Miscellaneous Clinical Roles

PSG Global Solutions

Sanford (NC)

On-site

USD 40,000 - 60,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

A prominent solutions provider is looking for a Manufacturing Technician to operate and maintain equipment in a regulated pharma/biotech environment. This role requires a strong commitment to Good Manufacturing Practices (GMP) and is ideal for candidates with previous experience in bioprocessing. Responsibilities include cleaning and sterilization of equipment, operating machinery, and training new employees, along with performing basic lab work. This position offers opportunities for training and career development.

Qualifications

2+ years of direct regulated manufacturing pharma/biotech experience.
Experience in a cGMP environment is a must.
Ability to follow detailed written and verbal instructions.

Responsibilities

Operate and maintain production equipment in assigned areas.
Clean and sterilize process equipment as needed.
Train new employees on production processes.

Skills

GMP experience

Knowledge of Clean and Steam in Place Systems

Mechanical ability

Attention to detail

Education

BA/BS in Tech/Bus/Industry/Science

AAS in Science

High School or equivalent

Tools

Autoclave

Industrial washers

Job description

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.

As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.

Job Description

The person filling this position operates all equipment in two assigned Manufacturing areas.
He or she will also clean equipment and facilities, and provide documentation of all duties in accordance with Good Manufacturing Practices.
Incumbent will perform all duties in a manner consistent with site and corporate cGMP, safety, environmental and human resources policies and procedures.
The incumbent will be required to attend quality-training programs and orientations on an annual or as needed basis.
This individual will be required to become familiar with domestic and international regulatory requirements associated with manufacturing and biological processes.
Annual performance goals and objectives will be evaluated against specific quality performance requirements as defined by the Manufacturing Supervisor.
Mandatory commitment to report to management any potential or actual deviations from regulatory requirements.
Ongoing input regarding quality process improvements.
Master documentation procedures by following detailed written and verbal instructions in order to complete assigned tasks (follow area SOP’s).
Demonstrate knowledge of procedures by performing tasks and duties and maintaining detailed records in a manner compliant with cGMPs.
Perform routine job duties, which may include vacuuming, mopping ceilings, walls and floors, emptying trashcans, etc.
Prepare production glassware and other equipment by operating industrial washers, autoclaves and depyrogenation ovens.
Clean and sterilize process equipment (tanks, fermentors) as needed.
Demonstrate and instruct proper gowning and aseptic processing procedures.
Work with individuals as a team.
Work various shifts and some weekends.
Operate and troubleshoot production equipment in assigned area and report unusual conditions or concerns about the process or equipment to area Supervisor.
Train new employees on production processes.
Perform lab work, such as: performing sample dilutions, pH, and conductivity readings.
Moderate repetitive standing, ladder climbing, repetitive bending, pushing, and lifting (up to 40 lbs) required on a daily basis.
Basic understanding of the metric system.
Be able to rationalize by suggesting solutions to unusual conditions and/or process concerns.
Must possess mechanical ability to assemble and operate equipment.
Must pay attention to detail by following procedures and noting unusual conditions.
Must have written and oral communication to read procedures, write accurate observations and follow directions

Qualifications

The following combinations of education and work experience are considered acceptable:

BA/BS Tech/Bus/Industry/Science with minimum 2 years direct regulated manufacturing pharma/biotech experience
AAS Science related with minimum 4 years direct regulated manufacturing pharma/biotech experience
HS or equivalent with minimum 8 years direct regulated manufacturing pharma/biotech experience
Or progression from Bio-processing Technician Level I that includes additional internal development curriculum
A minimum of four years pharmaceutical experience in biological manufacturing is preferred.

Additional Skills: