Hamlyn Williams have partnered with a unique manufacturing organisaton. They are responsible for developing and manufacturing generic pharmaceuticals products.

As the Director of Validation your role will be predominantly leadership focused and where appropriate you willl be responsible for cleaning, facilities, execution of process, aseptic and and automation validation for the local manufacturing sites.

As a Director of Validation you will be responsible for, but not limited to:

-Reviewing and approving validation test protocols

-Developing and updating Validation Master Plans for the clients manufacturing sites

-Providing leadership in a fast paced environment

-Keep to date with cGMP regualtory issue in relation to validation, ensuring all validation policies are updated accordingly

You will be required to have:

8+ years Pharmaceuticals experience

5+ years of management experience

The client are offering a very competitive salary range with a rather generous relocation package, if required.

Please note, the client does NOT offer visa sponsorships at this moment in time.

If interested, please apply directly through the apply button below or alternatively reach out to me on k.kazerouni@hamlynwilliams.com or +1 646-847-2703

Job