United BioSource Corporation

Manager, GQC Support

United BioSource Corporation$90K — $120K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences, Clinical, or Business with 5 years of quality assurance/compliance/auditing experience in a GCP environment.
  • Experience in a Contract Research Organization (CRO).
  • Proven experience hosting regulatory inspections and supporting client audits.
  • Minimum 5 years GCP experience and extensive knowledge of pharmaceutical regulatory requirements (e.g., ICH, GCP, GxP).
  • At least 1 year of managerial/supervisory experience preferred.
  • Strong proficiency in Microsoft Office Suite and experience in Quality Management Systems.
  • Experience in managing the corrective and preventive action (CAPA) lifecycle.

Responsibilities

  • Oversee the lifecycle of controlled documents and ensure compliance with policies and procedures.
  • Manage training activities and documentation related to SOPs and training matrices.
  • Assist with CAPA administrative tasks and maintain compliance processes.
  • Support GQC IT systems, including maintenance and change control.
  • Coordinate audit support functions, including scheduling and logistics for regulatory audits.
  • Review documentation for compliance prior to audits and ensure proper record storage.
  • Provide administrative support for the Global Quality Compliance department and assist in special projects.

Benefits

  • Competitive salaries
  • Growth opportunities for promotion
  • 401K with company match
  • Tuition reimbursement
  • Flexible work environment
  • Discretionary Paid Time Off (PTO)
  • Paid Holidays
  • Medical, Dental, and Vision coverage
  • Telemedicine services
  • Wellness program
  • Short-term and Long-term disability
  • Life insurance
Full Job Description
Manager Global Quality Compliance (GQC) Support

Brief Description:

The Manager Global Quality Compliance (GQC) Support oversees and manages the core support functions for the Quality Management System (QMS) set up and maintained by the Global Quality Compliance department including controlled documents management, training management, and continuous improvement (CAPA, audit). Audit support includes, but is not limited to, audit scheduling, logistics, and document preparation and support. There will be some travel for face to face inspections

Specific job duties:

Oversee and manage the controlled documents lifecycle and corresponding test assessments. Ensure compliance with internal policies and procedures and target review cycle frequency including appropriate formatting of SOP documents.
  • Support SOP review and approval process as deemed appropriate
  • Oversee and manage training related activities (e.g. SOP table of content, training matrix, training decks, other training documentation)
  • Oversee and provide assistance with CAPA administrative activities (data entry, effectiveness checks, process improvement, ensure process is managed in compliance with policies and procedures, etc.)
  • Support and assist with GQC IT systems maintenance and change control (CAPA, electronic Document and Learning Management System, other)
  • Oversee and manage the Regulatory/Client Audit Support functions
    1. Audit scheduling and audit calendar maintenance
    2. Meeting coordination/logistics
      • CDA Requests
      • Auditor Code of Conduct
      • Setting up internal trackers and portals
      • Setting up and providing secure Box access for auditor(s) when required
    3. Quality Compliance documentation review prior to and during audit.
    4. Ensure audit reports and responses are stored as per UBC record retention procedures.
  • Provide administrative support (i.e., agenda, minutes, metrics) for the Global Quality Compliance department.
  • Assist in department-related special projects.
  • Other duties as assigned.


Supervisory Responsibility:

None initially. May be a requirement in the future

Desired Skills and Qualifications:
  • Bachelor's degree required preferably in Life Sciences, Clinical, or Business area of study with 5 years quality assurance/compliance/auditing experience within a GCP environment.
  • Previous experience of working at a CRO
  • Experience hosting regulatory inspections and supporting client audits
  • Must have a minimum of 5 years GCP experience.
  • Extensive knowledge of applicable pharmaceutical/biotechnology regulatory requirements (e.g., ICH, GCP, GxP, FDA/CFR, EMA, MHRA, EU GVP)
  • Preferably at least 1 year of previous managerial/supervisory experience (i.e., experience managing teams and/or staff).
  • Proficient PC knowledge required including Microsoft Office Suite (i.e., Word, Excel, Powerpoint, Outlook), Internet, SharePoint.
  • Experience in management of the corrective and preventive action (CAPA) lifecycle
  • Experience in Quality Management Systems maintenance
  • Experience in management of standard operating procedures (SOPs)/policies
  • Experience in implementation and management of process improvement
  • Excellent verbal presentation and written communications skills.
  • Proven interpersonal and relationship building skills.
  • Proven skills in planning, analysis, and creative problem solving.
  • Strong organizational and time management skills.
  • Preferred exposure to software application development and maintenance. Demonstrated ability to:
    1. Always be honest with a high level of integrity.
    2. Communicate effectively and professionally
    3. Manage multiple tasks and competing priorities in accordance with business needs.
    4. Be a team player who motivates and educates other team members.
    5. Work independently.
    6. Be detailed oriented.
    7. Ensure confidentiality and discretion.


Benefits:

At UBC, employee growth and well-being are always at the forefront. We offer an extensive range of benefits to ensure that you have everything you need to thrive personally and professionally.

Here are some of the exciting perks UBC offers:
  • Competitive salaries
  • Growth opportunities for promotion
  • 401K with company match*
  • Tuition reimbursement
  • Flexible work environment
  • Discretionary PTO (Paid Time Off)
  • Paid Holidays
  • Employee assistance programs
  • Medical, Dental, and vision coverage
  • HSA/FSA
  • Telemedicine (Virtual doctor appointments)
  • Wellness program
  • Adoption assistance
  • Short term disability
  • Long term disability
  • Life insurance
  • Discount programs


#LI-HB1

#LI-REMOTE

About United BioSource Corporation

United BioSource Corporation is a leading provider of healthcare services and solutions. The company specializes in providing support for clinical trials, patient access programs, and post-approval research, helping pharmaceutical and biotech companies to bring new treatments to market more quickly and effectively. United BioSource Corporation has a global presence, with operations in North America, Europe, and Asia, and a team of over 1,500 professionals with expertise in a wide range of therapeutic areas. The company is committed to improving patient outcomes and advancing the field of healthcare through innovative solutions and collaborative partnerships.
Learn more about United BioSource Corporation
Size
1,500 employees
Industry
Net Income
$20 million
Founded
2003
5 Year Trend
+10%
Revenue
$300 million

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