Abzena

CDMO for complex biologics and ADCs

Production Services Associate 1

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours

Full-timeSan Diego, CA, USA$40k - $60k /yrIn-person

About the Job

Requirements

0–2 years of experience in manufacturing production.
A high school diploma is required.
Knowledge and understanding of current Good Manufacturing Practices (cGMPs).
Experience using single-use technologies and disposable systems.
Ability to perform basic arithmetic operations: addition, subtraction, multiplication, and division.
Ability to walk and stand for extended periods.
Ability to frequently lift or move objects weighing up to 30 pounds.
Ability to use arms, hands, and fingers to handle, feel, or reach.
Ability to climb, balance, stoop, kneel, crouch, or crawl.
Near and far sight, color, peripheral vision, depth perception, and ability to focus.

Responsibilities

Support both downstream and upstream production in a current Good Manufacturing Practice (cGMP) manufacturing environment.
Prepare buffers and media, clean and sanitize the facility, assemble equipment kits, and set up and break down operational equipment according to the operations schedule.
Perform complex tasks in accordance with cGMP requirements.
Operate and maintain production equipment using single-use materials for buffer and media preparation, including weighing and dispensing.
Perform daily, weekly, and monthly cleaning of the cleanroom and surrounding controlled areas, including floors, walls, ceilings, and equipment.
Maintain and stock supplies, including gowning and emergency kits.
Document and verify task completion according to current Good Documentation Practices (cGDP), standard operating procedures (SOPs), and batch records.
Manage a flexible work schedule where shift work may be required.
Conduct activities supporting production schedules as directed by senior staff.
Support floor operations for multiple projects simultaneously.
Cross-train on various tasks, including upstream and downstream cGMP manufacturing.
Set up equipment according to established practices, including RTP, STR, production bioreactors, AKTA systems, depth filters and pods, viral filtration, and UFDF.
Safely handle and transport raw materials, finished products, and equipment into and out of the cleanroom while adhering to aseptic technique.
Follow Abzena policies, procedures, quality standards, and applicable regulations.
Communicate and work effectively in a team environment.
Adhere to quality standards and perform other assigned duties.

Salary Range: 40000 to 60000 (Currency: USD) (Pay period: per-year-salary)

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.

Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.

We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.

We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.

The Production Services Associate I will be responsible for supporting both downstream and upstream production in a cGMP manufacturing environment. The Production Services team prepares buffers and media, cleaning and sanitization of the facility, assembling equipment kits to support manufacturing operations, setting up and breaking down of operational equipment, in accordance with the operations schedule. This role requires adherence to cGMP and standard operating procedures.

Example Plan Shift Schedule:

- First Day (Orientation): 9-5 am (Tuesday)

- Day after Orientation: 2:30-11 pm M-F

Schedule is subject to change based on needs.

Responsibilities

Perform a variety of complex tasks in accordance with cGMP.
Operate and maintain production equipment with single-use materials as it relates to buffer and media preparations, including weight and dispense.
Perform daily, weekly, and monthly cleanings of the cleanroom and surrounding controlled areas, including floors, walls, ceilings and equipment.
Maintain and stock supplies as directed. (i.e. gowning, and emergency kits, ect.)
Documentation/verification of task completion in accordance with cGDP, SOPs and Batch Records.
Manage a flexible work schedule where shift work may be required.
Conduct activities in support of production schedules as directed by senior staff.
Support floor operations for multiple projects simultaneously.
Crosstrain on various tasks including Upstream/Downstream cGMP manufacturing.
Operate in a team setting.
Follow detailed instructions and to maintain accurate records.
Set up equipment in accordance with established practices. (i.e. RTP, STR, Production Bioreactors, AKTA systems, Depth Filters and Pods, Viral Filtration, and UFDF)
Safely handle and transport raw materials, finished product and equipment in and out of the cleanroom, adhering to aseptic technique.
Operate to the highest ethical and moral standards.
Comply with Abzena's policies and procedures.
Communicate effectively in a team environment.
Participate effectively as a team player in all aspects of Abzena's business.
Adhere to quality standards set by regulations and Abzena policies, procedures, and mission.
Perform other duties as assigned.

Qualifications

0 – 2 years of experience in manufacturing production.
A high school diploma is required.
Knowledge and understanding of cGMPs.
Experience using single-use technologies and disposable systems.
Ability to compute basic arithmetic operations: addition, subtraction, multiplication, and division.

Physical Requirements

Physical ability to walk and stand for extended periods of time.
Frequently lift and or move objects up to 30 pounds.
Use arms, hands and fingers to handle, feel or reach.
Ability to climb, balance, stoop, kneel, crouch, or crawl.
Visual abilities include near and far sight, color, peripheral vision, depth and ability to focus.

FLSA: Non-Exempt

Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.

About the Company

Abzena

CDMO for complex biologics and ADCs

Abzena is a contract development and manufacturing organization (CDMO) that provides integrated services for complex biologics and bioconjugates, including antibody-drug conjugates, from discovery through GMP manufacturing for clinical trials and commercial supply. Its offerings cover antibody discovery, protein engineering, cell line development, process and analytical development, and cGMP manufacturing, often using its proprietary ThioBridge and Composite Human Antibody platforms. Abzena differentiates itself by delivering end-to-end development and manufacturing for complex biologics and by leveraging its proprietary technologies, with global facilities in the US and UK and a history of strategic acquisitions. Its goal is to help biotech and pharma programs progress efficiently from research to commercial supply by providing integrated services and potential licensing opportunities.

Company size: 201-500
Company stage: IPO
Headquarters: Babraham, United Kingdom
Founded: 2001

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