JOB REQUIREMENTS: 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. Summary of Objective: The Lead inspector will set an example by staying current on industry trends, informing team members of new policies or procedures and displaying integrity. Possess strong people skills with the ability to organize team members and delegate tasks. The team leader will serve as a link between team members across two manufacturing sites and Visual Inspection Management. They must be knowledgeable, kind, and a professional role model in order that team members respect their judgment. Must be responsible, dependable, self-motivated, pro-active and provide suggestions for improvement. Responsible for performing 100% manual visual inspection, labeling and packaging of sterile filled containers (vials) in accordance with all applicable procedures, regulations and safety directives across multiple sites. 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. Perform all job responsibilities in compliance with applicable regulations, standard operating procedures, and industry practice. Supports Visual Inspection, Packaging and Labeling of product as needed across multiple sites with minimal to no supervision. Follows written procedures as well as documentation of results in a neat and precise manner according to GMP standards and other regulations Monitor workers on site during production activities to ensure adherence to ethics and safety procedures * Motivate workers to enhance production quantity and at the same time maintain high production standards Collaborate with management to create work schedule for workers and ensure that it is within process capabilities. Initiates Quality System Event investigations (Event Reports / Deviations / CAPAs) and works with management to determine probable root causes Perform document changes within the Master Control system Review protocols and manufacturing batch records; provide insight for process improvements. Supports development and tracking of metrics (KPI\'s) relating to... For full info follow application link. LSNE is an EEO/AA Employer and all qualified applicants will receive consideration for employment without regard to, their race, color, religion, sex, age, national origin, ancestry, sexual orientation, gender identity, disability, protected genetic information, protected veteran status, military service, or other protected status. The Company\'s EEO policy, as well as its affirmative action obligations, include the full and complete support of The Company. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/6A725A9056634CB0