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Kia Biopharma Technologies
From company careers site

Assistant Manager

Location
Indore
Work mode
On-site
Employment type
Full-time

About the job

Purpose Recruitment of New Position.

Position / Job Title Assistant Manager (Sub Supervisor / Section In-Charge).

Department Quality Control

Reporting To Sr. Manager (P4) / AGM (M1)

Location Pithampur

Years of Experience 11 to 15 years.

Dosage Form Solid Oral

Job Responsibilities / Deliverables

•Responsible for leading the team of Approx 10+ members (Analyst + Reviewer) for respective section and release the batches after completion of analysis or any other given task as per target completion date. •Responsible for arranging a review of analytical raw data for correctness and completeness and to ensure final data submission to QA or other respective department as per specified timelines. •He is responsible for QMS handling (incidences, investigations, File notes, ratification, OOS, OOT, Change Control, CAPA etc.) and closing within stipulated timeline with proper root cause of his section. •To ensure and arrange all resources available to smooth line function as per planning and achieve deliverable task with minimum support. •He is responsible for facing the Audit (USFDA/MHRA/Client etc.) with respective section related work. •Should have good written and communication skills and perform the task given by the Sr. Leader as and when required. •Responsible for adherence of GLP and Health, Safety Environment system in Laboratory.

Qualifications & Pre-Requisites

•Preferably have following skill but not limit as mentioned below; •Bachelor / Master Degree of Science / Pharma. •He should have good experience of team handing (Analyst + Reviewer) for respective section. He should have past analytical experience of modern instruments like HPLC, GC, IR, UV, IC, KF, Dissolution etc. and requires knowledge of data review. •He should have experience of QMS Handling and know about GLP-GMP standard of analytical work. •The candidate having experience in US-FDA/MHRA approved company is preferable. •Knowledge of Chromleon 7.2 software will be an added advantage.

Additional notes •Role is expected to work in all shifts. •If required, the candidate should be ready to travel to all plant locations on work priority as per company policy. •Responsible to ensure compliance to GLP, Health, Safety and Environment. requirement.

From Kia Biopharma Technologies's careers page (Company careers page), checked 29 Oct 2026.

How to apply

  1. Select Apply on rubicon.co.in. It opens Kia Biopharma Technologies's own application form in a new tab, run on Company careers page.
  2. Fill in the form and upload your résumé there. Jobiwork never sees your application.
  3. Kia Biopharma Technologies will reply to you directly. No real employer asks you for money to apply.

Posted 14 Oct 2026 · checked 29 Oct 2026 · Report this job

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