Description:
Key Responsibilities:
Perform analytical testing on OSD products following GMP standards.
Support method verification, transfer, and validation activities.
Ensure accurate documentation and data integrity in lab records.
Assist with instrument calibration and troubleshooting.
Collaborate with cross-functional teams to support ongoing lab operations.
⚙️ Skills & Qualifications:
Bachelor’s degree in Chemistry, Biochemistry, or a related field.
1–4 years of hands-on QC laboratory experience (pharma or CDMO preferred).
Strong understanding of GMP and analytical techniques (HPLC, GC, dissolution, etc.).
Excellent attention to detail and documentation practices.
Ability to work onsite and in a team-oriented environment.
| Organization | United Pharma |
| Industry | Other Jobs Jobs |
| Occupational Category | Chemist |
| Job Location | Dayton,USA |
| Shift Type | Morning |
| Job Type | Full Time |
| Gender | No Preference |
| Career Level | Intermediate |
| Experience | 1 Year |
| Posted at | 2025-11-03 9:19 am |
| Expires on | 2026-03-06 |