Details:
- Job Type: Permanent
- Job Status: Full-Time
- Location: Manchester
- Date: 6 days ago
Description:
Position: Analytical Project Manager
Location: Manchester
Sector: Pharmaceutical
About Us:
A leading GMP pharmaceutical company dedicated to the development and manufacturing of high-quality pharmaceutical products is seeking a Senior Analytical Project Manager.
With a strong commitment to innovation and development the Analytical Project Manager will lead a team to deliver on global pharmaceutical development projects.
Role Overview:
The Analytical Project Manager will play a critical role in overseeing analytical development and validation activities within a GMP-compliant environment.
This role demands a deep technical understanding of analytical methodologies, coupled with the ability to draft comprehensive development and validation reports. Some of the responsibilities are outlined below.
Key Responsibilities:
Project Management: Oversee the planning, execution, and completion of analytical projects, ensuring alignment with project timelines and company objectives.
Technical Oversight: Provide technical guidance on analytical methods, ensuring robust design and validation of assays in compliance with GMP standards.
Report Drafting: Author and review detailed development and validation reports, ensuring clarity, accuracy, and regulatory compliance.
Team Leadership: Manage and mentor a team of analytical scientists, fostering a collaborative and productive work environment.
Stakeholder Communication: Liaise with cross-functional teams, including Quality Assurance, Manufacturing, and Regulatory Affairs, to ensure seamless project integration.
Problem-Solving: Address technical challenges and troubleshooting issues during analytical method development and validation.
Regulatory Compliance: Ensure all analytical activities adhere to GMP regulations and industry best practices.
Continuous Improvement: Identify and implement process improvements to enhance analytical efficiency and quality.
Qualifications:
Education: Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related field. A Ph.D. is preferred.
Experience: Minimum of 5 years’ experience in analytical development within a GMP pharmaceutical environment.
Technical Expertise: Strong understanding of analytical techniques (e.g., HPLC, GC, MS) and their application in pharmaceutical development and validation.
Project Management: Proven experience in managing analytical projects with a track record of successful project delivery.
Report Writing: Demonstrated ability to draft and review detailed development and validation reports.
Leadership: Prior experience in team management, with excellent leadership and interpersonal skills.
Regulatory Knowledge: Familiarity with GMP guidelines and regulatory requirements for pharmaceutical products.
Communication: Excellent verbal and written communication skills, with the ability to convey technical information clearly.
What We Offer:
Competitive Salary: £35,000 - £45,000
Professional Development: Opportunities for training and career advancement within a leading pharmaceutical company.
Innovative Environment: Work in a collaborative setting focused on cutting-edge pharmaceutical research and development