Pharmaceutical Development Lead

Location
Essex
Salary
£40000 to £50000 per annum
Posted
17 Oct 2018
Closes
14 Nov 2018
Ref
J563102
Contact
Chris Sowden
Contract Type
Permanent
Hours
Full Time
Hyper Recruitment Solutions are currently looking for a Pharmaceutical Development Lead to join a leading Pharmaceutical company based in the Essex area. As the Pharmaceutical Development Lead you will be responsible for leading product development projects from pre-formulation to commercialisation.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Pharmaceutical Development Lead will be varied however the key duties and responsibilities are as follows:

1. You will establish and develop manufacturing plans and processes to ensure NPD projects are completed to key deadlines by effectively liaising with Analytical Development and Production. This will also involve writing and amending manufacturing documentation (MBR's, Manufacturing Protocols, Manufacturing Reports).

2. The Pharmaceutical Development Lead will coordinate Production activities, train production teams on new documents/procedures and supervise manufacturing areas and oversee the development and validation of manufacturing processes for new products. They will also coordinate the manufacture of batches for submission/validation in the commercial plant.

3. Lead Product Developments at various stages from pre-formulation to industrialization to strengthen the business's product pipeline. You will coordinate product development activities to ensure compliance to cGMP and internal business standards.

4. Provide feedback and technical support to customers, senior management and internal teams on product and process development with the aim of ensuring an effective product launch phase.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Pharmaceutical Development Lead we are looking to identify the following on your profile and past history:

1. Relevant degree in a a Pharmaceutical/Scientific Discipline.

2. Proven industry experience in a GMP compliant Pharmaceutical Manufacturing setting.

3. A working knowledge and practical experience with Pharmaceutical Development and CMC guidelines. Experience with Sterile Manufacturing would be advantageous.

Key Words: Pharmaceuticals / Pharma / GMP / Manufacturing / CMC / Development / Dosage Forms / NPI / NPD / New Product Development / cGMP / SOP's / Batch Manufacturing Record / QC / QA / Dosage Forms / MHRA / FDA / EMA / New Product Introduction / Validation / Development / Product Pipeline / SOP / CAPA / CMC /

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.

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