BioPharma Consulting JAD Group

Advises drugmakers on engineering and compliance

Senior CQV Engineer - Oral Solid Dose, Spray Drying

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeCarolina, Puerto RicoNo salary listed

About the Job

Requirements

At least 10 years of CQV experience in pharmaceutical manufacturing.
Hands-on experience with oral solid dose and/or spray-drying equipment; experience with both is preferred.
A bachelor's degree in Engineering or a Life Science.

Responsibilities

Commission, qualify, and verify oral solid dose equipment, including tablet presses, coaters, and dispensing systems.
Commission, qualify, and verify spray-dried dispersion systems, spray dryers, and associated equipment.
Support equipment startup and write technical documentation.
Support other CQV areas as needed.

Desired Qualifications

Hands-on experience with both oral solid dose and spray-drying equipment.

Senior CQV Engineer - Oral Solid Dose and Spray Drying

BioPharma Consulting JAD Group · Carolina, Puerto Rico · Contract · Posted 2026-10-24

Workplace: on_site

Department: Eli Lilly

Description

Bring a new oral solid dose and spray-dried dispersion facility to life on a multi-year greenfield pharmaceutical program in Carolina, Puerto Rico. We have two openings for senior CQV engineers to commission and qualify tablet presses, coaters, dispensing systems and spray dryers.

What you'll do

Commission, qualify and verify OSD equipment (tablet presses, coaters, dispensing).
Commission, qualify and verify SDD systems, spray dryers and associated equipment.
Support equipment startup and write technical documentation.
Support other CQV areas as needed.

Requirements

10+ years of CQV in pharmaceutical manufacturing.
Hands-on OSD and/or spray drying (SDD) equipment experience; both is preferred.
Bachelor's degree in Engineering or a Life Science.

Benefits

Contract: 60 months (multi-year program), with possible extension
Shift: Administrative, Monday–Friday, on-site 5 days/week
Start: January 4, 2027

Apply

Apply at BioPharma Consulting JAD Group

About the Company

BioPharma Consulting JAD Group

Advises drugmakers on engineering and compliance

BioPharma Consulting JAD Group advises pharmaceutical and biotechnology businesses on engineering, quality and regulatory compliance. It works with companies operating under US Food and Drug Administration rules to develop technical solutions for their manufacturing plants and processes. Its engineering practice covers facility and equipment design, process improvements and project management, while validation work verifies and documents that production systems meet requirements. The firm sells tailored consulting and technical support for assignments and projects, with company managers involved in delivery. Founded in 2010, it is headquartered in Cambridge, Massachusetts.

Company size: 51-200
Company stage: Not listed
Total funding: Not listed
Headquarters: Cambridge, MA
Founded: 2010

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