Posts Tagged ‘CMC’

Analytical Team Leader – Northern Ireland

Tuesday, October 9th, 2012

Naynesh Mistry at CK Science is currently recruiting for an Analytical Team Leader to join a leading pharmaceutical company based in Northern Ireland on a permanent basis.

Responsibilities:

As an Analytical Team Leader you will provide technical leadership, management and coaching for operational analytical teams and enable the delivery of complex projects.  The post holder will manage the progress of Analytical work to GMP requirements and ensure that project schedules are met and that the work is carried out efficiently and accurately, providing regular updates to their Departmental Manager.

You will:

  • Provide technical and operational leadership, training and coaching to Technical Leaders, Senior Analysts, Analysts and Technicians.
  • Take full ownership for, the analytical activities required as part of their assigned projects. Identifying technical problems/issues, developing solutions and fully implementing these solutions with agreement from their departmental manager where appropriate.
  • Define the analytical strategy for new and ongoing projects (e.g. the strategy to develop, verify/validate or transfer analytical methods, stability study design etc). Support Technical leaders, and Senior Analysts with strategy setting and approve the approaches they propose (as appropriate).
  • Actively manage the performance of Technical Leaders, Senior Analysts, Analysts and Technicians assigned as their direct and indirect reports.
  • Take the lead in technical assessment for quotations, and support Business Development activities / visits (internal/external).
  • Provide support and front (as required) Client / Regulatory cGMP audits. And complete all assigned actions from audits promptly.
  • Prepare, review and approve any protocols, reports and other associated project / GMP documentation (e.g. data packs, Methods, specs) that are required to fulfil the projects or departments needs.
  • Overall responsibility for team adherence to Quality Management System document closure timelines (e.g. CAPA, CRF etc etc).

Qualifications:

The successful Analytical Team Leader will have the following qualifications, skills and experiences:

  • A degree in Chemistry or a Life Science subject with a significant chemistry component.
  • Significant experience of analysing and leading analytical development activities for solid oral dose Pharmaceutical drug products in a GMP environment.
  • Significant experience of : Stability study design and testing, HPLC method Development, HPLC method Validation, Dissolution Method Development, Dissolution Method Validation
  • Significant experience of supervising and managing cGMP laboratory activities and staff.
  • A thorough understanding of the pharmaceutical drug development process, and experience preparing regulatory CMC dossier sections.
  • Previous experience of using statistical data analysis techniques.
  • Experience in cGMP audits and knowledge of Microsoft Office (Word, Office, Excel etc)

Benefits:

If successful you will be joining one of the leading API manufacturer in Northern Ireland. Other benefits include:

  • An attractive remuneration package will reflect the importance of this role
  • 6.8 weeks annual leave
  • Company pension scheme
  • Enhanced sick pay and maternity entitlements,
  • Healthcare plan and opportunities for learning and development
  • Access to a company restaurant and parking facilities.

    Naynesh Mistry - Northern Ireland Scientific Recruitment

    Please contact Naynesh for more details.

How to apply:

To apply for this Analytical Team Leader position contact Naynesh Mistry via email nmistry@ckscience.co.uk or telephone: 0114 283 9956.  Please quote reference SH25404 in all correspondence.

 

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Analytical Team Leader - Northern Ireland        Analytical Team Leader - Northern Ireland

 

Pharmaceutical Technical Executive – London

Thursday, July 26th, 2012

Jason Johal at CK Science is currently recruiting for a Pharmaceutical Technical Executive to join an international speciality Pharmaceutical company based in London on a 6 month contract initially.

Responsibilities:

As a Pharmaceutical Technical Executive you will:

  • Provide a technical support service to the Medical and Regulatory Affairs Unit
  • Advise on all relevant product issues
  • Approve technical documentation provided by third parties
  • Investigate and resolve technical issues from manufacturers
  • Be involved in site transfer projects
  • Be responsible for compliance documents
  • Be responsible for expert document writing
  • Apply for licences

Qualifications:

The successful Pharmaceutical Technical Executive will have the following qualifications, skills & experiences:

  • BSc in Pharmacy or Chemistry or equivalent
  • Relevant technical experience gained in the pharmaceutical industry
  • Regulatory experience of CMC documentation (essential)
  • Manufacturing experience (essential)
  • CMC sections experience
  • Document control experience (essential)
  • Regulatory knowledge needed including regulatory licensing
  • Product development experience
  • Technical knowledge across a range of dosage forms (tableting experience is essential)
  • Auditing experience
  • Problem solving experience (essential)
  • Experience dealing with 3rd party manufacturers (advantageous)
  • Technical Transfer knowledge
  • API & Finished product experience

Benefits:

If successful for this Pharmaceutical Technical Executive, you will be joining a rapidly growing pharma company with several new product realised already this year and several more in the pipeline.  In return you will gain excellent development experience an attractive salary and if successful career progression opportunities.

