Job Purpose The Senior Specialist Drug Product and Device (GxP) provides comprehensive support to Technical Operations and perform essential oversight of Good Manufacturing Pratice (GMP) compliance for Drug Product (DP) …
Skills: GxP Compliance, Complaint Handling, Root Cause Analysis, CAPA Management, Change Control
Job Purpose The Senior Specialist Drug Product and Device (GxP) provides comprehensive support to Technical Operations and perform essential oversight of Good Manufacturing Pratice (GMP) compliance for Drug Product (DP) …
Overview Bruker is enabling scientists and engineers to make breakthrough post-genomic discoveries and develop new applications that improve the quality of human life. Bruker’s high performance scientific instruments and…
Skills: SAP, Salesforce, Order Administration, Microsoft Excel, Microsoft Office
Otis Elevator Co.
TÉCNICO DE MANUTENÇÃO (H/M) OTIS PORTO
Porto, Portugal · On-site
Mid level$1.2B raised
Date Posted: 2026-06-22 Country: Portugal Location: Delegação Porto, Portugal Gostarias de fazer parte de um setor estável, com muitas oportunidades de desenvolvimento profissional? Na OTIS, empresa multinacional de refe…
WHAT YOU WILL DO In this full-time permanent position based in Porto and reporting directly to an Operational Manager, you will be trained on a MES software from a technical perspective in order to be able to work on pro…
Skills: C#, SQL, React, Web Application Development, Database Schema Design
#WeAreIn for jobs that impact everyone’s life Behind every success, there is a plan: your strategic thinking, creative skills, and ability to communicate with others will drive innovation and turn ideas into impact. As a…
Skills: Sales Operations, Demand Creation, Revenue Fulfilment, Data Analysis, Microsoft Excel
Customer Care Assistant | Importação Automóvel (m/f/d)
Porto, Portugal · On-site
Mid level
A Salvador Caetano é um grupo internacional presente em 3 continentes, com mais de 75 anos dedicados à indústria e setor automóvel. Emprega mais de 7000 pessoas, em mais de 43 países. Na Salvador Caetano criamos valor no…
Role: Branch Manager Location: Porto, Portugal Full/Part-time: Full-time Construa uma carreira com confiança A Carrier Global Corporation, líder global em soluções inteligentes de climatização e energia, está comprometid…
A Salvador Caetano é um grupo internacional presente em 3 continentes, com mais de 75 anos dedicados à indústria e setor automóvel. Emprega mais de 7000 pessoas, em mais de 43 países. Na Salvador Caetano criamos valor no…
Skills: Parts Management, Invoicing, Customer Support, Continuous Improvement, English Language
Bem-vindo ao universo Caetano. Somos a organização que reúne as empresas da Salvador Caetano dedicadas à distribuição e reparação automóvel, com forte presença em Portugal e Espanha. Representamos 21 marcas automóveis, c…
Skills: Mechanical Repair, Brake Adjustment, Steering System Maintenance, Diagnostics, Oil and Filter Changes
Bem-vindo ao universo Caetano. Somos a organização que reúne as empresas da Salvador Caetano dedicadas à distribuição e reparação automóvel, com forte presença em Portugal e Espanha. Representamos 21 marcas automóveis, c…
Skills: Mechanical Repair, Brake Adjustment, Steering System Maintenance, Diagnostics, Oil and Filter Changes
Engenheiro Mecânico Automóvel (m/f/d) | Sports & You
Porto, Portugal · On-site
Mid level
A Sports & You é uma referência no mundo automóvel, onde a paixão pelo desporto motorizado se alia à excelência e à inovação. Com sede em Paredes, trabalhamos diariamente para superar desafios e elevar os padrões do seto…
A Salvador Caetano é um grupo internacional presente em 3 continentes, com mais de 75 anos dedicados à indústria e setor automóvel. Emprega mais de 7000 pessoas, em mais de 43 países. Na Salvador Caetano criamos valor no…
Skills: English Proficiency, MS Office, Power BI, Interpersonal Skills, Organization
Técnico de Mecatrónica Automóvel (m/f/d) | Sports & You
Porto, Portugal · On-site
Mid level
A Sports & You é uma referência no mundo automóvel, onde a paixão pelo desporto motorizado se alia à excelência e à inovação. Com sede em Paredes, trabalhamos diariamente para superar desafios e elevar os padrões do seto…
A Hyundai pertence à Salvador Caetano desde 2015 e é uma das mascas mais cresceu no top de vendas de veículos ligeiros em Portugal. Assumimos a liderança na ECO Mobilidade – na Hyundai não esperamos pelo futuro da mobili…
