113 Quality Assurance Control in Lisbon lowest at $14000.0+

Production Operator – Pataias64840394160513120

Indeed

Production Operator – Pataias

Do you have industrial experience and are looking for a new challenge? We are recruiting a Production Operator for a company operating in the field of molds and forms for the cosmetics industry. **Responsibilities:** \- Assist in production finishing; \- Check product quality. **Requirements:** \- Minimum compulsory education level; \- Experience in an industrial/factory environment (preferred); \- Availability to work Monday to Friday, from 8:00 a.m. to 5:00 p.m.; \- Personal transportation (preferred); \- Immediate availability to start work. **Offer:** \- Temporary employment contract with an expected duration of 3 months; \- Base salary: €870.00; \- Food allowance: €6.00; Type of position: Full-time Benefits: * Meal card/Ticket

Rua dos Mestres de Obras BA, 2450-065 Nazaré, Portugal

€ 870/month

Quality Administrator (m/f) - Entroncamento64840394176769121

Indeed

Quality Administrator (m/f) - Entroncamento

The **ANEXXA®**, a company specialized in Human Resources Solutions, is recruiting for a prestigious client: **Quality Administrator (m/f) \- Entroncamento** **FUNCTIONS** * Verification of quality-related procedures; * Identification of inconsistencies and nonconformities; * Proposal of alternative corrective actions for identified issues; * Follow-up of audited departments to verify implementation of recommended changes; * Evaluation of results following the implementation of new approaches; * Review of audit processes conducted by other auditors; * Organization of all documentation required for audits; * Other tasks inherent to the role. **PROFILE** * Education: Minimum of 12th grade; * Minimum professional experience of 2 to 5 years in similar roles (preferred); * Knowledge of ISO 9001, ISO 19443, and other relevant standards; * Proficiency in computer applications from an end-user perspective; * Teamwork skills; * Effective communication skills; * Organizational ability; * Good time management skills; * Willingness to travel nationwide; * Valid driver’s license for light vehicles (preferred); * Ability to commute independently to the headquarters/office in Alenquer; * Immediate availability (preferred); * Bilingual in Portuguese and English, with knowledge of French. **CONDITIONS** * Opportunity for professional career development; * Integration into a dynamic, diverse, and continuously evolving environment. If you believe you meet the stated requirements, please: * Send your CV with the subject line **"Quality Administrator (m/f) \- Entroncamento"**; * Submit your application via anexxa.pt; * For any questions, contact us at 915742071. You will be contacted if your profile matches our requirements; otherwise, your application will remain in our database for future opportunities. Your application will be processed in accordance with the General Data Protection Regulation (GDPR), Regulation (EU) 2016/679 of 27 April 2016. By submitting your application, you consent to the processing of your personal data for employment and recruitment purposes. Type of position: Full-time

R. Camilo Castelo Branco 5, 2005-472 Santarém, Portugal

Negotiable Salary

Production Assistant (M/F) - Valado dos Frades64684240532354122

Indeed

Production Assistant (M/F) - Valado dos Frades

Serlima Target, part of the Serlima Group, is the business unit specialized in temporary staffing solutions. We are recruiting a **Production Assistant (M/F)** for a client located in Valado dos Frades – Nazaré. **Responsibilities:** * Operate and monitor injection molding machines; * Support production and assembly of thermoplastic components; * Package finished parts; * Perform product quality inspections. **Requirements:** * Immediate availability; * Availability to work rotating shifts; * Prior factory experience working rotating shifts; * Minimum compulsory education level; * Own vehicle required; **Conditions:** * Employment contract with Serlima; * Initial and ongoing training; * Integration into a young and dynamic work environment. We’re waiting for you! Apply now! Job type: Full-time Work location: On-site

Rua dos Mestres de Obras BA, 2450-065 Nazaré, Portugal

Negotiable Salary

Industrial Maintenance Technician - Milharado (Mafra)64663306523394123

Indeed

Industrial Maintenance Technician - Milharado (Mafra)

