187725 - Senior Operator, Manufacturing
Industry
MAN
Region
NJ-New Jersey
City
Princeton
State
NJ
Rate
Up to $35.00 DOE
Duration
12 Months
Description
Chipton-Ross is seeking a Senior Operator, Manufacturing for an opening in Princeton, NJ.

RESPONSIBILITIES:
· Execution of manufacturing batch records, work instructions and/or SOPs, with minimal instruction on a day-to-day basis and a focus on proactive ‘right the first time’ executions. Assist with batch record reconciliation and timely documentation.

· Performance of all manufacturing activities in clean room (ISO 7) environment with specialized sterile gowning.

· Execution of cell manufacturing and cell processing activities in closed systems and maintaining aseptic technique during processing to ensure highest integrity, viability and sterility of cellular product until release.

· Work as a part of the team to execute all necessary GMP runs for cell manufacturing in an accurate and timely manner

· Perform accurate and error-free calculations of cell concentrations, cell and media dilutions and cell viability throughout the entire cell manufacturing process workflow.

· Able to execute all Department functions, such as maintaining suite, supplies, equipment, logbooks and data in accordance with site SOPs and policies.

· Acts as On-The-Job-Trainer for a variety of job functions

· Documentation of all activities to meet cGMP requirements. Execute document reviews and revisions. Daily record review, tasks, and databases. Actively provide feedback.

· Critical evaluation of processes, including foresight and thinking ahead.

· Complete preventative maintenance and work notifications tasks on time. Perform equipment testing and routine trouble-shooting.

· Ensure tasks are executed with a method of prioritization - interpret production schedules and complete tasks accordingly.

· Perform timely consumption of materials and completion of quality documentation in appropriate systems

· Identify deviations, aid in investigations/root cause analysis, and provide input on major/critical deviations. · Work to complete documentation of deviations and events in appropriate systems

· Execute validation protocols with minimal supervision or direction

· Participate in cross-functional teams to complete projects

REQUIRED EXPERIENCE:
· 3-5 years of relevant cGMP experience in a manufacturing pharmaceutical/biotech environment or related areas

· Experience in aseptic cell culture processing in IOS 5 biosafety cabinets while using universal precautions for handling of human-derived materials preferred

· Experience in cell therapy manufacturing required

· Experience in cell therapy automation technologies, closed system culture vessels, cell washers, cell separation technologies for autologous/allogenic product manipulation preferred

· Experience in handling, propagation, isolation, activation and cryopreservation of human primary cells including T cells preferred

· Strict adherence to SOPs, GMP regulations, FDA guidance and ability to accurately complete associated documentation required

Knowledge

· Understanding ‘why’ and not just the ‘how’ of processes and practices

· Knowledge of cGMP practices required

· Knowledge of deviation investigations preferred

· Knowledge of cell culture and aseptic techniques strongly preferred

Skills

· Mechnical Skills/ Analytical Skills/Method Automation

· MS Office

· Strong math skills

· Strong prioritization skills

· Detail oriented

· Results driven

Abilities

· Able to read, write, and communicate in English

· Able to understand and carry out instructions

· Reliable

· Strong communication (written and verbal)

· Effectively multi-task

· Able to work in an environment of change

· Able to work independently and as part of a team

· Able to recognize problems developing, not just occurring

EDUCATION:
Accredited High School Diploma/GED, Bachelor’s degree in Biological Sciences, Medical Technology, Applied Health Sciences or closely related field is preferred.

WORK HOURS:
1st Shift
Full-Time

Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.

Contact
Tyler Harrell
tharrell@chiptonross.com
CHIPTON-ROSS, INC.
420 Culver Boulevard
Playa Del Rey, CA 90293

Phone: (310) 414-7800 x307 or (800) 927-9318 x307

Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.

Employment will be contingent on candidate clearing pre-employment drug screen and background check.

Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.