Manufacturing Supervisor, Upstream

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.

WORKING AT GENEZEN

Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.

JOB SUMMARY

Promote a safe working environment, training, and development of the manufacturing team; plan on-time execution of batch activities; deliver quality and safe viral vector products; and continuously improve manufacturing processes.

This position is located in Indianapolis, Indiana (City of Fishers) and will report to the Director of Manufacturing.

ESSENTIAL JOB FUNCTIONS

Provide leadership, coaching, and mentoring of Upstream manufacturing personnel.

Oversee and execute Vector Upstream Manufacturing activities including the scheduling of resources, material staging, equipment preparation, batch execution, cleaning/sanitization, inventory transactions, and batch record review.

Provide on the floor training and support for upstream manufacturing operations for clinical viral vector batches.

Hire, coach, and develop Manufacturing team members, including performance management and periodic reviews.

Strong knowledge of cGMP and GDP requirements for Drug Substance Manufacturing (Viral Vector Manufacturing preferred).

Strong technical knowledge of both adherent and suspension cell lines including cell thawing, scale-up, bioreactor inoculation, transfection, harvest, and clarification.

Preferred knowledge and experience with the use and troubleshooting of Cytiva XDR 50L, Cytiva XDR 500L, Univercells Scale-X Carbo, and Cytiva iCELLis 500 bioreactors.

Monitor and report on area performance, identifying opportunities for improvement and implementing process improvements.

Design, implement, maintain, and continuously improve vector manufacturing systems, policies, procedures, and programs that ensure compliance to company and regulatory body standards for Quality and EHS.

Identify and mitigate risks in Manufacturing operations that could negatively impact product and personnel safety.

Manage the Manufacturing Production system including but not limited to personnel development, problem solving, investigation of deviations, root cause analysis, CAPAs, Change Controls, 6S, etc.

Ensure safe working environment and compliance with OSHA, EHS, Quality, and cGMP procedures and policies within the Manufacturing department

JOB QUALIFICATIONS

Prior leadership experience in GMP manufacturing facility

Preferably work experience in a comparable position (similar type of work, similar group dynamics), preferentially in an industrial organization

Ability to adhere to company internal and regulatory (EMA, FDA) policies, processes, and procedures

Hands -on experience in writing and reviewing the documentation

Experience in (bio)-manufacturing unit operations

Good writing and oral communication skills

The work schedule may require adjustments to support production activities

SPECIAL WORK REQUIREMENTS

Adaptability required as work schedule may change based on business needs

Criminal background check required

Other duties as assigned

KNOWLEDGE, SKILLS AND EXPERIENCE

EDUCATION / CERTIFICATIONS / LICENSES

Essential/Desired

BS in Biology, Microbiology, Chemistry, Virology, or any other relevant field of study

Desired

In-depth knowledge of aseptic processing, GxP, cell culture, and bioreactor operation and troubleshooting

Essential

ON-THE-JOB EXPERIENCE

4-6 years of related work experience in a GMP environment

Essential

1 year of supervisory experience

Desired

Drug Substance experience with cell culture and upstream viral vector manufacturing

Strongly Desired

Experience using single use systems

Desired

SKILLS / ABILITIES

• Demonstrated interpersonal skills to build relationships, act as change agent, manage conflict, and adapt to rapidly changing organizational and business needs
• Essential

• Ability to manage multiple priorities
• Essential

Work Environment:

Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning

Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities

Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock

Occasionally exposed to extremely loud noise levels

Spending time on the floor during activity execution (manufacturing, maintenance, construction, commissioning, and qualification) is required

Movement:

Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms

Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl

Lifting:

Frequently lift and/or move up to 25 pounds

Occasionally lift and/or move up to 40-50 pounds

Vision:

Frequently utilize close vision and the ability to adjust focus

Corrected 20/20 vision to assist with visual inspection of Drug Products

Communication:

Frequently required to communicate by talking, hearing, using telephone and e-mail

Strong communication skills to efficiently collaborate and coordinate within manufacturing and cross-functional

GENEZEN'S CURES VALUE-BASED COMPETENCIES

• C ommitted to Science
• We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.

• U rgency in action for the patients
• We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.

• R esilience & Grit in operations
• We are committed to overcoming challenges, learning from failures, and persistently striving for success.

• E xecute with Excellence & Integrity
• We are dedicated to delivering quality results and upholding ethical principals.

• S olutions driven for our partners
• We are committed to being a proactive, collaborative, creative and open-minded partner.

GENEZEN'S BENEFITS

Paid vacation days, amount based on tenure

Paid sick time

10 observed holidays + 2 floating holiday + 1 volunteer day

401(k) plan with company match up to 6% of salary

Share Appreciation Rights

Choice of several healthcare plans

FSA and HSA programs

Dental & vision care

Employer-paid basic term life/personal accident insurance

Voluntary disability, universal life/personal accident insurance

Accidental Death & Dismemberment (AD&D) Insurance

ADDITIONAL DETAILS

Nothing in the job description for this role restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

This position requires a criminal background check.

Genezen is an Equal Opportunity Employer.

Genezen participates in EVerify.

Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.

Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.

Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indi