Manufacturing Associate
Job Responsibilities:
- Manage own time and professional development, be accountable for own results and begin to prioritize own workflow.
- Cross-functional communication with tech transfer team, quality and engineering as necessary.
- Implement {Current} Good Manufacturing Practices {part of GxP} procedures and safe handling techniques for solid dosage processing within the continuous manufacture /PCMM work stream.
- Ability to follow Standard Operating Procedures and work under minimal supervision.
- Identify and support continuous improvement initiatives and root cause analysis tools.
- Generate, assist and execute documentation associated with solid dosage manufacture, such as, working batch record documentation, in-process run sheets.
- Complete activities identified as Operator care tasks associated with the maintenance and operation of complex pharmaceutical manufacturing equipment.
- Actively participate in shift exchange activities and communication channels.
- Complete training to take part in safety inspections within the facility.
- Manage solution preparation and laboratory consumables.
- Understand and comply with the policies, procedures and working practices of Environment, Health & Safety and where necessary contribute to the review and implementation of the practices in the plant.
- Help to coordinate shipments of solutions and medias to other sites.
Skills:
- Demonstrated experience in a biotechnology manufacturing or laboratory environment
- Operational knowledge of computerized systems, Familiarity with Production Control Systems, Enterprise Resource Planning Systems and other business systems
- Maintains a safe work environment
- Demonstrated capability to work as a team member in a matrix development team
- Excellent oral and written communication skills
- Strong computer skills in Microsoft Office required, especially MS Word, MS Excel
Education/Experience:
- High School
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