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Contract GMP QA Validation Consultant – Multinational Pharma – Ireland, Dublin – 3 Days Per Week - 3 Month Contract – Excellent Rates

Company: Meet
Location:
Reference: MD-HE-QAV-IRE-4
Closing Date: 06 Dec 17
Type: Contract
Salary (£): Competitive
Benefits:

Job Summary:

Exciting opportunity to join a global pharmaceutical company in Dublin on a 6 month contract role. Role is focused on QA review of Validation protocols as part of a wider site expansion project. Call Matt Dixon on 0203 019 6006 or email matt@peoplewithchemistry.com for more information.

Requirements:

This multinational Pharmaceutical company is looking for a contractor that is experienced in GMP QA review of Validation documents to come in and hit the ground running on a 3 month contract. This part-time role, working 3 days per week, is based at their manufacturing site in Dublin, Ireland.

This is a fantastic opportunity to get on board with a company that has a global presence in the industry and has a reputation as being a great company to work for.

 

Background

My client is building a brand new high-containment production facility for a high profile drug that is in a Phase 3 clinical trial. The API is a highly potent material, therefore the manufacturing site will be designed for high-containment in order to achieve their target of 1µg/m3 containment.

Get in touch with Matt Dixon at matt@peoplewithchemistry.com or call on 0203 019 6006 to find out more about this opportunity. This will be 100% confidential.

 

Role Responsibilities

Working as a QA Validation Consultant your main responsibilities will be:

  • Approval of the validation documentation drafted by various departments (QC, manufacturing, engineering)
  • Ensure that all QA activities relating to Validation are carried out in accordance with approved procedures.
  • Ensure the scientific integrity of the Validation study and ensure Validation work is completed to GMP compliance.
  • Final approval of Validation documentation.
  • Ensure that all compliance activities in relation to Validation are carried out in accordance of Helsinn internal procedures and industry standards.
  • Approval of Validation deviations.

 

Suitable For

This role is ideal for a consultant that has experience working in a high potency manufacturing environment and is also experienced with solid-dosage tablet production. If you have experience of writing and reviewing validation protocols for manufacturing equipment and conducting QA review of said protocols and manufacturing documentation you will be ideal for this opportunity!

Get in touch with Matt Dixon at matt@peoplewithchemistry.com or call on 0203 019 6006 to find out more about this opportunity. This will be 100% confidential.

 

Skills Required

  • Bachelor's degree in science, pharmacy, biological science or related field is preferred.
  • Hands-on international Quality Assurance experience in a solid-dose tablet manufacturing environment is essential
  • Experience working with high potency products from QA/Validation perspective is essential.
  • Strong understanding of cGMP requirements and the ability to implement and actions needed to implement this within the QMS.
  • Experience of writing and executing validation protocols for solid-dose manufacturing equipment (DQ, IQ, OQ, PQ).
  • Excellent verbal and written communication skills, ability to work well in teams or independently and the ability to prioritise work and manage multiple projects while maintaining quality and compliance.

Get in touch with Matt Dixon at matt@peoplewithchemistry.com or call on 0203 019 6006 to find out more about this opportunity. This will be 100% confidential.

 

Commutable Locations: Republic of Ireland, Dublin.

Rate: Competitive

Full job description and company details are available upon application, apply below. The position is being dealt with by Matt Dixon at Meet, call us on 0203 019 6006 or email directly at matt@peoplewithchemistry.com to discuss in confidence.

Meet are good people wo are great at recruitment. We’re proud to partner with the industry’s leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available. We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way.

Find out more about us at www.peoplewithchemistry.com https://uk.linkedin.com/in/matthew-dixon-34aab863

Apply for this job: Contract GMP QA Validation Consultant – Multinational Pharma – Ireland, Dublin – 3 Days Per Week - 3 Month Contract – Excellent Rates

Contact Information:

Address:  meet
Irongate House, 30 Dukes Place, London
EC3A 7HX
England
Tel:  +44 203 178 7488
Website:  Visit Our Web Site

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