Lead Technician - Manufacturing

Erytech Pharma, Inc.; Princeton (NJ); On-site; USD 65,000 - 85,000; Full time

Job summary

JobRx, Inc. in Princeton, New Jersey, is seeking a skilled technician to provide technical support in Clean Rooms and the Pilot Lab. The ideal candidate will have a BS in Immunology or related field with relevant experience, and must be able to effectively communicate across departments.

The role involves ensuring the availability of supplies, assisting in technical reporting, and conducting experiments to support new product development, while adhering to cGMP regulations.

Flexibility in work shifts and a commitment to maintaining high standards of operation are essential.

Qualifications

• Proficient in cGMP regulations and FDA standards.
• Ability to work aseptically in a clean room environment.
• Experience in biopharmaceutical manufacturing preferred.

Responsibilities

• Provide technical support to manufacturing technicians in clean rooms.
• Maintain and improve reporting of technical issues and work orders.
• Perform pilot plant experiments for new product development.

Skills

Technical communication skills

Project management

Flexibility in shifts

Analytical thinking

Education

BS in Immunology, Cell or Molecular Biology, Chemistry, or related field with 2 years experience

Associate degree with over 4 years of relevant industry experience

Tools

Microsoft Office

EMS system

Job description

Key Responsibilities

• Provide technical support to Manufacturing Technicians while processing in Clean Rooms or Pilot Lab.
• Process regularly and be a back‑up in case team members are not available as needed.
• Ensure supplies and materials needed for projects are available and organized.
• Follow up regarding manufacturing technical situations/issues throughout the day and initiate escalation process as needed.
• Assist Manufacturing Management in maintaining and improving the reporting of technical issues, work orders, equipment tag outs, equipment swaps etc.
• Perform pilot plant experiments to support New Product Development or Process Innovation projects as needed.
• Collaborate with facilities to ensure work orders are resolved and closed in a timely manner.
• Responsible for equipment tracker Excel file in MS Teams.
• Collaborate with SME to ensure manufacturing internal trackers are easily accessible, accurate and up to date.
• Responsible to oversee and ensure all equipment is calibrated, validated, and qualified as required.
• Ensure equipment is returned "as found" while maintaining its calibration/qualification/validation.
• SME in writing, revising, and reviewing SOP's Instructions and Forms to better improve process.
• SME to Initiate, assess impact and produce root cause analysis related to Deviations. Initiate and oversee CAPA and Change Controls as needed, collaborate with other team members and QA to perform appropriate investigations and analysis.
• Participate in investigations regarding equipment issues, providing an SME assessment to the main investigator.
• Be the back‑up SME for manufacturing data for trending and key performing attributes.
• Ensure data is collected and entered in the appropriate spreadsheet at the end of each production run with minimum delay.
• Be a back‑up in the absence of a supervisor as needed.

Knowledge, Skills, and Experience

• BS in Immunology, Cell or Molecular Biology, Chemistry, Biochemistry, Biology or Bioengineering with 2 years of relevant industry experience or an associate degree with over 4 years of relevant industry experience preferred but not required.
• Ability to foster culture of continuous improvement and operation excellence.
• High technical proficiency. Knowledge or COBE cell processor and cell encapsulation is a plus.
• Excellent technical communication skills, both verbal and written, and the ability to constructively interface effectively with all departments, all levels of organization and external vendors.
• Knowledge of Microsoft office and EMS system.
• Flexibility to work different shifts.
• Ability to aseptically gown in an ISO 8/ISO 7 clean room environment.
• Prior experience in clinical/commercial biopharmaceutical manufacturing and regulatory agencies inspections desired.
• Proficient in cGMP regulations as well as FDA.

• Demonstrated ability to manage multiple projects independently.
• Flexibility to handle and manage both long‑term development projects and short‑term troubleshooting needs.
• Critical analytical thinking and problem‑solving capabilities.
• Strong computer and communication skills, both written and oral.

Candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation prior to the commencement of employment to support the well‑being of our employees, their families, and the communities in which we live and work.