INTERNSHIP DETAILS

Tech Transfer Intern

CompanyMeiraGTx
LocationLondon
Work ModeOn Site
PostedDecember 19, 2025
Internship Information
Core Responsibilities
The intern will assist the Tech Transfer department in collecting and analyzing data from Tech Transfer and manufacturing processes. They will also help in establishing systems for data collation and contribute to general Tech Transfer activities.
Internship Type
full time
Company Size
409
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
MeiraGTx (Nasdaq: MGTX) is a vertically integrated, clinical-stage genetic medicine company with a broad pipeline of late-stage clinical programs supported by end-to-end manufacturing capabilities. MeiraGTx has an internally developed manufacturing platform process, internal plasmid production for GMP, two GMP viral vector production facilities as well as an in-house Quality Control hub for stability and release, all fit for IND through commercial supply. MeiraGTx has core capabilities in viral vector design and optimization and a potentially transformative riboswitch gene regulation platform technology that allows for the precise, dose-responsive control of gene expression by oral small molecules. MeiraGTx is focusing the riboswitch platform on delivery of metabolic peptides including GLP-1, GIP, Glucagon and PYY using oral small molecules, as well as cell therapy for oncology and autoimmune diseases. Although initially focusing on the eye, central nervous system, and salivary gland, MeiraGTx has developed the technology to apply genetic medicine to more common diseases, increasing efficacy, addressing novel targets, and expanding access in some of the largest disease areas where the unmet need remains great.
About the Role

Your mission

  • To assist the Tech Transfer department in collection and analysis of data from Tech Transfer and manufacturing processes.
  • To assist in putting in place systems of work in MeiraGTx for collation and creation of data sets from Tech Transfer and manufacturing processes.
  • To contribute in general Tech Transfer activities.


Job Description

Major Activities

  • Creation and maintenance of appropriate data storage and analytical systems.
  • Identification of key data in MeiraGTx documentation.
  • Systemic gathering of data from manufacturing documentation.
  • Systemic gathering of data from Tech Transfer documentation.
  • Transcription of data into data storage and analytical systems.
  • Analysis of data from manufacturing and Tech Transfer processes.
  • Creation and maintenance of data trend systems.
  • Communication of data trends.
  • Assisting in general Tech Transfer like protocol/reports drafting for instance.
  • Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures
  •  Responsible for ensuring that own training is undertaken in a timely and GMP compliant manner before the task is undertaken
  • Responsible for ensuring that any GMP documentation assigned to me e.g. (but not limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions is closed timely and in a RFT state

Key Job Competencies

  • Ability to translate practical process data into electronic data
  • Oral Communication - speaks clearly and persuasively in positive or negative situations; listens and gets clarification; responds well to questions; demonstrates good presentation skills; participates effectively in meetings.
  • Written Communication - writes clearly and informatively; edits work for spelling and grammar; varies writing style to meet needs; presents numerical data effectively; able to read and interpret written information
  • Motivation - sets and achieves challenging goals; demonstrates persistence and overcomes obstacles; measures self against standard of excellence;
  • Planning/Organizing - prioritizes and plans work activities; uses time efficiently; plans for additional resources; sets goals and objectives; organizes or schedules other people and their tasks; develops realistic action plans.
  • Professionalism - approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments.
  • Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures
  • Responsible for ensuring that own training is undertaken in a timely and GMP compliant manner before the task is undertaken
  • Responsible for ensuring that any GMP documentation assigned to me e.g. (but not limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions is closed timely and in a RFT state

Job Background

  • Educated to degree level, with industrial experience preferred in pharmaceuticals, biotechnology or scientific manufacture.  
  • Experience with data systems in either academia or industry would be advantageous.  
  • Experience of quality management systems would be advantageous.  


Why us?

Key Skills
Data AnalysisData ManagementCommunicationWritten CommunicationPlanningOrganizationProfessionalismGMP ComplianceData IntegrityDocumentation PracticeTranscriptionTrend AnalysisProblem SolvingTeam CollaborationAttention to DetailQuality Management
Categories
Science & ResearchHealthcareManufacturingData & AnalyticsTechnology