Operational QA Manager - 2nd Shift
Rockville, MD 
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Posted 1 month ago
Job Description
Site Name: USA - Maryland - Rockville
Posted Date: May 16 2024

GSK is currently looking for an Operational Quality Manager to join our team in Rockville, MD. OQ Manager will be responsible for Operational Quality's day to day activities at LSM/SSM site including batch record review and day to day Quality Operations. The OQ Manager will manage a team of Quality professionals accountable for batch record reviews confirmation of GMP operations in production and support groups i.e. laboratory and engineering. The job holder will be the main liaison with production management team and will participate in daily planning meetings, approve deviations to processes, to support LSM/SSM activities

Key Responsibilities:

  • Manage team of Operational Quality professionals (24/7) to support production activities and shop floor presence
  • Ensure Operational Quality schedules and activities support batch record review and batch disposition needs Review and approve deviation reports, corrective actions, to support GMP decisions and material disposition.
  • Review and approve SOPs, batch records, forms and all other GMP documentation to support day to day operations
  • With the Operational Quality Associate Director, the OQ Manager will serve as QA representative at product team meetings (PTM, CMC, POMM), participate in facility design teams and specific drug product development teams
  • Support Data Integrity and Human Performance efforts to reduce incidents and increase engagement with employees
  • Ensure that Quality risks in productions areas are understood and appropriately mitigate to support production schedules
  • Actively support performance initiatives to support performance improvements in the BDS release area to achieve site service goals.

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • BS Degree
  • 5+ years in a GMP pharmaceutical environment
  • 2+ years of Quality Assurance, or Operational Quality experience
  • Supervisory or management experience.
  • Must be able to work 2nd Shift hours (5:00 PM - 2:00 AM, Mon - Fri)

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • Biopharm experience preferred
  • 2+ years supervisory experience strongly preferred
  • Experience managing deviations and changes to processes as author, reviewer, or approver
  • Knowledge in Performance Improvements tools i.e. Six Sigma or equivalent
  • Ability to interpret and apply GMP, ICH and other regulatory guidelines. Critically evaluate individual processes and projects, then synthesize their insights to arrive at a summary of overall organizational status
  • Excellent organization skills - spearhead both the planning and implementation stages of multiple projects
  • Effective oral and written communication skills - able to speak, actively listen, and write/present well to different levels of the organization
  • Sound leadership skills and the ability to work effectively in a cross-functional team environment; Ability to manage appropriate resources (personnel, projects, budget, etc...) toward accomplishment of department and corporate goals.
  • Ability to handle multiple projects and interface with individuals from various departments at various levels.
  • Ability to work in a fast-paced environment in a results-oriented fashion.
  • Technical expertise - a firm understanding and application of process improvements, Biopharm technical elements and Quality Compliance requirements for the role.
  • Organization skills
  • Leadership skills - coach and company game-changer, inspiring other team members to give their best effort and setting the direction for improvement initiatives

#LI-GSK

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).

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Job Summary
Company
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
Bachelor's Degree
Required Experience
2+ years
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