Vaccines Process Associate (VPA)

at  WuXi Biologics

Dundalk, County Louth, Ireland -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate09 Feb, 2025Not Specified10 Nov, 2024N/ABatch Records,Interpersonal Skills,OperationsNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

VACCINE PROCESS ASSOCIATE (VPA), DRUG PRODUCT

WuXi Vaccines, a subsidiary of WuXi Biologics, focuses on human vaccine discovery, development and manufacture. An exciting new addition to the WuXi Biologics family, WuXi Vaccines will bring to the global vaccine industry the world-class integrated platforms and CDMO business model on which WuXi Biologics reputation is based. In development is an integrated vaccine manufacturing facility with 240 million US Dollar investment, including drug substance manufacturing (DS), drug product manufacturing (DP), Manufacture Science and Technology Labs (MS&T) as well as Quality Control labs (QC), dedicated to manufacturing our partner’s vaccine products for the global market.

EXPERIENCE & EDUCATION:

  • A keen interest and desire to develop a career in the pharma industry
  • Experience working as part of a team
  • Experience with recording information in real time using electronic or manual systems
  • Experience in executing operations while following SOPs, Batch Records and Manufacturing Controls Systems desirable
  • Experience in biopharmaceutical industry is an advantage
  • Experience of working in Grade CNC, C and D environment is an advantage.
  • Certificate, Diploma, Degree, Trade qualification or equivalent demonstrated experience of 12 months or more experience in a regulated environment
  • Excellent interpersonal skills, positive influence, team orientation, attention to detail, documentation skills, problem identification and problem-solving skills
  • An ability to work independently, and as a member of a self - managed shift team in a dynamic, fast-paced environment that requires flexibility and initiative

Responsibilities:

  • Perform all core production activities in DP facility
  • Manufacturing processes include Formulation of Buffer, Stabilizer and Drug Product Filling, Capping and Inspection
  • Support the development, commissioning & qualification of a new vaccines drug substance manufacturing equipment and subsequent transition to commercial manufacturing
  • Assist in maintaining a safety orientated Culture, cGMP compliant work environment always
  • Responsible for completion of manufacturing tasks according to SOPs and batch records (paper and electronic)
  • Perform initial troubleshooting of issues identified during routine operations
  • Assist with the investigation of manufacturing deviations through Quality System, engaging with all relevant personnel and functions as appropriate
  • Write, review, revise and approve of area SOPs, Batch Records, Logbooks, Training Competencies and Work Instructions
  • Training and mentoring of colleagues in SOPs, process execution and equipment operation
  • Seek opportunities for Continuous Improvement using Lean/Six Sigma tools as part of daily operations (Standard Work, TPM, 5S, etc.)
  • Where necessary assist in any in Facility and Equipment start up and Validation activities
  • Provide input on equipment installation, start-up, operation and troubleshooting to support introduction of new products into sustaining operations
  • Capable of working with individuals and with a team of up to 20 people
  • Provide technical leadership by acting as ‘Champion’ to drive improvements and excellence within specific aspects of the manufacturing operation within the shift team e.g. Environmental Monitoring, Lean, etc.
  • Provide manufacturing status update during shift handovers
  • Support Manufacturing team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g. Safety, Quality, Schedule adherence, Overall Equipment Effectiveness (OEE), and team training
  • Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested
  • Conduct all activities that are in accordance with Company policies & SOPs, WuXi values, & global regulatory guidelines (including cGMP/cGLP/cGCP), environmental guidelines, as appropriate, etc.
  • The role will be shift working
  • Due to the start-up nature of the project, there will be an expectation for flexibility and an ability to take on varied tasks at short notice not covered extensively within this job description


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Trade Certificate

A regulated environment

Proficient

1

Dundalk, County Louth, Ireland