JOB DESCRIPTION
Position: Production Operator
Department: Operations
Reports To: Production Manager
Location: Cranbury, NJ
Classification: Full time-On site
FLSA Status: Non-Exempt
SUMMARY/OBJECTIVE:
Under minimal supervision, this position is responsible for operation of pharmaceutical manufacturing equipment in a GMP environment for the purpose of making clinical supplies and performing development experiments. Incumbent is also responsible for leading manufacturing activities in assigned production rooms.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
QUALIFICATIONS AND EXPERIENCE:
Requires a bachelor's degree in an Engineering or Scientific Field with one (1) year of experience in Pharmaceutical or Life Science area or a High School Diploma and four (4) years of experience in pharmaceutical manufacturing with an emphasis on working on the implementation of new equipment and processes.
COMPETENCIES/SKILLS:
Read and interpret documents such as standard operating procedures, manuals, batch records, work instructions and specifications.
Legible Handwriting
Communicate clearly in writing and orally including in the creation of standard operating procedures and work instructions.
Apply concepts of basic arithmetic such as addition, subtraction, fractions, percentages, ratios, and proportions to practical solutions.
Graph data using spreadsheets and perform simple statistical analyses (means, standard deviations, linear regression).
Identify simple and moderate problems related to job function.
Scientific Reasoning the ability to gather data based on observations and measurement, formulate hypotheses, propose experimental tests, and draw conclusions, systematically.
Deductive Reasoning: Demonstrated experience applying general and complex rules to specific problems to produce answers that make sense.
Inductive Reasoning: Demonstrated experience applying a logical process in which multiple premises, all believed true or found true most of the time, are combined to obtain a specific conclusion (includes finding a relationship among seemingly unrelated events).
Knowledge of cGMP. o Familiar with Pharmaceutical Manufacturing.
Successfully completes regulatory and job training requirements.
Enter data into computer using software applications for data entry and word processing. Work and be proficient with e-mail systems.
Ability to perform repetitive tasks while maintaining speed of work and attention to detail without loss to production.
Ability to work individually in a self-directed manner with less than daily oversight.
Ability to work with others in a team environment.
SUPERVISORY RESPONSIBILITIES: None
WORK ENVIRONMENT:
This job operates in a manufacturing/packing/warehouse setting.
PHYSICAL DEMANDS:
TRAVEL:
Travel will be required less than 10% of the time, domestic and international.
SALARY RANGE:
From $25 to $28 per hour
If you’re interested in this position, please email [email protected] with your resume and any relevant documentation, including proof of certifications if specified in the job description.
Be sure to include the position title in the subject line of your email.
We look forward to connecting with you!
The job demands described here are representative of those that must be met by an employee to successfully perform the functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This job description is not intended and should not be construed to be exhaustive list of all responsibilities, skills, efforts, or working conditions associated with the job. It is intended to be a reflection of those principal job elements essential for recruitment and selection, for making fair job evaluations and for establishing performance standards. The percentage of time spent performing the various job duties is not absolute. The incumbent shall perform all other functions and/or be cross trained as shall be determined by the sole discretion of management, who has the right to amend, modify, or terminate this job in part or in whole. This document is not a contract for employment.
EXPERIC is an Equal Opportunity Employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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