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Per Diem Analytical Method Development Jobs in Rhode Island

Pharmaron

Scientist II, Analytical Chemistry

Coventry, RI · On-site

$90K - $120K/yr

What You'll Do The Scientist II will support process chemistry and manufacturing activities through analytical method development, validation, transfer, and sample testing in compliance with all ...

Pharmaron

Scientist II, Analytical Chemistry

Coventry, RI · On-site

$90K - $120K/yr

What You'll DoThe Scientist II will support process chemistry and manufacturing activities through analytical method development, validation, transfer, and sample testing in compliance with all ...

Pharmaron

Scientist II, Analytical Chemistry

Coventry, RI · On-site

$90K - $120K/yr

What You'll Do The Scientist II will support process chemistry and manufacturing activities through analytical method development, validation, transfer, and sample testing in compliance with all ...

Brownhealth

Per Diem BHS II

Riverside, RI · On-site

$19.97 - $32.96/hr

... development stages and cultural patterns in each step of the care process.Bradley Hospital Safety ... approved methods only, to maintain safety for extended periods of time. Specifically, such ...

Rehab Alliance

Physical Therapist - Per Diem

Woonsocket, RI · On-site

$1.5K - $2.0K/wk

Per Diem Setting: Skilled Nursing Facility | Long-Term Care Exciting opportunity with Rehab ... Join a leading therapy organization with 30+ years of excellence in care and team development. Why ...

Tier1usa

Physical Therapist - Per Diem

North Kingstown, RI · On-site

$1.6K - $2.0K/wk

Join a leading therapy organization with 30+ years of excellence in care and team development. Why ... Per Diem to join their client's in-house therapy program. Just as you're committed to delivering ...

Rehab Advisors

Physical Therapist - Per Diem

Woonsocket, RI

$1.5K - $2.0K/wk

Join a leading therapy organization with 30+ years of excellence in care and team development. Why ... Per Diem to join their client's in-house therapy program. Just as you're committed to delivering ...

RehabAdvisors.org

Physical Therapist - Per Diem

Woonsocket, RI · On-site

$1.5K - $2.0K/wk

Join a leading therapy organization with 30+ years of excellence in care and team development. Why ... Per Diem to join their client's in-house therapy program. Just as you're committed to delivering ...

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Per Diem Analytical Method Development information

What is the difference between Per Diem Analytical Method Development vs Per Diem Quality Control Analyst?

AspectPer Diem Analytical Method DevelopmentPer Diem Quality Control Analyst
Primary RoleDevelops and validates analytical methods for testing pharmaceuticalsPerforms routine testing and analysis of pharmaceutical products
Work EnvironmentLaboratory focused on method creation and validationLaboratory conducting routine quality testing
Required CredentialsBachelor's degree in Chemistry or related field; experience in method developmentBachelor's degree in Chemistry or related field; experience in quality testing

Per Diem Analytical Method Development specialists focus on creating and validating new analytical methods, while Per Diem Quality Control Analysts perform routine testing to ensure product quality. Both roles require similar educational backgrounds but differ in their primary responsibilities and work focus.

Per Diem Analytical Method Development jobs near you
Infographic showing various Per Diem Analytical Method Development job openings in Rhode Island as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution.

Scientist II, Analytical Chemistry

Coventry, RI • On-site

Pharmaron
Chemical Manufacturing • 10K+ employees
Learn more about Pharmaronexternal

$90K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 hours ago

Job description

Position: Scientist II, Analytical Chemistry
Salary Range: $90,000 - $120,000/yr.
Location: Coventry, RI (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 .
What You'll Do
The Scientist II will support process chemistry and manufacturing activities through analytical method development, validation, transfer, and sample testing in compliance with all applicable guidelines. Will also solve moderate complexity analytical development issues for assigned projects and/or initiatives.
Key Responsibilities
  • Demonstrate expertise in the core analytical laboratory skills, support development and/or scale up of chemical processes in assigned projects.
  • Demonstrate and apply sound understanding of the application of all available analytical tools and techniques.
  • Design and execute core experiments, interpret results, and plan additional experiments in a timely manner to solve assigned problems of moderate complexity. More complex problems will require additional guidance from a scientific supervisor/line manager.
  • Review experimental data, notebooks, and instrument qualification protocols/reports.
  • Support client projects as an individual contributor and as an analytical project leader: performing analyses, reporting results, trending and presenting data at project meetings, delegating work, being accountable for project deliverables and demonstrating leadership behaviors. In addition, may supervise one or more individual contributors and oversee their technical progress.
  • System ownership of equipment and instrumentation, including supporting qualification activities. Participate in software validation.
  • Support departmental or site audits, as required.
  • Follow all policies governing the business activities, key internal business practices, and external regulations governing the role.
  • Maintain good laboratory practices and GMP in compliance with safety and environmental requirements.
  • Write, revise, develop, and evaluate SOPs.
  • Perform other related assignments and duties, as required and assigned.

What We're Looking For
  • D. in Chemistry or related field with no industry experience
  • MS with 3+ years of experience or BS with 5 years of experience in pharmaceutical industry.
  • Evidence of experience in successful application of analytical skill sets to resolve scientific problems related to method design, development, and/or implementation.
  • Experienced troubleshooter of technical problems
  • 3 years of experience (may include Ph.D. experience) with core analytical instrumentation such as HPLC, GC, FTIR, UV, Mass Spectrometry.
  • Evidence of ability to effectively contribute to multi-disciplinary scientific teams
  • Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance
  • Evidence of ability to effectively scientifically supervise staff
  • Expert application of core laboratory techniques and instrumentation to impact API, intermediates and starting materials

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, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent 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.
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