Oper I, Production
2 weeks ago
**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.
1.To follow the proper entry-exit procedure with gowning.
2.To monitor temperature or humidity of clen room and if any non-conformance found informed to engineering department through work request.
3.To ensure the respective area in terms of cleanliness, all equipment’s are well maintained.
4.To ensure preventive maintenance of machine is performed in defined frequency.
5.After completion of maintenance activity ensure the proper cleaning activity shall be done if require. Perform the routine cleaning activity as mentioned in SOP.
6.To perform the verification activity (As witness) during manufacturing operation. (i.e. Cleaning /manufacturing verification) To perform the cleaning and lubrication of machines regularly.
7.To ensure that machines are working smoothly and performing as per standards.
8.To ensure that production activities (Like washing and DPT) are being performed as defined in the Standard Operating Procedure (SOP) / Batch Manufacturing Record (BMR).
9.To follow the SOP and guide the workers for the same. To check the status label of all equipment to avoid mix-up.
10.To check & verify the rejection generated are being handled as per SOP and resolve the problem immediately.
11.To acknowledge intervention, break-down and report to supervisor. To ensure the GMP norms are followed and maintained throughout the manufacturing.
12.To perform good documentation and follow the GDP.
13.To co-operate the other department in terms of validation activity.
14.To remove the material scrap from time to time as per Standard Operating Procedure (SOP).
15.To perform parts change and trial activity of machine within the timeline respect to production planning.
16.To report technical department and IT regarding any kind of maintenance work or computer System/network related issue.
17.To stop the activity if any non
- conformance or non - compliance is observed & escalate to production supervisor.
18.To preserve the machine parts in good condition and check periodically.
**Reasonable Accommodations**
**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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