Production Specialist

Title: Production Specialist Location: Warren, NJ Schedule: 8:00 am - 4:30 pm Type: Temporary Start date: ASAPENTRY LEVEL role seeking recent college grads with a BS Degree in the sciences! Will also consider AS Degree candidates with some industry lab experience preferably within a GMP regulated environment. Responsibilities:Day-to-day operations support in a cGMP manufacturing environment for the production of BeadChip and NGS products including formulation of bead intermediates, bulk reagents, and filled vials

As a Production Specialist, you will perform setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency

Responsible for the fulfillment of daily / weekly production support schedule and adapt to schedule and personnel changes to ensure internal and external customers' needs and deliveries made

Perform the following activities in a quality focused cGMP manufacturing environment: BeadChip carrier assembly - involves manual and automated equipment processes

Formulate custom bulk reagents - involves working with pipettes and balances

Bulk and fill reagent manufacturing

Weighing, diluting, measuring and verifying chemicals for in-process solutions

Packaging of carrier and reagent boxes

Ensure materials and equipment are available in inventory for production as required

Follow manufacturing schedule, report issues and concerns to management

Perform equipment setup, operation, re-supply, documentation, cleaning, minor equipment adjustments and minor preventative maintenance tasks to meet standards for safety, quality and efficiency

Follow GMP documents (e.g., SOPs, Work Instructions, Manufacturing Records) with strict adherence to safety and compliance

Create legible written records within batch records/forms

Write, revise and update manufacturing documentation

Maintain a clean and organized working lab environment

Responsible for training on all procedures assigned

Ensure all training is up to date and properly documented

The ability to be cross trained to assist in other production areas /departments as needed

Follows OSHA safety regulations for bloodborne pathogens

Interacts cooperatively with coworkers, supervisors, or managers of other departments

Requirements:

ENTRY LEVEL - AS / BS recent grads with laboratory experience OR AS degree with some GMP experience ideal.

AS / BS degree in science field

GMP experience a plus

Ability to read and interpret documents such as safety rules, operating and maintenance instructions and procedure manuals

Ability to write routine reports and correspondence

Ability to speak effectively before a group of employees

Ability to apply common sense understanding to carry out instruction furnished in written, oral and diagram form

Ability to deal with problems involving several concrete variables in standardized situation

Preferred CGMP Manufacturing Experience and / or Training

Basic knowledge of MS Office and software systems used in product support

Joule, a System One division is a leader in specialized workforce solutions and integrated services. With more than 6,000 employees and roughly 50 offices throughout the U.S. we provide scientific, clinical, engineering, energy, IT, legal and administrative staffing services. For more than 40 years, we have delivered workforce solutions and integrated services to clients nationally.

System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.