Job Details

ID #45869502
State New Jersey
City Southplainfield
Job type Contract
Salary USD TBD TBD
Source IKCON TECHNOLOGIES Inc.
Showed 2022-09-21
Date 2022-09-20
Deadline 2022-11-18
Category Et cetera
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Sr. Quality Engineer

New Jersey, Southplainfield, 07080 Southplainfield USA

Vacancy expired!

IKCON PHARMA, INC, an affiliate of IKCON TECHNOLOGIES, INC provides innovative services & solutions to our clients who develop novel, modern medicines to improve the lives of patients globally. By utilizing digital technologies, we can transform how sponsors approach clinical development by improving the patient experience, enhancing clinical trial productivity, increasing the quality of data collected in trials, and incorporating valuable insights from multiple sources of data. IKCON TECHNOLOGIES INC delivers exceptional IT services and solutions that provide clients with definite edge over competitors and promoting highest standards of quality. We are currently looking for a Sr. Quality Engineer with one of our clients in Remote, Remote If you are actively looking for opportunities, please send us your updated resume with your contact details. JOB TITLE Sr. Quality Engineer CITY Remote STATE Remote TAX TERMS C2C/W2 EXPERIENCE 7+ INTERVIEW MODE Telephonic and skype Required Skills: Key Duties and Responsibilities of a Sr. Quality Engineer: 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 Company, as needed Helps represents Company Quality on cross-functional working teams, applying strong communication and collaboration skills. Support continuous improvement projects Knowledge and Skills of a Sr. Quality Engineer: 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 Education and Experience of a Sr. Quality Engineer: Bachelor's Degree is Science or Allied Health 7-10 years direct experience Medical Device Experience is a MUST Educational Qualification: Bachelor's degree in a related field from an accredited college or university, with a minimum of 5 years of related experience.

Vacancy expired!

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