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Alcami

Pharmaceutical and biologics CDMO services

Scientist 2 - Analytical Testing

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeDurham, NC, USANo salary listed

About the Job

Requirements

  • A Master’s degree in Chemistry or a similar field with 0 or more years of related experience, or a Bachelor’s degree in Chemistry or a similar field with at least 4 years of related experience, or an Associate’s degree in Chemistry or a related field with at least 10 years of related experience.
  • Demonstrated hands-on experience with high-performance liquid chromatography (HPLC).
  • Excellent verbal and written communication and documentation skills.
  • Strong attention to detail and organizational skills.
  • Problem-solving and basic troubleshooting ability.
  • Basic knowledge of laboratory equipment and safety.
  • Basic knowledge of laboratory documentation.
  • Proficiency with Microsoft Word, Excel, and PowerPoint.
  • Ability to apply job skills, company policies, and standard operating procedures to complete a variety of tasks.
  • Ability to safely handle potent compounds and comply with required training, including initial and annual Resource Conservation and Recovery Act (RCRA) hazardous-waste training.
  • Ability to meet the physical demands of the role, including regularly lifting or moving up to 10 pounds, frequently up to 25 pounds, and occasionally up to 50 pounds, and to use required personal protective equipment.

Responsibilities

  • Perform routine and non-routine analytical testing in support of pharmaceutical product development or manufacturing, and may work on method development or validation projects.
  • Develop analytical methods for analysis using HPLC, dissolution, gas chromatography (GC), ultraviolet (UV), and/or Karl Fischer (KF) techniques.
  • Perform techniques such as residual-solvent testing, potency and related-substance assays, dissolution, elemental-impurity testing, moisture-content measurement, identification, and other wet-chemistry measurements.
  • Evaluate and interpret generated data and assess information for technical correctness and accuracy.
  • Understand the theoretical basis of methods and experiments and solve problems requiring evaluation of identifiable factors in data.
  • Write test procedures, protocols, and reports.
  • Maintain working knowledge of the instrumentation, equipment, and scientific methodologies needed for assigned tasks.
  • Assist with hazardous-waste removal, routine equipment cleaning, and restocking consumables and reagents.
  • Use laboratory software packages such as Empower3, ProCal, MasterControl, and electronic laboratory notebooks.
  • Maintain a safe, clean, and organized work environment; safely handle potent compounds.
  • Supervise, handle, or process hazardous waste in accordance with applicable Resource Conservation and Recovery Act guidelines and training requirements, including familiarity with emergency response procedures, equipment, and systems.
  • Complete required company training on time and comply with current Good Manufacturing Practices (cGMP) and other applicable requirements.
  • Perform other assigned duties.
  • Work on-site Monday through Friday, 8:00 a.m. to 5:00 p.m., and travel up to 5% as required.

Desired Qualifications

  • Prior laboratory or work experience in pharmaceutical, contract development and manufacturing organization (CDMO), or cGMP settings.
  • Working knowledge of cGMP in a pharmaceutical or regulated environment.

About the Company

Alcami

Pharmaceutical and biologics CDMO services

Alcami is a contract development and manufacturing organization supporting pharmaceutical and biologics companies from early development through commercial production. Services span drug product manufacturing (sterile fill-finish and oral solid dose), analytical and microbiology lab testing, and cGMP storage with validation and environmental monitoring. What sets Alcami apart is its integrated, end-to-end capabilities across the development lifecycle. The goal is to help pharma and biotech partners deliver safe, high-quality therapies to patients.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Pepperell, MA
Founded
1984

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