A leading company in the food industry is seeking to strengthen its operational team by hiring an Industrial Maintenance Technician to work in the Milharado area (Mafra). If you have experience in industrial maintenance, an interest in machinery, and are looking for stability within a solid and growing environment, this could be your ideal opportunity. **Responsibilities** * Perform preventive and corrective maintenance on industrial refrigeration, freezing, and preservation equipment; * Identify technical faults and carry out repairs to ensure proper machine operation; * Work on highly complex equipment while strictly adhering to all safety regulations; * Carry out minor welding tasks and support electrical work (valued); * Follow internal maintenance, quality, and safety procedures; * Record and report all interventions performed, collaborating with the production team. **Candidate Profile** * Proven experience in industrial maintenance (mandatory); * Knowledge of industrial refrigeration, freezing, and preservation systems; * Skills in electricity and/or welding will be valued; * High sense of responsibility, precision, and attention to detail; * Ability to work effectively in a team and communicate well; * Personal vehicle for commuting to the workplace. **Terms** * Indefinite-term employment contract; * Salary commensurate with experience and demonstrated competencies; * Opportunities for career progression and long-term employment; * Workplace location: Milharado (Mafra). An excellent opportunity to join a solid, historic, and continuously evolving company in the food industry, strongly committed to the professional development of its teams. Job type: Full-time Salary: €950.00 – €1,100.00 per month Benefits: * Meal card/voucher

R. Canal 6, 2640 Mafra, Portugal

€ 950-1,100/month

Indeed

Administrative

We are looking for a dedicated and organized Administrative professional to join our team in the food quality area at Receitas d'Avó. Our company, a leader in the food industry, values professionalism and rigor in product quality control. Responsibilities: * Assist in managing and organizing documents related to quality control. * Ensure compliance with food standards and regulations. * Provide administrative support to the quality department. * Collaborate in internal audits. * Help monitor and track process indicators. Requirements: * High school education (12th grade or equivalent). * Knowledge in food quality will be valued. * Analytical skills, ability to monitor indicators, and proficiency in Microsoft Office tools. * Strong sense of responsibility. * Proactive, motivated, and determined. We offer: * A dynamic and collaborative work environment. * Opportunities for professional development. * Competitive salary based on experience. Interested candidates should send their CV to the email: rdacandidaturas@gmail.com Type of offer: Full-time

R. João de Deus 1, 2630-247 Arruda dos Vinhos, Portugal

Negotiable Salary

Mechanical Welder (M/F) - Alverca do Ribatejo, Lisbon64278039129347125

Indeed

Mechanical Welder (M/F) - Alverca do Ribatejo, Lisbon

Part of the Serlima Group, Serlima Target is the business area specialized in Recruitment \& Selection and Temporary Work solutions. We are recruiting a **Mechanical Welder (M/F)** for a client company in the heavy vehicles sector located in **Alverca do Ribatejo, Lisbon**. **Main Responsibilities:** * Perform metal cutting, bending, fitting, drilling, and welding; * Assemble, adjust, and align mechanical components; * Provide assistance, when requested, in tasks carried out by mechanical workshops; * Carry out finishing and fine adjustments on metal parts to ensure proper fit and function; * Comply with company safety and quality standards. **Requirements:** * Proven experience in similar roles; * Ability to work in a team; * Sense of responsibility and attention to detail; **Offers:** * Direct contract with the client company; * Productivity bonuses; * Integration into a solid and growing company. Type of offer: Full-time/Full\-time Benefits: * Meal card/Ticket * Health insurance

Av. 5 de Outubro 4, 2615-063 Alverca do Ribatejo, Portugal

Negotiable Salary

QUALITY CONTROL (M/F) - CARREGADO64089052624643126

Indeed

QUALITY CONTROL (M/F) - CARREGADO

Integrated into the Serlima Group, Serlima Target is the business area specialized in temporary staffing and direct assignments, operating both as support for operations and for the other companies within the Group. Under the motto "We provide the right professional!" we are recruiting a Quality/Production Controller (M/F) for a client company in the Carregado area. **RESPONSIBILITIES:** * Quality control of automotive components; * Visual inspection of parts; * Use of metrology in quality control; * Feeding production lines; **REQUIREMENTS:** * Minimum 9th grade education; * Valid driver's license and own vehicle (**mandatory requirement**); * Experience in quality control and production within the automotive sector (**preferred**); * Experience in part polishing (**preferred**); * Immediate availability; * Availability for overtime; * Dynamic and proactive; **OFFER:** * Working hours from Monday to Friday; * Fixed shifts; * **Salary Package:** Base salary \+ Meal allowance \+ Overtime pay Type of offer: Full-time

