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Gmp Jobs (NOW HIRING)

GMP Pros General Application

Omaha, NE ยท On-site

$91K - $125K/yr

At GMP Pros, Inc., we're not here to do things the way they've always been done. We're here to innovate, push boundaries, and build a future that challenges the norm. If you're bold, driven, and ...

At GMP Pros, Inc. ยฎ , we're not here to do things the way they've always been done. We're here to innovate, push boundaries, and build a future that challenges the norm. If you're bold, driven, and ...

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GMP Cleaner

Oceanside, CA ยท On-site

$25 - $30/hr

Our client is seeking experienced GMP Commercial Cleaners to support cleaning operations in a GMP-regulated manufacturing facility in Oceanside, CA. Candidates must have previous GMP cleaning ...

The Guaranteed Maximum Price (GMP) Accountant is an integral member of the project team and plays a key role in reviewing and tracking GMP Trade Partner billings, collaborating with team members ...

At GMP Pros, Inc., were not here to do things the way they've always been done. We're here to innovate, push boundaries, and build a future that challenges the norm. If you're bold, driven, and ready ...

At GMP Pros, Inc. ยฎ , we're not here to do things the way they've always been done. We're here to innovate, push boundaries, and build a future that challenges the norm. If you're bold, driven, and ...

GMP Cleaning

Pearl River, NY ยท On-site

$18 - $22/hr

RK Pharma Inc. is hiring Cleanroom Technicians to support GMP cleaning , cleanroom sanitation , and visual inspection in our pharmaceutical manufacturing facility. This role is essential to ...

GMP Coordinator

Apex, NC ยท On-site

$26 - $29/hr

GMP Coordinator Job Overview The GMP Coordinator will be responsible for coordinating and managing project tasks in the GMP Program to ensure project delivery within allotted budget and timelines.

GMP Coordinator Job Overview The GMP Coordinator will be responsible for coordinating and managing project tasks in the GMP Program to ensure project delivery within allotted budget and timelines.

GMP Material Handler

Salisbury, NC ยท On-site

$15 - $18.25/hr

GMP Material Handler Salisbury, NC, United States $ 34.00 - 35.00 (US Dollar) GMP Material Handler needs 3+ years GMP warehouse inspection experience GMP Material Handler requires: Requires travel ...

GMP Coordinator

New Albany, OH ยท On-site

$17 - $18/hr

GMP Coordinator Job Overview The GMP Coordinator will be responsible for coordinating and managing project tasks in the GMP Program to ensure project delivery within allotted budget and timelines.

Bioassay GMP scientist will interact with other departments to maintain continuous project flow while complying with GLP/GMP standards. Essential Functions Reasonable accommodations may be made to ...

GMP Scientist I / GMP Operations Technician I The GMP Scientist I / GMP Operations Technician I supports all aspects of Good Manufacturing Practices (GMP) and production within a Clinical ...

GMP Technician

Indianapolis, IN ยท On-site

$18.05 - $19.05/hr

GMP Technician Job Overview The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly condition. The tech will work successfully with fellow employees and others ...

GMP Coordinator

Reading, PA ยท On-site

$23 - $24/hr

Strong knowledge of GMP regulations and guidelines * Excellent attention to detail and organizational skills * Strong communication and interpersonal abilities * Proficiency in using various software ...

GMP Cleaning Associate

Germantown, MD ยท On-site

$45K - $55K/yr

GMP Cleaning Associate will require a professional who thrives in a dynamic team environment, brings meticulous attention to detail in the quality of their work and is proactive in implementing ...

GMP Technical Writer

Tampa, FL ยท On-site

$60 - $70/hr

GMP Technical Writer Contract: 5 months duration with potential for extension Location: Tampa, FL - onsite Role Summary ASI is seeking a GMP Technical Writer / SQA Specialist to support our client ...

GMP Technician

Cairo, NY ยท On-site

$17 - $18/hr

The GMP Tech will be responsible for keeping assigned areas within GMP in clean and orderly condition. The tech will work successfully with fellow employees and others while understanding and ...

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Gmp information

See salary details

$13

$33

$47

How much do gmp jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for gmp in the United States is $33.28, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $44.47 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Gmp position, and why are they important?

To excel in a GMP (Good Manufacturing Practices) specialist role, individuals typically need a strong background in life sciences, quality control, and regulatory compliance, often requiring a relevant bachelor's degree or industry experience. Familiarity with quality management systems, documentation software, and industry-specific certifications like GMP or Six Sigma is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this position. These competencies ensure strict adherence to regulatory standards, product safety, and continuous improvement within pharmaceutical or food manufacturing environments.

