=EF=BB=BF

Hello Timothy,

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

Cordially,

Joyce Barreto

Escala= te Life Sciences

Administrative Assistant/Recruiter

C= ell: (407) 987-7529

Office: (877) 213-7740

www.escalatesciences.com

CONFIDENTIAL NOTICE: This may contain c= onfidential and privileged information for the sole use of the intended reci= pient. If you have received this message in error, please notify us immediat= ely by replying to this message and deleting it from your information system= .

On Wed, Feb 4, 2026 at 12:43=E2=80=AF= PM TJ Bourdeau <tjphuhs@gmail.com> wrote:

Joyce,

Just checking in if there are any upda= tes to my application or if there is any other information you need from me?=

Thanks,
TJ

On Jan 29, 2026, at 12:10=E2=80=AFPM, Joyce Barreto &= lt;jbarre= to@escalatesciences.com> wrote:

=EF=BB=BF

Thank you&nbs= p;for that information Timothy, I will be forwarding this to our operations m= anager and let you know if they request anything else or if we can move forw= ard with the secondary screening/interview.

C= ordially,

Joyce= Barreto

Escalate Life Sciences

Administrative&nbs= p;Assistant/Recruiter

Cell: (407) 987-7529

Office: (= 877) 213-7740

www.escalatesciences.com

CONFIDENTIAL NOT= ICE: This may contain confidential and privileged information for the sole u= se of the intended recipient. If you have received this message in error, pl= ease notify us immediately by replying to this message and deleting it from y= our information system.

On Thu, Jan 29, 2026 at 1:30=E2=80=AF= AM TJ Bourdeau <tj= phuhs@gmail.com> wrote:

Joyce,

Below is my response to your te= xt sent on 01/28/26:

At Formulated Sol= utions, I=E2=80=99ve supported GMP manufacturing operations for approximatel= y 3+ years, with direct involvement in quality oversight of controlled envir= onment and aseptic-adjacent manufacturing, including nasal spray production l= ines.
My experience includes o= n-floor Quality support of manufacturing operations conducted in controlled e= nvironments where we required the dawning and doffing of =E2=80=9Cbunny suit= =E2=80=9D gowning, where I provided IPQA and FPQA oversight during active pr= oduction runs. While I was not an aseptic operator, I was responsible for en= suring aseptic technique, procedural adherence, and documentation accuracy w= ere maintained throughout manufacturing activities. This included line clear= ance verification, batch record review, real-time documentation support, and= escalation of quality concerns during production.
<= p style=3D"margin-right:0in;margin-left:0in;font-size:medium;font-family:&qu= ot;Times New Roman",serif">As I progressed into Quality Supervisor and then QA M= anager roles, my responsibilities expanded to include review and approval of= batch records associated with aseptic/controlled-environment steps, deviati= on investigations related to aseptic practices or documentation errors, and C= APA implementation to strengthen right-first-time execution. I also supporte= d 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 per= formed under GMP-controlled environments, with a strong focus on compliance,= documentation integrity, and risk-based decision-making during live product= ion.
<= br>

Let me know if you need anything else from me, =
TJ