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Primary Responsibilities:
- Work in a cGMP environment to aid the peptide purification processes through solution preparation and preparative chromatography.
- Understand the metric system to perform calculations.
- Work with preparative scale chromatography.
- Collaborate with a team to complete specific projects in a timely manner.
- Follow approved cGMP manufacturing directions such as production batch records, SOPs, and test procedures.
- Perform scheduled clean room activities as per SOPs.
- Manage time effectively to perform daily tasks promptly, enhancing productivity and minimizing idle time.
- Willingness to work shifts and weekends as necessary.
- Responsibilities may adapt based on business needs and organizational changes.
Qualifications:
- Associate degree in sciences or at least 1 year of relevant laboratory experience.
ADA-Conditions of Employment:
- Ability to push, pull, squat, stand, sit, and walk throughout the day.
- Ability to lift up to 80 lbs.
- Wearing safety shoes and glasses in designated areas (provided by the company).
- Physician clearance to wear a respirator in designated areas.
- Ability to work in a chemical environment.
Additional Details:
- Role is 2nd shift only (4:30PM - 3:30AM).
- Entry-level candidates with lab experience or an associate degree are encouraged to apply.
- Employment type: Full-time.
- Industry: Pharmaceutical Manufacturing.
- Job function: Engineering and IT.
- Seniority level: Entry level.