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  • Job reference: RMS0227652

Scientist - Drug Production

  • Sector: Petrochemical & Chemical
  • Location: Dundalk, Louth
  • Job type: Permanent
  • Date posted: 05/10/2020
  • Duration: permanent
  • Time left:
    d h m s
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A rapidly growing R&D pharma technology business, are continuing their meteoric rise of becoming a global force in technology, contract manufacturing and drug production. With a recent $500 million investment in in facilities across Europe, 2 brand new purpose built sites and the acquisition of an established production facility, this innovative and forward thinking pharmaceutical are looking for the top talent in engineering, science and commercial to join their quest in becoming a global leader.

Technology and drug development has seen astronomical increase in hedge funds and private investments over the past 5 years, and with the demand increasing for positive human health, we are looking now more than ever to companies for help and support in drug development and drug production. Knowledge and experience is even more valuable to the public as well as businesses who are trying to make a difference, and our client is certainly one of knows.

With the investment of new sites and expansions comes a requirement for talented individual to join them and share their knowledge, and this case we are looking for a Scientist with Drug Product experience.

 Provide technical expertise and specialized knowledge in drug product (DP) process technology transfer, validation, troubleshooting and improvement to support production
 Write and review protocols, reports, batch records, standard operating procedures, and other technical documents to support DP operation
 Lead or coordinate the deviation investigation and control the progress to ensure initiate and close the deviation investigation timely and ensure execute the following CAPA smoothly
 Coordinate DP manufacturing technology transfer from external and internal costumers to DP production facility in Dundalk, Ireland
 Participate in laboratory work for manufacturing troubleshooting and process improvement as needed
 Support DP production CPV program through data reviewing, analyzing, and trending
 Take initiative to optimize the operation and continuous improvement

 Have DP formulation, DP freezing, DP filling, DP inspection, and/or DP lyophilization development and/or commercial manufacturing operation experience
 Have a working experience at GMP environment

(Indicate the mini. requirement & preferred
 Advanced Degree in Life Sciences, chemical engineering, biochemical engineering or related field is required
 Doctorate and Master degree with 5-year biopharmaceutical industry experience in the area of drug product formulation, fill, freezing, lyophilization, or product inspection
 Bachelor degree with 7-year biopharmaceutical industry experience in the area of drug product formulation, fill, freezing, lyophilization, or product inspection

 Excellent written, verbal communication and computer skills
 Excellent analytical skills and problem-solving skills
 Excellent organizational, time management, and multi-tasking skills
 Ability to function independently and exercise good judgement
 Ability to identify problems and solutions then act to resolve
 Work effectively in a cross-functional matrix environment, with internal and external collaborators and proactively communicate with internal and external stakeholders
 Have statistic data analysis capability and experience will be a plus

About Fircroft:
Fircroft has been placing people in specialist technical industries for over 50 years, focusing on mid to senior level engineers for contract and permanent roles worldwide. By applying for this job you give consent for Fircroft to contact you, via email & telephone, to discuss your application along with future positions and Fircroft's services.

Fircroft is registered as a Data Controller with the Information Commissioner as required under the General Data Protection Regulation 2016/679. Fircroft will only process your personal data for the specific purposes of managing your application.

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