Quality Vacancy At Organo pharmaceutical
ORGANO Pharma is hiring qualified and experienced QA professionals to join our growing team. If you have a strong background in GMP and a passion for pharmaceutical quality systems — we want to hear from you!
✔ 𝙌𝘼 𝘿𝙤𝙘𝙪𝙢𝙚𝙣𝙩𝙖𝙩𝙞𝙤𝙣 𝙎𝙪𝙥𝙚𝙧𝙫𝙞𝙨𝙤𝙧
📌 𝙌𝙪𝙖𝙡𝙞𝙛𝙞𝙘𝙖𝙩𝙞𝙤𝙣𝙨:
➖bachelor's degree in pharmacy or science.
➖Minimum 4 years of experience in pharmaceutical documentation or QA.
➖Experience managing controlled documents, SOPs, batch records, and archiving systems.
➖Strong knowledge of documentation practices and GMP standards.
➖Excellent attention to detail and organizational skills.
✔𝙌𝘼 𝙑𝙖𝙡𝙞𝙙𝙖𝙩𝙞𝙤𝙣 𝙎𝙪𝙥𝙚𝙧𝙫𝙞𝙨𝙤𝙧
📌 Qualifications:
➖bachelor’s degree in pharmacy, or Science.
➖Minimum 4 years of experience in pharmaceutical validation.
➖Hands-on experience with validation protocols (IQ, OQ, PQ).
➖Good knowledge of validation master plans and regulatory expectations.
➖Strong documentation and problem-solving skills.
✔𝙌𝘼 𝘾𝙤𝙢𝙥𝙡𝙞𝙖𝙣𝙘𝙚 𝙎𝙪𝙥𝙚𝙧𝙫𝙞𝙨𝙤𝙧
📌𝙌𝙪𝙖𝙡𝙞𝙛𝙞𝙘𝙖𝙩𝙞𝙤𝙣𝙨
➖bachelor’s degree in pharmacy, Science.
➖Minimum 4 years of QA or compliance experience in pharmaceuticals.
➖Strong knowledge of deviation management, CAPA, change control, and audit processes.
➖Familiarity with FDA/EU/WHO GMP guidelines.
➖Excellent analytical and communication skills.
📍 Location: El Obour
🕒 Job Type: Full-time
📩 How to Apply:
Send your updated CV to job@organo-pharma.com
Kindly mention the job title (e.g., "QA Documentation Supervisor", "Validation Supervisor", or "Compliance Supervisor") in the subject line.
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📌𝙌𝘼 𝙄𝙋𝘾 𝙎𝙪𝙥𝙚𝙧𝙫𝙞𝙨𝙤𝙧 & 𝙌𝘼 𝙄𝙋𝘾 𝙎𝙥𝙚𝙘𝙞𝙖𝙡𝙞𝙨𝙩 𝙑𝙖𝙘𝙖𝙣𝙘𝙞𝙚𝙨
➖ 𝙅𝙤𝙗 𝙎𝙪𝙢𝙢𝙖𝙧𝙮:
We are currently looking to expand our Quality Assurance In-Process Control (QA IPC) team with Ideal candidates who have hands-on experience in in-process quality control within a GMP-regulated environment and a strong understanding of quality systems in manufacturing operations.
📌 𝙌𝙪𝙖𝙡𝙞𝙛𝙞𝙘𝙖𝙩𝙞𝙤𝙣𝙨:
QA IPC Supervisor:
➖ Bachelor's degree in Pharmacy or Science.
➖ Minimum 4 years of experience in QA IPC or related QA/QC roles
➖ Strong leadership and communication skills
➖ Proficient in reviewing IPC documentation and managing a QA team
➖ In-depth knowledge of cGMP and regulatory requirements
QA IPC Specialist:
➖ Bachelor’s degree in Pharmacy or Science.
➖ Minimum 2 years of experience in QA IPC or QA/QC roles
➖ Familiarity with in-process checks, sampling, and documentation
➖ Strong observational and problem-solving skills
➖ Understanding of GMP and production processes
📍 Location: El Obour
🕒 Job Type: Full-time
📩 How to Apply:
Send your updated CV to job@organo-pharma.com
Kindly mention the job title (QA IPC Supervisor / QA IPC Specialist) in the subject line.