Pharma / Manufacturing Operations Manager at VANRATH
Newry, Northern Ireland, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

10 Aug, 25

Salary

50000.0

Posted On

10 May, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

VANRATH are delighted to be assisting a Major Pharmaceutical Manufacturing Company with the Recruitment of a high level role within a growing and exciting company. The role is for a Senior Operational Site Lead based in their HQ at Newry.
This is a fantastic opportunity for a high level candidate who is at a point in their career where they can put their specialist experience to use and help mould a brand new role within the company.
Salary - Fully Negotiable Depending on Experience + Fantastic Benefits
Hours - Mon-Fri 09:00 - 17:00 (onsite due to nature of the role)
Overview: The Senior Operational Lead - Sterile and Aseptic Manufacturing will oversee teams responsible for producing products to the highest standards, ensuring timely global distribution. They will drive performance and foster a culture of compliance and continuous improvement across key manufacturing areas to meet customer order deadlines.

Responsibilities

RESPONSIBILITIES:

  • Lead and manage large teams in a complex, highly regulated environment, driving performance and compliance
  • Identify development needs and skills gaps within the team, fostering growth and continuous learning.
  • Spearhead significant operational transformations, including site turnarounds and large scale process optimisations.
  • Maintain a deep knowledge and understanding of regulatory authority expectations (MHRA, FDA, EU GMP) for aseptic manufacturing.
  • Ensure products are manufactured in compliance with Good Manufacturing Practices (GMP) and within the parameters of the Quality Management System.
  • Lead and successfully navigate regulatory audits in sterile and aseptic production environments.
  • Implementing Lean, Six Sigma, or other efficiency methodologies that we are adopting in an aseptic/sterile environment.
  • Work closely with departments such as Engineering, Process Excellence, Validations, and Quality to ensure full compliance with GMP and customer requirements.
  • Support external audits and inspections as needed, ensuring all necessary documentation and procedures are up to date and in compliance with regulatory standards.

leadership role overseeing sterile operations ? Please Detail:

  • Do you have a Strong understanding of pharmaceutical manufacturing processes, including solid oral dose,
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