QC Reviewer, Sample Management (18 Months contract)

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery development and manufacturing of new drug therapies to get them faster to people who need them. No matter your role we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development Customer Focus Quality and Excellence Respect and Integrity we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people like you to join our growing team! Whether youre a recent college graduate or seeking your next career opportunity its time to discover your future at Altasciences.

We are better together and together We Are Altasciences.

About the role
The Quality Control Reviewer Sample Management Department is responsible for the quality control review of documentation related to the Sample Management team. He/she also conducts audits within the team to ensure that quality standards are met. He/she participates in the drafting and/or revision of standard operating procedures for sample management and glass washing.

What youll be doing here

• Perform 100% quality control on documentation generated by the sample management team.

• Responsible for quality within the sample management team.

• Perform audits within the team: develop execute and write reports.

• Completes additional information forms as necessary to ensure documentation is accurate and complete.

• Complete documentation necessary to track deviations and non-conformance reports within the team.

• Respond to QA citations.

• Archive documentation.

• Write revise and/or review standard operating procedures for sample management and glass washing.

• Write revise and/or update training materials.

• Keep abreast of relevant regulatory developments in the industry.

• Perform all work in accordance with applicable SOPs GCPs and GLPs and adhere to all company guidelines and policies.

• Keep abreast of new SOPs procedures and techniques through training sessions meetings and internal communications.

What you need to succeed

• You have a high school diploma or higher in health sciences or equivalent with at least 3 years experience.

• You must have in-depth knowledge of FDA-GLP GCP and TPD regulations.

• Experience in the medical or pharmaceutical field is an asset.

• Excellent management organizational communication (written and oral) and interpersonal skills.

• Strong GLP/GCP focus.

• Detail-oriented.

• Strong leadership decision-making and problem-solving skills.

• Customer oriented.

• Must be bilingual (French and English).

• Software: Access Outlook MS-Office Watson.

What we offer

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences benefits package includes:

• Health/Dental/Vision Insurance Plans

• RRSP with Employer Match

• Paid Vacation and Holidays

• Paid Sick and Bereavement Leave

• Employee Assistance & Telehealth Programs

Altasciences incentive programs include:

• Training and development programs

• Employee orientation bonus program

• Annual performance reviews

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MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract develop and retain highly talented employees from diverse backgrounds allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age race color religion creed sex sexual orientation gender identity national origin disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!