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Job Description
Target Pay Rate: $40-48.76/hr — salary will be commensurate with experience.
- Solid understanding of pharmaceutical operations within API (cell culture and purification), FPM (fill/finish, packaging), QC (environmental and product monitoring and sampling, assays, specification setting), Supply Chain and Warehouse Management, Validation, and Quality Systems (Deviation and CAPA management, Change Control, Audit & Observation management, Risk Management, etc.).
- Expertise in cGMP and regulatory requirements (FDA, EMEA, ICH, etc.).
- Excellent written, verbal, and presentation skills with the ability to adjust presentation style for various audiences.
- Builds partnerships internally.
- Ability to plan and prioritize complex daily activities, work under pressure, anticipate and assess risks, and proactively address issues.
- Demonstrates a Safety, Compliance, and Continuous Improvement mindset.
- Knowledge/experience with Microsoft Office Suite (Word, Excel, Outlook, PowerPoint, Teams), SAP, Dev@Com, ValGenesis, PharmDoss, and MES.
Work onsite involves review of documentation, archiving, and collaboration with MSAT partners on data trending.
Responsibilities include organizing work to meet department goals, contributing to team efforts, training staff, scheduling, and releasing Work Orders.
Requires 4-10 years of experience.
The Planet Group of Companies is an equal opportunity employer, celebrating diversity and fostering an inclusive environment.
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