SYMPA Pharma Private Limited | Dhamnod, Madhya Pradesh (near Indore)

About us

SYMPA Pharma is a new greenfield manufacturing facility for IV fluids (Large Volume Parenterals) in Dhamnod, Madhya Pradesh. Our QC lab is built and fully equipped, and we’re now looking for a Quality Control skilled to qualify the lab and get it production-ready.

The role

You’ll take the QC lab from “installed” to “operational”: qualifying instruments, building the documentation system, and setting up validation and stability programs ahead of commercial production. You’ll work alongside an experienced Plant Head and QA team who will support and guide you through the start-up.

Growth path: As the plant moves into commercial production, this role is intended to grow into the QC Manager position, based on performance.

What you’ll do

Before production start-up

- Execute IQ/OQ/PQ for QC instruments (HPLC, UV, KF, TOC, conductivity, particle counters, etc.) and set up the calibration program
- Prepare QC documentation from scratch: SOPs, specifications, standard test procedures, sampling plans, and formats/logbooks
- Carry out analytical method validation and verification
- Design and initiate stability study protocols for initial batches
- Support analytical testing for water system qualification (purified water, WFI) and process validation batches
- Set up data integrity controls (ALCOA+), audit trails,



and reference standard management

After start-up

- Manage routine testing of raw materials, packaging materials, in-process, and finished products
- Handle OOS/OOT investigations, deviations, and change controls for QC
- Coordinate with microbiology for BET, sterility testing, and environmental monitoring
- Prepare the lab for regulatory inspections and customer audits
- Build and lead the QC team

What we’re looking for

- B.Sc./B.Pharm/M.Sc. / M.Pharm in Chemistry, Analytical Chemistry, or Pharmaceutical Sciences
- 4–7 years of QC experience in pharmaceutical manufacturing, preferably in injectables or LVP
- Experience in a new plant or lab start-up is strongly preferred , especially instrument qualification, SOP preparation, and method validation
- Working knowledge of revised Schedule M, WHO-GMP, and ICH guidelines (Q1, Q2)
- Hands-on experience with HPLC and chromatography data systems
- Exposure to regulatory or customer audits

Why join us

- Set up a QC function from the ground up and own the systems you build
- Learn alongside an experienced Plant Head and QA team
- A clear path to QC Manager as the plant reaches commercial operation

To apply: Send your CV to [email protected] with the subject line “Assistant Manager – QC”. Please mention any plant start-up or lab qualification work you’ve done.

📌 Assistant Manager - Quality Control (Indore)
🏢 SYMPA Pharma Private
📍 Indore