Photocopy Operator jobs in Camden, NJ

PROCESS OPERATOR

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services.

SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements.

We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

• Title : Process Operator
• Location : Malvern , PA
• Industry : Pharmaceutical
• Hours : MON-THURS - 1 : 00PM - 11 : 30PM (potential OT on weekends)
• Salary : $23.00hr (Paid Weekly - Benefits Available)
• Employment Type : Contract to Hire

Environment : This client manufactures thousands of pharmaceutical, biologic, consumer health and beauty products utilizing superior and innovative drug delivery technologies to improve their value to patients and consumers.

Our customer believes in a Patient First culture putting patients at the center of their work to ensure the safety, reliable supply and optimal performance of our products.

Job Scope :

The Process Operator micronize mills client provided material including both active pharmaceutical ingredients and excipients as per Micron Technologies procedures and policies, client instructions and cGMP guidelines.

Essential Functions :

Micronization and milling of both hazardous and non-hazardous pharmaceutical actives and excipients.

Set up, operate equipment, and monitor production processes and report production on batch records in accordance with good documentation procedures (GDPs)

Review documentation (batch records, SOPs, Logbooks) for completeness, clarity, accuracy and submit edits to documents for revision as required.

Ability to work in a regulated environment with adherence to standard operating procedures

Capable of reading and following defined SOPs and policies and executes tasks accordingly.

Work in accordance with cGMP. Identify and communicate non-routine events, deviations and GMP deficiencies to supervisor in a timely manner.

Cleaning of the entire processing area and processing equipment.

Produce thorough, clear & consistence documentation in compliance with Quality Standards (Attributable, Legible, Contemporaneous, Original and Accurate)

Willingness to accept change, learn, and work with new processes.

Stops and asks questions or suggests improvements when something is unclear.

Participate in shift change meetings, site / team meetings, sending / receiving emails, offering suggestions for improvements, and participating in projects.

Strives for First Time Right

Remains current with CompliaceWire and other site training

Position Requirements :

Education or Equivalent :

High School Diploma or GED

Knowledge / Skills Requirements :

Physical strength, stamina and dexterity while wearing fully enclosed air suite

Employees be able to lift or move items up to 44 lbs. (20kg) individually, or with a two-person lift between 45 lbs and 76 lbs.

35kg). 77 lbs and over with a lift assistance device.

Ability to work safely with high potency active pharmaceutical ingredients (HPAPI) as well as novel compounds of unknown potency and toxicity

Work Environment

EOE / ADA

IND123

LI-SRG14

Last updated : 2024-04-23