Manager Chemical

Abbott Laboratories; Karachi Division; On-site; PKR 1,004,000 - 1,451,000; Full time

Job summary

Abbott Laboratories in Karachi is seeking a quality control professional to support the QC Manager, Validation team, Stability, Packaging Materials and Finish Goods across QC activities and technical problem resolution.

The role focuses on ensuring all physical, chemical, and instrumental testing is performed as per approved procedures for Finished Goods, Raw Materials, Packaging and in-process products, with emphasis on timely problem-solving and adherence to schedules.

Qualifications

• Science Graduate or Master; Pharm D preferred.
• 5-6 years’ experience in QC/validation/related roles.
• Proficient in MS Office.
• Teamwork and problem-solving skills.

Responsibilities

• Assist QC Manager to ensure no delays or non-availability of product/material and smooth introduction of new products.
• Ensure all Physical, Chemical, and instrumental testing are performed per approved procedures for Finished Goods, Stability, Packaging, Raw materials and in-process products.
• Review daily QC Lab planning and support EHS activities.
• Disposition of Finished Goods, Raw Materials, Packaging Materials within agreed lead times; review analytical data before final disposition.
• Support QC Manager/QC staff for technical problem resolution in QC Lab.
• Ensure timely completion of Non-Volume Related Activities (Test Method Validation, Cleaning validation, CSV, Training Schedule, Reference Standards, annual Calibration/Maintenance Schedule, LIR preparation, ER/CR raises).
• Plan and implement certification and reorientation schedules for all analysts and maintain records.
• Ensure one yearly or per-procedure testing for skip-tested raw materials.

Skills

Teamwork

Problem-solving

Analytical thinking

Education

Science Graduate/Master; preferably Pharm D

Tools

MS Office

Job description

Provide support to Quality Control Manager, Validation team, Stability Section, Packaging Materials and Finish Goods for all activities taking place in QC and technical problem resolution.

Major Responsibilities:

• Assist Quality Control Manager to make sure the QC activities do not result in delay or non-availability of product/material, delay in introduction of new products, delay in implementation of CIP


• To ensure that all Physical, Chemical, and instrumental testing are being performed as per authorized procedures for Finished Goods, Stability, Packaging and Raw materials and in process products


• Review of daily planning of QC Lab and support for EHS activities


• Disposition of Finished Goods, Raw Materials, Packaging Materials within agreed upon lead time and review of analytical data before final disposition


• Support Quality Control Manager / QC Staff for technical problem resolution in QC Lab


• To ensure timely completion of Non-Volume Related Activities (Test Method Validation, Cleaning validation, CSV, Training Schedule, Reference Standards, annual Calibration/Maintenance Schedule and adherence, LIR preparation, ER/CR raises and activities)


• Plan and implement certification and reorientation schedule for all analysts and maintain the record


• To ensure that one lot of raw materials which are included in list of skip testing must be tested (full specification) at least once a year or as required by procedure

Education/Knowledge & Experience:

• Science Graduate/Master; preferably Pharm D


• 5-6 years’ experience in the same capacity


• Proficient in MS Office


• Teamwork and problem-solving skills