Analyst I, Microbiology

Proclinical; La Tuilière; On-site; CHF 42,000 - 62,000; Full time

Job summary

Proclinical is seeking an Analyst I, Microbiology on a contract basis in Philadelphia, PA. The role focuses on performing laboratory assays and data documentation in line with cGMP and cGLP requirements.

You will contribute to routine lab operations, ensuring accuracy, compliance and timely completion of tasks with strong attention to data integrity. The position requires foundational lab experience, a biology degree, and proficiency in MS Office.

Qualifications

• Bachelor's degree in Biological Sciences or equivalent is required.
• Experience with biosafety concepts and analytical assays is preferred.
• Familiarity with GDP, cGMP and cGLP regulatory expectations.

Responsibilities

• Conduct biosafety and analytical assays following established protocols.
• Complete testing records in GDP-compliant format with attention to detail.
• Perform lab techniques and data analysis for assays.
• Report observations to supervisors or scientists.
• Prepare reagents and maintain laboratory supplies.
• Maintain equipment logs and perform routine cleaning.
• Assist in training new team members on processes.
• Coordinate daily tasks with supervisors to meet deadlines.
• Uphold cGMP, cGLP and SOPs in all activities.
• Support quality events and perform self/peer reviews of records.
• Conduct technical reviews for accuracy and completeness.
• Collaborate with other departments as needed.

Skills

Biosafety knowledge

cGMP/cGLP familiarity

Data recording & documentation

MS Office proficiency

Excellent communication

Team collaboration

Laboratory techniques

Bachelor's in Biological Sciences

Education

Bachelor's degree in Biological Sciences or equivalent

Tools

Microsoft Office

Job description

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.