{"id":4326,"date":"2023-07-28T11:56:23","date_gmt":"2023-07-28T03:56:23","guid":{"rendered":"https:\/\/credevo.com\/s\/?page_id=4326"},"modified":"2025-08-01T10:17:40","modified_gmt":"2025-08-01T02:17:40","slug":"quality-assurance-associate","status":"publish","type":"page","link":"https:\/\/credevo.com\/s\/quality-assurance-associate\/","title":{"rendered":"Quality Assurance Associate"},"content":{"rendered":"\n

Job Description<\/h3>\n\n\n\n
Job Title<\/strong><\/td>Quality Assurance Associate<\/td><\/tr>
Reports to<\/strong><\/td>CEO<\/td><\/tr>
Department<\/strong><\/td>Clinical Trials<\/td><\/tr>
Location<\/strong><\/td>Remote<\/td><\/tr>
Supervises <\/strong><\/td>None<\/td><\/tr>
Job Type<\/strong><\/td>On Contract<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n

Company Overview<\/h3>\n\n\n\n

Credevo<\/a> is a consulting company that supports organizations in their business development and assists healthcare companies with their product development, from clinical development to commercialization. Credevo provides strategic support in areas such as regulatory, clinical development, licensing (out-\/in-), and feasibility support, for products including pharmaceuticals, biologics, nutraceuticals, and medical devices.<\/p>\n\n\n\n

Job Summary:<\/h3>\n\n\n\n


The Quality Assurance Associate plays a vital role in ensuring adherence to Good Clinical
Practice (GCP), Standard Operating Procedures (SOPs), regulatory requirements, and
company policies in clinical trials. This position is responsible for supporting QA processes,
conducting audits, and assisting in risk management to uphold high-quality standards in clinical
research.<\/p>\n\n\n\n

Key Responsibilities:<\/strong><\/p>\n\n\n\n

Quality Process Maintenance & Improvement:<\/h3>\n\n\n\n

\u25cf Maintain and enhance quality processes to ensure compliance with GMP, GDP, and
GCP standards.
\u25cf Collaborate with cross-functional teams to manage change controls, CAPA, deviations,
complaints, and internal audit follow-ups.
\u25cf Investigate GxP non-compliances and customer product quality complaints.
\u25cf Utilize quality tools and techniques to perform root cause investigations and resolve
quality issues.<\/p>\n\n\n\n

Compliance & Documentation:<\/h3>\n\n\n\n

\u25cf Develop and implement corrective and preventive action (CAPA) plans to address
non-conformances.
\u25cf Update, maintain, and improve QMS process documents.
Perform data analysis, prepare quality trend reports, and communicate insights to
internal stakeholders.
\u25cf Oversee product specification creation and control.
\u25cf Conduct Product Quality Reviews (PQRs) as required.<\/p>\n\n\n\n

Regulatory & Quality Assurance:<\/strong><\/p>\n\n\n\n

\u25cf Ensure regulatory compliance in distribution supply chain operations for commercial drug
products.
\u25cf Support GMP\/GDP service providers in maintaining post-approval compliance.
\u25cf Implement Standard Operating Procedures (SOPs) and oversee their adherence.
\u25cf Provide QA support to pharmacovigilance and regulatory departments.<\/p>\n\n\n\n

Skills & Competencies:<\/strong><\/p>\n\n\n\n

Essential:<\/strong>
\u25cf Strong knowledge of GMP and GDP operational quality systems.
\u25cf Experience in pharmaceutical or life sciences organizations.
\u25cf Familiarity with quality system processes (e.g., Audits, Deviations, CAPA, Change
Control).
\u25cf Strong experience in writing, implementing, and maintaining SOPs & quality documents.
\u25cf Ability to analyze, research, and report independently across diverse topics.
\u25cf Excellent organizational and communication skills.
\u25cf Strong attention to detail and ability to work under pressure.
\u25cf Ability to work autonomously and prioritize tasks effectively.
\u25cf Flexible and adaptable to changing business needs.
Desirable:<\/strong>
\u25cf Experience managing communications projects (graphics, online, video, etc.) and
working with creative contractors.
\u25cf Native or fluent English proficiency
\u25cf Degree in a relevant scientific discipline (e.g., Pharmaceutical Sciences, Life Sciences,
Chemistry, or related fields).
\u25cf An inquisitive mindset with a proactive approach to problem-solving and continuous
improvement.<\/p>\n\n\n\n

\n
Apply Using Gmail \/ Google Account<\/a><\/div>\n<\/div>\n\n\n\n

IMPORTANT:<\/em><\/strong> You will need to login to your gmail \/ google account for authentication to apply.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"

Job Description Job Title Quality Assurance Associate Reports to CEO Department Clinical Trials Location Remote Supervises  None Job Type On Contract Company Overview Credevo is a consulting company that supports organizations in their business development and assists healthcare companies with their product development, from clinical development to commercialization. Credevo provides strategic support in areas such […]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-4326","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nQuality Assurance Associate<\/title>\n<meta name=\"description\" content=\"We are hiring for Quality Assurance Associate. 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