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Pharmaceutical Spray Drying Jobs (NOW HIRING)

Merck

Experience with pharmaceutical processing equipment and utility systems (OSD equipment such as tablet compression, encapsulation, spray drying, film coating, isolators; compressed gas systems and ...

Catalent, Inc.

Director of Quality

Chelsea, MA · On-site

$168K - $257K/yr

The site features inhaled powder spray drying, as well as multiple commercial-scale lines for ... As a member of the site leadership team ensure an effective Pharmaceutical Quality Management ...

Catalent Pharma Solutions

Director of Quality

Chelsea, MA · On-site

$168K - $257K/yr

The site features inhaled powder spray drying, as well as multiple commercial-scale lines for ... As a member of the site leadership team ensure an effective Pharmaceutical Quality Management ...

Catalent Pharma Solutions

Project Manager

Chelsea, MA · On-site

... and advanced spray drying equipment, including multiple largescale GMP spray dryers. The site ... Previous pharmaceutical or biotech industry experience is preferred Pay The anticipated salary ...

Catalent, Inc.

Commercial Account Manager

Chelsea, MA · On-site

Knowledge of PPQ, commercial manufacturing, inhalation products, oral solid dose (OSD), or related pharmaceutical operations is preferred but not required. * Experience with inhalation, spray drying ...

MSD Malaysia

... pharmaceutical processing equipment and utility systems (OSD equipment such as tablet compression, encapsulation, spray drying, film coating, isolators; compressed gas systems and purified water ...

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Pharmaceutical Spray Drying information

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How much do pharmaceutical spray drying jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for pharmaceutical spray drying in the United States is $19.43, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $21.15 per hour, depending on experience, location, and employer.

What is pharmaceutical spray drying?

Pharmaceutical spray drying is a process used to convert liquid drug formulations into dry powders by rapidly drying them with a hot gas. This technique is commonly used to improve the stability, solubility, and bioavailability of pharmaceutical compounds. The process involves atomizing the liquid into fine droplets, which are then exposed to hot air, causing the solvent to evaporate quickly and leaving behind dry particles. It is widely used in the production of inhalable drugs, oral formulations, and for encapsulation of sensitive ingredients.

What are the key skills and qualifications needed to thrive in pharmaceutical spray drying, and why are they important?

To excel in Pharmaceutical Spray Drying, a solid background in pharmaceutical sciences, chemical engineering, or a related field is essential, often supported by a relevant degree. Familiarity with spray drying equipment, process analytical technology (PAT), and adherence to Good Manufacturing Practices (GMP) are typically required, along with knowledge of regulatory standards. Strong problem-solving abilities, attention to detail, and effective communication help professionals optimize processes and ensure product quality. These skills are crucial for maintaining product efficacy, meeting regulatory requirements, and ensuring safe and efficient pharmaceutical manufacturing.

What are some common challenges faced by professionals working in pharmaceutical spray drying, and how can they be addressed?

Professionals in pharmaceutical spray drying often encounter challenges such as maintaining consistent particle size, ensuring product stability, and controlling moisture content. These issues can affect the efficacy and shelf life of the final product. To address these challenges, it is essential to closely monitor process parameters, collaborate with quality assurance teams, and regularly calibrate equipment. Working in multidisciplinary teams with formulation scientists and process engineers also helps in troubleshooting and optimizing the spray drying process.

What is the difference between Pharmaceutical Spray Drying vs Pharmaceutical Quality Control?

AspectPharmaceutical Spray DryingPharmaceutical Quality Control
Primary RoleOperates spray drying equipment to produce powdered pharmaceuticalsTests and inspects pharmaceutical products for quality and compliance
Required SkillsKnowledge of manufacturing processes, equipment operation, safety protocolsUnderstanding of testing methods, regulations, analytical techniques
Work EnvironmentManufacturing plant, production lineLaboratory or quality assurance department
CertificationsGMP training, equipment operation certificationsQuality assurance certifications, GMP knowledge

Pharmaceutical Spray Drying focuses on the manufacturing process of powdered drugs, while Pharmaceutical Quality Control ensures the final products meet quality standards. Both roles are essential in pharmaceutical production but differ in responsibilities and work environments.

Infographic showing various Pharmaceutical Spray Drying job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 2% Contract, and 1% Nights. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $40,423 per year, or $19.4 per hour.

Sr. Principal Scientist, Oral Drug Product Development

Cambridge, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Job description

Director, Oral Drug Product DevelopmentResponsibilities:
  • Lead formulation design, process development, manufacturability assessment, scale-up, technology transfer, and clinical manufacturing of small molecule oral dosage forms across all stages of development.
  • Develop enabling formulation approaches for challenging compounds (poorly soluble, poorly permeable, unstable, or complex molecules such as orally delivered peptides).
  • Serve as the senior drug product representative on cross‑functional CMC and asset teams; align regulatory, quality, manufacturing, analytical, clinical pharmacology, DMPK, and external partner functions.
  • Influence portfolio decisions based on developability, manufacturability, biopharmaceutical performance, technical risk, and investment priorities.
  • Champion technology transfer, clinical manufacturing readiness, and scale‑up at internal and external manufacturing sites; provide strategic oversight and establish manufacturing strategies.
  • Mentor and develop scientists and engineers supporting oral drug product development.
  • Oversee completion of drug product sections for regulatory submissions and related technical documentation.
  • Identify and implement new formulation technologies, predictive tools, digital workflows, and best practices to improve development efficiency and portfolio execution.
Required Skills/Qualifications:
  • PhD in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or related discipline; minimum 12 years' oral drug product development experience.
  • Track record leading formulation and process development for oral solid dosage forms (early through clinical manufacturing and/or late‑stage).
  • Experience with scale‑up, technology transfer, clinical manufacturing, and external manufacturing organizations.
  • Strong knowledge of CMC development, regulatory expectations, technical documentation, and phase‑appropriate development strategies.
  • Ability to lead cross‑functionally, influence strategy, manage technical risk, and communicate effectively.
  • Experience mentoring, developing, or leading scientists and engineers.
Preferred Skills:
  • Enabling tech expertise (amorphous solid dispersions, spray drying, hot‑melt extrusion, lipid‑based formulations, modified release, particle engineering).
  • Late‑stage development, commercial readiness, process characterization, and/or process validation experience.
  • Experience supporting at least one NDA/MAA and regulatory agency interactions.
  • Hands‑on oral solid dose manufacturing unit operations and manufacturability experience.
  • Experience implementing new technologies/digital tools/knowledge platforms across programs.
  • Experience managing external CDMO/CMO relationships and technology transfer.
Benefits (if included):
  • Medical, Dental, Vision, & Life insurances; fitness & wellness (reimbursement); short- and long-term disability; paid vacation (15+ days) and end‑of‑year shutdown; paid holidays; sick time; paid maternity and parental leave; 401(k) match; employee stock purchase plan; tuition reimbursement (up to $10,000/year); Employee Resource Groups participation.
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