Environmental Monitoring (EM) Sampling Analyst - ENTRY LEVEL - Travel Required

Boston Analytical

Environmental Monitoring (EM) Sampling Analyst - ENTRY LEVEL - Travel Required

Job Label:Environmental Monitoring (EM) Sampling Analyst 0220

Boston Analytical is a premier cGMP compliant laboratory, FDA and DEA registered for pharmaceutical analytical testing. We provide the highest quality analytical testing services to Pharmaceutical, Biopharmaceutical, and Medical device companies worldwide. Since 1987, Boston Analytical has been and remains dedicated to customer satisfaction, and to the fast and accurate analysis of our clients' products.

Boston Analytical is a growing pharmaceutical contract lab providing quality Analytical and Microbiological testing services. We are known for our quality and believe our success is driven by our employees. We provide our employees with a state-of-the-art work environment, excellent benefits and opportunities for development.

The Environmental Monitoring Microbiologist conducts cleanroom monitoring activities to ensure the air, surfaces, and critical utilities utilized for pharmaceutical product manufacturing meet cGMP requirements. These samples are collected according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures.

Travel is required in this position.Opportunities available will require youto temporarily relocate (on the company expense) for up to 6 weeks or more at a time.

PRIMARY DUTIES AND RESPONSIBILITIES:

Collects Environmental Monitoring Samples at client manufacturing sites on a daily basis.

Sample collection types include: air viable, surface viable, water and compressed gas samples. Samples are then subsequently submitted to the lab for analysis.

Understands the importance of aseptic technique and the critical role it plays in EM sample collection.

Documents work in a clear and organized manner.

Follows all safety rules and regulations and conducts periodic safety audits.

Follows all cGMP rules and regulations.

Under close supervision will be trained to become proficient at assigned tasks in order to become subject matter experts.

Performs routine data generation and problem solving with a minimal rework.

Works under close supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.

Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.

Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.

REQUIREMENTS & QUALIFICATIONS:

Qualifications include a BA or BS degree in Microbiology or related science discipline with 0-2 years of related experience is required. Knowledge of cGMP and related compliance regulations and guidances is preferred.

MINIMUM SKILLS REQUIREMENTS

Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.

A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.

Must have excellent organizational, verbal communication and technical documentation skills.

Solid computer skills.

Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.

Must be a team player with integrity and concern for the quality of Company products, services and staff members.

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Related Keywords:micro, microbiology, quality, biology, testing, cGMP, GMP, entry level, entry-level, microbiologists, Pharma, pharmaceutical, NH, MA