Manufacturing Associate, Cell & Gene Therapy job in Philadelphia, USA

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Contract

Discipline: Manufacturing

Location: United States

This vacancy has now expired. Please see similar roles below...

Manufacturing Associate, Cell and Gene Therapy - Contract - Philadelphia PA

Proclinical is seeking a dedicated Manufacturing Associate for Cell and Gene Therapy.

Primary Responsibilities:

This role focuses on the manufacturing of Master and Working Cell Banks and performing activities within production facilities to support the manufacture of Cell & Gene Therapy products. The ideal candidate will have a solid understanding of regulatory compliance and experience in aseptic techniques and cGMP.

Skills & Requirements:

Associates' or a Bachelor's degree, preferably in a scientific field alongside with relevant working experience
Experience performing cell culture
Knowledge of aseptic techniques
Ability to work in a Lab setting with Biohazards and various other chemicals
Ability to wear appropriate PPE as required
Solid understanding of Good Laboratory Practices and Good Manufacturing Practices

The Manufacturing Associate for Cell and Gene Therapy's responsibilities will be:

Manage and keep an eye on the overall performance of aseptic technique ensuring compliance with standards
Train, coach and mentor others on basic aseptic operational techniques
Identify aseptic technique gaps and implement improvements
Operate and maintain equipment, perform complex troubleshooting
Support sourcing and purchasing of standard, new, and complex equipment
Perform solution and material preparation, analyze results and resolve issues
Participate in and perform technical transfer activities
Execute in-house and offsite validation activities, provide input and review validation documentation
Schedule, receive and organize materials, perform material procurement activities
Follow compliance and regulatory requirements and current Good Manufacturing Practices (cGMPs)
Author and improve the efficiency and execution of Standard Operating Procedures (SOPs) and Batch Records (BRs)
Train others on SOPs, equipment, all unit operations and non-manufacturing SOPs and systems
Lead and oversee the manufacturing process

Compensation:

$21 - $26 per hour

If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.