Job Information
Curia Quality Investigations Specialist II in Albuquerque, New Mexico
Quality Investigations Specialist in Albuquerque, NM.
Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries.
The Quality Investigations Specialist is an integral part of the Curia team, contributing to our success by providing Quality Assurance oversight and subject matter expertise for current Good Manufacturing Process (cGMP) investigations.
Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture.
We proudly offer:
Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401k program
Learning platform
And more!
Supervisory Responsibilities:
This role does not have supervisory responsibilities, yet it may involve mentoring, guiding, and advising.
Responsibilities:
Provides QA oversight/leads and subject matter expertise for GMP investigations
Works with Quality and Operations to assure facilities and processes are in a constant state of readiness for regulatory and customer inspections
Works with Quality and Operations to assure on-time and “right the first time” execution of production activities
Supports product complaints, deviations, and failure investigations.
Subject matter expert for all related analytical and technical Quality Assurance
Contributes to CURIA’s core values of Curiosity, Urgency, Respect, Integrity and Accountability
Reviews and closes investigations and customer concerns
Performs root cause analysis and implementation of corrective action for process-related concerns
Recommends and initiates changes to applicable SOPs
Supports CURIA Compliance department during FDA and other agency inspections as well as customer and internal audits
Maintains a working knowledge of government and industry quality assurance codes and standards
Participates in the site or global projects and improvement efforts, as needed.
Read/interpret SOPs to ensure compliance
Maintain up to date trainings
Other duties as assigned
Required qualifications:
Provides guidance and mentorship to team members
Fosters a collaborative and positive work environment
Champions change
Promotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.
Demonstrates strong attention to detail
Education and Experience:
Bachelor’s Degree in Science, Chemistry, Biology or related field of study, preferred
Associate’s Degree in Science, Chemistry, Biology or related field of study
Minimum of three (3) years of experience in quality assurance and/or regulatory experience in the Pharmaceutical industry with demonstrated understanding of laboratory, manufacturing, packaging, regulatory, compliance, and quality assurance requirements for biological and drug product manufacturing
Must know the US, European and Japanese Compendia requirements for a pharmaceutical facility and an analytical/microbiological laboratory
Other Qualifications:
Must pass a background check
Must pass a drug screen
May be required to pass Occupational Health Screening
Education, experience, location and tenure may be considered along with internal equity when job offers are extended.
We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.
All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.
#LI-MM2
#CUR8b