Jason Johal - Manager at CK ScienceHow to apply:

Apply online:

For more information or to apply for this Pharmaceutical Technical Executive position, please contact Jason Johal jjohal@ckscience.co.uk or 01438 723 500. Please quote reference ST24799 in all correspondence.

 

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Pharmaceutical Technical Executive – London, UK

Friday, July 20th, 2012

Jason Johal at CK Science is recruiting for a Pharmaceutical Technical Executive to join an international speciality Pharmaceutical company based in London on a 6 month initial contract.

This is an excellent opportunity to join a growing pharmaceutical company with several new products launched this year and several more in the pipeline. As Pharmaceutical Technical Executive you will gain excellent development experience, and attractive salary and excellent personal development opportunities.

The Role:

As Pharmaceutical Technical Executive you will:

- Provide a technical support service to the Medical and Regulatory Affairs Unit

- Advise on all relevant product issues

- Approve technical documentation provided by third parties

- Investigate and resolve technical issues from manufacturers

- Be involved in site transfer projects

- Be responsible for compliance documents

- Be responsible for expert document writing

- Apply for licences

 

Qualifications, Skills and Experience:

The successful Pharmaceutical Technical Executive will have the following qualifications, skills & experiences:

- BSc in Pharmacy or Chemistry or equivalent

- Relevant technical experience gained in the pharmaceutical industry

- Regulatory experience of CMC documentation (essential)

- Manufacturing experience (essential)

- CMC sections experience

- Document control experience (essential)

- Regulatory knowledge needed including regulatory licensing

- Product development experience

- Technical knowledge across a range of dosage forms (tableting experience is essential)

- Auditing experience

- Problem solving experience (essential)

- Experience dealing with 3rd party manufacturers (advantageous)

- Technical Transfer knowledge

- API & Finished product experience

 

 

How to Apply:

 

Jason Johal at CK Science is recruiting for a Pharmaceutical Technical Executive – London

Please contact Jason for more details.

Click here to apply online now.

For more information regarding this Pharmaceutical Technical Executive position, contact Jason Johal via email: jjohal@ckscience.co.uk or telephone: 01438 723 500.Please quote reference ST24799 in all correspondence.

 

 

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Pharmaceutical Technical Executive – London   Pharmaceutical Technical Executive – London   Pharmaceutical Technical Executive – London   Pharmaceutical Technical Executive – London

 

Regulatory Manager – East Anglia

Monday, March 19th, 2012

Jason Johal at CK Science is currently recruiting for a Regulatory Manager to join a global Biopharma company in East Anglia and close to Cambridge

The Job:

The role of this Regulatory Manager job is to provide effective regulatory and strategic input during product development and product life cycle management to support manufacturing activities on site and to ensure regulatory compliance for final product release. This is a dual reporting role to the Director of Quality Operations and to the Director of RA CMC Europe.

Responsibilities:

As a Regulatory Manager  you will have responsibility for 5 Quality Assurance and Regulatory Affairs professional staff and a budget up to $1MM key responsibilities include:

  • Partnering with Global RA CMC to deliver the strategy and execution for the preparation of CMC components for investigational medicinal products, new marketing applications, MAA variations and responses to agency questions.
  • Evaluation of post-approval CMC changes that affect EU MAA and International filings. Good working knowledge of EMA centralized variation system and variation application form. Scientific assessment of all relevant product related documents in compliance with EU regulatory requirements. Preparation of the EU quality components for CMC variations and maintenance of CMC sections in CTD format for EU MAA.
  • Collecting and developing responses to questions from regulatory authorities in close cooperation with project team members in US and EU.
  • Developing and maintaining a knowledge and understanding of current regulatory requirements for manufacture of API and testing, release and distribution of licensed medicinal products.
  • Maintaining regulatory compliance system for therapeutic products to support final product release and distribution to market.
  • Maintaining a high quality standards and a continuous improvement approach in responding to the evolving regulatory environment.
  • Maintaining CMC regulatory documents and liaison with appropriate Regulatory Authorities. This includes Site Master Files and manufacturing licenses and other regulatory approvals are maintained and available for regulatory agency and Customer Inspections.

