Quality Control Analyst

Established in 1836, Acino is a pharmaceutical company headquartered in Zurich, with a clear focus on selected markets in the Middle East, Africa, the CIS Region and Latin America. With over 3,000 people across 90 countries, we deliver quality pharmaceuticals to promote affordable healthcare in these emerging markets and 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 toadvance innovation in linewith the Emirate's 2030 vision for the sector and beyond.The PositionThe RoleQuality Control Analyst will be responsible for performing analytical testing, maintaining laboratory resources, ensuring compliance with quality and safety standards, and supporting product release, method transfers, and validations. He /She will work with advanced analytical instruments, uphold data integrity principles, and ensure full compliance with GMP requirements to maintain product quality, safety, and efficacy.Perform analysis of raw materials, packaging materials, bulk products, finished products, in-process samples, stability samples, process/cleaning validation samples, and miscellaneous samples as per approved methods and protocols.Ensure all activities comply with GLP, GMP, and ALCOA++ principles.Operate major analytical instruments including HPLC, GC, Dissolution Apparatus, UV-Vis Spectrophotometer, and IR.Perform daily verification, calibration, and routine maintenance of instruments as per SOPs.Maintain an up-to-date inventory of reference standards, working standards, impurity standards, analytical columns, reagents, chemicals, and consumables.Conduct qualification of working standards against reference or primary standards.Prepare volumetric solutions and standardize them for routine use.Prepare, review, and update SOPs, test methods, and specifications as needed.Record all data accurately, clearly, and in real-time following GLP requirements.Report and support investigations for any OOS, OOT, incidents, or non-compliance activities.Initiate and support Change Control, CAPA, and Deviation processes as required.Follow safety procedures and use the recommended PPE for all QC activities.Ensure compliance with EHS policies and safe work practices in the laboratory.Support analytical validation/verification and cleaning validation studies.Participate in laboratory improvement initiatives.Carry out additional tasks assigned by the QC Manager in line with department objectives.Who You AreBachelor's degree in chemistry, pharmaceutical sciences, or related discipline.1–3 years of experience in a pharmaceutical QC laboratory.Hands-on experience with HPLC, GC, Dissolution, UV, and IR instruments.Knowledge of LIMS and SAP systems is preferred.Good understanding of GMP, GLP, and data integrity principles (ALCOA++).Strong attention to detail, analytical thinking, and problem-solving skills.Effective communication and teamwork abilities.We Are AcinoAt 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.How To ApplyNote that only direct applications via our HR system (follow the link above) will be considered.#J-18808-Ljbffr