Quality jobs

• United States of America
• Negotiable
• Posted 1 day ago

Job Summary: The VP Technical Development Consultant will be responsible for overseeing and guiding technical operations, process development, and scale-up activities for small molecules, specifically solid oral dosage forms. This role requires a deep understanding of Good Manufacturing Practices...

• United States of America
• Negotiable
• Posted 3 days ago

Position Overview: We are seeking a highly skilled and experienced Drug Product Process Development Consultant to join our team. The ideal candidate will have a strong background in small molecule drug product development, with a focus on early-stage development. This role involves providing tech...

• United States of America
• Negotiable
• Posted 3 days ago

Position Overview: We are seeking a highly skilled and experienced Drug Substance Process Development Consultant to join our team. The ideal candidate will have a strong background in small molecule drug development, with a focus on early-stage development. This role involves providing technical ...

• Denmark
• Negotiable
• Posted 7 days ago

Project Coordinator / Junior Project Manager (Operational Readiness - Downstream) Duration: 12 months, possible extension Location: Denmark - on-site Start Date: ASAP -12month contract We are looking for an experienced Project Coordinator or Junior Project Manager with pharmaceutical industry exp...

• Copenhagen
• Negotiable
• Posted 7 days ago

We are working with a leading pharmaceutical company based in Copenhagen that are dedicated to the development, manufacturing, and commercialisation of small molecule therapeutics. Their mission is to improve patient outcomes through innovative and high-quality products. We are seeking a detail-o...

• Visp
• Negotiable
• Posted 8 days ago

We are currently seeking a highly skilled and dedicated Lab Scientist to join our client's Analytical Department. If you have a strong background in analytical chemistry and a passion for process optimization, we would love to hear from you! Responsibilities Provide analytical support for chemica...

• Visp
• Negotiable
• Posted 8 days ago

We are currently seeking a highly skilled and dedicated Lab scientist to join our client's Analytical department. Main tasks and responsibilities: Analytical support of chemical process development and process optimisation. Preparation, execution and documentation of analyses, method developments...

• Cork
• Up to €50 per hour
• Posted 8 days ago

Responsibilities Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Conducts feasibility studies to verify capability and functionality. Develops new concepts from initial design to market release. Write an...

• Cork
• Up to €50 per hour
• Posted 8 days ago

Responsibilities Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Conducts feasibility studies to verify capability and functionality. Develops new concepts from initial design to market release. Write an...

• New Jersey
• Negotiable
• Posted 9 days ago

We are seeking a highly skilled Computer System Validation (CSV) Engineer to join our client on a contract basis. This role is crucial for ensuring the validation and compliance of computerized systems in a regulated, GxP-compliant environment, contributing to the production of innovative oncolog...

• Limerick
• Negotiable
• Posted 9 days ago

Acting as a Quality Lead for all phases of production realization including NPD, NPI, Commercialisation, Sustaining, End to Life. Monitor and drive compliance within the development process and/or operations to GMP and the requirements of the QMS within assigned area. Trouble shooting quality iss...

• Deutschlandsberg
• Negotiable
• Posted 15 days ago

Exciting Career Opportunity: Freelance CQV Consultant We are currently seeking an experienced Freelance CQV Consultant to join our client in Germany for a 12-month contract role. This is a full-time, on-site position with an immediate start. Key Details: Location: On-site, Germany Contract Durati...

• Valais
• Negotiable
• Posted 15 days ago

We are currently looking for a Project Engineer - Black Utilities to join the Global Engineering Team based in Valais, Switzerland! Summary: Your tasks will include developing and verifying ideas and requests, generating feasibility and conceptual studies, considering regulatory requirements and ...

• Stein
• Negotiable
• Posted 15 days ago

We are currently seeking a highly skilled and motivated GMP High Bay Warehouse Specialist to join our client's team in Stein. The Specialist will be driving the execution and coordination of the defined CQV activities in the warehouse for both cold and ambient temperatures and support building. R...

• Stein
• Negotiable
• Posted 15 days ago

We are seeking a skilled and motivated Instrumentation & Controls Engineer to join our client's team in Stein. Summary: The Instrumentation and Control (I&C) Engineer will report directly to the Automation Technical Lead and is responsible for providing hands on support to the commissioning and q...

• Philadelphia
• Negotiable
• Posted 19 days ago

We are working with a leading pharmaceutical company dedicated to the development, manufacturing, and commercialization of small molecule therapeutics. Their mission is to improve patient outcomes through innovative and high-quality products. We are seeking a detail-oriented Quality Assurance Spe...

