Quality Control Data Analyst (Toxicity)

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Always Connecting, Always Evolving.

TECHEAD is seeking qualified applicants for the following Contract position – Quality Control Data Analyst (Toxicity) / Richmond VA – (JOB-21143). If you are looking for a new opportunity and this position looks to be a fit, please apply to see the TECHEAD difference that has made us successful for 30+ years!

You can find more about our team and values by checking us out at TECHEAD.com or on Glassdoor

Job Description:

Flexible, Part-time hours
Remote

Techead has partnered with a manufacturing client in Richmond, VA to help them hire a part-time Quality Control Data Analyst for a contract position.  This role may average 20 hours per week with the potential to increase to 40 depending on the needs of the department.

Ideal candidates will be available during normal business hours (9 – 5) during training period, however there will be flexibility in creating your own scheduled once training is complete.

Responsibilities: 

• The Quality Control Data Reviewer will provide ad hoc technical data review with their Preclinical and Editorial Services (Regulatory Affairs) department.
• Review (laboratory) records and study data results or calculations, both paper-based and in electronic format (e.g., Excel), including audit trails, for completeness and accuracy
• Ensure the assay records and related information are compliant to test methods (e.g., OECD), procedures (e.g., GLP), specifications, cGMP, and applicable SOP requirements and scientifically sound
• Ensure the assay records and related information are compliant to test methods (e.g., OECD), procedures (e.g., GLP), specifications, cGMP, and applicable SOP requirements and scientifically sound
• Communicate with Scientist(s), Analysts, and Manager(s) to proactively address quality impacting issues
• Provide support as required to address data related issues internally or in collaboration with other departments as a member of a cross-functional team
• The Quality Control Data Reviewer will provide ad hoc technical data review with their Preclinical and Editorial Services (Regulatory Affairs) department.

Requirements: 

• Must have 3-5 years of experience with Regulatory Quality Control of toxicity data/results in Vitro and in Vivo data/results
• PhD in Toxicology, Chemistry, Biology or related field needed (Retiree OR student in process of obtaining PhD in current field will be considered) 

TECHEAD’s mission is to make our on-site associates successful by placing them in the right environment so they can grow and prosper. How we treat and respond to our clients and employees is a reflection of who we are and makes us stand out from the rest. Keeping our business focused on building and maintaining relationships with our employees and clients is the key to our success. We won’t strive for anything less.

TECHEAD provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

For more information on TECHEAD please visit www.techead.com.

No second parties will be accepted.

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