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Hourly Cmc Consultant Jobs (NOW HIRING)

Ecolab

Biopharma Regulatory Strategist

King Of Prussia, PA · On-site

$138K - $208K/yr

... consulting talent focused on biopharma compliance, innovation, and CMC strategy. What You Will Do ... Annual or Hourly Compensation Range The base salary range for this position is $138,700.00 - $208 ...

Ecolab

Biopharma Regulatory Strategist

King Of Prussia, PA · On-site

$138K - $208K/yr

... consulting talent focused on biopharma compliance, innovation, and CMC strategy. What You Will Do ... Annual or Hourly Compensation Range The base salary range for this position is $138,700.00 - $208 ...

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$10

$38

$82

How much do hourly cmc consultant jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for hourly cmc consultant in the United States is $38.02, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $48.08 per hour, depending on experience, location, and employer.

What is the difference between Hourly Cmc Consultant vs Contract Cmc Specialist?

AspectHourly Cmc ConsultantContract Cmc Specialist
CredentialsTypically requires a degree in life sciences, with industry certificationsSimilar credentials, often with additional specialized training
Work EnvironmentConsulting firms, biotech or pharma companies, project-basedContract roles within biotech or pharma companies, project-specific
Employer & Industry UsageUsed by consulting firms and biotech companies for temporary expertiseEngaged directly by companies for specific projects

Both roles involve working on CMC (Chemistry, Manufacturing, and Controls) projects in the biotech and pharmaceutical industries. The main difference lies in employment type: Hourly Cmc Consultants typically work on a flexible, hourly basis through consulting firms, while Contract Cmc Specialists are hired directly for specific projects on a contractual basis. Both require similar credentials and industry experience, but their work arrangements and employer relationships differ.

What cities are hiring for Hourly Cmc Consultant jobs? Cities with the most Hourly Cmc Consultant job openings:
What are the most commonly searched types of Cmc Consultant jobs? The most popular types of Cmc Consultant jobs are:
What states have the most Hourly Cmc Consultant jobs? States with the most job openings for Hourly Cmc Consultant jobs include:
What job categories do people searching Hourly Cmc Consultant jobs look for? The top searched job categories for Hourly Cmc Consultant jobs are:
Hourly Cmc Consultant jobs near you
Infographic showing various Hourly Cmc Consultant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 51% Full Time, 44% Part Time, 1% Temporary, and 3% Contract. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $79,074 per year, or $38 per hour.

Contract: Manager, CMC Stability Management and Analysis

Immunome, Inc.

Bothell, WA • On-site

$88.10 - $100.05/hr

Full-time

Re-posted 10 days ago

Job description

Company Overview
Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.
Position Overview
Immunome is seeking an experienced Contract: Manager, CMC Stability Management and Analysis to oversee execution of outsourced stability programs. This contract role will be responsible for maintaining stability pull schedules, data review, and vendor oversight activities across mAb intermediate, drug substance, and drug product.
The successful consultant will bring practical expertise in GMP stability operations, biologics and large-molecule stability requirements, understanding of ADC stability indicating assays and outsourced laboratory management. This position requires a hands-on program manager who can translate technical and regulatory expectations into actionable plans, manage timelines and risks across external partners, and ensure stability deliverables are met.
Responsibilities
Study Execution and Operational Oversight
  • Review stability protocols for long-term and accelerated studies.
  • Create and maintain stability plans, master schedules, pull calendars, and study trackers across multiple development programs.
  • Oversee execution of stability studies and ensure timely sample pulls, testing initiation, data delivery, and escalation of schedule or quality risks.

Data Review, Trending, and Technical Assessment
  • Review stability data for completeness, accuracy, data integrity, trend behavior, specification compliance, and consistency with expected product quality attributes.
  • Support evaluation of OOS/OOT results and atypical trends.
  • Prepare stability summaries, trend reports, shelf-life assessments, retest/expiry recommendations, and technical risk assessments to support program decision-making.

Qualifications
  • Bachelor's or advanced degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Chemical Engineering, or a related field.
  • 8+ years of experience in stability, QC, Analytical Development, CMC, or technical operations within the biotechnology or biopharmaceutical industry, or equivalent.
  • Demonstrated experience managing GMP stability programs for biologics, monoclonal antibodies, fusion proteins, or other large molecules; ADC experience preferred.
  • Hands-on experience with stability data review, trending, shelf-life assessment.
  • Prior experience managing external CTLs, CDMOs, CROs, or stability storage vendors supporting regulated studies.
  • Working knowledge of GMP requirements, data integrity expectations, ICH stability guidance, and regulatory expectations for biologics stability studies.
  • Contract or consultant experience in a matrixed biotech environment preferred.

Knowledge and Skills
  • In-depth understanding of biologics stability program management, including drug substance and drug product stability, retest/expiry dating, storage condition justification, and ongoing stability commitments.
  • Working knowledge of ICH Q1A(R2), Q1B, Q1D, Q1E, Q5C, relevant FDA/EMA expectations, and phase-appropriate application of stability requirements.
  • Strong understanding of biologics product quality attributes.
  • Familiarity with analytical technologies used in biologics stability testing, including HPLC/UPLC, SEC, CE-SDS/cIEF/icIEF, ELISA, binding and potency assays.
  • Strong project management skills with the ability to manage detailed schedules, multiple vendors, cross-functional dependencies, and competing program priorities.
  • Ability to interpret stability trends, identify risks, escalate issues appropriately, and drive practical solutions in collaboration with technical and quality stakeholders.
  • Excellent documentation, communication, and stakeholder management skills.
  • Comfort with ambiguity and dynamic timelines; ability to operate independently and drive execution with limited supervision.

WA State Contract Pay Transparency (Hourly Rate)
$88.10-$100.05 USD
E/E/O
Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
E-Verify
Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).

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