Supervisor, cGMP Manufacturing

CSBio Co.; Milpitas (CA); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

401k

PTO

Medical, dental, and vision insurance

Holiday pay and paid time off

Disability insurance

Life insurance

Carpool / transportation assistance

Team building activities

Job summary

CSBio is seeking a Supervisor of cGMP Peptide Manufacturing at its Milpitas facility. You will lead production operations, oversee SPPS, purification, lyophilization, and packaging for clinical and commercial campaigns, reporting to the Head of Manufacturing.

This is a hands-on leadership role with responsibility for schedule, quality, and compliance. You will manage production staff, drive improvements, ensure 21 CFR 210/211 and ICH Q7 adherence, and support tech transfer and regulatory data

Qualifications

• Bachelors degree in Chemistry, Biochemistry, Chemical Engineering or related discipline.
• 3+ years of cGMP manufacturing experience in pharmaceutical, biopharmaceutical or peptide manufacturing.
• Hands-on experience with SPPS, prep HPLC purification, and lyophilization.

Responsibilities

• Lead and mentor manufacturing team; establish performance metrics and training.
• Direct cGMP peptide production operations including SPPS, cleavage, purification, lyophilization, and packaging.
• Own production scheduling and on-time delivery; allocate resources across programs.
• Drive yield, throughput, and cost improvements using process capability data.

Skills

SPPS

cGMP manufacturing

Leadership

HPLC purification

Lyophilization

MES/eBR systems

Education

Bachelors in Chemistry/Biochemistry/Chemical Engineering or related

Tools

MES/eBR systems

Job description

Description

CSBio is a peptide contract manufacturing founded in 1993. Our initial products were a complete line of automated synthesizers for manufacturing and process development, with a focus on cGMP production. In 1994, we opened our custom peptide facility and began producing high quality compounds for research organizations and pharmaceutical companies worldwide. In 2004, we opened our peptide production facility in Menlo Park, CA and in 2014, we expanded our production capability through the addition of a new, state of the art building dedicated to cGMP peptide production. In 2017, we passed a FDA inspection and were recommended to be approved for commercial drug substance manufacturing. In 2023, we added additional cGMP clinical production capacity in Milpitas, CA.

Position Summary

As Supervisor of cGMP Peptide Manufacturing, you will lead our peptide production operations during a critical growth phase. You will be responsible for executing and scaling solid-phase peptide synthesis (SPPS), downstream purification, lyophilization, and packaging operations across clinical and commercial campaigns at our Milpitas cGMP facility. This is a hands-on technical and leadership role reporting to the Head of Manufacturing, with direct authority over manufacturing operations, production staff, scheduling, and floor execution.

You will oversee day-to-day GMP production, in-process execution, campaign delivery, and operational excellence that ensure product quality, on-time delivery, and regulatory compliance. This role bridges peptide chemistry expertise with manufacturing operations, directly impacting batch success, CDMO customer confidence, and manufacturing efficiency.

Key Responsibilities

Site Operations

• Lead and mentor manufacturing team of 1-2 chemists, operators, and technicians; establish performance metrics, career development, technical training programs, and ensure high-throughput production operations
• Direct cGMP peptide production operations including SPPS, cleavage, prep HPLC purification, lyophilization, and final packaging across clinical and commercial campaigns
• Own production scheduling and on-time delivery; establish campaign plans, sequencing, and resource allocation across multiple concurrent programs to support manufacturing commitments
• Drive yield, throughput, and cost efficiency improvements; establish process performance targets based on capability analysis, historical data, and ICH guidance
• Ensure manufacturing operations comply with cGMP, internal SOPs, and master batch records per 21 CFR 210/211 and ICH Q7
• Manage production equipment (synthesizers, prep HPLC systems, lyophilizers, packaging lines); oversee equipment qualification, preventive maintenance, and vendor relationships
• Author and maintain master batch records, SOPs, and work instructions; establish justified process parameters based on process capability and development data
• Lead investigation of deviations, failed batches, and process excursions; conduct root cause analysis and implement corrective actions
• Support process characterization, scale-up, and tech transfer activities; partner with Process Development on new product introductions and PPQ campaigns
• Prepare manufacturing data packages for regulatory submissions (IND, CMC dossiers); ensure data integrity compliance (21 CFR Part 11, ALCOA+)
• Manage manufacturing execution systems (MES) and electronic batch records; drive digitalization of production operations
• Support CDMO customers with campaign execution, tech transfer, and manufacturing troubleshooting; maintain customer confidence through responsive operational support

