Descrizione dell'offerta
Job Opportunity: Quality Assurance Associate, Master Data
Location: Latina, Italy (Borgo San Michele production site, 12‑month fixed‑term contract). Responsibilities
Approve production documentation (Master Batch Record and recipes) and the master data of materials, equipment and resources, ensuring timely delivery and overall process quality. Control and guarantee the management of critical master data in compliance with GMP, quality and compliance requirements defined by company procedures. Collaborate with cross‑functional project teams (New Product Introduction, Technology Transfer, Technical Launch, Validation Process) to ensure market launch dates. Support quality processes by managing non‑conformities, monitoring corrective / preventive actions and change control requests linked to assigned projects. Resolve issues across plant departments related to product, process and equipment/facilities/utilities management to maintain quality, safety and efficacy. Act as the Quality representative in corporate projects, overseeing quality aspects. Provide effective support to the Production Service, offering solutions to overcome critical situations. Qualifications / Requirements
Master’s degree in Pharmaceutical Chemistry and Technologies, Pharmacy, Chemistry or Biology; Engineering; Computer Science. Minimum 12 months of experience in the pharmaceutical sector or a similar field. Excellent command of the English language. Good knowledge of Microsoft Office suite. Compensation and Benefits
Base pay range: €29,800.00 – €48,530.00. Additional benefits include an annual bonus, vacation days, a minimum of 12 weeks parental leave, bereavement leave, caregiver leave, volunteer leave, well‑being reimbursement, insurance plans, service anniversary rewards and recognition awards.
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Location: Latina, Italy (Borgo San Michele production site, 12‑month fixed‑term contract). Responsibilities
Approve production documentation (Master Batch Record and recipes) and the master data of materials, equipment and resources, ensuring timely delivery and overall process quality. Control and guarantee the management of critical master data in compliance with GMP, quality and compliance requirements defined by company procedures. Collaborate with cross‑functional project teams (New Product Introduction, Technology Transfer, Technical Launch, Validation Process) to ensure market launch dates. Support quality processes by managing non‑conformities, monitoring corrective / preventive actions and change control requests linked to assigned projects. Resolve issues across plant departments related to product, process and equipment/facilities/utilities management to maintain quality, safety and efficacy. Act as the Quality representative in corporate projects, overseeing quality aspects. Provide effective support to the Production Service, offering solutions to overcome critical situations. Qualifications / Requirements
Master’s degree in Pharmaceutical Chemistry and Technologies, Pharmacy, Chemistry or Biology; Engineering; Computer Science. Minimum 12 months of experience in the pharmaceutical sector or a similar field. Excellent command of the English language. Good knowledge of Microsoft Office suite. Compensation and Benefits
Base pay range: €29,800.00 – €48,530.00. Additional benefits include an annual bonus, vacation days, a minimum of 12 weeks parental leave, bereavement leave, caregiver leave, volunteer leave, well‑being reimbursement, insurance plans, service anniversary rewards and recognition awards.
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