MSAT Engineer - Tampa, FL

In this role, you will support GMP manufacturing operations for oral solid dose products, ensuring processes run efficiently, safely, and with the highest quality standards. · ...

This role supports GMP manufacturing operations for oral solid dose products at Lonza. · Key responsibilities include providing technical support, · planning project timelines, · applying chemical engineering principles, · and analyzing complex data sets. ...

United States, Tampa (Florida) · MSAT Technical Writer · Location: Tampa, FL · Join our Manufacturing Sciences and Technology (MSAT) team and play a key role in supporting the production of high‑quality solid oral dosage (OSD) medicines. In this role, you will contribute directl ...

MSAT Technical Writer · Location: Tampa, FL · Join our Manufacturing Sciences and Technology (MSAT) team and play a key role in supporting the production of high‑quality solid oral dosage (OSD) medicines. In this role, you will contribute directly to compliant, efficient, and re ...

QA Documentation Engineer (Validation & GMP) · Tampa, FL, 33634 · 100% On-Site · We are seeking a detail-oriented QA Engineer to support validation, engineering documentation, and GMP quality systems in a regulated manufacturing environment. This role plays a critical part in ens ...

Job Description: · Are you a hardworking and dedicated QA Engineering professional located in Tampa, FL? Do you have experience in a Pharmaceutical Manufacturing environment? · Apply today to join a team where your growth, well-being, and success are our top priority · Details: · ...

: · 100% on-site · The QA Engineer is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle documentation, (i.e. SOPs, Change Controls, CAPAs, Deviations), ensuring compliance with corporate procedures, SOPs, cGMP, stand ...

The QA Engineer is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle documentation, (i.e. SOPs, Change Controls, CAPAs, Deviations), ensuring compliance with corporate procedures, SOPs, cGMP, standards and implementi ...

The QA Documentation Specialist is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle documentation, (i.e. SOPs, Change Controls, CAPAs, Deviations), ensuring compliance with corporate procedures, SOPs, cGMP, standard ...

MSAT Technical Writer · Location: Tampa, FL · Join our Manufacturing Sciences and Technology (MSAT) team and play a key role in supporting the production of high‑quality solid oral dosage (OSD) medicines. In this role, you will contribute directly to compliant, efficient, and re ...

JOB TITLE: QA Documentation Specialist III · LOCATION: Tampa, FL · DURATION: 12 Months · Pay rate: $40-$41 per hour · 100% on-site · Summary: · The QA Engineer is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle d ...

QA Documentation Specialist III/QA Engineer · Location: Tampa, FL (ONSITE) · Duration: 6+ MONTHS (possibility of extension) · The QA Engineer is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle documentation, (i.e. ...

QA Documentation Specialist III/QA Engineer · Location: Tampa, FL (ONSITE) · Duration: 12+ MONTHS (possibility of extension) · The QA Engineer is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle documentation, (i.e. ...

Title: QA Documentation Specialist III · Location: Tampa, FL 33634 · Duration: 10 Months · Payrate: 25 - $40/an hr. · 100% on-site · The QA Engineer is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle documentation, ...

The QA Documentation Specialist III is responsible for the timely development, review, and approval of engineering, validation, and lifecycle documentation (SOPs, Change Controls, CAPAs, Deviations). This role ensures compliance with corporate procedures, cGMP regulations, and in ...

Job Title: QA Documentation Specialist III · Location: Tampa, FL (Onsite) · Duration: Contractual till Marc 2027 with the possibility of extension · ONLY W2 PLEASE...... NO C2C · 100% on-site · The QA Engineer is responsible for ensuring the timely development, review and appro ...

QA Engineer · Location: Tampa, FL · Duration: Contract till March 2027 with possibility to extend · 100% on-site · The QA Engineer is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle documentation, (i.e. SOPs, Chan ...

Job Description · The QA Engineer is responsible for ensuring timely development, review, and approval of engineering, validation, and lifecycle documentation in alignment with corporate procedures, SOPs, cGMP, and industry best practices. This role supports manufacturing, engine ...

"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment". · Job Title: QA Documentation Specialist III · Location: Tampa, FL % Onsite) · Duration: 12 months · Pay rate: $35-40/ ...

Title: QA Documentation Specialist III · Location: Tampa, FL 33634 · Duration: 10 Months · Payrate: 25 - $40/an hr. · Find out more about the daily tasks, overall responsibilities, and required experience for this opportunity by scrolling down now. · 100% on-site · The QA Enginee ...