Miramar, Florida, United States · On-site
Job DetailsJob Location: Miramar, FL 33025Position Type: Full TimeJob Shift: Any Supports release and stability testing for raw materials, components, standards, intermediate/finished products Prepares and executes verif…
Skills: Release Testing, Stability Testing, Verification Protocols, Technology Transfer, Method Validation
Miramar, Florida, United States · On-site
Job DetailsJob Location: Miramar, FL 33025Position Type: Full TimeJob Summary: The QC Scheduler/Planner is responsible for coordinating and optimizing Quality Control laboratory activities to ensure timely testing and re…
Skills: QC Scheduling, Sample Workflow Coordination, GMP Compliance, Capacity Planning, KPI Tracking
Miramar, Florida, United States · On-site
Job DetailsJob Location: Miramar, FL 33025Position Type: Full TimeJob Shift: DayJob Summary: The Design Controls Specialist is responsible for establishing, maintaining, and ensuring compliance of design control processe…
Skills: Design Controls, DHF Management, FDA 21 CFR Part 820, ISO 13485, ISO 14971
Tamarac, Florida, United States · On-site
Job DetailsJob Location: Tamarac, FL 33321Job Shift: Swing Gains and uses qualifications to perform process steps as necessary to support continuous operations, in accordance with Batch manufacturing record instructions …
Skills: cGMP, Batch Manufacturing Records, SAP, Equipment Cleaning, Material Weighing
Hyderabad, Telangana, India · On-site
Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Position Type: Internship Assist in the preparation and submission of regulatory documents to health authorities for product registrations…
Skills: Regulatory Documentation, Regulatory Research, Compliance Review, Cross-functional Collaboration, Regulatory Intelligence
Tamarac, Florida, United States · On-site
Job DetailsJob Location: Tamarac, FL 33321Position Type: Full TimeJob Shift: SwingDescription: The Aseptic Cleaner will be responsible for daily, weekly and overnight sanitization of the clean room manufacturing areas. T…
Skills: Aseptic Cleaning, CGMP Practices, SOP Compliance, Sterile Gowning, Sanitization
Tamarac, Florida, United States · On-site
Job DetailsJob Location: Tamarac, FL 33321Job Shift: SwingJob Summary: The Supervisor, Production Operations is responsible for all aspects of a specific shift within the Transdermal Manufacturing and Packaging facility,…
Skills: Leadership, cGMP, Production Planning, Performance Metrics, Continuous Improvement
Tamarac, Florida, United States · On-site
$90k–$110k/yr
Job DetailsJob Location: Tamarac, FL 33321Salary Range: $90,000.00 - $110,000.00Job Shift: DayJob Summary: This position is responsible for authoring and executing process validation protocols related to drug manufacturi…
Skills: Process Validation, Compliance Engineering, PPQ, FMEA, CAPA
Tamarac, Florida, United States · On-site
$85k–$95k/yr
Job DetailsJob Location: Tamarac, FL 33321Salary Range: $85,000.00 - $90,000.00 Salary/yearJob Shift: DayJob Summary: Under general direction will write, execute, or review and approve equipment commissioning and qualifi…
Skills: Commissioning and Qualification, Statistical Analysis, Design of Experiments, CAPA, GMP
Miramar, Florida, United States · On-site
$75k–$85k/yr
Job DetailsJob Location: Miramar, FL 33025Salary Range: $75,000.00 - $80,000.00 Salary/yearAbout Us: Aveva Drug Delivery Systems is a pharmaceutical manufacturer at the forefront of innovative drug delivery technologies.…
Skills: GMP Compliance, Deviation Investigation, CAPA, Validation, Qualification
Miramar, Florida, United States · On-site
$38/hr–$48/hr
Job DetailsJob Location: Miramar, FL 33025Salary Range: $75,000.00 - $80,000.00 HourlyAbout Us: Aveva Drug Delivery Systems is a pharmaceutical manufacturer at the forefront of innovative drug delivery technologies. We a…
Skills: cGMP Compliance, Deviation Investigation, CAPA, Validation and Qualification, Root Cause Analysis
Hyderabad, Telangana, India · On-site
Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Be a Subject Matter Expert in method development of HPLC and GC techniques. Basic instrument operational skills. QualificationsM .Pharm .
