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Quality Control Chemistry Jobs in Washington (NOW HIRING)

Initiation of quality records (e.g. deviation, OOS/OOT). * Perform CAPA actions as assigned by ... Bachelors degree in Chemistry or other science-related discipline. * 1+ years of practical related ...

Perform other duties as needed EDUCATION AND EXPERIENCE: * BS degree in the Biological Sciences, Bioengineering, or Chemistry. * 7+ years of experience performing QC activities in the pharmaceutical ...

Define and maintain QC/QMP objectives, targets, processes and review new targets, plans, and ... Bachelor's degree in medical technology, chemistry, biology, or related science. * Four years ...

... chemistry, or related environments. * Working knowledge of Good Manufacturing Practices (GMPs), Good Laboratory Practices (GLPs), and food safety principles. * Understanding of quality control and ...

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Quality Control Chemistry information

What is quality control chemistry?

Quality Control Chemistry is a branch of chemistry focused on ensuring that products, especially in industries like pharmaceuticals, food, and manufacturing, meet quality and safety standards. Quality Control (QC) Chemists analyze raw materials, in-process samples, and finished products using a variety of analytical techniques to verify their composition and purity. Their work helps identify any deviations from regulatory or company standards, ensuring that products are safe and effective for consumers. QC Chemistry is crucial for compliance with government regulations and maintaining a company's reputation.

What are the key skills and qualifications needed to thrive as a quality control chemist, and why are they important?

To thrive as a Quality Control Chemist, you need a solid understanding of analytical chemistry, laboratory techniques, and a bachelor's degree in chemistry or a related field. Familiarity with instruments such as HPLC, GC, FTIR, and LIMS, as well as knowledge of GMP/GLP regulations, is typically required. Attention to detail, critical thinking, and effective communication are valuable soft skills that enhance accuracy and teamwork. These competencies are crucial for ensuring product quality, regulatory compliance, and reliable laboratory operations.

What are some common challenges faced in a quality control chemistry role, and how can they be addressed?

Quality Control Chemists often face challenges such as tight deadlines for product release, maintaining compliance with changing regulatory standards, and managing complex testing protocols. To address these, effective time management, continuous training on regulations, and strong attention to detail are essential. Additionally, collaborating with production and R&D teams helps resolve discrepancies quickly and ensures that quality standards are consistently met.

What is the difference between Quality Control Chemistry vs Quality Assurance Specialist?

AspectQuality Control ChemistryQuality Assurance Specialist
CertificationsOften requires a Bachelor's in Chemistry or related field, with certifications like ASQ CQE or similarSimilar certifications, with focus on process audits and compliance
Work EnvironmentLaboratory settings, testing labs, manufacturing plantsOffice-based, audits, documentation, and process review environments
Primary FocusTesting raw materials, in-process, and finished products for quality and complianceDeveloping, implementing, and maintaining quality systems and procedures
Industry UsageCommonly used in manufacturing, pharmaceuticals, and chemical industriesUsed across similar industries but with a broader focus on quality systems

While both roles aim to ensure product quality, Quality Control Chemistry focuses on laboratory testing and analysis, whereas Quality Assurance Specialists develop and oversee quality systems and processes to prevent defects.

How much do quality control chemistry chemists make in the US?

Quality control chemistry chemists in the US typically earn a median annual salary of around $60,000 to $70,000, with entry-level positions starting lower and experienced professionals earning higher wages. Salaries can vary based on education, certifications, industry, and location, and the role often involves analyzing samples, using laboratory instruments, and ensuring product quality.

How to become a quality control chemist?

To become a quality control chemist, typically a bachelor's degree in chemistry, biochemistry, or a related field is required. Gaining experience with laboratory techniques, quality assurance processes, and relevant certifications such as ASQ or Six Sigma can enhance job prospects. Strong attention to detail, analytical skills, and familiarity with laboratory instruments are essential for this role.

Is a Quality Control Chemistry a good job?

A Quality Control Chemistry position involves testing and analyzing products to ensure they meet quality standards, often requiring knowledge of laboratory techniques and regulatory compliance. It can offer stable employment with opportunities for advancement, especially in industries like pharmaceuticals and manufacturing. The role typically requires attention to detail, analytical skills, and sometimes certifications such as a bachelor's degree in chemistry or related fields.

