Pharmaron Jobs Hiring Now
Pharmaron is hiring for 26 open roles on Migrate Mate as of August 31, 2026, concentrated in biotech & life sciences and laboratory research, with listed salaries up to about $170,000. Migrate Mate updates Pharmaron's live openings daily. Pharmaron is a contract research, development, and manufacturing organization serving the pharmaceutical and biotechnology industries across drug discovery, process chemistry, and preclinical research.
Find Pharmaron JobsOverview
Pharmaron hiring data on Migrate Mate, as of August 31, 2026.
- Open jobs
- 26
- Top team
- Biotech & Life Sciences
- Seniority
- Across all levels
- Work type
- 8% remote or hybrid
- Top location
- Coventry
- Salary range
- $55,000–$170,000
Listed salaries for Pharmaron roles on Migrate Mate range from about $55,000 to $170,000 per year across 26 open roles, as of August 31, 2026. Some roles list hourly contract rates.
Open Roles at Pharmaron
Showing 25 of 26+ Pharmaron jobs
Position: Scientist I/II – LC-MS/MS Bioanalysis
Salary Range: $55,000-$70,000
Location: Exton, PA (On-site)
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.
Job Overview:
As a Scientist I/II – LC-MS/MS Bioanalysis, you will develop, optimize, troubleshoot, and validate bioanalytical methods supporting DMPK and regulated studies. You'll work with advanced LC-MS/MS and high-resolution mass spectrometry platforms while gaining exposure to a broad range of therapeutic modalities-from traditional small molecules to peptides, oligonucleotides, PROTACs, biologics, and emerging therapies.
This opportunity is ideal for an early-career bioanalytical scientist who wants to expand beyond routine sample analysis and develop deeper expertise in method development, complex bioanalysis, scientific problem-solving, and study execution within a global CRO/CDMO environment.
Key Responsibilities
- Develop, optimize, troubleshoot, and validate LC-MS/MS bioanalytical methods supporting drug discovery and development programs.
- Perform bioanalytical sample analysis for DMPK, method development, validation, and regulated studies.
- Operate LC-MS/MS and HPLC platforms and gain exposure to advanced mass spectrometry technologies.
- Design and execute scientifically sound experiments aligned with client objectives, study requirements, and internal quality standards.
- Process, analyze, interpret, and report bioanalytical data while identifying and resolving technical challenges.
- Review and execute study protocols and ensure accurate documentation of experimental procedures, results, and conclusions.
- Author and contribute to protocols, validation reports, technical summaries, study reports, and other scientific documentation.
- Support GLP and regulated bioanalytical activities in accordance with applicable procedures and quality requirements.
- Collaborate with scientists, project teams, management, Business Development, and clients to support successful project execution.
- Participate in scientific project reviews, technical discussions, and continuous improvement initiatives.
- As experience develops, take on increasing scientific ownership and opportunities to support studies in a Principal Investigator and/or Study Director capacity, as appropriate.
What We're Looking For
- Bachelor's degree or higher in Chemistry, Pharmaceutical Sciences, Biochemistry, Life Sciences, or a related scientific discipline.
- 1–3+ years of relevant bioanalytical laboratory experience; position level will be determined based on experience and demonstrated technical capabilities.
- Hands-on experience with LC-MS/MS bioanalysis, including exposure to method development, optimization, validation, and/or sample analysis.
- Understanding of chromatographic and mass spectrometric principles.
- Strong analytical thinking and ability to troubleshoot scientific and technical challenges.
- Ability to accurately analyze, interpret, document, and communicate scientific data.
- Strong organizational skills and attention to detail.
- Ability to manage multiple priorities and work effectively in a fast-paced, collaborative scientific environment.
Preferred Qualifications
- Experience developing and validating LC-MS/MS bioanalytical methods.
- Experience working within a GLP or regulated bioanalytical environment.
- Experience with SCIEX Triple Quad platforms, including 6500+ and/or 7600 systems, or comparable LC-MS/MS instrumentation.
- Experience with high-resolution mass spectrometry platforms.
- Experience supporting DMPK and regulated bioanalytical studies.
- Experience analyzing complex modalities such as peptides, oligonucleotides, PROTACs, biologics, or other emerging therapeutic modalities.
- Experience with HPLC and other analytical detection platforms.
- Experience authoring protocols, validation reports, technical summaries, or study reports.
- Previous CRO, pharmaceutical, or biotechnology industry experience.
- Experience collaborating directly with clients or cross-functional scientific teams.
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
- Comprehensive Medical, DentalVision Insurance with significant employer contributions
- 401(k) Retirement Plan with generous employer matching
- Generous Paid Time Off (PTO), Paid Sick LeaveCompany Holidays to support work-life balance
- Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus HealthcareDependent Care Flexible Spending Accounts
- 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
- Employee Assistance Program (EAP), mental health resources, and wellness programs
- Family-friendly benefits, including fertility support and maternity resources
- Professional development and career growth opportunities within a leading global CRO/CDMO
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
#LI-MC1
Position: Scientist I/II – LC-MS/MS Bioanalysis
Salary Range: $55,000-$70,000
Location: Exton, PA (On-site)
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.
Job Overview:
As a Scientist I/II – LC-MS/MS Bioanalysis, you will develop, optimize, troubleshoot, and validate bioanalytical methods supporting DMPK and regulated studies. You'll work with advanced LC-MS/MS and high-resolution mass spectrometry platforms while gaining exposure to a broad range of therapeutic modalities-from traditional small molecules to peptides, oligonucleotides, PROTACs, biologics, and emerging therapies.
This opportunity is ideal for an early-career bioanalytical scientist who wants to expand beyond routine sample analysis and develop deeper expertise in method development, complex bioanalysis, scientific problem-solving, and study execution within a global CRO/CDMO environment.
