• United Kingdom, Uk

Job Description:

Project Manager / Study Director

Job Information Job Title Project Manager / Study Director
Job Code
Job Category Project Management
Job Location Manchester

Do you have previous knowledge and experience as a Project Manager in a Good Practice (GxP) regulatory laboratory within the chemical, pharmaceutical, biopharmaceutical industry

Do you have specialist expertise in method development & validation of methods

Are you looking for your next challenge in Manchester, where you can strive to deliver projects on time, on budget whilst maintaining excellent working relationship both internally and externally

ABOUT THE ROLE Intertek Pharma Services Manchester (IPSM) has an extensive range of analytical instrumentation and provides analytical services to customers in the pharmaceutical, biopharmaceutical, personal care and speciality chemical sectors in a GLP, GCP and GMP regulated laboratory The Project Manager role is an integral part of the Laboratory team and will be accountable for leading, managing and driving our Total Quality Assurance customer promise every day

As Project Manager (PM) you will coordinate and manage a range of GLP and/or GCP regulated analytical studies, ensuring delivery is on time and within budget The role will require the ability to demonstrate both project management and technical skills by acting as a direct liaison in terms of delivery and quality between both colleagues and clients

The role will be based at Hexagon Tower, Blackley, North Manchester where the site offers a variety of on-site amenities including a gym and restaurant In addition to generous paid annual holidays we proactively support work life balance for all our employees by operating flexible working opportunities

ABOUT YOU BSc / MSc/ PhD in Chemistry (or related scientific discipline)

Excel at managing scientific projects within a Good X Practice (GxP) regulated environment

Understanding of the regulatory requirements or Good Working Practices which apply to the pharmaceutical Industry

Experience and good working knowledge of the Chemical and Pharmaceutical Industry with good commercial understanding and natural business acumen

Good experience of preparing documents with technical support or guidance across multiple projects

ABOUT INTERTEK Global pioneers in the Quality Assurance industry, they are the only company in the world that delivers on a truly global scale a fully integrated portfolio of Assurance, Testing, Inspection and Certification services

Over 44,000 employees located in 1,000 laboratories and offices across the world

Our innovation-led, end-to-end Total Quality Assurance (TQA) proposition helps organisations operate safely, effectively and with complete peace of mind in an increasingly complex, fast-changing world across all industries

A focused strategy and culture that gives employees the right platform to grow and develop their careers

HOW TO APPLY Please provide a CV, Covering Letter (outlining your suitability for the role) and Salary Expectations to mailtocpukhrcareersintertekcom All candidates will be required to confirm eligibility to work in the UK before starting employment

All the personal data we process will be in line with our Privacy Policy as per link - http//wwwintertekcom/privacy-policy/ We will use your data to make a decision about assessing qualifications and work suitability for a particular job and your possible appointment for an interview

As a matter of courtesy, we will try to respond to all applications However, due to the volume of applications received, we may not be able to respond to individual candidates If you have not been contacted within four weeks unfortunately, your application has been unsuccessful Please do not let this deter you from applying for vacancies in the future should you meet the minimum requirements of the role

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Research/Surveyor/MR
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 11th Apr 2020

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