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Ppd Scientist Jobs (NOW HIRING)

Data Scientist

Renton, WA · On-site

$104.10 - $146.63/hr

Data Scientist Company: PACCAR Requisition Summary As a Data Scientist you'll support the growth of ... to shape PPD's current business and long‑term analytics strategy. Job Functions ...

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Ppd Scientist information

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$37K

$91K

$160K

How much do ppd scientist jobs pay per year?

As of Aug 20, 2026, the average yearly pay for ppd scientist in the United States is $90,961.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $100,000.00 per year, depending on experience, location, and employer.

What is a PPD scientist?

PPD Scientists are professionals who work in Pharmaceutical Product Development (PPD), focusing on research, development, and testing of new drugs and therapies. They are involved in designing studies, analyzing data, and ensuring that products meet regulatory and quality standards. PPD Scientists play a critical role in bringing safe and effective pharmaceutical products to market, collaborating with clinicians, regulatory specialists, and manufacturing teams throughout the development process.

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

To thrive as a PPD Scientist, you need a strong background in analytical chemistry, biology, or a related scientific field, typically supported by a relevant degree and laboratory experience. Familiarity with laboratory instrumentation (such as HPLC, GC, and mass spectrometry), data analysis software, and compliance with regulatory standards (e.g., GMP, GLP) is essential. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities set successful candidates apart. These skills ensure accurate data generation, compliance with industry regulations, and efficient collaboration within product development teams.

What are some typical challenges a PPD scientist faces when working on new pharmaceutical formulations?

A PPD Scientist often encounters challenges such as optimizing formulations for stability and efficacy while meeting regulatory requirements and tight project timelines. Balancing the need for innovative solutions with cost-effectiveness is also common, as is troubleshooting unexpected results during analytical or scale-up phases. Collaboration with cross-functional teams, including analytical chemists, regulatory affairs, and manufacturing, is essential to address these obstacles efficiently and ensure successful product development.

What is the difference between Ppd Scientist vs Pharmacovigilance Scientist?

AspectPpd ScientistPharmacovigilance Scientist
Required CredentialsBachelor's or Master's in Life Sciences, Pharmacology, or related fields; often requires certification in pharmacovigilanceSimilar educational background; certifications like PV or drug safety are common
Work EnvironmentResearch labs, clinical trial settings, pharmaceutical companiesRegulatory agencies, pharmaceutical companies, CROs
Industry UsageFocuses on drug development, safety data analysis, and clinical researchMonitoring, assessing, and reporting adverse drug reactions and safety signals

Both roles involve drug safety and require similar educational backgrounds and certifications. However, Ppd Scientists typically focus on clinical trial data analysis, while Pharmacovigilance Scientists concentrate on post-market safety monitoring and regulatory reporting. The roles often overlap but differ mainly in their specific focus within the drug safety spectrum.

More about Ppd Scientist jobs

What cities are hiring for Ppd Scientist jobs?

Cities with the most Ppd Scientist job openings:

What states have the most Ppd Scientist jobs?

States with the most job openings for Ppd Scientist jobs include:

Infographic showing various Ppd Scientist job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $90,961 per year, or $43.7 per hour.

Senior Scientist - GMP Laboratory

Thermo Fisher Scientific

Middleton, WI • On-site

$91K - $125K/yr

Full-time

Posted 22 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 427 frontline employees who took The Breakroom Quiz

