Executive

Aveva Drug Delivery Systems; Hyderabad; On-site; INR 300,000 - 500,000; Full time

Job summary

Aveva Drug Delivery Systems in Hyderabad seeks a QA/Documentation focused candidate for full-time roles in the lab. The position emphasizes SOP management, GLP/GMP compliance, and meticulous document control within a dynamic pharmaceutical lab environment.

Candidate should hold an M Pharmacy with up to 4 years of experience and be prepared to support training and induction for new joiners, while ensuring accurate logbooks, master copies, and file numbering meet regulatory standards.

Qualifications

• M Pharmacy degree with less than 4 years of experience.
• Experience in GMP/cGLP environment preferred.

Responsibilities

• Assign instrument/equipment IDs and SOP numbers.
• Prepare/review ARD, FRD and DQA related SOPs and sign-off.
• Maintain the Stability Chamber.
• Issue RLD samples and maintain RLD logbooks.
• Allot numbering for specifications, STP, test methods for finished products and API.
• Provide SOPs for new joiners, induction and training activities.
• Manage documentation cell activities like master copy filing and file numbering.
• Ensure cGLP/cGMP compliance and good documentation practice.
• Maintain laboratory cleanliness and assist head of department as required.

Skills

Documentation

SOP documentation

Compliance

Lab maintenance

Education

M Pharmacy

Job description

Job Details: Job Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072, Position Type: Full Time, Salary Range: ₹300,000.00 - ₹500,000.00 Salary/year, Job Shift: Day,

Responsibilities

• Responsible for assigning of Instrument / Equipment ID and their SOP Number.
• Responsible for preparation/ review of all ARD, FRD and DQA related SOP and their sign off activity.
• Responsible for Maintenance the Stability Chamber Maintenance.
• Responsible for RLD samples issuance and maintenance of RLD logbooks.
• Responsible for Allotment of Numbering of Specification, Standard Test Procedure, Test Method of Finished products and API of various product of OSD as well as Injectables, change control number, Instrument / Equipment ID and their SOP Number.
• Responsible for providing SOP’s for new joiners, Induction and Training related Activity.
• Responsible for All the Formats and Logbook issuance related Activity of All Departments along with Employee training record Lab Not book issuance for ARD, FRD and PRD.
• Responsible for Documentation Cell related Activity like Filing of the Master copy, CCF’s in Files, Numbering all the Files and keeping them in Documentation cell alphabet wise. (Over all Maintenance of Documentation Cell)
• Responsible for following cGLP/cGMP compliance in the Laboratory and maintenance of Document cell.
• Responsible for following good documentation practice and general cleanliness in the laboratory.
• Responsible for any other work assigned by head of the department / designee as on when required.

Qualifications

M Pharmacy with less than 4 years of experience.