Analytical Method Transfer Specialist

Posted 20 Days Ago
Be an Early Applicant
Dorado, PRI
In-Office
Senior level
Pharmaceutical
The Role
Supports analytical method transfers between laboratories by developing plans and protocols, coordinating samples, equipment, standards, training, and documentation, executing transfer testing, evaluating results against acceptance criteria, and authoring technical reports. The role also supports method validation, troubleshooting, investigations, CAPAs, change controls, deviations, audit readiness, and compliant laboratory recordkeeping in FDA-regulated pharmaceutical, biotechnology, medical device, or combination-product environments.
Summary Generated by Built In

For Analytical Method Transfer Specialist services in the Laboratory area.

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, Biology, or a related scientific discipline.
  • Five or more years of relevant experience in an FDA-regulated pharmaceutical, medical device, biotechnology, or combination-product laboratory environment.
  • Bilingual: English & Spanish.
  • Shift: Administrative and according to business needs. 
  • Experience in:
    • Analytical technologies such as HPLC or UPLC, GC, FTIR, UV-Visible spectrophotometry, balances, pH meters, microscopy, and associated sample-preparation equipment.
    • Transferring methods between internal sites or between a company laboratory and a contract laboratory.
    • Release, stability, assay, impurities or degradation products, residual solvents, physical testing, or cleaning-verification methods, based on project scope.
    • Supporting laboratory expansion, remediation, product transfer, audit readiness, or regulatory inspections.

The Personality Part:    

  • If you have a commitment to serving customers with high-quality research and products, to embracing a diverse work culture, and even to the environment, you might just be what we’re looking for!
     

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

  • Support development of analytical method transfer plans, transfer assessments, protocols, comparative-testing strategies, acceptance criteria, and final reports.
  • Coordinate transfer activities between the transferring and receiving laboratories, including schedules, samples, standards, reagents, equipment, training, and documentation readiness.
  • Execute or support approved transfer testing using current procedures, specifications, worksheets, and laboratory controls.
  • Confirm that required equipment is qualified and calibrated and that assigned analysts are trained before protocol execution.
  • Prepare samples, standards, reagents, solutions, mobile phases, and laboratory materials accurately and in accordance with approved methods.
  • Operate qualified laboratory equipment and generate, process, review, and document analytical results.
  • Compile and compare results from transferring and receiving laboratories against protocol acceptance criteria.
  • Support analytical method verification, qualification, validation, revalidation, troubleshooting, and lifecycle activities associated with method implementation.
  • Evaluate method performance characteristics included in the approved protocol and determine whether the receiving laboratory meets established acceptance criteria.
  • Document deviations and protocol exceptions occurring during method-transfer activities and support timely resolution before study closure.
  • Contribute technical information to laboratory investigations, root-cause assessments, nonconformances, CAPAs, and change controls associated with transferred methods.
  • Author and revise transfer protocols, reports, assessments, data summaries, procedures, worksheets, technical justifications, and supporting records.
  • Maintain complete, accurate, contemporaneous, attributable, legible, and traceable laboratory records in the applicable paper or electronic systems.

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 in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, Biology, or a related scientific discipline
  • Five or more years of relevant experience in an FDA-regulated pharmaceutical, medical device, biotechnology, or combination-product laboratory environment
  • Bilingual proficiency in English and Spanish
  • Experience with analytical technologies including HPLC or UPLC, GC, FTIR, UV-Visible spectrophotometry, balances, pH meters, microscopy, and sample-preparation equipment
  • Experience transferring analytical methods between internal sites or between company and contract laboratories
  • Experience with release, stability, assay, impurities or degradation products, residual solvents, physical testing, or cleaning-verification methods
  • Experience supporting laboratory expansion, remediation, product transfer, audit readiness, or regulatory inspections
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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