Dr.Reddys Laboratories Ltd Hiring Bpharm/ Mpharm for Team Member_Packing

Dr.Reddys Laboratories Ltd Walk-in Interview 2024.Dr.Reddys Laboratories Lt Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue… 

Important Details :

• Post of date:27/12/2024
• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Vacancy details:

• Department: Team Member_Packing
• Educational qualification: A Bpharm/ Mpharm
• Minimum work experience: 4 to 6 years of experience in qualification activities
• Job Location: Pydibimavaram

Job Description : Greeting from Dr.Reddys Laboratories Ltd..!!!!

• Execution of Qualifications/Validations of packing equipment

You will be responsible for documentation and execution of qualification activities. This includes preparation, review and execution of URS (User Requirement Specification), DQ (Design Qualification), FDS (Functional Design Specification), UTM (User Traceability Matrix), IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), RQ and (Requirement Qualification) documents.

• Your responsibilities include review of miscellaneous qualification documents and preparation and review of risk assessments for equipment and systems.

• You will be responsible for new project related FAT (Factory Acceptance Test) and SAT (Site Acceptance Test).

• You will review and compile raw data, relevant certificates, analysis test reports and

• preparation and review of final summary report.

• You will be responsible for preparation and review of protocols and reports for media fill validation and cleaning validation.

• Your role involves initiation of relevant CRN (Change Request Number) for new or existing activity, timely closure of assigned action plans as per CRN, and CRN review and approval.

To ensure and adhere Organization Safety/Quality policies, Procedures, norms and its effective implementation from time to time.

Ensure the adherence of SHE standards and policies across the plant with respect to MSI.

To follow the personnel hygiene practices and discipline.

Maintaining cGMP practices in production area and report any discrepancies/incidents to immediate supervisor.

Skills & attributes

Technical Skills

• Experience in working with sterile product facility related validations such as equipment validation, media fill, cleaning validation, process validation, area qualification, and other miscellaneous qualifications.

• Expertise in preparation, review, and execution of documents, including URS, DQ, FDS, UTM, IQ, OQ, PQ, RQ.

Behavioral skills

Effective listening skills, ensuring a comprehensive understanding of information.

A keen eye for detail, ensuring accuracy and precision in tasks.

Awareness and sensitivity to deadlines, ensuring timely completion of tasks.

Analytical skills and the ability to troubleshoot, enabling effective problem-solving.

Strong interpersonal skills and the ability to work well in a team, fostering collaboration and positive team dynamics.

Apply Online