1

Quality Control Pharma Jobs in Washington (NOW HIRING)

Quality Control Data Reviewer I Salary Range : $68,000- 75,000 Location : Germantown, MD About ... pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide ...

Quality Control Data Reviewer I Salary Range : $68,000- 75,000 Location : Germantown, MD About ... pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide ...

Quality Control Data Reviewer I Salary Range : $68,000- 75,000 Location : Germantown, MD About ... pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide ...

... fastest growing generic pharma company in the US! With our sites in Chantilly and Manassas ... Quality Control within a Pharmaceutical Manufacturing company. Skills Requirements: Working ...

Biochemist

Chantilly, VA ยท On-site

$69K - $73K/yr

... fastest growing generic pharma company in the US! With our sites in Chantilly and Manassas ... Quality Control within a Pharmaceutical Manufacturing company. Skills Requirements: Working ...

Biochemist

Chantilly, VA ยท On-site

$69K - $73K/yr

... fastest growing generic pharma company in the US! With our sites in Chantilly and Manassas ... Quality Control within a Pharmaceutical Manufacturing company. Skills Requirements: Working ...

next page

Showing results 1-20

Quality Control Pharma information

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

Is Quality Control Pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It requires attention to detail, knowledge of laboratory techniques, and often involves certifications such as GMP training. The role offers stable employment opportunities in the pharmaceutical industry with potential for career advancement.

What are popular job titles related to Quality Control Pharma jobs in Washington?

For Quality Control Pharma jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Quality Control Pharma jobs in Washington look for?

The top searched job categories for Quality Control Pharma jobs in Washington are:

What cities in Washington are hiring for Quality Control Pharma jobs?

Cities in Washington with the most Quality Control Pharma job openings:

Infographic showing various Quality Control Pharma job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 10% Part Time, 2% Temporary, 8% Contract, and 1% Nights. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution.

Quality Control Data Reviewer I

Pharmaron

Germantown, MD โ€ข On-site

$68K - $75K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Job description

Position: Quality Control Data Reviewer I
Salary Range: $68,000- 75,000
Location: Germantown, MD
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
  • Perform comprehensive quality review of bioanalytical assay data for accuracy, completeness, data integrity, and compliance with GLP/GCP requirements, study protocols, SOPs, and client expectations.
  • Review datasets generated from method development, method validation, and sample analysis studies.
  • Review study reports, protocols, protocol amendments, and supporting documentation for accuracy and compliance.
  • Review sample management documentation and verify samples are appropriately documented and stored in LIMS.
  • Review laboratory equipment calibration records, logbooks, and other quality documentation.
  • Ensure laboratory records and documentation accurately reflect actual laboratory activities and events.
  • Work closely with analysts and scientific staff to investigate and resolve data discrepancies, sample management questions, and documentation issues.
  • Maintain accurate QC review records in accordance with SOPs and quality best practices.
  • Initiate and coordinate quality events in TrackWise with Lead Scientists.
  • Communicate with management and internal departments regarding data review findings and study status.
  • Support the development and revision of SOPs, work instructions, methods, study plans, and training materials.
  • Assist with training and mentoring team members as appropriate to experience level and qualification.
  • Track QC metrics, identify recurring errors or trends, and contribute to continuous improvement initiatives that enhance quality and efficiency.
  • Support internal and external audits and maintain awareness of applicable regulatory requirements and industry best practices.
  • Complete required training within established timelines and maintain compliance with laboratory safety policies.
What We're Looking For
  • Bachelor's degree in a relevant scientific field.
  • QC Data Reviewer I: Some laboratory or quality experience.
  • QC Data Reviewer II: 2+ years of relevant quality experience.
  • QC Data Reviewer III: 5+ years of relevant quality experience.
  • Experience working in a Quality Control or Quality Assurance capacity within a bioanalytical laboratory preferred.
  • Experience working in a regulated laboratory environment.
  • Knowledge of GLP, GCP, 21 CFR Part 11, 21 CFR Part 58, and ICH guidelines.
  • Strong attention to detail, organizational skills, critical thinking, and problem-solving abilities.
  • Strong written and verbal communication skills.
  • Strong computer skills, particularly Microsoft Word and Excel, including intermediate to advanced knowledge of Excel formulas and functions.
  • Experience with LIMS, laboratory/instrument software, and quality management systems preferred.
  • Experience with TrackWise or similar quality systems preferred.
  • Experience with project management tools such as Smartsheet preferred.
  • Ability to work independently while collaborating effectively with scientists, analysts, and cross-functional teams.
  • For senior-level roles, demonstrated ability to handle complex data-review issues, mentor team members, support process improvements, and represent the QC function during audits.
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.
#LI-PR1