Quality Assurance Senior Associate #26-20776

"US Tech Solutions•West Greenwich, RI

14h•Onsite

About The Position

In this vital role, will be responsible for PQA (Plant Quality Assurance) On the Floor in support of Manufacturing activities. This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations.

Requirements

GMP experience is a must
Proficient in Microsoft Office (e.g., Outlook, Word, Excel, PowerPoint, MS Teams)
Knowledge of data integrity requirements
High school/GED + 4 years work experience or Associate + 2 years work experience or Bachelor + 6 months work experience or Masters Degree
cGMP experience
Excellent written and verbal communication skills

Nice To Haves

Drive
Independent but able to work within a team structure
Experience working in a cGMP environment
Experience with decision making
Experience with analytical testing and/or general compendia testing
Experience working with batch records and other GMP documentation
Knowledge of Good documentation practices and data integrity requirements
Experience collaborating within and across functional areas and demonstrated customer service focus
Ability to prioritize and navigate ambiguity, with minimal oversight, in a fast-paced environment
Bachelor’s degree and 2 years of Quality/Manufacturing work experience

Responsibilities

Provide Quality oversight to ensure that operations products are manufactured, tested, stored, and distributed according to current applicable regulations.
Ensure that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations.
Performs review and approval of cGMP processes, procedures, documents and records.
Review logbooks, batch records, attachments, work orders, and other GMP documentation.
Ensure that deviations from established procedures are documented per procedures.
Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements.
Alert management of quality, compliance, supply and safety risks.
Complete required assigned training to permit execution of required tasks.
Responsible for being in clean room space for majority of time on shift which includes gowning in and out of frocks and coveralls.
Communicating and collaborating with the PQA shift to ensure required tasks are completed