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HomeCompaniesHcfa Fa Us2 Oraclecloud Com CX 5001Officer, Manufacturing Process Operations

Officer, Manufacturing Process Operations

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

Job facts

FieldValue
CompanyHcfa Fa Us2 Oraclecloud Com CX 5001
TitleOfficer, Manufacturing Process Operations
Normalized title-
Department / teamManufacturing Process Operations
LocationGujarat, IN, United States
Work modelOn Site
Employment typeFull Time
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-06-04 / 2026-06-04
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Hcfa Fa Us2 Oraclecloud Com CX 5001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Oracle Recruiting Cloud / Fusion HCM.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Gujarat.Open
Department jobsActive postings in Manufacturing Process Operations.Open
Work model jobsActive On Site postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyHcfa Fa Us2 Oraclecloud Com CX 5001
Source55674fbb-0c45-4fea-a514-ebaecaf9c870
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description Description: This role is responsible for supporting injectable manufacturing operations by executing processing, equipment operation, and aseptic production activities within a regulated sterile pharmaceutical environment. The role operates manufacturing equipment such as autoclaves, washing machines, sterilizers, filtration systems, mixing vessels, and filling-related equipment to ensure timely batch execution. The incumbent handles raw materials, components, intermediates, and finished injectable products in accordance with approved procedures, aseptic practices, and quality standards. It ensures accurate batch documentation, equipment cleanliness, and compliance with cGMP and global regulatory requirements. The role contributes to safe and efficient production, supports equipment upkeep, and participates in continuous improvement initiatives to enhance productivity, quality, and schedule adherence in injectable manufacturing operations. Essential Functions: Operate manufacturing equipment such as autoclaves, sterilizers, filtration units, mixing vessels, washing machines, and filling support systems as per SOPs Execute injectable manufacturing activities including solution preparation, filtration, sterilization, filling support, and component handling as per batch records Handle raw materials, containers, closures, intermediates, and finished injectable products in compliance with aseptic and GMP standards Maintain accurate batch manufacturing records, equipment logbooks, and production documentation in line with GDP requirements Perform equipment cleaning, sanitization, line clearance, and basic maintenance as per approved procedures Ensure compliance with cGMP, aseptic practices, safety guidelines, and regulatory requirements including FDA and EMA standards Support environmental control practices and maintain cleanliness of general and classified manufacturing areas Identify and report deviations, equipment malfunctions, or process abnormalities to supervisors promptly Participate in in-process checks and sampling activities to support product quality and batch release requirements Contribute to process improvement initiatives focused on productivity, quality enhancement, cost control, and schedule adherence Additional Responsibilities: Qualifications Education: Bachelors Degree (BA/BS) B.E. - Required M. Pharm M. Pharm - Preferred Experience: 2 years or more in 2 - 5 Years Specialized Knowledge: Licenses:

Full job record

Job IDc68ff7e4cc3182b69147d89b6e49df0a5eb118a0
Org ID822a1eaf-b950-4323-90f0-79f735f12603
Source ID55674fbb-0c45-4fea-a514-ebaecaf9c870
Board ID55674fbb-0c45-4fea-a514-ebaecaf9c870
Provideroracle_hcm
Provider Job Key8123
TitleOfficer, Manufacturing Process Operations
Normalized Title
Statusactive
Activeyes
Location TextDahej, Bharuch, Gujarat, IN
DepartmentManufacturing Process Operations
Team
Employment Typefull_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionIN
CityGujarat
Salary RawDescription Description: This role is responsible for supporting injectable manufacturing operations by executing processing, equipment operation, and aseptic production activities within a regulated sterile pharmaceutical environment. The role operates manufacturing equipment such as autoclaves, washing machines, sterilizers, filtration systems, mixing vessels, and filling-related equipment to ensure timely batch execution. The incumbent handles raw materials, components, intermediates, and finished injectable products in accordance with approved procedures, aseptic practices, and quality standards. It ensures accurate batch documentation, equipment cleanliness, and compliance with cGMP and global regulatory requirements. The role contributes to safe and efficient production, supports equipment upkeep, and participates in continuous improvement initiatives to enhance productivity, quality, and schedule adherence in injectable manufacturing operations. Essential Functions: Operate manufacturing equipment such as autoclaves, sterilizers, filtration units, mixing vessels, washing machines, and filling support systems as per SOPs Execute injectable manufacturing activities including solution preparation, filtration, sterilization, filling support, and component handling as per batch records Handle raw materials, containers, closures, intermediates, and finished injectable products in compliance with aseptic and GMP standards Maintain accurate batch manufacturing records, equipment logbooks, and production documentation in line with GDP requirements Perform equipment cleaning, sanitization, line clearance, and basic maintenance as per approved procedures Ensure compliance with cGMP, aseptic practices, safety guidelines, and regulatory requirements including FDA and EMA standards Support environmental control practices and maintain cleanliness of general and classified manufacturing areas Identify and report deviations, equipment malfunctions, or process abnormalities to supervisors promptly Participate in in-process checks and sampling activities to support product quality and batch release requirements Contribute to process improvement initiatives focused on productivity, quality enhancement, cost control, and schedule adherence Additional Responsibilities: Qualifications Education: Bachelors Degree (BA/BS) B.E. - Required M. Pharm M. Pharm - Preferred Experience: 2 years or more in 2 - 5 Years Specialized Knowledge: Licenses:
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealIndiaCareers/job/8123
Apply URLhttps://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealIndiaCareers/job/8123
First Seen At2026-06-04 10:30:40Z
Last Seen At2026-06-06 20:23:04Z
Last Checked At2026-06-06 20:23:04Z
Last Changed At2026-06-06 20:23:04Z
Inactive At
Source Posted At2026-06-04 06:57:40Z
Source Updated At
Raw Payload Uris3://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
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Native Structured
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