1

Internship Computer System Validation Csv Jobs in New York

CSV Lead

Raritan, NJ · On-site

Advanced knowledge of Computer Systems Validation (CSV). * Strong understanding of GXP, 21 CFR Part 11, EU GMP Annex 11, GAMP 5, and Data Integrity. * Hands-on experience with risk-based validation ...

New

Lead or assist in Computer System Validation (CSV), equipment qualification, and periodic review processes. Generate and review technical documentation, protocols, and reports. * Compliance ...

... Computer Systems Validation (CSV) • Deep understanding of FDA regulations, GxP requirements, and data integrity • Experience supporting FDA approval processes and regulatory submissions • ...

CSV Engineer Location: Raritan, NJ(Hybrid) Mandatory - Validation experience with ERP applications ... in Computer System Validation (Based on the role selected) * Experience in FDA and/or Global ...

CSV Engineering Lead

Manhattan, NY · On-site

$90 - $120/hr

As a CSV Engineering Lead, you will make sure the systems Neko relies on are validated, fit for ... Computer system validation at Neko is not only about compliance. It is equally about making our ...

Showing results 21-40

Internship Computer System Validation Csv information

What is an internship in computer system validation (CSV)?

An Internship in Computer System Validation (CSV) is a temporary position, typically for students or recent graduates, that provides hands-on experience in ensuring that computer systems used in regulated industries (like pharmaceuticals or healthcare) meet required standards and regulations. Interns assist with validating software and hardware, documenting processes, and ensuring compliance with industry guidelines such as FDA 21 CFR Part 11 or EU Annex 11. This role helps interns understand the lifecycle of computer systems in a regulated environment and prepares them for careers in quality assurance, compliance, or IT within highly regulated sectors.

What are the typical responsibilities of an intern in computer system validation (CSV)?

As a Computer System Validation (CSV) intern, you can expect to assist with tasks such as reviewing and drafting validation documentation, executing test scripts, and collecting evidence to ensure compliance with regulatory requirements. You may also support the maintenance of validation records and participate in team meetings to discuss project progress or findings. These responsibilities are crucial in ensuring that computer systems used in regulated industries, like pharmaceuticals or healthcare, function as intended and meet quality standards. Working closely with senior validation specialists, you'll gain hands-on experience with industry guidelines and learn how cross-functional teams collaborate to achieve compliance.

What are the key skills and qualifications needed for an internship in computer system validation (CSV)?

To thrive as an Internship Computer System Validation CSV specialist, you need foundational knowledge in computer science, life sciences, or engineering, along with an understanding of regulatory standards like GxP or FDA 21 CFR Part 11. Familiarity with validation documentation, software testing tools, and quality management systems is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for interpreting requirements and collaborating with cross-functional teams. These skills ensure compliance, data integrity, and the successful validation of computerized systems in regulated environments.

What is the difference between Internship Computer System Validation Csv vs Computer System Validation Specialist?

AspectInternship Computer System Validation CsvComputer System Validation Specialist
CredentialsTypically pursuing or recent graduate, basic understanding of validationRelevant certifications (e.g., GAMP, ISPE), experience preferred
Work EnvironmentInternship setting, supervised, entry-level tasksFull-time role, independent responsibilities in regulated industries
Industry UsageUsed in pharmaceutical, biotech, and medical device companies for trainingUsed for maintaining compliance, validating systems in regulated environments

In summary, the Internship Computer System Validation Csv is an entry-level position focused on learning and supporting validation tasks, while the Computer System Validation Specialist is a more experienced role responsible for ensuring system compliance and validation in regulated industries.

What are the most commonly searched types of Computer System Validation Csv jobs in New York?

The most popular types of Computer System Validation Csv jobs in New York are:

What are popular job titles related to Internship Computer System Validation Csv jobs in New York?

For Internship Computer System Validation Csv jobs in New York, the most frequently searched job titles are:

What cities in New York are hiring for Internship Computer System Validation Csv jobs?

Cities in New York with the most Internship Computer System Validation Csv job openings:

Infographic showing various Internship Computer System Validation Csv job openings in New York as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 100% In-person job distribution.

Specialist, Metrology and Validation (On-site)

MSD

Rahway, NJ

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago


Job description

Job Description

The Pharmaceutical Analysis & Digital Technologies (PADT) Analytical Capabilities & Operations (ACO) department of our Research and Development Division is seeking applicants for a Metrology and Validation Specialist position available at the Rahway, New Jersey research facility.

The Metrology and Validation Specialist will work as part of the integrated US Metrology and Validation team and drive a culture of quality and operational excellence across the global Development Sciences & Clinical Supply (DSCS) network. The role oversees and supports the onboarding, qualification, validation, and routine maintenance of analytical equipment and instrumentation within a GMP environment.

The key responsibilities of this role will include:

  • Partner with scientific teams across DSCS to drive compliance and operational excellence.

  • Onboard, qualify, and maintain laboratory equipment and instrumentation in both GMP and non-GMP environment.

  • Participate in laboratory computer system validation activities associated with new or upgraded instrumentation or software packages in compliance with 21CFR11 compliance requirements.

  • Prepare, review, and approve documentation such as master inventory lists, qualification documentation, calibration documentation, computer system inventories.

  • Support internal and external quality audits and maintain laboratory state of permanent inspection readiness.

  • Author or contribute to Standard Operating Procedures (SOP).

  • Originate and own Investigations and Change Management records.

  • Collaborate with cross-functional teams to deliver department level prioritiesand initiatives.

The successful candidate must function both independently and be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. Strong communications skills and eagerness to adapt and learn are essential attributes. As a member of our team, you will be joining scientific and technical problem solvers who are dedicated to creating the life-changing medicines of tomorrow.

Education Minimum Requirements (standard for each level)

  • Bachelor's degree, or higher, in analytical chemistry or related field with 3+ years relevant industry experience.

Required Experience and Skills

  • A strong team player with the ability to work both independently and cross-functionally to deliver on complex objectives.

  • Proven track record of strong technical and innovative problem solving.

  • Desire and ability to learn new concepts outside of core expertise and training.

  • Excellent verbal and written communication skills, demonstrated creativity, and strong interpersonal skills.

  • Related industry experience with metrology and equipment maintenance and calibration.

  • Experience working within a GMP environment.

  • Understanding of GMP policies and procedures.

Preferred Experience and Skills

While not required, experience in one or more of the following areas is beneficial.

  • Demonstrated commitment to multiculturalism and inclusion.

  • Experience leading a team for a common goal.

  • Experience in Auditing and Compliance within pharmaceutical industry, including change management and deviation management.

  • Experience supporting internal and external quality audits.

  • Experience in Instrument commissioning, qualification, and validation (CQV).

  • Experience in instrument computer system validation.

  • Experience with IT, computerized systems, software and applications, including Secure Desktop.

  • Experience with developing tools (e.g., Power Apps) or utilizing AI.

ARD

EligibleforRP

Required Skills:

Analytical Instrumentation, Analytical Laboratory Equipment, Calibration Procedures, Change Controls, Computer System Validation (CSV), Data Analysis, Equipment Calibrations, Equipment Maintenance, Equipment Qualification, GMP Environments, Laboratory Instrumentation, Metrology, Regulatory Compliance, Technical Writing, Validation Activities

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$96,200.00 - $151,400.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

09/5/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.