Quality Control Analyst III
Catalent’s Chelsea, Massachusetts site—often referred to as the Boston location—is a global Center of Excellence for spray dry dispersion (SDD) and dry powder inhaler (DPI) capsule manufacturing and packaging, supporting inhalation drug products from clinical development through commercial launch. Located at 190 Everett Avenue, the approximately 96,000‑square‑foot GMP facility features ISO 8 production suites, high‑potency containment capabilities, and advanced spray drying equipment, including multiple large‑scale GMP spray dryers. The site offers integrated services such as powder processing, capsule filling, blister packaging, and on‑site quality control and analytical testing, with capacity to produce up to 100 million capsules annually. Strategically positioned just minutes from Boston Logan International Airport and within the Greater Boston life sciences hub, the Chelsea site plays a critical role in Catalent’s global inhalation network and regulatory‑compliant manufacturing operations.
Position Summary
We have an opportunity for a Quality Control Analyst III to join our team supporting product development, release, and stability testing. This role involves performing chemical and physical analyses of raw materials, in-process materials, and drug products following standard operating procedures. The position includes compiling data for documentation, participating in investigations and reports, and ensuring compliance with specifications. The Quality Control Analyst also contributes to revising and updating standard operating procedures as needed.
Shift: Monday - Friday, 8:00am to 5:00pm
Location: Chelsea, MA
100% Onsite
The Role
Operate analytical instrumentation such as HPLC, UPLC, GC, UV-vis, FTIR, laser diffraction, and KF
Statistically and critically analyze data for trending and reporting into regulatory filings; Participate in laboratory and/or quality investigations
Monitor equipment and instrumentation daily to ensure proper operation and calibration
Participate in the construction and/or revision of standard operating procedures; Assist in writing and updating analytical test procedures, protocols, log books, and checklists
Identify, alert, and propose solutions to issues on instruments and/or test executions; lead and implement recommended solutions and/or corrective actions
Independently organize workflows to accomplish objectives, provide guidance and support to colleagues, and promote new policies and programs effectively
Other duties may be assigned
The Candidate
Minimum Requirements
Bachelor’s Degree is required, preferably in Physical or Chemical Sciences (life sciences)
Minimum of 4–6 years of experience in a cGMP regulated environment is required
Chromatography skills using Empower is required
Proficiency in Microsoft Office is required
Ability to lift up to 20 lbs. is required
Ability to stand for long periods of time is required
Preferred Skills & Background
Experience in MDI/DPI analytical test methods such as Andersen Cascade Impactor and Emitted Dose techniques is preferred
Experience with analytical method development and validation is preferred
Pay
The anticipated salary range for this position in MA is $90,000 – $110,000 plus bonus. The final salary offered to a successful candidate may vary and will depend on factors such as experience, skillset, education, and business needs. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Why You Should Join Catalent
Defined career path and annual performance review and feedback process.
Diverse, inclusive culture.
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
Competitive paid time off plus 8 paid holidays.
Community engagement and green initiatives.
Medical, dental, and vision benefits effective day one of employment.
Tuition reimbursement.
Catalent offers rewarding opportunities to further your…