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

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

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

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

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

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

Infographic showing various Quality Control Chemistry 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.

QC Chemist

Rockville, MD • On-site

Supernus Pharmaceuticals, Inc.
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago


Job description

Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. We currently have 8 products in the market that are making a real impact on patient outcomes.
Job Summary:
Responsible for performing testing pharmaceutical solid dosage forms for release and stability, primarily by dissolution, and HPLC; maintaining proper GMP documentation for logbooks and report writing as necessary.
Essential Duties & Responsibilities:
  • Initiation of quality records (e.g. deviation, OOS/OOT).
  • Perform CAPA actions as assigned by management.
  • Support senior staff members in their responsibilities and tasks.
  • Revise Standard Operating Procedures or Test Methods as needed.
  • Perform testing (including dissolution, spectroscopy, HPLC analysis, and visual inspection).
  • Maintain equipment logbooks in accordance with company guidelines designed to comply with cGMP.
  • Utilize laboratory data systems for acquiring and processing data (e.g. Empower, LIMS, etc).
  • Perform data management, data review and report writing assignments as needed.
  • Supports senior staff members in their responsibilities and tasks.
  • Maintain data within company data integrity standards.
  • Other duties as assigned.

Non-Essential Duties & Responsibilities:
  • Calibration of laboratory instruments.
  • Performing chemical inventories.
  • Serve as a backup for training activities to newer employees.

Supervisory Responsibilities:
  • N/A

Knowledge & Other Qualifications:
  • Bachelors degree in Chemistry or other science-related discipline.
  • 1+ years of practical related experience preferred.
  • Experience with HPLC and/or dissolution testing preferred.
  • Experience with GMPs, GCPs, and/or GLPs is preferred.
  • Experience with a Quality Management system is preferred.
  • Ability to understand and follow written procedures.
  • Computer literate with proficiency of Microsoft Office package including Word, Outlook, and Excel.
  • Knowledge of Good Documentation Practices and ALCOA+.
  • Detail oriented, strong laboratory documentation skills.
  • Strong communication and technical writing skills in English language.
  • Ability to accept personal accountability for successful job performance.
  • Ability to work efficiently and accurately to meet set goals and timelines, and ability to pay attention to detail.
  • Ability to work in a fast paced and flexible work environment where priorities can change.

Other Characteristics:
  • Ability to work independently and as part of a team and maintain high ethical standards of integrity and quality.
  • Ability of having an innovative and dynamic approach to work.
  • A self-starter able to work independently but comfortable working in a team environment.
  • Ability to consistently exhibit Supernus Values in interactions with employees at all levels of the organization, vendors, customers, and others.
  • Capable of performing other duties as assigned by Management.
  • Authorized to legally work in the United States without visa sponsorship.

Physical Requirements/Work Environment/Travel Requirements:
  • Sedentary work. Exerting up to 10 pounds of force occasionally and/or carry objects. Sedentary work involves sitting most of the time.
  • The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer screen, iPad, or other electronic device; and extensive reading.
  • The worker is not substantially exposed to adverse environmental conditions.
  • Will be required to work in a clean and/or sterile laboratory environment occasionally and wear personal protective equipment to include but not limited to: gloves, safety glasses or goggles, face shields, lab coats, aprons, ear plugs and mask to include respirators.

Compensation:
At Supernus, we offer a competitive compensation package that reflects your experiences and contributions. The expected salary range for fully qualified candidates applying for this role is $50,000 to $60,000. This range is what the Company reasonably expects to offer for the position and is not reflective of the full compensation scale of the role. This range may be modified in the future. An individual's salary within the range is based on multiple factors, which may include and are not limited to education, relevant experience, knowledge, length of industry experience and organizational needs.
You also will be able to participate in a competitive benefits package, including but not limited to: health, dental, vision, paid time off, 401k company match, company paid life insurance and health and wellness benefits. The total compensation package for this position also includes other compensation elements such as stock equity awards, employee stock purchase programs and participation in our Company's discretionary annual bonus program.
Supernus Pharmaceuticals is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.