General Consideration - Pinnaql
About the role
Pinnaql is a trusted consulting partner to regulated life sciences companies, providing deep technical, validation, and quality expertise across the product lifecycle. We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity, accelerate timelines, and maintain compliance and audit readiness. As our client portfolio continues to grow, we’re building a network of professionals for upcoming projects and long-term opportunities. This posting is for future opportunities which could be onsite or hybrid. While this is not tied to an immediate opening, we actively review submissions and connect with candidates as project needs arise.
Why Connect with Pinnaql: At Pinnaql, people come first. When you're empowered to do your best work, bold ideas thrive and real progress happens. Our team partners closely with consultants and clients to deliver meaningful impact across critical life sciences projects. Excited to build something meaningful together? We look forward to hearing from you.
Skills
- Automation & Digital Transformation
- CQV & CSV Engineering
- Quality Systems & Lifecycle Solutions
- Quality Operations & Assurance
- Lab Technical Operations
- Manufacturing Technical Operations
- Project Management & Capital projects
Requirements
- Experience in GxP-regulated environments (pharma, biotech, medical device)
- Involvement in validation, engineering, quality systems, or project delivery
- Exposure to manufacturing, laboratory, or capital project environments
- Ability to collaborate across technical and cross-functional teams
- Experience with systems such as DeltaV, Rockwell/Allen-Bradley, Siemens, MES (Syncade, PharmaSuite, PAS-X), or similar platforms
- Experience with validation and quality systems/tools (e.g., Kneat, Veeva, MasterControl, TrackWise, ValGenesis, etc.)