Qualifications and Skills:

This Regulatory Manager role will require good working relationships with internal customers from QA/QC/Production/ Materials Management to improve regulatory compliance and awareness as well as collaboration with global regulatory personnel to ensure best practices and knowledge of global activities are communicated to site.

The company require someone capable of working independently to achieve goals and objective and with the ability to prioritise and organise daily work to meet overall deadlines. They must be able to influence others in a positive way and to identify and manage their own projects to completion. They will need the following:

  • A good knowledge of Pharmaceutical manufacturing processes and cGMP is essential as is knowledge and experience of international regulatory affairs environment for product life cycle management.
  • Practical experience of European regulatory procedures and the EU centralized procedure both pre and post approval are expected as is a good understanding of global change control management and regulatory compliance.
  • The ability to work on a number of projects with tight timelines, good scientific writing skills and the ability to work independently with minimal guidance are also required.

How to apply:

Apply online now

For more information or to apply for this Regulatory Manager role please contact Jason Johal on 01438 723 500 or email jjohal@ckscience.co.uk.  Please quote reference ST23896 in all correspondence.

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Head of Quality & Compliance Job (CMC Services) – Cambridge, UK

Tuesday, December 7th, 2010

As the Head of Quality and Compliance you will ensure the departments in the division are operating in accordance with appropriate GMP standards and review procedures to identify and implement changes to achieve continuous improvement in quality and compliance. This role is based in Cambridge, UK.

 

Responsibilities:

By working with Heads of Departments you will review operational procedures, SOPs and training in each department and identify and implement changes to improve quality and compliance. You will evaluate whether departmental errors have the potential to occur across the Division or Company and ensure they are investigated thoroughly and appropriate actions put in place to prevent a reoccurrence. You will also ensure that all GMP services provided by the Division meet current and future world-wide regulatory compliance and internationally recognised quality standards.

Key responsibilities of this Head of Quality & Compliance will include reviewing department and divisional quality metrics on a monthly basis and identifying trends and potential issues, reviewing departmental QC procedures and evaluating their effectiveness and robustness, training staff in GMP regulations and quality standards and Identify regulatory and quality training needs. You will also review all CAPA investigations and act as a source of advice for regulatory/quality queries from any member of staff within the Division.

The key aim of this role is to build, lead and motivate an effective quality and compliance team and to co-ordinate and respond to quality queries for both internal and external clients.

 

Person Specification:

The ideal candidate will have a thorough working knowledge of GMP, good communication skills and will be trained in LEAN or Six Sigma. Significant experience of quality management systems is essential as is experience in CMC and commercial drug manufacture.

 

Apply Now

For more information, or to apply for this Head of Quality and Compliance position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST20961 in all correspondence.

CMC Project Manager Job – Cambridge, UK

Tuesday, December 7th, 2010

As CMC Project Manager you will be responsible and accountable for the planning co-ordination and management of CMC projects within “NDA”. You will be based in Cambridge, UK.

 

Responsibilities:

Further responsibilities of this CMC Project Manager job will include:

  • Organising, and co-ordinating CMC projects at NDA and to act as the main interface between the client /sponsor and the technical/laboratory staff supporting the study.
  • Continually seeking to identify opportunities for and to lead by example, improvements in quality, productivity, new techniques and automation, where applicable and to participate in business reviews, identifying areas of service development, particularly with respect to project and programme management.

In addition as CMC Project Manager you will be the key interface between NDA and the client/third party suppliers/manufacturers delivering a comprehensive service to customers on scientific and GMP matters.

 

Person Specification:

The ideal candidate will have detailed knowledge of CMC requirements with either a Quality Control or Manufacturing background. They will have extensive knowledge of CMC stability studies/ drug development process and demonstrated knowledge of GMP. Excellent communication and customer service skills are essential as is Experience in CMC development for biologics gained in either a CRO, manufacturer or scientific project planning role. Demonstrated experience in working with colleagues in a matrix environment is also required.

 

Apply Now

For more information, or to apply for this CMC Project Manager position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk.

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