Production Operator

ppAs a Production Operator, you will play a key role in the manufacturing of Tensive’s implantable medical devices. You will contribute to production activities carried out in a controlled environment, ensuring compliance with quality standards, operating procedures, and regulatory requirements. As part of the Production team, you will collaborate closely with the Quality Assurance Regulatory Affairs and Engineering teams to support manufacturing operations and drive continuous process improvement. /ph3Key Responsibilities /h3ulliPerform manufacturing activities for implantable medical devices in an ISO Class 7 cleanroom environment. /liliExecute production processes according to approved procedures and work instructions. /liliEnsure production traceability through the accurate and timely completion of production records and manufacturing documentation. /liliParticipate in the management of production nonconformities, contributing to root cause investigations and supporting the implementation of corrective and preventive actions (CAPA). /liliWork closely with the Quality Assurance Regulatory Affairs (QARA) team on the management of quality system documentation. /li /ulh3Required Skills Qualifications /h3h3bMandatory Requirements (Must Have) /b /h3pWe are looking for motivated individuals who enjoy hands-on manufacturing activities, have strong attention to detail, and are eager to contribute to the production of innovative medical devices. /pullibEducation: /b Technical diploma (e.g., Industrial, Chemical, Biomedical, or Biotechnology Technician) or a Bachelor’s degree in a scientific or technical discipline. /lilibLanguage: /b Basic proficiency in English. /lilibSafety: /b Knowledge of safety principles related to the handling of chemical substances. /lilibCommunication: /b Ability to communicate effectively and collaborate with cross-functional teams. /lilibSoft Skills: /b Precision, reliability, a problem-solving mindset, and the ability to work both independently and as part of a team. /lilibIT Skills: /b Good knowledge of Microsoft Office applications. /li /ulh3bPreferred Requirements (Nice to have) /b /h3ulliPrevious experience in medical device, pharmaceutical, biotechnology, or other regulated manufacturing environments. /liliPrevious experience working in cleanroom environments. /liliKnowledge of ISO 13485 and Good Manufacturing Practices (GMP). /liliExperience in drafting technical documentation. /li /ulh3What We Offer Recruitment Process /h3pApplications for the Production Operator position will be collected throughout June and July, with screening and selection activities taking place during the application period. The successful candidate is expected to join the company in July. The selection process includes an initial introductory interview, followed by a more in-depth discussion focused on the candidate’s knowledge and experience, as well as a brief interview in English. /ppThe company offers a structured onboarding program, including a two-month induction, training, and mentoring period designed to support the successful integration of the selected candidate. Depending on the candidate’s profile and assessment, the company offers either an apprenticeship contract or a permanent employment contract under the Chemical Industry SME collective agreement (CCNL Chimico Confapi). The gross annual salary (RAL) will range from b€23,500 to €28,000 /b, depending on the selected candidate’s qualifications, knowledge, and experience. /ppThe compensation package also includes: /pulliAnnual company performance bonus of €2,300 gross /liliAnnual welfare allowance of €1,000 /lili€8 meal vouchers for each working day /liliHybrid work policy with one day of remote work per week /liliAccident and supplementary health insurance coverage /li /ulpIn accordance with applicable regulations, this position is open to candidates of all genders and is offered without discrimination of any kind. /p /p #J-18808-Ljbffr