| junior Process Validation Contract at Junior, West Virginia, USA |
| Email: [email protected] |
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From: Avinash kumer, stellentit [email protected] Reply to: [email protected] Role :- junior Process Validation Location : Onsite in Trumbull CT - 5 days a week Job type : Contract RAte : $35 to $40/hr on c2c Note :- The process with AC is a little bit different than other companies. All candidates who are submitted to them must have an active and up to date LinkedIn profile. Please share their LinkedIn profile on submission. Job Description :- Can you help on the below role Fairly junior Process Validation role. Only 3 years of Medical Device experience is needed to be considered, hence the low rate. To perform this job successfully, an individual must be able to execute each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Must have strong working knowledge in: 21CFR820, ISO13485:2016, ISO14971 Process validation (IQ/OQ/PQ/TMV/MSA) Ideally both in transferring/scaling up existing processes as well as developing new processes NCMR, CAPA, Change control and GDP experience At least 3 years of experience in the medical device industry Experience in integrations/acquisitions with respect to ensuring quality requirements are preserved pre-post integration. Presentation of results in a logical and clear manner Ability to analyze information and come to conclusions based on presented data Ability to communicate effectively both orally and in writing Strong organizational and interpersonal skills Ability to learn and utilize computer in standard business applications including electronic document control, word processing, spreadsheets and databases. Background in statistics with respect to process control (reliability, capability, SPC, etc.) BS Degree in Life Science, Engineering or equivalent program is preferred Qualifications Background in statistics with respect to process control (reliability, capability, SPC, etc.) BS degree in Life Science, Engineering or equivalent program is preferred General Comments Onsite in Trumbull CT - 5 days a week 12 months duration to start Someone with Strong Process Validation knowledge IQ OQ PQ TMV/MSA (Validation Master PLAN VMP-Manufacturing process experience) NCMR Capa experience crucial here MSA (GR&R) protocol and report writing, execution PFMEA execution Statistics general knowledge very Important here with respect to process control (sampling for validations, Sampling for in process inspections) Med Device experience Must have bachelors degree Avinash Kumar Sr. IT Recruiter Email- [email protected] Phone Number : +1 321 7856 062 STELLENT IT A Nationally Recognized Minority Certified Enterprise " Happiness can be found, even in the darkest of times, if one only remembers to turn on the light ." - JK Rowling Keywords: rlang information technology Connecticut junior Process Validation Contract [email protected] |
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| 12:38 AM 17-Jan-25 |