ZipRecruiter

Log In

1

Gmp Manufacturing Jobs (NOW HIRING)

Intellectt INC

Manufacturing Technician

Harmans, MD · On-site

Execute GMP manufacturing batch records, SOPs, SMPs, and work instructions with a "right the first time" approach Accurately document activities to meet cGMP standards and quality expectations ...

Lonza

Manufacturing Process Expert

Walkersville, MD · On-site

$103K - $175K/yr

Own day-to-day execution of GMP manufacturing operations, ensuring safety, quality, and on-time delivery * Serve as area SME, driving right-first-time performance and data-driven problem solving

Merck & Co.

BS in Engineering, Computer Science or related field with 2 years of experience (GMP Manufacturing and/or Manufacturing Automation)OrHigh School Diploma and with 4 years of experience (GMP ...

LifeSprout

Manufacturing Technician

Baltimore, MD · On-site

$45K - $60K/yr

Team members gain direct exposure to cutting‑edge materials science, GMP manufacturing, and the development of products designed to restore form and function for patients with soft‑tissue loss.

next page

Showing results 1-20

All JobsGmp Manufacturing Jobs

Gmp Manufacturing information

See salary details

$13

$24

$34

How much do gmp manufacturing jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for gmp manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What is a GMP Manufacturing job?

A GMP Manufacturing job involves producing pharmaceutical, biotechnology, or medical device products while following Good Manufacturing Practices (GMP) regulations. Responsibilities typically include operating equipment, maintaining sterile environments, documenting processes, and ensuring product quality and compliance. These roles are essential for maintaining safety and regulatory standards in healthcare-related manufacturing industries.

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

To excel in GMP Manufacturing, you need a solid understanding of Good Manufacturing Practices, attention to detail, and experience in regulated production environments, often backed by a degree in life sciences or engineering. Familiarity with quality management systems, batch record documentation, and equipment such as bioreactors or chromatography columns is typically required, and certifications like GMP or Six Sigma can be beneficial. Strong teamwork, communication skills, and the ability to follow precise procedures are essential soft skills for this position. These competencies ensure safe, compliant, and efficient production of pharmaceuticals or biotechnology products within strict regulatory frameworks.

What are some common challenges faced in GMP Manufacturing roles?

Employees in GMP Manufacturing often encounter challenges such as maintaining meticulous documentation, adapting to changing regulatory requirements, and adhering to strict cleanliness and safety standards. The production process must be tightly controlled and deviations must be reported and resolved promptly, which requires a high level of diligence and accountability. Additionally, working collaboratively with quality assurance, engineering, and other cross-functional teams can add complexity to daily operations. Overcoming these challenges helps ensure product quality and regulatory compliance, while also providing valuable professional experience in one of the most highly regulated industries.

More about Gmp Manufacturing jobs
What cities are hiring for Gmp Manufacturing jobs? Cities with the most Gmp Manufacturing job openings:
What are the most commonly searched types of Gmp Manufacturing jobs? The most popular types of Gmp Manufacturing jobs are:
What states have the most Gmp Manufacturing jobs? States with the most job openings for Gmp Manufacturing jobs include:
What job categories do people searching Gmp Manufacturing jobs look for? The top searched job categories for Gmp Manufacturing jobs are:
Gmp Manufacturing jobs near you
Infographic showing various Gmp Manufacturing job openings in the United States as of June 2026, with employment types broken down into 1% Internship, 50% Full Time, 42% Part Time, 3% Temporary, 2% Contract, and 2% Nights. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.
API Manufacturing Process Safety Engineer

API Manufacturing Process Safety Engineer

Phlow Corp

Petersburg, VA • On-site

$72K - $96K/yr

Full-time

Posted 4 days ago

Job description

Phlow Corp is seeking an API Manufacturing Process Safety Engineer to own and build the API Manufacturing Process Safety program from the ground up for small-molecule API manufacturing at the Petersburg, VA campus. This position is directly responsible for the process safety activities associated with technology transfer, process design, and GMP startup, and works hand in hand with the Tech Transfer team and the GMP Manufacturing Operations team to ensure safe, compliant, and reliable operations. The role leads process safety assessments, Management of Change (MOC), and the implementation and verification of safeguards in GMP manufacturing.
Requirements
Essential Job Duties & Responsibilities
  • Build, implement, and continually improve the API Process Safety program in alignment with OSHA PSM, EPA requirements, and Phlow procedures.
  • Own and lead PFMEAs, PHAs, and PSSRs for new and existing API processes; translate outcomes into practical engineered and administrative controls for GMP operations.
  • Identify and control hazards typical to API operations (e.g., exotherms, overpressure, vacuum collapse, flammable/toxic releases, static, dust deflagration) and ensure safeguards are in place and effective.
  • Coordinate thermal hazard characterization (e.g., DSC/ARC/RC1) and ensure data are integrated into equipment design, operating limits, automation strategies, interlocks, and procedures.
  • Develop and support relief and vent strategies (PSVs/rupture discs, vent sizing, scrubbers/containment) and contribute to LOPA/SIL evaluations and verification of assumptions.
  • Own the process safety portion of the MOC process by evaluating risk impacts, defining required safeguards, and confirming PSI updates, training, and startup readiness.
  • Define mechanical integrity expectations for critical protective systems and instrumented functions; work closely with Maintenance and Engineering to prioritize and validate testing.
  • Lead or participate in incident and near-miss investigations related to process and equipment; perform root cause analysis and track corrective/preventive actions to closure.
  • Develop and deliver training and coaching for employees and contractors on process safety and life safety requirements related to API manufacturing.
  • Collaborate closely with Tech Transfer, GMP Manufacturing GMP Manufacturing Operations, Process Engineering, Quality & Regulatory, Facility Security, and local emergency responders to support drills, pre-incident planning, and safe execution of campaigns.

Requirements:
  • Bachelor's degree in Chemical Engineering or a closely related engineering discipline.
  • Experience in process safety, chemical engineering, or EHS in manufacturing (pharma/API or chemical processing preferred).
  • Practical experience with exothermic/reactive chemistry, overpressure protection, or cryogenic/flammable systems.
  • Working knowledge of OSHA/EPA regulations and core PSM elements (PHA/HAZOP, LOPA/SIL concepts, MOC, PSSR, incident investigation).
  • Proficiency with process safety tools and documentation (PSI, risk assessments, action tracking).
  • Strong analytical and problem-solving skills with the ability to collaborate in cross-functional teams.
  • Ability to work in a fast-paced environment with regular field presence in manufacturing areas.

Competencies/Skills:
  • Solid technical proficiency in process safety methods and engineering fundamentals.
  • Ability to perform structured risk assessments and recommend practical mitigation strategies.
  • Effective communication and interpersonal skills at all organizational levels.
  • Strong organizational skills and the ability to manage multiple tasks and priorities.
  • Continuous improvement mindset and attention to detail.

Working Conditions:
  • Work environment includes GMP manufacturing suites, technical areas, and utilities with potential exposure to chemical materials and elevated noise.
  • Must maintain a high level of awareness for personnel and equipment safety.
  • Use of personal protective equipment (PPE) may be required, including respirators, gloves, safety glasses, and protective clothing.

Physical Requirements
  • Work in various positions such as walking, standing, or sitting for prolonged durations, including reaching, bending, twisting, turning, and climbing.
  • Exposure to indoor factory conditions and outdoor environments with varying temperatures.
  • Ability to lift objects up to 25-35 pounds occasionally.
  • Frequent walking, standing, bending, and climbing stairs or ladders to access equipment and platforms

Apply