Reagent Change Specialist

Joulé

Oro Valley, AZ

JOB DETAILS
SALARY
$28.48–$28.48 Per Hour
SKILLS
Agile Programming Methodologies, Change Control, Change Management, Communication Skills, Continuous Improvement, Cross-Functional, Current Good Manufacturing Practice (cGMP), Document Change Management, Document Control, Documentation, Establish Priorities, Functional Analysis, GLP (Good Laboratory Practices), GMP (Good Manufacturing Practices), ISO (International Organization for Standardization), Maintain Compliance, Manufacturing, Manufacturing/Industrial Processes, Microsoft Office, Operations Processes, Organizational Skills, Outsourcing, Presentation/Verbal Skills, Regulations, Regulatory Compliance, Requirements Management, SAP Administration, Scientific Principles, Service Delivery, Supply Chain, Surveillance, Technical Analysis, Technical Writing, Time Management, Writing Skills
LOCATION
Oro Valley, AZ
POSTED
5 days ago

Job Title: Reagent Change Specialist
Location: Oro Valley, AZ
Contractor Work Model: Onsite
Hours: 8:00AM - 5:00PM M-F
Compensation: $28.48/hr
Type: Contract, Potential for extension or conversion to permanent


Responsibilities

  • Coordinate and manage change control activities related to supplier product/process changes, CAPAs, non-conforming events, product obsolescence, and continuous improvement initiatives.
  • Partner with cross-functional stakeholders to assess change requirements, prioritize implementation activities, and ensure compliance with quality and regulatory standards.
  • Update and revise documents including Work Instructions, Operating Procedures, Production Documents, Temporary Deviations, Stability & Surveillance Memos, Technical Assessments, Protocols, and Reports using current templates and revision controls.
  • Facilitate stakeholder review and approval processes, track approvals, and address reviewer comments.
  • Support preparation of Change Control Board (CCB) requests and coordinate implementation activities with the Change Management Office (CMO).
  • Participate in cross-functional change control review teams as needed.
  • Adhere to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP), ensuring compliance with quality systems and regulations.
  • Collaborate with cross-functional teams, support continuous improvement initiatives, and contribute to team and departmental meetings.
  • Perform additional duties as assigned.

Requirements
  • Bachelor's Degree in a scientific, manufacturing, supply chain, or related discipline.
  • 4+ years of experience in production, manufacturing, supply chain, quality, or a related field; Master's Degree with 2+ years of relevant experience preferred.
  • Strong understanding of scientific principles and manufacturing processes.
  • Advanced technical writing and documentation skills.
  • Excellent verbal and written communication abilities.
  • Strong organizational and time management skills.
  • Ability to work independently and collaboratively across functions.
  • Proficiency with Google Suite, Microsoft Office, Agile, EtQ, SAP, experience managing document control and change management processes.
  • Experience in GLP, cGMP, or ISO-regulated environments preferred.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M-


#LI-


Ref: #558-Scientific


About the Company

J

Joulé

With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:

  • Scientific staffing for hard-to-find skills

Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.

  • Clinical lifecycle recruiting

From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.

  • Equipment calibration, maintenance and validation

Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.

  • National healthcare recruitment

Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
WEBSITE
https://www.jouleinc.com/