Walk in Drive for M.Pharm, B.Pharm, MSc in QA, QC at Felix Generics Pvt Ltd- on 29th October, 2023

Felix Generics Pvt Ltd
  • Full Time
  • Anywhere

Felix Generics Pvt Ltd

About Felix Generics Pvt Ltd

Felix Generics Pvt Ltd is a pharmaceutical generics company specializing in veterinary medicines. Their facility received approval from the Health Products Regulatory Authority (HPRA) in April 2021. The parent company is based in Ireland, with the Indian corporate office situated in Gurgaon and the Research and Development Center located in Greater Noida. The manufacturing facility is based in the Special Economic Zone (SEZ) in Pithampur, Indore.

1. QC Validation Analyst

  • Experience

    : 4-8 years

  • Qualification

    : M.Sc / M.Pharma / B.Pharma

  • Responsibilities:

    • Analytical methods validation, verification, and methods transfer
    • Validation of cleaning methods
    • Handling HPLC, GC, DR, and other instruments
    • Preparing method validation verification protocol and report
    • Reviewing analytical hard copy and electronic data

2. QC Sr. Officer / Executive

  • Experience

    : 4-8 Years

  • Qualification

    : M.Sc / M.Pharma / B.Pharma

  • Responsibilities

    :

    • Working in QC analyzing, Stability, In process, FR RM sample
    • Handling instruments like HPLC, GC, FTIR, UV, DR, SSA, etc.
    • Versatile in handling SAR documentation like preparing STPs and review of analytical hard copies and electronic data

3. QA / QC / Microbiology – Injectable

  • Designation

    : Officer / Sr. Officer / Executive / Sr. Executive

  • Experience

    : 4-8 years in Injectable plants

  • Qualification

    : M.Sc. (Microbiology/ Biotechnology/ Chemistry) / M.Pharma / B.Pharma

  • Responsibilities

    :

    • Quality assurance, quality control, and microbiology tasks related to injectables

4. Quality Assurance (IPQA / QMS/ Q&V)

  • Experience

    : Candidate should have experience in handling of IPQA activities.

  • Responsibilities

    :

    • Batch record review, Audit trail review, Batch release, Process validation
    • Cleaning validation, Media fills, Control sample management
    • Preparation & review of SOPs / protocols
    • Handling of change controls, Deviation, CAPA, Quality Risk Management, Market complaint
    • Qualification of Equipment’s and Utilities
    • Review of Layouts / drawings, Validation Master planner

5. Microbiology (Analyst)

  • Experience

    : Candidate should have experience in all microbiological testing and method validations

  • Responsibilities

    :

    • Proficient in BET testing
    • GPT, Environment Monitoring, Culture handling
    • Experience in Qualification of Microbiology Equipment’s/Instruments

6. Quality Control (Analyst)

  • Experience

    : Candidate should have experience in instruments qualification & calibration

  • Responsibilities

    :

    • Handling quality control instruments; HPLC, GC, FTIR, UV, etc.
    • Experience in chemical analysis, water analysis, RM/PM analysis, FP/ln-process, and stability analysis
    • Method validation / verification / transfer activity & Cleaning method validation
    • Preparation of documents; Protocols, reports, SOP’s, STP’s, etc.
    • Eligibility: Candidate having experience to work in USFDA approved unit with good communication skills.

Walk-in Interview

To apply for this job email your details to grandirpharma@gmail.com