Want to join our team? Have a look at our current job offerings or just send in your CV to jobs@trevalco.com.

We also work with freelancers.

Quality Assurance Consultants

Belgium

As a quality assurance consultant you work with customers in the pharmaceutical industry to ensure quality on projects or during routine operations. Depending on your background and your level of experience you give advise on regulatory requirements, facilitate risk assessments and investigations, you assist during regulatory inspections, give training and might even be asked to conduct internal or supplier audits on behalf of our customers.

Needs:
  • good knowledge of cGMP
  • good writing skills in english
  • strong analytical skills, well organized, studious and precise
  • minimum 2 years experience in the pharmaceutical industry is a must
  • master or bachelor degree
Offer:
  • work in a great team
  • interesting projects
  • professional development through coaching, self-study, in-house and external training
  • attractive salary package, adapted to suit your needs
  • work / life balance
Those interested and meet the above conditions, please send your CV together with personal details by e-mail address jobs@trevalco.com.

CSV consultants (different levels)

Belgium

As CSV consultant you are responsible to execute computer validation projects from our offices or on-site with a customer. You are involved in the analysis of user requirements, design, testing and implementation of new software solutions. Our customers count on your knowledge and experience regarding regulatory requirements, and your capability to manage project risks.

Needs:
  • minimum 2 years of experience in validation
  • strong affinity with computer systems
  • good technical writing skills in english
  • strong analytical skills, well organized, studious and precise
  • experience in the pharmaceutical industry and knowledge of cGMP is a plus
  • master or bachelor degree
Offer:
  • work in a great team
  • interesting projects
  • professional development through coaching, self-study, in-house and external training
  • attractive salary package, adapted to suit your needs
  • work / life balance
Those interested and meet the above conditions, please send your CV together with personal details by e-mail address jobs@trevalco.com.

Project Engineers

Belgium

As Project Engineer, you are responsible for determining the technical and user requirements, the selection, tendering and/or design of pharmaceutical equipment, facilities, utilities or automation. You ensure the follow-up during the different phases (design, construction, commissioning, etc.), as well as the proper and timely delivery of the project. You manage the change control process, the definition and execution of the validation strategy, Commissioning & Qualification.
You manage and keep the oversight of involved contractor companies, and ensure that their work is done on time, with the required quality and safety on site. You ensure the handover and support at start of operations.

Needs:
  • minimum 2 years experience in engineering for one or more of the following areas: HVAC, cleanrooms, utilities, pharmaceutical production equipment, packaging equipment, logistic equipment, automation
  • good spoken and writing skills in english, dutch and/or french are a plus
  • strong analytical skills, well organized, studious and precise
  • experience in the pharmaceutical industry and knowledge of GMP are a plus
  • master or bachelor degree
Offer:
  • work in a great team
  • interesting projects
  • professional development through coaching, self-study, in-house and external training
  • attractive salary package, adapted to suit your needs
  • work / life balance
Those interested and meet the above conditions, please send your CV together with personal details by e-mail address jobs@trevalco.com.

Project Leads / Project Managers

Belgium

As Project Lead or Project Manager you ensure the delivery of projects in the Pharmaceutical Industry on time, with the required quality and within budget. You define the roles and responsibilities, and assign resources based on timeline, workload and required knowledge/skill. As problem solver, you support and lead the team and assure stability in the execution through the different phases (scope, layout, preliminary/detailed design, execution, verification until hand-over). You drive the decision-making process and ensure a positive environnement for and within the team. You use good PM Practices & Tools to keep schedule, budget control, resolve issues, escalation to stakeholders and management, etc. You ensure clear communication at all required levels: within the project team, feedback to resources manager/ lead engineer and to project manager/coordination teams.

Needs:
  • you are a true leader and you excel in communication
  • proven track record that shows competency in project management software and methods: PM certification (e.g. PMI, PRINCE2), risks management tools (e.g. FMEA, HAZOP)
  • proven project management experience with capability of working independently on multiple projects, and able to prioritize tasks and meet strict deadlines within budget
  • good spoken and writing skills in english and dutch
  • solution-oriented, customer focus and attitude to problem-solving
  • experience in the pharmaceutical industry and knowledge of GMP are a plus
Offer:
  • work in a great team
  • interesting projects
  • professional development through coaching, self-study, in-house and external training
  • attractive salary package, adapted to suit your needs
  • work / life balance
Those interested and meet the above conditions, please send your CV together with personal details by e-mail address jobs@trevalco.com.

Consultant QC Analytical Method Validation

Belgium

As a QC Analytical Method Validation Consultant you support and execute routine and project related analytical method validation activities. You perform Root Cause Analysis and support the implementation of preventive and corrective actions. You support the development, improvement and/or transfer of QC methods and assist in the writting of reports. You support the organization during internal and external audits.

Needs:
  • minimum 2 years of experience in QC laboratory or validation function
  • technical expertise in one or more of the following areas: ELISA, MDS, HPLC, nephelometry, cleaning validation, sample management
  • proven experience in Method Transfer
  • good technical writing skills in english
  • strong analytical skills, well organized, studious and precise
  • good knowledge of cGMP, knowledge of GCP is a plus
Offer:
  • work in a great team
  • interesting projects
  • professional development through coaching, self-study, in-house and external training
  • attractive salary package, adapted to suit your needs
  • work / life balance
Those interested and meet the above conditions, please send your CV together with personal details by e-mail address jobs@trevalco.com.