Manufacturing Quality Inspector I

Otsuka ICU Medical; Austin (TX); On-site; USD 42,000 - 62,000; Full time

Job summary

Otsuka ICU Medical is seeking a Manufacturing Quality Inspector for the 3rd shift (Sun-Wed, 6:00pm-4:30am) to monitor production lines in a clean-room environment and ensure adherence to cGMP standards. The role requires inspecting materials, batch records, and finished products, performing functional and dimensional tests, and documenting results.

Candidates should be detail-oriented, able to work independently and in teams, and have at least a High School Diploma with 1 year of

Qualifications

• Must pass written and practical area requirements for area/certification.
• Must be able to read, understand, and communicate well with others in person and over the phone.
• Must have working knowledge of mathematical calculations (adding, subtracting, multiplying, dividing).
• Capable of working with fractions, decimals, and percentages.
• Must be able to input data into a computer, as required.
• Must be able to work independently and in a team environment.

Responsibilities

• Inspects materials, batch record documents and final products during the production process or offline.
• Performs and records release functional and dimensional testing.
• Restarts automated equipment that stopped for quality issues.
• Evaluates products for defects and recognizes unacceptable product.
• Makes decisions regarding product conformity and determines if MQ batch record criteria is met.
• Collects file samples, stability testing samples, and laboratory samples.
• Inputs data into batch records, reports and electronic databases.
• Monitors production lines for irregularities and reports to supervisor.

Skills

Attention to detail

Mathematical calculations

Independent work

Team collaboration

Data entry

Equipment handling

Problem solving

Communication

Education

High School Diploma

Tools

Laboratory equipment

Job description

Position Summary

The Manufacturing Quality (MQ) Inspector's responsibility will be to monitor production processes for compliance to cGMP standards. He/she will perform a variety of quality control checks to ensure appropriate utilization of equipment, commodities, product and procedures for the assigned production area. Conduct and document a variety of visual, functional and dimensional testing in support of commodity/product release - particularly in the bag fabrication, overwrap and packaging areas of production. 3rd shift: Sunday - Wednesday (6:00pm - 4:30am)

Essential Duties & Responsibilities

• Inspects materials, batch record documents and final products during the production process or off line (APQR, re-inspection, batch records).
• Performs and records release functional and dimensional testing.
• Restarts automated equipment that stopped for quality issues.
• Evaluates products for defects and recognize unacceptable product.
• Makes decision regarding product conformity and determines if MQ batch record criteria is met.
• Performs testing on commodities and final product and determines acceptance according to specifications.
• Collects file samples, stability testing samples, and laboratory samples in accordance with established procedures.
• Inputs data (numerical/informational) into batch records, reports and electronic data bases.
• Recognizes unacceptable product.
• Monitors production lines for irregularities and reports to area supervisor, accordingly.
• Works with both internal and external customers.
• Shares information and provides feedback on material, operational, and mechanical related issues.
• Performs mathematical calculations such as adding, subtracting, multiplying and dividing and therefore must have working knowledge of mathematical applications.
• Uses good problem solving and interpersonal skills for effective communications.
• Follows up on activities to ensure quality is maintained.
• Assists in area improvements, department changes and meetings.
• Follows prescribed uniform and gowning requirements.
• Maintains a safe, orderly, clean work environment.
• Reports all accidents to the supervisor.
• Ensures all PPE (personal protective equipment) is used, as required.
• Adheres to cGMP guidelines, SOP's and plant policies/guidelines.
• Assists in monitoring area for cGMP compliance.
• Perform other related duties or special assignments as directed by supervisor.

Knowledge & Skills

• Must pass written and practical area requirements for area/certification.
• Must have the ability to follow verbal and written instructions and read, understand, and communicate well with others in person and over the phone.
• Must have a working knowledge of mathematical calculations, such as adding, subtracting, multiplying, and dividing.
• Capable of working with fractions, decimals, and percentages.
• Must be able to input data into a computer, as required.
• Possesses good mechanical skills to handle lab equipment.
• Must be able to work independently and in a team environment.
• Must be dependable, competent and show good attendance.
• Must be a detail-oriented person.
• Requires strong focusing skills on in-process work activities to detect irregularities.
• Adapts positively to a changing environment and/or situation.
• Must be able to maintain confidentiality with personal and business information.
• The incumbent will be expected to function independently with minimum supervision.

Minimum Qualifications, Education & Experience

• Must be at least 18 years of age
• High School Diploma required
• Minimum one years' experience as a production operator or similar production or quality experience.

Work Environment

The MQ Inspector position can directly impact the QA organization relative to business goals and documentation compliance. Non-compliance with government regulations (FDA, GMP, etc.), can negatively impact the organization with adverse audit observations.

• Work is performed in a clean room environment
• While performing the duties of this job, the employee may be required to sit or stand for long periods of time
• Must be able to occasionally move and lift objects of up to 25 lbs
• Typically requires travel less than 5% of the time

About Us

Innovation, Impact, and Purpose. Find Your Future Here. We manufacture the critical IV solutions providers count on to deliver consistent, reliable care. Each product we make helps ensure patients receive the therapies they need without disruption. When you work here, you become part of something bigger-a team dedicated to reliability and innovation. No matter the role, your work directly strengthens the healthcare supply chain and impacts patients nationwide. We offer opportunities for growth, collaboration, and meaningful contributions, all in pursuit of a mission that truly matters. Join us and help shape the future of IV solutions.

EEO Statement:

Otsuka ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status. If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at [e-mail]. We are committed to providing equal access and opportunities for all candidates.

Otsuka ICU Medical EEO Policy Statement

Know Your Rights: Workplace Discrimination is Illegal Poster

Otsuka ICU Medical CCPA Notice to Job Applicants