Quality Control Manager

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    "description": "<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt; font-weight: bold\"><span style=\"text-decoration: underline\">Qualifications:</span></span></p>\n<ul>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Bachelor’s degree or higher in Chemistry, Chemical Engineering, or Pharmacy.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">At least 10 years of experience in the field, including a minimum of 5 years in managerial positions within Quality Control or R&amp;D laboratories in the pharmaceutical industry.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Advanced proficiency in English.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Strong analytical thinking skills; team-oriented, well-organized, responsible, and possessing strong interpersonal skills.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Experienced in managing large teams.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Knowledgeable in current GMP practices and data integrity/security requirements.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Advanced knowledge of chromatographic techniques, spectrophotometric techniques, and other fundamental analytical methods.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Knowledge and experience in raw material and finished product chemical controls.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Able to adapt to flexible working hours.</span></li>\n</ul>\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt; font-weight: bold\"><span style=\"text-decoration: underline\">Job Description:</span></span></p>\n<ul>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Ensure that chemical analyses of raw materials, intermediates, and finished products; in-process controls; primary–secondary–tertiary packaging material inspections; and physical controls (packaging IPC, finished product and bulk AQL inspections) are performed and reported in accordance with approved methods, company procedures, and current GMP rules and guidelines.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Monitor the updates of reference documents related to the department (e.g., pharmacopoeias, standards such as ISO, ICH, TSE, etc.) and initiate change control forms (DTF) when necessary to adapt local and international guideline/standard updates into the system.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Track department-related changes, deviations, internal and external audit actions, DOFIs, and OoS/OoT cases; ensure they are completed accurately and within the required timelines.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Identify the department’s needs for materials, equipment, physical modifications, investments, training, and staffing; prepare investment budgets; and create and monitor the consumables budget in line with departmental and company objectives.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Prepare chemical analysis methods used for quality control based on customer requirements, current practices, and necessary changes; manage their transfer to QC laboratories; perform applicability checks and verifications; and ensure that methods remain up to date.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Organize and oversee calibration and qualification activities of instruments used in quality control analyses to ensure timely completion in accordance with current GMP expectations and company procedures.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Ensure that QC analyses, related documentation, and raw data are completed fully and on time, following current data integrity practices, local and international standards, GMP guidelines, and company procedures—without delaying production or shipment schedules.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Ensure onboarding and continuous training of assigned personnel; support the acquisition and implementation of up-to-date technical knowledge; manage team productivity, performance, and motivation; and report on employee development and performance evaluations.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Represent the department during internal and external audits, as well as local and international authority inspections.</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Participate in internal audits and domestic/international supplier audits when required.</span></li>\n</ul>\n<p><br><br></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">In connection with your application, Arcera will collect, process and store personal data about you. Our <a href=\"https://www.arceralifesciences.com/wp-content/uploads/sites/5/2026/03/Arcera-Privacy-Notice-for-Candidates.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">Privacy Notice for Prospective Employees</a>, provides an overview of the personal data that Arcera processes during the application process. Note: This Privacy Notice may be updated by Arcera, we therefore invite you to consult the latest versions via the above link.</span><br></p>\n<p><br></p>",
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