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Quality Associate I (5th Shift: 7AM-7PM)
$57k-73k (estimate)
Full Time 2 Months Ago
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Marion, North Carolina is Hiring a Quality Associate I (5th Shift: 7AM-7PM) Near Marion, NC

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

This is where your creativity addresses challenges

Responsible for working with the manufacturing departments to address defects with the finished products

Your Team at Baxter

Within Quality, every role makes a difference. Products that Baxter makes are shipped worldwide for patients in need. Whether it's building a new process from scratch or facing a never-before-seen production hurdle, individuals within Quality are given the trust and opportunity to bring creativity to the table. Regardless of your specific role with a product, it is sure to touch a portion of our global operation.

The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. Our patients come first, always.

What we offer from Day One

  • Medical, Dental and Vision coverage
  • 160 hours of Paid Time Off and Paid Holidays
  • 401K match
  • Employee Stock Purchase Program
  • Paid Parental Leave
  • Tuition Reimbursement

What you'll be doing

  • Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Baxter quality practices.
  • Leads ongoing, daily departmental operations.
  • May include the supervision of assigned personnel in achieving defined quality goals in an efficient, accurate and timely manner; Interview/hire, evaluate, train and develop direct reports
  • Perform in-depth internal assessments and evaluations by collecting and analyzing accurate, objective evidence regarding risks and their magnitude.
  • Assessments and information gathering may be through in-depth employee interviews, flow charting and other informational gathering techniques.
  • Determine the logic, adequacy and effectiveness of processes, systems and related requirements.
  • Develop plans to correct identified risks including areas of non-conformance, advise management and implement approved corrective action plans.
  • Write, review, analyze and revise written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc.
  • Support external assessments or audits. Assist with audits of various reports (Protocols, Qualifications, Regulatory Submissions, etc.)
  • Serve as Subject Matter Expert (SME) and provide training to local employees as needed on relevant area(s) Other duties, tasks or projects as assigned. Sustain a clean and safe work area using 6S principles
  • Learn, understand and apply thorough quality standards, Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP)

What you'll bring

  • Bachelor's degree strongly preferred. Degree in engineering or life science preferred.
  • Must be at least 18 years of age.
  • Strong interpersonal skills and phenomenal attention to detail are needed.
  • Must be a strong teammate with good problem solving, and good verbal and written communication skills.
  • Must have the ability to manage people, encourage partnership and drive decisions.
  • Must be able to handle multiple projects concurrently, have computer experience and have knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices as appropriate
  • Understand verbal and written safety and quality instructions and read and comprehend written work instructions including words and drawings.
  • Must have basic English written and oral communication skills adequate to communicate with other team members.

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 employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $56,000 - $77,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

Other Duties as Assigned

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. Overtime is worked as required.

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.

131158

Qualifications:

Highway 221 North PO Box 1390|Marion, NC 28752|United States of America

Job Summary

JOB TYPE

Full Time

SALARY

$57k-73k (estimate)

POST DATE

03/27/2024

EXPIRATION DATE

05/25/2024

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The job skills required for Quality Associate I (5th Shift: 7AM-7PM) include Problem Solving, Written Communication, Attention to Detail, Innovation, etc. Having related job skills and expertise will give you an advantage when applying to be a Quality Associate I (5th Shift: 7AM-7PM). That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Quality Associate I (5th Shift: 7AM-7PM). Select any job title you are interested in and start to search job requirements.

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The following is the career advancement route for Quality Associate I (5th Shift: 7AM-7PM) positions, which can be used as a reference in future career path planning. As a Quality Associate I (5th Shift: 7AM-7PM), it can be promoted into senior positions as a Quality Assurance Specialist IV that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Quality Associate I (5th Shift: 7AM-7PM). You can explore the career advancement for a Quality Associate I (5th Shift: 7AM-7PM) below and select your interested title to get hiring information.

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If you are interested in becoming a Quality Associate, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Quality Associate for your reference.

Step 1: Understand the job description and responsibilities of an Accountant.

Quotes from people on Quality Associate job description and responsibilities

Perform regular quality assessments on all incoming materials from vendors and outgoing products for shipping.

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Reject all products and materials that fail to meet quality expectations.

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The QA associate helps Quality Engineering and Quality Manager to complete corrective action tasks.

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Read blueprints, plans, and specifications to understand the requirements of products and services.

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Measure product dimensions, examine functionality, and compare the final product to the specifications.

05/11/2022: Lowell, MA

Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.

Career tips from people on Quality Associate jobs

Create a “Theme of the Month” Strategy.

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Stay Positive and Reward Best Practice.

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Deliver Feedback, Coaching And Training.

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