• Basel
• Negotiable
• Posted 22 days ago

We are currently searching for a Scientist QC Raw Materials to join our client's team in Basel, Switzerland on a 9-month contract. This is an exciting opportunity to become part of the Primary Packaging and Raw Material QC team, where you will play a critical role in ensuring the quality and comp...

• Basel
• Negotiable
• Posted 22 days ago

We are searching for a Scientist QC Raw Materials to join our team on a 9-month contract. This role plays a key part in the Primary Packaging and Raw Material QC team, ensuring the quality and compliance of raw materials used in drug product manufacturing. The successful candidate will be respons...

• Galway
• Negotiable
• Posted 22 days ago

Senior Validations Engineer The requirements of this role within the wider project are to cover the validation activities with respect to the testing and manufacture of the client's device. Role/ Responsibilities: Develop, and/or approve, validation documentation, including protocol, records, and...

• New York
• Negotiable
• Posted 23 days ago

We are seeking a highly skilled QA Supervisor to join a leading Medical Device company. In this role, you will be responsible for: Maintaining a Quality Management System compliant with FDA regulations and driving continuous improvement. Managing complaint handling and adverse event reporting, en...

• Visp
• Negotiable
• Posted 25 days ago

We are seeking a Quality Assurance Manager to oversee compliance and customer Quality Agreement (QAA) activities for Drug Product manufacturing in Visp. This role involves collaboration with Drug Product Services and Drug Substance teams, acting as the primary QA contact for customer-related qual...

• Negotiable
• Posted about 1 month ago

We have a current opportunity for a Senior Quality Engineer on a contract basis. - To start ASAP - Fully on-site (hands on role) - Must have injection moulding experience - Previous contract Manufacturing environment would be suitable - CAPA's - Medical Device standard - ISO13485 - Monday - Frida...

• Spain
• Negotiable
• Posted about 1 month ago

QARA Consultant - Diagnostics Software Specialist We are excited to announce a contract opportunity for an experienced QARA Consultant specialising in diagnostics software within the medical device sector. This role is fully remote and requires proficiency in Spanish, aligning with our commitment...

• Spain
• Negotiable
• Posted about 1 month ago

🚀 Exciting Opportunity - QARA Consultant - Software Diagnostics 🚀 📅 Contract Length: 12 Months 🌎 Location: Remote 💼 Hours: 20 Hours per week I am partnering with a leading medical device client who is looking for a QARA Consultant focusing on Software Diagnostics Compliance. 🔍 Key Skills & Experi...

• Germany
• Negotiable
• Posted about 1 month ago

Urgent Freelance Quality Assurance Engineering Consultant (Pharmaceutical Industry) Location: Northern Germany Duration: Immediate Start - 12-Month Contract Language: Must be German-speaking We are working exclusively with a large pharmaceutical client to find a highly skilled Quality Assurance E...

• Germany
• Negotiable
• Posted about 1 month ago

Urgent Freelance CQV Engineering Consultant (Pharmaceutical Industry) Location: Northern Germany Duration: Immediate Start - 12-Month Contract Language: Must be German-speaking Company Overview: We are working exclusively with a leading pharmaceutical client to find a highly skilled CQV Engineeri...

• Huntersville
• Negotiable
• Posted about 1 month ago

Job Summary: We are seeking a Quality Engineer with knowledge of Medical Device Manufacturing and a compliance background. This role demands a solid understanding of quality system requirements for medical device companies. The primary responsibility will be to execute Corrective and Preventive A...

• Dublin
• Negotiable
• Posted about 1 month ago

I'm currently looking for an experienced DeltaV Automation Lead with expertise in spray drying and a background in API manufacturing for a full-time, on-site role in the South of Ireland. The client is eager for an immediate start but is open to some flexibility for the right candidate. Ideal Can...

• Negotiable
• Posted about 1 month ago

𝗗𝗲𝗹𝘁𝗮𝗩 𝗕𝗮𝘁𝗰𝗵 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿 - 12-𝗠𝗼𝗻𝘁𝗵 𝗖𝗼𝗻𝘁𝗿𝗮𝗰𝘁 | 𝗗𝘂𝗯𝗹𝗶𝗻 | 𝗙𝗟𝗦 𝗦𝗵𝗶𝗳𝘁 Currently seeking an experienced 𝗗𝗲𝗹𝘁𝗮𝗩 𝗕𝗮𝘁𝗰𝗵 𝗘𝗻𝗴𝗶𝗻𝗲𝗲𝗿 for a 12-𝗺𝗼𝗻𝘁𝗵 𝗰𝗼𝗻𝘁𝗿𝗮𝗰𝘁 at a leading 𝗽𝗵𝗮𝗿𝗺𝗮 site in Dublin. This role is key to supporting critical manufacturing operations in a fast-paced, high-tech environment. 🔹12-𝗺𝗼𝗻𝘁𝗵 𝗰𝗼𝗻𝘁...

