- 214077 - QA Engineer
- Industry
- ENG
- Region
- NY-Upstate
- City
- Skaneateles
- State
- NY
- Rate
- Up to $31.81 DOE
- Duration
- 12 months
- Description
Chipton-Ross is seeking a QA Engineer for a hybrid contract opportunity in Skaneateles, NY.
BASIC QUALIFICATIONS (REQUIRED SKILLS/EXPERIENCE):
· Must have computer proficiency with solid experience in Microsoft Word, Excel, Trackwise, SAP, and other systems.
· Ability to work effectively as part of a cross functional team.
· Ability to relate and work well with people.
· Excellent organizational, presentation, and verbal/written communication skills.
· Attention to detail.
· Ability to multi-task and work well under pressure.
· Expertise in interpreting regulations and familiarity with GDP and GMP
· Experience with working in an environment subject to compliance with 21 CFR Parts 7, 11, 803, 806, 810, 820 strong preferred.
· Must be able to sit for most of the work day.
· Ability to stand or walk for long periods as well.
· Must have good hand to eye coordination and dexterity
· Physical Requirements: Dynamic Lifting capability: Must have the ability to lift 40 pounds at a time.
POSITION RESPONSIBILITIES:
This position manages the project investigations and day-to-day task assignments within the Corrective and Preventive Action (CAPA) program within their assigned site. The position also has responsibility to work closely with various managers at the facility to monitor, manage and maintain metrics for the CAPA program in their specific area. Additionally, this position is responsible for standardizing the CAPA program across different sites in the Front Line Care (FLC) division. Specific responsibilities may include, but are not limited to:
· Ensures efficient processing of nonconformance management for the Quality Management System in Trackwise.
· Maintain Quality Metrics for NCR/CAPA timeliness and makes recommendations for improvement.
· Leads and facilitate discussions with CAPA owners to drive completion of investigations, root-cause analysis, impact analysis, and closure of events.
· Write, review, analyze and revise written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc.
· Identifies areas for process/quality improvements and supports those efforts.
· Owns and manages several project investigation records at one time.
· Analyze trends to monitor the effectiveness of the CAPA process and drive remediation for improvement
· Follows Good Documentation Practices (GDP) and ensures compliant documentation related to area of responsibility.
REQUIRED EDUCATION:
Accredited Associate or BS in business, science, or engineering
WORK HOURS:
Full-Time 1st Shift
Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.
- Contact
-
Johnnie Barrientos
jbarrientos@chiptonross.com
CHIPTON-ROSS, INC.
420 Culver Boulevard
Playa Del Rey, CA 90293
Phone: (310) 414-7800 x290 or (800) 927-9318 x290
Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.
Employment will be contingent on candidate clearing pre-employment drug screen and background check.
Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.