Skills: After Sales Management, Team Leadership, KPI Monitoring, Customer Satisfaction, Strategic Planning
A Midas é a empresa líder mundial em manutenção e serviços automóvel multimarca. Fazemos parte da Salvador Caetano e a nossa missão é cuidar dos condutores e dos seus veículos, de forma sustentável, contribuindo para a s…
A Lusilectra, empresa inserida na Salvador Caetano, disponibiliza produtos e serviços no âmbito dos acessórios especiais automóvel, equipamentos para oficinas e centros de inspeção, ferramentas profissionais e máquinas d…
Bem-vindo ao universo Caetano. Somos a organização que reúne as empresas da Salvador Caetano dedicadas à distribuição e reparação automóvel, com forte presença em Portugal e Espanha. Representamos 21 marcas automóveis, c…
Skills: Mechanical Repair, Diagnostics, Vehicle Maintenance, Tool Usage, Quality Control
A Salvador Caetano é um grupo internacional presente em 3 continentes, com mais de 75 anos dedicados à indústria e setor automóvel. Emprega mais de 7000 pessoas, em mais de 43 países. Na Salvador Caetano criamos valor no…
A Academia de Verão Midas está de volta | Candidaturas abertas És o mecânico Top que procuramos? As candidaturas para a 4ª edição da Academia de Verão Midas abriram e voltam a desafiar os alunos dos cursos de mecatrónica…
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Full-time
bachelor degree
Learning Environment, Impactful Work, Flexibility and Balance, Career Growth
Posted 50d ago
~40 hrs/week
Responsibilities
The role provides oversight of GMP compliance for Drug Product and Device vendors, managing quality issues, CAPAs, and change controls. It specifically focuses on the receipt, investigation, and closure of technical complaints within the electronic Quality Management System.
Requirements
Requires a degree in Life Sciences, Engineering, Pharmacy, or a related field with experience in a GxP-regulated environment. Candidates should have hands-on experience with complaint handling and familiarity with eQMS platforms.
Full job description
Job Purpose
The Senior Specialist Drug Product and Device (GxP) provides comprehensive support to Technical Operations and perform essential oversight of Good Manufacturing Pratice (GMP) compliance for Drug Product (DP) and Device vendors. They will manage all Quality-related issues, oversee CAPAs, Change Controls, and handle GMP-related Temperature Excursions and Technical Complaints, collaborating effectively with the rest of the MoonLake Quality team, the Technical Operations team and consultants (where necessary). This role is responsible for the receipt, assessment, investigation, documentation, and closure of technical complaints in accordance with GxP regulations (including GMP, GCP, and GDP, as applicable). The role ensures that all technical complaints, such as device issues, temperature excursions, packaging defects, or product quality concerns, are managed in compliance with internal procedures and regulatory expectations and are appropriately recorded, investigated, trended, and reported within the electronic Quality Management System (eQMS). This role supports patient safety, product quality, and regulatory compliance across clinical and commercial activities.
Key Accountabilities:
Technical Complaint Management
Act as the primary coordinator for technical complaints, ensuring complaints are logged, assessed, investigated, and closed within defined timelines using the eQMS (e.g., Qualio).
Ensure accurate completion of complaint records, including complaint details, product information, batch/lot numbers, and classification
Perform initial assessment and classification of complaints (e.g., technical vs safety‑related) and ensure appropriate escalation when required
Investigation & Root Cause Analysis
Coordinate and document complaint investigations, working with internal stakeholders and external vendors as required.
Support or lead root cause analysis, ensuring conclusions are evidence‑based and adequately justified.
Ensure CAPAs, change controls, or quality issues are raised and tracked where required following investigation outcomes.
GxP Compliance & Documentation
Ensure all complaint handling activities comply with applicable GxP regulations, internal SOPs, and Quality Management System requirements.
Maintain inspection‑ready documentation, ensuring complaint records are complete, traceable, and auditable.