• Negotiable
• Posted about 1 month ago

I'm currently looking for an experienced DeltaV Automation Lead with expertise in spray drying and a background in API manufacturing for a full-time, on-site role in the South of Ireland. The client is eager for an immediate start but is open to some flexibility for the right candidate. Ideal Can...

• Sweden
• Negotiable
• Posted about 1 month ago

About the Role: We are seeking an experienced CQV (Commissioning, Qualification & Validation) Consultant to support Factory Acceptance Testing (FAT) and commissioning for a key project. The successful candidate will play a critical role in ensuring that equipment and systems meet regulatory and o...

• Visp
• Negotiable
• Posted about 1 month ago

Our client is seeking a skilled Thermal Validation Subject Matter Expert to join their BIO Biologics Division Services (BDS) team for a 9-month contract in Visp. The successful candidate will be responsible for ensuring the qualification and validation of process and support equipment, including ...

• Visp
• Negotiable
• Posted about 2 months ago

Unser Kunde sucht einen qualifizierten Biotech Associate, der für einen spannenden 10-Monats-Vertrag dem Team der BIO Biologics Division Services (BDS) beitritt. Dies ist eine hervorragende Gelegenheit für eine detailorientierte Fachkraft, die im Bereich der Qualitätssicherung in einer hochmodern...

• Visp
• Negotiable
• Posted about 2 months ago

Unser Kunde sucht einen qualifizierten Biotech Associate, der für einen spannenden 10-Monats-Vertrag dem Team der BIO Biologics Division Services (BDS) beitritt. Dies ist eine hervorragende Gelegenheit für eine detailorientierte Fachkraft, die im Bereich der Qualitätssicherung in einer hochmodern...

• Negotiable
• Posted about 2 months ago

We are seeking a DeltaV Automation Engineer with 3+ years of experience in DeltaV Batch systems within pharma manufacturing for a 12-month contract in Dublin. Key Responsibilities: Support automation operations and ensure GMP compliance. FLS Shift Role - supporting 24/7 operations Troubleshoot an...

• Visp
• Negotiable
• Posted about 2 months ago

Our client is seeking a skilled Supplier & Material Qualification Specialist to join their BIO Mammalian team for a 6-Month contract to ensure the efficient and compliant supplier and material qualification process in line with regulatory requirements, corporate standards, and agreements with sta...

• United States of America
• Negotiable
• Posted about 2 months ago

ry: We are seeking an experienced GMP Auditor to join our Quality Assurance team. The successful candidate will be responsible for ensuring compliance with Good Manufacturing Practices (GMP) and conducting thorough audits of our processes and systems. Key Responsibilities: Conduct internal and ex...

• United States of America
• Negotiable
• Posted about 2 months ago

Responsibilities: Minimum 7 years of experience in quality assurance in the biotech or pharmaceutical industry Small Molecules, Solid Oral Dosage experience. Develop, implement, and maintain quality assurance programs, policies, and procedures in compliance with regulatory standards (e.g., FDA, E...

• Nyon
• Negotiable
• Posted about 2 months ago

Our client is seeking a skilled QC Validation Scientist to join their Product Innovation team for a 2-year contract. This position is ideal for someone with extensive experience in process, cleaning, and analytical validation within the pharmaceutical industry. As a QC Validation Scientist, you w...

• Vienna
• Negotiable
• Posted about 2 months ago

Job Title: Freelance eQMS Specialist Duration: 6 Months Industry: Pharmaceutical We are looking for a Project Quality Management Specialist to support the modernisation and update of our Electronic Quality Management System (eQMS) on a freelance basis. This is a contract position for six months, ...

• Negotiable
• Posted about 2 months ago

CQV - HVAC Specialist Required in Dublin, UK (Contract Position) Are you a seasoned CQV professional with expertise in the pharmaceutical sector? We are seeking an experienced Freelance Commissioning, Qualification and Validation (CQV) specialist to fill a contract role focusing on Heating, Venti...

• North Carolina
• Negotiable
• Posted about 2 months ago

. The Contractor Quality Associate, Biologics plays a critical role in data management of commercial biologics executed by contract laboratories. The position requires familiarity with data review, data management in Excel or Minitab, and understanding of LIMS systems. Some understanding or famil...