Quality Assurance Specialist

Acino International AG; Dubai; On-site; AED 120,000 - 160,000; Full time

Benefits offered by this job

Equal Opportunity Employer

Dynamic work environment

Job summary

Acino International AG is seeking a professional to ensure GMP compliance during manufacturing and packaging. The role involves managing documentation and supporting batch release activities, while adhering to compliance standards. Candidates should have a Bachelor’s degree in pharmacy and relevant experience in the pharmaceutical industry.

Join a dynamic environment at Acino where your contributions can significantly impact healthcare access. Competitive compensation and growth opportunities are available, fostering an inclusive workplace.

Qualifications

• Bachelor’s degree in pharmacy required.
• Knowledge of GMP compliance and regulatory standards.
• Experience in Quality Assurance or Quality Control is essential.

Responsibilities

• Ensure GMP compliance during manufacturing.
• Manage documentation related to batch production.
• Monitor manufacturing and packing activities.

Skills

GMP compliance

Document management

Analytical techniques

Technical writing

Data analysis

Shift work

Teamwork

Communication skills

Education

Bachelor’s degree in pharmacy

Tools

Microsoft Excel

Microsoft Word

Microsoft PowerPoint

Job description

Established in 1836, Acino, part of Arcera, is a pharmaceutical company headquartered in Zurich, with a clear focus on selected markets in the Middle East, Africa, and Latin America, as well as Ukraine and Eurasian countries. With over 3,000 people across 90 countries, we deliver quality pharmaceuticals to promote affordable healthcare in these emerging markets. We also leverage our high-quality pharmaceutical manufacturing capabilities and network to supply leading companies through contract manufacturing and out‑licensing.

Acino is part of Arcera , a diversified life sciences holding company, established by ADQ in Abu Dhabi in 2024 with the purpose to advance innovation in line with the Emirate’s 2030 vision for the sector and beyond.

The Position

The Role

Ensures on‑floor GMP compliance during manufacturing and packaging and supports batch release activities through in‑process oversight, batch record review, deviation escalation, and verification of compliance prior to batch disposition.

• Responsible for document management such as issuance, storage, retention and destruction of documents and records as per defined procedure.
• To ensure good documentation by all concerned personnel and all the documents are as per current GMP requirements and in‑house SOPs.
• Preparation of standard operating procedure and provide training on SOPs.
• Responsible for maintaining audit documents such as regulatory and customer audit report and response.
• To ensure that batch production operations are carried out in accordance with cGMP and procedure mentioned in respective batch record.
• Monitoring of manufacturing/packing activities on routine basis.
• Ensure compliance in Warehouse, Manufacturing and Packing.
• To review the batch records including associated data, logbooks etc and to track monthly batch release activities.
• Ensure that cGMP requirements are been followed and monitored in the critical process areas.
• To ensure good documentation by all the concerned and all the documents are as per current GMP requirements and in‑house SOPs.
• To participate and ensure satisfactory technology transfer, process validation, cleaning validation and hold time studies.
• To implement CAPA for internal & external audits.
• Responsible to participate in investigations.
• To participate in audits and to provide relevant information, when required.
• To prepare Product quality review.
• Ensure safe work practices, and usage of recommended PPE during activity.
• Ensure compliance to EHS policy and its requirements.
• Responsible for management of document room including labelling and arrangement of files, storage, issuance, and retrieval on approved request.
• Issuance of batch manufacturing and packaging records to production department as per request.
• Any other responsibilities assigned by department head.

Who You Are

• Bachelor’s degree in pharmacy
• Working knowledge of Microsoft excel, word, power point etc.
• Relevant experience in the regulated pharmaceutical industry, specifically including Quality Assurance, Quality Control, and/or Drug Regulatory Affairs
• Experience with health authority inspections and third‑party audits
• Understanding of pharmaceutical manufacturing and laboratory work (including familiarity with various analytical techniques) a strong asset
  • Decision‑making skills.
  • Excellent communications skills in English (verbal, written, listening, email writing)
• Technical writing skills
• Understanding of manufacturing processes and/or quality systems elements
  • Data analysis skills are required
• Able to work in shifts
• Ability to work as part of a team.

We Are Acino

At Acino, we push the boundaries to deliver high‑quality pharmaceutical products that improve patients’ lives. Driven by our collective purpose to provide access to medicines to those in need, our strength lies in our unique expertise and presence in emerging and high‑growth markets. We are proud to be challenging the status quo in the pharmaceutical industry, always looking ahead to the future with an open mind.

Join Acino, a dynamic and rapidly growing environment where your contributions can make a real difference.

Acino is an Equal Opportunity Employer.