What are the typical daily responsibilities of a Gmp specialist in a manufacturing facility?

As a GMP specialist, your day may involve overseeing production processes to ensure compliance with regulatory standards, conducting regular audits, and maintaining detailed documentation of all manufacturing activities. You will likely work closely with quality assurance, production, and engineering teams to identify and rectify any deviations from established protocols. Additionally, you may be responsible for training staff on GMP procedures and supporting investigations into product quality issues. This role requires a proactive approach to problem-solving, a keen eye for detail, and frequent interaction with various departments to maintain product quality and safety.

What skills are needed for Gmp jobs?

GMP (Good Manufacturing Practice) jobs require strong attention to detail, knowledge of regulatory standards, and good documentation skills. Familiarity with manufacturing processes, quality control, and relevant certifications such as GMP training or ISO standards are also important. Effective communication and the ability to work in a regulated environment are essential for success in GMP roles.

Are GMP jobs in demand?

GMP (Good Manufacturing Practice) jobs are in demand in the pharmaceutical, biotech, and food manufacturing industries due to strict regulatory requirements. These roles often require knowledge of quality control, compliance, and relevant certifications, and employment opportunities tend to grow with industry expansion and regulatory updates.

What is a typical day in a GMP job?

A GMP (Good Manufacturing Practice) job typically involves monitoring manufacturing processes, inspecting facilities, ensuring compliance with safety and quality standards, and documenting procedures. The work often requires attention to detail, adherence to protocols, and the use of quality management systems, with shifts varying based on the role and company needs.

What is a Gmp?

A GMP (Good Manufacturing Practice) job typically involves ensuring that products, especially in industries like pharmaceuticals, biotechnology, and food production, are consistently produced and controlled according to quality standards. Employees in GMP roles follow strict guidelines to maintain safety, hygiene, and compliance with regulatory requirements. Common GMP job positions include quality control specialists, manufacturing technicians, and regulatory compliance officers.

More about Gmp jobs
What cities are hiring for Gmp jobs? Cities with the most Gmp job openings:
What are the most commonly searched types of Gmp jobs? The most popular types of Gmp jobs are:
What states have the most Gmp jobs? States with the most job openings for Gmp jobs include:
Infographic showing various Gmp job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, 1% Part Time, 1% Temporary, 6% Contract, and 6% Nights. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $69,222 per year, or $33.3 per hour.

GMP Pros General Application

GMP Pros

Omaha, NE โ€ข On-site

$91K - $125K/yr

Full-time

Vision, Life, Retirement

Re-posted 24 days ago


Job description

Ready to Shatter the Status Quo?


At GMP Pros, Inc., we're not here to do things the way they've always been done. We're here to innovate, push boundaries, and build a future that challenges the norm. If you're bold, driven, and ready to make real impact- join us.


We exist to shatter the status quo - redefining what's possible in our industry, empowering our team to think differently, and creating solutions that break barriers and spark change.

We are proud to be a GreatPlaceToWorkUS-Certified company!Culture: Check out what our employees say makes working here so great!


Ready to make an impact?


GMP Pros seeks experienced Formidable Leaders - W-2 & 1099, Full-time


ValuePeople Benefits:(W-2's)

Enjoyacomprehensive,high-valuebenefitspackagethatincludes:

401(k) with a generous 5% company contribution - no employee match required and immediate vesting.

Flexibletimeoffandpaidfloatingholidays,designedtoenhanceyourwork-lifebalance.

Healthcareplanoptions,plusdental,vision,life,AD&Dcoverage,etc.

HSA/FSAoptionsandanEmployeeAssistanceProgram(EAP).

CompetitivecompensationandparticipationinourStockAppreciationRights(SAR)Plan.


Thrive in a collaborative, inclusive, and diverse culture that champions open communication, transparency, and team connection through engaging events-where every voice is heard, and innovation flourishes.

LifeSciencesIndustry!


Join an innovative, fast-growing company supporting the world's top pharmaceutical, medical device, food, animal health, and manufacturing organizations.


Here, you'll experience the best of both worlds-opportunities to lead impactful projects for global clients while thriving in an agile environment, supported by a highly collaborative, results-driven team.

WhatYou'llExperience:

  • A fast-paced, high-energy environment with exciting challenges and the thrill of exceeding expectations.
  • Major recognition for your successes, and unwavering support to help you overcome any hurdles.
  • Ajourneythatwillexpandyourlimitsandlaunchyouintonewpossibilities.
  • The chance to make a real, lasting impact and leave your mark on something extraordinary.
  • Theenergyandcamaraderieofapassionate,driventeamthatthrivestogether.

