Supervisor, Microbiology

Curia

Albuquerque (NM)

On-site

USD 80,000 - 95,000

Full time

14 days+

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Benefits offered by this job

Generous benefits available immediately
Paid training, vacation, and holidays
Career advancement opportunities
Education reimbursement
401(k) program with matching contributions
Learning platform and other employee resources

Job summary

Curia in Albuquerque, NM is seeking a Supervisor for the Microbiology laboratory. The role involves overseeing daily operations, ensuring compliance with cGMP and regulatory standards while training and mentoring staff.

The ideal candidate will have a Bachelor’s degree in microbiology or a related field, with at least three years of relevant experience, two of which must be in a leadership capacity.

Join Curia and help deliver life-saving treatments to patients while enjoying generous benefits and opportunities for career advancement.

Qualifications

  • Bachelor's degree in microbiology or related field preferred.
  • Minimum three years of related work experience; at least two years in leadership.
  • Proficient in validation/qualification of lab microbiological techniques.

Responsibilities

  • Supervise daily operations of the microbiology laboratory.
  • Ensure compliance with cGMP and regulatory requirements.
  • Train and mentor laboratory staff in test methods and equipment operation.

Skills

Leadership
Microbiological techniques
Communication
Organizational skills
Problem-solving

Education

Bachelor’s degree in a scientific discipline

Tools

Microsoft Office
Laboratory information management software

Job description

Supervisor, Microbiology – Albuquerque, NM

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life‑saving treatments to patients. This role oversees the daily operations of the microbiology laboratory, ensuring compliance with cGMP, regulatory standards, and company policies.

Benefits
  • Generous benefits available immediately
  • Paid training, vacation, and holidays (vacation accrual starts first day)
  • Career advancement opportunities
  • Education reimbursement
  • 401(k) program with matching contributions
  • Learning platform and other employee resources
Responsibilities
  • Supervise daily operations of the microbiology laboratory, including scheduling and task assignments for analysts and technicians.
  • Ensure completion of microbiological testing, environmental monitoring, and isolate identification in compliance with cGMP and regulatory requirements.
  • Train, mentor, and qualify laboratory staff in test methods, equipment operation, and documentation practices.
  • Monitor laboratory equipment performance, troubleshoot technical issues, and report unresolved problems to the Microbiology Manager.
  • Maintain inventory of reagents, media, and test materials; oversee aseptic preparation, ordering, and documentation.
  • Approve attendance records, vacation schedules, and other administrative requirements; enforce corrective or disciplinary actions when necessary.
  • Prepare, revise, and maintain SOPs, protocols, and related documentation.
  • Coordinate specialized laboratory activities such as quarterly gamma‑sterilization dose audits, bioburden audits, and routine analyses.
  • Perform and review cGMP documentation and calculations; support investigations and audit activities.
  • Collaborate with cross‑functional groups (R&D, Technical Services, Laboratory Systems) to support laboratory initiatives and company projects.
  • Promote continuous improvement by identifying opportunities to streamline processes and improve efficiency.
  • Perform other related duties as assigned.
Qualifications
  • Bachelor’s degree in a scientific discipline, preferably microbiology or related field.
  • Minimum of three (3) years of related work experience, including at least two (2) years in a leadership role.
  • Proven experience and proficiency in the validation/qualification of lab microbiological techniques.
  • Experience in a GMP or GLP environment, preferably pharmaceutical clean‑room.
  • Strong written and verbal communication skills, with the ability to present information to managers, clients, and the public.
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook) and laboratory information management.
  • Ability to read and interpret SOPs, technical procedures, and regulatory documents.
  • Strong attention to detail and organizational skills.
  • Background check and drug screen required; additional occupational health screening may be required.
Skills & Abilities
  • Leads with integrity and respect.
  • Provides guidance, coaching, and mentorship to team members.
  • Demonstrates business acumen and fosters a collaborative work environment.
  • Champions change and promotes a safe and healthy workplace.
  • Organizes multiple projects and priorities effectively.

Curia is an Equal Opportunity Employer and a covered E‑Verify employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability.

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