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HomeCompaniesHcfa Fa Us2 Oraclecloud Com CX 5001Executive, Manufacturing Documentation

Executive, Manufacturing Documentation

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

Job facts

FieldValue
CompanyHcfa Fa Us2 Oraclecloud Com CX 5001
TitleExecutive, Manufacturing Documentation
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 seen2026-05-07 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-06

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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 preparing, maintaining, and controlling manufacturing documentation within a regulated pharmaceutical manufacturing environment, ensuring that all batch records, standard operating procedures, and related documents are accurate, complete, and compliant with current Good Manufacturing Practices and applicable regulatory requirements. The position supports the documentation lifecycle including creation, review, revision, and archival of manufacturing documents in accordance with established document control procedures. It ensures that all manufacturing documentation accurately reflects executed processes and meets the requirements of regulatory agencies including FDA and EMA. The role collaborates with manufacturing, quality, and regulatory teams to ensure documentation integrity and compliance across all production activities. It performs reviews of completed batch records to identify discrepancies, errors, or deviations and escalates findings as required. Accurate and timely completion of documentation tasks is a core accountability of this position. The role participates in process improvement initiatives and functional team projects aimed at enhancing documentation quality, efficiency, and compliance. It operates within a highly regulated pharmaceutical environment, ensuring all documentation outputs meet defined quality and regulatory standards. Essential Functions: Prepare, review, and maintain manufacturing batch records, standard operating procedures, and related documentation in compliance with cGMP and regulatory requirements Support the documentation lifecycle including creation, revision, review, and archival of manufacturing documents in accordance with document control procedures Review completed batch records to identify discrepancies, errors, or deviations and escalate findings to relevant stakeholders Ensure all manufacturing documentation accurately reflects executed processes and meets the requirements of regulatory agencies including FDA and EMA Collaborate with manufacturing, quality, and regulatory teams to ensure documentation integrity and compliance across all production activities Maintain accurate and complete documentation records including batch record logs and document revision histories Ensure all documentation activities comply with current Good Manufacturing Practices (cGMP) and applicable regulatory requirements Participate in process improvement projects and functional team initiatives to enhance documentation quality, efficiency, and compliance Support training activities related to documentation standards and cGMP requirements as required Additional Responsibilities: Qualifications Education: Bachelors Degree (BA/BS) B. Sc. - Required Master Degree (MS/MA) M.Sc. - Preferred Experience: 5 years or more in 5 - 8 Years Specialized Knowledge: Licenses:

Full job record

Job ID9edc96b6f1e891dc3b2679bc682e661a6de05c33
Org ID822a1eaf-b950-4323-90f0-79f735f12603
Source ID55674fbb-0c45-4fea-a514-ebaecaf9c870
Board ID55674fbb-0c45-4fea-a514-ebaecaf9c870
Provideroracle_hcm
Provider Job Key7913
TitleExecutive, Manufacturing Documentation
Normalized Title
Statusactive
Activeyes
Location TextSachana, Mehsana, 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 preparing, maintaining, and controlling manufacturing documentation within a regulated pharmaceutical manufacturing environment, ensuring that all batch records, standard operating procedures, and related documents are accurate, complete, and compliant with current Good Manufacturing Practices and applicable regulatory requirements. The position supports the documentation lifecycle including creation, review, revision, and archival of manufacturing documents in accordance with established document control procedures. It ensures that all manufacturing documentation accurately reflects executed processes and meets the requirements of regulatory agencies including FDA and EMA. The role collaborates with manufacturing, quality, and regulatory teams to ensure documentation integrity and compliance across all production activities. It performs reviews of completed batch records to identify discrepancies, errors, or deviations and escalates findings as required. Accurate and timely completion of documentation tasks is a core accountability of this position. The role participates in process improvement initiatives and functional team projects aimed at enhancing documentation quality, efficiency, and compliance. It operates within a highly regulated pharmaceutical environment, ensuring all documentation outputs meet defined quality and regulatory standards. Essential Functions: Prepare, review, and maintain manufacturing batch records, standard operating procedures, and related documentation in compliance with cGMP and regulatory requirements Support the documentation lifecycle including creation, revision, review, and archival of manufacturing documents in accordance with document control procedures Review completed batch records to identify discrepancies, errors, or deviations and escalate findings to relevant stakeholders Ensure all manufacturing documentation accurately reflects executed processes and meets the requirements of regulatory agencies including FDA and EMA Collaborate with manufacturing, quality, and regulatory teams to ensure documentation integrity and compliance across all production activities Maintain accurate and complete documentation records including batch record logs and document revision histories Ensure all documentation activities comply with current Good Manufacturing Practices (cGMP) and applicable regulatory requirements Participate in process improvement projects and functional team initiatives to enhance documentation quality, efficiency, and compliance Support training activities related to documentation standards and cGMP requirements as required Additional Responsibilities: Qualifications Education: Bachelors Degree (BA/BS) B. Sc. - Required Master Degree (MS/MA) M.Sc. - Preferred Experience: 5 years or more in 5 - 8 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/7913
Apply URLhttps://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealIndiaCareers/job/7913
First Seen At2026-05-31 18:02:43Z
Last Seen At2026-06-06 20:23:04Z
Last Checked At2026-06-06 20:23:04Z
Last Changed At2026-05-31 18:02:43Z
Inactive At
Source Posted At2026-05-07 05:34:33Z
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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