Principal Quality Control Specialist, Master Data

Welcome to Holly Springs North Carolina home to Roche/Genentechs largest-ever investment: a $2B greenfield start-up where next-generation technology high-performing teams and Operational Excellence converge to create the global standard for high-volume highly-efficient Drug Product manufacturing.

The facilitys core is defined by Innovation - leveraging advanced automation robotics digital tools real-time data analytics and simple streamlined processes to produce the highest quality medicines. This plant meets todays demand for CVRM (Cardiovascular Renal and Metabolism) medicines and is scalable to grow with the portfolio which focuses on next-generation metabolic medicines specifically targeting the global obesity epidemic and Type 2 diabetes. This is a fast-paced entrepreneurial environment with a high-level of accountability with planned launch in 2028.

Are you a problem-solver and change-agent who thrives in a Team environment eager to tackle the most complex manufacturing challenges If so this is a once-in-a-lifetime opportunity to launch a state-of-the-art facility from the ground-up and shape the culture of our organization for the next generation.

Join us in Holly Springs where you wont just build a plantyou will build the future of medicine.

The Opportunity:

The Holly Springs QC Team is seeking an individual to create and sustain a fully digital QC laboratory key to this is simple to moderately complex sets of Master Data that support QC operations. This role will collaborate with internal and external departments (e.g. QC Operations Database System Developers Business Analysts Manufacturing Packaging External Quality Control System Scientists Product Technical Leads etc.) to maintain and improve contemporary relevance of QC Master Data. This role will have a deep understanding of how QC master data is utilized and how it can be improved. As a key SME in QC IT systems the role will develop and deliver end user training for the site. The role will own deviation investigations Corrective and Preventive Actions (CAPAs) Change Requests perform periodic reporting periodic system evaluations audit trail review and analytical equipment administration.

• You will create update and test Master Data and end-user defined system settings to enable consistent execution collection transaction storage analysis and reporting of QC data. Software Systems include: Labware (LIMS) Binova (LES) SAP Mettler Toledo LabX Waters Empower Chromatography Data System Veeva and ValGenesis.

• You will be the site representative on System Enhancement and User Communities of Practice Teams communicating system changes and best practices to local system users

• You will be accountable for end user training for supported systems.

• You will lead or participate in Quality Control Investigations using established Root Cause Analysis tools and generating data-based impact assessments within established timelines.

• You will own Corrective and Preventive Action Plans and Change Controls.

• You will author review and/or approve standard operating procedures work instructions monitoring protocols monitoring reports gap assessments and risk assessments.

• You will participate in cross functional teams that ensure safety quality delivery engagement and cost objectives are sustained/exceeded.

Who You Are

• You have a B.S./B.A. degree in Chemistry Biochemistry or relevant scientific discipline and a minimum of five years of experience in a GMP setting.

• You have a proven experience building and maintaining complex static data (Specifications Methods Sampling Plans) in a production environment.

• You possess a working understanding of database management/relational tables preferably with experience working with Labware (LIMS) Binova (LES) SAP Mettler Toledo LabX Waters Empower Chromatography Data System or similar cGMP QC systems.

• You have sound knowledge of cGMPs or equivalent Regulations.

• You must have the ability to interpret and apply quality standards to operational activities.

• You must have strong verbal and written communication skills.

Work Environment/Physical Demands/Safety Considerations

• You will be working on site in a flexible open space work environment and QC laboratories requiring gowning (lab coat eye protection gloves)

• You will work on/interact with analytical instruments and computerized systems/screens for long periods of time (6-8 hours)

• You may be required to lift up to 25lbs

• You may have to work with hazardous materials and chemicals.

The expected salary range for this position based on the primary location for this position of Holly Springs NC is $98000 - 182000. Actual pay will be determined based on experience level qualifications geographic location and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

Link to Benefits

There are no relocation benefits available for this position

Genentech is an equal opportunity employer. It is our policy and practice to employ promote and otherwise treat any and all employees and applicants on the basis of merit qualifications and competence. The companys policy prohibits unlawful discrimination including but not limited to discrimination on the basis of Protected Veteran status individuals with disabilities status and consistent with all federal state or local laws.

If you have a disability and need an accommodation in relation to the online application process please contact us by completing this form Accommodations for Applicants.