Qualifications
- Qualified candidates will possess a Bachelor’s degree in scientific or engineering discipline along with 3-5 years related industry experience.
- Proficient in Microsoft Word, Excel, Power Point and Project.
- General knowledge of quality system elements and cGMP regulations.
- Experience providing support to clients with quality issues such as OOS results, deviations and non-conformances arise.
- Ability to write and revise Standard Operating Procedures.
- Effective written and oral communication skills; ability to write, type, express or exchange ideas; ability to convey information/instructions accurately.
- Carry out duties and responsibilities with limited supervision.
- Flexibility to work occasional weekends and evenings.
- Ability to walk, stand and move about for long periods of time; work with equipment in the field including basic hand tools, lift and manipulate reasonable weights (approximately 35 lbs.), ability to sit and type for long periods of time.
- Ability to plan and manage own work
Additional Information
All candidates must be legally eligible to work in the United States.
We are an equal opportunity employer. M/F/D/V
ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.