Job description

ABOUT US:

Altus Quality is a top-tier consulting group headquartered in the dynamic commonwealth of Massachusetts, and just a few miles outside of the biotech hub of Cambridge. Altus provides Quality and Compliance advisory services to the Clinical and Life Science sector. Our Passionate Professionals provide GxP Auditing, Process Development/Technical Writing and QMS Support.

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Altus Quality is actively seeking experienced Regulatory Affairs professionals with experience in SOP development. This position is remotely based.

Regulatory Affairs professional should have experience with :

• SOPs - Process Development
• Submission Management

Position Expectations:

• Write SOPs and WIs from scratch
• Update documents to align with current standards
• Finalize documents within timeframe

Requirements

• Understanding of Clinical Regulatory Affairs processes
• Excellent communication skills, both written and oral

Interested in joining Altus Quality Consulting? Please submit your resume.

EEO Statement
Altus Quality is an equal opportunity employer to all individuals regardless of their race, color, religion, creed, sex, sexual orientation, gender identity, national origin, age, disability, veteran, marital, or domestic partner status, citizenship, genetic information or any other status or characteristic covered by federal, state or local law. Further, the company takes affirmative action to ensure that applicants are employed and employees are treated during employment without regard to any of these characteristics. Discrimination of any type will not be tolerated.

Job Types: Full-time, Part-time, Contract

Pay: From $100,000.00 per year

Benefits:

• Flexible schedule

Schedule:

• 8 hour shift
• Monday to Friday
• Self-determined schedule

Work Location: Remote

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