Dei BioPharma Ltd., a Drugs and Vaccines Manufacturing Plant is seeking eligible and qualified applicants for the position of Quality Control Finished Products Analyst.  The candidate will be responsible for testing of semi-finished, finished products and stability samples in the Quality Control laboratory in an effective, efficient and compliant manner so as to fulfill marketing... requirements.

To perform the chemical analysis of samples of Semi-Finished and Finished product in accordance with current approved standard test methods and specifications.
To perform the chemical analysis of stability samples kept at accelerated and long term conditions in accordance with current approved standard test methods.
To prepare the stability protocols of samples of products
To help out the team leader for the management of inventory of lab consumable, like reagents and HPLC columns, to facilitate smooth testing of samples of products.
To perform analytical method validations.
To prepare the Standard testing method and specifications for finished products.
To prepare the standard operating procedures relevant to quality control systems.
To report monthly KPIs of finished product testing on prescribed format. more

Dei BioPharma Ltd., a Drugs and Vaccines Manufacturing Plant is seeking eligible and qualified applicants for the position of Granulation Officer. The Granulation Officer will be responsible for overseeing the granulation process within the pharmaceutical production unit. This includes the preparation, operation, and optimization of granulation equipment used in the manufacturing of solid dosage... forms such as tablets and capsules. The role ensures adherence to Good Manufacturing Practices (GMP) and compliance with safety and quality standards.

Adhere to and follow the SOP’s, current Good Manufacturing Practices, and good documentation practices throughout the Granulation/blending process.
Follow entry – exit procedure, personnel hygiene requirement and cleaning of change room as per SOP.
Daily Maintenance and record of machine change parts of granulation and Tool room
Set up equipment such as high-shear mixers, fluid bed dryers, and granulators as required for production.
To perform the Batch-to-Batch cleaning and Product to Product cleaning of granulation/ blending area and equipment as per SOP.
Record temperature, humidity, and pressure differential of  granulation/blending and related
To perform the daily balance verification and Monthly calibration in granulation/blending and respective area.
Receiving of raw material from Dispensing stores to granulation/blending area and granules store to blending area
Filling of necessary documents, labeling, checklist, and annexure for each step of granulation / blending processes.
Verification of API, raw materials, and granules against the batch manufacturing record.
To fill up the data in PLC as per BMR and check
it by concern production Chemist.
To do granulation and blending of batch as per the BMR and SOP.
On-line entry in all daily record accurately and in legible way.
In-process checks of granulation/blending parameters as per the frequency given in BMR
Ensure all granulation processes comply with GMP, regulatory requirements, and Dei BioPharma’s internal quality standards.
Monitor the granulation process to detect any quality issues and take corrective actions.
To intimate immediate supervisor for if any rejection during operation and to follow instruction for rectification.
Weighing of granules and transfer blending area with proper labeling.
Weighing of blend and transfer to granules stores/ capsule blend stores area.
To follow systematic charge handover as per the shift schedule.
Responsible for any other job assigned by reporting authority. more

Dei BioPharma Ltd., a Drugs and Vaccines Manufacturing Plant is seeking eligible and qualified applicants for the position of Quality Control Packing Material Analyst. The candidate will be responsible for sampling and testing of incoming supplies of packaging materials in an effective, efficient and compliant manner and fulfill the need of internal customers.

To organize and perform sampling... and testing of all incoming supplies of packaging materials that are intended for packaging of different products at the site in accordance with the current approved methods.
To scrutinize the draft artworks of printed packaging components against the approved labeling text, technical drawings and company policy & procedures and get authorize from relevant stake holders.
Maintain the repository of approved, valid Artworks and ensure that only current versions are issuing to the printers / suppliers.
To monitor the validities of the approved packaging materials and plan their re-sampling and re-testing at stipulated time intervals till the allocated expiry dates.
To prepare material specifications and standard test methods for packaging materials in accordance with the current/established standards and requirements.
To prepare the standard operating procedures for the activities pertinent to the sampling & testing of packaging materials and Artworks management.
Maintain the analytical & checking records as per the Quality Control system.
Manage the retention samples of packaging components for future references.
Maintain the analytical equipment in workable conditions at all times, to facilitate timely analysis.
To report monthly KPIs of packaging material laboratory on prescribed format more

Dei BioPharma Ltd., a Drugs and Vaccines Manufacturing Plant is seeking eligible and qualified applicants for the position of Quality Assurance Officer. The candidate will be responsible for implementing the Quality Management Systems at the shop floor and to ensure that Change requests, Deviation & Failure Investigations, Product Complaints, Quality Risks and CAPA are efficiently & timely managed... as per the cGMP requirements.

