production executive 2

PeopleStrong

India

On-site

INR 600,000 - 900,000

Full time

11 days ago
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Job summary

Sekhmet Pharmaventures is seeking an Executive 2 for the Production team at Optimus Drugs (P) Ltd in Vishakapatnam. The role requires 3–8 years of experience, a B.Sc/Graduation, and full-time employment.

You will implement cGMP practices, assist in validation activities, draft SOPs, and support process development and trials within the production unit. Based in Vishakapatnam, the position integrates with Operations and Production sub-departments, with responsibilities spanning document creation,

Qualifications

  • Must follow cGMP and safety norms.
  • Must be able to prepare and review validation protocols and reports.
  • Prepare and review SOPs.

Responsibilities

  • Execute process development, trials and validations as per protocol/BMR.
  • Follow company policies and ensure compliance with SOPs and GMP.

Skills

Document Creation
SAP
BMR

Education

Graduation
B.Sc

Job description

  • Sekhmet Pharmaventures>Optimus Drugs (P) Ltd>ODPL - 02>Operations>Production>U2 Production Common>2200201001
  • Vishakapatnam

End Date 15 Sep 2026

Required Experience 3 - 8 years

Basic Section

No. Of Openings 1

Grade L6E

Designation Executive 2

Campus/Non Campus Non Campus

Employment Type Full Time

Requisition Type New

Median 1 - 9999999

Comp off OT Applicability Comp off & Overtime

TAT 30

Confidential No

Closing Date 15 Sep 2026

Organisational

Company Sekhmet Pharmaventures

Entity Optimus Drugs (P) Ltd

Department Operations

Sub- Department Production

Cost Centre 2200201001

Country India

Region South

State Andhra Pradesh

City Vishakapatnam

Unit Unit-2

Working Location Vishakapatnam

Skills
Skill

Document Creation SAP BMR

Graduation

B.Sc

Working Language
Job Description

To follow cGMP and safety norms adhere to the company policy.

Making sure that validation protocols and reports are preparation review.

Preparation and review of SOP’s.

To execute process development /Trial/Validation batches as per the specific steps mentioned in the concerned protocol/BMR.

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