Analyst I, Microbiology - Contract - Philadelphia, PA
Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful research that drives healthcare innovation!
Proclinical is seeking an Analyst focusing on microbiology to perform laboratory assays and procedures in compliance with regulatory guidelines, including Good Manufacturing Practices (cGMP) and Good Laboratory Practices (cGLP).
Primary Responsibilities:
In this role, you will contribute to the daily operations of the lab, ensuring accuracy, compliance, and efficiency in testing and documentation. This position requires a detail-oriented individual who can work independently on routine tasks while collaborating effectively with team members.
Skills & Requirements:
- Foundational laboratory experience and knowledge of biosafety and analytical assays.
- Familiarity with GDP and general understanding of cGMP and cGLP requirements.
- Ability to manage multiple tasks and meet deadlines with guidance.
- Strong skills in evaluating and recording technical data accurately and clearly.
- Effective communication skills, both verbal and written.
- Team-oriented mindset with positive interpersonal skills.
- Proficiency in Microsoft Office applications (Excel, Word, Outlook).
- Bachelor's degree in Biological Sciences or equivalent education.
- Ensure compliance with FDA and global quality regulations in all aspects of work.
- Adhere to established procedures and protocols, prioritize continuous training, and uphold high standards of data integrity.
The Analyst's responsibilities will be:
- Conduct biosafety and analytical assays following established protocols and regulatory guidelines.
- Accurately complete testing records and documentation in compliance with Good Documentation Practices (GDP).
- Perform laboratory techniques and data analysis for assays.
- Report observations and findings to supervisors or scientists.
- Prepare reagents and maintain laboratory supplies.
- Perform equipment cleaning and maintenance, including updating logs.
- Assist in training and onboarding new team members by sharing knowledge of processes and procedures.
- Coordinate daily work activities with supervisors to ensure timely completion of tasks.
- Maintain laboratory upkeep in accordance with cGMP, cGLP, and Standard Operating Procedures (SOPs).
- Support quality events and perform self and peer reviews of testing records after appropriate training.
- Conduct technical reviews of executed testing records for accuracy and completeness.
- Collaborate with other departments as needed to achieve organizational goals.
- Exhibit professional behavior and adhere to company policies and practices.
- Perform additional duties as assigned by supervisors or managers.
If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at m.raletz@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
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