Home › Companies › Hcfa Fa Us2 Oraclecloud Com CX 5001 › Executive, 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
| Field | Value |
|---|---|
| Company | Hcfa Fa Us2 Oraclecloud Com CX 5001 |
| Title | Executive, Manufacturing Documentation |
| Normalized title | - |
| Department / team | Manufacturing Process 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 | 2026-05-07 / 2026-05-31 |
| Changed / last seen | 2026-05-31 / 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 Process 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 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 ID | 9edc96b6f1e891dc3b2679bc682e661a6de05c33 |
| 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 | 7913 |
| Title | Executive, Manufacturing Documentation |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Sachana, Mehsana, Gujarat, IN |
| Department | Manufacturing Process 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 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 URL | https://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealIndiaCareers/job/7913 |
| Apply URL | https://hcfa.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/AmnealIndiaCareers/job/7913 |
| 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 | 2026-05-31 18:02:43Z |
| Inactive At | — |
| Source Posted At | 2026-05-07 05:34:33Z |
| 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 |
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