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Cpps Jobs in Massachusetts (NOW HIRING)

Sail Biomedicines

Sr. Engineer, Drug Product

Cambridge, MA · On-site

$130K - $150K/yr

Support definition and refinement of CPPs, KPPs, CMAs, IPCs, IPTs, and release-relevant process controls. * Collaborate with Analytical Development, Quality, Manufacturing, Supply Chain, Regulatory ...

Sail Biomedicines

Sr. Engineer, Drug Product

Cambridge, MA · On-site +1

$130K - $150K/yr

Support definition and refinement of CPPs, KPPs, CMAs, IPCs, IPTs, and release-relevant process controls. * Collaborate with Analytical Development, Quality, Manufacturing, Supply Chain, Regulatory ...

Syner-G

Process Engineer

Plainville, MA · On-site

Define Critical Process Parameters (CPPs), Key Process Parameters (KPPs), Critical Quality Attributes (CQAs), and operating ranges. * Support process characterization activities and process ...

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Cpps information

See Massachusetts salary details

$83.5K

$147.3K

$229.9K

How much do cpps jobs pay per year?

As of Aug 22, 2026, the average yearly pay for cpps in Massachusetts is $147,274.00, according to ZipRecruiter salary data. Most workers in this role earn between $119,000.00 and $168,200.00 per year, depending on experience, location, and employer.

What is a CPPS?

A CPPS (Certified Professional in Patient Safety) job typically involves ensuring and improving patient safety within healthcare settings. Professionals in this role work to identify risks, implement safety protocols, and promote best practices to reduce medical errors. They may collaborate with healthcare teams, analyze incidents, and develop strategies to enhance overall patient care quality. This role is common in hospitals, healthcare organizations, and regulatory agencies.

What are the key skills and qualifications needed to thrive as a CPPS?

To thrive as a Certified Patient Payment Specialist (CPPS), you need a strong understanding of healthcare billing processes, insurance claims, and basic accounting principles, often supported by formal training or certification. Proficiency with healthcare billing software, electronic medical records (EMR), and familiarity with HIPAA regulations are commonly required. Strong attention to detail, effective communication, and problem-solving abilities set top performers apart. These skills are essential to ensure accurate processing of payments, seamless patient interactions, and compliance with industry standards.

What are some common challenges faced by Certified Patient Payment Specialists (CPPS) and how are they addressed?

Certified Patient Payment Specialists often encounter challenges such as handling complex insurance claims, managing denied or delayed payments, and clarifying patient billing inquiries. Staying current with frequently changing insurance policies and payment regulations can also be demanding. Success in this role usually involves ongoing education, effective use of billing software, and close collaboration with healthcare providers and insurance companies. Most organizations provide regular training and encourage teamwork to help specialists stay updated and resolve challenges efficiently.

What are popular job titles related to Cpps jobs in Massachusetts?

For Cpps jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Cpps jobs in Massachusetts look for?

The top searched job categories for Cpps jobs in Massachusetts are:

Cpps jobs near you
Infographic showing various Cpps job openings in Massachusetts as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $147,274 per year, or $70.8 per hour.

Sr. Engineer, Drug Product

Sail Biomedicines

Cambridge, MA • On-site

$130K - $150K/yr

Full-time

Re-posted 16 days ago

Job description

Position Summary
We are seeking an Engineer / Scientist to support drug product process development, process characterization, technology transfer, and manufacturing support for targeted lipid nanoparticle (tLNP) drug product processes. This role will focus on transferring complex LNP manufacturing processes to CDMOs, building and maintaining process models, supporting scale-up and process performance monitoring, and leading technical assessments for deviations, investigations, and process improvements.
The ideal candidate has hands-on experience with biologics, nanoparticle, RNA, sterile drug product, or advanced therapy manufacturing processes and is comfortable working across process development, analytical data, manufacturing execution, and quality systems.
Key Responsibilities
Process Development
  • Support process optimization and characterization activities for LNP formulation, TFF, mAb sterile filtration, and final fill.
  • Support definition and refinement of CPPs, KPPs, CMAs, IPCs, IPTs, and release-relevant process controls.
  • Collaborate with Analytical Development, Quality, Manufacturing, Supply Chain, Regulatory, and external partners to ensure process knowledge is captured and applied consistently.

Technology Transfer to CDMOs
  • Lead LNP/tLNP drug product unit operations to external manufacturing partners, including formulation, TFF/UF-DF, conjugation, sterile filtration, and final fill.
  • Role will communicate and align internal process knowledge to CDMO's through development of process descriptions and ensure alignment on CPPs, KPP, CMAs, equipment fit, single-use assembly design, and hold times. Review documentation from CDMOs surrounding batch execution at all relevant scales.
  • Review executed batch records, deviations, process data, and analytical results to confirm process performance and identify improvement opportunities.
  • Provide person-in-plant or remote technical support

Process Modeling & Data Analysis
  • Develop and maintain process models for mass balance, IPCs/IPTs, and process parameters. Use process models to support scale-up, tech transfer, batch planning, deviation impact assessments, and manufacturing readiness.
  • Support continued process verification by identifying trends, process drifts, and relationships between process inputs and product quality attributes.

Required Qualifications
  • BS with 6+ years of relevant experience or MS with 4+ years of relevant experience. Advanced degree in Chemical Engineering, Bioengineering, Pharmaceutical Sciences, or related field.
  • Experience in process development, manufacturing sciences, technical operations, or GMP manufacturing support.
  • Experience with biologics, RNA, LNPs, nanoparticles, sterile drug product, vaccines, cell/gene therapy, or other complex parenteral products.
  • Experience supporting CDMO manufacturing campaigns, engineering runs, GMP batches, GLP tox batches, or clinical supply manufacturing.
  • Ability to analyze process data and build mass balance or process models using Excel, JMP, Python, MATLAB, Spotfire, or similar tools.
  • Strong technical writing skills with experience authoring technical reports, deviation assessments, process descriptions, or transfer documentation.
  • Ability to work cross-functionally with internal teams and external CDMOs in a fast-paced development environment.

Preferred Qualifications
  • Experience with process risk assessments, FMEA, continued process verification, process characterization, or control strategy development.
  • Familiarity with GMP documentation, change control, CAPA, deviation systems, and regulatory expectations for biologics or sterile drug products.

Salary Range: $130,000 - $150,000
Sail Biomedicines is an Equal Opportunity Employer. Sail does not discriminate based on race, religion, color, sex, gender identity, sexual orientation, age, national origin, veteran status, or any other status protected under federal, state, or local law.

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