Supervisor, Manufacturing at Cellares

South San Francisco, California, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, Cell Therapy, Pharmaceutical ManufacturingIndustries

Requirements

Proven leadership to drive effective communication, coordination, and collaboration across cross-functional groups
Ability to interface with all levels of the organization, including Manufacturing, Quality, MSAT, QC, Process/Analytical Development, Supply Chain, Warehouse, Training, Engineering/Facilities, and EH&S
Experience working in a fast-paced, mission-driven environment
Ability to operate in a controlled GMP environment and perform gowning as per procedure
Ability to perform routine procedures following written instructions (SOPs, batch records, solution documents, protocols, etc.)
Ability to execute manufacturing processes in both R&D and GMP environments, following protocols and/or SOPs
Understanding of all operations, functions, capability of equipment and ancillary support to equipment, ability to operate said equipment, and perform complex troubleshooting
Knowledge of compliance and regulatory requirements and current Good Manufacturing Practices (cGMPs), including understanding the ‘why’ behind the regulations
Ability to coach and mentor others on compliance, procedures, aseptic techniques, equipment, and troubleshooting skills

Responsibilities

Lead, direct, coach, and develop an effective manufacturing team responsible for daily clinical and commercial/clinical production of autologous and allogeneic cell therapy products, ensuring safe and compliant operations according to cGMP requirements
Provide technical and managerial leadership by effectively interfacing and collaborating with key stakeholders and functions across the organization to successfully manufacture and disposition products to patients in a timely manner
Lead and oversee manufacturing processes including engineering runs, PPQ, and APS
Ensure manufacturing processes in both R&D and GMP environments follow appropriate protocols and/or standard operating procedures (SOPs)
Responsible for on-the-floor operation performance, overall performance of aseptic technique and process execution, ensuring compliance with standards
Make spot corrections and provide feedback on process and procedure adherence to employees in the cleanroom
Review in-process and completed documents for accuracy, including SAP issuance of materials, and assure documentation is turned in to area management within specified days of completion
Initiate, investigate, and support the closure of Deviation Reports, CAPAs, and Change Controls
Revise and originate production records, standard operating procedures, protocols, and reports
Accountable for schedule preparation, adjustments, and performance of work assignments for team
Coordinate and perform routine cleanroom and laboratory activities including ordering, cleaning, restocking, and equipment qualification/maintenance
Oversee the hiring, development, and performance management of staff within team
Train and mentor new manufacturing associates on procedures, aseptic techniques, equipment, and troubleshooting skills
Responsible for team’s training status to be compliant
Actively participate in all health authority, customer, and internal audits of the facility
Work closely with other functions

Skills

Key technologies and capabilities for this role

cGMPGMPCell Therapy ManufacturingManufacturing LeadershipSOPsPPQEngineering RunsMSATQCSupply ChainCross-functional CollaborationTeam Coaching

Questions & Answers

Common questions about this position

Is this a full-time position?

Yes, this is a full-time employment position.

What is the work location or remote policy for this role?

This information is not specified in the job description.

What key skills and experience are required for the Manufacturing Supervisor role?

The role requires proven leadership in cGMP manufacturing operations, experience with cell therapy products, aseptic technique, process execution, troubleshooting equipment, and collaboration across functions like Quality, MSAT, QC, and Engineering.

What is the company culture like for this position?

The role is in a fast-paced, mission-driven environment focused on cell therapy manufacturing, where the successful candidate should enjoy tackling a broad selection of challenges as the company grows.

What makes a strong candidate for this Manufacturing Supervisor position?

A strong candidate is innovative, highly motivated, with proven leadership to coach and develop manufacturing teams, ensure cGMP compliance, and collaborate across multidisciplinary functions in cell therapy operations.

Cellares

Develops and manufactures cell therapies efficiently

About Cellares

Cellares develops and manufactures cell therapies in the biotechnology sector, operating as an Integrated Development and Manufacturing Organization (IDMO). Its proprietary "Smart Factory" technology features an automated single-use cartridge system, which increases productivity and reduces costs and process failures compared to traditional methods. The company serves a range of clients, including pharmaceutical companies, and aims to provide efficient and cost-effective manufacturing services for cell therapies. Cellares stands out by combining development and manufacturing processes under one roof, making it a competitive option in the industry.

South San Francisco, CaliforniaHeadquarters

2019Year Founded

$345.3MTotal Funding

SERIES_CCompany Stage

Industrial & Manufacturing, BiotechnologyIndustries

201-500Employees

Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Company Match

Stock Options

Risks

Emerging biotech startups threaten Cellares' market share with similar solutions.

Potential regulatory delays could impact scaling of new automated systems like Cell Q.

Supply chain vulnerabilities may disrupt production timelines for Cell Shuttle and Cell Q.

Differentiation

Cellares' Cell Shuttle offers 10x scalability over manual cell therapy manufacturing.

The Smart Factory technology integrates development and manufacturing, unlike traditional CDMOs.

Cell Q automates QC processes, addressing bottlenecks in cell therapy quality control.

Upsides

Partnership with Sony enhances precision in cell therapy manufacturing processes.

Strategic partnership with Bristol Myers Squibb provides financial boost and validation.

Ossama Eissa's appointment as COO accelerates global expansion and operational capabilities.

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