What are the responsibilities and job description for the Manufacturing Line Specialist Lead – (1st/2nd/3rd Shift) position at BioSpace?
Position Summary
We are looking for a Manufacturing Line Specialist Lead who will play a part in the facility start-up with primary responsibilities focused on leading daily manufacturing activities on the floor, performing routine equipment, production, and line activities, and the timely production of pharmaceuticals according to qualification, compliance, and business requirements.
Duties & Responsibilities
We are looking for a Manufacturing Line Specialist Lead who will play a part in the facility start-up with primary responsibilities focused on leading daily manufacturing activities on the floor, performing routine equipment, production, and line activities, and the timely production of pharmaceuticals according to qualification, compliance, and business requirements.
Duties & Responsibilities
- Led the day-to-day production activities on the line, responsible for aligning and scheduling personnel and resources to meet the daily and weekly production and equipment demands.
- Collaborate with Manufacturing, Quality Operations, Environmental Health and Safety, and other cross-functional teams to meet production needs.
- Support the onboarding and technical training of Manufacturing Operators on process equipment, including high-speed fill lines with integrated Isolators, Terminal Sterilizers, ATEC commodities processing, Parts Washers, Autoclaves, Single-Use Technology, and Aseptic Process Simulations (media fills).
- Assist R&D and MSAT on new product introduction and tech transfer activities to ensure a steady stream of products to meet commercial demand.
- Initiate and complete manufacturing investigations, including root cause analysis and product impact assessment.
- Assist in the revision and management of manufacturing documents such as Batch Records and SOPs.
- Provide technical expertise and support to production teams, addressing issues and challenges as they arise while working closely with Engineering and other support teams.
- Supports regulatory inspections.
- Ability to quickly adapt and adjust priorities in response to changes in the production schedule due to unforeseen disruptions to minimize impact on operations.
- A minimum of 4 years’ experience in biopharmaceutical manufacturing in a GMP environment.
- An associate’s degree or higher in Pharmaceutical Sciences, Biology, or a related field is preferred.
- Experience with sterile fill-finish manufacturing. Knowledge of GMP, regulatory requirements, and industry best practices.
- Detailed-oriented with a focus on accuracy in creating and updating production documents.
- Experience in using ERP systems.
- Experience performing as a shift lead of a team, training others, and developing training material.
- Knowledge of high-speed aseptic filling and barrier system technology (isolator, RABS).
- Experience with single-use components in drug product formulation, sterile filtration, and aseptic filling applications.
