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Job Requirements of Associate Director, Quality Operations:
-
Employment Type:
Contractor
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Location:
Cambridge, MA (Onsite)
Do you meet the requirements for this job?
Associate Director, Quality Operations
Careers Integrated Resources Inc
Cambridge, MA (Onsite)
Contractor
Pay Rate: $68.00/hr to $101/hr on w2
Summary / purpose of the position
The Quality Operations Associate Director role is responsible for supporting commercial distribution activities, maintaining current Good Distribution Practices related to commercial product distribution for the *** Biopharmaceuticals, Inc. US affiliate office, including:
a) Management of outsourced third-party logistics service provider operations involved in managing commercial drug distribution.
b) Release of commercial products for distribution
c) Management of and response to temperature excursions, product replacement requests, serialization issues, and logistics complaints for commercial products
d) Deviations, CAPAs and change controls related to GDP operations.
e) Annual GDP training development
f) Ownership of local Vendor Management and external audit program
g) Maintaining KPIs and metrics related to GDP.
h) Other tasks as assigned related to GDP Quality Operations, including documentation management assistance, SOP writing and revision, audits and inspection support, and new product launches.
i) Adherence to all applicable *** SOP’s, policies, and regulatory requirements
This role, reporting to the Sr. Director Quality Operations, will work in collaboration with GDP and GxP functions at the USA affiliate office, including Trade/Supply Chain and Regulatory. The Associate Director, Quality Operations is responsible for the release of commercial product into the US market and potential outbound shipments for global markets. This role is responsible for establishing and maintaining relationships with manufacturing and distribution channels. This role is also responsible for ensuring compliance with policies and procedures relevant to appropriate distribution of commercial drug, as well as working with corporate to ensure external vendors involved in GDP storage and distribution are audited.
Responsibilities will include, but are not limited to the following:
Education / Certifications:
Bachelor’s degree or higher, preferably in science related area
Experience:
Languages:
Fluent in English
Key Technical Competencies Required - Knowledge of US GDP regulations and DSCSA requirements, cold chain shipping and shipper qualifications, and vendor qualification - Highly organized - Strong demonstrated communication skills - Agile in decision making, - Ability to collaborate across departments and levels. - Proficiency in Microsoft Office suite, including Word, Excel, and PowerPoint required. - Up to 10% travel required for this role.
Summary / purpose of the position
The Quality Operations Associate Director role is responsible for supporting commercial distribution activities, maintaining current Good Distribution Practices related to commercial product distribution for the *** Biopharmaceuticals, Inc. US affiliate office, including:
a) Management of outsourced third-party logistics service provider operations involved in managing commercial drug distribution.
b) Release of commercial products for distribution
c) Management of and response to temperature excursions, product replacement requests, serialization issues, and logistics complaints for commercial products
d) Deviations, CAPAs and change controls related to GDP operations.
e) Annual GDP training development
f) Ownership of local Vendor Management and external audit program
g) Maintaining KPIs and metrics related to GDP.
h) Other tasks as assigned related to GDP Quality Operations, including documentation management assistance, SOP writing and revision, audits and inspection support, and new product launches.
i) Adherence to all applicable *** SOP’s, policies, and regulatory requirements
This role, reporting to the Sr. Director Quality Operations, will work in collaboration with GDP and GxP functions at the USA affiliate office, including Trade/Supply Chain and Regulatory. The Associate Director, Quality Operations is responsible for the release of commercial product into the US market and potential outbound shipments for global markets. This role is responsible for establishing and maintaining relationships with manufacturing and distribution channels. This role is also responsible for ensuring compliance with policies and procedures relevant to appropriate distribution of commercial drug, as well as working with corporate to ensure external vendors involved in GDP storage and distribution are audited.
Responsibilities will include, but are not limited to the following:
- Day-to-day management of third-party logistics service provider operations involved in commercial drug distribution.
- Distribution release of commercial batches to trade and for shipment to other markets, including review of shipping records and temperature traces for all international and domestic shipments of commercial product, certificates of analysis for accuracy and compliance, shipment and receipt documentation, and disposition of commercial drug product
- Establishing and maintaining relationships with manufacturing and distribution channels
- Review, assessment and responses to temperature excursions, product replacement requests, serialization issues, and logistics complaints for commercial products
- Development and maintenance of Quality Technical Agreements
- Quality oversight of temperature-controlled shipper qualifications
- Ownership of local Vendor Management and external audit program
- Communication, initiation, and management of any GDP related Deviations, CAPAs and change controls
- Review and update Annual GDP training materials.
- Maintain and report on KPI metrics.
- Other tasks as assigned related to GDP Quality Operations, including documentation management assistance, SOP writing and revision, audits and inspection support, and new product launches.
- Completing and maintaining up-to-date training and training records on functions performed
- Adheres to all applicable *** SOP’s, policies, and regulatory requirements
- Knowledge, abilities & experience
Education / Certifications:
Bachelor’s degree or higher, preferably in science related area
Experience:
- Minimum 12+ years of experience in Quality responsible for oversight of Good Distribution Practices and third-party logistics in a pharmaceutical or similar setting
- SAP experience is preferred.
- Experience with electronic platforms for quality systems management and training
Languages:
Fluent in English
Key Technical Competencies Required - Knowledge of US GDP regulations and DSCSA requirements, cold chain shipping and shipper qualifications, and vendor qualification - Highly organized - Strong demonstrated communication skills - Agile in decision making, - Ability to collaborate across departments and levels. - Proficiency in Microsoft Office suite, including Word, Excel, and PowerPoint required. - Up to 10% travel required for this role.
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