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Fda Project Jobs in Nevada (NOW HIRING)

The Clorox Company

Sanitation Manager

Reno, NV · On-site

... projects. The Sanitation Supervisor / Manager can coordinate other technical and functional ... FDA audit experience * Sanitarian certification - preferred * Lean manufacturing experience

Clorox

Sanitation Manager

Reno, NV

... projects. The Sanitation Supervisor / Manager can coordinate other technical and functional ... FDA audit experience * Sanitarian certification - preferred * Lean manufacturing experience

The Clorox Company

Sanitation Manager

Reno, NV

... projects. The Sanitation Supervisor / Manager can coordinate other technical and functional ... FDA audit experience * Sanitarian certification - preferred * Lean manufacturing experience

Hamilton Medical

Principal Regulatory Affairs

Reno, NV · On-site

... FDA or other regulatory authorities. Respond to inquiries and requests for information in a timely manner with complete and accurate information. * Participate in the required Project Team (P-Team ...

Stord

Continuous Improvement Engineer I

Reno, NV

$78K - $105K/yr

Develop and implement continuous improvement projects for our Fulfillment Center to reinforce the ... Working knowledge of ISO:9001, GMP, and FDA guidelines. * Strong numerical, analytical, and ...

Stord, Inc.

Continuous Improvement Engineer I

Reno, NV · On-site

$78K - $105K/yr

Develop and implement continuous improvement projects for our Fulfillment Center to reinforce the ... Working knowledge of ISO:9001, GMP, and FDA guidelines. * Strong numerical, analytical, and ...

Sun Technical

Assembler

Reno, NV · On-site

$16 - $19.75/hr

... projects * Adhere to general safety rules, manufacturing procedures, company policies and procedures, QSR, and FDA Regulations. * Identify and report any product quality problems * Facilitate ...

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Fda Project information

What is an FDA Project?

An FDA Project typically refers to a project that involves compliance with the U.S. Food and Drug Administration (FDA) regulations. These projects can include developing, testing, or bringing to market medical products such as drugs, medical devices, biologics, or food items. The goal of an FDA Project is to ensure that products meet safety, efficacy, and quality standards set by the FDA before they are approved for public use. Such projects often require extensive documentation, clinical trials, and regulatory submissions to obtain FDA approval.

What is the difference between Fda Project vs Fda Reviewer?

AspectFda ProjectFda Reviewer
Required CredentialsTypically requires a background in life sciences, engineering, or related fields; often includes project management certificationsRequires a degree in life sciences, pharmacy, or medicine; often needs FDA-specific training or experience
Work EnvironmentProject teams within pharmaceutical or biotech companies, regulatory agencies, or consulting firmsRegulatory agencies, pharmaceutical companies, or biotech firms reviewing submissions
Employer & Industry UsageUsed in project management contexts to oversee regulatory submissions and complianceUsed in regulatory review processes to evaluate drug, device, or food applications

In summary, Fda Project roles focus on managing regulatory initiatives and ensuring compliance within organizations, while Fda Reviewers are responsible for evaluating and approving submissions directly for regulatory approval.

What are the key skills and qualifications needed to thrive as an FDA Project Manager, and why are they important?

To thrive as an FDA Project Manager, you need a strong background in regulatory affairs, project management, and a degree in life sciences or a related field. Familiarity with FDA submission requirements, electronic common technical document (eCTD) systems, and project management tools like MS Project or Asana is essential. Excellent communication, organization, and problem-solving abilities help manage cross-functional teams and ensure compliance. These skills ensure that projects meet regulatory standards, progress efficiently, and achieve timely FDA approvals.

What are some common challenges faced by professionals working on FDA project teams?

Professionals working on FDA project teams often encounter challenges related to regulatory compliance and shifting guidelines. Navigating complex documentation requirements, coordinating with cross-functional teams (such as clinical, regulatory, and quality assurance), and meeting strict submission deadlines are all common hurdles. Effective communication and adaptability are essential, as projects frequently involve collaboration across departments and ongoing updates based on regulatory feedback. Successfully managing these challenges helps ensure product approval and supports career advancement within regulatory affairs.
What are popular job titles related to Fda Project jobs in Nevada? For Fda Project jobs in Nevada, the most frequently searched job titles are:
What job categories do people searching Fda Project jobs in Nevada look for? The top searched job categories for Fda Project jobs in Nevada are:
What cities in Nevada are hiring for Fda Project jobs? Cities in Nevada with the most Fda Project job openings:
Fda Project jobs near you
Sanitation Manager

