Heparin Coating Process Technician II

ZEISS Group•Ontario, CA

13d•$24 - $30•Onsite

About The Position

About Us: How many companies can say they’ve been in business for over 177 years?! Here at ZEISS, we certainly can! As the pioneers of science, ZEISS handles the everchanging environments in a fast-paced world, meeting it with cutting edge of technologies and continuous advancements. ZEISS believes that innovation and technology are the key to a sustainable future and solutions for global change. We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology. We are a global company with over 42,000 employees and have over 4,000 in the US and Canada alone! Make a difference, come join the team! What’s the role? This position is responsible for performing assigned duties in compliance with all applicable Heparin Coating and Heparin-related procedures, quality standards, and regulatory requirements while supporting production objectives. The role is assigned to Second Shift with the following schedule expectations: Regular Schedule: Monday through Friday, 1:30 PM – 10:00 PM Extended Hours: Based on business and production needs, shift end times may extend up to 12:00 AM. Saturday Overtime: When required, scheduled hours will be 11:30 AM – 8:00 PM and will not exceed eight (8) hours per shift. Overtime Requirement: Participation in overtime is mandatory when business or production demands require additional coverage.

Requirements

Minimum of two (2) years of experience working in a chemical laboratory environment; or
Minimum of two (2) years of coursework toward an Associate’s degree in a science-related field; or
Minimum of two (2) years of experience working within the ZEISS Heparin Coating process.
Ability to effectively communicate with individuals across all organizational levels, including management, supervisors, coworkers, inspectors, and external auditors (e.g., FDA and other regulatory agencies).
Ability to read, analyze, and interpret technical procedures, work instructions, and regulatory documentation.
Ability to prepare reports, complete documentation, and contribute to procedure development.
Ability to present information clearly and respond effectively to questions from leadership and cross-functional teams.
Ability to apply basic algebraic concepts and perform calculations required for batch formulation, process control, and data recording.
Ability to solve practical problems and manage multiple variables in a manufacturing or laboratory environment.
Ability to interpret instructions provided in written, verbal, diagrammatic, or schedule formats, including Material Safety Data Sheets (MSDS/SDS).
Ability to effectively prioritize tasks and manage multiple responsibilities in a fast-paced production environment.
Light to moderate physical effort required.
Ability to lift and carry equipment up to approximately 25 pounds.
Frequent standing and walking required.
Repetitive hand usage including grasping, fine manipulation, and controlled handling of materials.
Vision requirements include close vision, distance vision, peripheral vision, depth perception, and ability to adjust focus.

Responsibilities

Perform assigned duties in compliance with all applicable Quality Control Standard Operating Procedures (QCSOPs), Good Manufacturing Practices (GMP), and regulatory requirements, including ISO 9001 and EN 46001 standards.
Load and unload lenses from fixtures in accordance with established procedures and quality standards.
Prepare, weigh, and accurately record batch formulations following defined batch record requirements.
Stage, process, and document work orders in accordance with batch record and traceability requirements.
Perform plasma treatment on lenses and verify power output during test runs to ensure process accuracy and consistency.
Maintain full traceability for multiple work orders within each batch.
Collect and submit samples for batch testing in accordance with quality protocols.
Accurately and legibly document processing parameters and production data in batch records and associated documentation.
Maintain completed batch records and forward documentation to Quality Assurance (QA) for review and archival in a timely manner.
Support continuous improvement initiatives by reviewing, updating, and recommending revisions to process documentation as needed.
Conduct routine diagnostic testing and monitoring of process equipment to support performance trending and preventative maintenance efforts.
Prepare and maintain required process materials, including 15% Ethyl Alcohol and Blocking Fluid, and ensure proper disposal of used Heparin Coating solutions in accordance with safety and environmental procedures.
Monitor and maintain inventory levels of process supplies and coordinate chemical and material replenishment as required.
Provide support to Production Supervisors as needed.
Participate in cross-training and perform lens production operations across multiple workstations.
Support engineering and production teams with special projects, new product introductions, and process development initiatives.
Perform other duties as assigned to support departmental and organizational objectives.