R. Cap. Ten. Oliveira e Carmo 29, 2580-499 Carregado, Portugal

Negotiable Salary

Quality Assurance Associate64088838966530127

Indeed

Quality Assurance Associate

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: Guarantees cGMP compliance in all activities and systems related to Projects and Products execution. Applies technical knowledge and expertise in quality and current Good Manufacturing Practices (cGMPs) to provide support to the operational area. Acts as the primary point of contact on QA side during manufacturing operations, ensuring compliance throughout operations. * Regular presence on manufacturing floor, providing on\-the\-job support, developing a sense of collaboration with operational areas and performing a general oversight of activities, as required * Provide real\-time quality assurance support on the production floor over two shifts (07:00/15:00 and 15:00/23:00\) * Identify, document and escalate deviations or any other non\-conformities * Support investigations to the shop floor, including to the root cause analysis and the implementation of corrective and preventive actions (CAPAs) * Rigorously, accurately, efficiently and professionally manage all quality activities for the assigned projects and / or products in accordance with applicable cGMP, quality operational standards / procedures and legal regulations, ensuring the site is always “audit ready” * Promote the importance of high\-quality levels and the importance of a continuous improvement culture in relevant company activities * Act as a catalyst for change and improvement in performance/quality * Provide an example of professionalism * Efficiently, accurately and reliably ensure that project and / or product activities are delivered in compliance with cGMP requirements and maintenance of the company Quality Management System is assured * Manage and participate in Quality Product key activities for the assigned product / projects, and introduction of new products; including (but not limited to) preparation, review and approval of auxiliary documentation, protocols and quality related reports * Prepare for and support internal and external site audits and inspections, conducting regular reviews and periodically following\-up action plans as necessary * Ensure inspection readiness in work completed and Act in an advisory capacity for all internal and external site audits * Periodic follow\-up of ongoing deviations and Change Controls (PdAs) to assure timely closure of deviations and approval of PdAs, as appropriate * Prepares SOPs, department IOPs, quality related reports and change control documents (PdAs) as required and appropriate * Review process master documentation, revision of executed batch documentation and product specifications as required and appropriate * Ensures that SOPs and IOPs are up to date, compliant and supports efficient production. * Review regulatory documentation and co\-ordination of site documentation to support regulatory requirements * Authorize the usage of production equipment/utilities when qualification required * Solve challenges related to compliance problems by providing collaborative and timely support to all areas and departments, escalating as required * Ensure the effective and proactive flow of information between stakeholders, representing the team as appropriate * To assure and promote compliance on Health, Safety and Environment in the area and activities for which is responsible, or in which participates * Accurately use and maintain all information systems * Support the generation / reporting of KPIs for the team * Develop and accumulate strong QA expertise, sharing knowledge of new developments and methodologies within the area * Co\-ordinate and assist with the analysis and investigation of customer complaints that may arise, ensuring all complaints are investigated and closed out within specified timeframes * Be an advocate for safe operating and high\-quality performance, alerting ascending colleagues to any potential risks, discrepancies, deviations or non\-conformance in accordance with Hovione internal procedures, suggesting optimizations or improvements, including those that have the potential to mitigate unnecessary complexity * Apply and develop knowledge of Quality Assurance and participate in area processes, procedures and projects with the guidance of more senior colleagues * Perform to ensure all assigned tasks are delivered on time, safely, efficiently, reliably and in a cost\-effective manner * Execute professional activities in compliance with GMP and HSE guidelines, internal and external requirements as well as promote the implementation and maintenance of Hovione´s policies, systems and procedures (COPs, HBR, SOPs and others) * Undertake any additional tasks commensurate with the role as and when required * Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health \& safety rules/procedures, regulations and codes of practice. We are looking to recruit a Candidate:: * University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar scientific field (mandatory) * Requires educational / training experience in a QA GMP environment within the Pharmaceutical Industry (desirable) * Experience of working in a GMP operational environment (desirable) * Training and experience of GMP standards (desirable) * Experience of working with Regulatory Affairs and a basic knowledge of the function (desirable) * Knowledge of GMP practices * Fluency in English is a requirement * Computer literate with good working knowledge of the MS Office package * Good documentation skills and attention to detail * Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

