Experience Inc. Jobs

Quality Engineer II - Onsite

• Bioengineering

• Biotechnology

• Change Control

• Chemistry

• Immunology

• Inspections

• ISO

• ISO Standards

• Medical Device

• Peoplesoft

• QMS

• Root Cause Analysis

• SAP

• SIX Sigma

• SOPS

• Statistical Analysis

• Virology

Description:

This job posting is for a contingent resource on assignment with Corning Incorporated. This position could provide you with an opportunity to help Corning push the boundaries of technology while enjoying the benefits of working for Magnit. Magnit is a leading, global professional services and technology company and a certified “Great Place to Work” Magnit has been a leader in contingent workforce management since 1991 and work with leading Fortune 500 companies and other large organizations across the world.

Job Title: Quality Engineer II

Scope of Position:

Develop and support all Quality Management System (QMS) / Regulatory Affairs (RA) activities and functions supporting the quality goals and quality metrics for site. Responsible for new product setup, quality project management, and regulatory compliance of serum products. Ensure compliance to in-house and/or external specifications and standards such as cGMPs, 21 CFR 820, ISO 13485, and Quality System Procedures.​

Day to Day Responsibilities:

• Ensure compliance to new and changing regulations affecting products and processes

• including, but not limited to, QSR’s, global import/export regulations, etc.

• New product setup and management of related projects

• Assist with Supplier audits, as needed

• Maintenance of BSE Serum Certificates of Suitability filing with EDQM

• Collaborates with USDA on regulatory compliance activities including regulatory

• approvals, import/export compliance, traceability, quarantine, safety testing and affidavits

• Serve as a resource for customer’s regulatory and technical inquiries

• Ongoing maintenance of ISO 13485 based quality system

• Implement and handle CAPA (Corrective and Preventive Actions) and problem resolution

• Coordinates and leads Quality Documentation, Nonconformance Reports, Inspection

• Activities, and Product Disposition

• Coordinates the review and revision of procedures, specifications, and forms to maintain and improve the QMS

• Quality Help Desk and customer complaint point of contact and problem resolution including Questionnaires, Certificates and Customer Surveys, etc.

• Perform Internal Audits in support of internal requirements, 21 CFR 820 and ISO 13485 compliance

• Assists in representing in customer quality audits, supplier quality audits and regulatory inspections

• Performs investigations and analysis activities to support resolution of quality issues

• Collaborates with organizational teams to support quality system implementation

• Creation of new product master files satisfying customer and quality system requirements

• Ensures quality standards by following company & departmental policies & procedures including, but not limited to: Product performance & quality verification; Identifying, recording, and investigating problems related to and product, process & quality systems; Evaluating processes for improvements and standardization and Initiating action to prevent non-conformance in products, process, and quality systems

• Training on quality systems and applicable regulations as identified by supervisor and required by position

• Tracking/trending aspects of the QMS

Other job duties as required:

• Travel Requirements: Less than 10%

• Hours of work/work schedule/flextime: Standard business hours, Monday – Friday

• Required Education: Minimum of Bachelor’s degree in Science, Engineering, Bioengineering or related field

• Prefer Chemistry or Biology degree programs

• Preferred Education, Years and Area of Experience: Minimum 3 years’ experience in Quality or Regulatory, preferably in a medical device, pharmaceutical or biotechnology environment/industry

Required Skills:

• Thorough knowledge and practical application of Quality Systems Regulations 21 CFR 820 and ISO 13485

• Ability to develop, update and train on SOPs

• Working knowledge of ISO standards and Quality Management Systems (QMS)

• Problem solving techniques to perform investigations and drive root cause analysis

• Related work experience performing internal/external audits

• Ability to monitor the QMS such as: Change Control, CAPA, Complaints, Nonconforming Materials and Products

• Experience with Continuous Improvement, Lean or Six Sigma

Desired Experience / Qualifications / Skills:

• SAP, EtQ and/or PeopleSoft experience

• Experience with statistical analysis

• Project management experience

• Animal by-product import/export regulations

• Animal health and/or virology, immunology, epidemiology knowledge

Soft Skills:

• Ability to multi-task with ability to be organized

• Strong interpersonal and communication skills

• Strong time management skills and attention to detail

• Ability to influence others in a team environment while collaborating with peers and functional areas

• Ability to work independently with minimal supervision

Pay Transparency:

• This is the pay range that Magnit reasonably expects to pay someone for this position is $40.18/hour - $53.57/hour.

• Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met).

QUALIFICATION/ LICENSURE :

• Work Authorization : Green Card, US Citizen

• Preferred years of experience : 3+ Years

• Travel Required : 25% or less

• Shift timings: 9 AM to 5 PM

Job Location

Woodland, California

Pay

USD 40.18 - USD 53.57 Per Hour

CONTRACT DURATION

11 month(s)

Apply

We prohibit discrimination on the basis of race, color, gender, age, religion, national origin, sexual orientation, gender identity or expression, disability, veteran status or any other legally protected status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.