U6-Production-Executive 3

Sekhmet Pharmaventures; Thiruvallur District; On-site; INR 250,000 - 500,000; Full time

Job summary

Sekhmet Pharmaventures Pvt Ltd. in Tamil Nadu is seeking an Executive to support production operations at Gummidipoondi. The role focuses on GMP/cGMP compliance, raw material handling, and document control to ensure manufacturing quality.

The candidate will participate in QA/QC interactions, maintain BMR/SOP adherence, and assist in master formula records, equipment status, and CAPA investigations. A BSc is required, with 1–4 years of relevant experience.

Qualifications

• Bachelor’s degree in science (BSc) required or equivalent.
• Experience in GMP/cGMP manufacturing environments preferred.
• 1–4 years of relevant production experience.

Responsibilities

• Compliance with GMP norms and to be following cGMP in manufacturing area.
• To prepare and approval of material requisition order to store and follow-up till receipt of raw materials.
• Verification of raw material/packing material during dispensing as per BMR and receipt of raw materials and packing material as per BMR from warehouse.
• Manufacturing, packing and Documentations as per BMR and SOP.
• To verify quality system in the production department.
• Preparation and review of master formula record, process records, reprocess record, repacking record, regular BMRs and ECR.
• Responsible for initiation of QMS documents like change controls, deviations, OOS, OOT, CAPA and conduct failure mode investigations.
• Preparation of URS, PQ documents and review of DQ, IQ, OQ and other qualification documents.

Skills

Team building

Working in teams

Production Support

Education

Bachelor of Science (BSc)

Job description

• Gummidipoondi

End Date 17 Nov 2026

Required Experience 1 - 4 years

Basic Section

No. Of Openings 1

Grade L6F

Designation Executive 3

Campus/Non Campus Non Campus

Employment Type Full Time

Requisition Type Replacement

Median 1 - 999999999

Comp off OT Applicability Comp off & Overtime

TAT 30

Confidential No

Organisational

Company Sekhmet Pharmaventures

Department Operations

Sub- Department Production

Cost Centre 5200201001

Country India

Region South

State Tamil Nadu

Unit Unit-6

Working Location Gummidipoondi

Skills

Skill

Team building and working in teams Production Support

Undergraduate (Bachelor’s Level) Qualifications

Bachelor of Science (BSc)

Working Language

Job Description

• Compliance with GMP norms and to be following cGMP in manufacturing area.
• To prepare and approval of material requisition order to store and follow-up till receipt of raw materials.
• Verification of raw material/packing material during dispensing as per BMR and receipt of raw materials and packing material as per BMR from warehouse.
• Manufacturing, packing and Documentations as per BMR and SOP.
• To verify quality system in the production department.
• Preparation and review of standard operating procedures relevant to production department and to review of List of equipment and equipment re-qualification planner.
• Wearing appropriate PPE and following safety procedures for personnel/product safety as per Safety SOP.
• Preparation and review of master formula record, process records, reprocess record, repacking record, regular BMRs and ECR.
• Responsible for initiation of QMS documents like change controls, deviations, OOS, OOT, CAPA and conduct failure mode investigations.
• Preparation of URS, PQ documents and review of DQ, IQ, OQ and other qualification documents.
• Responsible to comply the requirements of technical audits and safety audits.
• Preventive maintenance and calibration planning according to schedule.
• Responsible for complying with all production-related documents.
• Interaction with warehouse/quality assurance for material availability / release of raw material and packing materials intermediate and finished goods.
• Co-ordination with engineering for maintenance / machine breakdown / modification / calibration.
• Check on production yields and re-conciliation at various stages of manufacturing.
• Responsible for production planning and achieving maximum production by utilizing all resources to deliver the API on target timelines to fulfill customer needs.
• Maintaining harmonious relations with employees .
• Updating of equipment status board, u sage logbook & relevant records as per BMR/ECR/SOP .
• Proper segregation of material, labelling and identification, area cleaning and disinfection.
• Raising test requisition to QA / QC and follow-up till release of test report.
• Ensure cleanliness of hard to clean parts of equipments during cleaning for product-changeover (campaign cleaning) and to ensure regular cleaning between batch to batch of the same product.
• To assure batch uniformity and integrity of drug products through written procedures followed by in process controls and tests of each batch.
• Submission of completed BMR, other completed records and raising BMR/ECR requisition to QA as per production planning.
• Maintaining equipments and area cleanliness as per requirement.
• To monitor outputs and to validate the performance of manufacturing process.
• Responsible for exploring ideas and implementing latest technologies in the production and keeping on update with the regulatory requirements and latest guidelines.
• Attending training as per annual training calendar.