The Position
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 autoinjector assembly 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 autoinjector assembly 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 assembly of autoinjectors following cGMP, PQS and Safety standards while maintaining a teamwork attitude to effectively manage production needs and meet the production schedule. The Master Assembly 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. The successful candidate will need to demonstrate the following traits:
Perform visual and dimensional inspections of autoinjector components and COA-released materials, ensuring compliance with quality standards.
Identify and resolve discrepancies, contribute to investigations, troubleshoot technical issues, and address system gaps.
Execute autoinjector tasks like device insertion, labeling and cap insertion, along with receiving and delivering materials, while focusing on quality and efficiency.
Complete and review process-related documentation, communicate effectively with teams, and support training activities and departmental metrics reporting.
Participate in safety inspections, scheduling meetings, project discussions, and other assigned tasks to maintain compliance and efficiency.
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 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.
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.
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 packaging work for extended periods of time.
Must be able to perform visual label inspection for extended periods of time.
Must be able to lift 40lbs, push/pull >75lbs of force.
Relocation benefits are available for this job posting.
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.
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 (https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform) .
