Manufacturing Senior Executive / Assistant Manager

6 - 10 years

10 - 15 Lacs

Posted:4 days ago| Platform: Naukri logo

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Work Mode

Remote

Job Type

Full Time

Job Description

Position Summary

The Manufacturing Senior Executive / Assistant Manager will provide documentation and process support to the on-site manufacturing team. This role includes preparing essential documents, initiating quality system events, and coordinating with cross-functional teams to ensure smooth manufacturing operations. The role requires strong documentation skills, understanding of manufacturing processes, and the ability to work independently in a virtual environment.

Key Responsibilities

Documentation Support

  • Provide comprehensive backend documentation support to the manufacturing team and collaborate virtually with on-site teams.
  • Prepare, review, and update

    Standard Operating Procedures (SOPs)

    in accordance with cGMP and organizational requirements.

Quality Systems

  • Initiate

    Change Controls

    ,

    Deviations

    , and

    Corrective and Preventive Actions (CAPA)

    as part of the Quality Management System.
  • Ensure timely and accurate documentation of all quality-related activities.

Cross-Functional Coordination

  • Maintain effective communication with

    Cross Functional Teams (CFTs)

    such as QA, QC, Production, Supply Chain, and Engineering to support coordinated manufacturing activities.
  • Assist in resolving documentation and process-related queries raised by different departments.

Administrative Responsibilities

  • Complete any task assigned by the Head of Department (HOD) in alignment with organizational priorities and timelines.
  • Support continuous improvement initiatives within the manufacturing department.

Qualifications & Requirements

  • Bachelors or Master’s degree in Pharmacy, Biotechnology, Chemistry, or related field.
  • 3–7 years of experience in pharmaceutical manufacturing or documentation roles (Senior Executive).
  • 6–10 years of experience for Assistant Manager level.
  • Good understanding of

    cGMP

    , documentation practices, and manufacturing processes.
  • Familiarity with quality systems such as Change Control, Deviations, and CAPA.
  • Excellent written and verbal communication skills.
  • Strong organizational skills and attention to detail.
  • Ability to work independently and as part of a cross-functional virtual team.

Key Competencies

  • Documentation & Compliance
  • Communication & Coordination
  • Time Management
  • Problem-Solving Skills
  • Adaptability
  • Team Collaboration

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