Job Overview
We are seeking a skilled professional to lead and/or participate in projects focused on developing strategy with respect to chemistry, manufacturing, and controls (CMC) of combination drug devices.
The ideal candidate will have a strong background in FDA, US Pharmacopeia and/or European Pharmacopeia and ICH guidelines related to CMC regulatory topics, as well as experience in method development and validation, compendial method verification and transfer, specification/acceptance criterion development, stability testing, out of specification (OOS) investigation, post-approval manufacturing changes, verification of active pharmaceutical ingredient (API) components to recognized compendial standards and API vendor qualifications and audit.
1. Maintain high level of expertise in FDA, US Pharmacopeia and/or European Pharmacopeia and ICH guidelines related to CMC regulatory topics.
2. Provide oversight in the development of CMC strategies to support global regulatory strategy and submissions and Support submissions pertinent to CMC for global regulators.
3. Technically review data and reports for accuracy and consistency with regulator's expectations (including, but not limited to stability data and lot release data such as HPLC, Particulate, Dissolution).
4. Provide CMC expertise and collaborate with stakeholders to identify contract manufacturers, API vendor selection, qualification and support audits of same.
5. Lead or participate in engineering projects serving as subject matter expert within the field of CMC and test method development.
6. Provide input on new product introduction and assessing proposed manufacturing changes and provide guidance during implementation of product changes.
7. Support the Investigation / Root Cause Analysis of OOS API results ensuring consistency in terms of methodology and regulatory expectations.
8. Collaborate with other Post Market / Manufacturing Engineering Teams to ensure the effective completion of all activities associated with Post Market Engineering projects / objectives.
9. Collaborate and interact effectively with other internal companies and global functions within the organisation (e.g., Regulatory Affairs, Engineering, Operations (Manufacturing), and Quality) to develop and implement CMC strategies.
10. Ensure effective reporting to the Post Market Engineering management team.
11. Work closely to build effective relationships with other functions in particular Production, Quality and Regulatory teams.