General Consideration - Pinnaql

Posted 2 Months Ago
Be an Early Applicant
Hiring Remotely in United States
Remote
Mid level
Biotech • Consulting • Pharmaceutical • Manufacturing
The Role
Pinnaql is building a talent network for future life-sciences consulting projects across validation, automation, quality, lab and manufacturing operations. Candidates with GxP experience in validation, CQV/CSV, MES/automation platforms, and quality systems are sought for on-site or hybrid engagements supporting pharmaceutical, biotech, and medical device clients.
Summary Generated by Built In

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.

Areas We Support

We work across a range of functions, including:

  • Automation & Digital Transformation
  • CQV & CSV Engineering
  • Quality Systems & Lifecycle Solutions
  • Quality Operations & Assurance
  • Lab Technical Operations
  • Manufacturing Technical Operations
  • Project Management & Capital projects

Typical Backgrounds

  • 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.)

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 Required

  • 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 automation and control systems (DeltaV, Rockwell/Allen-Bradley, Siemens) and MES platforms (Syncade, PharmaSuite, PAS-X)
  • Experience with validation and quality systems/tools (Kneat, Veeva, MasterControl, TrackWise, ValGenesis, etc.)
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The Company
HQ: Geneva
154 Employees
Year Founded: 2019

What We Do

Pinnaql, Inc. is a professional services consulting firm providing quality, regulatory, and operational excellence solutions to biopharmaceutical, medical device, and CDMO companies worldwide. The company specializes in laboratory validation, engineering, and compliance, helping regulated life sciences organizations navigate manufacturing challenges, reduce execution risks, and accelerate the transition from lab innovation to commercial market readiness.

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