Team Member - Quality Control at Dr Reddy's Laboratories Limited

Baddi, Himachal Pradesh, India -

Full Time

Start Date

Immediate

Expiry Date

31 Mar, 26

Salary

0.0

Posted On

31 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, HPLC, Documentation, Calibration, Inventory Management, GMP, Lab Safety, SOP Preparation, Incident Investigation, Change Control, CAPA, LIMS, Analyst Qualification, Data Tracking, Compliance Response, Training

Industry

Pharmaceutical Manufacturing

Description

Company Description DRL FT06 Baddi Job Description To carry out the following routine checks in the laboratory on daily basis: Carry out verification of chemical (in-stock and in-use). Qualification of working standards. Glassware verification & labelling. Routine calibration and verification of all instruments. Logbooks verification. To ensure that the documentation done is online and error free. To ensure the correctness of the document before submitting it for the review of Group Leader/AQA reviewer. Column stock, inventory, indent, requirement and routine usage verification. Reference/Working standard and impurities verification. Area upkeep and maintenance. Calibration schedule/document/labels routine verification. Carrying out qualification of equipment and timely incorporation in system. Preparation and review of standard operating procedure and other GMP documents. Carry out investigation related to incident/OOS/OOT and ensuring timely closure. Handling of change control, CAPA related to quality control department, ensuring timely closure and effectiveness check of implemented CAPAs. Ensuring that all changes related to specifications/STPs/SOPs are evaluated and percolated in an effective manner to all concerned. Responsible for stock preparation and its inventory i.e. chemical, standards, column etc. in LIMS. Responsible for execution of masters and its requirements, highlighting issues and their support for way forward in LIMS. Maintain analyst qualification record and instrument registration in LIMS. Responsible for Lab Safety and follow the JSA. Ensure to use the proper PPE at workplace. Periodic review / SPOT check of specifications / STPs in use. Any other responsibility assigned by Group Leader. Review closure of audit trails. Verification of outside calibration and their report. Tracking and updation of data related to Kaizen, Near Miss, LDM. Compliance Response preparation and closure support. Timely closure of observations related to SOI and QOI. Ensuring timely availability of accessories and Lab consumables for routine use (PO creation and other SAP related activities). Ensuring timely completion of all the training assigned to self. Above mentioned all activities should be performed in the presence of buddy. Qualifications B.Sc /M.Sc/B. Pharma Additional Information Basic knowledge of HPLC is required. Job Family: Quality Sub Job Family: Quality Control Preferred type of working: On-Premise Years of Experience: 3 - 6 Business unit: GMO

Responsibilities

The Team Member in Quality Control is responsible for routine checks in the laboratory, including verification of chemicals, calibration of instruments, and ensuring documentation accuracy. They also handle incident investigations and manage change controls within the quality control department.