QA Specialist II - Floor Support

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 QA Operations Specialist II - Floor Support is responsible for providing QA support of Manufacturingand Visual Inspection activities for clinical and commercial drug product in a GMP facility. The work scopeincludes on-the-floor Quality oversight of manufacturing activities including observing formulation andaseptic processes, performing AQL visual inspection of finished drug product vials, GMP documentationand Batch Record review, line clear and product changeover activities, disposition of incoming rawmaterials, review and approval of facility work orders, and other various QA functions as needed. Realtime continuous monitoring of manufacturing related systems and processes to ensure compliance withapplicable regulatory and industry standards, needed quality improvements, and safety/efficacy forphase appropriate GMP manufacture of drug products.

Essential Duties and Responsibilities Include:

* Perform QA on-the-floor activities supporting client projects, including room release, auditingcritical processes, reviewing GMP documentation in real time, and resolving issues that occur during manufacturing.
* Consult with internal teams such as Operations, QC, Facilities/Engineering, Project Management, and Materials Management to resolve complex situations or problems.
* Perform frequent walkthroughs and internal audits of manufacturing and support areas to ensureadherence to policies and procedures. May include management from groups such as Operations,Facilities, Quality, and Materials Management.
* Batch record review for adherence to internal procedures and Good Documentation Practices
* Support the evaluation and disposition of intermediates, finish bulk drug substance and drugproduct.
* Review, approval and disposition of incoming materials such as consumables, excipients, and ActivePharmaceutical Ingredient.
* QA review and approval of new and revised GMP documents such as SOP's and raw materialspecifications.
* Act as first responder for on the floor quality issues in a timely manner, documentation of allevents/investigations and required immediate corrective actions.
* Co-ownership of nonconforming material investigations.
* Review of Quality Control environmental and utility monitoring data and test results
* Review and approval of work orders impacting manufacturing facilities and utilities
* Root cause analysis using methodologies, such as: fishbone, 5 whys, etc.
* Advise and coach internal customers on proper documentation of tasks
* Initiation of Quality Systems (deviations, CAPA, Nonconformances).
* Perform Acceptable Quality Limit (AQL) visual inspection of final drug product
* Support Visual Inspection, packaging, and labeling operations

* Create, review, and approve final product labels
* Perform inspection of final product retains
* SOP revision as it pertains to process improvements.
* Participate in site quality and process improvement initiatives. Represent QA on project teams andrepresent QA perspective as necessary.
* Support internal, client, and regulatory audits and inspections.
* Obtain Qualified Trainer status on department specific training tasks; train new and less experienced team members.
* Recommend and support improvement ideas and projects
* Interact with clients during client visits
* Guide personnel indirectly and directly involved in GMP operations pertaining to cGMP compliance, internal procedures, regulatory requirements and industry best practices.

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 work in a dynamic, fast paced work environment

* Honesty, integrity, respect, and courtesy with all colleagues

* Creative with the ability to work with minimal supervision and balanced with independent thinking

* Resilient through operational and organizational change

* Exceptional organizational skills and attention to detail

* Ability to make risk-based decisions and resolve issues with minimal guidance

* Excellent interpersonal skills and the ability to communicate well orally and in writing

* Proficiency in MS Office including Word, and Excel

* Excellent verbal and written communication skills required

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.

* Ability to don cleanroom garments and pass aseptic gowning qualification.

Frequent reading, writing, and verbal communication

* Must be able to travel between multiple local production facilities

* Able to translate ideas to actual concepts and processes

* Proven ability to manage multiple projects (duties) simultaneously

* Able to work in a highly complex environment with competing demands and priorities

* Cross functional staff, members of management, internal and external clients, members of the Quality organization

* No managerial responsibilities. This is an individual contributor role.

* < 10% 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.

* Bachelor's degree in a relevant scientific field.

* Minimum 3 years' experience in relevant GMP industry, with minimum 1 year experience in Quality, preferred.

* Equivalent combination of education and experience considered.

ASQ certification is a plus

* Exposure to RCA, technical writing, and working with quality related investigations

* Exposure to lean operation excellence highly desirable

* Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as ICH

* Knowledge and ability to apply basic scientific principles to solve operational, as well as routine quality tasks

* Experience using Risk Management Tools (FMEA, HACCP, PHA, etc.) and familiarity with ICH Q9 preferred

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, 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.