Senior MSAT Engineer
- East
- Contract
- CAPEX Projects
This vacancy has now expired
Do you want to work for one of the world’s fastest growing pharmaceutical companies?
With heavy investment year on year, this company are expanding at a rapid pace. They are becoming a household name within the Pharmaceutical and Bio-Pharmaceutical sectors. With manufacturing sites around the world, they regularly win awards to confirm their status as a market leader. This facility in Massachusetts is a trademark facility which is bringing great attention to the company in the US.
Currently they are looking for a Senior MSAT Engineer to join their team.
Responsibilities:
- Develop, generate, and execute TT protocols and reports independently. Review and approve documents prepared by other MSAT colleagues.
- Independently lead, the company Vaccines process performance qualification (PPQ) and relative studies with DP manufacturing. Support Manufacturing to perform any scale-up or process adaptations during PPQ.
- Collaborate with different functional groups (e.g. Supply Chain, Production Unit, Quality Control, HSE, other sites.) to complete PPQ with no delay on project schedule.
- Regularly liaise with customer and represent MSAT department as required, acting at key strategy meetings to inform and decide correct path through TT, with respect to current regulatory best practices and requirements, cost, and schedule.
- Factory floor support for manufacturing during critical stage operation execution during PPQ batches.
- Leads new product introductions and lifecycle changes into a vial processing plant, from a Process Development perspective and then acts as process and technical SME during CV stage.
- Troubleshoots issues with drug product processing technologies and equipment, in the scale up and commercialisation, during NPI.
- Leads and collaborates on cross functional investigation teams, utilising root cause analysis: 5-
Requirements:
- BS/MS with major in Biology, Chemistry or Pharmaceutical Engineering or related Science or Engineering major or person with equivalent experience.
- Have prior development or commercial experience in one or more of the following areas: Formulation, Filling and/or Lyophilization. Vaccine experience desirable.
- Have prior experience in the generation of validation protocols, analysis of validation data, and technical writing of validation reports.
- Have process development or process validation experience, having worked on NPI and TT projects previously.
- Have the experience to perform, lead, and close variation/deviation investigation for development or commercial product.
- Minimum 6 years working in a cGMP pharmaceutical, biological, or vaccine clinical or commercial production facility within a technical support role.
- Have knowledge and understanding of biopharmaceutical cGMP quality systems and operations.
If this role is of interest to you, please apply now!
#LI-JS4
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
Save as job alert
WE’RE NOT JUST
ABOUT THE WORK
Although That’s Pretty Awesome
We’re about an unmatched company culture and a huge range of benefits you’ll love, both on and off the clock.
Check out all our perks hereSimilar Jobs
Salary
Competitive
Location
Illinois
Salary
Competitive
Sector
CAPEX Projects
Job type
Contract
Location
North America
East Coast
Description
Project Controls Manager – Illinois – Contract – Pharmaceuticals This is a fantastic opportunity for a Project Controls Manager to join our major, global pharmaceutical client on their
Reference
36337
Expiry Date
01/01/0001
Author
Kristen ScottAuthor
Kristen ScottSalary
Competitive
Location
Illinois
Salary
Competitive
Sector
CAPEX Projects
Job type
Contract
Location
North America
East Coast
Description
Project Controls Professional – Illinois – Contract – Pharmaceuticals This is a fantastic opportunity for a Project Controls Professional to join our major, global pharmaceutical client on
Reference
33641
Expiry Date
01/01/0001
Author
Kristen ScottAuthor
Kristen ScottSalary
Competitive
Location
Toulouse
Salary
Competitive
Sector
CAPEX Projects
Job type
Contract
Location
France
Description
Technical Project Manager - Life Sciences - Contract - France A global leading biopharmaceutical client requires a Project Manager experienced in large biotech projects to join their new bio
Reference
36344
Expiry Date
01/01/0001
Author
Caroline O’SullivanAuthor
Caroline O’SullivanInsights
Send us your CV
Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.
James
I manage this role.