Support internal and external audits and inspections by providing complaint data, metrics, and documentation as required
Work with the MoonLake Quality Team to manage and develop Quality Systems and procedures within the company
Cross‑Functional Collaboration
Liaise with Clinical Operations, Technical Operations, Quality Assurance, Pharmacovigilance, and external vendors/CDMOs to support timely resolution and Drug Product / Device assembly, labelling and packaging activities, including complaints.
Support alignment between technical complaints and related quality processes such as deviations, recalls, and serious breaches, where applicable.
Work with the Drug-Device Development Team to define and oversee activities sub contracted to vendors by MoonLake, with specific emphasis on quality and compliance requirements
Trending & Reporting
Support trend analysis of technical complaints, contributing to periodic quality reports and management review activities.
Identify recurring issues and contribute to continuous improvement initiatives within the Quality System.
Your profile
Education:
Degree in Life Sciences, Engineering, Pharmacy, or a related scientific discipline (or equivalent experience).
Experience:
Experience working in a GxP‑regulated environment (pharmaceutical, biotech, medical device, or clinical research).
Hands‑on experience with complaint handling, quality issues, or deviation management within a Quality Management System.
Familiarity with electronic QMS platforms (e.g., Qualio or similar).
Experience with device or combination product complaints (desirable).
Exposure to temperature excursions, packaging complaints, or technical product issues (desirable).
Experience supporting regulatory inspections or audits (desirable).
Skills/knowledge/behavioural competencies:
Strong understanding of GxP principles and quality system processes.
Excellent documentation and technical writing skills.
Ability to manage multiple complaints simultaneously while meeting regulatory timelines.
Strong attention to detail and a structured, risk‑based approach to problem solving.
Effective communication and stakeholder‑management skills.
Work Location:
2 days a week in our brand new Porto or Cambridge office
Why us?
An exciting job opportunity awaits you!
MoonLake is a dynamic and innovative company pushing the boundaries of possibility, and we are looking for passionate individuals to join our stellar team.
What we offer: Learning Environment: An opportunity to learn and grow alongside experienced professionals in a supportive and innovative biotech environment.
Impactful Work: Contribute to ground-breaking projects that have the potential to transform global healthcare.
Flexibility and Balance: Work remotely/hybrid, enjoying a healthy work-life balance while making meaningful contributions to our team.
Career Growth: A clear path for career progression, with the chance to take on more responsibilities as you develop your skills.
Our Core Values
We look for potential MoonLakers that embody our three core values that drive our pursuit of excellence:
We do Stellar Science: We aspire to create novel therapies that elevate treatment horizons, with innovative science, and high quality, always.
We go beyond: We aspire to be positively disruptive in our field, and bold in the way we challenge the norms and each other.
We unlock value: We aspire to create long-term value for investors and communities.
About us
MoonLake Immunotherapeuticsis a clinical-stage biopharmaceutical company unlocking the potential of sonelokimab, a novel investigational Nanobody® for the treatment of the inflammatory disease, to revolutionize outcomes for patients.
We continue to make significant progress in our Global Clinical Development Programs. The company’s focus is on inflammatory diseases with a major unmet need, including hidradenitis suppurativa and psoriatic arthritis – conditions affecting millions of people worldwide with a large need for improved treatment options. MoonLake was founded in 2021 and is headquarted in Zug, with hubs in Cambridge & Porto.
Creating next-level therapies for inflammatory skin and joint diseases with Nanobody® science
Industry
Biotechnology Research
Company size
11-50 employees
Founded
2021
Headquarters
Zug, Zug
LinkedIn followers
9,399
MoonLake Immunotherapeutics AG is a clinical-stage biopharmaceutical company leveraging revolutionary Nanobody® technology to develop next-level medicines for immunologic diseases, including inflammatory skin and joint diseases.
How many Manufacturing jobs are open in Porto, Portugal right now?
There are currently 62 open manufacturing positions in Porto, Portugal listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Porto, Portugal?
Companies currently hiring include Caetano Auto, AAM - American Axle & Manufacturing, SINGLE BUOY MOORINGS INC., Infineon Technologies, Amcor, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Manufacturing jobs in Porto, Portugal?
Yes — 18 of the 62 open manufacturing positions offer remote or hybrid work (0 remote, 18 hybrid).
How do I apply for Manufacturing jobs in Porto, Portugal?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.