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Quality Investigations Specialist II

Curia IncAlbuquerque, NM

Overview

Schedule
Full-time
Career level
Senior-level
Remote
On-site
Benefits
Paid Holidays
Paid Vacation
Career Development

Job Description

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

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.

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FAQs About Quality Investigations Specialist II Jobs at Curia Inc

What is the work location for this position at Curia Inc?
This job at Curia Inc is located in Albuquerque, NM, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Curia Inc?
Employer has not shared pay details for this role.
What employment applies to this position at Curia Inc?
Curia Inc lists this role as a Full-time position.
What experience level is required for this role at Curia Inc?
Curia Inc is looking for a candidate with "Senior-level" experience level.
What benefits are offered by Curia Inc for this role?
Curia Inc offers following benefits: Paid Holidays, Paid Vacation, Career Development, 401k Matching/Retirement Savings, and Tuition/Education Assistance for this position. Actual benefits may vary depending on the employer's policies and employment terms.
What is the process to apply for this position at Curia Inc?
You can apply for this role at Curia Inc either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.