Key Responsibilities
- Develop, optimize, troubleshoot, and validate LC-MS/MS bioanalytical methods supporting drug discovery and development programs.
- Perform bioanalytical sample analysis for DMPK, method development, validation, and regulated studies.
- Operate LC-MS/MS and HPLC platforms and gain exposure to advanced mass spectrometry technologies.
- Design and execute scientifically sound experiments aligned with client objectives, study requirements, and internal quality standards.
- Process, analyze, interpret, and report bioanalytical data while identifying and resolving technical challenges.
- Review and execute study protocols and ensure accurate documentation of experimental procedures, results, and conclusions.
- Author and contribute to protocols, validation reports, technical summaries, study reports, and other scientific documentation.
- Support GLP and regulated bioanalytical activities in accordance with applicable procedures and quality requirements.
- Collaborate with scientists, project teams, management, Business Development, and clients to support successful project execution.
- Participate in scientific project reviews, technical discussions, and continuous improvement initiatives.
- As experience develops, take on increasing scientific ownership and opportunities to support studies in a Principal Investigator and/or Study Director capacity, as appropriate.
What We're Looking For
- Bachelor's degree or higher in Chemistry, Pharmaceutical Sciences, Biochemistry, Life Sciences, or a related scientific discipline.
- 1–3+ years of relevant bioanalytical laboratory experience; position level will be determined based on experience and demonstrated technical capabilities.
- Hands-on experience with LC-MS/MS bioanalysis, including exposure to method development, optimization, validation, and/or sample analysis.
- Understanding of chromatographic and mass spectrometric principles.
- Strong analytical thinking and ability to troubleshoot scientific and technical challenges.
- Ability to accurately analyze, interpret, document, and communicate scientific data.
- Strong organizational skills and attention to detail.
- Ability to manage multiple priorities and work effectively in a fast-paced, collaborative scientific environment.
Preferred Qualifications
- Experience developing and validating LC-MS/MS bioanalytical methods.
- Experience working within a GLP or regulated bioanalytical environment.
- Experience with SCIEX Triple Quad platforms, including 6500+ and/or 7600 systems, or comparable LC-MS/MS instrumentation.
- Experience with high-resolution mass spectrometry platforms.
- Experience supporting DMPK and regulated bioanalytical studies.
- Experience analyzing complex modalities such as peptides, oligonucleotides, PROTACs, biologics, or other emerging therapeutic modalities.
- Experience with HPLC and other analytical detection platforms.
- Experience authoring protocols, validation reports, technical summaries, or study reports.
- Previous CRO, pharmaceutical, or biotechnology industry experience.
- Experience collaborating directly with clients or cross-functional scientific teams.
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
- Comprehensive Medical, DentalVision Insurance with significant employer contributions
- 401(k) Retirement Plan with generous employer matching
- Generous Paid Time Off (PTO), Paid Sick LeaveCompany Holidays to support work-life balance
- Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus HealthcareDependent Care Flexible Spending Accounts
- 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
- Employee Assistance Program (EAP), mental health resources, and wellness programs
- Family-friendly benefits, including fertility support and maternity resources
- Professional development and career growth opportunities within a leading global CRO/CDMO
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
#LI-MC1
Job Roles at Pharmaron
Working at Pharmaron
Pharmaron's 26 open roles are across all levels, and about 8% are remote or hybrid. The most active teams are biotech & life sciences, laboratory research, and maintenance & repair. Pharmaron provides contract research, development, and manufacturing services to pharmaceutical and biotechnology companies, supporting programs across analytical chemistry, process chemistry, preclinical sciences, and life sciences manufacturing. Most Pharmaron roles are based in Coventry, with some in Baltimore and Exton.
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Browse jobs by rolePharmaron Jobs: Frequently Asked Questions
How many jobs is Pharmaron hiring for right now?
Pharmaron is hiring for 26 open roles on Migrate Mate as of August 31, 2026, updated daily, concentrated in biotech & life sciences and laboratory research. Roles span scientific, technical, and operational functions including chemistry, preclinical research, quality control, facilities, and procurement.
What kinds of roles does Pharmaron hire for?
The most active teams are biotech & life sciences, laboratory research, and maintenance & repair. Pharmaron hires scientists, researchers, and technical specialists across process chemistry, analytical chemistry, and preclinical sciences, as well as maintenance technicians, procurement specialists, facilities managers, and finance staff. Most postings are across all levels, ranging from associate-level researchers to principal scientists and investigators.
Are Pharmaron jobs remote or in-person?
Mostly on-site. About 8% of Pharmaron's open roles on Migrate Mate are remote or hybrid as of August 31, 2026, with the rest based in Coventry. Each Pharmaron listing shows its work location so you can filter before applying.
How do I apply to a job at Pharmaron?
Find a Pharmaron role on Migrate Mate, then follow the listing through to Pharmaron's own careers page to complete the application. Pharmaron manages its own hiring process directly, including screening, interviews, and offers. Migrate Mate keeps Pharmaron's openings current so you can browse what is actively available before applying.
What do Pharmaron jobs pay?
Listed salaries for Pharmaron roles on Migrate Mate range from about $55,000 to $170,000 per year as of August 31, 2026, with most postings at across all levels. Some roles list hourly contract rates. Exact pay is set by Pharmaron and shown on each listing.
Does Pharmaron hire entry-level?
Most of Pharmaron's open roles on Migrate Mate are across all levels as of August 31, 2026. Check individual Pharmaron listings for stated experience requirements.
Where is Pharmaron hiring?
Most Pharmaron roles are based in Coventry, with some in Baltimore and Exton, and about 8% offer remote or hybrid work as of August 31, 2026. Migrate Mate shows the location on each listing.