QC Instrument Validation

Position Details:
Job Title:
Quality/Validation Engineer III / Laboratory Instrument Validation
Duration: 09 months contract, extendable up to 18 months

Location:

Rocky Mount, NC
Note:
Client has the right-to-hire you as a permanent employee at any time during or after the end of contract.
You may participate in the company group medical insurance plan which includes dental and vision.
Job Description:
The Quality Engineer III - Instrument Validation will be responsible for:
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.
ROLE RESPONSIBILITIES
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. Previous experience with PR/CAPA systems preferred.
Reviews validation deliverables created by others for adherence to site validation SOPs and acts as validation approver as needed.
All other duties as assigned.
QUALIFICATIONS
Bachelor's degree in a science or engineering related discipline with knowledge in quality operations laboratory processes.
5-7 years of experience in the validation of laboratory instruments including those with computerized systems attached in a cGMP environment (required).
5-7 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.
Ability to follow a variety of instructions furnished in written, oral, diagram, or schedule form.
PHYSICAL/MENTAL REQUIREMENTS (not all roles will have physical or mental requirements)
Use a computer terminal for up to 8 hours per shift, occasionally lift a maximum…