Master Manufacturing Technician, Autoinjector Assembly

F. Hoffmann-La Roche AG; Holly Springs (MS); On-site; USD 61,600 - 114,400; Full time

Benefits offered by this job

Discretionary annual bonus

Relocation benefits

Job summary

F. Hoffmann-La Roche AG in Holly Springs seeks a Master Manufacturing Technician to support the startup of high volume autoinjector assembly lines. This role involves providing technical input and collaborating with various departments to ensure equipment readiness and compliance.

The ideal candidate should have significant production experience and knowledge of SAP/ERP systems. The position offers a competitive salary range of $61,600–$114,400 based on qualifications and experience.

Qualifications

• Minimum of High School and 7+ related years of production experience.
• Proficient knowledge of SAP or ERP system.
• Experience with drug product manufacturing preferred.

Responsibilities

• Support process design, qualification, startup of autoinjector assembly lines.
• Provide technical input for the new manufacturing facility.
• Train colleagues and provide knowledge on complex processes.

Skills

Production experience

SAP or ERP system knowledge

Collaboration skills

Quality compliance

Education

High School diploma or AA degree

Bachelor’s Degree in science, manufacturing or engineering

Job description

Overview

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.

Responsibilities

• Support the process design, qualification, startup and registration of our high volume autoinjector assembly lines at our state‑of‑the‑art facility.
• Provide hands‑on technical input for the new large volume manufacturing facility in Holly Springs.
• 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 design and startup activities for a new Drug Product Fill and Finish facility.
• Provide knowledge and training on complex process and equipment technologies to all required partners.
• Provide training materials and training for people joining the organization.
• Act as a coach for colleagues with less experience and help them develop skills/expertise.
• Support authoring of standard operating procedures for new equipment.
• Support acceptance testing to ensure that equipment is suitable for end‑user execution.
• After go‑live of the facility, transition into a routine position on the site and extend into daily operation responsibilities.
• During the operational phase, 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.
• 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 such as 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.

Qualifications

• Minimum of High School and 7+ related years of production experience and/or AA degree and 5+ years technical related experience in the pharma industry, supply chain management or in manufacturing.
• Proficient knowledge and experience of SAP or ERP system.
• Bachelor’s Degree in science, manufacturing or engineering (preferred). 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.

Salary and 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. Relocation benefits are available for this job posting. This position also qualifies for the benefits detailed at the link provided below.

EEO Statement

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.