QC Associate - Temporary64088838985219128

Indeed

QC Associate - Temporary

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines. * Apply and develop QC knowledge while participating in procedures and projects under guidance from senior staff. * Ensure all tasks comply with GMP, quality standards, and legal regulations, escalating issues when needed. * Plan and execute method development, transfer, validation, and reporting activities accurately and on time. * Resolve analytical issues collaboratively and escalate unresolved problems per defined procedures. * Maintain clear, proactive communication with internal and external stakeholders, representing the team when required. * Propose new methodologies and suggest optimizations to improve processes and performance. * Support onboarding of new team members and ensure high professional standards across the lab. * Maintain laboratory records, logbooks, and data systems in accordance with GLP and internal procedures. * Conduct instrument maintenance, calibration, and qualification, while adhering to HSE and GMP guidelines. * Work effectively in cross\-functional teams, support audits, and contribute to KPI tracking and continuous improvement initiatives. * Use analytical techniques and instrumentation, such as gas and high\-performance liquid chromatography (HPLC) amongst others. We are looking to recruit a Candidate:: * University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar Chemistry, Biochemistry or Health Sciences field (mandatory). * Requires educational / training experience in a QC laboratory environment. * Hands\-on experience in Analytical Chemistry and QC procedures (desirable). * Training and experience of GMP and ICH guidelines standards (desirable). * Knowledge on HPLC and GC, and familiarity with Empower Software (desirable). * Technical understanding of GMP practices, analytical theory and techniques. * Documentation skills and attention to detail \- Fluency in English is a requirement. * Computer literate with good working knowledge of the MS Office package. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity. ***Notice to Agencies and Search Firms Representatives*** *Hovione does not accept unsolicited résumes from agencies or search firms for this job posting. Any resumes submitted to Hovione by a third\-party agency or search firm without a valid written and signed search agreement will become the sole property of Hovione. No fees will be paid if a candidate is hired for this position as a result of an unsolicited referral. Thank you for your understanding.*

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Indeed

Analyst

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines. * To organize and define daily priorities within their assigned tasks in order to accurately and promptly perform the allocated sample analysis to meet the requirements of the periodic laboratory plan and area KPIs. * To adhere to the laboratory testing schedule in order to achieve an efficient Quality Control (QC) system. * Take responsibility for all data individually generated and ensure it is in accordance with all applicable GMP requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities. * To maintain all checklists, laboratory records and notebooks in which he/she is involved to an acceptable GMP standard and in accordance with Hovione internal procedures. * To maintain good hygiene and housekeeping within the laboratory. * To perform routine calibration and both corrective and preventative maintenance of designated laboratory instruments, requesting any instrument parts and consumables required by the area. * Comply with the high standards in the QC Laboratories. * To bring any discrepancies, deviations or non\-conformance in testing or work practice to the attention of QC management in accordance with Hovione internal procedures. * To issue events and support the investigation of OOS/OOT/atypical results, deviations and QC incidents generated in the QC Laboratories. * Ensure appropriate communication with other internal department in relation to QC work by using the appropriate Hovione processes and their IT platforms. * Assist with audits as required, following the instruction of QC Management. * Undertake any additional tasks to support the laboratory activities as and when required. * Seek out additional information when one feels that the available information is not enough. * Follow all annual performance review requirements, including completion of the self\-assessment. * Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health \& safety rules/procedures, regulations and codes of practice. * Ensure facility activities are carried out in compliance with all GMP, legal and HSE regulations and applicable standards in the country of operation, complying with and enforcing all Hovione processes and good practice. We are looking to recruit a Candidate:: * High School diploma (mandatory) * Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical\-related or other science\-related field (mandatory) * Chromatography HPLC/GC experience * Relevant work experience in similar position * Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (mandatory) * Experience of GMP practices and HSE standards (preferable) \- Technical understanding of GMP practices, analytical theory and techniques \- Clear and open communication skills (written and verbal) * Competent (written and verbal) English (preferable for sites where English is not the first language) * Ability and availability to work in shift patterns, as required by business needs * Computer literate with knowledge of the MS Office package AK382 * Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Engº/ Quality Technician (m/f)_Mafra638227356860171210

Indeed

Engº/ Quality Technician (m/f)_Mafra

Group of companies in the pastry and confectionery sector with several production units located in Mafra, Óbidos and Benedita is seeking to integrate an Engº/Quality Technician (m/f) into its team. Main responsibilities: * Execution of food control, monitoring of manufacturing processes and internal quality procedures; * Minimum qualifications at Bachelor's level in one of the following fields: Food Engineering, Biotechnology, Biology, or Biochemistry; * Team management and production optimization; * Quality control from raw materials to finished product; * Internal training and awareness initiatives regarding Food Safety and Good Manufacturing Practices; Requirements: * Immediate availability; * Experience in an industrial environment within the Food Production area (eliminatory criterion); * Experience in developing quality and HACCP procedures and processes; Knowledge of BRC and/or IFS standards; * Fluency in English (preferable); * Leadership skills; * Critical thinking and sense of responsibility; * Flexibility to adjust working hours according to specific demands; * Knowledge of PHC software (preferable); * Proficiency in Microsoft Office tools (Excel, Word, PowerPoint) Interested candidates should send their CV and applicable certificates to recrutamento@pastelariarolo.pt with the subject line: “Engº/ Quality Technician \- Mafra”. Type of offer: Full-time

R. Canal 6, 2640 Mafra, Portugal

Negotiable Salary