Are you a GMP Pros?!

  • Are you a proactive doer?
  • Do you need variety and change to keep from getting bored?
  • Do you build relationships easily and are you able to communicate information so that it is easily understandable?
  • Do you like working in a team supportive environment where others want to help you succeed?
  • Do you try to find a better way for everything because that is the way it should be?
  • Do you thrive in organized chaos and high-pressure situations?
  • Do you quickly become an expert in any subject matter you are working in?
  • Can you stay motivated and help motivate others in the face of adversity and change? Are you resilient?


Some other things that you will need to be successful:

  • Experienced in an FDA-regulated environment.
  • Excellent communication and organization skills, with an analytical and problem-solving mindset.
  • Ability to multi-task and complete multiple projects on time.


These positions require at least 3 years of experience in the Food, Pharmaceutical, Animal Health, Medical Device, or Bio-Pharmaceutical manufacturing sectors.


Preferred Qualities and Traits:

  • Self-Motivated- Must be driven to seek out new opportunities, ask questions and keep pursuing things when information is limited or not given at all.
  • Creative Thinker- Corrective actions require new thoughts and ideas on existing equipment or problems. Approach things with a broad scope at first and engineer solutions.
  • Positive Attitude -This is a tough position. You are in the trenches doing work a lot of others don't want to do. It's a great opportunity to grow and learn a wide variety of skills but if you let things get to you it will show in your attitude towards others. Real positivity within you will show and make others more willing to work with you and drop their guards.
  • Technical Writing Skills - Must be able to quickly turn information received into concise verbiage on paper. Complete stories must be told of events that occurred and actions to be taken but should not use "fluff."
  • Listening Skills -ACTUALLY listen to everyone's input before forming your thoughts or replies. Operators and others in the plant have a wealth of process and product knowledge. Some are limited to their specific trade so it's your job to take their information to the next level and fit it into the bigger puzzle.
  • Adaptable -In the fast moving and changing industry of OTC and Pharma, things will change continuously. Must be able to adapt to the changes and continue making progress.
  • Project Management -General knowledge of project timelines and cost is important, but don't let that limit you in the investigation and problem-solving phases.
  • Willingness To Always Be Learning -You won't always be right, and that's okay. There is a steep learning curve in this industry. Take in as much as possible and it will only benefit your future.
  • Methodically Fast-Paced-Must be patient and focused while also having a continuous sense of urgency.



Pre-Employment Requirements:

  • Pass and maintain pre-employment/contract background check and safety certification, including but not limited to outstanding professional references.
  • Subject to motor vehicle report review.
  • Maintain valid driver's license and endorsements as required per position.
  • Pass pre-employment/contract physical, medical evaluation, and drug screen due to the safety sensitive nature of this position.
  • Successfully complete and maintain any required safety certification and testing on an annual basis.


GMP Pros is an Equal Opportunity Affirmative Employer (EEO/AA) and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status are strongly encouraged to apply. It is the policy of GMP Pros to provide equal opportunity in employment for all qualified individuals regardless of race, color, religion, ethnicity, national origin, ancestry, disability, medical condition, age, citizenship, sex, sexual orientation, gender, gender identity, gender expression, marital status, pregnancy, genetic information, military status, veteran status, and any other characteristic protected by law.


By submitting material for consideration for this position you are attesting that no material or interaction with GMP Pros Team Members establishes any obligation for GMP Pros to hire you. If you are hired, you understand that either GMP Pros or you can terminate your employment at any time and for any reason, with or without cause and without prior notice. Further, you understand that no representative of GMO Pros has the authority to make any assurance to the contrary.


By submitting your application for this position, you attest that you have given GMP Pros true and complete information on this application. No requested information has been concealed. You are authorizing GMP Pros to contact references provided for employment reference checks. If any information you have provided is untrue, or if you have concealed material information, you understand this will constitute cause for the denial of employment or immediate dismissal.


Accessibility: If you need help accessing this page, please contact:Email:HR@gmppros.comIf you want to view the EEO is the Law poster, please choose your language:English-Spanish-Arabic-Chinese


This company participates in the United States Department of Homeland Security E-Verify program. The E-Verify program is an internet-based employment eligibility verification system operated by the U.S. Citizenship and Immigration Services. Please use the links provided for important information when applying for work with this company:Everify English / Spanish


Key words: GXP, engineer, pharma, BioTech, Biologics, eBR, MES, PAS-X


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About GMP Pros

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

Omaha, NE, US

Year founded

2013