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Quality Control Stability Jobs in Virginia (NOW HIRING)

Granules

Quality Control Manager

Chantilly, VA · On-site

$100K - $120K/yr

Supervise the testing of bulk release, finished product and stability testing * Manage and supervise QC laboratory personnel with varying levels of experience, assigning the work schedule and ensure ...

Klockner Pentaplast

QC Technician

Gordonsville, VA

$18.50/hr

The QC Technician utilizes standard operating procedures and specifications to evaluate products ... Determines dimensional stability by time and temperature in percent; Conducts any other specialized ...

Klöckner Pentaplast

QC Technician

Gordonsville, VA · On-site

$18.50/hr

The QC Technician utilizes standard operating procedures and specifications to evaluate products ... Determines dimensional stability by time and temperature in percent; Conducts any other specialized ...

Granules

Biochemist I/II (QC Analyst)

Chantilly, VA · On-site

$55K - $80K/yr

The role of Biochemist I/II (QC Analyst) is responsible for supporting the operations and ... stability samples, method development and/or transfers, and cleaning validations. Follows standard ...

Thermo Fisher Scientific

QC Technician II

Middletown, VA

$16.95 - $25.42/hr

Testing and documentation of raw materials, in-process, final kits, and stability samples on ... Minimum of 1 year of work experience in QA or QC or related field * Preferred: Experience in a cGMP ...

New

Prestige Brands

Quality Inspector

Lynchburg, VA · On-site

Responsibilities also include completion of documentation, stability program support, and issuance ... QC Lab. * Evaluate inspection results against established specifications. * Review physical ...

System Soft Technologies

Senior Service Engineer

Ashburn, VA · On-site

$106K - $146K/yr

Quality Assurance - Develop, implement, and maintain quality control processes and procedures to ... Servant leader who demonstrates integrity, reliability, and stability. * Focused and driven ...

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Quality Control Stability information

What career paths are possible in QC?

Career paths in Quality Control (QC) include roles such as QC Technician, QC Analyst, Quality Assurance Specialist, and Quality Manager. Advancement often involves gaining experience, certifications like ASQ certifications, and developing skills in inspection, testing, and data analysis within manufacturing, pharmaceuticals, or food industries.

What is the difference between Quality Control Stability vs Quality Control Inspector?

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

Which pays more, QA or QC?

In the field of Quality Control Stability, Quality Assurance (QA) roles generally offer higher salaries than Quality Control (QC) positions due to their broader responsibilities and focus on process improvement. QA jobs often require more experience and may involve certifications like Six Sigma or ISO standards, which can also influence pay. However, salaries vary based on industry, location, and level of experience.

What are some common challenges faced in a Quality Control Stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

What are the key skills and qualifications needed to thrive as a Quality Control Stability specialist, and why are they important?

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

What is a Quality Control Stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.

Is QC analyst a stressful job?

A QC analyst role involves inspecting and testing products to ensure quality standards are met, which can be demanding during tight deadlines or when addressing product issues. The job often requires attention to detail, adherence to safety protocols, and sometimes working in environments with strict regulatory requirements, which can contribute to stress levels.

What is quality control salary?

The salary for a quality control stability role typically ranges from $40,000 to $70,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced professionals with certifications can earn higher wages. Salaries often include benefits such as health insurance and paid time off.
What are the most commonly searched types of Quality Control Stability jobs in Virginia? The most popular types of Quality Control Stability jobs in Virginia are:
What are popular job titles related to Quality Control Stability jobs in Virginia? For Quality Control Stability jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability jobs in Virginia look for? The top searched job categories for Quality Control Stability jobs in Virginia are:
What cities in Virginia are hiring for Quality Control Stability jobs? Cities in Virginia with the most Quality Control Stability job openings:
Quality Control Stability jobs near you

QC Lab Tech (Stability Coordinator) (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA

$19 - $22/hr

Other

Re-posted 21 hours ago

Job description

Description


Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.

Job Summary:

Perform a variety of activities to administer the stability program and manage data generated in support of the company's quality program. 


Essential Responsibilities:


  • Comply with the requirements of stability standard operating procedure.
  • Data entry and usage of stability software.
  • Review stability program annually and recommend revision when necessary.
  • Provide stability summary to QC Director upon completion of study.
  • Assures that stability samples are disposed of according to GMP guidelines.
  • Will assist in preparing and maintaining batch records, certificate of analysis, maintain/control and file records of raw material specification and finished product specification.
  • Responsible for ensuring stability chambers and monitoring system are performing within set requirements. 
  • Employee uses professional skills and concepts to solve a variety of often complex situations. Able to make clear and concise decisions of vast importance in limited period of time. Must be able to perform multiple tasks in the proper sequence to effectively reach desired goals.


Requirements:


  • Minimum Associate's Degree, Bachelor's degree preferred in pharmacy, chemistry or related scientific field
  • 0-2 years' experience in Quality control laboratory.
  •  Knowledge of and ability to work with equipment, supplies, components and technical areas that are utilized in the    pharmaceutical industry.
  • Knowledge of FDA guidelines on Stability requirements is a plus;
  • Must be able to analyze data and work with a high degree of accuracy; 
  • Organized and able to perform duties in a timely manner; 
  • Must be flexible and able to handle multiple activities;
  • Must have excellent computer skills and verbal and written commutation skills.
  • Must be able to work in a team environment; team player.


Additional Preferred: 


  •  Experience in GMP quality control and/or pharmaceutical manufacturing facility; 
  • Pharmaceutical stability operations experience


Physical Conditions



Long periods of sitting, standing, walking, bending, stooping, reaching, and lifting. Will work around powders and other chemicals. Protective eyewear is necessary to wear in the laboratory or manufacturing.

Requirements


Preferred Knowledge & Skills:


  • Strong knowledge of the major analytical techniques: HPLC/UPLC, GC, dissolution, etc. FT-IR, FDA/ICH regulations.
  • Solid knowledge of FDA/ICH regulations.


Required Experience & Education:


  • BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Biotechnology or related field.
  • Minimum 2 - 5 years of experience in using analytical instrument techniques including HPLC/GC/FT-IR, UV-Vis, Dissolution Apparatus, Ovens/Auto Titrators/KF Titrator/Particle size analyzers/ Ion-Chromatography.


We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.



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