Aseptic Compliance Specialist

Global-Technical-Talent-1

Thousand Oaks (CA)

Sur place

USD 44 000 - 52 000

Temps partiel

Il y a 5 jours
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Avantages offerts par ce poste

Medical, Vision, and Dental Insurance
401k Retirement Fund

Résumé du poste

GTT is seeking an Aseptic Compliance Specialist in Thousand Oaks, CA to support 24/7 aseptic drug product manufacturing with data review, compliance, and media fill protocol development.

Qualified candidates will have hands-on aseptic experience, drug product filling, and strong communication skills; the role involves document revisions, data analysis, and collaboration with the 24/7 readiness team.

Qualifications

  • Hands-on experience with aseptic practices and drug product filling.
  • Drug product manufacturing experience.
  • Aseptic compliance/contamination control experience.
  • Outstanding communication skills.

Responsabilités

  • Serve as aseptic processing technical resource for 24/7 manufacturing.
  • Revise controlled documents to support process changes and improvements.
  • Own aseptic-related deviations.
  • Develop metrics and outputs that translate data into decisions.
  • Provide on-the-floor support during aseptic operations.
  • Prepare media fill protocols, including scope and incubation conditions.

Connaissances

aseptic practices
drug product filling
communication skills

Formation

Doctorate degree
Master's degree + 2 years experience
Bachelor's degree + 4 years experience
Associate's degree + 8 years experience
High school diploma / GED + 10 years experience

Description du poste

Aseptic Compliance Specialist

Location: Thousand Oaks, CA

Onsite Flexibility

Onsite

Contract Details
  • Position Type: Contract
  • Contract Duration: 12 months
  • Pay Rate: $32.00–$38.00 / Hour (USD)
  • Shift / Schedule: Monday–Friday, 8:00 AM–5:00 PM initially; transitioning to Wednesday–Sunday, 8:00 AM–5:00 PM once 24/7 operations commence in 2027
  • Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Job Summary

Candidates must have experience with aseptic practices and drug product filling. Suppliers must screen for this experience beyond familiarity. This role serves as a drug product aseptic processing technical resource supporting 24/7 drug product manufacturing. The function focuses on data review, compliance, and media fill protocol development within a drug production facility.

Key Responsibilities
  • Serve as a drug product aseptic processing technical resource supporting 24/7 drug product manufacturing.
  • Support continuous improvement initiatives that strengthen aseptic compliance, process robustness, and operational efficiency.
  • Revise controlled documents, including SOPs, work instructions, and related records, to support process changes and improvements.
  • Own aseptic-related deviations.
  • Support the 24/7 Ways of Working Lead to evaluate 1 years of aseptic call log data from the floor and identify recurring trends, root causes, and improvement opportunities.
  • Develop clear metrics, summaries, and actionable outputs that convert operational data into decisions, priorities, and follow-up actions.
  • Establish and maintain a cyclic process for gathering information, addressing challenges, implementing improvements, and assessing effectiveness.
  • Analyze production data to identify bottlenecks and risks for 24/7 operations in 2027.
  • Write reports and perform compliance reviews related to aseptic manufacturing.
  • Collaborate with the 24/7 operational readiness team.
  • Prepare media fill protocols, including scope, batch size, interventions, acceptance criteria, and incubation conditions.
  • Provide on-the-floor support during aseptic operations.
  • Develop metrics, actionable outputs, and manage completion of those outputs.
Required Skills
  • Experience with aseptic practices and drug product filling (beyond familiarity — must be hands-on)
  • Drug product manufacturing experience
  • Aseptic compliance/contamination control experience
  • Outstanding communication skills
Preferred Skills
  • Prior involvement in 24/7 operational readiness or continuous manufacturing operations
  • Familiarity with regulatory expectations for aseptic processing (FDA/EMA) and GMP documentation practices
Education Requirements
  • Doctorate degree; OR
  • Master's degree and 2 years of experience; OR
  • Bachelor's degree and 4 years of experience; OR
  • Associate's degree and 8 years of experience; OR
  • High school diploma / GED and 10 years of experience
Required Experience
  • Project management within drug production/manufacturing (sterile or aseptic environment strongly preferred)
  • Hands-on experience with media fill / aseptic process simulation activities
  • Demonstrated experience in CAPA reviews (corrective and preventive actions) or similar quality/compliance investigations
Benefits
  • Medical, Vision, and Dental Insurance Plans
  • 401k Retirement Fund
Important Notes
  • Interview process: Phone/virtual interviews — initial phone screen conducted by the recruiter, followed by interviews with the hiring team.
About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

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