Drug Product Coordinator (100% remote)

Do you like working in a pharma context and does a 100% remote job opportunity sounds like music to your ears? Then this position as a Drug Product Coordinator is the right fit for you.

Please send me your resume (pdf): ben.veulemans@professionals.randstad.be

• 
  Bachelor’s Degree in engineering, science, or an equivalent technical discipline
• Minimum of 4 years working in an FDA-regulated environment, preferably in a pharmaceutical or biologics manufacturing environment
• Basic understanding of of aseptic processing principles
• Proficiency in computer applications such as Microsoft Office Suite
• Must have strong ability to maintain high efficiencies and accuracy in data entry
• Detail-oriented, with ability to quickly process complex information and make critical decisions with limited information at times
• Strong interpersonal, written, and oral communication skills

Experience / Knowledge Preferred:

• Experience in the NCL/OMCL process for vaccine government approval/release
• Previous experience in work environment under cGMP regulation highly desirable
• Experience in Vaccine Production/QA
• Proficient in applying process excellence tools and methodologies
• Experience working with external manufacturers or laboratories

As an answer to your high performance & flexibility, AUSY offers you an interesting salary package, with some interesting extra’s like:

• Meal vouchers of 7
• Net representation cost of 50
• Hospitalization insurance
• Car + unlimited fuel card OR home-work compensation
• 32 holidays
• End-of-year bonus
• Pension plan
• ECO vouchers
• Opportunities to follow trainings

This big pharma company is looking for a Drug Product Coordinator to maintain an oversight of all drug products. This role is 100% remote.

Do you have some pharma experience and are you familiar with GMP and aseptic processing principles? Please send me your resume (pdf) and I help you one step closer to this challenging opportunity.

ben.veulemans@professionals.randstad.beor call me on 03 317 19 51.

• 
  Maintain high-level oversight of all Drug Substance (DS) and Drug Product (DP) lots manufactured throughout the production network
• Liaise with samples coordinators at external manufacturers to schedule and execute samples shipments to NCL/OMCLs (National Control Laboratories/Official Medicines Control Laboratories)
• Schedule shipping route verification studies and review/approve shipping route verification reports to validate shipping lanes across the network in timely manner
• Should samples arrive with alarmed temperature monitor, advise on product disposition
• Ensure samples are tracked in eLIMS accurately and in a timely manner
• Lead process improvement initiatives to streamline samples sending/receipt processes
• Manage process for sending/receiving backup samples as needed
• Complete and pass all applicable training required for access to quality and information management systems (i.e. ETS Trackwise, eLIMS etc.)
• Complete and pass all applicable Good Manufacturing Practice training and general quality management training
• Learning and remaining current with local regulations, guidelines and quality practices associated with the vaccines industry is required