Sanitation Manager

The Clorox Company

Reno, NV • On-site

Full-time

Medical, Retirement, PTO

Posted 12 days ago

Job description

Clorox is the place that's committed to growth - for our people and our brands. Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can make a positive impact on consumers, communities, and teammates. Join our team. #CloroxIsThePlace
Your role at Clorox:
The position will manage the Sanitation functions at the Food BU Reno, NV manufacturing facility. This position will focus on providing sanitation, cGMP, and microbiological expertise to the Plant Management Team. This role will be part of the Plant Quality Team and will establish, maintain, and continuously improve the policies and procedures to ensure that our cleaning and sanitation programs are robust. They will provide support to all departments including quality, operations, maintenance, engineering, logistics, and learning management. Focus areas include identifying and eliminating conditions to prevent contamination and non-compliance to regulatory requirements. This role will need to effectively interface with all levels of the plant workforce to effectively communicate and align on product and operations risks. This role requires the ability to apply standard quality and troubleshooting principles and practices to assigned projects. The Sanitation Supervisor / Manager can coordinate other technical and functional disciplines, as needed, to effectively solve problems. This role will provide training in functional areas of expertise and will require communication of technical material to non-technical people, both oral and written.
In this role, you will:
  • Operations Support - Ensure that the plant cleaning and sanitation procedures are effective and efficient. Provides operational support and analytical problem-solving at the Food BU Reno, NV manufacturing site, drawing on internal and external experts as appropriate, and managing improvement plans and activities. Ensure practices are in place and standardized to ensure that stable conditions exist that ensure product safety and quality assurance standards are maintained in compliance with Federal regulations. Performs plant environmental, and sanitation audits and testing. Manages plant master sanitation schedule (MSS). Ensures documentation adherence and compliance. This position manages 3rd party suppliers and is accountable for the chemical and pest control services. The sanitation team reports to this position.
  • People Management and Development - Provides strategic leadership and direction for site sanitation roles and responsibilities. Identifies current gaps and develops long and short-term plans to serve the team's development and future.
  • Drive Continuous Improvement - Supports the continuous improvement of the Sanitation function by identifying and resolving gaps/waste in systems, tools, and processes. Identified as the SME for key Sanitation processes to ensure they are effectively managed, standardized, maintained, and continuously improved.
  • Training and Support - Ensures plant personnel are appropriately trained on sanitation methods. Provides approval for the cleaning and sanitation validation aspects of new equipment, products & processes. Ensures sanitation of lines for new or changes to formulations meet plant and Federal standards for documentation.
  • Strategic Leadership - Provides strategic leadership and functional vision to help develop the plant and quality journey milestones. This role identifies key leverage points within organization to drive sanitation improvements. Lead processes to improve sanitation by establishing credibility with business management team.
  • Foster a strong food safety culture by emphasizing that food safety is everyone's responsibility.
  • Ensure teams are in compliance and accountable to food safety and GMP requirements.
  • Emphasize continual improvement and open communications about food safety concerns.

#LI-Onsite
What we look for:
  • 5 plus years' experience in FDA regulated (Cosmetics, Food or Beverage) in a combination of Quality and/or Sanitation - Direct manufacturing, operations, sanitation, and product testing preferred.
  • FDA audit experience
  • Sanitarian certification - preferred
  • Lean manufacturing experience
  • Knowledge of cGMP's, FDA regulations, microbiology and analytical testing.
  • Knowledge of government regulatory documentation requirements for Food Manufacturing
  • Knowledge of sanitation in a FDA regulated plant
  • Knowledge of microbiology
  • Knowledge of pathogen environmental monitoring
  • Knowledge of sanitation practices and procedures in a Food Manufacturing plant
  • Knowledge of analytical testing requirements and test methodologies preferred.
  • Strong problems solving skills, issue resolution and root cause analysis.
  • Strong written and verbal business communication skills
  • Strong independent leadership skills.
  • Excellent organization, time management and project management skills
  • Proven experience on cross-functional teams- R&D, Manufacturing, Quality Control, and Technical Services
  • Highly Flexible and Adaptable. Able to work independently in a fast-paced multitasking environment.
  • Work Schedule must be flexible throughout work week and some weekend work.
  • Ability to travel if necessary
  • Bachelor's degree or a combination of education/industry experience indicating an ability to successfully perform the essential functions of the position.

Workplace type:
Onsite - 5 Days a week
Our values-based culture connects to our purpose and empowers people to be their best, professionally and personally. We serve a diverse consumer base which is why we believe teams that reflect our consumers bring fresh perspectives, drive innovation, and help us stay attuned to the world around us. That's why we foster an inclusive culture where every person can feel respected, valued, and fully able to participate, and ultimately able to thrive. Learn more
[U.S.]Additional Information:
At Clorox, we champion people to be well and thrive, starting with our own people. To help make this possible, we offer comprehensive, competitive benefits that prioritize all aspects of wellbeing and provide flexibility for our teammates' unique needs. This includes robust health plans, a market-leading 401(k) program with a company match, flexible time off benefits (including half-day summer Fridays depending on location), inclusive fertility/adoption benefits, and more.
We are committed to fair and equitable pay and are transparent with current and future teammates about our full salary ranges. We use broad salary ranges that reflect the competitive market for similar jobs, provide sufficient opportunity for growth as you gain experience and expand responsibilities, while also allowing for differentiation based on performance. Based on the breadth of our ranges, most new hires will start at Clorox in the first half of the applicable range. Your starting pay will depend on job-related factors, including relevant skills, knowledge, experience and location. The applicable salary range for every role in the U.S. is based on your work location and is aligned to one of three zones according to the cost of labor in your area.
-Zone A: $88,700 - $165,900
-Zone B: $81,300 - $152,100
-Zone C: $73,900 - $138,300
All ranges are subject to change in the future. Your recruiter can share more about the specific salary range for your location during the hiring process.
This job is also eligible for participation in Clorox's incentive plans, subject to the terms of the applicable plan documents and policies.
Please apply directly to our job postings and do not submit your resume to any person via text message. Clorox does not conduct text-based interviews and encourages you to be cautious of anyone posing as a Clorox recruiter via unsolicited texts during these uncertain times.
To all recruitment agencies: Clorox (and its brand families) does not accept agency resumes. Please do not forward resumes to Clorox employees, including any members of our leadership team. Clorox is not responsible for any fees related to unsolicited resumes.

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