Environmental Monitor - Marietta, United States - GSK

GSK

Verified Company

Marietta, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Site Name:
USA - Pennsylvania - Marietta

Posted Date:
Apr

Are you looking for an opportunity to support a Quality Management team in the day to day operations in a manufacturing environment? If so, this is the role for you.

As Environmental Monitor, you will be responsible for the collection of environmental monitoring samples and identifying deviations and potential problems and communicating these situations with appropriate personnel.

This role will provide YOU the opportunity to lead key activities to progress YOUR career.

These responsibilities include some of the following:

Perform Environmental Monitoring duties related to viable air, viable surfaces, swabs, and nonviable air sample collection.
Coordination of daily sampling activities for environmental monitoring (including generation of sample collection paperwork, labels, sample submission, etc) to meet SOP requirements.
Responsible for maintaining and ordering sufficient supplies, maintain EM media inventories, ordering equipment to perform all monitoring, and maintaining the equipment in good working conditions in a calibrated status.
Handle special projects such as abnormal test results, validation studies as needed.
Assure that all required documentation including records and logs, is complete and accurate according to the current GMP rules.
Maintain required records and logs.
Revise and write SOP's specific to monitoring as required and assist/lead the training of new personnel.
Assist with and participate in development of training programs and conduct training sessions for new and less experienced staff as necessary.
When assigned to rotating shift work; work independently and without direct supervision to perform normal operating routines and emergency response procedures.
Communicate and report status of operations as well as variances from specifications to area manager. Take appropriate actions and escalate issues immediately.
Perform all job responsibilities in compliance with applicable EHS and GMP regulations, guidelines, policies, GSK standard operating & safety procedures, and industry practice and Industrial Excellence initiatives.

Why you?:

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

Bachelor's degree

HS diploma and 5 years of experience in quality control or production within the pharmaceutical or biotechnology industry

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

2 years of experience in quality control or production within the pharmaceutical or biotechnology industry preferred
Knowledge of standard aseptic technique.
Must meet the Office of Health & Safety (OHS) Medical Guidance for working in production environment.
Computer skills required in Excel and Word.
Ability to follow written procedures and document results in a neat and precise manner.
Position may require employees to work in a 24/7 rotational schedule. This schedule will include holidays, and weekends; overtime may be required.
Must be well organized, flexible, openminded and dynamic.
Must have demonstrated selfdirect work habits and strong communication skills.
Must be a committed team player prepared to work in and embrace a team based culture.
Ability to work within a multiskilled team.
Maintain attention to detail, while completing multiple or repetitive tasks.
Demonstrate a serious commitment to accuracy and quality while meeting goals or deadlines.
Maintain a high level of integrity while balancing multiple priorities and responsibilities.
Some experience in analytical systems including quality control/production, validation, documentation and compliance preferred.
Experience with SAP system
Strong interpersonal skills. Solid team player able to function within team based organization.
Able to interact with peers, subordinates and senior personnel in multidisciplinary environment including engineering, facility operations, validation, production and QA and QC.
Able to prioritize and decide appropriate course of actions.
Ability to understand client's needs (producers) and to interact with people from various domains (Regulatory, QA, other analytical groups inside the Company.)
Demonstrated familiarity with cGMP's, facility regulatory guidelines and standard operating procedures.

LI-GSK

MariettaVaccines

vaccinessupplychain

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive.

We prevent a