Senior GMP Analytical PM

CV-Library

Posted on Jun 20, 2024 by CV-Library
Manchester, Greater Manchester, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
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

Reference: 221862120

https://jobs.careeraddict.com/post/92150558
CV-Library

Senior GMP Analytical PM

CV-Library

Posted on Jun 20, 2024 by CV-Library

Manchester, Greater Manchester, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
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

Reference: 221862120

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