilled in a range of manufacturing processes and procedures through on the job training and significant on the job experience
Detail oriented with strong mechanical aptitude
Sets the example for fostering collaboration and teamwork
Assertive, self-directed, and results oriented
Honesty, integrity, respect and courtesy with leadership and peers
Strong commitment to conducting PCI PHARMA SERVICES business according to the highest legal and ethical standards, and to continually pursue excellence in the manufacturing and delivery of PCI PHARMA SERVICES products and services
Resilient, can quickly move forward despite challenges, thrives on challenges to improve skills and abilities
Must have ability to work as self-starter and handle multiple priorities in a dynamic cross-functional team-based environment
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, 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.
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
