hirly

Amneal

Assistant General Manager, Manufacturing Injectables

Hyderabad, Telangana, India

Apply through hirly

Upload your resume and get a version tailored to this job, plus a cover letter, in about thirty seconds — before you create an account.

Apply with hirly

hirly's read of this role

Seniority
Lead / management
Country
IN
Work mode
On-site / unstated
First seen by hirly
25 Sept 2026

Derived automatically from the posting. Sign up to see how the role scores against your own resume.

the posting

  • Description
  • To review, develop and introduce systems, practices and cultural changes that enable the production
  • department to meet business demands within agreed time frames and expected GXP standards.
  • To prepare production planning on monthly basis as per the production requirement and availability of
  • materials.
  • To discuss production plans with subordinates and scheduling weekly plans / allocation of weekly shift
  • schedule.
  • Daily work allocation to supervisors & workmen. Achieving set targets of daily/weekly /monthly
  • manufacturing/packaging plan.
  • To interact with Warehouse/QC/QA for the material availability / release and schedule the production
  • plan.
  • To propose and implement innovative ideas towards improvements in process efficiency, productivity,
  • delivery, quality, yield, safety resulting in successful operations.
  • To manage the troubleshooting activity, ensuring identification of appropriate corrective measures and
  • driving structured implementation of these measures through cross-functional teams.
  • To perform Gap analysis of defined procedures in Batch Manufacturing Record / Batch Packing Record /
  • Standard Operating Procedure / Protocol and initiation of corrective actions.
  • To impart continuous training to the workforce for enhancing their productivity & operational efficiencies
  • through knowledge enhancement / skill building.
  • To ensure effective execution of new product introduction and technology transfer of any product to the
  • Site.
  • To prepare & review of SOPs related to production department.
  • To review of documents like log books, BMR, BPR for error free online documentation and timely
  • submission to QA.
  • To co-ordinate with all concerned departments for providing cost efficient services and achieving
  • excellence.
  • Planning and execution of media fill validation along with Validation Team.
  • To ensure timely execution of equipment qualification along with Validation Team.
  • To review the annual validation plan, preventive maintenance plan and calibration plan.
  • Ensure timely initiation and closure of QMS documents of production department like change control,
  • deviations, CAPA and Risk Assessments with the stipulated timeframes.
  • To involve and implement in self-inspection of the system and use the findings from such audits for
  • overall improvement of facility, systems and documentation process.
  • Compliance to the regulatory authorities with respect to the investigations.
  • Qualifications
  • Qualification - B Pharma / M Pharma
Original posting on Amneal's site ↗

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job