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Production / QC / QA / Engineering & Maintenance Roles

Date Posted: Aug 02, 2025
Job is expired

Job Detail

  • location_on
    Location Freelance
  • desktop_windows
    Job Type: Full Time/Permanent
  • schedule
    Shift: Rotating
  • analytics
    Career Level: Experienced Professional
  • group
    Positions: 10
  • calendar_view_day
    Experience: 2 years
  • male
    Gender: No Preference
  • school
    Degree: Masters
  • calendar_month
    Apply Before: Sep 04, 2025

Job Description

Maintenance


  • 🧾 Job Description
  • Cohance Lifesciences Limited is hiring experienced professionals for key departments in its pharmaceutical manufacturing operations:
  • 1. Production
  • Functions: Capsule/liquid filling, tablet compression, coating, granulation, secondary packing
  • Responsibilities:
  • Operate and maintain production equipment
  • Follow cGMP & SOP guidelines
  • Ensure documentation and process adherence during batch execution
  • 2. Quality Control (QC)
  • Functions: Raw material, in-process, and finished product analysis
  • Responsibilities:
  • Conduct sampling and testing
  • Maintain lab instruments
  • Perform stability studies, impurity profiling, and documentation
  • 3. Quality Assurance (QA)
  • Functions: In-process quality assurance, compliance, documentation
  • Responsibilities:
  • BMR/BPR review
  • Hold time and process validation studies
  • Handle deviations, OOS, CAPA, and change control
  • 4. Engineering & Maintenance
  • Functions: Utilities, equipment maintenance, breakdown and preventive maintenance
  • Responsibilities:
  • Oversee facility maintenance and utility systems
  • Ensure equipment calibration, upkeep, and documentation
  • Coordinate with production and EHS teams

  • 🎓 Eligibility Criteria
  • Educational Qualifications:
    B.Sc, M.Sc, B.Pharm, M.Pharm, B.Tech, Diploma
  • Experience Required:
    2 to 14 years (depending on department and role seniority)

  • 💼 Key Skills Required
  • Functional Area Key Skills & Tools
    Production cGMP operations, granulation, compression, coating, batch documentation
    QC HPLC, UV, dissolution, analytical chemistry, LIMS, stability studies
    QA IPQA, deviation handling, CAPA, SOPs, line clearance, audit preparedness
    Engineering Preventive/corrective maintenance, AutoCAD, HVAC, water systems, BMS

  • 🎁 Benefits
  • Competitive industry-aligned compensation
  • Opportunity to work in FDA-regulated, global CDMO environment
  • Career growth in formulation, API, and specialty chemical divisions
  • Cross-functional exposure and training across units

  • Venue:
    Cohance Lifesciences Ltd
    GMR Hyderabad Aviation SEZ,
    Mamidipally, Balapur Shamshabad,
    Ranga Reddy, Telangana

  • 📄 Documents to Carry
  • Updated Resume
  • Educational Certificates
  • Aadhar & PAN Card
  • Passport-size Photograph
  • Last 3 Months’ Payslips / CTC Details

Benefits

  • Competitive salary
  • Exposure to a global API & pharmaceutical CDMO environment with state-of-the-art plants
  • Professional growth in FDA‑regulated, high-quality production facilities
  • Multi-disciplinary experience across QA, QC, Engineering, and Production lines

Company Overview

Hyderabad, Telangana, India

Company Name Cohance Lifesciences Limited  Company Summary Cohance Lifesciences (formerly Suven Pharmaceuticals until May 2025) is an integrated, global CDMO (contract development and manufacturing organization) and API manufacturing platform head... Read More

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