AHMEDABAD · FULLTIME
Jr Executive, Quality Control
Amneal Pharmaceuticals
Ahmedabad · onsite · Posted 12d ago
Sourced from
Undisclosed0–4 yrsfulltimeAhmedabad
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Section · 01
About this role
Department: Analytical Quality control
Role: QC (Raw Material/Packing Material)
Roles Responsibilities
Responsibiliti es:
- Sample management, including sample in/out, Entry/Exit of samples, Test sample requests, and management of sample request forms for QC laboratory activity.
- Ensure that all raw material and packing material testing and method verification activity is carried out per schedule and per GMP. Ensure that records are maintained to appropriate requirements.
- Sampling of Raw material, packing material and Physical verification of consumable as per priority of production and release in accordance with quality standards and procedures.
- Preparation of Raw material/ Packing material specifications and DRS. Analysis of Packing material (Primary, Secondary and Tertiary packing materials).
- Support laboratory operations including but not limited to method verification, equipment qualification, calibration, cleaning and maintece, purchase and receipt of reagents and consumables and document management.
- Responsible for analysis of samples, following test methods, generation and compilation of results, data packets preparation and submission for review of results in a timely manner.
- Reading and understanding the test procedure and the requirements per USP, EP, JP and IP.
- Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness.
- To assist in writing SOP documents, change plan or change records (document revisions) supporting continuous improvement of test procedures.
- To carry out completion and review of GMP Documentation of data sheets or LIMS software.
- To carry out QC sample receipt, assay and release procedures.
- Support Audit preparation and any audit related activity
- Responsible for maintaining and Training records for the QC laboratory in accordance with GLP compliance and any other work assigned by the Supervisor or Head of Department.
- Qualification: Master s degree in science
- Good verbal and email communication skills
- Attention to detail and strong compliance mindset
- Curiosity to read, learn and working across cross-functional teams
- Basic MS Office: Word, Excel, PowerPoint
- Flexible to work in shifts as per operational requirements.
Basic Requirements:
Qualification: Masters in Science( Chemistry/ Analytical/ Biotechnology)
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
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Section · 02
Skills
Document Managementaudit preparationAssayCompilationChemistryEquipment QualificationBiotechnologylaboratory operationsCommunication SkillsoperationsmaintenancePhysical VerificationcomplianceQCPacking Material
Section · Company
About Amneal Pharmaceuticals
Amneal Pharmaceuticals
Pharma
5.5k+
employees
2002
24 years old
Bridgewater, New Jersey
United States (USA)
About
Amneal Pharmaceuticals operates in the pharmaceutical sector, focusing on developing accessible and affordable medicines to address critical healthcare challenges.
Industries
PharmaBiotechnologyClinical Research
Employee ratings
1,455 reviews
4.2/ 5
Culture
4.0
Career growth
3.5
Work-life
4.2
Employees rate it well for
Work Culture190Senior Management93Work Life Balance87Work Environment69HR Policies65
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