Skills: HPLC, GC Techniques, Method Development, Instrument Operational Skills
Hyderabad, Telangana, India · On-site
Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Position Type: Internship Assist in the preparation and submission of regulatory documents to health authorities for product registrations…
Skills: Regulatory Documentation, Regulatory Research, Compliance Review, Cross-functional Collaboration, Regulatory Intelligence
Hyderabad, Telangana, India · On-site
Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Position Type: Internship Assist in the preparation and submission of regulatory documents to health authorities for product registrations…
Skills: Regulatory Documentation, Regulatory Research, Compliance Review, Cross-functional Collaboration, Regulatory Intelligence
Hyderabad, Telangana, India · On-site
$400k–$700k/yr
Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Salary Range: $400,000.00 - $700,000.00 Salary/yearJob Shift: Any Responsible for identifying project requirements and request for indenti…
Skills: Formulation Development, GLP Procedures, Pre-formulation Study, Scale-up Execution, Sterile Dosage Forms
Miramar, Florida, United States · On-site
$125k–$145k/yr
Job DetailsJob Location: Miramar, FL 33025Position Type: Full TimeSalary Range: $125,000.00 - $145,000.00 SalaryJob Summary –Manager, Supply Chain The Manager, Supply Chain is responsible for overseeing and driving…
Skills: Supply Chain Strategy, Production Planning, Logistics Management, Warehouse Operations, Inventory Control
Tamarac, Florida, United States · On-site
$50k–$80k/yr
Job DetailsJob Location: Tamarac, FL 33321Salary Range: $50,000.00 - $65,000.00Job Shift: Day Review, approve, and release manufacturing, packaging, and clinical batch records along with auxiliary documentation. Prepare …
Skills: Batch Record Review, Product Release, Quality Assurance, SOP Compliance, Deviation Management
Tamarac, Florida, United States · On-site
$16/hr–$18/hr
Job DetailsJob Location: Tamarac, FL 33321Salary Range: $16.00 - $18.25 HourlyJob Shift: DayJob Summary: Provide administrative/secretarial support to the executive team (Aveva/DifGen). This role is responsible for being…
Skills: Administrative Support, Microsoft Office Suite, Front Desk Management, Calendar Management, Filing
Miramar, Florida, United States · On-site
Job DetailsJob Location: Miramar, FL 33025Job Shift: DayJob Summary: The Blender Operator I is responsible for performing pharmaceutical blending and compounding operations involving active pharmaceutical ingredients (AP…
Skills: Pharmaceutical Blending, Compounding Operations, cGMP Compliance, Good Documentation Practices, Hazardous Material Handling
Hyderabad, Telangana, India · On-site
Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Position Type: Full TimeJob Shift: DayJob Description To lead and manage analytical development activities for complex injectable and soli…
Skills: HPLC, UPLC, GC, PSD, SEM
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Supports release and stability testing for raw materials and finished products while executing verification and technology transfer protocols. Responsible for writing technical reports, training analysts, and maintaining QC compliance systems.
Requires a degree in a scientific field with 2 to 7 years of QC laboratory experience depending on the level of education (Bachelor's, Master's, or PhD). Must possess strong mathematical abilities and deep knowledge of FDA and cGMP regulations.
Job DetailsJob Location: Miramar, FL 33025Position Type: Full TimeJob Shift: Any
Supports release and stability testing for raw materials, components, standards, intermediate/finished products
Prepares and executes verification protocols for in-house/compendia test methods
Executes technology transfer protocols and assists in evaluations
Analytical support to ARD for qualification/validation of test methods
Reviews laboratory work and approves data packages as designated by the Supervisor
Maintains a heighten proficiency with data acquisition systems;
Execute methods for calibration of analytical instrumentation
Writes and reviews STPs, SOPs, Specifications and technical reports
Trains analysts on methods and instrumentation
Independently troubleshoots instrumentation
Maintains QC compliance systems with guidance of Supervisor
Coordinates testing schedules and monitors status of sample testing as assigned by the Supervisor
Works as a member of a team to achieve all outcomes
Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements
All other relevant duties as assigned
Qualifications
Ability to apply advances mathematical concepts such as exponents, logarithms, quadratic equations, linear regression, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, and correlation techniques..
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
Ability to read, analyze, and interpret common scientific and technical journals, specifications, standard operating procedures, and standard testing procedures. Ability to write presentations and articles that conform to prescribed style and form. Ability to effectively present information to middle management.
Knowledge FDA, cGMPs, and SOPs
Experience
A minimum of five to seven (5)-7 years of QC laboratory experience (Bachelor’s degree)
A minimum of two to five (2 -5) years of QC laboratory experience (Master’s degree)
A minimum of two (2) years lab experience (Ph. D. degree)
AVEVA is a global leader in transdermal drug delivery located in the United States. The company has an extensive history of providing pharmaceutical partners with fully integrated, controlled-release transdermal products that fulfill unmet market needs or supply high-quality, affordable brand equivalents. By leveraging this experience, AVEVA offers a full range of research, development and manufacturing capabilities to produce transdermal pharmaceutical products that can improve the quality of life, usage and compliance rates for patients.
Offices: 3250 Commerce Parkway, Miramar, FL 33025, US
AVEVA is a global leader in transdermal drug delivery located in the United States. The company has an extensive history of providing pharmaceutical partners with fully integrated, controlled-release transdermal products that fulfill unmet market needs or supply high-quality, affordable brand equivalents. By leveraging this experience, AVEVA offers a full range of research, development and manufacturing capabilities to produce transdermal pharmaceutical products that can improve the quality of life, usage and compliance rates for patients.
Offices: 3250 Commerce Parkway, Miramar, FL 33025, US
