Technical Services Specialist (Drug Substance)

Tandem Project Management Ltd.; Dublin; On-site; EUR 70,000 - 110,000; Full time

Job summary

Tandem Project Management Ltd. seeks a Technical Services Specialist to support technology transfer, process validation and routine manufacturing for Upstream and Downstream DS processes in West Dublin.

Role involves collaborating with Process Development, DS operations, QA, Regulatory and other teams to ensure successful facility start-up, process qualification and timely material release.

Qualifications

• B.Sc./M.Sc. in Biochemistry, Biology, Chemistry or Engineering.
• 3+ years’ experience in Technical Services/Process Development/Manufacturing Support in a biopharma bulk DS setting.
• Technical/operational knowledge of multiple unit operations in cell culture processing.

Responsibilities

• Provide process expertise in Upstream and/or Downstream disciplines.
• Author and review transfer documentation, protocols and reports; support validation.
• Identify study requirements and liaise with Global Process Development and CMOs.

Skills

Tech transfer

Process development

cGMP knowledge

Biopharma manufacturing

Education

B.Sc. in Biochemistry/Biology/Chemistry or Eng

M.Sc. in Biochemistry/Biology/Chemistry or Eng

Job description

Bulk Drug Substance - Technical Services Specialist (Upstream/Downstream)

A Technical Services Specialist is required for a biopharmaceutical company in West Dublin. The successful candidate will provide processing expertise to support technology transfer, process validation and routine commercial manufacturing for Upstream and/or Downstream manufacturing. The ideal candidate will be responsible for providing support for the technology transfer of new/existing drug substance (DS) manufacturing processes to our clients' facility, and will be required to work in close collaboration with Process Development, DS Process Sending unit, Operations, Engineering, Supply Chain, Quality, Quality Control, Regulatory and other involved departments to ensure successful facility start-up and process qualification

Responsibilities:

• Provide process expertise in one, or both of the following disciplines: Upstream (Cell culture focus) to include media preparation, large-scale cell culture bulk drug substance manufacturing process (vial thaw, scale up, seed reactors and production bioreactors and harvest centrifugation/clarification; Downstream: to include buffer preparation, purification and viral reduction steps including chromatography, ultrafiltration viral reduction filtration and viral inactivation technologies and DS formulation and bulk fill.
• Author and review process transfer documentation, gap assessments, technical protocols and reports, process validation documentation, strategy documents
• Identify requirements for laboratory studies to support process fit, decisions or process transfer, and liaise closely with Global Process Development and CMO’s to oversee the design and execution of studies
• Support the introduction of new raw materials and consumables through the generation of materials lists, Bills of Materials, material specifications and outline testing requirements
• Work closely with colleagues in Quality, Supply Chain and Manufacturing Operations to ensure the availability and release of materials to meet technology transfer and routine manufacturing timelines
• Identify and implement process improvements, e.g. yield, cycle time reduction
• Generate documentation protocols and lead the execution of plant-supporting studies and technical studies on the manufacturing floor at a commercial scale
• May be required to work periodically out of normal business hours (temporary shift working) during periods of engineering and validation batch execution and provide on-call support to manufacturing.
• Provide on the floor support for troubleshooting processing issues and to lead manufacturing investigations into process deviations and resolution
• Lead any key process changes using change control system
• Adherence to highest standards for Compliance (Quality and Safety), implement corporate standards and liaise effectively with global groups and provide technical support during audits
• Ensure compliance with site EHS policy, cGMP and other business regulations and participate in risk assessments, audits, and incident investigations
• Author and review common technical document (CTD) sections and reports for regulatory agency submissions
• Serve as a subject-matter expert (SME) on technology transfer and process support during regulatory agency inspections.

Qualifications & Experience:

• B.Sc. in Biochemistry, Biology, Chemistry or equivalent, or B.Eng. Process or Chemical Engineering. M.Sc. or other postgraduate qualification in Biochemistry, Biology, Chemistry or equivalent, or B.Eng. Process or Chemical Engineering.
• Minimum 3+ years’ experience in Technical Services / Process Development / Manufacturing Support in a biological bulk drug substance manufacturing organisation.
• Technical and operational knowledge of multiple unit operations in cell culture processing.
• Comprehensive understanding of cGMP requirements for biopharmaceutical manufacturing.
• Experience in Technology Transfer activities is advantageous
• Knowledge or experience of start-ups or systems would be ideal.
• Experience in authoring CMC sections of regulatory submissions.