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Granules

Vertically integrated API and dosage manufacturer

Lab Assistant - Stability Coordinator, Pharmaceutical Manufacturing

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeChantilly, VA, USA$19 - $22 /hrIn-person

About the Job

Requirements

  • An Associate’s degree is required; a Bachelor’s degree in pharmacy, chemistry, or a related scientific field is preferred.
  • Zero to two years of experience in a quality control laboratory.
  • Knowledge of equipment, supplies, components, and technical areas used in the pharmaceutical industry.
  • Ability to analyze data accurately.
  • Strong organizational skills and ability to complete duties in a timely manner.
  • Flexibility to handle multiple activities.
  • Computer skills and verbal and written communication skills.
  • Ability to work in a team environment.
  • Ability to work around powders and other chemicals and to wear protective eyewear in laboratory or manufacturing areas.
  • Experience in Good Manufacturing Practice (GMP) quality control and/or a pharmaceutical manufacturing facility is preferred.
  • Pharmaceutical stability operations experience is preferred.

Responsibilities

  • Comply with the requirements of the stability standard operating procedure.
  • Enter data and use stability software.
  • Review the stability program annually and recommend revisions when necessary.
  • Provide a stability summary to the Quality Control Director upon completion of a study.
  • Ensure stability samples are disposed of according to Good Manufacturing Practice guidelines.
  • Assist in preparing and maintaining batch records and certificates of analysis, and maintain, control, and file raw material and finished product specification records.
  • Ensure stability chambers and their monitoring systems perform within established requirements.
  • Perform multiple tasks in the proper sequence to achieve work goals and make clear, concise decisions in complex situations within limited timeframes.

Desired Qualifications

  • Knowledge of Food and Drug Administration guidelines on stability requirements is a plus.

About the Company

Granules

Vertically integrated API and dosage manufacturer

Granules India manufactures Active Pharmaceutical Ingredients, Pharmaceutical Formulation Intermediates, and Finished Dosages for customers in more than 80 countries, leveraging large-scale, cost-efficient production. Its vertical integration means it controls the production chain from base chemicals to final packaged medicines, while also marketing its own label products in the US via Granules Pharmaceuticals Inc. The company differentiates itself through a global manufacturing footprint, scale, and an integrated supply chain that supports both contract manufacturing and branded products, including advanced areas like MUPS, oncology, and peptide therapeutics. Its goal is to provide globally accessible, affordable medicines by maintaining secure supply and expanding capabilities in complex therapies, while pursuing sustainability through green chemistry and net-zero emissions.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Not listed
Founded
2014

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