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Validation Associate Jobs in Puerto Rico (NOW HIRING)

Artisan Associate III Pay Rate: $11.48 Monday through Friday 40 hrs. 1st Shift: 5:00 am - 1:30 pm ... Validation. piece and any others that apply to your work area, making sure that the finished work ...

Description The Sr. Associate Technical Engineering will provide technical engineering support on ... issues, validation issues, electrical issues and process maintenance issues. 4. Assist the ...

Execute routine validation protocols. * Regularly draft and revise routine documents, e.g., MPs ... Apply to be a Manufacturing Associate today! Kelly PR Offers! * Exposure to a variety of career ...

The Associate Technical Engineering will provide automation support on all system/equipment ... validation, electrical and process automation issues. * Assist during FDA and other regulatory ...

PR

$11/hr

Hiring Immediately!        Store Sales Associate in San Juan, Puerto Rico Starting Pay ... Must have a valid, unrestricted driver's license issued by the state in which the position is ...

PR

$15 - $17.25/hr

Hiring Immediately!      Store Sales Associate in Guaynabo, PR Starting Pay Rate: $ 11.00 ... Must have a valid, unrestricted driver's license issued by the state in which the position is ...

PR

$13 - $14.75/hr

Hiring Immediately!      Store Sales Associate in Guaynabo, PR Starting Pay Rate: $ 11.00 ... Must have a valid, unrestricted driver's license issued by the state in which the position is ...

PR · On-site

$14.75 - $16.75/hr

Hiring Immediately!      Store Sales Associate in Caguas, PR Starting Pay Rate: $ 11.00 ... Must have a valid, unrestricted driver's license issued by the state in which the position is ...

Store Associate

Isabela, PR · On-site

$12.13/hr

Store associates are also expected to promptly resolve any customer concerns and ensure maximum ... Must have a valid, unrestricted Driver's License * Must be able, with or without reasonable ...

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Validation Associate information

What are the key skills and qualifications needed to thrive as a Validation Associate, and why are they important?

To thrive as a Validation Associate, you need a background in life sciences or engineering, strong analytical skills, and knowledge of regulatory compliance standards such as GMP or FDA guidelines. Familiarity with validation software, laboratory instrumentation, and documentation management systems is typically required, and certifications like Lean Six Sigma can be beneficial. Attention to detail, problem-solving abilities, and effective communication are essential soft skills in this role. These skills ensure that processes, equipment, and systems meet regulatory requirements and quality standards, which is critical for product safety and organizational compliance.

How does a Validation Associate typically collaborate with other departments during a project?

A Validation Associate frequently works cross-functionally with teams such as Quality Assurance, Manufacturing, and Research & Development. They coordinate to gather essential documents, understand process requirements, and ensure that all validation activities meet regulatory standards. Effective communication and organization are key, as Validation Associates often facilitate meetings, resolve discrepancies, and provide updates to stakeholders. This collaborative approach helps maintain compliance and supports the successful launch or improvement of products and processes.

What are Validation Associates?

Validation Associates are professionals responsible for ensuring that processes, equipment, and systems in industries like pharmaceuticals, biotechnology, and manufacturing meet required standards and regulations. They plan and execute validation protocols to confirm that products are produced consistently and meet quality specifications. Their work involves documenting procedures, performing tests, analyzing data, and maintaining compliance with regulatory agencies such as the FDA. Validation Associates play a critical role in quality assurance and risk management within their organizations.

What is the difference between Validation Associate vs Quality Control Analyst?

AspectValidation AssociateQuality Control Analyst
Required CredentialsBachelor's degree in life sciences or related field; certifications like CQE or ASQ often preferredBachelor's degree in chemistry, biology, or related field; certifications like CQE or ASQ common
Work EnvironmentPharmaceutical, biotech, or medical device manufacturing facilities; focus on validation processesLaboratories, manufacturing plants; focus on testing and quality assessment
Employer & Industry UsageUsed in regulated industries requiring validation of processes and systemsCommon in quality testing, inspection, and product release processes

While both roles require a background in science and similar certifications, a Validation Associate primarily focuses on validating processes and systems to ensure compliance, whereas a Quality Control Analyst concentrates on testing products and materials to verify quality. Both roles are essential in regulated industries but serve different functions within the quality assurance framework.

What are the most commonly searched types of Validation jobs in Puerto Rico? The most popular types of Validation jobs in Puerto Rico are:
What job categories do people searching Validation Associate jobs in Puerto Rico look for? The top searched job categories for Validation Associate jobs in Puerto Rico are:
Artisan Associate III

Artisan Associate III

Adecco

Vega Baja, PR • On-site

$11.48/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago


Job description

Artisan Associate III

Pay Rate: $11.48


Monday through Friday 40 hrs.
1st Shift: 5:00 am - 1:30 pm
Braiding practical exam
Interview after the candidate has passed the test. (same day)

Requirements:
Fourth year of High School.
Be able to read, write, and follow instructions in both languages (English/Spanish).
Manual dexterity, a high level of concentration, and the ability to follow instructions
consistently are required.
Work under minimal supervision.
Responsibilities:
Responsible for carrying out the corresponding operations according to Production Order, Kanban Card, Standard Operation Sheet, 1st. Grade Validation. piece and any others that apply to your work area, making sure that the finished work meets the established requirements.
It makes sure that the Production Order and the material in the containers are correct. Verify that the material is properly identified, as specified in the Production Order.
Responsible for the quality of their work. While performing the work, it inspects, separates, identifies, and reports, correctly, the material, parts, or products that do not meet the established quality requirements.
Note: In our manufacturing work environment, safety glasses, ear protectors and safety shoes are required.


Pay Details: $11.48 per hour
Benefit offerings available for our associates include short-term disability and additional voluntary benefits including medical, dental, vision, life insurance, commuter benefits and a 401K plan.
Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave and Vacation Leave or any other paid leave required by Federal, State, or local law where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance