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Gmp Consultant Jobs (NOW HIRING)

Advanced Cleanroom Solutions

GMP Cleaner

San Diego, CA · On-site

$14.75 - $17.50/hr

The company also offers contamination consulting, audits, training, certification, and testing to support clients' quality and compliance needs. Role Description The GMP Cleaner is a part-time, on ...

New

Eliquent Life Sciences, Inc

Consultant 1

Montrose, CA · On-site

Execute validation testing and document results in compliance with GMP/GLP standards. * Support ... Consultant I (Entry-Level / Junior) * Experience: 0-3 years CSV or validation experience in GMP ...

Techtrueup

Machine Operator (GMP)- 2nd shift

Clinton, PA

$16.75 - $20/hr

Our wide network of consultants and contract-to-hire engineers brings deep expertise across ... The GMP Associate I supports the manufacturing of high-quality medical devices by operating ...

GMP Pros

Technical Sales Representative

Omaha, NE · On-site

If that's you - GMP Pros wants to hear from you. Who We Are GMP Pros, Inc. is a fast-growing ... consultative polish of an account manager who earns trust in a complex, regulated industry.That ...

Techtrueup

Machine Operator (GMP)- 2nd shift

Clinton, PA · On-site

$16.75 - $20/hr

Our wide network of consultants and contract-to-hire engineers brings deep expertise across ... The GMP Associate I supports the manufacturing of high-quality medical devices by operating ...

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How much do gmp consultant jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for gmp consultant in the United States is $66.73, according to ZipRecruiter salary data. Most workers in this role earn between $55.53 and $80.77 per hour, depending on experience, location, and employer.

Are GMP consultant jobs in demand?

GMP (Good Manufacturing Practice) consultant jobs are in demand due to ongoing regulatory requirements in the pharmaceutical, biotech, and food industries. Professionals with expertise in compliance, quality assurance, and relevant certifications are sought after to ensure manufacturing processes meet strict standards.

What is a GMP consultant?

A GMP (Good Manufacturing Practice) Consultant is a professional who helps businesses comply with regulatory standards for the production of pharmaceuticals, medical devices, food, and cosmetics. They assist in quality assurance, regulatory compliance, audits, and process improvements to ensure safety, consistency, and legal adherence. Their role often includes training staff, identifying compliance gaps, and preparing companies for inspections by regulatory bodies like the FDA or EMA.

What does a GMP consultant do?

A GMP Consultant’s daily responsibilities often include conducting facility audits, reviewing and developing SOPs, analyzing compliance gaps, and providing recommendations for process improvements. They may also deliver training sessions to staff, ensure documentation aligns with regulatory standards, and support client teams during inspections or regulatory submissions. GMP Consultants frequently collaborate with quality assurance, production, and regulatory affairs personnel, making strong interpersonal skills and clear communication crucial. This diverse mix of tasks provides opportunities to solve challenges and help organizations maintain high-quality standards.

What are the key skills and qualifications needed to thrive as a GMP consultant?

To thrive as a GMP Consultant, you need in-depth knowledge of Good Manufacturing Practices, quality assurance, and regulatory compliance, typically backed by a degree in life sciences or related fields. Familiarity with regulatory frameworks (such as FDA, EMA), audit processes, and systems like CAPA management or electronic QMS is essential, and certifications like GMP Professional or Six Sigma are advantageous. Strong analytical thinking, project management, and excellent communication skills are key soft skills for excelling in this role. These abilities ensure consultants can effectively guide organizations through complex regulatory landscapes, drive continuous improvement, and maintain compliance within highly regulated industries.

How to become a GMP consultant?

To become a GMP (Good Manufacturing Practice) consultant, individuals typically need a background in life sciences, pharmacy, or engineering, along with experience in pharmaceutical or biotech manufacturing. Obtaining certifications such as the Certified Quality Auditor or GMP-specific training can enhance credibility, and strong knowledge of regulatory requirements from agencies like the FDA is essential. Gaining practical experience and staying current with industry standards are key steps in establishing a career as a GMP consultant.
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Gmp Consultant jobs near you
Infographic showing various Gmp Consultant job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 7% Part Time, and 6% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $138,790 per year, or $66.7 per hour.

GMP QC Systems Consultant

Stark Pharma Solutions Inc

Frankford, DE • On-site

Contractor

Posted 17 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on GMP QC Systems Consultant position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: GMP QC Systems Consultant

Location: Frankford, DE (100% Onsite)
Duration: 12+ Month Contract

Job Overview

We are seeking an experienced GMP QC Systems Consultant to support the implementation, integration, and validation of Quality Control laboratory systems in a regulated pharmaceutical environment. The ideal candidate will have strong expertise in GMP laboratory systems, Computer System Validation (CSV/CSA), and cross-functional project execution.

Key Responsibilities

  • Lead implementation and integration of GMP QC laboratory systems.
  • Coordinate system configuration, data migration, deployment, and go-live activities.
  • Manage project timelines, risks, budgets, and stakeholder communications.
  • Support Computer System Validation (CSV/CSA), including IQ/OQ/PQ execution and documentation.
  • Perform risk assessments, testing, and validation activities in compliance with GAMP5 and GxP requirements.
  • Collaborate with QA, IT, laboratory teams, vendors, and business stakeholders to ensure successful project delivery.
  • Ensure compliance with GxP, Data Integrity, and internal quality standards.
  • Prepare project status reports and support release readiness activities.

Required Qualifications

  • 8+ years of experience in Pharmaceutical, Biotechnology, or other GMP-regulated environments.
  • Strong experience implementing and validating QC/Laboratory systems.
  • Hands-on knowledge of CSV, CSA, GAMP5, GxP, IQ/OQ/PQ, and risk-based validation.
  • Experience with system integration, data migration, and cross-functional project coordination.
  • Familiarity with laboratory platforms such as LIMS, SDMS, Empower, LabX, QuantStudio, SoftMax Pro, or similar systems.
  • Excellent communication, documentation, and stakeholder management skills.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com