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Internship Gmp Pharmaceuticals Jobs (NOW HIRING)

Chemist- II

West Point, PA · On-site

$72K/yr

... Introductory knowledge of GMP concepts through coursework, training, or internships. • ... pharmaceutical drug products • Support method development, method optimization, and method ...

Experience * Entry-level position; internships, academic research, or co-op experience in microbiology or GMP environments preferred. * Exposure to pharmaceutical manufacturing, quality, validation ...

Manufacturing Engineer

Maryland Heights, MO · On-site

$70K - $90K/yr

Internship or co-op experience in pharmaceutical manufacturing or packaging operations. * Knowledge ... Experience working in a cleanroom or GMP environment What We Offer * Competitive base salary ...

Engineering Intern

York, PA · On-site

$16.50 - $21.50/hr

Your Role Our engineering internships provide hands-on exposure to working alongside experienced professionals in a GMP-regulated pharmaceutical manufacturing environment. Engineering Interns support ...

... internship or co-op experience will be considered * Proficiency in AutoCAD 2D and AutoCAD 3D ... Experience in a GMP-regulated biotech or pharmaceutical manufacturing environment * Familiarity ...

... internship or co-op experience will be considered * Proficiency in AutoCAD 2D and AutoCAD 3D ... Experience in a GMP-regulated biotech or pharmaceutical manufacturing environment * Familiarity ...

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Internship Gmp Pharmaceuticals information

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How much do internship gmp pharmaceuticals jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for internship gmp pharmaceuticals in the United States is $15.54, according to ZipRecruiter salary data. Most workers in this role earn between $12.50 and $17.55 per hour, depending on experience, location, and employer.

What is an internship GMP pharmaceuticals?

Internship GMP Pharmaceuticals positions are entry-level roles designed for students or recent graduates to gain practical experience working in pharmaceutical companies that follow Good Manufacturing Practice (GMP) standards. These internships provide hands-on training in areas such as quality assurance, production, research, and regulatory compliance. Interns learn about industry regulations, laboratory techniques, and documentation processes essential for producing safe and effective medicines. The goal is to prepare interns for future full-time roles in the pharmaceutical industry by exposing them to real-world challenges and best practices.

What do interns at a GMP pharmaceutical company do?

As an intern in a GMP pharmaceutical company, you can expect to be involved in a variety of hands-on projects that support quality assurance, manufacturing operations, and regulatory compliance. Typical responsibilities might include assisting with documentation review, participating in laboratory testing, supporting process improvement initiatives, and learning about batch record management. Interns often collaborate closely with experienced scientists, quality control, and production teams, gaining exposure to cross-functional workflows in a regulated environment. This role provides valuable insight into industry standards and helps build a foundation for future roles in pharmaceutical manufacturing or quality assurance.

What skills and qualifications are needed to thrive as an intern at a GMP pharmaceutical company?

To thrive as an intern in a GMP pharmaceutical company, you need a background in life sciences or pharmacy, a basic understanding of laboratory techniques, and knowledge of Good Manufacturing Practices (GMP). Familiarity with laboratory information management systems (LIMS), documentation protocols, and standard operating procedures is often expected. Attention to detail, strong communication, and a willingness to learn are vital soft skills that help interns excel in this setting. These skills and qualities ensure compliance, data integrity, and effective teamwork in a highly regulated and quality-driven industry.

What is the difference between Internship Gmp Pharmaceuticals vs Pharmaceutical Sales Representative?

AspectInternship Gmp PharmaceuticalsPharmaceutical Sales Representative
CredentialsTypically pursuing or recent graduate in life sciences or pharmacyBachelor's degree in life sciences, pharmacy, or related field
Work EnvironmentLaboratory, manufacturing, or quality control settingsField-based, visiting healthcare providers and pharmacies
Industry UsageInternship role within pharmaceutical companies for trainingSales and marketing within pharmaceutical companies

Internship Gmp Pharmaceuticals focuses on gaining hands-on experience in pharmaceutical manufacturing, quality assurance, or regulatory compliance, often in a lab or production setting. In contrast, Pharmaceutical Sales Representatives primarily engage in promoting products to healthcare professionals in the field. Both roles are essential in the pharmaceutical industry but serve different career paths and skill sets.

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What are the most commonly searched types of Gmp Pharmaceuticals jobs?

The most popular types of Gmp Pharmaceuticals jobs are:

What states have the most Internship Gmp Pharmaceuticals jobs?

States with the most job openings for Internship Gmp Pharmaceuticals jobs include:

Infographic showing various Internship Gmp Pharmaceuticals job openings in the United States as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 100% In-person job distribution, with an average salary of $32,333 per year, or $15.5 per hour.

$72K/yr

Temporary

Medical, Dental, Vision, Retirement

Re-posted 29 days ago


Job description

Education & Experience
Required Education:
• BS or MS in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related scientific discipline.
Required Experience:
• No prior pharmaceutical industry experience required.
• Academic laboratory experience, undergraduate or graduate research, or internships may substitute for industry experience.
Preferred Experience:
• Academic or internship exposure to HPLC.
• Chemistry training and experience as a pharma intern in an analytical lab would be ideal.
• Introductory knowledge of GMP concepts through coursework, training, or internships.
• Familiarity with chromatography data systems such as Empower or ChemStation.
• Exposure to analytical techniques such as dissolution testing, GC, or Karl Fischer titration.
Core Technical Competencies
• Fundamental understanding of analytical and scientific principles.
• Ability to follow SOPs, test methods, and laboratory safety requirements.
• Strong attention to detail and commitment to data accuracy and integrity.
• Willingness to learn GMP documentation and electronic laboratory notebook practices.
Software & Digital Tools
Required:
• Microsoft Office Suite (Word, Excel, PowerPoint) for documentation, data review, and communication.
Preferred:
• Empower or other chromatography data systems (e.g., ChemStation).
Key Responsibilities
Under the supervision of senior scientific staff, the contractor will:
• Perform GMP and non GMP analytical testing on pharmaceutical drug products
• Support method development, method optimization, and method validation activities.
• Accurately document experimental work in electronic laboratory notebooks in compliance with data integrity and regulatory requirements.
• Assist with preparation, review, and maintenance of technical documentation and reports.
• Follow laboratory safety, quality, and compliance procedures.
• Learn and adhere to laboratory safety procedures; may support work with Beta Lactam and OEB 4-5 compounds under appropriate supervision and training
Behavioral & Professional Competencies
• Detail oriented, well organized and good time management skill
• Ability to manage multiple tasks with guidance
• Team oriented with effective communication skills
• Demonstrates professionalism, reliability, and compliance mindset
• Strong learning agility and openness to feedback Equal Opportunity Employer / Disabled / Protected Veterans
The Know Your Rights poster is available here:
https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf
The pay transparency policy is available here:
https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdf
For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required.
We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team.
AllSTEM Connections participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program.
https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf
We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
Additional Skills
(none specified)
AllSTEM Representative Contact Info
Account Executive:
Broughton
Branch Phone:
(909) 244-1777
Location:
Ontario, CA