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Repligen

Bioprocessing solutions for biologics manufacturing

Manufacturing Associate 1

Machine & Process OperationConfirmed live in the last 24 hours
Full-timeWaterford, IrelandIn-person

About the Job

Requirements

  • A Leaving Certificate is required.
  • The ability to follow written and oral instructions and operate equipment is required.
  • Good understanding and knowledge of Corrective and Preventive Action (CAPA), cleanroom operations, continuous improvement, Good Manufacturing Practice (GMP), Environmental Health and Safety (EHS), press operations, packaging and labelling, and quality is preferred.
  • Previous moulding experience is highly desirable.
  • Previous experience is desirable but not essential; full training will be provided.

Responsibilities

  • Assemble products in accordance with approved procedures, quality standards, and production requirements.
  • Follow standard operating procedures and work instructions, and complete required documentation accurately.
  • Maintain a safe and organized work area and support the team in achieving daily production targets.
  • Use, store, process, and control materials within relevant manufacturing operations areas according to approved documentation, including standard operating procedures, batch documents, manufacturing orders, and manufacturing drawings.
  • Use, store, maintain, and clean equipment within relevant manufacturing operations areas according to approved documentation, including standard operating procedures, batch documents, manufacturing orders, and manufacturing drawings.
  • Achieve operational targets, including efficiency, right-first-time performance, final pass yield, and documentation error measures.
  • Be responsible for hourly and daily performance of the assigned manufacturing cell.
  • Participate in manufacturing-cell-based teams and teamwork initiatives, including designing, developing, and implementing projects such as audits, inspections, and project implementation.
  • Participate actively in continuous-improvement projects to improve manufacturing-process quality and efficiency.
  • Maintain thorough knowledge of moulding processes, in-process inspection, assembly, and packaging, as agreed through shift training versatility goals.
  • Accurately report assigned department measures, metrics, and controls.
  • Maintain and control specialized equipment and tools in relevant areas according to applicable standard operating procedures.
  • Complete manufacturing and packaging in-process testing according to approved documentation, standard operating procedures, batch documents, and policies.
  • Comply with safety standards, policies, and procedures while carrying out normal duties and work practices.
  • Report near misses, accidents, and dangerous occurrences to the department manager or supervisor immediately or as soon as practicable, and document them with the team leader or supervisor.
  • Comply with quality standards, procedures, policies, standard operating procedures, and other approved documentation.
  • Investigate production problems or process deviations, conduct root-cause analysis, and implement corrective or preventative actions to reduce recurrence.
  • Communicate current line performance, shift issues, upcoming changeovers, and line and documentation status during shift changes.
  • Participate in weekly communication meetings with wider shift members and communicate supportively during training activities.
  • Communicate respectfully, courteously, openly, honestly, and consistently with fellow employees, contractors, and visitors.
  • Perform other duties as assigned in response to developments or changes to the role.

Desired Qualifications

  • Operate at pace and make agile decisions.
  • Deliver high-quality results, overcome challenges, focus on priorities, and execute effectively.
  • Continuously seek opportunities to learn, build skills, and share learning.
  • Sustain energy and well-being.
  • Build strong relationships and collaborate through honest and open conversations.

About the Company

Repligen

Bioprocessing solutions for biologics manufacturing

Repligen provides products and services to support biotherapeutic manufacturing. It offers filtration, chromatography systems, process analytics, fluid management, and protein solutions that help develop and produce biologics such as cell and gene therapies, mRNA, monoclonal antibodies, antibody–drug conjugates, bispecific antibodies, and fusion proteins. Its offerings are designed to fit the full bioprocess workflow—from upstream filtration and purification to downstream analytics and process control—through a portfolio of systems, consumables, and services. Repligen differentiates itself by maintaining a broad, integrated suite of bioprocessing technologies and global manufacturing support across 22 sites, enabling clients to scale from development to commercial production. The company’s goal is to advance and accelerate the manufacturing of biologics by providing reliable, end-to-end solutions that streamline development and scale-up.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Waltham, MA
Founded
1981

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