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ATTENTION JOB SEEKERS!

BE PART OF AN ORGANIZATION WORKING WITH COMPANIES WHO ARE FINDING CURES AND TRANSFORMING MEDICINE!

Full-time hourly position - competitive salaries, career advancement opportunities, a bonus plan, excellent benefits package including a matching 401K, health, dental, vision and tuition reimbursement.

Full-time and hourly positions - competitive salaries, career advancement opportunities, a bonus plan, excellent benefits package including a matching 401K, health, dental, vision and tuition reimbursement. 

Job Summary:

Responsibilities for this position involve validation equipment operation, protocol development, protocol execution and associated activities.This position will support a wide range of validation activities, including laboratory and manufacturing equipment of all types, laboratory and manufacturing technical support services, facilities/utilities, computerized systems and data integrity assessment/remediation.

This full-time position works with supervision to gain experience with more experienced staff.

This position is for day shift but may require some occasional off shift overnight and/or weekend coverage to accommodate schedules and/or project timelines.

Essential Duties and Responsibilities:

• Directly support validation projects at external client sites
• Operate validation test equipment: process meter, data logging systems
• Independently develop and execute validation protocols and procedures
• Perform CSV (computer software validation) and data integrity assessment/remediation
• Support deviation resolution and troubleshooting strategies with client
• Provide technical support to laboratory and/or manufacturing areas
• Support positive client interaction and communication
• All other duties as assigned

Education, Experience and Qualifications:

• BA/BS in technical or science field of study. Candidates with an HSD/GED, technical training, or an Associate’s degree combined with mechanical aptitude or relevant industry experience
• Strong working knowledge of IT concepts, strategies, and methodologies
• Proficient with Microsoft Office (Word Excel, Powerpoint)
• Strong written and verbal communication skills
• Strong mechanical skills
• Strong reporting, organizational and interpersonal skills
• Ability to multitask and to perform tasks with high quality and accuracy
• Validation experience or experience working in a GMP regulated environment is a plus, including working knowledge of ISO 9001, ISO 17025, GMP, GLP, GAMP 5 and 21 CFR Part 11
  

Additional Information:

• Drug testing
• Inoculations specific to customer sites
• Travel required
• Valid driver’s license