Job Details

ID #45838634
State Rhode Island
City Rhode island
Job type Contract
Salary USD competitive competitive
Source Real Staffing
Showed 2022-09-20
Date 2022-09-20
Deadline 2022-11-18
Category Et cetera
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Contract - Quality Engineer

Rhode Island, Rhode island, 02901 Rhode island USA

Vacancy expired!

Title: Contract - Quality Engineer

Location: Providence, RI

(100% Onsite)

Duration: 12+ Month contract

About the Company: A global pharmaceutical company

Benefits: Real Staffing offers medical, dental, vision, 401K, voluntary life insurance, short term/long term disability.

About the Role: The GMP Operational Senior Quality Engineer supports the principles and application of quality assurance and regulatory compliance. The incumbent supports or executes a wide range of straightforward activities, and supports new/existing project initiatives.

Your Main Responsibilities:
  • Supports quality oversight for root-cause analysis and product impact assessment for investigations as a result of deviations, OOS, and OOT investigations ensuring appropriate CAPA actions are identified.
  • Supports change control assessments, implementation and closure
  • Identifies and facilitates continuous improvement efforts
  • Supports drafting and revising Quality Agreements between CMOs/Suppliers and Vertex, as needed
  • Helps represents Quality Assurance on cross-functional working teams, applying strong communication and collaboration skills.
  • Support continuous improvement projects

Requirements
  • Bachelors Degree is Science or Allied Health
  • 7-10 years direct experience
  • Experience supporting multiple projects/teams within stated objectives and timelines
  • Experience supporting cross-functional team members and collaborate effectively
  • Good communication skills (written and verbal) and the ability to exchange potentially complex information
  • Able to integrates activities with other groups, departments and project teams as needed
  • Demonstrated ability to support evaluation of quality matters and solve straightforward problems using technical experience and judgement based on precedent
  • Ability to work in a fast-paced environment and meet quality, accuracy, and timeliness objectives
  • Expanded conceptual knowledge of cGMP's in a pharmaceutical setting
  • Proficient in leading event investigations, Root Cause Analysis (RCA), and CAPA

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

To find out more about Real please visit

Vacancy expired!

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