Log in, investigate and close all event and deviations within allocated timelines as per approved procedure and issue the final report after getting signed off.
Log in, review the proposed change requests, get evaluated from relevant stake holders, and monitor the progress on implementation and close them as per approved procedure.
Log in, review the identified potential risks, evaluate and assess them for criticality and suggest mitigation plan get authorized it, monitor the implementation of action plan and close as per approved procedure.
Log in, define action items, responsibilities and timelines, get approved and close all initiated CAPA on approved format and in accordance with the approved procedure.
Log in, investigate and close all reported product technical complaints on approved format, in accordance with the approved procedure.
Maintenance and retention of all records related to Quality Systems.
To participate in the internal audit of the facility in the capacity of lead or assist auditor.
Develop and report the monthly KPIs of event & deviation, Change control, CAPA and product technical complaint on monthly basis. more

Dei BioPharma Ltd., a Drugs and Vaccines Manufacturing Plant is seeking eligible and qualified applicants for the position of Purified Water Operator. The Purified Water Operator is responsible for operating, monitoring, and maintaining the purified water system used in pharmaceutical manufacturing. This includes the generation, storage, and distribution of purified water (PW) and water for... injection (WFI) to ensure compliance with Good Manufacturing Practices (GMP) and water quality standards required for pharmaceutical production processes.

Adhere and follow the SOP’s, current Good Manufacturing Practices, and good documentation practices throughout the Water System – (Operation & Cleaning).
To follow entry – exit procedure, personnel hygiene requirement and cleaning of change room & Water system area as per SOP.
Daily Monitor, maintain, and operate Water Treatment Plant processes and equipment.
Daily maintain cleanliness of system and daily records of Water Treatment Plant processes and equipment as per SOP of Water Treatment Plant & generated water parameters.
Conducts daily rounds and inspections at the Water Treatment Plant.
Assistance in Collection, inspection, testing, and evaluation incoming and outgoing water supplies with QC/Micro/Production/engineering supervisors.
Receives & Maintain the inventory, and stores hazardous chemicals, related to a water treatment plant operation.
To perform the cleaning & maintenance of area, Water Treatment Plant and accessories as per SOP.
Filling of necessary documents, labelling, checklist, and annexure for each step of Water Treatment Plant processes.
Regulates and records flow of water, and checks water levels in sedimentation, tanks, filters and distribution reservoir.
Operates water system, controls required dosing at all levels and arrange the samples of water to QC/Micro lab for testing and other basic chemical and microbiological tests as SOP.
On-line entry in all daily record accurately and in legible way.
Fill up the data in PLC as per requirements and check it by concern supervisor.
Intimate immediate supervisor for if any issues during operation and to follow instruction for rectification
Ensure plant adheres to safety and environmental rules.
Monitor and troubleshoot operating equipment
Conceptualize, design, and implement plant improvement projects as when required.
Identify process deviations and perform root cause/corrective action
Perform preventive and routine maintenance
Use scientific rules and methods to solve problems.
Observe gauges, dials, or other indicators to make sure a machine is working properly.
Replenish inventory as needed
Follow systematic charge handover as per the shift schedule.
Responsible for any other job assigned by reporting authority. more

Dei BioPharma Ltd., a Drugs and Vaccines Manufacturing Plant is seeking eligible and qualified applicants for the position of Quality Control Raw Material Analyst. The candidate will be responsible for sampling and testing of incoming supplies of Raw materials in an effective, efficient and compliant manner and fulfill the need of internal customers.

To organize and perform sampling and testing... of all incoming supplies of raw materials that are intended for the manufacturing of different products at the site in accordance with the current approved methods.
To monitor the validities of the approved Raw materials and plan their re-sampling and re-testing at stipulated time intervals till the allocated expiry dates.
To prepare material specifications and standard test methods for Raw materials in accordance with the current/established standards and requirements.
To prepare the standard operating procedures for the activities pertinent to the sampling & testing of Raw materials.
Maintain the analytical records as per the Quality Control system.
Manage the retention samples of Raw materials for future references.
Maintain the analytical equipment in workable conditions at all times, to facilitate timely analysis.
To report monthly KPIs of Raw material laboratory on prescribed format more

Qualifications, Skills and Experience:

Qualifications, Skills and Experience: