Fresenius Kabi Oncology Limited has announced a Walk-In Interview for experienced professionals in Production, Engineering, and Quality Assurance (QA) at its Baddi, Himachal Pradesh facility. This hiring drive offers excellent career opportunities for candidates with experience in injectable pharmaceutical manufacturing.

If you have relevant qualifications and experience in sterile manufacturing, engineering utilities, validation, or quality systems, this is a great opportunity to join a globally recognized pharmaceutical company.

Walk-In Interview Detai

Particular Details

Company

Fresenius Kabi Oncology Limited

Industry

Pharmaceutical (Injectable Manufacturing)

Job Location

Baddi, Himachal Pradesh

Interview Date

12 July 2026 (Sunday)

Interview Time

9:30 AM to 4:00 PM

Interview Venue

Hotel Solitaire, S.C.O. 902-903, NAC, Housing Board Light, Sector-13, Manimajra, Chandigarh – 160101

Departments Hiring

Production

Engineering

Quality Assurance (QA)

Production Openings

1. Executive / Assistant Manager / Manager – Production

Qualification

M.Pharm / B.Pharm / M.Sc

Experience

6–15 Years in Injectable Manufacturing

Required Skills

Aseptic filling operations

Vial washing

Terminal sterilization

Lyophilization

Bulk manufacturing

FIT

cGMP

Data Governance

QMS

Equipment Qualification & Validation

Team Handling

2. Executive / AM – QMS

Qualification

M.Pharm / B.Pharm

Experience

6–8 Years

Required Skills

cGMP

Data Governance

QMS Elements

Deviation Investigation

CAPA

Change Control

SOP Preparation

Documentation

Aseptic Manufacturing Knowledge

3. Operator – Production

Qualification

Diploma

ITI

D.Pharm

Experience

2–5 Years

Required Skills

Filling Machine Operation

Vial Washing Machine

Depyrogenation Tunnel

Terminal Sterilization

Lyophilization

FIT

cGMP

GDP

Basic QMS Awareness

Aseptic Isolator Technology

Engineering Openings

Electrician ITI – Electrical

Experience

8–10 Years

Skills

Electrical Cabling

Equipment Erection

Commissioning

Equipment Shifting

Work on Vial Lines

Isolators

Sterilizers

AHUs

LAFs

Utility Executive

Qualification

B.Tech Electrical Engineering

Experience

7–10 Years

Skills

DG Sets

Compressors

Chillers

Transformers

HT/LT PCC

ISO 50001

Utility Maintenance

Team Leadership

Utility Electrician ITI

Experience

7–10 Years

Skills

Electrical Utility Systems

Power Distribution

HT/LT Panels

PCC

MCC

ACB

VCB Panels

Transformers

DG Sets

UPS

Executive – Engineering

Qualification

B.Tech Electrical / Instrumentation

Experience

7–10 Years

Skills

Vial Filling Lines

Isolators

Lyophilizers

Sterilizers

Pipeline Installation

Equipment Erection & Commissioning

Electrical Cabling

AHUs

LAFs

SOP Creation

Cross-functional Execution

Quality Assurance (QA) Openings

Sr. Executive / Assistant Manager – Validation QA

Qualification

B.Pharm / M.Pharm / M.Sc

Experience

8–12 Years

Skills

Equipment Validation

Utility Validation

Facility Validation

Cleaning Validation

Process Validation

Media Fill Validation

Risk Assessment

CSV

GxP Software Qualification

CAPA

Executive – MQA

Experience

3–8 Years

Skills

In-Process QA

Line Clearance

Batch Record Review

GMP Compliance

Deviation Investigation

CAPA

Data Integrity

Regulatory Audit Support

Executive – LQA

Experience

3–8 Years

Skills

QC Oversight

Analytical Documentation

OOS/OOT Investigation

Laboratory Compliance

Data Integrity

Regulatory Audit

Inspection Readiness

QA Executive

Experience

3–8 Years

Skills

Quality Review

CAPA Management

Internal & External Audits

SOP Documentation

GMP Training

Risk Assessment

Quality Compliance

PPT & Excel Knowledge

Documents Required

Candidates should carry:

Updated Resume/CV

Passport-size Photograph

Latest Salary Slip

Contact Person

Shikha Sharma

Email: Shikha.Sharma@fresenius-kabi.com

Why Join Fresenius Kabi?

Global pharmaceutical organization

Modern sterile injectable manufacturing facility

Career growth opportunities

Exposure to international quality standards

Competitive compensation

Learning and development programs

Technical FAQs

1. What is aseptic filling in injectable manufacturing?

Aseptic filling is the sterile filling of pharmaceutical products into containers without terminal sterilization. It requires strict environmental control, sterile equipment, and trained operators to prevent microbial contamination.

2. What is CAPA in pharmaceutical quality systems?

CAPA (Corrective and Preventive Action) is a quality management process used to investigate deviations, identify root causes, implement corrective actions, and prevent recurrence while maintaining regulatory compliance.

3. What is the purpose of cleaning validation?

Cleaning validation demonstrates that equipment cleaning procedures consistently remove product residues, cleaning agents, and contaminants to predefined acceptable limits, preventing cross-contamination.

4. What is Data Integrity in GMP?

Data Integrity ensures that all pharmaceutical data is accurate, complete, consistent, attributable, legible, contemporaneous, original, and accurate (ALCOA+ principles) throughout the product lifecycle.

5. What is the difference between IQ, OQ, and PQ in equipment qualification?

IQ (Installation Qualification): Verifies that equipment is installed correctly.

OQ (Operational Qualification): Confirms the equipment operates within specified limits.

PQ (Performance Qualification): Demonstrates that the equipment consistently performs effectively under routine production conditions.