Construction Manager Brabant Walloon – contracting Our partner is looking for a Construction Manager to join its team. This international company is well-known for its pharmaceuticals. Your responsibilities?
Coordinate construction activities and liaise with the Host Site EHS team
Review safe methods of working ahead of work starting
Lead daily safe work planning sessions e.g. SPA, RAMS, PTW
Participate in daily prestart workforce safety briefings
Participate in safety meetings and lead daily safety walks of the site
Participate in toolbox talks
Assist in incident investigation
Induct / orientate the workers
Identify and control new workers
Identify general and specific safety hazards to the workers
Inspect and conduct safety audits of tasks and safe systems / processes
Ensure that all incidents are reported
Participate in incident investigations
Ensure workers only carry out tasks for which they are trained and qualified
Ensure risk assessments and method statements are in place and in use
Encourage and participate in the behavioral safety system
Intervene and correct any unsafe conditions
Participate in safety meetings
Ensure good housekeeping and organised tidiness (5S) at all times
Your profile?
Experience in construction management of medium and large capital projects
EHS experience
Project and people management skills with thorough knowledge of construction
Communication and collaboration skills
Our offer? Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to training in technical matters and soft skills. We will be your career partner for each step along the way.
Validation Engineer Brabant Walloon – contracting Our partner is looking for a Validation Engineer to join its team. This international company is well-known for its pharmaceuticals. Your responsibilities? The department is, amongst other expertise, in charge of the implementation of health authorities Facility Design requirement for all manufacturing building in the Belgium sites. A new task is required : implementing internal standards of the company (Engineering Standard) You will be responsible for leading the implementation of this new standard in several steps :
Gap analysis between Engineering Standard and Belgium SOP’s
Support and lead risk assessment issuing for each unit with local SMEs
Follow up and track progress on assessment issuing as per milestone.
Participating in the assessment to standardize inter manufacturing units evidences and assessment (same answer for requirement, adding and suggest control or mitigations, identifying gaps).
Possibly, support the Unit to edit remediation plans for gaps identified.
Furthermore, the candidate leads the reporting to Engineering Standard Duty holder and sponsor.
Your profile?
Scientific university degree (Engineer in Chemistry, biochemistry, or Pharmacist,…)
Experience in Product & Process
Experience in project management
Risk assessment
Successful experience in stakeholders management
Excellent organization skills and ability to operate effectively in a multicultural, matrix organization where the workload requires balancing multiple responsibilities simultaneously
Fluent in French et English
Our offer? Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to training in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply. Do you have any questions? You can contact Anaïs Malikian, [email protected]
Your responsibilities: Commissioning and Qualification: Review IQOQ protocols and reports to ensure the qualification of CPP, support the team for risk analysis creation (SRA), review equivalence certificate, write validation plans…
Validation: According to the client’s standards and procedures, design the validation strategy through PQ protocol redaction, ensure the readiness for PQ validation, coordinate validation (on the floor job expected), manage unplanned events associated with validation, be the contact with QC.
Product validation: Understand the product validation lifecycle and ensure that the validation strategy is in line with the product validation strategy, support the product steward in product related topic (E&L, holding time, …).
Change Control: Assessment of the validation impact through eCC assessment (Stakeholder role expected), Coordinate eCC, and be responsible of eCC tasks.
Project management: Plan and manage PQ activities (material, documentation, people…), support the project planner, animation of meetings/workshops, help the production representative in the understanding of validation requirements.
Your profile:
University degree (Biotechnology, Agronomy, Chemistry or Pharmacy).
At least 5 years’ professional experience in pharmaceutical environment, in quality and validation environment.
Good oral and written communication skills in French & English (for efficient communication with engineering office and suppliers).
Good Knowledge of GMP Regulated environment related to validation activities.
Good interpersonal relationship skills – To be a good team player to success in each validation.
Problem solving and achievement oriented.
Be organized.
Nice to have:
Knowledge of freezer dryers, filling lines and isolators would be an asset.
To maintain and keep up to date its knowledge and experience necessary to the function.
Ability to take decisions in stressful conditions.
Proactive and ready to take the lead to make things happen.
Ability to work under pressure on multiple deliverables within project timelines.
Our offer? Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. Are you interested in this job? I kindly invite you to apply or send me your CV, [email protected]
