Quality Systems Inspector III

Fresenius Medical Care North America; Oregon (OH); On-site; USD 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a dedicated Quality Control Inspector to ensure the highest standards for incoming materials. This role involves conducting thorough inspections, maintaining accurate records, and collaborating with cross-functional teams to address quality issues. The ideal candidate will possess strong organizational skills and attention to detail, ensuring compliance with GMP regulations and quality control standards. Join a dynamic team that values excellence in quality assurance, and contribute to the production of safe and effective products that make a difference in people's lives.

Qualifications

• 2-4 years' experience in a quality-related role in manufacturing.
• Ability to interpret drawings/specifications and apply inspection techniques.

Responsibilities

• Conduct inspections of incoming materials and maintain inspection records.
• Participate in failure investigations and root cause analysis.

Skills

Organizational Skills

Detail Oriented

Mathematical Aptitude

GMP Regulations Knowledge

Quality Control Techniques

Education

High School Diploma

Associate's Degree

Job description

PURPOSE AND SCOPE:

Ensures inspections are completed for all incoming materials. These inspections confirm that the incoming materials meet specific characteristics and specifications and associated procedures. Assigns and or performs daily spot-checking of process controls and other processes, such as label control activities and preparation of product samples for internal laboratory analysis or shipment to testing facilities. Reviews quality/production records for accuracy, completeness, and conformance to all applicable procedures.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

• Under limited supervision, applies considerable knowledge in quality systems inspection to prepare, perform, and control raw material/packaging material incoming inspections and Material Inspection Reports.
• Performs and maintains process ownership of supplier evaluation activities.
• Participates in cross functional failure investigations and facilitate root cause analysis.
• Performs and maintains calibration service and activities
• Verifies and records the receipt of components and their condition upon arrival. Documents condition of nonconforming components (description, photographs, etc.) for Material Review Board (MRB) disposition.
• Assigns lot control identification to all incoming production components (chemical components, packaging components, etc.).
• Samples and inspects packaging and chemical components according to approved procedures to ensure conformance with specifications.
• Performs inspections/audits of the process to ensure conformance with SOP procedures and identification as needed.
• Prepares, issues, and reconciles all finished product labels in accordance with established label control procedures.
• Prepares samples for internal laboratory testing or for shipment to an appropriate testing facility.
• Reconciles all finished product labels.
• Records, counts, and interfaces with issuing facility, and maintains/adjusts the label inventory as necessary.
• Receives and inspects incoming product labels.
• Maintains effective communication with vendors.
• Enters data in spreadsheets, as assigned for QS records and trending.
• Assist with validations as required.
• Maintains a clean inspection work area.
• Assembles device history records (DHR) for issuance to production.
• Reviews finished DHR's for completeness and correctness.
• Responsible for DHR post production review and compiling - Dry and Liquid.
• Participates in QS Internal Audits to monitor the effectiveness of controls.
• Performs functions that require full knowledge of general aspects of the job.
• Normally receives no instruction on routine daily work, and general instructions on newly introduced assignments.
• May provide assistance to junior staff with more complex support tasks that require a higher level of understanding of functions, as directed by immediate supervisor.
• May escalate issues to supervisor for resolution, as deemed necessary.
• Reviews and complies with the Code of Business Conduct and all applicable company policies and procedures, local, state and federal laws and regulations.
• Assists with various projects as assigned by direct supervisor.
• Other duties as assigned.

Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions.

PHYSICAL DEMANDS AND WORKING CONDITIONS :

• The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• May occasionally be required to lift and/or move up to 50 pounds.

EDUCATION :

High School Diploma required; Associate's Degree desirable

EXPERIENCE AND REQUIRED SKILLS:

• 2 - 4 years' related experience in a chemical, food, or drug manufacturing facility, or in a quality related role.
• Must have good organizational skills, and ability to perform work in a team environment with a minimum level of supervision.
• Must be detail oriented and be capable of interpreting drawings/specifications.
• Must be capable of applying inspection/sampling plans/techniques to verify if materials/components conform to the applicable drawings/specifications.
• Must have an aptitude for math with basic algebraic skills and measurement skills.
• General knowledge of GMP regulations and standard quality control inspection techniques.
• Ability to prepare routine administrative paperwork.
• Records maintenance skills.
• Knowledge of the structure, policies and procedures of FDA regulated facilities (21 CRD Part 820 Medical Devices), and Health Canada regulated facilities, if applicable.

EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity

Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.

EOE, disability/veterans