Role: Laboratory Instrument Validation – QE Only H4 EAD, GC, USC
Locations: Richmond, VA
Onsite from Day 1 (5 days a week)
Qualifications
•Bachelor's degree in a science or engineering related discipline with knowledge in quality operations laboratory processes
•7-9 years of experience in the validation of laboratory instruments including those with computerized systems attached in a cGMP environment (required)
•7-9 years of experience in the Pharmaceutical industry or relevant business experience within Quality Assurance or Validation cGMP Compliance
•Hands on experience operating instrument systems
•Demonstrated attention to detail
•Good oral and legible written communication skills
•Must be able to work independently
•Mastery of core computer software/systems (Word, Excel, Sharepoint, etc.)
•Demonstrated ability to work in a team environment and manage workload to meet deadlines
•Mathematical and scientific reasoning ability
Responsibilities
•Serving as validation representative for instruments
•Partnering with the laboratories, quality system administrators, BT, instrumentation and quality on implementing new instruments at the site
•Performing analytical instrument validation including computerized system validation if applicable
•Performing any validation change control during the life-cycle of the system
•Performing system periodic review
•Performing system decommissioning
•This position will be responsible for providing end-user support for all Quality Laboratory groups as well as compliance to global and site internal policies and procedures
•Initiates and leads change control for implementation of new instruments or changes to existing analytical instrumentation and associated instrument control software where applicable in Quality Control laboratories
•Authors cGMP risk assessments, user requirements & functional specifications, validation plans, protocols (i.e •IQ, OQ, PQ), reports, addendums and other validation deliverables as required by the site validation SOPs
•Assist the system owner with evaluating recommending the appropriate user roles and privileges for data integrity (where applicable), writing instrument operation instructions and preventive maintenance plans
•Ensures lab instrument's adherence to national and international regulatory guidelines on Electronic Records and Electronic Signatures and Data Integrity, cGMP, FDA 21 CFR Part 11/210/211, EU Annex 11, MHRA guidelines
•Authors protocol to challenge the main aspects of these requirements during validation to demonstrate adherence
•For systems found unable to fully comply, formulate workarounds/strategies with core stake holders to mitigate the gaps
•Initiates and leads risk assessment, gap analysis, and deviation management associated with validation of lab instruments
•Completes periodic reviews of instruments and instrument control software with focus on change control, deviation investigations, and CAPA to ensure compliance and validated state of the instrument
•Reviews validation deliverables created by others for adherence to site validation SOPs and acts as validation approver as needed
•All other duties as assigned
•Position interacts with laboratories within the Quality unit and impacts their compliance and continuous improvement
•Other functions key to the instrument validation process includes Laboratory System Administrators, Calibration and Documentation
Manager (Operations)
Suite #204, 8405 Sterling Street,
Irving - Texas - 75063.
linkedin.com/in/chandu-akkineni-51a512198
Hangouts: aforakkineni
You received this message because you are subscribed to the Google Groups "SureShotJobs" group.
To unsubscribe from this group and stop receiving emails from it, send an email to sureshotjobs+unsubscribe@googlegroups.com.
To view this discussion on the web visit https://groups.google.com/d/msgid/sureshotjobs/CA%2BRonb-gQZ1%3Dpp%2BVEF_-h-2TGx9%2By0i1bZdmCKaAOv1YZE%2BX4Q%40mail.gmail.com.
No comments:
Post a Comment