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mallinckrodtpharmaceuticals1

mallinckrodtpharmaceuticals1

Quality Control Analyst

Company

mallinckrodtpharmaceuticals1

Role

Quality Control Analyst

Location

Madison, WI, us

Job type

Full-time

Found on Mokaru

92 months ago

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Salary

Not disclosed by employer

Job description

The Quality Control (QC) Analyst will work both independently and within a team to perform daily analysis of in-process samples, finished product and raw materials via established test methods while following cGMP and GDP in the QC laboratory.  Typical analysis consists of pH, Osmolality, ELISA, PCR, sterility, UV/Vis spectroscopy and other general chemical and bioanalytical assays.

Principal Responsibilities

  • Conducts routine analysis of in-process samples, finished products, and raw materials according to standard operating procedures (SOPs) and Master Specifications.
  • Utilizes proper aseptic technique during the execution of analysis.
  • Performs stability testing according to established schedules.
  • Documents and investigates any OOS results.
  • Follows cGMP and GDP to perform all tasks.
  • Documents and assesses data against established specifications.
  • Perform inventory, stock and clean QC laboratories.
  • Perform QC review of data records.

Department specific/Non-essential responsibilities:

  • Assist with calibrating and maintaining laboratory equipment.
  • May perform training of new and existing QC team on established methods and procedures
  • May provide technical expertise for method optimization, verification, qualification, and validation.
  • May develop and qualify testing methods and SOPs.
  • May assist with or lead QC projects for process improvements.
  • May draft reports, plans and protocols.
  • May revise and updates SOPs.
  • Additional duties as assigned.

Experience / Skills:

  • Bachelor’s degree in a scientific discipline or equivalent and a minimum of three years’ related experience required.
  • Knowledge of cGMP is required.
  • Must possess skills and knowledge of general chemical and bioanalytical test methods.
  • Knowledge of ELISA, PCR, UV/Vis spectroscopy, cell culture and aseptic technique is preferred.

Competencies:

  • Attention to detail: able to organize and maintain data and information.
  • Ability to work in a controlled environment with gowning/PPE requirements.
  • Ability to learn through observation and hand’s on experience.
  • Ability to work independently in a fast-paced, team oriented organization.
  • Strong written and verbal communication skills.

Organizational Relationship/Scope:

  • Reports to Quality Control leadership team.
  • Work is performed within a team of QC Analysts.
  • Regular communication with QC, manufacturing, technical operations among others.

Working Conditions:

  • 70% laboratory and manufacturing environment
  • 30% normal office and meeting room conditions
  • Must be able to perform work while aseptically gowned with the appropriate PPE

All your information will be kept confidential according to EEO guidelines.

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