199th of 542 rated manufacturers


Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
Position: Senior Scientist
Location: Middleton, Wisconsin
Details: Fully Onsite; Full-Time
This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.
Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
Discover Impactful Work:
The Senior Scientist independently performs complex laboratory testing and provides hands-on technical coaching and mentorship within the laboratory. This role is focused on being an in-lab proven contributor who actively executes, troubleshoots, and improves testing activities while developing in-depth subject matter expertise in assigned methods, assays, or analytical platforms.
A Senior Scientist may operate either as a non-routine technical contributor for method development, transfer, or validation activities or as a key technical resources for complex or priority routine testing. In all cases, the Senior Scientist remains directly involved in laboratory execution and testing oversight, owns non-routine technical deliverables within defined scope, and mentors Scientist I and II staff to ensure high-quality, consistent laboratory performance.
This role serves as a senior technical contributor and escalation resource within the laboratory. The Senior Scientist is responsible for the quality and technical accuracy of assigned deliverables (data, reports, methods, and protocols) but does not own overall program delivery, routine study management, or primary technical client communication. Client interaction may occur for method-specific technical discussions but does not include ownership of broader client relationships or project coordination. Scientific decisions that impact method lifecycle, validation strategy, or broader testing models are escalated to Staff Scientist + for approval. This role is distinct from a Study Lead and does not own routine study/program management, project coordination, or primary client-facing responsibilities.
A day in the Life:
  • Independently performs complex laboratory testing, including challenging routine testing, analytical investigation support, development, transfer, or validation activities.
  • Communicates analytical needs, resources, and/or barriers with relevant stakeholders.
  • Maintains a strong hands-on laboratory presence and serves as a technical resource during test execution.
  • Actively assists with testing execution, troubleshooting, and optimization rather than directing work from outside the lab.
  • Applies advanced scientific judgment to execution strategy, data interpretation, and problem resolution.
  • Develops and maintains subject matter expertise in one or more analytical methods, assays, or platform technologies.
  • Serves as a technical escalation point for execution level testing issues encountered during routine (release, stability, quality control) or non-routine (development, transfer, validation) work.
  • Identifies method, execution, or workflow improvements that enhance data quality and downstream routine testing robustness.
  • May independently execute or technically lead defined components of method development, transfer, or validation work.
  • Authors and/or reviews non-routine technical deliverables such as methods, protocols, reports, and quality records.
  • Supports transition of improved or newly established methods into routine testing by strengthening clarity, robustness, and usability.
  • Acts as a key in-lab technical resource for complex or escalated routine testing.
  • Assists analysts with execution strategy, atypical results, and troubleshooting for established methods.
  • Supports quality management through hands-on data review and root cause analysis.
  • Trains, mentors, and equips Scientist I and II staff through direct laboratory involvement and technical coaching.
  • Reinforces best practices through example and active participation in testing activities.

Keys to Success:
Education
  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Experience
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years' experience) or equivalent combination of education, training, & experience.

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills, Abilities
  • Previous GMP Laboratory experience strongly preferred
  • Previous experience with HPLC, CE, iCE, or ELISA strongly preferred
  • Previous experience with cell culture, mammalian cell culture, flow cytometry, PCR, ELISA, or cell-based bioassays strongly preferred
  • Previous experience with method troubleshooting, optimization, and/or validation preferred
  • Advanced knowledge of analytical testing techniques, laboratory instrumentation, and method execution in a regulated environment.
  • Demonstrated ability to independently execute complex testing, investigations, and non-routine laboratory activities.
  • Strong troubleshooting, problem-solving, and critical thinking skills, with the ability to identify analytical challenges at the source and implement effective solutions.
  • Proven ability to develop and maintain subject matter expertise in assigned methods, assays, or analytical platforms.
  • Versed in data analysis with the ability to identify trends, outliers, and atypical results.
  • Strong attention to detail and commitment to data integrity, quality, and accuracy.
  • Working knowledge of GMP requirements and data integrity principles.
  • Excellent organizational skills with the ability to adapt to changing priorities
  • while maintaining focus, composure, and productivity.
  • Ability to prioritize and execute multiple assignments with challenging or conflicting deadlines in a dynamic laboratory environment.
  • Ability to mentor and technically develop scientific staff through hands-on guidance and knowledge transfer.
  • Strong written and verbal communication skills, particularly for technical documentation and scientific discussion.
  • Demonstrated ability to work collaboratively, maintain a positive attitude, and contribute effectively within a team environment.
  • Demonstrated experience in identifying and resolving conflicts in a professional and constructive manner.
  • Ability to maintain a high degree of confidentiality with client information and data.
  • Proficiency with Microsoft Office applications (e.g., Word, Excel, Power BI, PowerPoint, Teams, SharePoint).
  • Familiarity with data collection and laboratory software used to support analytical testing.
  • Demonstrated ability to receive, apply, and act on constructive feedback to continuously improve performance.
  • Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

Work Environment
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
  • Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
  • Able to work upright and stationary and/or standing for typical working hours.
  • Able to lift and move objects up to 25 pounds.
  • Able to work in non-traditional work environments.
  • Able to use and learn standard office equipment and technology with proficiency.
  • May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
  • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Accessibility/Disability Access
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.
*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

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