Environmental Monitoring Associate - Quality Control

Tandym Group Internal; Bedford (TX); On-site; USD 45,000 - 65,000; Full time

Job summary

A leading pharma company is seeking an Environmental Monitoring Associate in Bedford, TX. The role involves performing environmental monitoring, documenting tasks within laboratory systems, and ensuring compliance with GMP standards. Candidates with relevant degrees and experience in laboratories are especially encouraged to apply.

Qualifications

• Bachelor’s Degree with no experience; or, Associate’s Degree with 2+ years of experience; or, High School Diploma/GED with 4+ years of experience.
• Must maintain aseptic qualifications.

Responsibilities

• Perform environmental monitoring tasks for aseptic environment and controlled areas.
• Document all tasks within LIMS or standard laboratory documentation.
• Ensure tasks are completed in a GMP compliant manner.

Skills

Basic mathematical skills

Computer savvy

Data Entry skills

Interpersonal skills

Communication skills

Attention to detail

Organizational skills

Education

Bachelor’s Degree

Associate’s Degree

High School Diploma / GED

Job description

A recognized pharma company in Massachusetts is actively seeking a new Environmental Monitoring Associate, Quality Control to join their growing team in Bedford.

About the Opportunity:

• Schedule: Wednesday to Saturday
• Hours: 7am to 5:30pm
• Setting: Onsite

***Note: During training period, the qualified professional selected for this role will be required to work a Monday to Friday schedule from 7:30am to 4pm.***

Responsibilities:

• Perform environmental monitoring (EM) tasks for the aseptic environment, other controlled areas, and plant utility systems following specified instructions and techniques from Standard Operating Procedures (SOP), Training Material, and other GMP documents
• Incubate and enumerate microbial growth on EM plates
• Ensure all tasks are completed in a GMP compliant and safe manner
• Document all tasks within LIMS or standard laboratory paper documentation utilizing GDP principles
• Enter information into logbooks as applicable for tasks per SOP
• Partner and communicate with operations, manufacturing, facilities, and other site departments as required for support of operations and GMP processes
• Actively participate in daily and weekly laboratory meetings
• Accurately complete task management tools and handover communications
• Perform general lab tasks, including cleaning and equipment preparation
• Maintain training for all required tasks
• Perform other duties, as needed

Qualifications:

• Bachelor’s Degree with no experience; or, Associate’s Degree with 2+ years of experience; or, High School Diploma / GED with 4+ years of experience
• Basic mathematical skills
• Computer savvy and Data Entry skills
• Great interpersonal skills
• Excellent communication skills (written and verbal)
• Strong attention to detail
• Highly organized
• Must maintain aseptic qualifications