Manufacturing Associate I-OSD 1st Shift

AlkermesWilmington, OH
Onsite

About The Position

This entry-level position involves working with a small team in a GMP environment to manufacture commercial and/or clinical-scale batches. The hours for this position are Monday to Friday 7:30a to 4:00p.

Requirements

  • High School diploma or equivalent
  • Basic knowledge of the Scientific Method
  • Basic math skills including addition, subtraction, multiplication, division, and percentages
  • Basic knowledge of and adherence to current GMPs and GDPs
  • Basic knowledge of chemistry and biology
  • Basic knowledge of HAZCOM, RCRA, and other Safety requirements
  • Basic level of mechanical aptitude
  • Good documentation skills
  • Ability to learn how to operate all types of production equipment (i.e. Blenders, HMIs, Tablet presses, Coaters, Wash off lines, Comils, etc.)
  • Ability to read, understand, and accurately follow company SOPs and guidelines
  • Basic knowledge of computer systems (Microsoft Suite, SAP, Veeva Vault, LMS)
  • Understanding and comprehension of Master Batch Records
  • Detail-oriented
  • Willingness to learn new tasks and skills
  • Ability to work well in a team environment
  • Ability to respond quickly and execute assignments
  • Willingness to readily adapt to changing job duties
  • Positive attitude
  • Understanding of and promotion of company and customer objectives
  • Ability to follow all procedures to ensure a high-quality product
  • Ability to push and/or pull equipment or product using a pallet jack
  • Ability to lift/move 40 lbs. overhead.
  • Ability to properly gown and don PAPR for potent controlled substance formulations for extended periods of time
  • Must be able to be medically cleared for respirator use (PAPR)
  • Ability to operate different types of production equipment.
  • Ability to gown correctly for clean room manufacturing operations.
  • Ability to stand or sit for extended periods (up to 4 hours at a time).
  • Must be able to work in an office and a manufacturing environment.

Nice To Haves

  • 0-1 years of experience in a pharmaceutical manufacturing operation, preferably in OSD
  • A bachelor's degree is preferred; other relevant work experience, education, and training will be considered.

Responsibilities

  • Production, bulk packaging, and inspection of pharmaceutical drug formulations
  • Assisting with facility cleaning and operational maintenance
  • Cleaning all manufacturing equipment and areas
  • Assisting with facility and process validations as required
  • Assisting with environmental and water system monitoring as required
  • Assisting with RCRA and safety inspections as required
  • Documenting all work as required by cGMPs and GDPs on a timely basis
  • Reading and following all Company SOPs and guidelines
  • Abiding by all safety requirements as defined by the company
  • Completing other tasks as assigned by supervision
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