This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives- where your purpose accelerates our mission.
Hours: 7 am – 3 pm
This is where you save and sustain lives
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives- where your purpose accelerates our mission.
Your role at Baxter
Perform final review and determine acceptability of documentation concerning plant systems, processes, and finished product by using SOPs, Specifications, and Master Documentation Manuals (MDMs). Responsible for performing batch release and expediting batch release to facilitate cost effective inventory.
Your team
Baxter’s employees are united in a mission to save and sustain lives. We are passionate about applying scientific innovation to meet the needs of the millions of people worldwide who depend on our medically necessary therapies and technologies. We focus on increasing access to healthcare, innovating in crucial areas of unmet need, and pursuing creative collaborations that bring our mission to life for patients every day.
What you’ll be doing
- Must follow strict guidelines per specifications, SOPs and MDMs.
- Must be expert at Good Documentation Practices.
- Must plan own workload releasing and reviewing of system documents and production folders by priority.
- Must plan own workload releasing and reviewing production documents by priority.
- Independently plans, schedules, and activates, document requests.
- Perform final review of test results for completeness and assurance that product is within limits per specifications.
- Perform final review of Mold start-up packages, Molding Daily Quality, and Product Records.
- Read Bills of Materials and Temporary Substitutions to assure correct parts have been used.
- Perform final review of sterilization charts, records and graphs to assure product has been sterilized by the correct specifications and parameters.
- Must ensure all supporting documents and correct signatures are present before releasing systems and production records.
- Perform final review of cleaning records, equipment, and temperature verification records.
- Must maintain files such that documents are readily available for area of responsibility.
- Must ensure that documents removed from the area are corrected and returned in a timely manner.
- Accumulate all required documentation for a batch and perform cross checks on documents with a specific batch
- Release batches in a timely manner with a focus on due dates and performance metrics.
- Resolve issues with supervisor to assure acceptability of product.
- Maintain files in the Record Repository according to record retention requirements.
- Interact with peers, Production personnel, and Quality Management at all levels.
- Jointly prioritizes documentation activity with team members daily.
- Aids in the process and issuance of complex new documents.
- Must perform review of all documentation packages.
- Resolve issues with supervision to assure acceptability of documentation.
- Must perform all other duties and responsibilities as determined by management/supervision.
What you’ll bring
- High School Diploma required
- Must have strong interpersonal and communication skills, direct interaction with team members, management, and other plant personnel (Internal and External).
- Must have strong clerical background and excellent typing skills.
- Must be inquisitive and able to formulate plans to solve problems.
- Must be highly proficient in computer operations.
- Willing to work a flexible work schedule and overtime as required.
- Must have knowledge of both plant and department Environmental, Health and Safety regulations and comply with said regulations accordingly.
- Must have experience multi-tasking, prioritizing and handling large volumes of incoming work.
- Ability to work without supervision.
- Must meet deadlines.
- Must be able to work with speed.
- Must have good knowledge of the Cleveland Documentation System.
- Must be a team player
- Ability to do a considerable amount of walking.
- Evidence of experience using Microsoft Office applications including Excel, Power Point and word to create or update spreadsheets, presentations and documentation.
- Must have a good attitude.
- Meet visual acuity requirements as documented in Baxter Cleveland Visual Acuity procedure CL-01-01-037.
- Ability to sit for long periods of time
- Ability to reach above the shoulder
- Ability to bend/stoop
- Ability to climb ladders
We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all our employees, and we strive to be more transparent with our pay practices. To that end, this position has a salary range of $33,000 to $76,000. The above range represents the expected salary range for this position. The actual salary may vary based upon several factors including, but not limited to, relevant skills/experience, time in the role, business line, and geographic/office location.
#IND-USOPS
The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
EEO is the Law
EEO is the law – Poster Supplement
Pay Transparency Policy
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
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