Master Manufacturing Technician, Inspection

F. Hoffmann-La Roche AG; Holly Springs (MS); On-site; USD 62,000 - 114,000; Full time

Benefits offered by this job

Relocation benefits

Discretionary annual bonus

Benefits package

Job summary

Roche/Genentech in Holly Springs, NC, is building a state-of-the-art, high-volume drug product manufacturing site. We seek a Master Manufacturing Technician to support design, qualification, startup and registration of automated visual inspection lines, collaborate with engineering, MSAT, Quality and Regulatory, and help train teams.

You will master AVI equipment, perform visual product inspections, support SOPs, conduct acceptance testing, and transition to daily operation, ensuring cGMP

Qualifications

• You possess a minimum of High School and 7+ related year production experience and/or AA degree and 5+ years technical related experience in the pharma industry, supply chain management or in manufacturing.
• You have proficient knowledge and experience of SAP or ERP system.

Responsibilities

• Master the daily operation, setup, and troubleshooting of high‑speed Automated Visual Inspection (AVI) machines.
• Perform manual visual inspections of filled drug products and classify defects.
• Maintain, audit, and re‑certify defect kits for daily machine challenges and validation activities.
• Identify and resolve discrepancies, contribute to investigations, and troubleshoot technical issues.
• Manage material staging and movement for inspection lines to maintain continuous flow.
• Complete and review process‑related documentation and support training activities.

Skills

Production experience

SAP/ERP

Education

High School diploma

AA degree

Bachelor's Degree in science/manufacturing/engineering

Job description

Welcome to Holly Springs, North Carolina— home to Roche/Genentech's 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 facility's 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 today’s 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 won't just build a plant—you will build the future of medicine.

The Opportunity

We're seeking a Master Manufacturing Technician to support the process design, qualification, startup and registration of our high volume automated visual inspection lines at our state of the art facility. In this exciting role, you will support the User Team and will provide hands‑on technical input for the new large volume manufacturing facility in Holly Springs. In partnership with the Engineering and the start‑up project (user) team, you will partner and collaborate with our partner organizations (Engineering and MSAT, Quality, Supply Chain, Technical Development, Regulatory, CMO, Strategy) to provide input as the end‑user for activities related to design and start‑up a new Drug Product Fill and Finish facility. This role specifically is about the design, qualification, start‑up and registration of the facility’s high volume automated visual inspection lines. You will provide knowledge and training on complex process and equipment technologies to all required partners. You will provide training materials and training for people joining the organization. You will act as a coach for colleagues with less experience and help them develop skills/expertise. You will support authoring of standard operating procedures for new equipment. You will support acceptance testing to ensure that equipment is suitable for end‑user execution. Following go‑live of the facility, you will transition into a routine position in the site and will extend into daily operation responsibilities. During the operational phase, you will be responsible for the visual inspection process following cGMP, PQS and Safety standards while maintaining a teamwork attitude to effectively manage production needs and meet the production schedule. The visual inspection process is inclusive of high speed automated visual inspection, manual inspection, inspection kit management, and the processes associated with operating this equipment. The Master Inspection Technician role will be expected to bring technical expertise in one or more GMP systems, a detailed process understanding of the function and good people skills across the organization.

Responsibilities

• You will provide knowledge and training on complex process and equipment technologies to all required partners.
• You will provide training materials and training for people joining the organization.
• You will act as a coach for colleagues with less experience and help them develop skills/expertise.
• You will support authoring of standard operating procedures for new equipment.
• You will support acceptance testing to ensure that equipment is suitable for end‑user execution.
• You will transition into a routine position in the site and will extend into daily operation responsibilities.
• You will master the daily operation, setup, and troubleshooting of high‑speed Automated Visual Inspection (AVI) machines and secondary Visual Robotics units in a high‑volume manufacturing setting.
• You will perform manual visual inspections of filled drug products, classifying defects to ensure compliance with cGMP standards.
• You will maintain, audit, and re‑certify operational and qualification defect kits required for daily machine challenges, routine operation, and validation activities.
• You will identify and resolve discrepancies, contribute to investigations, troubleshoot technical issues, and address system gaps.
• You will manage material staging and movement for inspection lines to maintain continuous operational flow and consistently meet production schedules.
• You will complete and review process‑related documentation, communicate effectively with teams, and support training activities and departmental metrics reporting.
• You will participate in safety inspections, scheduling meetings, project discussions, and other assigned tasks to maintain compliance and efficiency.
• You will leverage strong interpersonal skills to train and mentor junior technicians, support onboarding, and drive departmental metrics.

Qualifications

Who You Are: You possess a minimum of High School and 7+ related year production experience and/or AA degree and 5+ years technical related experience in the pharma industry, supply chain management or in manufacturing. You have proficient knowledge and experience of SAP or ERP system.

Preferred Qualifications

• You possess a Bachelor's Degree in science, manufacturing or engineering.
• You have experience with high volume, low cost, drug product manufacturing and or supply chain.

Work Environment / Physical Demands / Safety Considerations

• This role requires you to be onsite full time, initially at the Genentech project office before transitioning on‑site once the site buildings are built and equipment delivered.
• Travel of up to 30% of the time is expected during the project phase to support facility acceptance testing.
• The environment requires gowning, gloves, steel toe boots and safety glasses (as required).
• Ability to work in controlled environments, as required.
• Candidates must be flexible to work overtime and adjust working schedule beyond normal work week.
• Work schedule may be subject to change based on the phase of the project and/or commercial demand.
• Ability to perform computer work and RF equipment, as required.
• Standing and Sitting is required for extended periods of time.
• Must be able to perform repetitive manufacturing work for extended periods of time.
• Must be able to perform visual inspection for extended periods of time.
• Must be able to lift 40lbs, push/pull >75lbs of force.

Benefits

The expected salary range for this position based in North Carolina is $61,600 - $114,400. Actual pay will be determined based on experience, 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. Relocation benefits are available for this job posting.

Link to Benefits

Equal Opportunity & Accessibility

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 company's 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.