QC Data Reviewer

Join Our Team as a QC Data Reviewer in Andover!

We are seeking a detail-oriented professional to fill the role of QC Data Reviewer on a temporary basis in Andover, United States. This position is perfect for individuals who thrive in a dynamic environment and are committed to maintaining high quality standards. The ideal candidate will be instrumental in ensuring the accuracy and consistency of our data, which is crucial for our ongoing projects and overall operational success.

Job Description:

• Reviewing and validating data quality and integrity to ensure that all information is accurate and reliable.
• Ensuring compliance with established data standards and protocols to uphold the company's commitment to quality data management practices.
• Identifying, documenting, and addressing any discrepancies in data to prevent and correct data anomalies.

This role is an excellent opportunity for those looking to enhance their career in quality control and data management. The position offers exposure to various facets of data review processes and provides a platform to develop expertise in data quality assurance. By joining our team, you will play a key role in supporting our mission to deliver outstanding results through rigorous data accuracy. We invite you to apply if you meet the criteria and are enthusiastic about contributing to our team's success!

Key Responsibilities:

• Meticulously examining datasets for accuracy and coherence.
• Collaborating with team members to discuss findings and recommendations for data improvement.
• Utilizing specialized software tools to facilitate effective data review and management.
• Desired Education and Skills:
• Contract QC Reviewer II: B.S. or M.S. degree in molecular biology or cell biology with at least 2-5 years relevant experience.
• Working experience in a cGMP environment is preferred.
• Experience with Advanced Therapeutic Medicinal Products (ATMPs, gene therapies) is highly desired.
• Understanding of relative potency assays, infectious titer assays, and replication competent vector assays is highly desired.
• An understanding of cell culture, relative potency testing, infectious titer testing, replication competent vector assays, SDS-PAGE, PCR, qPCR, ddPCR, and DNA sequencing (Sanger and NGS) is highly desired.

If you are passionate about data quality and keen on making a significant impact in a thriving and supportive environment, we would love to hear from you. Apply today and help us uphold our commitment to excellence in data management!

Desired Skills and Experience

Desired Education and Skills:
· Contract QC Reviewer II: B.S. or M.S. degree in molecular biology or cell biology with at least 2-5 years relevant experience. 
· Working experience in a cGMP environment is preferred.
· Experience with Advanced Therapeutic Medicinal Products (ATMPs, gene therapies) is highly desired.
· Understanding of relative potency assays, infectious titer assays, and replication competent vector assays is highly desired.
· An understanding of cell culture, relative potency testing, infectious titer testing, replication competent vector assays, SDS-PAGE, PCR, qPCR, ddPCR, and DNA sequencing (Sanger and NGS) is highly desired.
· An understanding of relevant FDA, EU, and ICH regulatory guidelines and pharmacopeia as applicable to bioassays, nucleic acids data review and method qualification/validation is necessary.
· Attention to detail with exceptional and demonstrable record keeping / documentation skills.
· Project management skills including the ability to manage one's project resource requirements (material, manpower, time, etc.), and ability to elevate relevant issues to project lead and line-management.
· Strong interpersonal skills and a proven ability to communicate effectively through verbal and written formats.
· Self-starter with the ability to work in a fast-paced, cross-functional, highly collaborative environment.
· Extensive technical writing skills. Experience drafting GMP SOPs, protocols and reports.
Operate as a part of a team with experience supervising and or training individuals in a functional, safe working environment while maximizing efficiency.

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

To find out more about Real, please visit www.realstaffing.com