Re: Aseptic Experience

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Hello Timothy,

No new updates from the client, however, in the time being, our operations
manager would like to know if you have managerial or supervisor experience.
How many people and what experience do you have?

Cordially,

*Joyce Barreto*
Escalate Life Sciences
Administrative Assistant/Recruiter
Cell: (407) 987-7529
Office: (877) 213-7740
www.escalatesciences.com
[image: Escales Life Sciences New Logo Firma.jpg]
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On Wed, Feb 4, 2026 at 12:43 PM TJ Bourdeau <tjphuhs@gmail.com> wrote:

> Joyce,
>
> Just checking in if there are any updates to my application or if there is
> any other information you need from me?
>
> Thanks,
> TJ
>
> On Jan 29, 2026, at 12:10 PM, Joyce Barreto <jbarreto@escalatesciences.com>
> wrote:
>
> 
> Thank you for that information Timothy, I will be forwarding this to our
> operations manager and let you know if they request anything else or if we
> can move forward with the secondary screening/interview.
>
> Cordially,
>
> *Joyce Barreto*
> Escalate Life Sciences
> Administrative Assistant/Recruiter
> Cell: (407) 987-7529
> Office: (877) 213-7740
> www.escalatesciences.com
> [image: Escales Life Sciences New Logo Firma.jpg]
> CONFIDENTIAL NOTICE: This may contain confidential and privileged
> information for the sole use of the intended recipient. If you have
> received this message in error, please notify us immediately by replying to
> this message and deleting it from your information system.
>
>
>
> On Thu, Jan 29, 2026 at 1:30 AM TJ Bourdeau <tjphuhs@gmail.com> wrote:
>
>> Joyce,
>>
>>
>> Below is my response to your text sent on 01/28/26:
>>
>>
>> At Formulated Solutions, I’ve supported GMP manufacturing operations for
>> approximately 3+ years, with direct involvement in quality oversight of
>> controlled environment and aseptic-adjacent manufacturing, including nasal
>> spray production lines.
>>
>> My experience includes on-floor Quality support of manufacturing
>> operations conducted in controlled environments where we required the
>> dawning and doffing of “bunny suit” gowning, where I provided IPQA and FPQA
>> oversight during active production runs. While I was not an aseptic
>> operator, I was responsible for ensuring aseptic technique, procedural
>> adherence, and documentation accuracy were maintained throughout
>> manufacturing activities. This included line clearance verification, batch
>> record review, real-time documentation support, and escalation of quality
>> concerns during production.
>>
>> As I progressed into Quality Supervisor and then QA Manager roles, my
>> responsibilities expanded to include review and approval of batch records
>> associated with aseptic/controlled-environment steps, deviation
>> investigations related to aseptic practices or documentation errors, and
>> CAPA implementation to strengthen right-first-time execution. I also
>> supported inspection readiness and participated in FDA and customer audit
>> shadowing, including on-floor support and follow-up documentation.
>>
>> Overall, my aseptic manufacturing experience is rooted in quality
>> governance and oversight of nasal spray manufacturing performed under
>> GMP-controlled environments, with a strong focus on compliance,
>> documentation integrity, and risk-based decision-making during live
>> production.
>>
>>
>>
>> Let me know if you need anything else from me,
>>
>> TJ
>>
>