Baxter looking for Technical Trainee | M.Pharm, MSc, B.Pharm apply

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries.

Post : Technical Trainee

Job Description
• To ensure the implementation and maintenance of Current Good Manufacturing Practice (cGMP) standards and all
• In Process Quality Assurance Activities i.e Line Clearance, In-Process Sampling, FP Sampling, Shop Floor Compliance, Quality Risk Assessment, Quality Management system i.e Incident, Investigations, CAPA, Change Control.
• To take instructions from shift in-charge daily and report the activity done, shift wise to Shift in-charge.
• To verify sample / good destruction process and report any gap to Department Head and take corrective and preventive action in coordination with respective Department Head.
• To raise request for stability batch destruction after expiry period is over.
• To receive and handle data loggers and to place the data loggers in consignment at the time of shipment.
• To carry out reconciliation and physical verification of the returned goods.
• To verify headspace oxygen and dissolve oxygen during in-process monitoring.
• To verify logbooks, online documents, records, analysis report and other supporting documents related to products manufactured in the plant.
• To provide support to shift in-charge and Section Head in investigation, in case of any product complaints or deviation.

• To execute the Corrective and Preventive Action (CAPA) defined by Quality Management System (QMS), as per instruction of Executive.
• To verify secondary packing material at the time of issuance against Technical Package / Standard Material Requirement Form and approve the process step.
• To execute line clearance for routine packing activity, monitor each packing line at regular time interval and sample collection.
• To support in trend analysis of the packing line monitoring and keep track of Out of Trend (OOT) results and report to Sub-department Manager.
• To execute the CAPA defined by QMS and as per instruction of Sub-department Manager.
• To give non-compliance reports to the respective departments in case of internal quality audits and report it to Section Head and Department Head.

Candidate Profile : M.Pharm, MSc, B.Pharm, Bio Tech Graduates/Post Graduates

Additional Information
Qualification : M.Pharm, MSc, B.Pharm
Location : Ahmedabad, Gujarat
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Quality Control
End Date : 30th May, 2021