Home › Companies › Acino › QA Sr. Specialist (Sterile Area)
QA Sr. Specialist (Sterile Area)
Acino · Cairo, Cairo, -, Egypt · Active · BambooHR
Job facts
| Field | Value |
|---|---|
| Company | Acino |
| Title | QA Sr. Specialist (Sterile Area) |
| Normalized title | - |
| Department / team | Quality Assurance |
| Location | Cairo, Cairo |
| Work model | - |
| Employment type | Active |
| Salary | - |
| Status | active |
| ATS provider | BambooHR |
| Posted / first seen | 2026-06-11 / 2026-06-12 |
| Changed / last seen | 2026-06-12 / 2026-06-22 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Acino. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through BambooHR. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Cairo. | Open |
| Department jobs | Active postings in Quality Assurance. | 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 | Acino |
| Source | 52cd711a-66b4-4a8f-8258-b2616c280158 |
| ATS provider | BambooHR |
Description
Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide.
As QA Senior Specialist your focus will be on the sterile production area, and you will be responsible for monitoring the manufacturing and packaging process to ensure the agreement with GMP procedures and report any violations during the manufacturing activities. The position reports to QA Senior Section Head of the sterile area and the location are based in our Cairo site in Al Obour City.
Your responsibilities:
Monitor production processes against batch records to ensure GMP compliance and prevent deviations.
Enter manufacturing and expiry dates for the monthly ampoule plan in SAP.
Review and approve monthly ampoule films for printing.
Collect and review batch record documents for market release, record data in annual product review template.
Report violations to the compliance team, ensure root causes are identified, and corrective actions implemented.
Participate in annual quality self-inspection plans to detect and address deviations in manufacturing practices.
Qualification and Experience:
Bachelor’s degree of pharmacy or science (Chemistry)
Work experience: 2-5 years
Decision-making and problem-solving skills
Ability to handle stress effectively
Excellent English proficiency and communication skills
Highly detail-oriented
This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!
Full job record
| Job ID | 9f5ed586bb7433e9e9ca979cc66c5647ee19c529 |
| Org ID | 93549f0c-9a11-444d-9afa-31eefd63bbdb |
| Source ID | 52cd711a-66b4-4a8f-8258-b2616c280158 |
| Board ID | 52cd711a-66b4-4a8f-8258-b2616c280158 |
| Provider | bamboohr |
| Provider Job Key | 828 |
| Title | QA Sr. Specialist (Sterile Area) |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Cairo, Cairo, -, Egypt |
| Department | Quality Assurance |
| Team | — |
| Employment Type | Active |
| Workplace Type | — |
| Remote Policy | — |
| Country | — |
| Region | Cairo |
| City | Cairo |
| Salary Raw | — |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://acino.bamboohr.com/careers/828 |
| Apply URL | https://acino.bamboohr.com/careers/828 |
| First Seen At | 2026-06-12 10:27:25Z |
| Last Seen At | 2026-06-22 11:08:39Z |
| Last Checked At | 2026-06-22 11:08:39Z |
| Last Changed At | 2026-06-12 10:27:25Z |
| Inactive At | — |
| Source Posted At | 2026-06-11 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=bamboohr/board=acino/date=2026-06-22/2026-06-22T11-08-33-053Z-05a7a26cc40a03776ff7c2e232d2b1a622a3d143bcc1f7382dfbffcf4bfc2564.json |
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"description": "<p><span>Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide.</span></p>\n<p><br></p>\n<p><span>As QA Senior Specialist your focus will be on the sterile production area, and you will be responsible for monitoring the manufacturing and packaging process to ensure the agreement with GMP procedures and report any violations during the manufacturing activities. </span>The position reports to QA<span> Senior Section Head of the sterile area </span>and <span>the location are based in our Cairo site in Al Obour City. </span></p>\n<p><br></p>\n<p><span><span style=\"font-weight: bold\">Your responsibilities:</span></span></p>\n<ul>\n<li><span>Monitor production processes against batch records to ensure GMP compliance and prevent deviations.</span></li>\n<li><span>Enter manufacturing and expiry dates for the monthly ampoule plan in SAP.</span></li>\n<li><span>Review and approve monthly ampoule films for printing.</span></li>\n<li><span>Collect and review batch record documents for market release, record data in annual product review template.</span></li>\n<li><span>Report violations to the compliance team, ensure root causes are identified, and corrective actions implemented.</span></li>\n<li><span>Participate in annual quality self-inspection plans to detect and address deviations in manufacturing practices.</span></li>\n</ul>\n<p><span><br></span></p>\n<p><span><span style=\"font-weight: bold\">Qualification and Experience:</span></span></p>\n<ul>\n<li>Bachelor’s degree of pharmacy or science (Chemistry)</li>\n<li>Work experience: 2-5 years</li>\n<li><span>Decision-making and problem-solving skills</span></li>\n<li><span>Ability to handle stress effectively</span></li>\n<li><span>Excellent English proficiency and communication skills</span></li>\n<li><span>Highly detail-oriented</span></li>\n</ul>\n<p><br></p>\n<p><span>This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</span></p>",
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