BioProcess Associate

Overview

Support large‑scale biopharma manufacturing operations, validation and process improvement.

Key Responsibilities

• process execution
• equipment operation
• batch review
• procedure documentation
• process optimization
• project validation

Tasks

-Execution of commercial manufacturing processes according to established work instructions. -Operates all production equipment within the assigned functional area -Assists with reviewing batch and exception reports for each manufacturing lot in conjunction with Quality representative and provide input to related investigations and QA audit activities. -Creation of operating procedures & other relevant documentation for large scale manufacturing -Engages in and supports culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and safe work environment. -Takes part in investigations and optimisations of processes using scientific, engineering and lean principles -Working with the manufacturing operations group, project design team, the CQV team, & the Automation/CSV reps to facilitate the implementation of the project design and validation of the MPCC manufacturing facility.

Requirements

• level 6
• cgmp
• delta v
• sap
• biopharma
• problem solving

What You Bring

-The successful candidate will ideally possess a minimum of Level 6 qualification in an Engineering/Science related discipline; however, relevant experience in a similar regulated industry will also be considered (e.g. cGMP, ISO or similar cleanroom industry experience strongly preferred) -The successful candidate must demonstrate an ability to work independently and also as part of a team. -Effectively uses process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.). -Excellent communication skills and the ability to work in a cross functional collaborative environment are required. -Adheres to Good Manufacturing Practices and Standard Operating Procedures. -Requires extensive working experience in a large-scale biopharmaceutical manufacturing facility -The successful candidate must demonstrate problem solving ability and to adhere to scheduled timelines.

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About Qcs Staffing

-Founded with the aim of providing top-tier staffing solutions for diverse sectors. -Focus on long-term partnerships with clients, ensuring the right talent for specialized roles. -Expert in recruiting for both large-scale projects and niche, high-demand sectors. -Has become a trusted partner in sectors such as Industrial, Energy, and Infrastructure. -Notable for a rapid response to market demands and changing industry trends. -Experience in delivering recruitment services for large infrastructure and energy projects. -Specializes in sourcing skilled professionals for both permanent and temporary roles. -Recognized for working on complex and large-scale projects with a diverse client base.

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