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CIQA is seeking for professionals with the education and experience in a variety of disciplines to be part of our team. 

The following positions are available in Puerto Rico, United Status, Europe and others.  

VALIDATION PROFESSIONAL II:

VALIDATION PROFESSIONAL I:

Text Box: Since it foundation in 1996, CIQA had employed over 500 engineers mainly from the University of Puerto Rico, Mayagüez Campus.  Bringing the first job opportunity to our young professionals in PR.
Text Box: Excellent Job Opportunities

CIQA is willing to invest in the most qualified personnel and provide the technical training required to develop successful professional in the pharmaceutical engineering field. 

 

VALIDATION PROFESSIONALS:

Minimum Requirements:


B.S., M.S., Ph.D. Engineering, Chemistry, Biology, Computer or Natural Sciences, license preferred. Oriented to high technology with solid analytical and organizational skills, as well as good communication and writing documentation abilities. Proficiency in English and Spanish. Good knowledge in computer applications (such as
MS Word, MS Excel, MS Project, Statgraphics, and others).  Excellent understanding and interpretation of current pharmaceutical regulations and standard operating procedures. No experience required for entry level positions: training opportunities.

 

Willing to travel or relocate within Puerto Rico, if required.  CIQA provides apartment facilities and travel allowance.

 

Additional and Optional Requirements:

Good documentation practices with knowledge in computer and process validation of solid dose, biologics, parenteral, bulk and medical devices according to FDA guidelines cGMP, GAMP4, cGLP and 21 CFR part 11. Knowledge in new process computerized equipment such as HVAC, WFI, Steam/Dry Heat sterilization, PLC/controllers (AB, Wonderware, DeltaV, EBI, WebControl,  etc.), freezers / incubators, mixers, blenders, granulators, tablet compression machines, cleaning validation KAYE Validator 2000, and others. In addition, knowledge in new laboratory computerized instrumentation such as HPLC, GC, FT-IR, UV/vis, Dissolution, NIR and others. Professional certifications: PE, CQE and CQA

 

Strong practical understanding of regulatory compliance, statistical analysis and process optimization.

 

Professional Benefits:

In addition to an excellent compensation and growing opportunities, CIQA offers unique benefits such as exposure to new process and high technology equipment for solid dose, parenteral, biologics, bulk and medical devices.  The benefits offered are competitive and proportional to the education, experience and professional aptitude compatible with the expected pharmaceutical requirements.


Be part of an excellent pharmaceutical validation team, You can send us your resume by e-mail to:


Text Box: CIQA Recruitment Offices: 
Street 2 A-27 Urb. Porta Coeli, San German, PR. 00683

IMPORTANT INFORMATION:

 

Please be patient,  NO follow-up phone calls, faxes, unsolicited or unscheduled visits are allowed.  All resumes will be received by e-mail, exclusively.

 

After received your resume by e-mail, we need some time to evaluate it.  If you are a potential candidate for an employment position, we will contact you to gather more information, coordinate a visit to fill an electronic formulary and/or interview. 

We are an Equal Opportunity Employer, and take affirmative action to employ women, Vietnam Era Veterans and people with disabilities. AA/EEO Employer M/F/V/HAA/EEO Employer M/F/V/H