Description The Principal Scientist, QC Analytical serves as a senior scientific expert within the Quality Control organization, providing advanced technical leadership, method development oversight, and subject-matter e…
Description The Scientist I, QC Analytical, is an experienced individual contributor responsible for independent execution, maintenance, and scientific oversight of GMP analytical methods supporting raw material, in-proc…
Skills: HPLC/UPLC, ELISA, Protein Characterization, GMP Compliance, Data Integrity
Company: Gerber Collision & Glass Great Teams Don’t Happen by Accident Built with Intent. Driven by YOU. At the Gerber Collision & Glass, our teams work to provide the elite infrastructure and supportive environment you …
Skills: Vehicle Disassembly, Vehicle Reassembly, Body Repair, Frame Realignment, Welding
Why Work for Saddle Creek? Saddle Creek Logistics Services succeeds by promoting a diverse, friendly, and respectful teamwork environment. As a vital service provider, we not only make a difference in our community but o…
Skills: Order Picking, Packing, RF Scanning, Product Assembly, Cycle Counting
Location: Sanford, FL (On-site) Schedule: Monday–Friday, 7:00 AM–3:30 PM (core hours) About Omega Medical Imaging Omega Medical Imaging designs and manufactures advanced image-guided interventional systems used in hospit…
Company: Gerber Collision & Glass Great Teams Don’t Happen by Accident Built with Intent. Driven by YOU. At the Gerber Collision & Glass, our teams work to provide the elite infrastructure and supportive environment you …
Skills: Vehicle Disassembly, Vehicle Reassembly, Body Repair, Frame Realignment, Welding
Company: Gerber Collision & Glass Great Teams Don’t Happen by Accident Built with Intent. Driven by YOU. At the Gerber Collision & Glass, our teams work to provide the elite infrastructure and supportive environment you …
Skills: Vehicle Disassembly, Body Repair, Frame Realignment, Welding, Painting
Additional Locations: Requisition ID: 27425 REV-O is the manufacturer of two industry-leading ambulance brands that build Type 1, Type 2, Type 3, and medium-duty models: Road Rescue & Wheeled Coach. With a legacy and pas…
Overview As a Shift Lead, you’ll help ensure your team of co-workers are maximizing their overall productivity during each shift, while adhering to the highest safety standards. Hourly Pay: $19.00/hr. Shift(s): 4th Shift…
Skills: Team Leadership, Safety Compliance, Recruiting, Employee Development, Forklift Operation
Maschmeyer Concrete Company of Florida is currently seeking highly-motivated, dependable Block Plant Laborers to join our team at our Concrete Block Production Plants in major cities throughout Florida. Availability for …
Skills: Quality Inspection, Defect Removal, Palletizing, Industrial Cleaning, Production Line Operation
Application close date: Applications will be accepted on an ongoing basis until the requisition is closed. At Blue Origin, we envision millions of people living and working in space for the benefit of Earth. We’re workin…
We take pride in our culture and strive to make Bobcat - GDN a place where people want to work, achieve excellence, remain curious and humble, and build lifelong relationships. ** Bobcat is Hiring in the South Fort Pierc…
Company: Gerber Collision & Glass Great Teams Don’t Happen by Accident Built with Intent. Driven by YOU. At the Gerber Collision & Glass, our teams work to provide the elite infrastructure and supportive environment you …
Skills: Vehicle Disassembly, Body Repair, Chassis Realignment, Welding, Painting
CURRENT EMPLOYEES - Please apply using "Jobs Hub" in Workday. This career site is for external applicants only. Employee Type: Regular Repairs electrical mining equipment and facilities. Job Description: Title: Electrici…
Skills: Electrical Troubleshooting, High Voltage Systems, AC/DC Circuits, MSHA Regulations, National Electric Code
**This is a contract position** (We have openings at both our Davie and Fort Lauderdale locations with multiple shifts available.) Davie: 3370 Davie Rd #601, Davie, FL 33314Fort Lauderdale: 276 SW 34th St, Fort Lauderdal…
Skills: Shipping and Receiving, Inventory Management, SAP, Forklift Operation, Microsoft Excel
PSG® is the global pump, metering and dispensing-solution expert, enabling the safe and efficient transfer of critical and valuable fluids that require optimal performance and reliability in applications where it matters…
Skills: Supervision, Mentoring, Training, Production Scheduling, ERP Software
Date Posted: 2026-07-01 Country: United States of America Location: US-FL-JUPITER-ADR ~ 17900 Beeline Hwy ~ ADR BLDG Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizens…
Skills: Dimensional Inspection, Visual Inspection, Power Tool Operation, Mechanical Tool Operation, Technical Data Interpretation
ELECTRONICS TECHNICIAN About You The person we are looking for is dynamic, driven, motivated, and has deep technical expertise. You have exemplary electrical/electronic trouble shooting and problem-solving skills. You ar…
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Full-time
postgraduate degree
Posted 39d ago
~40 hrs/week
Responsibilities
Provides senior technical leadership for QC analytical activities, overseeing the development, validation, and transfer of complex analytical methods. Acts as a subject matter expert during regulatory inspections and leads high-level investigations into atypical results.
Requirements
Requires a Ph.D. or Master's degree in biological sciences or analytical chemistry with 8-10 years of experience in a GMP, FDA-regulated environment. Must possess expert-level knowledge of analytical methodologies such as HPLC, CE, and MS.
Full job description
Description
The Principal Scientist, QC Analytical serves as a senior scientific expert within the Quality Control organization, providing advanced technical leadership, method development oversight, and subject-matter expertise for analytical activities supporting raw materials, intermediates, drug substances, and final products. This role drives the development, qualification, and validation of complex analytical methods, supports technology transfer activities, and ensures analytical programs meet regulatory, corporate, and scientific standards. The Principal Scientist leads high-level investigations, provides technical mentorship across departments, and contributes to strategic initiatives supporting continuous improvement of QC Analytical operations.
Requirements
Provide expert leadership in analytical testing for biologics, vaccines, cell/gene therapies, or APIs, including techniques such as HPLC/UPLC, GC, CE, ELISA, compendial methods, spectroscopy, and bioassays.
Provide expert guidance for method lifecycle management, including phase-appropriate validation strategies and regulatory expectations.
Lead technical transfer of analytical methods from Process Development, Protein Characterization, and external partners into QC, ensuring successful integration into routine testing operations.
Act as primary scientific reviewer of QC analytical data, reports, protocols, and investigations to ensure accuracy, compliance, and scientific integrity.
Support the design, review, and execution of stability studies; develop stability-indicating methods and oversee evaluation of long-term and accelerated data.
Serve as the QC Analytical SME during audits, regulatory inspections, client meetings, and cross-functional technical discussions.
Provide advanced technical support for atypical results, including OOS, OOT, and ABT investigations; lead root cause analysis and propose scientifically sound corrective and preventive actions.
Contribute to continuous improvement initiatives, including new technologies, workflow optimization, data integrity enhancements, and analytical efficiency improvements.
Collaborate with QA, Manufacturing, Process Development, and Protein Characterization groups to resolve complex analytical issues and ensure alignment across teams.
Prepare and review scientific documentation including method development reports, validation protocols, stability reports, and analytical risk assessments.
Mentor and guide QC Analysts and Scientists, providing training in new methods, instrumentation, regulatory expectations, and scientific best practices.
Maintain deep knowledge of compendial, ICH, and FDA guidance and ensure analytical strategies align with current regulatory expectations.
This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.
Education and Skills Required:
Ph.D. in biological sciences, biochemical sciences, analytical chemistry, or related field preferred or Master’s degree with extensive relevant experience may be considered.
Minimum of 8–10 years of experience in a GMP, FDA-regulated environment with a strong focus on analytical development, validation, and QC laboratory operations
Proven track record of leading analytical teams and complex technical projects
Expert-level knowledge of analytical methodologies such as HPLC/UPLC, CE, MS, ELISA, qPCR, and other characterization techniques.
Strong organizational, documentation, and time-management capabilities with high attention to detail.
Your CDMO Partner for On-Time Process Development and cGMP Manufacturing.
Industry
Biotechnology Research
Company size
51-200 employees
Headquarters
Fort Lauderdale, Florida
LinkedIn followers
6,267
GBI, based near Fort Lauderdale, Florida, is a fully integrated, customer-focused cGMP Contract Development Manufacturing Organization (CDMO) of Biosimilar and innovative monoclonal antibodies, recombinant proteins, vaccines, Antibody Drug Conjugates (ADCs), and other bioconjugates.
GBI offers a wide range of Single Source Solution services, including cell line development, GMP master cell banking, proof-of-concept development, cell culture, purification, and bioconjugation process development, scale-up, GLP pilot manufacturing for Tox animal studies, and cGMP manufacturing with fill & finish for human clinical trials.
These core services are complemented by full support relative to assay development and qualification, analytical and microbiological Quality Control (QC), and Quality Assurance and Regulatory Affairs (QA/RA). With over 20 years of experience as an independent contract development and manufacturing service provider, GBI has worked with organizations of all sizes, from academic research institutions and virtual biotech start-ups to large, established multinational corporations.
Offices: 1850 NW 69th Ave, Fort Lauderdale, Florida 33313, US
BiosimilarsBioconjugationMonoclonal AntibodiesRecombinant ProteinsCell CultureVaccinesAntibody Drug ConjugatesRadioimmunoconjugatesPurificationQbD
Based on 1495 listings with disclosed salaries, most manufacturing jobs in Florida pay between $66k–$178k per year. Individual offers vary with seniority, company size, and specialization.
How many Manufacturing jobs are open in Florida right now?
There are currently 8,779 open manufacturing positions in Florida listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Florida?
Companies currently hiring include Blue Origin, Northrop Grumman, Northrop Grumman Mission Systems, Inc., Coca-Cola Beverages Florida, L3Harris Technologies, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Manufacturing jobs in Florida?
Yes — 541 of the 8779 open manufacturing positions offer remote or hybrid work (197 remote, 344 hybrid).
How do I apply for Manufacturing jobs in Florida?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.