Synokem Pharma Walk-In Interview – Production, Packing, Quality Control & Quality Assurance Jobs | Haridwar

Synokem Pharmaceuticals Ltd. has announced a Walk-In Interview Drive for experienced pharmaceutical professionals across Production & Packing, Quality Control (QC), and Quality Assurance (QA) departments. The company is offering exciting career opportunities at its Haridwar, Uttarakhand manufacturing facility. Eligible candidates with relevant pharmaceutical manufacturing experience are invited to attend the interview with the required documents.

Synokem Pharma Recruitment – Overview

Particulars Details

Company Name

Synokem Pharmaceuticals Ltd.

Job Type

Walk-In Interview

Industry

Pharmaceutical Manufacturing

Job Location

Haridwar, Uttarakhand

Interview Date

19th July 2026 (Sunday)

Interview Time

09:00 AM – 05:00 PM

Interview Venue

Hotel Le Mariet, Kishanpura, Baddi-Nalagarh Highway (NH-105), Tehsil Nalagarh, District Solan, Himachal Pradesh

Departments & Positions

Production & Packing Department

Position

Experience

Compression Operator – Bylayer

3–8 Years

Granulation Operator

3–8 Years

Executive

8–10 Years

QMS Executive

5–6 Years

Packing Sr. Officer

5–6 Years

Almach 3015 Machine Operator

3–7 Years

Stripe Machine Operator

3–7 Years

Quality Control (QC)

HPLC Officer / Sr. Officer – 3–5 Years

Microbiology Officer / Sr. Officer – 3–5 Years

GC/GLP Officer / Sr. Officer – 3–5 Years

RM & PM Officer / Sr. Officer – 3–5 Years

Quality Assurance (QA)

Process/Cleaning Validation – 4–6 Years

QMS – 4–6 Years

IPQA – 4–6 Years

Equipment & Utility System Validation – 4–6 Years

Documents Required

Candidates should carry:

Updated Resume/CV

Last 3 Months Salary Slips

Last 6 Months Bank Statement

Recent Passport Size Photograph

Aadhaar Card

Contact Details

Email: jobs@synokempharma.com

Mobile: 8689011329, 9258157446

Why Join Synokem Pharmaceuticals?

Established pharmaceutical manufacturing company

Career growth opportunities

Modern manufacturing facility

Exposure to GMP-regulated operations

Opportunity to work with experienced pharmaceutical professionals

Important Tips for Candidates

Reach the interview venue before the reporting time.

Carry original and photocopies of all educational and experience documents.

Update your resume with current responsibilities and achievements.

Dress professionally for the interview.

Candidates should have relevant pharmaceutical manufacturing experience for the applied position.

Technical FAQs

1. What analytical instruments are commonly used in the QC department at pharmaceutical companies?

Quality Control laboratories primarily use HPLC (High Performance Liquid Chromatography), Gas Chromatography (GC), UV-Visible Spectrophotometer, FTIR, Dissolution Test Apparatus, pH Meter, Karl Fischer Titrator, and Stability Chambers for testing raw materials, in-process samples, and finished products.

2. What is the role of IPQA in pharmaceutical manufacturing?

In-Process Quality Assurance (IPQA) ensures manufacturing activities comply with Good Manufacturing Practices (GMP). IPQA performs line clearance, in-process checks, batch documentation review, deviation monitoring, sampling, and process verification to maintain product quality.

3. What is Process Validation and Cleaning Validation?

Process Validation demonstrates that a manufacturing process consistently produces products meeting predetermined quality standards. Cleaning Validation verifies that cleaning procedures effectively remove residues and contaminants, preventing cross-contamination between products.

4. What responsibilities does a Compression Operator perform?

A Compression Operator sets up and operates tablet compression machines, monitors tablet weight, hardness, thickness, friability, and disintegration, performs machine adjustments, maintains production records, and follows cGMP and SOP requirements.

5. What are GMP and GLP, and why are they important?

Good Manufacturing Practices (GMP) ensure medicines are consistently produced and controlled according to quality standards. Good Laboratory Practices (GLP) ensure laboratory testing is reliable, accurate, traceable, and compliant with regulatory requirements. Both are essential for regulatory compliance and patient safety.