- Lead CQV activities for pharmaceutical manufacturing projects.
- Develop and execute commissioning, qualification, and validation protocols.
- Ensure compliance with industry regulations and standards, such as cGMP and FDA guidelines.
- Collaborate with cross-functional teams to ensure the successful implementation of CQV activities.
- Conduct risk assessments and develop mitigation strategies.
- Document and report on CQV activities, findings, and corrective actions.
- Support continuous improvement initiatives related to CQV processes.
- Bachelor's or Master's degree in Engineering or a related field.
- Minimum of 5 years of industrial experience in CQV roles.
- At least 2 years of experience in the pharmaceutical industry.
- Strong understanding of industry regulations and standards.
- Excellent analytical and problem-solving skills.
- Effective communication and interpersonal skills.
- Ability to work effectively within cross-functional teams.
-
CONSULTYS Cambridge, Cambridgeshire, United KingdomConsultys is a global engineering and services consulting company dedicated exclusively to the Life Sciences industry. · Below covers everything you need to know about what this opportunity entails, as well as what is expected from applicants. · Since 2005, Consultys has been wor ...
-
Validation Consultant
1 week ago
PM Group Cambridgeshire, United Kingdom**Validation Consultant**: · - Contract · - Onsite · - Cambridgeshire, United Kingdom · - CQV · - 7090 · **Overview · - PM Group is looking for a validation engineer to support a secondary pharmaceuticals site in East Anglia · **Responsibilities · **Responsibilities** · Validatio ...
-
Validation Engineer
2 weeks ago
PM Group Sawston, United Kingdom Contract, Full timePM Group is seeking a Validation Engineer to join an API Manufacturing facility in Suffolk for 3-4 months. · Responsibilities: · * Work closing with Capital Project, Production, QA, and R&D departments to get the validation scopes and agreements to release the desired production ...
-
Validation Engineer
2 weeks ago
PM Group Sawston, United Kingdom ContractPM Group is seeking a Validation Engineer to join an API Manufacturing facility in Suffolk for 3-4 months.Responsibilities: * Work closing with Capital Project, Production, QA, and R&D departments to get the validation scopes and agreements to release the desired production statu ...
-
Commissioning & Validation Engineer
1 week ago
CONSULTYS Cambridge, Cambridgeshire, United KingdomConsultys · Increase your chances of an interview by reading the following overview of this role before making an application. · is a global engineering and services consulting company dedicated exclusively to the Life Sciences industry. · Since 2005, Consultys has been working o ...
-
Validation Engineer
5 days ago
PM Group Hertfordshire, United KingdomA clinical-stage biopharmaceutical company developing next-generation, programmed T cell therapies based in the South West of the UK are seeking an Equipment Validation Consultant. · Responsibilities: · Process equipment qualification and related activities to support new manu ...
-
Validation Engineer
2 weeks ago
PM Group South Cambridgeshire, United KingdomPM Group is seeking a Validation Engineer to join an API Manufacturing facility in Suffolk for 3-4 months.Responsibilities: · Work closing with Capital Project, Production, QA, and R&D departments to get the validation scopes and agreements to release the desired production stat ...
-
Validation Engineer
1 day ago
PM Group Hertfordshire, United KingdomJob Description A clinical-stage biopharmaceutical company developing next-generation, programmed T cell therapies based in the South West of the UK are seeking an Equipment Validation Consultant. · Responsibilities: · Process equipment qualification and related activities to ...
CQV (Commissioning, Qualification & Validation) Engineer - cambridgeshire, United Kingdom - CONSULTYS
Description
Consultys is a global engineering and services consulting company dedicated exclusively to the Life Sciences industry.
Since 2005, Consultys has been working on technical projects with some of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada.
Thanks to our excellent team, we support manufacturers in all stages of drug development.
Respect, transparency, and gratitude. These are the values that made Consultys one of the most high-performing Life Sciences consulting companies.
Do you want to be part of a human-sized company that values every individual? Do you want to work on long-term innovative projects, working closely with global Life Sciences product companies in the world? Join us
We offer an attractive salary and benefits. You will work in a stimulating environment, with a lot of opportunities for your professional and personal development.
Job Summary
We are seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to join our team. The CQV Engineer will play a crucial role in ensuring that all systems and equipment are properly commissioned, qualified, and validated according to industry standards and regulatory requirements.
Responsibilities
Qualifications