Manufacturing Technician I/II/III (2nd Shift)

Up Closets of North Cincinnati; Indianapolis (IN); On-site; USD 40,000 - 80,000; Full time

Job summary

Join a forward-thinking company at the forefront of gene therapy as a Manufacturing Technician. In this role, you will be integral to the production of clinical and commercial products, working closely with various teams to ensure compliance and efficiency. This position offers a dynamic work environment where innovation and collaboration are key. You'll engage in cGMP operations, troubleshooting, and maintaining equipment, all while contributing to groundbreaking advancements in healthcare. If you're passionate about making a difference and thrive in a fast-paced setting, this opportunity is perfect for you.

Benefits

Paid vacation days

401(k) plan with company match

Choice of several healthcare plans

FSA and HSA programs

Employer-paid basic term life insurance

Voluntary disability insurance

Qualifications

• 2-4 years of related cGMP industry experience required.
• Hands-on experience in writing and reviewing documentation.

Responsibilities

• Perform routine and non-routine manufacturing operations.
• Document operations according to GDP principles.

Skills

cGMP manufacturing operations

aseptic techniques

troubleshooting

documentation skills

communication skills

process-oriented thinking

Education

High School Diploma

Associate’s Degree in Life Sciences/Engineering

Bachelor’s Degree in Life Sciences/Engineering

Job description

Manufacturing Technician I/II/III (2nd Shift)

Lexington, MA

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

Manypeople 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

Manufacturing performs all required process steps and in process controls, in close collaboration with MSAT, QC, QA, Engineering and Validation. With general supervision the individual will perform routine and non-routine manufacturing operations, including but not limited to work functions in Cell Culture, Purification, Solution & Equipment Prep areas. Operates production equipment according to SOPs for the production of clinical and/or commercial products.

This position is located in Lexington, MA and reports to the MFG Supervisor.

ESSENTIAL JOB FUNCTIONS

This individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Batch Production Records and Solution prep records. Primary responsibilities include the following:

• Attend daily meetings including shift hand off and ensure relevant information is shared between shifts.
• Perform weekly/monthly walkthroughs and ensure areas are maintained in a safe and compliant state.
• Maintaining orderliness of process area and stocking production area with supplies from collaboration with Supply Chain.
• Demonstrating general knowledge of aseptic techniques.
• Perform troubleshooting activities according to SOPs.
• Execute routine and non-routine production operations according to MFG schedule, including off shift production activities when needed.
• Document operations according to GDP principles in Batch Production Record (BPR), Solution records (SLR), Logbooks and Forms.
• Perform page reviews in BPRs, SLRs, Logbooks, and Forms.
• Carry out work in a safe manner, notifying management of safety issues and risks.
• Required to work holidays and overtime as needed to support the manufacturing process.

This individual will manage equipment and support facility related projects by:

• Perform scheduled cleaning of equipment.
• Perform standardization of equipment.
• Support product change over activities.
• Support equipment and process qualifications if needed.
• Escalate work requests to Senior or Lead Technicians for submission in work request management system.

SPECIAL JOB REQUIREMENTS

• Normally requires a high school diploma and 2-4 years related cGMP industry experience or an Associate’s Degree in Life Sciences/Engineering field with 1 year of cGMP Manufacturing experience or Bachelor’s degree in life Sciences/Engineering field.
• Preferably working 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 documentation.
• Experience in (bio)-manufacturing unit operations (USP and/or DSP).
• Good writing and oral communication skills.
• Applies experience and skills to complete assigned work within own area of expertise.
• Works within standard operating procedures and/or scientific methods.
• Comfortably able to lift up to 40lbs.
• 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

High School Diploma

Associate’s Degree in Life Sciences/Engineering

Bachelor’s Degree in Life Sciences/Engineering

ON-THE-JOB EXPERIENCE

2-4 years related industry experience

SKILLS / ABILITIES

Has process-oriented way of thinking and working.

Is self-organized.

Is able to communicate in professional way on diverse levels and channels.

Is capable of taking initiative when necessary.

Has a flexible attitude in a challenging environment.

Is intrinsically motivated.

PHYSICAL DEMANDS

While performing the duties of this job, the employee is required to meet the following physical demands:

• Regularly sit for long periods of time.

Movement

• Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; 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 20 pounds.
• Rarely lift and/or move up to 40 pounds.

Vision

• Frequently utilize close vision and the ability to adjust focus.

Communication

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

GENEZEN'S CURES VALUE-BASED COMPETENCIES

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

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

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

Execute with Excellence & Integrity
We are dedicated to delivering quality results and upholding ethical principles.

Solutions 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.
• 401(k) plan with company match up to 6% of salary, vested immediately.
• Choice of several healthcare plans.
• FSA and HSA programs.
• Employer-paid basic term life/personal accident insurance.
• Voluntary disability, universal life/personal accident 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.