Specialist Quality Control

Posted 5 Days Ago
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Juncos, PRI
In-Office
Senior level
Pharmaceutical
The Role
Provide technical leadership for QC laboratory operations in a pharmaceutical/regulated environment. Perform method validation, transfer and qualification; troubleshoot assays; analyze data and author reports. Ensure GMP/GLP compliance, develop controlled documents and programs, lead audits and investigations, and support regulatory interactions. May train, supervise staff, and manage multi-site action items and special projects.
Summary Generated by Built In

 For QC Services in the Laboratory area.

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor's Degree with five (5) years of experience within the pharmaceutical or regulated industry.
  • Bilingual (English & Spanish).
  • Project Management skills.
  • Shift: Administrative and according to business needs.
  • Experience in:
    • Method Validation, Method Transfer, Method Qualification. 
    • Scientific, Chemistry or Microbiologist. 

The Personality Part:    

  • Picture yourself in a lab… with all the equipment you need to put your multitasking, scientific, creative (to come up with all those experiments!) skills to work. Picture as well an environment of healthy competition, teamwork, being ethical and of using the scientific method in all ways possible. If you like how this sounds, then this might be the job for you. Bring it on!

AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)

  • Responsible for providing technical guidance, Provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise.
  • Resolve technical issues and troubleshoot for assays as necessary.
  • Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety.
  • Manage existing and/or develop and implement new programs, processes and methodologies.
  • Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact.
  • Approve lab investigations, Lead audit teams.
  • May serve as subject matter expert to develop technical training.
  • May perform routine work in a specific area of responsibility as necessary.
  • Represents the department/organization on various teams, Independently responsible for following through on multi-site action items.
  • May interact with regulatory agencies regarding area(s) of responsibility including written responses.
  • May resolve issues with outside resources.
  • Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements.

WHO WE ARE:

We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! 

Are you the next piece?

Skills Required

  • Bachelor's degree with five years' experience in the pharmaceutical or regulated industry
  • Bilingual English and Spanish
  • Project management skills
  • Experience with method validation, method transfer, and method qualification
  • Background in chemistry, microbiology, or scientific discipline
  • Knowledge and experience implementing GMP and GLP procedures
Am I A Good Fit?
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The Company
HQ: Guaynabo, PR
76 Employees
Year Founded: 2008

What We Do

We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are We The Right Piece For You? We are: Experienced and knowledgeable in the Industry Committed to Safety Always compliant with FDA Regulations & Audits Cost Effective Proven successful track record Over ten (10) years of experience If you'd like to apply to any of our open positions, send us your updated resume in Word or PDF Format to [email protected]

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