Associate Director of AOC Process Development & Manufacturing
Confidential
Associate Director of AOC Process Development & Manufacturing
About the Company
Top-tier pharmaceutical firm
Industry
Pharmaceuticals
Type
Privately Held
About the Role
The Company is in search of an Associate Director for AOC Process Development and Manufacturing, with a focus on Oligo-linker. This senior leadership role is pivotal in overseeing all aspects of oligonucleotide process development and manufacturing, from the initial stages to Phase 3 and commercial scale-up. The successful candidate will be responsible for the technical aspects of oligonucleotide CMO process development, providing expert guidance, and ensuring the execution of late-stage manufacturing strategies. A strong background in oligonucleotide synthesis, and purification, and a deep understanding of cGMP, FDA, and EMA guidelines are essential. The role also involves authoring and reviewing regulatory filings, leading tech transfer activities, and managing a team to meet the demands of the advancing pipeline. Applicants for this role at the company should hold a minimum of a Bachelor's degree in a relevant field, with a Master's or PhD preferred, and have at least 8 years of experience in the pharmaceutical industry, specifically in oligonucleotide synthesis and purification at a large scale. The ideal candidate will have a proven track record in process development, manufacturing, and technology transfer, as well as experience with IND and BLA filings. Strong communication, interpersonal skills, and the ability to work effectively in a fast-paced environment are required. The role demands a leader who can identify and mitigate risks, ensure compliance with regulations, and foster collaboration both internally and with external partners.
Travel Percent
Less than 10%
Functions
- Product Management
- Medical Care/Hospital Administration
$123k - $180.4k
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...activities for assigned products including development and maintenance of RMPs, ARMMs, and... ...utilization and consistency of detailed GPS processes and quality systems. Mentor and... ...responsibilities of the EU Qualified Person and associated regulatory expectations. Provide...Full timeLocal areaFlexible hours
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