Qa Specialist I - Ops

PCI Pharma Services•Bedford, NH

2d•Onsite

About The Position

The QA Operations Specialist I – Floor Support is responsible for providing QA support of Manufacturing and Visual Inspection activities for clinical and commercial medical device products in a GMP facility. The work scope includes on-the-floor Quality oversight of manufacturing activities including observing formulation and fill processes, GMP documentation and Batch Record review, line clearance, disposition of incoming raw materials, review and approval of facility work orders, and other various QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of Medical device products.

Requirements

Exposure to RCA, technical writing, and working with quality related investigations.
Minimum 2 years’ experience in relevant GMP industry preferred.
An equivalent combination of experience and education may be considered
Exposure to lean operation excellence highly desirable
Knowledge of FDA regulations (i.e., 21CFR Part 820)
Knowledge and ability to apply basic scientific principles to solve operational, as well as routine quality tasks.
Knowledge and exposure to using Risk Management Tools (FMEA, PHA, etc.)
Scientific, technical, and mechanical subject matter comprehension and aptitude
Able to articulate scientific and technical subject matter

Nice To Haves

ASQ certification is referred.
Strong organizational skills and attention to detail
Ability to make risk-based decisions and resolve issues with minimal guidance.
Demonstrated positive interpersonal skills and the ability to communicate well orally and in writing.
Proficiency in MS Office including Word, and Excel
Ability to work in a dynamic, fast-paced work environment.
Honesty, integrity, respect and courtesy with all colleagues
Able to work with some limited supervision, able to escalate issues as needed.
Is flexible and adaptable through operational and organizational change.

Responsibilities

Perform QA on-the-floor activities supporting client projects, including room release, auditing critical processes, reviewing GMP documentation in real time.
Perform periodic walkthroughs of manufacturing and support areas to ensure adherence to policies and procedures.
Batch record review for adherence to internal procedures and Good Documentation Practices
Review, approval and disposition of incoming materials such as consumables, excipients, and bulk device Ingredient, as applicable.
QA review and approval of new and revised GMP documents such as SOP’s and raw material specifications.
Act as first responder for on the floor quality issues in a timely manner, documentation of all events/investigations and required immediate corrective actions.
Assist in nonconforming material investigations.
Review of Quality Control Environmental Data
Review and approval of work orders impacting manufacturing facilities and utilities
May participate in root cause analysis using methodologies, such as: fishbone, 5 whys, etc.
Advise and coach internal customers on proper documentation of tasks
Assist in the initiation of Quality Systems (deviations, CAPA, Nonconformances).
Support Visual Inspection, packaging, and labeling operations
Create, review, and approve final product labels
Participate in SOP revision as it pertains to process improvements.
Participate in site quality and process improvement initiatives.
Represent QA on project teams and represent QA perspective as necessary.
Guide personnel indirectly and directly involved in GMP operations pertaining to cGMP compliance, internal procedures, regulatory requirements and industry best practices