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Formulation Development Cmc Jobs in Philadelphia, PA

Globus Medical

Analytical Scientist

Audubon, PA · On-site

Collaborate cross-functionally with upstream/downstream process development, formulation, and quality teams to support CMC development. * Analyze and interpret complex data, provide scientific ...

Globusmedical

Analytical Scientist

Audubon, PA

Collaborate cross-functionally with upstream/downstream process development, formulation, and quality teams to support CMC development. * Analyze and interpret complex data, provide scientific ...

Pace

Analytical Chemist- Small Molecule

Norristown, PA · On-site

$75K - $85K/yr

Pace ® Life Sciences delivers a comprehensive suite of contract CMC development, CTM manufacturing ... May interpret analytical data to guide formulation and process development decisions. ESSENTIAL ...

Pacelabs

Analytical Chemist- Small Molecule

Norristown, PA · On-site

$75K - $85K/yr

Pace Life Sciences delivers a comprehensive suite of contract CMC development, CTM manufacturing ... May interpret analytical data to guide formulation and process development decisions. ESSENTIAL ...

MSD

Senior Configuration Engineer (Hybrid)

West Point, PA

$118K - $156K/yr

Strong CMC domain knowledge across analytical, process, formulation, and drug substance/product development * Experience supporting enterprise data model or platform implementations, including source ...

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All JobsFormulation Development Cmc JobsFormulation Development Cmc Jobs in Philadelphia, PA

Formulation Development Cmc information

See Philadelphia, PA salary details

$30

$51

$97

How much do formulation development cmc jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for formulation development cmc in Philadelphia, PA is $51.35, according to ZipRecruiter salary data. Most workers in this role earn between $34.95 and $82.21 per hour, depending on experience, location, and employer.

What is the role of CMC in drug development?

In formulation development, CMC (Chemistry, Manufacturing, and Controls) ensures the quality, safety, and efficacy of a drug by establishing manufacturing processes, quality standards, and regulatory documentation. Formulation scientists and CMC teams collaborate to develop stable, scalable drug products that meet regulatory requirements throughout development and commercialization.

What is the salary of formulation R&D?

The salary for a Formulation Development CMC professional typically ranges from $70,000 to $130,000 annually, depending on experience, education, and location. Entry-level roles may start lower, while senior positions with specialized skills or certifications can earn higher salaries. Compensation often includes benefits such as health insurance and bonuses.

What is the highest paying job in pharmaceuticals?

In pharmaceuticals, senior roles such as Vice President of Research and Development or Chief Scientific Officer typically have the highest salaries, often exceeding several hundred thousand dollars annually. These positions require extensive experience, advanced degrees, and leadership skills, and they oversee drug development, regulatory strategies, and company innovation.

What is the difference between Formulation Development Cmc vs Formulation Scientist?

AspectFormulation Development CmcFormulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fields; industry certificationsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields
Work EnvironmentPharmaceutical or biotech R&D labs, manufacturing settingsResearch labs, development facilities, pharmaceutical companies
Industry UsageRegulatory submissions, product development, manufacturing supportFormulation research, experimental design, product optimization

Formulation Development Cmc focuses on developing formulations suitable for regulatory approval and manufacturing, often involving documentation and compliance. Formulation Scientists primarily conduct research and experiments to create and optimize formulations. While both roles require similar educational backgrounds and work in related environments, Cmc roles emphasize regulatory and manufacturing aspects, whereas Scientists focus on experimental research and innovation.

Is formulation part of CMC?

In formulation development roles within CMC (Chemistry, Manufacturing, and Controls), formulation is a core component, involving the design and optimization of drug formulations to ensure stability, efficacy, and manufacturability. These professionals work with analytical tools, quality standards, and regulatory requirements to develop suitable formulations for clinical and commercial products.

What is Formulation Development CMC?

Formulation Development CMC (Chemistry, Manufacturing, and Controls) refers to the process of designing and optimizing the composition of a drug product, ensuring it is safe, effective, and stable for patient use. This role involves selecting appropriate excipients, developing the manufacturing process, and generating the data required to support regulatory submissions. CMC professionals collaborate with research, quality, and regulatory teams to ensure that the drug product meets all necessary standards throughout its lifecycle.

What are the key skills and qualifications needed to thrive as a Formulation Development CMC specialist, and why are they important?

To thrive as a Formulation Development CMC specialist, you need expertise in pharmaceutical sciences, chemistry, and regulatory guidelines, often supported by an advanced degree in a relevant field. Familiarity with analytical techniques, formulation equipment, and regulatory submission systems like eCTD is crucial. Strong problem-solving skills, attention to detail, and effective collaboration are essential soft skills in this role. These competencies ensure the successful development, optimization, and regulatory approval of safe and effective pharmaceutical products.

What are some typical challenges faced by professionals in Formulation Development CMC, and how are they addressed?

Professionals in Formulation Development CMC often encounter challenges such as ensuring formulation stability, meeting regulatory requirements, and scaling up from laboratory to manufacturing. Addressing these challenges requires close collaboration with analytical, regulatory, and manufacturing teams, as well as staying current with evolving guidelines. Effective project management, rigorous experimental design, and proactive risk assessment are key strategies to successfully navigate these complexities and ensure timely progress of drug development projects.
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What cities near Philadelphia, PA are hiring for Formulation Development Cmc jobs? Cities near Philadelphia, PA with the most Formulation Development Cmc job openings:
Formulation Development Cmc jobs near you
Associate Director/Director-BD

Associate Director/Director-BD

Frontage Laboratories

Exton, PA • On-site

Full-time

Medical, Dental, Life, Retirement

Posted 12 days ago

Job description

Associate Director/Director, Business Development, CMC Services

Associate Director/Director, Business Development, CMC Services

Full time

Remote

Location – United states (Mid-west to Northeast), Preferred Boston Area

Reports to: Director, Scientific Strategy & Business development

Frontage Laboratories Inc.

Frontage Laboratories Inc. (Frontage) is a global CRDMO with broad expertise in supporting pre-clinical and clinical drug development. Frontage operates out of several different locations within the USA, Canada, and China. Frontage’s core competencies include drug metabolism, pharmokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.


Frontage CMC:

At Frontage, we leverage over 25 years of expertise to develop specialized solutions that address CMC challenges across all dosage forms, encompassing drug product development, analysis, clinical trial materials, submission batches, and commercial manufacturing. Our state-of-the-art facilities are equipped with advanced CDMO operations and manufacturing equipment for oral solid doses, semisolids, ophthalmic products, sterile injectables and biologics. We also provide comprehensive analytical testing services—including API and product release, stability studies, dissolution testing—and maintain fully equipped in-house microbiological laboratories.

Responsibilities:

  • Prioritize the promotion of CMC services while integrating Frontage's broader capabilities within the differentiation framework.
  • Manage the entire business development process, from lead generation through to contract completion.
  • Attain sales objectives through a strategic approach focused on securing profitable opportunities.
  • Secure and retain business through professional, consultative, and proactive sales activities directed at key decision makers
  • Strong negotiating skills, knowledge of legal contracts and experience with RFIs/RFPs and competitive bidding processes
  • Formulate and implement a competitive strategy driven by market analysis and intelligence.
  • Proactively identify and develop project prospects, new clients to ensure a robust sales pipeline.
  • Assess customer challenges and collaborate with subject matter experts to deliver customized solutions.
  • Commit to frequent travel for client meetings, industry conferences, and seminars as required.
  • Continuously analyze the competitive landscape and formulate tactics to strengthen market position.
  • Work closely with technical and operational teams to uncover and pursue up-selling opportunities.
  • Establish and maintain account management plans and actions to foster relationships with prospective and key clients.
  • Develop and adhere to a structured client engagement cycle to expand the client portfolio and exceed sales targets.
  • Identify and communicate cross-selling opportunities for other Frontage business units.
  • Utilize the CRM tool to accurately document all stages of the sales cycle and provide reliable sales forecasts (Opportunities, CDA, MSA, Site Visits, Face to Face Meetings, Proposal requests, Proposal issued, Closed won or lost, etc.)


Requirements:

  • BS degree or above, life science preferred.
  • 3-8 years’ working experience of commercial sales or technical expertise in formulation development, analytical testing, or commercial manufacturing in a Pharmaceutical CDMO company.
  • Self-starter with proven ability to develop a territory strategy for quota attainment.
  • Solid understanding of the drug products and dosage forms such as OSD, Injectables, Semi solids, Ophthalmic Dosage forms
  • Fair knowledge in Biologicals, Cell and Gene therapy market
  • Excellent interpersonal and communications skills required.
  • Very strong work ethic and comfortable with travels (50%)
  • Knowledge and understanding of FDA, GXP, and ICH regulations and guidance
  • Highly proficient in using Microsoft Office Suite: MS PowerPoint, MS Word, and MS Excel


Salary and Benefits:

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability