Interim Manufacturing Manager

Recruiter
Juice Resource Solutions Limited
Location
Maidenhead
Salary
45.00 - 53.00 GBP Hourly
Posted
09 Oct 2018
Closes
16 Oct 2018
Position/Level
Professional / Specialist
Responsibilities
Information Technology
Sector
Technology
Contract Type
Contract / Interim
Language
English
Interim Manufacturing Manager
Global Pharmaceutical Company
6 months initial contract
ASAP Start
Location: Maidenhead area, Berkshire
Rate: Up to GBP 53p.h. (or GBP 425 p.d.)

Our client is seeking an interim manufacturing manager (Pharmaceuticals) for an initial 6-12 month contract. The company are one of the world's largest and best known Pharmaceutical companies.

KEY ACCOUNTABILITIES:

* Evaluate the potential impact of proposed changes on quality and efficacy
* Support the change control process when applicable
* Participate where necessary in QA-led investigations of process deviations and customer complaints. Support manufacturing troubleshooting activity and propose CAPA where applicable
* Evaluate manufacturing instructions, specifications and amendment to each.
* Ensure that current pharmacopeial requirements are met where applicable
* Perform and support raw material evaluation and qualification
* Investigate process improvements and oversee the process validation, ensuring adequate documentation is available to support successful registration of projects
* Support request for information requests which may arise on regulatory variation submission
* Support request for information requests which may arise on regulatory variation submission
* Update company Specification systems such as GSS, CONNECT, etc.
* Manage the APR process
* Create pharmaceutical reports.
* Participate in various cross-disciplinary groups in an expert capacity.
* Support local manufacturing plant in an expert capacity
* Actively participate in the Tech Transfer Team
* Contribute expertise on product and process engineering.
* Support Process and Analytical optimization, development and validation as required
* Ensure transfer compliance with current company procedures
* Develop product development strategies for current products on market
* Contribute Expertise on product and process development
* Actively participate in establishing and developing the process on a production scale
* Create and/or Review up-scaling reports
* Ensure that adequate documentation is available to support successful registration of products
* Support commercialization of secondary market launches of new product introductions
* Ensure that adequate documentation is available to support successful registration of projects
* Management of Third Parties
* Actively participate in the selection, due diligence and evaluation of Third Party partners
* Management of technical relationship with Third Party and provide technical supervision to assure that company products are produced according to company and International standards
* Maintain necessary good manufacturing practice (GMP) skills through training, technical review and SOPs
* Have a close collaboration with the Supply Chain
* Continuously update new research findings and techniques
* Be responsible for personal development (active participation in planning and employee reviews as well as creation and implementation of personal development plans)

SKILLS/EXPERIENCE REQUIRED:

Educational: Minimum of Bachelors degree with a major in chemistry, chemical engineering or pharmaceutics or equivalent degree.

Work Experience:
* A minimum of 8 years in a pharmaceutical manufacturing or product development environment with a major emphasis on multi-ingredient finished dose formulations.
* Experience with non-prescription ingredients used in cough, cold & allergy preparations and analgesics is a distinct advantage.
* Comprehensive understanding of quality compliance knowledge within EU and good understanding of GxP systems
* A demonstrated business partner and ability to bring together multi-disciplined technical staff in order to problem-solve.
* Technical writing and documentation review abilities
* Project management, communication and prioritization skills.
* Demonstrable experience of working with external manufacturers

Due to the high volume of applications we receive we are not able to get back to everyone who applies. Therefore if you have not heard back from Juice Resource Solutions within 7 days please assume that your application has been unsuccessful however we will contact you if suitable roles come up that match your skill set.

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