Looking for a career in the pharmaceutical injectable industry? Fresenius Kabi Oncology Limited is conducting a Walk-in Interview for experienced professionals in Production, Engineering, Validation QA, Manufacturing QA (MQA), Laboratory QA (LQA), QMS, and Utility Engineering. Candidates with experience in sterile injectable manufacturing are invited to attend this recruitment drive.

Walk-in Interview Details

  • Company: Fresenius Kabi Oncology Limited
  • Location: Baddi, Himachal Pradesh
  • Interview Date: 12 July 2026 (Sunday)
  • Interview Time: 9:30 AM to 4:00 PM

Interview Venue

Hotel Solitaire
(A Unit of K.K. Resorts Pvt. Ltd.)
S.C.O. 902-903, NAC, Housing Board Light Point,
Sector 13, Mani Majra, Chandigarh – 160101


Current Open Positions

Production Department

Executive / Assistant Manager / Manager – Production

Qualification

  • M.Pharm / B.Pharm / M.Sc.

Experience

  • 6–15 years in Injectable Manufacturing

Key Skills

  • Aseptic filling operations
  • Aseptic interventions
  • Vial washing
  • Terminal sterilization
  • Lyophilization
  • Bulk manufacturing
  • FIT
  • cGMP
  • Data Governance
  • QMS
  • Equipment Qualification
  • Validation
  • Team handling

Executive / Assistant Manager – QMS

Qualification

  • M.Pharm / B.Pharm

Experience

  • 6–8 years in Injectable Manufacturing

Key Skills

  • cGMP
  • Data Governance
  • QMS
  • Deviation Investigation
  • CAPA
  • Change Control
  • SOP Preparation
  • Documentation
  • Aseptic manufacturing compliance

Operator – Production

Qualification

  • Diploma / ITI / D.Pharm

Experience

  • 2–5 years

Key Skills

  • Filling Machine
  • Vial Washing Machine
  • Depyrogenation Tunnel
  • Terminal Sterilization
  • Lyophilization
  • FIT
  • cGMP
  • GDP
  • Basic QMS
  • Aseptic Isolator Technology

Engineering Department

Electrician (ITI – Electrical)

Experience

  • 8–10 years in Injectable Plant

Skills Required

  • Electrical cabling
  • Equipment erection
  • Commissioning
  • Equipment shifting
  • Experience with vial lines, isolators, sterilizers, AHUs and LAFs

Utility Executive

Qualification

  • B.Tech (Electrical Engineering)

Experience

  • 7–10 years in Pharmaceutical Industry

Skills Required

  • DG Sets
  • Compressors
  • Chillers
  • Transformers
  • HT/LT PCC
  • Team Leadership
  • ISO 50001

Utility Electrician (ITI – Electrical)

Experience

  • 7–10 years

Skills Required

  • Electrical Utility Systems
  • Power Distribution
  • HT/LT Panels
  • PCC
  • MCC
  • ACB
  • VCB Panels
  • Transformers
  • DG Sets
  • UPS
  • Auxiliary Equipment

Executive – Engineering

Qualification

  • B.Tech (Electrical Engineering / Instrumentation)

Experience

  • 7–10 years in Injectable Industry

Skills Required

  • Vial Filling Lines
  • Isolators
  • Lyophilizers
  • Sterilizers
  • Pipeline Installation
  • Equipment Commissioning
  • AHUs
  • LAFs
  • Process Design
  • SOP Preparation
  • Cross-functional Coordination

Quality Assurance Department

Senior Executive / Assistant Manager – Validation QA

Qualification

  • B.Pharm / M.Pharm / M.Sc.

Experience

  • 8–12 years

Key Responsibilities

  • Equipment Qualification
  • Utility Qualification
  • Facility Qualification
  • Cleaning Validation
  • Process Validation
  • Media Fill Validation
  • Regulatory Compliance
  • Risk Assessment
  • Investigation
  • SOP Review
  • CAPA Management
  • CSV
  • GxP Software Qualification

Executive – Manufacturing QA (MQA)

Qualification

  • B.Pharm / M.Pharm / M.Sc.

Experience

  • 3–8 years

Key Responsibilities

  • In-process QA Monitoring
  • Line Clearance
  • Batch Record Review
  • GMP Compliance
  • Deviation Investigation
  • CAPA
  • Data Integrity
  • Regulatory Audit Support

Executive – Laboratory QA (LQA)

Experience

  • 3–8 years

Key Responsibilities

  • QA Oversight of QC Laboratory
  • Analytical Document Review
  • OOS/OOT Investigation
  • Laboratory Data Integrity
  • Audit Trail Review
  • Inspection Readiness

QA Executive

Qualification

  • B.Pharm / M.Pharm / M.Sc.

Experience

  • 3–8 years

Key Responsibilities

  • Quality Review
  • Management Review Meetings
  • CAPA Management
  • Internal & External Audit Support
  • SOP and Document Management
  • GMP Training
  • Effectiveness Monitoring
  • Risk Assessment
  • Quality Compliance
  • Advanced MS PowerPoint & MS Excel

Documents Required

Candidates should carry:

  • Updated Resume/CV
  • One Passport Size Photograph
  • Latest Salary Slip

Contact Details

HR Contact: Shikha Sharma

Email: Shikha.Sharma@fresenius-kabi.com


Why Join Fresenius Kabi?

Fresenius Kabi is a globally recognized pharmaceutical company specializing in injectable medicines, oncology products, clinical nutrition, and medical technologies. Professionals joining the organization gain exposure to advanced sterile manufacturing technologies, global quality systems, and regulatory standards including USFDA, EU GMP, MHRA, and other international agencies.

If you have experience in Injectable Manufacturing, Aseptic Processing, Validation, Engineering, Utility, or Quality Assurance, this walk-in interview is an excellent opportunity to advance your pharmaceutical career.

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