System Optimization

• Support the design, implementation, and continuous improvement of core manufacturing systems.
• Ensure systems are compliant, practical, efficient, and usable for front-line teams; identify opportunities to simplify workflows, reduce inefficiencies, and improve adoption.

Audit/Inspection Support

• Support manufacturing audit and inspection follow-up, including drafting and driving effective responses, CAPAs, commitments, and remediation plans, and ensuring actions are completed on time and are operationally practical and sustainable.

Hands-On Leadership

• Model CSBio's expectation that leaders understand operations at a task level; to observe workflows, understand bottlenecks, and identify where quality or execution is breaking down.
• Demonstrate willingness to roll up sleeves, dive into operational details, and help solve problems directly when needed; use firsthand operational knowledge to recommend practical solutions and realistic milestones.

Team Development

• Foster a culture of initiative, urgency, accountability, and continuous improvement within the manufacturing team; ensure issues are surfaced early, discussed openly, and resolved with practical, sustainable solutions.
• Provide coaching and support to chemists to strengthen operational understanding, problem solving, and execution.

Competencies:

To perform the job successfully, an individual should demonstrate the following competencies:

Problem Solving - Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations.

Teamwork - Balances team and individual responsibilities; Exhibits objectivity and openness to others' views; Gives and welcomes feedback; Supports everyone's efforts to succeed.

Organizational Support - Follows policies and procedures; Completes tasks correctly and on time; Supports organization goals and values.

Motivation - Sets and achieves challenging goals; Demonstrates persistence and overcomes obstacles; Measures self against standard of excellence.

Adaptability - Adapts to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events.

• Bachelors Chemistry, Biochemistry, Chemical Engineering, or related discipline.
• 3+ years of cGMP manufacturing experience in pharmaceutical, biopharmaceutical, or peptide manufacturing
• Hands-on experience with solid-phase peptide synthesis (SPPS), prep HPLC purification, and lyophilization unit operations
• 1+ years in a leadership role managing manufacturing operations or production teams
• Expertise in cGMP batch execution, master batch record authoring, and campaign management
• Strong understanding of FDA cGMP expectations for manufacturing operations, data integrity (21 CFR Part 11), and batch record documentation
• Experience supporting process validation, PPQ campaigns, and tech transfer of new peptide products into GMP manufacturing
• Demonstrated manufacturing management skills including budget oversight, capital project management, vendor management, and staffing
• Strong problem-solving and investigative skills; ability to troubleshoot process and equipment issues in real time on the manufacturing floor
• Excellent communication skills; ability to communicate manufacturing status, deviations, and risks clearly to quality, operations, and regulatory teams
• Demonstrated ability to work effectively in a small, hands-on, fast-moving organization.
• Experience with MES/eBR systems and continuous improvement initiatives is preferred.

• Medical, dental, and vision insurance (Kaiser HMO or BlueShield PPO. Employer pays 90% for Employee and 75% for Employee's family; Dental: Aetna Dental, Delta Dental, Guardian Dental, MetLife Dental. Vision: VSP and Aetna EyeMed)
• 401k 10% 1:1 match
• PTO policy. 10 days PTO
• Companywide paid holiday during: Week of July 4, Thanksgiving (2 days), Week of December 25Basic life ($20,000 paid by company) and supplemental life insurance (optional supplemental).
• Disability insurance 50% standard employer paid.
• Carpool, clean air vehicle, and cell phone reimbursement
• Employee rewards and recognition program
• Company organized social events
• Quarterly sponsored team building activities