Baxter Off Campus Drive 2023 | Hiring Freshers as Technical Trainee(Quality Assurance) for Gurgaon location
Join Baxter's Off Campus Drive 2023 in Gurgaon as a
Technical Trainee (Night Shift) in the field of Quality Assurance. Make a
difference in patients' safety and contribute to saving and sustaining lives.
Gain valuable experience in processing complaint files and regulatory reports,
while working with a globally renowned healthcare organization. Fluent
communication, strong problem-solving skills, and attention to detail are key
attributes for success. Freshers are encouraged to apply for this opportunity
to kick-start their career in the medical products industry.
Technical Trainee (Night Shift)
Req #: JR –
101279
Location Gurgaon,
Haryana, India
Job Category: Quality
Date Posted: 05/18/2023
Overview
This is where you make a difference in our patients’
safety. As a member of the Baxter Quality team, you will play an essential part
in our mission of saving and sustaining lives. Quality is important throughout
the entire product lifecycle and works collaboratively with all areas of the
organization. Because Quality touches everything Baxter does, a role in Quality
provides many opportunities for growth, learning and a successful career that
has a daily impact on people’s lives.
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Success
Profile
What makes a successful Quality team member at Baxter?
Take a look at some of the top traits we’re looking for and see if you’re a
fit.
Technical
Trainee (Night Shift)
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 position is responsible for processing complaint
files and/or Regulatory Reports
Essential Duties and Responsibilities:
- Effectively
manage and process complaints, which includes performing daily tasks
associated with processing complaint files across multiple product lines,
which may include:
- Opening
complaint records.
- Collecting
necessary complaint information.
- Performing
follow-up with the customer (written and verbal).
- Determining
reportability of complaints.
- Evaluating
complaints for need to investigate and coordinating sample retrieval.
- Responding
to customer complaints (written and verbal).
- Timely
closure of complaints, as per procedure.
- Effectively
manage and process MDRs (Medical Device Reports) and more complex
complaints under supervision
- Effectively
manage workflow, identifying and escalating issues.
- Triaging
internal and external communication for complaints.
- May
participate in continuous improvement efforts and projects, as assigned
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Skills: -
- Fluent
in English: solid written and verbal communication skills.
- Ability
to prioritize and multitask.
- Proficient
with computers.
- Ability
to work with cross-functional teams to interact effectively with peers,
management, and customers.
- Readily
accepting of assignments to new/different products.
- Strong
critical thinking and problem-solving skills.
- Ability
to work independently.
- Detail
oriented
Education and/or Experience
- Minimum
of an Associate’s Degree required in nursing, pharmacy, medical
technology, engineering or scientific background MLT (Medical Laboratory
Technician), LPN- Licensed Practical Nurse, RN-Registered Nurse or
equivalent experience (defined as a minimum of 1 year of medical products
industry experience). Bachelor’s degree and/or clinical
certification (MT, RN) preferred
- 0-1
year work experience in a cGMP(Current Good Manufacturing Practice)
related industry or in a clinical setting
- Project
Management experience and/or certification preferred
Reasonable Accommodations
Baxter is committed to working with and providing reasonable
accommodations to individuals with disabilities. If, because of a medical
condition or disability, you need a reasonable accommodation for any part of
the application or interview process, please send an e-mail to Americas_TTA@baxter.com and
let us know the nature of your request along with your contact information.
Click Here To Apply for
Baxter
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