What are the responsibilities and job description for the Other - Manufacturing Associate position at Infobahn SoftWorld Inc?
Job Description
Job Description
Job Title : Pharmaceutical Manufacturing Associate
Location : Andover, MA
Duration : 12 Months with possible extension
Overview :
Join Client's pharmaceutical manufacturing team, where your efforts will directly contribute to providing essential medicines to patients worldwide. As a key member of the team, you will play an important role in the cGMP production of phase I / II clinical drug substances, supporting the Biotherapeutics portfolio. Your expertise will ensure that medicines are delivered to patients and healthcare providers when they need them the most.
Key Responsibilities :
- Be an integral part of a multi-disciplinary team, focusing on mammalian bio-processing to support the production of clinical drug substances.
- Support manufacturing operations by reviewing and following Standard Operating Procedures (SOPs), batch records, and standard work.
- Collaborate with cross-functional teams, including tech transfer, quality, and engineering, to ensure seamless operations.
- Implement Current Good Manufacturing Practices (cGMP) and safe handling techniques for solid dosage processing within continuous manufacturing / PCMM work streams.
- Prioritize and manage workflows based on resource availability, ensuring tasks are completed accurately and efficiently.
- Participate in continuous improvement initiatives, including root cause analysis and troubleshooting.
- Assist with the generation, execution, and review of documentation related to solid dosage manufacturing, including batch records and in-process run sheets.
- Perform operator care tasks for the maintenance and operation of complex pharmaceutical manufacturing equipment.
- Take part in shift exchange activities and communication channels to ensure smooth transitions and operational success.
- Complete required training to participate in safety inspections within the facility and assist with safety protocols.
- Manage solution preparation and laboratory consumables, ensuring the proper handling and use of materials.
- Comply with Environmental, Health & Safety (EHS) policies and practices, contributing to reviews and implementation as needed.
- Coordinate the shipment of solutions and media to other sites to support ongoing operations.
Qualifications : Must-Have :
Nice-to-Have :
Physical / Mental Requirements :
Non-Standard Work Schedule / Travel Requirements :
