Design Verification Lead
- Worldwide
- Contract
- CAPEX Projects
This vacancy has now expired
This is a fantastic opportunity for a Design Verification Lead to join our major, global pharmaceutical client on their latest new-build project based in Puerto Rico, this is a large-scale greenfield capital project and investing more than $1bn.
Role & Responsibilities:
- Lead and manage design verification and CQV activities specifically for Oral Solid Dosage (OSD) manufacturing, focusing on capsules and tablets.
- Serve as the primary onsite technical resource, working hands-on with equipment and systems to ensure successful CQV processes.
- Work directly with vendors, challenging design decisions when necessary and ensuring alignment with project requirements and specifications.
- Communicate effectively in English and Spanish, coordinating across corporate teams, vendors, and stakeholders.
- Provide technical guidance and hands-on support in OSD core technologies, such as compression, granulation, compaction, and printing.
- Review and interpret Piping and Instrumentation Diagrams (P&IDs), offering insights and identifying improvements.
- Exhibit self-initiative and strong communication skills to convey technical information clearly,
- ensuring successful collaboration with designers and vendors.
Required Qualifications:
- Minimum of 5 years of experience in a Design Verification or CQV Lead role within pharmaceutical manufacturing, with a strong emphasis on Oral Solid Dosage (OSD) processes.
- In-depth knowledge of core OSD technologies, particularly compression, coding, granulation, and compaction.
- Demonstrated experience with OSD manufacturing technologies and processes used by major pharmaceutical companies
- Ability to read, interpret, and utilize P&IDs to support CQV processes and design verification.
- Strong communication skills with fluency in both English and Spanish, enabling seamless interaction with corporate teams and vendors.
- Proven ability to work onsite full-time and engage in a dynamic, consultant role where adaptability and proactive problem-solving are essential.
If this role is of interest to you, please apply now!
#LI-KS1
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
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
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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