Mechanical Work Package Owner
- North America, United States
- Contract
- CAPEX Projects
Are you looking for the opportunity to work with a global biopharmaceutical company? This is your chance! Our client develops and delivers life changing medicines to millions of people globally and as part of their growth, they are looking for a Mechanical Work Package Owner to help support operations at their Maryland facility.
With their Drug Substance (DS) manufacturing network growing rapidly, they are committed to growing their portfolio of commercial biologics products supplied worldwide – and this is your opportunity to be involved!
Responsibilities:
- Assists project manager or line manager within project leadership in planning and delivering defined work scope on a project to meet agreed schedule and budget.
- Coordinates with all project related members on day-to-day progress of work activities to ensure timely completion of a project.
- Acts as a package lead or area lead within a project.
- Prepares regular project reports and presentations for key stakeholders.
- Follows-up closely on actions and mitigations activities in the project risk management plan.
- Organizes and conducts effective work sessions (like PDR meetings; etc.).
- Supports the PM in ensuring compliance to the project management process (CPDP) throughout project life cycle.
- Ensures compliance with engineering, SHE and work standards and associated procedures, to ensure the assets meet business needs and satisfy external regulators.
- Assist the PM in planning, managing and controlling allocation of resources, to ensure that Customer requirements are met at the optimum cost.
- Contributes to the planning and execution of sourcing strategy for projects or programs, including negotiation, appointment, control and integration of multiple vendors and internal partners.
Requirements:
- 10+ years of experience in people management or working as a senior engineer e.g. as team leader, line manager or project manager.
- Proven experience within the pharmaceutical/biopharmaceutical industry.
- Documented experience within contractor supervision activities
- Degree in engineering within mechanical, chemistry-/production engineering or similar.
- Knowledge of regulatory requirements (GMP and GEP).
- Have strong inter-personal skills and the ability to bring people together around a common purpose.
- Are result-oriented, have a well-structured work approach.
If this role is of interest to you, please apply now!
#LI-NR1
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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