Environmental Monitoring Associate I

Proclinical; Pennsylvania; On-site; USD 30,000 - 41,000; Part time

Job summary

Proclinical is seeking an Environmental Monitoring Associate I for a contract position in Philadelphia, PA. You will support manufacturing and validation activities by performing environmental monitoring, sampling, testing, and ensuring compliance with sterility programs.

The role involves collecting environmental samples, reading plates, and maintaining accurate documentation while collaborating with a cross-functional team to meet project timelines and quality expectations.

Qualifications

• Strong oral and written communication.
• Adaptability and ability to prioritize tasks.
• Ability to manage responsibilities while collaborating in a team.
• Capability to work on multiple projects simultaneously.
• Familiarity with FDA and quality compliance regulations.
• Commitment to continuous training and data integrity.

Responsibilities

• Collect environmental monitoring samples (particulate, viable surface, air, water).
• Perform laboratory and equipment cleanings.
• Read plates and interpret microbiological results.
• Complete laboratory data forms and documentation in compliance with cGMPs, CFR, and SOPs.
• Interact effectively with team members, supervisors, and lab customers.
• Meet established timelines and goals for data delivery.

Skills

Communication skills

Adaptability

Prioritization

Team collaboration

Multitasking

Data integrity

Education

Bachelor's degree in Biology or Microbiology

Job description

Environmental Monitoring Associate I - Contract - Philadelphia, PA

Help protect product quality and patient safety by playing a vital role in environmental monitoring within a cutting-edge pharmaceutical environment.

Proclinical is seeking an Environmental Monitoring Associate I for a contract position in Philadelphia, PA.

Primary Responsibilities:

The successful candidate will support manufacturing and validation activities by performing environmental monitoring, sampling, testing, and ensuring compliance with sterility assurance programs. You will work collaboratively in a team environment to maintain high-quality standards and contribute to the success of operational goals.

Skills & Requirements:

• Strong oral and written communication skills.


• Adaptability, flexibility, and ability to prioritize tasks effectively.


• Ability to manage individual responsibilities while collaborating as part of a team.


• Capability to work on multiple projects simultaneously.


• Bachelor's degree in Biology, Microbiology, or a related Life Science field.


• Familiarity with FDA and worldwide quality compliance regulations.


• Commitment to continuous training, skill development, and maintaining data integrity.

The Environmental Monitoring Associate I's responsibilities will be:

• Collect environmental monitoring samples, including particulate, viable surface, air, and water samples.


• Perform laboratory and equipment cleanings.


• Read plates and interpret results of microbiological testing assays.


• Accurately complete laboratory data forms, logbooks, and other required documentation in compliance with cGMPs, CFR, and SOPs.


• Interact effectively with team members, supervisors, and lab customers.


• Meet established timelines and goals for delivering data.


• Follow all general and laboratory SOPs.


• Report observations of ongoing tests to management.


• Provide operational support for manufacturing activities.


• Contribute to departmental goals and overall operations.