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Biopharma Scientific Jobs (NOW HIRING)

Ecolab

Biopharma Regulatory Strategist

King Of Prussia, PA · On-site

$138K - $208K/yr

High-impact global role with visibility across Life Sciences, Bioprocessing, Regulatory, Commercial, R&D, Digital, and senior leadership teams. * Opportunity to shape biopharma growth strategy by ...

Talentmark

Business Development Manager

Waltham, MA · On-site

The biggest advantage of working with our client is that your career will have the best combination of biopharmaceutical science and applications, and you will grow with confidence and strength. Job ...

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As of Sep 8, 2026, the average hourly pay for biopharma scientific in the United States is $31.48, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $40.14 per hour, depending on experience, location, and employer.

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A Biopharma Scientist researches, develops, and tests new drugs and therapies derived from biological sources such as proteins, cells, or genetic material. They work in laboratory settings to design experiments, analyze biological data, and ensure the safety and effectiveness of pharmaceutical products. Biopharma Scientists often collaborate with other scientists, regulatory agencies, and healthcare professionals to bring new treatments to market. Their work is crucial in advancing medical science and improving patient outcomes.

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Scientists in the biopharma industry often encounter challenges such as navigating complex regulatory requirements, working with rapidly evolving technologies, and managing cross-functional collaboration with teams like regulatory affairs, clinical development, and manufacturing. Addressing these challenges requires staying up-to-date with industry regulations, embracing continuous learning, and developing strong communication skills to ensure effective teamwork. Proactively seeking mentorship and participating in professional development opportunities can also help scientists adapt and advance in their careers.

What are the key skills and qualifications needed to thrive as a biopharma scientist, and why are they important?

To thrive as a Biopharma Scientist, you need a strong background in molecular biology, biochemistry, or related life sciences, usually supported by a relevant degree such as a PhD or MSc. Familiarity with laboratory instruments, data analysis software, and industry-specific regulations like GMP and GLP is typically required. Strong problem-solving, teamwork, and communication skills help drive innovation and collaboration across multidisciplinary teams. These skills and qualifications are vital for ensuring scientific rigor, regulatory compliance, and successful advancement of biopharmaceutical projects.
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Infographic showing various Biopharma Scientific job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 81% Physical, 3% Hybrid, and 16% Remote job distribution, with an average salary of $65,473 per year, or $31.5 per hour.

Biopharma Regulatory Strategist

Ecolab

King Of Prussia, PA • On-site

$138K - $208K/yr

Full-time

Re-posted 17 days ago

Ecolab rating

7.5

Company rating: 7.5 out of 10

Based on 212 frontline employees who took The Breakroom Quiz

57th of 104 rated chemical manufacturers

Job description

At Ecolab, we help customers solve some of the world's most critical challenges across clean water, safe food, and healthy environments. As biopharma continues to evolve, regulatory strategy is becoming an increasingly important lever for innovation, market access, customer value, and growth.
As the Biopharma Regulatory Strategist, you will help shape and execute regulatory strategies that accelerate growth across Ecolab's Life Sciences and Bioprocessing businesses. In this global role, you will partner across Regulatory, Commercial, R&D, Digital, Government Relations, and key account teams to position Ecolab as a trusted regulatory partner across the full biopharma lifecycle. You will bring external perspective, deep CMC expertise, and strong business acumen to translate regulatory change into measurable customer value, risk mitigation, and revenue impact.
What's in it For You
  • High-impact global role with visibility across Life Sciences, Bioprocessing, Regulatory, Commercial, R&D, Digital, and senior leadership teams.
  • Opportunity to shape biopharma growth strategy by helping accelerate regulatory-enabled growth across priority accounts and markets.
  • Ability to influence future regulatory frameworks across digital, ICH Q12, compliance models, and evolving biopharma market access needs.
  • Enterprise-level impact by connecting regulatory strategy to commercial growth, account strategy, innovation, and differentiated customer value.
  • Leadership opportunity to build and develop high-performing regulatory consulting talent focused on biopharma compliance, innovation, and CMC strategy.

What You Will Do:
  • Lead breakthrough biopharma regulatory strategies across digital, commercial, and advocacy priorities that create competitive advantage.
  • Drive profitability, sales growth, and risk mitigation through regulatory strategies for Biopharma accounts.
  • Serve as a strategic regulatory advisor to global Bioprocessing leadership.
  • Connect Regulatory, Commercial, R&D, and Digital teams to deliver differentiated, end-to-end customer solutions.
  • Shape global biopharma and chemical regulatory frameworks to help accelerate growth, remove structural barriers, and deliver value across markets, segments, and customers.
  • Develop Biopharma compliance, innovation, and CMC customer talent with a focus on business advantage through regulatory change management.
  • Bring external perspective from health authorities, industry forums, and customers to anticipate change and translate it into business and customer value.
  • Help define and execute regulatory strategies that support molecule conversion and growth across priority biopharma and CDMO accounts.
  • Enable scalable revenue through predictive compliance strategies for digital/AI software and services.

Minimum Qualifications
  • Advanced degree (PhD, PharmD, or MSc) in Life Sciences, Pharmaceutical Sciences, Chemistry, Biochemistry, Chemical Engineering, or a related discipline.
  • 15 years of progressive Regulatory Affairs experience within biopharma, with deep CMC regulatory strategy expertise for biologics.
  • Direct experience with global health authorities, including FDA, EMA, and PMDA, and experience leading advocacy efforts.
  • Strong commercial acumen with the ability to frame regulatory choices as business trade-offs.
  • Experience in digital strategy or digital transformation initiatives.
  • Excellent executive communication and influencing skills across all levels.

Preferred Qualifications
  • Experience with key account management, or commercial strategy in Life Sciences.
  • MBA.
  • Demonstrated ability to build, develop, and scale high-performing teams.
  • Ability to connect regulatory strategy to enterprise growth, commercial priorities, and business transformation.
  • Proven ability to simplify complex priorities and focus teams on the highest-value opportunities.
  • Experience leading transformation, innovation, and digital adoption across functions.
  • Strong ability to influence broadly and shape decisions beyond one function.

Annual or Hourly Compensation Range
The base salary range for this position is $138,700.00 - $208,100.00. This position is eligible for annual bonus and long-term incentives based on performance, per plan terms. Many factors are taken into consideration when determining compensation, such as experience, education, training, geography, etc. We comply with all minimum wage and overtime laws.
Benefits
Ecolab strives to provide comprehensive and market-competitive benefits to meet the needs of our associates and their families. Click here to see our benefits.
If you are viewing this posting on a site other than our Ecolab Career website, view our benefits at jobs.ecolab.com/working-here.
Potential Customer Requirements Notice
To meet customer requirements and comply with local or state regulations, applicants for certain customer-facing roles may need to:
- Undergo additional background screens and/or drug/alcohol testing for customer credentialing.
Americans with Disabilities Act (ADA)
Ecolab will provide reasonable accommodation (such as a qualified sign language interpreter or other personal assistance) with our application process upon request as required to comply with applicable laws. If you have a disability and require accommodation assistance in this application process, please visit the Recruiting Support link in the footer of each page of our career website.

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About Ecolab

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Ecolab is a global sustainability leader offering water, hygiene and infection prevention solutions and services that protect people and the resources vital to life.

Industry

Manufacturing

Company size

10,000+ Employees

Headquarters location

Saint Paul, MN, US

Year founded

1923

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