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Associate Director, cGMP Manufacturing Facilities Maintenance

Employer
Sutro Biopharma, Inc
Location
San Carlos, CA
Salary
180,000-195,000
Start date
Feb 21, 2024

Job Details

Sutro Biopharma, Inc. is looking for energetic and talented individuals to join its multidisciplinary research and development team. You will be working to develop new processes to maximize our technology and enhance our internal and collaborative product development initiatives in a fast-paced environment.    Responsibilities:    The Associate Director, cGMP Manufacturing Facilities Maintenance position will oversee Facility, Utility, Process and Lab equipment maintenance and calibration services at our cGMP facility. You will apply expert knowledge of cGMP process equipment and utilities, automated building systems (including lighting, HVAC, security systems) and building maintenance to establish/continue peak facility performance. This position will have responsibility for managing internal employees, vendors, and consultants as well as hands-on work.    
  • Monitor performance of critical utilities and process equipment in cGMP environment and perform or arrange necessary repairs, adjustments, calibrations, and preventative maintenance, including maintaining appropriate documentation.
  • Manage vendors and manage routine equipment repair and maintenance for: RO/DI water system, CIP system, clean steam, clean dry air, emergency generator, lighting, HVAC, janitorial, etc.
  • Manage complex maintenance and repair of plant and/or office facilities and equipment.  Knowledge of basic electrical, mechanical, air-conditioning, plumbing, etc using hand and power tools as required beneficial but not required.
  • Respond/Coordinate daily facilities work requests.
  • Coordinate equipment requisitions with internal departments for building services requirements, and carry out equipment and furniture installations.
  • Manage space planning process (for new hire and moves) by maintaining personnel location maps, physically moving and/or assisting in moving boxes and furniture as necessary, assisting in new hire orientation, and monitoring process to ensure efficient, effective completion with focus on excellent customer service.
  • Key participant in expansion and construction projects, managing design and installation of facility improvements with internal staff as well as outside consultants and vendors.
  • Manage the security and keycard systems consistently and according to protocols and policies.
  • Be available for on-call and weekend duties as assigned/needed.
  • Oversee conference room set-up and maintenance of clean conference rooms and kitchen areas.
  • Serve as a member of the Health and Safety Committee.
  • Manage and direct Shipping and Receiving function for the cGMP facility.
  • Back-up primary staff collecting and transporting full chemical waste containers to the storage building and providing hoods with empty chemical waste containers.
  • Back-up primary staff maintaining dry chemical storage.  Taking chemicals from bins, scanning the chemicals in and placing the chemicals in the correct storage container.   Scanning empty bottles and discarding of them properly.
  • Manage other vendors including: locksmith, recycle/shredding, electrician, food and beverage services.
  Qualifications:    
  • High school degree required, Bachelor’s degree preferred with at least 10 years of facilities experience.
  • Hands-on experience maintaining a cGMP facility is required.
  • Experience in a start-up environment, particularly in the biotech industry, is strongly preferred. Certification in maintenance trade, formal apprenticeship or on-the-job training is a plus.
  • Requires strong written and verbal communication skills; the ability to work independently on day-to-day activities.
  • Must have strong computer skills including experience with computerized HVAC, electronic keycard management, and Microsoft Office (Outlook, Word, Excel).
  • Must be able to leverage and work in a team environment.
  • Must be able to consistently follow established procedures, guidelines, and regulatory mandates.
  • Must have knowledge and ability to perform mechanical maintenance work on site.
Sound exciting? Apply today and join our team!  Sutro Biopharma, Inc. encourages all new hires to be fully vaccinated for COVID-19 prior to the first date of employment.  Sutro provides a competitive benefits package that includes a choice of health, dental, and vision insurance, life insurance, flexible spending accounts, 401K plan, PTO, ESPP (Employee Stock Purchase Plan) and stock options.  As an equal opportunity employer, we believe in fostering a culture that is inclusive and values diversity in background and opinions. Sutro Biopharma hires extraordinary individuals into every position in the company and is committed to the diversity of our team. Our company progresses without regard of race, ethnicity, gender, sexual orientation, religious belief, age, disability, or citizenship status. We are dedicated to creating a safe environment where our employees can grow and succeed together.     We look forward to hearing from candidates who are interested in exploring opportunities with Sutro! Our People & Culture team/hiring managers are unable to respond and do not accept solicitations from third-party agencies.  The anticipated salary range for fully qualified candidates applying for this role at Sutro Biopharma’s California-based locations will be [180,000-195,000] (not including bonus, equity, and benefits). The final salary offered will be dependent on several factors that include and are not limited to relevant previous experience, job responsibilities and duration of experience, the type and length of experience within the industry and education.  About Sutro BiopharmaSutro Biopharma, Inc., is a clinical-stage company relentlessly focused on the discovery and development of precisely designed cancer therapeutics, transforming what science can do for patients. Sutro’s fit-for-purpose technology, including cell-free XpressCF®, provides the opportunity for broader patient benefit and an improved patient experience. Sutro has multiple clinical-stage candidates, including luveltamab tazevibulin, or luvelta, a registrational-stage folate receptor alpha (FolRα)-targeting ADC in clinical studies. A robust pipeline, coupled with high-value collaborations and industry partnerships, validates our continuous product innovation. Sutro is headquartered in South San Francisco. For more information, follow Sutro on social media @Sutrobio, or visit www.sutrobio.com.  

Company

sutro

 

Sutro Biopharma, Inc., is a clinical-stage company relentlessly focused on the discovery and development of precisely designed cancer therapeutics, transforming what science can do for patients. Sutro’s fit-for-purpose technology, including cell-free XpressCF®, provides the opportunity for broader patient benefit and an improved patient experience. Sutro has multiple clinical stage candidates, including luveltamab tazevibulin, or luvelta, a registrational-stage folate receptor alpha (FolRα)-targeting ADC in clinical studies. A robust pipeline, coupled with high-value collaborations and industry partnerships, validates our continuous product innovation. Sutro is headquartered in South San Francisco. For more information, follow Sutro on social media @Sutrobio, or visit www.sutrobio.com.

Stock Symbol: STRO

Twitter

 

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Bill Newell, CEO Interviewed by Brad Loncar, Founder, Biotech TV – “Sutro Biopharma’s CEO on ADCs, non-cell protein synthesis, and more" - view it here 

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Company info
Website
Phone
650.881.6500
Location
111 Oyster Point Blvd
South San Francisco
California
94080
US

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