Job Description
Job Description :
In this role, you will be responsible for:
1. MFG Documentation: Initiate and monitor manufacturing documentation including Guides, SOPs, Work Instructions and other document types
2. Recipe: Coordinates and/or Makes revisions to recipes, both in DCS and MES, including parameters, resource text (RTE text) and resource groups
3. Support of the manufacturing process(including on floor support as needed) and represents MFG in cross functional groups. This includes but is not limited to:
• Investigating & Troubleshooting discrepancies on the floor, idenimplemtning corrective actions
•Identifies improvement opportunities for MFG
Support scheduling of MFG by ensuring production schedule reflects actual process
4. Support Training of MFG staff by writing, editing or designing training materials
5. Supports small projects by working in cross functional teams to collect data, analyse data, and execute various action items against set timelines. May lead some small projects via cross functional teams
Qualifications
An understanding of the manufacturing process and its equipment, current regulations, and cGMP’s are needed to perform this position effectively
Education
Bachelor’s degree in Biotechnologies / Pharma or Engineering Degree in Pharma/ Biotechnologies preferred