Home › Companies › Hcfa Fa Us2 Oraclecloud Com CX 5001 › Associate, Inspection

Associate, Inspection

Hcfa Fa Us2 Oraclecloud Com CX 5001 · Sachana, Mehsana, Gujarat, IN · On Site · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

Field	Value
Company	Hcfa Fa Us2 Oraclecloud Com CX 5001
Title	Associate, Inspection
Normalized title	-
Department / team	Manufacturing Product & Packaging Operations
Location	Gujarat, IN, United States
Work model	On Site
Employment type	Full Time
Salary	-
Status	active
ATS provider	Oracle Recruiting Cloud / Fusion HCM
Posted / first seen	2026-05-25 / 2026-05-31
Changed / last seen	2026-06-04 / 2026-06-06

Related slices

Page	What it contains	Open
Company jobs	Active postings from Hcfa Fa Us2 Oraclecloud Com CX 5001.	Open
Company breakdowns	Role, location, ATS, and work model facets for this company.	Open
ATS provider jobs	Active postings observed through Oracle Recruiting Cloud / Fusion HCM.	Open
Provider filtered search	The same provider as a filtered job collection.	Open
City jobs	Active postings in Gujarat.	Open
Department jobs	Active postings in Manufacturing Product & Packaging Operations.	Open
Work model jobs	Active On Site postings.	Open
Lifecycle events	Open, update, close, and reopen events for this posting.	Open
Original posting	Canonical source or apply URL captured from the ATS.	Open

Linked records

Company	Hcfa Fa Us2 Oraclecloud Com CX 5001
Source	55674fbb-0c45-4fea-a514-ebaecaf9c870
ATS provider	Oracle Recruiting Cloud / Fusion HCM

Description

Description Description: This role is responsible for performing inspection operations within pharmaceutical manufacturing environments, ensuring that pharmaceutical products and components meet defined quality and compliance standards in accordance with current Good Manufacturing Practices (cGMP). The incumbent conducts visual and mechanical inspection of pharmaceutical products, packaging materials, and components to identify defects, non-conformances, and deviations from established specifications. This position adheres to standard operating procedures and quality standards to maintain product integrity, safety, and compliance throughout the inspection process. The role supports the overall quality assurance function by identifying and segregating non-conforming products and reporting inspection findings accurately and in a timely manner. It contributes to maintaining a clean, organized, and compliant work area in accordance with area cleaning and sanitization protocols. The position participates in training programs to develop technical competencies in inspection techniques, regulatory requirements, and quality standards applicable to pharmaceutical manufacturing. It supports continuous improvement efforts by identifying and reporting deviations and contributing to corrective and preventive action processes. Essential Functions: Perform visual and mechanical inspection of pharmaceutical products, packaging materials, and components to identify defects and non-conformances. Adhere to current Good Manufacturing Practices (cGMP) and standard operating procedures during all inspection activities. Identify, segregate, and report non-conforming products and materials in accordance with established quality procedures. Maintain accurate and complete inspection records and documentation as required by regulatory standards. Contribute to maintaining a clean, organized, and compliant work area in accordance with area cleaning and sanitization protocols. Operate inspection equipment and tools in accordance with established procedures and safety guidelines. Participate in training programs to develop technical competencies in inspection techniques and quality standards. Support continuous improvement efforts by identifying and reporting deviations and contributing to CAPA processes. Comply with all regulatory requirements and internal policies applicable to pharmaceutical manufacturing and inspection operations. Additional Responsibilities: Qualifications Education: Bachelors Degree (BA/BS) B. Sc. - Required Master Degree (MS/MA) M. Sc.. - Preferred Experience: 2 years or more in 2 - 5 Years Specialized Knowledge: Licenses:

Full job record

Job ID	0476704d0ff346d17edeba22bc0d3d43dc2f27d8
Org ID	822a1eaf-b950-4323-90f0-79f735f12603
Source ID	55674fbb-0c45-4fea-a514-ebaecaf9c870
Board ID	55674fbb-0c45-4fea-a514-ebaecaf9c870
Provider	oracle_hcm
Provider Job Key	8068
Title	Associate, Inspection
Normalized Title	—
Status	active
Active	yes
Location Text	Sachana, Mehsana, Gujarat, IN
Department	Manufacturing Product & Packaging Operations
Team	—
Employment Type	full_time
Workplace Type	on_site
Remote Policy	—
Country	United States
Region	IN
City	Gujarat
Salary Raw	Description Description: This role is responsible for performing inspection operations within pharmaceutical manufacturing environments, ensuring that pharmaceutical products and components meet defined quality and compliance standards in accordance with current Good Manufacturing Practices (cGMP). The incumbent conducts visual and mechanical inspection of pharmaceutical products, packaging materials, and components to identify defects, non-conformances, and deviations from established specifications. This position adheres to standard operating procedures and quality standards to maintain product integrity, safety, and compliance throughout the inspection process. The role supports the overall quality assurance function by identifying and segregating non-conforming products and reporting inspection findings accurately and in a timely manner. It contributes to maintaining a clean, organized, and compliant work area in accordance with area cleaning and sanitization protocols. The position participates in training programs to develop technical competencies in inspection techniques, regulatory requirements, and quality standards applicable to pharmaceutical manufacturing. It supports continuous improvement efforts by identifying and reporting deviations and contributing to corrective and preventive action processes. Essential Functions: Perform visual and mechanical inspection of pharmaceutical products, packaging materials, and components to identify defects and non-conformances. Adhere to current Good Manufacturing Practices (cGMP) and standard operating procedures during all inspection activities. Identify, segregate, and report non-conforming products and materials in accordance with established quality procedures. Maintain accurate and complete inspection records and documentation as required by regulatory standards. Contribute to maintaining a clean, organized, and compliant work area in accordance with area cleaning and sanitization protocols. Operate inspection equipment and tools in accordance with established procedures and safety guidelines. Participate in training programs to develop technical competencies in inspection techniques and quality standards. Support continuous improvement efforts by identifying and reporting deviations and contributing to CAPA processes. Comply with all regulatory requirements and internal policies applicable to pharmaceutical manufacturing and inspection operations. Additional Responsibilities: Qualifications Education: Bachelors Degree (BA/BS) B. Sc. - Required Master Degree (MS/MA) M. Sc.. - Preferred Experience: 2 years or more in 2 - 5 Years Specialized Knowledge: Licenses:
Salary Min	—
Salary Max	—
Salary Currency	—
Salary Period	—
Source URL	https://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealIndiaCareers/job/8068
Apply URL	https://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealIndiaCareers/job/8068
First Seen At	2026-05-31 18:02:43Z
Last Seen At	2026-06-06 20:23:04Z
Last Checked At	2026-06-06 20:23:04Z
Last Changed At	2026-06-04 10:30:40Z
Inactive At	—
Source Posted At	2026-05-25 09:06:06Z
Source Updated At	—
Raw Payload Uri	s3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=hcfa.fa.us2.oraclecloud.com\|CX_5001/date=2026-06-06/2026-06-06T20-22-52-037Z-c8b76f7dadd2fd84e1ac9b9023fee1f40f3de46a882ea2c2b3ab7fb496a86529.json

Event Fields

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Parsed Structured

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Extensions

{}

Native Structured

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