Manufacturing Associate Downstream

Avid Bioservices; Costa Mesa (CA); On-site; USD 28,282 - 37,663; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) matching

Paid time off

Job summary

A leading biopharmaceutical company located in Costa Mesa, CA, is seeking a Manufacturing Associate to join their team. The role involves working in a multi-product facility in compliance with cGMP standards, overseeing tasks such as chromatography operations and meticulous documentation. Candidates with 2+ years of experience in related fields, especially in aseptic environments, are encouraged to apply. The position offers competitive pay ranging from $20.53 to $27.34 per hour, with opportunities for growth and development.

Qualifications

• Minimum of 2 years of experience with large-scale liquid chromatography.
• 1+ years of related experience in the life sciences industry.
• Proficiency in GMP production environments.

Responsibilities

• Ensure timely setup of equipment and materials for production runs.
• Operate and maintain chromatography skids.
• Conduct antibody and enzyme purification techniques.

Skills

Large-scale liquid chromatography

Aseptic techniques

Multitasking

Detail-oriented

Education

Bachelor’s or associate degree (A.A.)

Tools

BioProcess chromatography skids

Sartocheck 3/4 Filter Integrity Tester

ARS Frontier Autoclave

Job description

Looking to join a passionate team dedicated to developing and manufacturing life‑saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.

Your Role:

Join our dynamic team as a Manufacturing Associate, Downstream! In this role, you'll be a crucial part of our multi‑product manufacturing facility, working in strict compliance with cGMP and Standard Operating Procedures. Your responsibilities will encompass various tasks, including production, meticulous documentation, report writing, materials procurement, and equipment scheduling. You will be instrumental in ensuring the timely production and release of top‑quality products.

• Ensuring the timely setup of equipment and materials for each production run.
• Planning and preparing all necessary resources for various processes and activities.
• Operating and diligently maintaining BioProcess chromatography skids.
• Proficiently handling the packing, unpacking, and cleaning of production‑scale chromatography columns.
• Executing antibody and enzyme purification techniques using Affinity chromatography, Size Exclusion chromatography, Ion Exchange chromatography, Hydrophobic Interaction, and Tangential Flow Filtration (TFF).
• Conducting pH and conductivity meter calibration and testing.
• Managing product filtration processes, including sterile filtration, ultrafiltration, and viral filtration.
• Demonstrating exceptional aseptic techniques with precise, deliberate movements.
• Participating in product filling, including aseptic processing and media fill qualifications.
• Upholding the cleanliness and maintenance of cleanroom facilities and equipment.
• Monitoring and controlling raw material inventory levels.
• Ensuring compliance with Good Manufacturing Practices (GMP) documentation standards.
• Taking the initiative to revise and initiate Batch Production Records, Standard Operation Procedures, study protocols, and reports.
• Leading and managing independent projects as assigned, contributing to the overall success of the manufacturing team.
• Skillfully preparing media and buffer solutions critical for production processes.
• Conducting manual cleaning of small parts and equipment to maintain hygiene and efficiency.
• Performing thorough filter integrity testing using specialized equipment like the Sartocheck 3/4 Filter Integrity Tester.
• Operating and ensuring the proper maintenance of the ARS Frontier Autoclave.

Minimum Qualifications:

• 2+ years of experience with large‑scale liquid chromatography columns or similar equipment.
• 1+ years of related experience in the life sciences industry.
• Proficiency in working within a GMP production environment with aseptic techniques.
• Capability to gown for a class 10,000 cleanroom environment and work under aseptic conditions in a class 100 environment.

Preferred Qualifications:

• Bachelor’s or associate degree (A.A.) with a preference for biology or chemistry emphasis.

Position Type / Expected Hours of Work:

This role is a full‑time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5:00 p.m. unless otherwise stated by Supervisor. Must have the ability to be flexible working overtime, weekends and/or holidays when necessary.

Compensation:

We offer competitive compensation packages for this role, including a base salary, performance‑based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.

The compensation range for this role is $20.53 – $27.34 per hour depending on experience and qualifications. Additionally, we offer opportunities for career growth and development in a supportive and inclusive work environment.

Who you are:

• You have a “bring it on!” team‑player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
• Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
• You have exceptional multitasking skills and an unparalleled attention to detail that ensures the smooth running of everything.
• You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:

In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. Reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting.